<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2025</YEAR>
<VOL>11</VOL>
<NO>4</NO>
<MOSALSAL>0</MOSALSAL>
<PAGE_NO>384</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>Green Synthesis of Metallic Nanoparticles and Their Multifaceted Applications: A Review Study</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Nanotechnology, specially, metallic nanoparticles (NPs) has successively revolutionized many aspects of biomedical and industrial practices due to their distinct physiochemical and functional characteristics. Nonetheless, traditional methods of synthesis typically create toxic wastes and threaten the environmental safety. Green synthesis has since been developed as a sustainable solution, utilizing biological entities, including plants, bacteria, and fungi, in an environmentally-friendly way to produce NPs.&#160;
Objectives: This work critically examine green synthesis methodologies to determine the biological processes, and evaluate their effects on the quality of NPs, their bioactivity, and use in medical and industrial practice.
Methods: Google Scholar and PubMed were used for the literature review till April 30, 2025. The used keywords were &#8220;metallic nanoparticles,&#8221; &#8220;metal ions,&#8221; &#8220;green synthesis,&#8221; &#8220;bacteria,&#8221; &#8220;fungi,&#8221; and &#8220;plant.&#8221; The development of the manuscript was based on full-length research and review articles, which describe the rationale, technologies, methods and basic principles of &#8220;green chemistry.&#8221;
Results: The analysis of green methods of synthesizing NPs showed that it is possible to produce metal NPs (e.g. Ag, Au, Cu, Fe, Pd, Se) of controlled size and shape consistently. The biogenic sources were found to be reliably able to generate sufficiently pure and monodisperse particles and protocols. These NPs have potential antimicrobial, antioxidant, and anticancer efficacies. Also, the improved techniques of biodistribution evaluation suggest that they could be used in the medical field.
Conclusion: The review confirmed various strategies researchers have performed to manufacture metallic NPs using green synthesis method.&#160;</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>277</FPAGE>
			<TPAGE>298</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/18
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/4/27
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/29
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/9/8
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Ankush</Name>
				<MidName></MidName>
				<Family>Banalia</Family>
				<NameE>Ankush</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Banalia</FamilyE>
				<Organizations>
				<Organization>Department of Pharmaceutics, School of Pharmacy, Graphic Era Hill University, Dehradun, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>ankushbanalia8@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Dinesh</Name>
				<MidName></MidName>
				<Family>Puri</Family>
				<NameE>Dinesh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Puri</FamilyE>
				<Organizations>
				<Organization>Department of Pharmaceutics, School of Pharmacy, Graphic Era Hill University, Dehradun, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>puridinesh105@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Bacteria</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Fungi</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Green synthesis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Metallic Nanoparticles (NPs)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Metal ions</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Plant</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>From Beneficial to Pathogenic: Transformation of Our Gut Microbiota by Antibiotics</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: The gut microbiome highlights the significance of understanding the relationship between antibiotic use and microbial alterations. This knowledge is crucial for the current health status and future medical practices.&#160;
Objectives: This review examines the effects of antibiotics on gut microbiota, emphasizing the significant changes in microbial composition resulting from their use.
Methods: Relevant articles published until February 2025 were retreived from Medical databases, including PubMed/MEDLINE, ScienceDirect, Scopus, Web of Science, and Google Scholar, using keywords, such as &#8220;antibiotics,&#8221; &#8220;gut microbiota,&#8221; &#8220;dysbiosis,&#8221; &#8220;antibiotic resistance,&#8221; and &#8220;microbial diversity.&#8221;
Results: Antibiotics profoundly disrupt the microbiota balance, potentially leading to chronic diseases and metabolic changes. Dysbiosis, or microbial imbalance, can arise from factors like diet and antibiotic exposure, reducing microbial diversity and promoting pathogenic species over beneficial ones. Clinically, dysbiosis is linked to increased risks of autoimmune disorders, obesity, and inflammatory bowel diseases. Specific antibiotics, including amoxicillin and levofloxacin, exhibit varying effects on gut microbiota. Dietary interventions are suggested to restore beneficial bacteria and enhance gut health. Further research should explore the long-term consequences of antibiotic use on gut health and emphasize developing effective recovery strategies.
Conclusion: The main conclusion of this review is that antibiotics dramatically reduce gut microbial diversity and balance and accelerate dysbiosis, which is associated with long-term health risks that requires nutritional and therapeutic strategies to restore microbial balance.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>299</FPAGE>
			<TPAGE>310</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/16
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/4/25
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/3
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/8/12
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Ameneh</Name>
				<MidName></MidName>
				<Family>Omidi</Family>
				<NameE>Ameneh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Omidi</FamilyE>
				<Organizations>
				<Organization>Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>a.omidi@modares.ac.ir; amenehomidi86@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maedeh Hasanzadeh</Name>
				<MidName></MidName>
				<Family>Bafghi</Family>
				<NameE>Maedeh Hasanzadeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bafghi</FamilyE>
				<Organizations>
				<Organization>Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>DABIR_YALDA@YAHOO.COM</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Kobra</Name>
				<MidName></MidName>
				<Family>Shirani</Family>
				<NameE>Kobra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shirani</FamilyE>
				<Organizations>
				<Organization>Department of Toxicology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>k.shirani@modares.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Antibiotics</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Gut microbiota</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Dysbiosis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Microbial diversity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antibiotic resistance</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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[DOI:10.1016/j.jhazmat.2024.133714] [PMID]##Ziegler M, Han JH, Landsburg D, Pegues D, Reesey E, Gilmar C, et al.“ Impact of levofloxacin for the prophylaxis of bloodstream infection on the gut microbiome in patients with hematologic malignancy. Open Forum Infect Dis. 2019; 6(7):ofz252. [DOI:10.1093/ofid/ofz252] [PMID]##González-Chávez SA, Salas-Leiva JS, Salas-Leiva DE, López-Loeza SM, Sausameda-García J, Orrantia-Borunda E, et al. Levofloxacin induces differential effects in the transcriptome between the gut, peripheral and axial joints in the Spondyloarthritis DBA/1 mice: Improvement of intestinal dysbiosis and the overall inflammatory process. PLoS One. 2023; 18(2):e0281265. [DOI:10.1371/journal.pone.0281265] [PMID] ##Xin-Li L, Da-Chang W, Cui-Li Z, Yi X. Effects of levofloxacin hydrochloride on the intestinal microbiota of BALB/c mice by PCR-DGGE. Afr J Microbiol Res. 2012; 6(14):3455-60. [Link]##Zhan M, Yang X, Zhao C, Han Y, Xie P, Mo Z, et al. 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Gibel carp Carassius auratus gut microbiota after oral administration of trimethoprim/ sulfamethoxazole. Dis Aquat Organ. 2012; 99(3):207-13. [DOI:10.3354/dao02477] [PMID]##Dukaew N, Thongkumkoon P, Sirikaew N, Dissook S, Sakuludomkan W, Tongjai S, et al. Gut microbiota-mediated pharmacokinetic drug-drug interactions between mycophenolic acid and trimethoprim-sulfamethoxazole in humans. Pharmaceutics. 2023; 15(6):1734. [DOI:10.3390/pharmaceutics15061734] [PMID] ##Tahan S, Melli LC, Mello CS, Rodrigues MS, Bezerra Filho H, de Morais MB. Effectiveness of trimethoprim-sulfamethoxazole and metronidazole in the treatment of small intestinal bacterial overgrowth in children living in a slum. J Pediatr Gastroenterol Nutr. 2013;5 7(3):316-8. [DOI:10.1097/MPG.0b013e3182952e93] [PMID]##Kofteridis DP, Maraki S, Mixaki I, Mantadakis E, Samonis G. Impact of prolonged treatment with trimethoprim-sulfamethoxazole on the human gut flora. Scand J Infect Dis. 2004; 36(10):771-2. [DOI:10.1080/00365540410020956] [PMID]##Pilla R, Gaschen FP, Barr JW, Olson E, Honneffer J, Guard BC, et al. Effects of metronidazole on the fecal microbiome and metabolome in healthy dogs. J Vet Intern Med. 2020; 34(5):1853-66. [DOI:10.1111/jvim.15871] [PMID] ##Stübing H, Reisinger A, Suchodolski J, Werner M, Unterer S, Hartmann K, et al. [The effect of metronidazole compared to a synbiotic on selected intestinal bacteria and on clinical improvement in dogs with acute diarrhea (German)]. Tierarztl Prax Ausg K Kleintiere Heimtiere. 2023; 51(01):5. [Link]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Facile Biosynthesis of Gold Nanostructures Using Aqueous Extracts of Scutellaria multicaulis and Heracleum persicum Stems and H. persicum Fruits, and their Cytotoxicity Against Breast Cancer Cells</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: The introduction of highly specific drug nanoparticles (NPs) into cancer cells has demonstrated a broad therapeutic potential with diminished toxicity. Hence, the synthesis of nanoparticles has garnered significant interest among researchers
Objectives: This study presents an eco-friendly method for synthesizing gold NPs (AuNPs) using Scutellaria multicaulis and Heracleum persicum stem extracts, Sanguisorba officinalis root, and H. persicum fruit extracts, and evaluates their anticancer effects.
Methods: The characterization of AuNPs was studied using UV&#8211;visible, field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX) spectroscopy, X-ray diffraction (XRD), dynamic light-scattering (DLS), Zeta potential (ZP), and Fourier-transform infrared spectroscopy (FTIR). Total phenolic content (TPC) and total flavonoid content (TFC) of AuNPs were evaluated using colorimetric analysis. MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and apoptosis assays were used to assay their cytotoxic potential.&#160;
Results: The absorption peaks were between 535 and 545 nm. FE-SEM and EDX analyses revealed that the AuNPs were oval in shape with a crystal size of 10-30 nm. XRD data showed the crystal structures of AuNPs to be 7.41, 7.61, 7.61, and 7.84 nm for stems of S. multicaulis (Sm-S)-AuNPs, stems of H. persicum (Hp-S)-AuNPs, roots of S. officinalis (So-R)-AuNPs, and fruits of H. persicum (Hp-F)-AuNPs, respectively. FT-IR suggested that elements such as phenolics, aromatic compounds, and proteins played a role in the reduction and stabilization of AuNPs. The mean size of AuNPs was ascertained using a Zetasizer, with measurements of 60.46, 41.2, 51, and 50.27 nm for Sm-S-AuNPs, Hp-S-AuNPs, So-R-AuNPs, and Hp-F-AuNPs, respectively. ZP analysis showed that AuNPs are negatively charged, indicating good dispersion stability. AuNPs had a high content of phenolic and flavonoid compounds and exhibited strong inhibitory effects on MDA-MB231 cell proliferation. Sm-S-AuNPs demonstrated anticancer effects in vitro by inducing oxidative stress and apoptosis.
Conclusion: Overall, the results affirm the potential of the examined plant extract as a viable raw biomaterial for the synthesis of biologically active AuNPs. These could be instrumental in developing novel antitumor agents to combat breast cancer.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>311</FPAGE>
			<TPAGE>330</TPAGE>
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		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/162025/04/30
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/2/10
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/32025/09/30
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/7/8
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Zahra</Name>
				<MidName></MidName>
				<Family>Gharari</Family>
				<NameE>Zahra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Gharari</FamilyE>
				<Organizations>
				<Organization>Department of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>z.gharari@alzahra.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hanie</Name>
				<MidName></MidName>
				<Family>Sadeghinia</Family>
				<NameE>Hanie</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sadeghinia</FamilyE>
				<Organizations>
				<Organization>Department of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>h.sadeghinia@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Parichehr</Name>
				<MidName></MidName>
				<Family>Hanachi</Family>
				<NameE>Parichehr</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hanachi</FamilyE>
				<Organizations>
				<Organization>Department of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>p.hanachi@alzahra.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Anticancer</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antioxidant</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Apoptosis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Gold nanoparticles (AuNPs)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Green synthesis</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Deivayanai VC, Thamarai P, Karishma S, Saravanan A, Yaashikaa PR, Vickram AS, et al. Advances in nanoparticle-mediated cancer therapeutics: Current research and future perspectives. Cancer Pathog Ther. 2024; 3(4):293-308.[DOI:10.1016/j.cpt.2024.11.002] [PMID]##Gharari Z, Khoshnamvand M, Sadeghinia H, Hanachi P. Easy synthesis of gold nanoparticles using Allium ampeloprasum L. aqueous extract: Phytochemical characterization, in vitro antioxidant activities, and cytotoxic effects. Nat Prod Res. 2025; 18:1-5. [DOI:10.1080/14786419.2025.2493182] [PMID]##Kumar P, Chandra P, Verma N, Diksha, Sharma A, Mani M, et al. Gold Nanoparticles: An emerging novel technology for targeted delivery system for site-specific diseases. Curr Drug ther. 2025; 20:345-61. [Link]##Patil T, Gambhir R, Vibhute A, Tiwari AP. Gold nanoparticles: Synthesis methods, functionalization and biological applications. J Clust Sci. 2023; 34(2):705-25. [Link]##Madkour LH. Applications of gold nanoparticles in medicine and therapy. Pharm Pharmacol Int J. 2018; 6(3):157-74. [Link]##Mishra, S, Sundaram, B. Fate, transport, and toxicity of nanoparticles: An emerging pollutant on biotic factors. Process Saf Environ Prot. 2023; 174:595-607. [Link]##Dang Y, Guan J. Nanoparticle-based drug delivery systems for cancer therapy. Smart Mater Med. 2020; 1:10-19. [DOI:10.10.1016/j.smaim.2020.04.001] [PMID]##Adeyemi OS, Otuechere CA, Adewuyi A, Adeyanju AA, Awakan OJ, Otohinoyi DA. Gold nanoparticles in delivery applications. In: Mozafari M, editor. Nanoengineered Biomaterials for Advanced Drug Delivery. Amsterdam: Elsevier; 2020. [Link]##Hano C, Abbasi BH. Plant-Based Green Synthesis of Nanoparticles: Production, Characterization and Applications. Biomolecules. 2022; 12(1):31. [DOI:10.3390/biom12010031] [PMID]##Husen A, Rahman QI, Iqbal M, Yassin MO, Bachheti RK. Plant-mediated fabrication of gold nanoparticles and their applications. In: Husen A, Iqbal M, editors. Nanomaterials and Plant Potential. Cham: Springer; 2019. [Link]##Khan T, Ullah N, Khan MA, Mashwani ZU, Nadhman A. Plant-based gold nanoparticles; a comprehensive review of the decade-long research on synthesis, mechanistic aspects and diverse applications. Adv Colloid Interface Sci. 2019; 272:102017. [DOI:10.1016/j.cis.2019.102017] [PMID]##El-Sheekh MM, Hassan LHS, Morsi HH. Evaluation of antimicrobial activities of blue-green algae-mediated silver and gold nanoparticles. Rend Lincei Sci Fis Nat. 2021; 32(4):747-59. [DOI:10.1007/s12210-021-01016-x]##Godipurge SS, Yallappa S, Biradar NJ, Biradar JS, Dhananjaya BL, Hegde G, et al. A facile and green strategy for the synthesis of Au, Ag and Au-Ag alloy nanoparticles using aerial parts of R. hypocrateriformis extract and their biological evaluation. Enzyme Microb Technol. 2016; 95:174-84. [DOI:10.1016/j.enzmictec.2016.08.006] [PMID]##Huang X, Wu H, Liao X, Shi B. One-step, size-controlled synthesis of gold nanoparticles at room temperature using plant tannin. Green Chem. 2010; 12(3):395-9. [Link]##Cudalbeanu M, Peitinho D, Silva F, Marques R, Pinheiro T, Ferreira AC, et al. Sono-biosynthesis and characterization of AuNPs from Danube Delta Nymphaea alba root extracts and their biological properties. Nanomater. 2021; 11(6):1562. [DOI:10.3390/nano11061562] [PMID]##Botteon CEA, Silva LB, Ccana-Ccapatinta GV, Silva TS, Ambrosio SR, Veneziani RCS, et al. Biosynthesis and characterization of gold nanoparticles using Brazilian red propolis and evaluation of its antimicrobial and anticancer activities. Sci. Rep. 2021; 11(1):1974. [DOI:10.1038/s41598-021-81281-w] [PMID]##Huang Y, Zhang Y, Zhang Y, Liu W, Fang Y, Motlagh M. Novel biogenic preparation of gold nanoparticles decorated on sepiolite clay and evaluation of anticancer effect on gastric cancer cell and electrochemical sensing of nitrite. Environ. Res 2023; 238(Pt 2):117260. [DOI:10.1016/j.envres.2023.117260] [PMID]##Gharari Z, Hanachi P, Walker TR. Green synthesized Ag-nanoparticles using Scutellaria multicaulis stem extract and their selective cytotoxicity against breast cancer. Anal Biochem. 2022; 653:114786. [DOI:10.1016/j.ab.2022.114786] [PMID]##Gharari Z, Hanachi P, Sadeghinia H, Walker TR. Eco-Friendly Green Synthesis and Characterization of Silver Nanoparticles by Scutellaria multicaulis Leaf Extract and Its Biological Activities. Pharmaceuticals. 2023; 16(7):992. [DOI:10.3390/ph16070992] [PMID]##Hanachi P, Gharari Z, Sadeghinia H, Walker TR. Synthesis of bioactive silver nanoparticles with eco-friendly processes using heracleum persicum stem extract and evaluation of their antioxidant, antibacterial, anticancer and apoptotic potential. J Mol Struct. 2022; 1265:133325. [Link]##Charghadchi M, Gharari Z, Sadighian S, Yazdinezhad A, Sharafi A. Green Synthesized Silver Nanostructure Using Rhus coriaria Fruit Extract Inhibits the Growth of Malignant MCF-7 Cell Line. Braz Arch Biol Technol. 2021; 64:e21210069. [DOI:10.1590/1678-4324-2021210069]##Gharari Z, Hanachi P, Sadeghinia H, Walker TR. Cichorium intybus bio-callus synthesized silver nanoparticles: A promising antioxidant, antibacterial and anticancer compound. Int J Pharm. 2022; 625:122062. [DOI:10.1016/j.ijpharm.2022.122062] [PMID]##Keskin C, Atalar MN, Firat Baran M, Baran A. Environmentally friendly rapid synthesis of gold nanoparticles from Artemisia absinthium plant extract and application of antimicrobial activities. J Inst Sci Technol. 2021; 11(1):365-75. [DOI:10.21597/jist.779169]##Keskin C, Baran A, Baran MF, Hatipoğlu A, Adican MT, Atalar MN, et al. Green synthesis, characterization of gold nanomaterials using Gundelia tournefortii leaf extract, and determination of their nanomedicinal (antibacterial, antifungal, and cytotoxic) potential. J Nanomater. 2022; 2022(1):7211066. [Link]##Fouda A, Awad MA, Al-Faifi ZE, Gad ME, Al-Khalaf AA, Yahya R, et al. Aspergillus flavus-mediated green synthesis of silver nanoparticles and evaluation of their antibacterial, anti-candida, acaricides, and photocatalytic activities. Catalysts. 2022; 12(5):462. [Link]##TYAl-Abdullah Z, AL-SHAWI AA, Aboud MN, Al Abdul Aziz B, Al-Furaiji HQM, Luaibi IN. Synthesis and analytical characterization of gold nanoparticles using microwave-assisted extraction system and study their application in degradation. J Nanostruct. 2020; 10(4):682-90. [Link]##Kanchi S, Kumar G, Lo AY, Tseng CM, Chen SK, Lin CY, et al. Exploitation of de-oiled jatropha waste for gold nanoparticles synthesis: A green approach. Arab J Chem. 2018; 11(2):247-55. [Link]##Muddapur UM, Alshehri S, Ghoneim MM, Mahnashi MH, Alshahrani MA, Khan AA, et al. Plant-based synthesis of gold nanoparticles and theranostic applications: A review. Molecules. 2022; 27(4):1391. [DOI:10.3390/molecules27041391] [PMID]##Asariha M, Kiaie SH, Izadi S, Pirhayati FH, Fouladi M, Gholamhosseinpour M. Extended-release of doxorubicin through green surface modification of gold nanoparticles: In vitro and in ovo assessment. BMC Chem. 2022; 16(1):110. [DOI:10.1186/s13065-022-00895-x] [PMID]##Vinay S, Chandrasekhar N, Chandrappa C. Eco-friendly approach for the green synthesis of silver nanoparticles using flower extracts of Sphagneticola trilobata and study of antibacterial activity. Int J Pharm Biol Sci. 2017; 7:145-52.[Link]##Muniyappan N, Pandeeswaran M, Amalraj A. Green synthesis of gold nanoparticles using Curcuma pseudomontana isolated curcumin: Its characterization, antimicrobial, antioxidant and anti-inflammatory activities. Environ ToxicolChem. 2021; 3:117-24. [Link]##Arif H, Qayyum S, Akhtar W, Fatima I, Kayani WK, Rahman KU, et al. Synthesis and characterization of zinc oxide nanoparticles at different pH values from Clinopodium vulgare L. and their assessment as an antimicrobial agent and biomedical application. Micromachines. 2023; 14(7):1285. [DOI:10.3390/mi14071285] [PMID]##Kumar B, Smita K, Debut A, Cumbal L. Utilization of Persea americana (Avocado) oil for the synthesis of gold nanoparticles in sunlight and evaluation of antioxidant and photocatalytic activities. Environ Nanotechnol Monit Manag. 2018; 10:231-37. [Link]##Tungmunnithum D, Thongboonyou A, Pholboon A, Yangsabai A. Flavonoids and other phenolic compounds from medicinal plants for pharmaceutical and medical aspects: An overview. Medicines 2018; 5(3):93. [DOI:10.3390/medicines5030093] [PMID]##Marslin G, Siram K, Maqbool Q, Selvakesavan RK, Kruszka D, Kachlicki P, et al. Secondary metabolites in the green synthesis of metallic nanoparticles. Materials. 2018; 11(6):940. [DOI:10.3390/ma11060940] [PMID]##Ahmad T, Bustam MA, Irfan M, Moniruzzaman M, Asghar HMA, Bhattacharjee S. Mechanistic investigation of phytochemicals involved in green synthesis of gold nanoparticles using aqueous Elaeis guineensis leaves extract: Role of phenolic compounds and flavonoids. Biotechnol Appl Biochem. 2019; 66(4):698-708. [DOI:10.1002/bab.1787] [PMID]##Hasan MR, Sharma P, Pilloton R, Khanuja M, Narang J. Colorimetric biosensor for the naked-eye detection of ovarian cancer biomarker PDGF using citrate modified gold nanoparticles. Biosens Bioelectron. 2022; 11:100142. [Link]##Hamelian M, Hemmati S, Varmira K, Veisi H. Green synthesis, antibacterial, antioxidant and cytotoxic effect of gold nanoparticles using Pistacia Atlantica extract. J Taiwan Inst Chem Eng. 2018; 93:21-30. [DOI:10.1016/j.jtice.2018.07.018]##Kang Me, Weng Y, Liu Y, Wang H, Ye L, Gu Y, Bai X. A Review on the Toxicity Mechanisms and Potential Risks of Engineered Nanoparticles to Plants. Rev Environ Contam Toxicol. 2023; 261:5. [Link]##Liu N, Tang M. Toxic effects and involved molecular pathways of nanoparticles on cells and subcellular organelles. J Appl Toxicol. 2020; 40(1):16-36. [DOI:10.1002/jat.3817] [PMID]##Kumar R, Kumar A, Bhardwaj S, Sikarwar M, Sriwastaw S, Sharma G, Gupta M. Nanotoxicity unveiled: Evaluating exposure risks and assessing the impact of nanoparticles on human health. J Trace Elements Miner. 2025; 13:100252. [DOI:10.1016/j.jtemin.2025.100252]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Albumin Utilization Evaluation in a Teaching University Hospital in Iran</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Human albumin solution (HAS) is an expensive colloidal preparation that is commonly used in clinical practice. Given the high cost of albumin and its rising worldwide use, it is imperative to establish a practical protocol to improve the rational use of albumin products. This study aimed to identify albumin utilization patterns in a teaching hospital and to demonstrate the importance of revisiting strategies for albumin administration.
Objectives: This study aimed to identify albumin utilization patterns in a teaching hospital and to demonstrate the importance of revisiting strategies for albumin administration.
Methods: This retrospective study was conducted between March 20, 2023, and March 19, 2024, at Imam Khomeini Educational Hospital, an affiliated hospital of Mazandaran University of Medical Sciences, Sari City, Iran. All albumin forms completed during the study period were enrolled for appropriateness evaluation in accordance with the protocol developed by the Iranian Food and Drug Administration.
Results: In 82 patients (32.1%), serum albumin levels were greater than 2.5 g/dL at the time of albumin administration, of which 56% were above the recommended cut-off for the indication. Among 313 albumin prescriptions, in 7 cases (2.3%), albumin administration was not based on any official indication listed in the protocol. Albumin level less than 2.5 g/dL for 3 days (25.4%), ascites or generalized edema (24.4%), and hepatorenal syndrome (HRS) (13%) were the most common reasons for albumin administration. The daily albumin dose ranged from 1 vial of 20% to 5 vials, averaging 19 g/d. Only one patient (0.3%) had the duration of albumin treatment stated, and no patient had their albumin levels rechecked 72 hours after administration.
Conclusion: This study showed significant deviations from the albumin prescription protocol. Some aspects of albumin prescribing, including the minimum cut-off for starting albumin, the duration of use, and rechecking the albumin level, were not adequately considered by physicians. These findings highlight a more sophisticated focus on albumin prescribing in an attempt to minimize the irrational prescription of this expensive and valuable drug.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>331</FPAGE>
			<TPAGE>338</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/162025/04/302025/08/18
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/5/27
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/32025/09/302025/11/3
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/8/12
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Ebrahim</Name>
				<MidName></MidName>
				<Family>Salehifar</Family>
				<NameE>Ebrahim</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Salehifar</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pharmacy, Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Institute of Herbal Medicines and Metabolic Disorders, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Esalehifar@mazums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Zahra</Name>
				<MidName></MidName>
				<Family>Bagherzadegan</Family>
				<NameE>Zahra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bagherzadegan</FamilyE>
				<Organizations>
				<Organization>Department of Pharmaceutical Care, Emam Khomeini Hospital, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>ph.emam@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shahram</Name>
				<MidName></MidName>
				<Family>Ala</Family>
				<NameE>Shahram</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ala</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pharmacy, Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Institute of Herbal Medicines and Metabolic Disorders, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Sh204ala@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Sima</Name>
				<MidName></MidName>
				<Family>Ramezaninejad</Family>
				<NameE>Sima</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ramezaninejad</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pharmacy, School of Pharmacy, Babol University of Medical Sciences, Babol, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Sima.ramezaninejad@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Albumin</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Albumin guideline</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Drug utilization evaluation</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Caraceni P, Domenicali M, Tovoli A, Napoli L, Ricci CS, Tufoni M, et al. Clinical indications for the albumin use: Still a controversial issue. Eur J Intern Med. 2013; 24(8):721-8. [DOI:10.1016/j.ejim.2013.05.015] [PMID]##Mirici-Cappa F, Caraceni P, Domenicali M, Gelonesi E, Benazzi B, Zaccherini G, et al. How albumin administration for cirrhosis impacts on hospital albumin consumption and expenditure. World J Gastroenterol. 2011; 17(30):3479-86. [DOI:10.3748/wjg.v17.i30.3479] [PMID]##Bachhav SS, Kshirsagar NA. Systematic review of drug utilization studies &#38; the use of the drug classification system in the WHO-SEARO region. Indian J Med Res. 2015; 142(2):120-9. [DOI:10.4103/0971-5916.164223] [PMID]##WHO. WHO medicines strategy: Framework for action in essential drugs and medicines policy 2000-2003. Geneva: WHO; 2000. [Link]##Kazemi Y, Hadavand N, Hayatshahi A, Torkamandi H, Gholami K, Hadjibabaie M, et al. Albumin utilization in a teaching hospital in Tehran: Time to revise the prescribing strategies. J Pharm Care. 2015; 1(4):127-32. [Link]##Rothschild MA, Oratz M, Schreiber SS. Serum albumin. Hepatology. 1988; 8(2):385-401. [DOI:10.1002/hep.1840080234] [PMID] ##Liumbruno GM, Bennardello F, Lattanzio A, Piccoli P, Rossettias G; Italian Society of Transfusion Medicine and Immunohaematology (SIMTI). Recommendations for the use of albumin and immunoglobulins. Blood Transfus. 2009; 7(3):216-34. [DOI:10.2450/2009.0094-09] [PMID]##Shahbazi Khamas S, Mirbagheri I, Dehnadi Moghadam A, Jafari A, Ashouri A. Evaluation of albumin utilization in a major teaching hospital in Iran before and after guideline implementation. J Pharm Care. 2021; 9(2):67-73. [Link]##Javan-Noughabi J, Parnian E, Hajiesmaeili M, Salehiniya H, Setoodehzadeh F. The impact of a guideline to prevent inappropriate albumin administration in a hospital in Iran. Br J Heal Care Manag. 2020; 26(10):1-7. [Link]##Zolfagharian F, Ghazanfari S, Elyasi S, Iraji P, Saberi MR, Vahdati-Mashhadian N, et al. Drug utilization evaluation of albumin in a teaching hospital of Mashhad, Iran: An interventional pre-post design study. Int J Clin Pharm. 2017; 39(4):704-11. [DOI:10.1007/s11096-017-0458-y] [PMID]##Dastan F, Jamaati H, Emami H, Haghgoo R, Eskandari R, Hashemifard SS, et al. Reducing inappropriate utilization of albumin: the value of pharmacist-led intervention model. Iran J Pharm Res. 2018; 17(3):1125-9. [PMID]##Farasatinasab M, Amouzegar A, Safari S, Ghanbari B, Darkahian M, Emami S, et al. Albumin utilization evaluation in a major teaching hospital in Iran: Recommendations for guideline development. J Res Pharm Pract. 2018; 7(3):157-63. [DOI:10.4103/jrpp.JRPP_18_4] [PMID]##Lyu PF, Hockenberry JM, Gaydos LM, Howard DH, Buchman TG, Murphy DJ. Impact of a sequential intervention on albumin utilization in critical care. Crit Care Med. 2016; 44(7):1307-13. [DOI:10.1097/CCM.0000000000001638] [PMID]##Ishida TS, Sakai MC, de Melo DO. The Appropriate use of human albumin in a Brazilian university hospital: Therapeutic indication and dosage regimen. Braz J Pharm Sci. 2018; 54 (4). [DOI:10.1590/s2175-97902018000418008]##Buckley MS, Knutson KD, Agarwal SK, Lansburg JM, Wicks LM, Saggar RC, et al. Clinical pharmacist-led impact on inappropriate albumin use and costs in the critically Ill. Ann Pharmacother. 2020; 54(2):105-12. [DOI:10.1177/1060028019877471] [PMID]##Chiatti C, Bustacchini S, Furneri G, Mantovani L, Cristiani M, Misuraca C, et al. The economic burden of inappropriate drug prescribing, lack of adherence and compliance, adverse drug events in older people: A systematic review. Drug Saf. 2012; 35(Suppl 1):73-87. [DOI:10.1007/BF03319105] [PMID]##Noormandi A, Karimzadeh I, Mirjalili M, Khalili H. Clinical and economic impacts of clinical pharmacists' interventions in Iran: A systematic review. Daru. 2019; 27(1):361-78. [DOI:10.1007/s40199-019-00245-8] [PMID]##Yu YT, Liu J, Hu B, Wang RL, Yang XH, Shang XL, et al. Expert consensus on the use of human serum albumin in critically ill patients. Chin Med J (Engl). 2021; 134(14):1639-54. [DOI:10.1097/CM9.0000000000001661] [PMID]##Gatta A, Verardo A, Bolognesi M. Hypoalbuminemia. Intern Emerg Med. 2012; 7(Suppl 3):193-9. [DOI:10.1007/s11739-012-0802-0] [PMID]##Margarson MP, Soni N. Serum albumin: Touchstone or totem? Anaesthesia. 1998; 53(8):789-803. [DOI:10.1046/j.1365-2044.1998.00438.x] [PMID]##Aramwit P, Kasettratat N. Evaluation of serum albumin utilization in inpatient at a private hospital in Bangkok. Yakugaku Zasshi. 2004; 124(9):631-4. [DOI:10.1248/yakushi.124.631] [PMID]##Talasaz AH, Jahangard-Rafsanjani Z, Ziaie S, Fahimi F. Evaluation of the pattern of human albumin utilization at a university affiliated hospital. Arch Iran Med. 2012; 15(2):85-7. [PMID]##Delaney AP, Dan A, McCaffrey J, Finfer S. The role of albumin as a resuscitation fluid for patients with sepsis: A systematic review and meta-analysis. Crit Care Med. 2011; 39(2):386-91. [DOI:10.1097/CCM.0b013e3181ffe217] [PMID]##Abedi F, Zarei B, Elyasi S. Albumin: A comprehensive review and practical guideline for clinical use. Eur J Clin Pharmacol. 2024; 80(8):1151-69. [DOI:10.1007/s00228-024-03664-y] [PMID]##Jahangard Rafsanjani Z, Javadi MR, Torkamandi H, Alahyari S, Hajhossein Talasaz A, Gholami K, et al. The evaluation of albumin utilization in a teaching university hospital in Iran. Iran J Pharm Res. 2011; 10(2):385-90. [PMID]##Shafiee E, Rezaee H, Entezari-Maleki T, Hamishehkar H. The evaluation of albumin use in an Iranian University hospital. Pharma Sci. 2016; 22(3):186–9. [DOI:10.15171/PS.2016.29]##Farsad BF, Hadavand N, Masumi S, Salehi H. Albumin utilization review to evaluate the efficacy and cost, perform as a qualitative study in special wards in Shaheed Rajaei cardiovascular, medical &#38;research center. Biosci Biotechnol Res Asia. 2016; 13(3):1469-77. [Link]##Ibrahim DM, Shawki MA, Solayman MH, Sabri NA. The impact of clinical pharmacist implemented protocol on albumin utilization and cost in an Intensive Care Unit in Egypt. Front Pharmacol. 2022; 13:825048. [DOI:10.3389/fphar.2022.825048] [PMID]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Acute Respiratory Distress Syndrome in Drug and Chemical Poisoning: A Cross-sectional Study</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Poisonings are a major medical emergency, contributing to 15-20% of hospital visits. Acute respiratory distress syndrome (ARDS), defined by acute hypoxemia and non-cardiogenic pulmonary edema, presents significant challenges in diagnosis and management.&#160;
Objectives: This study investigates the incidence of ARDS in patients with drug and chemical poisoning hospitalized at Shah Vali Hospital in Yazd City, and Shahid Beheshti Hospital in Taft City, Iran from 2014 to 2023.
Methods: We conducted a descriptive cross-sectional study involving patients with drug and chemical poisoning presenting to the emergency departments of the two hospitals. After obtaining ethical approval, we reviewed medical records of eligible patients. Data were analyzed using SPSS software, version 25, presenting qualitative data as frequencies and percentages, and quantitative data as Mean&#177;SD. The chi-square test assessed statistical significance, with P&#60;0.05 deemed significant.
Results: Our analysis included 61 patients, comprising 77% men and 23% women, with a mean age of 46.1 years and an average hospitalization duration of 9.7 days. The primary cause of poisoning was suicide, accounting for 49.2% of cases, predominantly through oral ingestion (96.7%). Methadone was identified as the most common poisoning agent. Notably, 68.9% of patients had a history of addiction, and 27.9% required dialysis, while sepsis was present in 31.1% of cases. Among patients with ARDS, 21.3% had pre-existing pulmonary conditions. Elevated urea and creatinine levels were observed in 85.2% of cases, and metabolic acidosis was noted in all patients. Seizures occurred in 32.8% of individuals, with an overall mortality rate of 59%. Although no significant differences in mortality were associated with addiction history (P=0.310), a strong correlation was found with the type of poisoning agents (P&#60;0.001).
Conclusion: The study found 59% mortality rate among ARDS patients due to drug and chemical poisoning, emphasizing the need for effective management strategies. A significant proportion of cases were involved with addiction, primarily to methadone, yet no mortality correlation with addiction was observed. The findings underscore the complexities of treating ARDS in the context of poisoning, necessitating a diverse approach to improve patient outcomes.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
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			<TPAGE>346</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/162025/04/302025/08/182024/11/14
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1403/8/24
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/32025/09/302025/11/32025/08/16
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/5/25
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Saeed</Name>
				<MidName></MidName>
				<Family>Ghorbani</Family>
				<NameE>Saeed</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghorbani</FamilyE>
				<Organizations>
				<Organization>Department of Medical Science, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>dr.sa.ghorbani@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hamid</Name>
				<MidName></MidName>
				<Family>Owliaey</Family>
				<NameE>Hamid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Owliaey</FamilyE>
				<Organizations>
				<Organization>Department of Forensic Medicine &#38; Clinical Toxicology, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>hamid.owliaey@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Komeil</Name>
				<MidName></MidName>
				<Family>Aghazadeh-Habashi</Family>
				<NameE>Komeil</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Aghazadeh-Habashi</FamilyE>
				<Organizations>
				<Organization>Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>komeil.aghazade@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Razavi</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Razavi</FamilyE>
				<Organizations>
				<Organization>Department of Medical Science, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>fatmarazavi0@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Navid</Name>
				<MidName></MidName>
				<Family>Rostami</Family>
				<NameE>Navid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rostami</FamilyE>
				<Organizations>
				<Organization>School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>navidd.rostamii@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Sareh</Name>
				<MidName></MidName>
				<Family>Rafatmagham</Family>
				<NameE>Sareh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rafatmagham</FamilyE>
				<Organizations>
				<Organization>Department of Internal Medicine, Fasa University of Medical Sciences, Fasa, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Niloofarderavi@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hamid Reza</Name>
				<MidName></MidName>
				<Family>Ghasemirad</Family>
				<NameE>Hamid Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghasemirad</FamilyE>
				<Organizations>
				<Organization>Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>hr.ghasemirad@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Mahdizadeh Gazoui</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mahdizadeh Gazoui</FamilyE>
				<Organizations>
				<Organization>Department of Medical Science, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mdzdf962@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mehrdad</Name>
				<MidName></MidName>
				<Family>Kiasi</Family>
				<NameE>Mehrdad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kiasi</FamilyE>
				<Organizations>
				<Organization>Department of Medical Science, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>kiasimehrdad@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohsen</Name>
				<MidName></MidName>
				<Family>Jabbari</Family>
				<NameE>Mohsen</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Jabbari</FamilyE>
				<Organizations>
				<Organization>Department of Medical Science, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Mo.jabbari75@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Khashayar</Name>
				<MidName></MidName>
				<Family>Moravej</Family>
				<NameE>Khashayar</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Moravej</FamilyE>
				<Organizations>
				<Organization>Faculty of Dentistry, Is.C., Islamic Azad University, Isfahan, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Khashayarmoravej@hotmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Rouzina</Name>
				<MidName></MidName>
				<Family>Shabani</Family>
				<NameE>Rouzina</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shabani</FamilyE>
				<Organizations>
				<Organization>Department of Medical Science, Yaz.C., Islamic Azad University, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Rozhina.shabani@icloud.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Acute respiratory distress syndrome (ARDS)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Drug poisoning</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Chemical poisoning</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Mehrpour O, Akbari A, Jahani F, Amirabadizadeh A, Allahyari E, Mansouri B, et al. Epidemiological and clinical profiles of acute poisoning in patients admitted to the intensive care unit in eastern Iran (2010 to 2017). BMC Emerg Med. 2018; 18(1):30. [DOI:10.1186/s12873-018-0181-6] [PMID]##Ghasempoori K, Sharifi V, Hatami M. [Epidemiology of Acute Poisoning in Patients Admitted to Qaemshahr Razi Hospital, Iran, 2014 (Persian)]. J Mazandaran Univ Med Sci. 2016; 26(143):247-51. [Link]##Alinejad S, Zamani N, Abdollahi M, Mehrpour O. A Narrative Review of Acute Adult Poisoning in Iran. Iran J Med Sci. 2017; 42(4):327-46. [PMID]##Jayakrishnan B, Al Asmi A, Al Qassabi A, Nandhagopal R, Mohammed I. Acute drug overdose: Clinical profile, etiologic spectrum and determinants of duration of intensive medical treatment. Oman Med J. 2012; 27(6):501-4. [DOI:10.5001/omj.2012.120] [PMID]##Aghabiklooei A, Shadnia S, Hassanian-Moghaddam H, Zamani N. Acute respiratory distress syndrome caused by methadone syrup. Arh Hig Rada Toksikol. 2013; 64(3):439-43. [DOI:10.2478/10004-1254-64-2013-2347] [PMID]##Ramadori GP. Organophosphorus poisoning: Acute respiratory distress syndrome (ARDS) and cardiac failure as cause of death in hospitalized patients. Int J Mol Sci. 2023; 24(7):6658. [DOI:10.3390/ijms24076658] [PMID]##Raghavendran K, Napolitano LM. Definition of ALI/ARDS. Crit Care Clin. 2011; 27(3):429-37. [DOI:10.1016/j.ccc.2011.05.006] [PMID]##Huppert LA, Matthay MA, Ware LB. Pathogenesis of acute respiratory distress syndrome. Semin Respir Crit Care Med. 2019; 40(1):31-9. [DOI:10.1055/s-0039-1683996] [PMID]##Rocco PR, Pelosi P. Pulmonary and extrapulmonary acute respiratory distress syndrome: Myth or reality? Curr Opin Crit Care. 2008; 14(1):50-5. [DOI:10.1097/MCC.0b013e3282f2405b] [PMID]##Bellani G, Laffey JG, Pham T, Fan E, Brochard L, Esteban A, et al. 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Can fiberoptic bronchoscopy be applied to critically ill patients treated with noninvasive ventilation for acute respiratory distress syndrome? Prospective observational study. BMC Pulm Med. 2016; 16(1):89. [DOI:10.1186/s12890-016-0236-y] [PMID]##Combes A, Peek GJ, Hajage D, Hardy P, Abrams D, Schmidt M, et al. ECMO for severe ARDS: systematic review and individual patient data meta-analysis. Intensive Care Med. 2020; 46(11):2048-57. [DOI:10.1007/s00134-020-06248-3] [PMID]##Huber W, Findeisen M, Lahmer T, Herner A, Rasch S, Mayr U, et al. Prediction of outcome in patients with ARDS: A prospective cohort study comparing ARDS-definitions and other ARDS-associated parameters, ratios and scores at intubation and over time. Plos One. 2020; 15(5):e0232720. [DOI:10.1371/journal.pone.0232720] [PMID]##Bhardwaj H, Bhardwaj B, Awab A. Revisiting opioid overdose induced acute respiratory distress syndrome. Indian J Crit Care Med. 2014; 18(2):119-20. [DOI:10.4103/0972-5229.126095] [PMID]##Radke JB, Owen KP, Sutter ME, Ford JB, Albertson TE. The effects of opioids on the lung. Clin Rev Allergy Immunol. 2014; 46(1):54-64. [DOI:10.1007/s12016-013-8373-z] [PMID]##Zarei S, Jabalameli S, Moghimian M, Nikyar H. [The effectiveness of cognitive-behavioral therapy on drug beliefs and addiction memory in opioid addicts undergoing methadone maintenance treatment (Persian)]. J Mod Psychol Res. 2024; 19(73):74-83. [Link]##Ehsaei A, Hosseini Abardeh M, Ostadimoghaddam H, Yazdani N. [An investigation of the visual function in maintenance stage of treatment with methadone in drug addicted individuals (Persian)]. J Param Sci Rehabil. 2017; 6(3):44-50.[Link]##Noori R, Narenjiha H, Aghabakhshi H, Habibi G, Khoshkrood Mansoori B. Methadone maintenance therapy outcomes in Iran. Subst Use Misuse. 2012; 47(7):767-73. [DOI:10.3109/10826084.2010.517726]##Anan K, Ichikado K, Kawamura K, Johkoh T, Fujimoto K, Suga M. Clinical characteristics and prognosis of drug-associated acute respiratory distress syndrome compared with non-drug-associated acute respiratory distress syndrome: A single-centre retrospective study in Japan. BMJ Open. 2017; 7(11):e015330. [DOI:10.1136/bmjopen-2016-015330] [PMID]##Ghaffourian T, Barati L, Khajavi A, Mehrjerdian M. [Evaluation of Methadone Poisoning in Pediatric Emergency Department, Gorgan, North of Iran (2011-19) (Persian)]. J Gorgan UnivMed Sci. 2021; 23(4):95-8. [Link]##Ala A, Shams Vahdati S, Moosavi L, Sadeghi H. Studying the relationship between age, gender and other demographic factors with the type of agent used for self-poisoning at a poisoning referral center in North West Iran. J Acad Emerg Med. 2011; 10(3):100-2. [Link]##Bhadade RR, de Souza RA, Harde MJ, Khot A. Clinical characteristics and outcomes of patients with acute lung injury and ARDS. J Postgrad Med. 2011; 57(4):286-90. [DOI:10.4103/0022-3859.90077] [PMID]##Summers C, Singh NR, Worpole L, Simmonds R, Babar J, Condliffe AM, et al. Incidence and recognition of acute respiratory distress syndrome in a UK intensive care unit. Thorax. 2016; 71(11):1050-1. [DOI:10.1136/thoraxjnl-2016-208402] [PMID]##Panitchote A, Mehkri O, Hastings A, Hanane T, Demirjian S, Torbic H, et al. Factors associated with acute kidney injury in acute respiratory distress syndrome. Ann Intensive Care. 2019; 9(1):74. [DOI:10.1186/s13613-019-0552-5] [PMID]##Pilarczyk K, Huenges K, Bewig B, Balke L, Cremer J, Haneya A, et al. Acute kidney injury in patients with severe ARDS requiring extracorporeal membrane oxygenation: Incidence, prognostic impact and risk factors. J Clin Med. 2022; 11(4):1079. [DOI:10.3390/jcm11041079] [PMID]##Alenezi FK, Almeshari MA, Mahida R, Bangash MN, Thickett DR, Patel JM. Incidence and risk factors of acute kidney injury in COVID-19 patients with and without acute respiratory distress syndrome (ARDS) during the first wave of COVID-19: A systematic review and Meta-Analysis. Ren Fail. 2021; 43(1):1621-33. [DOI:10.1080/0886022X.2021.2011747] [PMID]##van den Akker JP, Egal M, Groeneveld AJ. Invasive mechanical ventilation as a risk factor for acute kidney injury in the critically ill: A systematic review and meta-analysis. Crit Care. 2013; 17(3):R98. [DOI:10.1186/cc12743] [PMID]##Peek GJ, Mugford M, Tiruvoipati R, Wilson A, Allen E, Thalanany MM, et al. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): A multicentre randomised controlled trial. Lancet. 2009; 374(9698):1351-63. [DOI:10.1016/S0140-6736(09)61069-2] [PMID]##Kim WY, Hong SB. Sepsis and acute respiratory distress syndrome: Recent update. Tuberc Respir Dis (Seoul). 2016; 79(2):53-7. [DOI:10.4046/trd.2016.79.2.53] [PMID]##Li S, Zhao D, Cui J, Wang L, Ma X, Li Y. Prevalence, potential risk factors and mortality rates of acute respiratory distress syndrome in Chinese patients with sepsis.J Int Med Res. 2020; 48(2):300060519895659. [DOI:10.1177/0300060519895659] [PMID]##Yang P, Wu T, Yu M, Chen F, Wang C, Yuan J, et al. A new method for identifying the acute respiratory distress syndrome disease based on noninvasive physiological parameters. Plos One. 2020; 15(2):e0226962. [DOI:10.1371/journal.pone.0226962] [PMID]##Bass CM, Sajed DR, Adedipe AA, West TE. Pulmonary ultrasound and pulse oximetry versus chest radiography and arterial blood gas analysis for the diagnosis of acute respiratory distress syndrome: A pilot study. Crit Care. 2015; 19(1):282. [DOI:10.1186/s13054-015-0995-5] [PMID]##Edriss H, Pfarr M. Acute respiratory distress syndrome, metabolic acidosis, and respiratory acidosis associated with citalopram overdose. Southwest Respir Crit Care Chron. 2014; 2(5):24-8. [Link]##Dai Q, Wang S, Liu R, Wang H, Zheng J, Yu K. Risk factors for outcomes of acute respiratory distress syndrome patients: A retrospective study. J Thorac Dis. 2019; 11(3):673-85. [DOI:10.21037/jtd.2019.02.84] [PMID]##Kraut JA, Madias NE. Metabolic acidosis: Pathophysiology, diagnosis and management. Nat Rev Nephrol. 2010; 6(5):274-85. [DOI:10.1038/nrneph.2010.33] [PMID]##Behnoush B, Taghadosinejad F, Arefi M, Shahabi M, Jamalian M, Kazemifar AM. Prevalence and complications of drug-induced seizures in Baharloo Hospital, Tehran, Iran. Iran J Toxicol. 2012; 6(16):588-93. [Link]##Aghili Mehrizi FS, Owliaey H, Ghasemirad H, Faress F, Asghari R, Talebi S. Emerging trends in drug-induced seizures: A pilot study. Razavi J Univ Med SCi. 2024; 12(4):13-23. [DOI:10.30483/rijm.2024.254489.1295]##Nosaka N, Ichiba S, Tsukahara K, Knaup E, Hayashi K, Kasahara S, et al. Acute respiratory distress syndrome in a child with severe epileptic disorder treated successfully by extracorporeal membrane oxygenation: A case report. BMC Pediatr. 2015; 15:29. [DOI:10.1186/s12887-015-0348-1] [PMID]##Traficante DC, Feibish G, Kashani J. Methadone-induced torsades de pointes masquerading as seizures. Clin Pract Cases Emerg Med. 2017; 1(1):40-3. [DOI:10.5811/cpcem.2016.11.32664] [PMID]##Asadi-Pooya AA, Emami M, Emami Y. Gender differences in manifestations of psychogenic non-epileptic seizures in Iran. J Neurol Sci. 2013; 332(1-2):66-8. [PMID]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>The Impact of N-acetylcysteine Supplementation on Spermatogenic Recovery and Biochemical Markers in Dexamethasone-administered Mice</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Dexamethasone (DEX), a widely used synthetic glucocorticoid, is associated with adverse effects on male reproductive health. N-acetylcysteine (NAC), as a glutathione precursor and potent antioxidant, helps neutralize free radicals, thereby preventing tissue damage and preserving sperm integrity.
Objectives: This study aimed to assess the effect of NAC on the undesired effects of DEX on the spermatogenesis indices and sperm parameters.
Methods: A total of 24 NMRI mice were divided into 4 groups: control, DEX (7 mg/kg/d, IP), NAC (100 mg/kg/d, IP), and DEX+NAC. They received treatments for 7 days. Testicular tissues were excised 24 hours after treatment completion for stereological evaluation and determination of mean daily sperm production (DSP). In addition, the mean numbers of spermatogonia, spermatocytes, spermatids, Leydig cells, and Sertoli cells, along with spermatogenesis indices, sperm tail length (STL), motility, and malondialdehyde (MDA) levels in serum and testicular tissues, and testosterone concentration were measured and analyzed.&#160;
Results: In the DEX-treated group, significant declines were detected in sperm motility, spermatogenesis indices, DSP, and the counts of spermatocytes, spermatids, and Leydig cells, along with a reduction in serum testosterone levels compared with the control (P&#60;0.05). Conversely, serum and testicular MDA concentrations increased markedly following DEX administration (P&#60;0.05). Co-treatment with NAC normalized these parameters to levels comparable to the control group.
Conclusion: The findings of this study suggest that NAC can mitigate the detrimental effects of DEX on spermatogenesis indices and sperm quality parameters, likely through its antioxidant and regulatory effects.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>347</FPAGE>
			<TPAGE>358</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/162025/04/302025/08/182024/11/142025/07/28
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/5/6
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/32025/09/302025/11/32025/08/162025/11/29
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/9/8
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Monireh</Name>
				<MidName></MidName>
				<Family>Mahmoodi</Family>
				<NameE>Monireh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mahmoodi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Faculty of Science, Arak University, Arak, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>m-mahmoodi@araku.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Malek Soleimani</Name>
				<MidName></MidName>
				<Family>Mehranjani</Family>
				<NameE>Malek Soleimani</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mehranjani</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Faculty of Science, Arak University, Arak, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>m-soleimani@araku.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Sepideh</Name>
				<MidName></MidName>
				<Family>Bakhshi</Family>
				<NameE>Sepideh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bakhshi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Faculty of Science, Arak University, Arak, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mehrad.bahmani2021@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Dexamethasone (DEX)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>N-acetylcysteine (NAC)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Spermatogenesis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Mice</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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[DOI:10.1007/s00101-019-00672-x] [PMID]##Iorgulescu JB, Gokhale PC, Speranza MC, Eschle BK, Poitras MJ, Wilkens MK, et al. Concurrent dexamethasone limits the clinical benefit of immune checkpoint blockade in glioblastoma. Clin Cancer Res. 2021; 27(1):276-87. [DOI:10.1158/1078-0432.CCR-20-2291] [PMID]##Ma Y, Fan X, Han J, Cheng Y, Zhao J, Fang W, et al. Critical illness and sex hormones: Response and impact of the hypothalamic-pituitary-gonadal axis. Ther Adv Endocrinol Metab. 2025; 16:20420188251328192.[DOI:10.1177/20420188251328192] [PMID]##Ignatiuk V, Izvolskaia M, Sharova V, Zakharova L. Disruptions in hypothalamic-pituitary-gonadal axis development and their igg modulation after prenatal systemic inflammation in male rats. Int J Mol Sci. 2023; 24(3):2726. [DOI:10.3390/ijms24032726] [PMID]##Kong Z, Zhu L, Liu Y, Liu Y, Chen G, Wang H. Effects of different stages, dosages and courses of prenatal dexamethasone exposure on testicular development in mice. Food Chem Toxicol. 2025; 201:115468. [DOI:10.1016/j.fct.2025.115468] [PMID]##Annie L, Gurusubramanian G, Kumar Roy V. Dexamethasone mediated downregulation of PGC-1α and visfatin regulates testosterone synthesis and antioxidant system in mouse testis. Acta Histochemica. 2019; 121(2):182-8. [DOI:10.1016/j.acthis.2018.12.004] [PMID]##Tenório MCDS, Graciliano NG, Moura FA, Oliveira ACM, Goulart MOF. N-Acetylcysteine (NAC): Impacts on human health. Antioxidants (Basel). 2021; 10(6):967. [DOI:10.3390/antiox10060967] [PMID]##Mokra D, Porvaznik I, Mokry J. N-Acetylcysteine in the Treatment of Acute Lung Injury: Perspectives and Limitations. Int J Mol Sci. 2025; 26(6):2657. [DOI:10.3390/ijms26062657] [PMID]##Abedini Bajgiran F, Khazaei Koohpar Z, Salehzadeh A. Effects of N-Acetylcysteine supplementation on oxidative stress and expression of apoptosis-related genes in testicular tissue of rats exposed to lead. Biol Trace Elem Res. 2023; 201(5):2407-15. [DOI:10.1007/s12011-022-03325-0] [PMID]##Mohammadi-Sardoo M, Mandegary A, Nabiuni M, Nematollahi-Mahani SN, Amirheidari B. Mancozeb induces testicular dysfunction through oxidative stress and apoptosis: Protective role of N-acetylcysteine antioxidant. Toxicol Ind Health. 2018; 34(11):798-811. [DOI:10.1177/0748233718778397] [PMID]##Malmir M, Soleimani Mehranjani M, Naderi Noreini S, Faraji T. Protective antioxidant effects of N‐acetylcysteine against impairment of spermatogenesis caused by paranonylphenol. Andrologia. 2018; 50(10):e13114. [DOI:10.1111/and.13114] [PMID]##Wang Y, Xu Y, Yang L, Yang Y, Guo AL, Han XJ, et al. N-acetylcysteine alleviated tris (2-chloroisopropyl) phosphate-induced sperm motility decline and functional dysfunction in mice through reversing oxidative stress and DNA damage. Ecotoxicol Environ Saf. 2024; 271:116000. [DOI:10.1016/j.ecoenv.2024.116000] [PMID]##Soleimani Mehranjani M, Azizi M, Sadeghzadeh F. The effect of melatonin on testis histological changes and spermatogenesis indexes in mice following treatment with dexamethasone. Drug Chem Toxicol. 2022; 45(3):1140-9. [DOI:10.1080/01480545.2020.1809672] [PMID]##Sadeghzadeh F, Mehranjani M, Mahmoodi M. Vitamin C ameliorates the adverse effects of dexamethasone on sperm motility, testosterone level, and spermatogenesis indexes in mice. Hum Exp Toxicol. 2019; 38(4):409-18. [DOI:10.1177/0960327118816137] [PMID]##Mohamadpour M, Mollajani R, Sarabandi F, Hosseini F, Mohsenkia M, Erfanizadeh M, et al. Protective effect of grape seed extract on dexamethasone-induced testicular toxicity in mice. Crescent J Med Biol Sci. 2020; 7(1):59-65. [Link]##Turkmen R, Akosman MS, Demirel HH. Protective effect of N-acetylcysteine on MK-801-induced testicular oxidative stress in mice. Biomed Pharmacother. 2019; 109:1988-93. [DOI:10.1016/j.biopha.2018.09.139] [PMID]##Shittu SA, Shittu ST, Akindele OO, Kunle-Alabi OT, Raji Y. Protective action of N-acetylcysteine on sperm quality in cyclophosphamide-induced testicular toxicity in male Wistar rats. JBRA Assist Reprod. 2019; 23(2):83-90. [DOI:10.5935/1518-0557.20180079] [PMID]##Björndahl L, Kirkman Brown J; other Editorial Board Members of the WHO Laboratory Manual for the Examination and Processing of Human Semen. The sixth edition of the WHO laboratory manual for the examination and processing of human semen: ensuring quality and standardization in basic examination of human ejaculates. Fertil Steril. 2022; 117(2):246-51. [DOI:10.1016/j.fertnstert.2021.12.012] [PMID]##Blutke A, Wanke R. Sampling strategies and processing of biobank tissue samples from porcine biomedical models. J Vis Exp. 2018; (133):57276. [DOI:10.3791/57276] [PMID]##Dehghani F, Sotoude N, Bordbar H, Panjeshahin MR, Karbalay-Doust S. The use of platelet-rich plasma (PRP) to improve structural impairment of rat testis induced by busulfan. Platelets. 2019; 30(4):513-20. [DOI:10.1080/09537104.2018.1478400] [PMID]##Zamani A, Saki F, Hatami N, Koohpeyma F. Stereological assessment of the effects of vitamin D deficiency on the rat testis. BMC Endocr Disord. 2020; 20(1):162. [DOI:10.1186/s12902-020-00642-0] [PMID]##Siervo GEML, Mariani NAP, Silva AAS, Punhagui-Umbelino APF, Costa IRD, Andrade AD, et al. Low dose of cyclosporine A disrupts sperm parameters and testosterone levels reversibly in mice. Toxicol Appl Pharmacol. 2023; 460:116374. [DOI:10.1016/j.taap.2023.116374] [PMID]##Tootian Z, Fazelipour S, Goodarzi N, Arab HA. The effect of pure phenol on sperm parameters and fertility rate in male mice. Iran J Vet Med. 2015; 9(4):295-301. [Link]##Buege JA, Aust SD. [30] Microsomal lipid peroxidation. In: Methods in enzymology. Amsterdam: Elsevier; 1978. [DOI:10.1016/S0076-6879(78)52032-6]##Tutar E, Pesen B, Coşkun ZM, Bolkent S. Oxidative stress status in testis of type-2 diabetic rats treated with Delta-9-tetrahydrocannabinol. Eur J Biol. 2021; 80(2):91-6. [Link]##Abouzaripour M, Daneshi E, Miri S. Effect of Nigella sativa on dexamethasone-induced testicular toxicity in mice. Avicenna J Phytomed. 2024; 14(5):520-6. [DOI:10.22038/AJP.2023.23584] [PMID]##Chaimontri C, Arun S, Kamollerd T, Lapyuneyong N, Taoto C, Innoi S, et al. Low sperm quality and increased testicular caspases in chronic stress mice induced by dexamethasone. Braz J Biol. 2025; 85:e289850. [DOI:10.1590/1519-6984.289850] [PMID]##Hajimirza SP, Forouzesh F, Shabani M. [Effect of dexamethasone on Fas/FasL and Bax/Bcl2 mRNA expression in human colorectal Cancer HT-29 cell line (Persian)]. Res Med. 2020; 44(2):352-9. [Link]##Deng S, Dai G, Chen S, Nie Z, Zhou J, Fang H, et al. Dexamethasone induces osteoblast apoptosis through ROS-PI3K/AKT/GSK3β signaling pathway. Biomed Pharmacother. 2019; 110:602-8. [DOI:10.1016/j.biopha.2018.11.103] [PMID]##Alahmar AT, Al Jothery AH, Al-Daami QJ, Abbas A, Al-Hassnawi AT. 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Ameliorative impacts of Allium cepa Linnaeus aqueous extract against testicular damage induced by dexamethasone. Andrologia. 2021; 53(4):e13955. [DOI:10.1111/and.13955] [PMID]##Gallo A, Esposito MC, Tosti E, Boni R. Sperm motility, oxidative status, and mitochondrial activity: Exploring correlation in different species. Antioxidants (Basel). 2021; 10(7):1131. [DOI:10.3390/antiox10071131] [PMID]##Ribeiro JC, Nogueira-Ferreira R, Amado F, Alves MG, Ferreira R, Oliveira PF. Exploring the role of oxidative stress in sperm motility: A proteomic network approach. Antioxid Redox Signal. 2022; 37(7-9):501-20. [DOI:10.1089/ars.2021.0241] [PMID]##Lara NL, Santos IC, Costa GM, Cordeiro-Junior DA, Almeida AC, Madureira AP, et al. Duration of spermatogenesis and daily sperm production in the rodent Proechimys guyannensis. Zygote. 2016; 24(5):783-93. [DOI:10.1017/S0967199416000137] [PMID]##Zirkin BR, Papadopoulos V. Leydig cells: formation, function, and regulation. Biol Reprod. 2018; 99(1):101-11. [DOI:10.1093/biolre/ioy059] [PMID]##Zhang J, Hu G, Huang B, Zhuo D, Xu Y, Li H, Zhan X, Ge RS, Xu Y. Dexamethasone suppresses the differentiation of stem Leydig cells in rats in vitro. BMC Pharmacol Toxicol. 2019; 20(1):32. [DOI:10.1186/s40360-019-0312-z] [PMID]##Hasona NA. Grape seed extract attenuates dexamethasone-induced testicular and thyroid dysfunction in male albino rats. Andrologia. 2018; 50(5):e13002. [DOI:10.1111/and.13002] [PMID]##Liu M, Chen B, Pei L, Zhang Q, Zou Y, Xiao H, et al Decreased H3K9ac level of StAR mediated testicular dysplasia induced by prenatal dexamethasone exposure in male offspring rats. Toxicology. 2018; 408:1-10. [PMID]##Dare JB, Ojewale AO, Olaniyan OT, Adole JA, Okotie GE, Akintayo CO, et al. Adansonia digitata aqueous leaf extract ameliorates dexamethasone-induced testicular injury in male Wistar rats. Asian Pac J Reprod. 2021; 10(3):113-20. [Link]##Azimi Zangabad E, Shomali T, Roshangar L. Effects of pharmacological doses of niacin on subacute glucocorticoid‐induced testicular damage in rats. Pharmacol Res Perspect. 2023; 11(5):e01128. [PMID]##Filippopoulou F, Habeos GI, Rinotas V, Sophocleous A, Sykiotis GP, Douni E, et al. Dexamethasone administration in mice leads to less body weight gain over time, lower serum glucose, and higher insulin levels independently of NRF2. Antioxidants (Basel). 2021; 11(1):4. [DOI:10.3390/antiox11010004] [PMID]##Schmitt B, Vicenzi M, Garrel C, Denis FM. Effects of N-acetylcysteine, oral glutathione (GSH) and a novel sublingual form of GSH on oxidative stress markers: A comparative crossover study. Redox Biol. 2015; 6:198-205. [DOI:10.1016/j.redox.2015.07.012] [PMID]##Xie C, Yi J, Lu J, Nie M, Huang M, Rong J, et al. N‐acetylcysteine reduces ROS‐mediated oxidative DNA damage and PI3K/Akt pathway activation induced by Helicobacter pylori infection. Oxid Med Cell Longev. 2018; 2018:1874985. [DOI:10.1155/2018/1874985] [PMID]##Malmir M, Faraji T, Noreini N, Mehranjani M. Protective antioxidant effects of N-acetylcysteine on testicular tissue and serum testosterone in paranonylphenol-treated mice (a stereological analysis). Reprod Syst Sex Disord. 2018; 7(2):225. [Link]##Ghafarizadeh A, Malmir M, Naderi Noreini S, Faraji T. Antioxidant effects of N-acetylcysteine on the male reproductive system: A systematic review. Andrologia. 2021; 53(1):e13898. [DOI:10.1111/and.13898] [PMID]##Shahrzad E, Shariati M, Naimi S, Edalatmanesh MA. Protective effect of N-acetylcysteine on changes in serum levels of Pituitary–Gonadal axis hormones and testicular tissue in acrylamide-treated adult rats. Adv Hum Biol. 2020; 10(1):16-21. [DOI:10.4103/AIHB.AIHB_65_19]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Determination of Serum Crocetin After Oral Administration of Krocina Tablets Using HPLC and LC–MS Method</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Saffron, derived from Crocus sativus, has long been used in traditional medicine because of its antioxidant, anti-inflammatory, and neuroprotective properties, which are primarily attributed to crocin, its major bioactive pigment. Crocin is extensively hydrolyzed to crocetin in the gastrointestinal tract, where it exhibits improved systemic absorption and acts as the principal circulating metabolite. However, pharmacokinetic data regarding commercially available crocin formulations remain limited.
Objectives: Crocin is the main active pigment in saffron and is responsible for its many therapeutic effects. A pharmaceutical product called Krocina is available on the Iran market, and this study aims to investigate the pharmacokinetics and absorption of Krocina 15-mg tablets.
Methods: A stock solution of crocetin at a concentration of 5 &#181;g/mL in methanol was prepared. Serum and urine standards were then prepared from this stock in the concentration range of 0.025 to 2.5 &#181;g/mL. Each standard was analyzed with high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS) with multiple reaction monitoring (MRM). A mobile phase composed of methanol, water, and acetic acid (85%, 14.5%, 0.5%), at a detection wavelength at 423 nm with a flow rate of 0.8 mL/min was employed. LC-MS measurements were performed in positive electrospray ionization mode (ESI+) using a Supelco analytical column (150&#215;4.6 mm, 3 &#181;m Discovery HS C18, USA).
Results: The intraday coefficient of variation (CV) measured by HPLC &#60;1.28%, and the interday CV&#60;3.44%. For the LC-MS/MRM method, intraday CV&#60;1.05% and interday CV was below 2.87%. The average peak serum concentration of crocetin after Krocina tablet administration occurred at 240 minutes, measured as 177.11 ng/mL by HPLC and 184.33 ng/mL by LC-MS/MRM.
Conclusion: Both HPLC and LC-MS methods demonstrated adequate capability for blood analysis and determination of pharmacokinetic parameters, and the obtained data were considered reliable. The clinical effects of Krocina tablets should be related to absorbed crocetin.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>359</FPAGE>
			<TPAGE>368</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/162025/04/302025/08/182024/11/142025/07/282025/08/16
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/5/25
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/32025/09/302025/11/32025/08/162025/11/292025/12/8
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/9/17
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Faezeh</Name>
				<MidName></MidName>
				<Family>Ghorbanzadeh</Family>
				<NameE>Faezeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghorbanzadeh</FamilyE>
				<Organizations>
				<Organization>Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>ghorbanzadeh.faezeh@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hossein</Name>
				<MidName></MidName>
				<Family>Kamali</Family>
				<NameE>Hossein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kamali</FamilyE>
				<Organizations>
				<Organization>Targeted Drug Delivery Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>kamalih@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mojgan</Name>
				<MidName></MidName>
				<Family>Nejabat</Family>
				<NameE>Mojgan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Nejabat</FamilyE>
				<Organizations>
				<Organization>Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>nejabatm2@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Majid</Name>
				<MidName></MidName>
				<Family>Ghayour Mobarhan</Family>
				<NameE>Majid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghayour Mobarhan</FamilyE>
				<Organizations>
				<Organization>Department of Nutrition, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>ghayourm@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Farzin</Name>
				<MidName></MidName>
				<Family>Hadizadeh</Family>
				<NameE>Farzin</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hadizadeh</FamilyE>
				<Organizations>
				<Organization>Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>hadizadehf@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Krocina</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Tablet</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pharmacokinetic</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>High-performance liquid chromatography (HPLC)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Liquid chromatography-mass spectrometry (LC-MS)</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Effect of Storage Period on the Bioactive Composition and Therapeutic Potential of Syzygium aromaticum Essential Oil</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Essential oil (EO) of Syzygium aromaticum is usually used for medicinal purposes. In most cases, it is kept for a long duration.&#160;
Objectives: The work aimed at examining how the duration of storage of the EO affects its medicinal quality of the essential oil.&#160;
Methods: The EO of S. aromaticum was extracted by hydrodistillation. The extracted EO was kept in a cupboard in amber bottles at room temperature for 4, 183, and 365 days. Chemical components of the EOs were determined by gas chromatography mass spectroscopy (GC-MS). The antioxidant activity was determined by using the 2,2-diphenyl-1-picryl-hydrazyl (DPPH), 2,2-azobis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS), and ferric reducing antioxidant power (FRAP) assays. Dopamine and butyrylcholinesterase (BCHE) assays were used to assess the anti-hypertensive activity. The anti-diabetic tendencies were evaluated with the &#945;-glucosidase and &#945;-amylase assays. Albumin denaturation and protease were used to estimate the anti-inflammatory activity.&#160;
Results: The results indicate that the EO shows a color change from light yellow in 4 and 183 days of storage to dark brown after 365 days. The results of the GC-MS show a higher value of eugenol in the EO stored for 183 and 365 days (93.15% and 93.46%, respectively). It also shows the presence of eugenol acetate (17.05%) in the EO stored for 4 days, but it was absent in 183 and 365 days of storage. The EO stored for 4 days had a higher inhibition of antioxidant, anti-inflammatory, anti-hypertensive, and anti-diabetic parameters tested.
Conclusion: The results indicate that the higher the period of storage of the essential oil, the less medicinal potency it possesses.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>369</FPAGE>
			<TPAGE>384</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/07/182025/07/162025/04/302025/08/182024/11/142025/07/282025/08/162025/08/19
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/5/28
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/11/292025/11/32025/09/302025/11/32025/08/162025/11/292025/12/82025/11/29
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/9/8
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Abayomi Gideon</Name>
				<MidName></MidName>
				<Family>Adeyemo</Family>
				<NameE>Abayomi Gideon</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Adeyemo</FamilyE>
				<Organizations>
				<Organization>Department of Pure and Applied Chemistry, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>adeyemoabayomi0205@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shola</Name>
				<MidName></MidName>
				<Family>Hezekiah Awojide</Family>
				<NameE>Shola</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hezekiah Awojide</FamilyE>
				<Organizations>
				<Organization>Department of Pure and Applied Chemistry, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>shola.awojide@uniosun.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Alilat</Name>
				<MidName></MidName>
				<Family>Ololade Tiamiyu</Family>
				<NameE>Alilat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ololade Tiamiyu</FamilyE>
				<Organizations>
				<Organization>Department of Pure and Applied Chemistry, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>ololadetiamiyu19@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Adebanjo Jacob</Name>
				<MidName></MidName>
				<Family>Anifowose</Family>
				<NameE>Adebanjo Jacob</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Anifowose</FamilyE>
				<Organizations>
				<Organization>Department of Pure and Applied Chemistry, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>adebanjo.anifowose@uniosun.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Adedayo Olubunmi</Name>
				<MidName></MidName>
				<Family>Adeboye</Family>
				<NameE>Adedayo Olubunmi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Adeboye</FamilyE>
				<Organizations>
				<Organization>Department of Food Science and Technology, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>adedayo.adeboye@uniosun.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ezekiel</Name>
				<MidName></MidName>
				<Family>Olumide Fadunmade</Family>
				<NameE>Ezekiel</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Olumide Fadunmade</FamilyE>
				<Organizations>
				<Organization>Learning and Development Bureau, Chatham, United Kingdom.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>o.fadunmade@learninganddevelopmentbureau.org.uk</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Oluwatumininu</Name>
				<MidName></MidName>
				<Family>Abosede Mutiu</Family>
				<NameE>Oluwatumininu</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Abosede Mutiu</FamilyE>
				<Organizations>
				<Organization>Industrial Chemistry Program, Bowen University, Iwo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mutiuoluwatumininu@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Yemisi</Name>
				<MidName></MidName>
				<Family>Elizabeth Asibor</Family>
				<NameE>Yemisi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Elizabeth Asibor</FamilyE>
				<Organizations>
				<Organization>Department of Pure and Applied Chemistry, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>yemisi.asibor@uniosun.edu.ng</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Syzygium aromaticum</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Essential oil</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antioxidant</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Anti-inflammatory</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Anti-hypertensive</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antidiabetic</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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