<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2026</YEAR>
<VOL>12</VOL>
<NO>1</NO>
<MOSALSAL>0</MOSALSAL>
<PAGE_NO>70</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>Oncogenic Potential of John Cunningham Virus (JCV) in Human Infection and Cancer Development</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: The John Cunningham virus (JCV), a prevalent and asymptomatic virus, can cause neurological complications, such as progressive multifocal leukoencephalopathy (PML) in immunocompromised individuals. Cancer is the second leading cause of death globally, with 10-15% of human cancers linked to viral infections, making JCV a significant tumor-inducing virus.
Objectives: This study aimed to examine the biology of JCV, its infection mechanisms, and the pathways that may facilitate tumorigenesis.
Methods: This narrative review employed a systematic approach to literature retrieval. Searches were conducted across major electronic databases, including PubMed, Scopus, Web of Science, and Google Scholar, to identify relevant publications up to early 2025. The search scope included a wide range of study designs, such as original research, reviews, systematic reviews, meta-analyses, and case reports. The search strategy utilized a combination of the following key terms: &#8220;John Cunningham virus&#8221; OR &#8220;JCV&#8221;, &#8220;JC virus&#8221;, &#8220;oncogenesis&#8221; OR &#8220;oncogenic&#8221;, &#8220;cancer development&#8221;, &#8220;infection&#8221;, and &#8220;human neoplasms.&#8221;
Results: The findings indicate that JCV disrupts key cellular pathways, including p53 and retinoblastoma protein (pRB) pathways, and its genomic integration into host DNA suggests its oncogenic potential. Its mechanisms include alterations in cell cycle control and Wnt signaling, promotion of cell proliferation, and potential interaction with &#946;-catenin, leading to various cancers.
Conclusion: A better understanding of virus-related carcinogenesis could provide new targets for developing viral therapies that address not only viral infections but also cancer.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>1</FPAGE>
			<TPAGE>8</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/05/1
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/2/11
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/12/2
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/9/11
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Abolfazl</Name>
				<MidName></MidName>
				<Family>Jafari-Sales</Family>
				<NameE>Abolfazl</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Jafari-Sales</FamilyE>
				<Organizations>
				<Organization>Department of Microbiology, Kaz.C., Islamic Azad University, Kazerun, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>a.jafari_1392@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Kosar</Name>
				<MidName></MidName>
				<Family>Hosseini-Karkaj</Family>
				<NameE>Kosar</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hosseini-Karkaj</FamilyE>
				<Organizations>
				<Organization>Infectious Diseases Research Center, TaMS.C., Islamic Azad University, Tabriz, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>kosar22hosseini@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mehrdad</Name>
				<MidName></MidName>
				<Family>Pashazadeh</Family>
				<NameE>Mehrdad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Pashazadeh</FamilyE>
				<Organizations>
				<Organization>Infectious Diseases Research Center, TaMS.C., Islamic Azad University, Tabriz, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mehrdadpashazadeh85@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>John Cunningham virus (JCV)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Polyomavirus</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Oncogenes</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Retinoblastoma protein (pRB)</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Takahashi K, Sekizuka T, Fukumoto H, Nakamichi K, Suzuki T, Sato Y, et al. Deep-sequence identification and role in virus replication of a JC virus quasispecies in patients with progressive multifocal leukoencephalopathy. J Virol. 2016; 91(1):e01335-16. [DOI:10.1128/JVI.01335-16] [PMID] ##Kartau M, Verkkoniemi-Ahola A, Paetau A, Palomäki M, Janes R, Ristola M, et al. The incidence and predisposing factors of John Cunningham virus-induced progressive multifocal leukoencephalopathy in Southern Finland: A population-based study. Open Forum Infect Dis. 2019; 6(2):ofz024. [DOI:10.1093/ofid/ofz024] [PMID] ##Suleman M, Khan TA, Ejaz H, Maroof S, Alshammari A, Albekairi NA, et al. Structural vaccinology, molecular simulation and immune simulation approaches to design multi-epitopes vaccine against John Cunningham virus. Microb Pathog. 2024; 189:106572. [DOI:10.1016/j.micpath.2024.106572] [PMID]##Vilibic-Cavlek T, Bogdanic M, Peric T, Radmanic L, Antolasic L, Milasincic L, et al. Prevalence of JC polyomavirus in patients with neuroinvasive disease of unknown etiology in Croatia. Medicina. 2023; 60(1):69. [DOI:10.3390/medicina60010069] [PMID] ##Zou W, Imperiale MJ. Biology of Polyomavirus miRNA. Front Microbiol. 2021; 12:662892. [DOI:10.3389/fmicb.2021.662892] [PMID] ##Delbue S, Comar M, Ferrante P. Review on the role of the human polyomavirus JC in the development of tumors. Infect Agent Cancer. 2017; 12:10. [DOI:10.1186/s13027-017-0122-0] [PMID] ##Maginnis MS, Atwood WJ. JC virus: an oncogenic virus in animals and humans? Semin Cancer Biol. 2009; 19(4):261-9. [DOI:10.1016/j.semcancer.2009.02.013] [PMID] ##Dwyer C, Sharmin S, Kalincik T. Rates of John Cunningham virus seroconversion greatly reduced in natalizumab-treated patients during COVID-19-related lockdowns. Eur J Neurol. 2024; 31(1):e16059. [DOI:10.1111/ene.16059] [PMID] ##Del Valle L, Khalili K. Induction of brain tumors by the archetype strain of human neurotropic JCPyV in a transgenic mouse model. 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[DOI:10.1016/B978-0-12-824156-1.00012-1]##Mohammed Ali SH, Mohammed Al-Alwany SH, Khalil Hussein A. Molecular Interplay of John Cunningham virus with interleukin 1 beta in colorectal carcinomatous tissues from a group of Iraqi patients. Arch Razi Inst. 2022; 77(6):2299-306. [DOI:10.22092/ARI.2022.358617.2267] [PMID]##Zheng HC, Xue H, Zhang CY. The oncogenic roles of JC polyomavirus in cancer. Front Oncol. 2022; 12:976577. [DOI:10.3389/fonc.2022.976577] [PMID] ##Ikegaya H. Geographical identification of cadavers by human parasites. Forensic Sci Int Genet. 2008; 2(2):83-90. [DOI:10.1016/j.fsigen.2007.10.184] [PMID]##Butic AB, Spencer SA, Shaheen SK, Lukacher AE. Polyomavirus wakes up and chooses neurovirulence. Viruses. 2023; 15(10):2112. [DOI:10.3390/v15102112] [PMID] ##Mettenleiter TC. Breaching the barrier-the nuclear envelope in virus infection. J Mol Biol. 2016; 428(10 Pt A):1949-61. [DOI:10.1016/j.jmb.2015.10.001] [PMID]##Cortese I, Reich DS, Nath A. Progressive multifocal leukoencephalopathy and the spectrum of JC virus-related disease. Nat Rev Neurol. 2021; 17(1):37-51. [DOI:10.1038/s41582-020-00427-y] [PMID] ##Ferenczy MW, Marshall LJ, Nelson CD, Atwood WJ, Nath A, Khalili K, et al. Molecular biology, epidemiology, and pathogenesis of progressive multifocal leukoencephalopathy, the JC virus-induced demyelinating disease of the human brain. Clin Microbiol Rev. 2012; 25(3):471-506. [DOI:10.1128/CMR.05031-11] [PMID] ##Torres C. Evolution and molecular epidemiology of polyomaviruses. Infect Genet Evol. 2020; 79:104150. [DOI:10.1016/j.meegid.2019.104150] [PMID]##Mouliou DS. John Cunningham virus and progressive multifocal leukoencephalopathy: A falsely played diagnosis. Diseases. 2024; 12(5):100. [DOI:10.3390/diseases12050100] [PMID] ##Bhattacharjee S, Chattaraj S. Entry, infection, replication, and egress of human polyomaviruses: An update. Can J Microbiol. 2017; 63(3):193-211. [DOI:10.1139/cjm-2016-0519] [PMID]##Imperiale MJ. The human polyomaviruses: An overview. In: Khalili K, Stoner GL, editors. Human polyomaviruses: Molecular and clinical perspectives. Hoboken: Wiley; 2001. [Link]##Ahye N, Bellizzi A, May D, Wollebo HS. The role of the jc virus in central nervous system tumorigenesis. Int J Mol Sci. 2020; 21(17):6236. [DOI:10.3390/ijms21176236] [PMID] ##Link A, Shin SK, Nagasaka T, Balaguer F, Koi M, Jung B, et al. JC virus mediates invasion and migration in colorectal metastasis. Plos One. 2009; 4(12):e8146. [DOI:10.1371/journal.pone.0008146] [PMID]##Ajuh ET, Wu Z, Kraus E, Weissbach FH, Bethge T, Gosert R, et al. Novel human polyomavirus noncoding control regions differ in bidirectional gene expression according to host cell, large T-antigen expression, and clinically occurring rearrangements. J Virol. 2018; 92(7):e02231-17. [DOI:10.1128/JVI.02231-17] [PMID] ##Khalili K, White MK, Sawa H, Nagashima K, Safak M. The agnoprotein of polyomaviruses: A multifunctional auxiliary protein. J Cell Physiol. 2005; 204(1):1-7. [DOI:10.1002/jcp.20266] [PMID]##Saribas AS, Coric P, Hamazaspyan A, Davis W, Axman R, White MK, et al. Emerging from the unknown: structural and functional features of agnoprotein of polyomaviruses. J Cell Physiol. 2016; 231(10):2115-27. [DOI:10.1002/jcp.25329] [PMID] ##Ricciardiello L, Baglioni M, Giovannini C, Pariali M, Cenacchi G, Ripalti A, et al. Induction of chromosomal instability in colonic cells by the human polyomavirus JC virus. Cancer Res. 2003; 63(21):7256-62. [PMID]##Mushtaq M, Darekar S, Kashuba E. DNA Tumor Viruses and Cell Metabolism. Oxid Med Cell Longev. 2016; 2016:6468342. [DOI:10.1155/2016/6468342] [PMID] ##He J, Liu L, Tang F, Zhou Y, Liu H, Lu C, et al. Paradoxical effects of DNA tumor virus oncogenes on epithelium-derived tumor cell fate during tumor progression and chemotherapy response. Signal Transduct Target Ther. 2021; 6(1):408. [DOI:10.1038/s41392-021-00787-x] [PMID] ##Moens U, Van Ghelue M, Ehlers B. Are human polyomaviruses co-factors for cancers induced by other oncoviruses? Rev Med Virol. 2014; 24(5):343-60. [DOI:10.1002/rmv.1798] [PMID]##White MK, Khalili K. Expression of JC virus regulatory proteins in human cancer: Potential mechanisms for tumourigenesis. Eur J Cancer. 2005; 41(16):2537-48. [DOI:10.1016/j.ejca.2005.08.019] [PMID]##Sinagra E, Raimondo D, Gallo E, Stella M, Cottone M, Rossi F, et al. JC virus and lung adenocarcinoma: Fact or myth? Anticancer Res. 2017; 37(6):3311. [DOI:10.21873/anticanres.11699]##Reiss K, Khalili K. Viruses and cancer: Lessons from the human polyomavirus, JCV. Oncogene. 2003; 22(42):6517-23. [DOI:10.1038/sj.onc.1206959] [PMID]##Ksiaa F, Ziadi S, Mokni M, Korbi S, Trimeche M. The presence of JC virus in gastric carcinomas correlates with patient&#039;s age, intestinal histological type and aberrant methylation of tumor suppressor genes. Mod Pathol. 2010; 23(4):522-30. [DOI:10.1038/modpathol.2009.184] [PMID]##Noch E, Sariyer IK, Gordon J, Khalili K. JC virus T-antigen regulates glucose metabolic pathways in brain tumor cells. Plos one. 2012; 7(4):e35054. [DOI:10.1371/journal.pone.0035054] [PMID] ##Muñoz-Mármol AM, Mola G, Ruiz-Larroya T, Fernández-Vasalo A, Vela E, Mate JL, et al. Rarity of JC virus DNA sequences and early proteins in human gliomas and medulloblastomas: the controversial role of JC virus in human neurooncogenesis. Neuropathol Appl Neurobiol. 2006; 32(2):131-40. [DOI:10.1111/j.1365-2990.2006.00711.x] [PMID]##White MK, Gordon J, Reiss K, Del Valle L, Croul S, Giordano A, et al. Human polyomaviruses and brain tumors. Brain Res Brain Res Rev. 2005; 50(1):69-85. [DOI:10.1016/j.brainresrev.2005.04.007] [PMID]##Soltani S, Farahani A, Shahbahrami R, Shateri Z, Emadi MS, Pakzad R, et al. Investigation of Epstein-barr virus, cytomegalovirus, human herpesvirus 6, and polyoma viruses (JC virus, BK virus) among gastric cancer patients: A cross sectional study. Health Sci Rep. 2024; 7(4):e2043. [DOI:10.1002/hsr2.2043] [PMID] ##Izi S, Youssefi M, Rahmani F, Roshan NM, Yari A, Avval FZ. Detection of JC Polyomavirus tumor antigen in gastric carcinoma: A report from Iran. Iran J Microbiol. 2018; 10(4):266. [PMID]##Yamaoka S, Yamamoto H, Nosho K, Taniguchi H, Adachi Y, Sasaki S, et al. Genetic and epigenetic characteristics of gastric cancers with JC virus T-antigen. World J Gastroenterol. 2009; 15(44):5579-85 [DOI:10.3748/wjg.15.5579] [PMID] ##Haghi Navand A, Teimoori A, Makvandi M, Nisi N, Seyedian SS, Ranjbari N, et al. Study on JV virus in patients with colon cancer type adenocarcinoma. Asian Pac J Cancer Prev. 2019; 20(4):1147-51. [DOI:10.31557/APJCP.2019.20.4.1147] [PMID] ##Prezioso C, Pietropaolo V, Moens U, Ciotti M. JC polyomavirus: A short review of its biology, its association with progressive multifocal leukoencephalopathy, and the diagnostic value of different methods to manifest its activity or presence. Expert Rev Mol Diagn. 2023; 23(2):143-57. [DOI:10.1080/14737159.2023.2179394] [PMID]##Shin SK, Li MS, Fuerst F, Hotchkiss E, Meyer R, Kim IT, et al. Oncogenic T-antigen of JC virus is present frequently in human gastric cancers. Cancer. 2006; 107(3):481-8. [DOI:10.1002/cncr.22028] [PMID]##Abdel-Aziz HO, Murai Y, Hong M, Kutsuna T, Takahashi H, Nomoto K, et al. Detection of the JC virus genome in lung cancers: possible role of the T-antigen in lung oncogenesis. Appl Immunohistochem Mol Morphol. 2007; 15(4):394-400. [DOI:10.1097/01.pai.0000213126.96590.64] [PMID]##Alibek K, Kakpenova A, Mussabekova A, Sypabekova M, Karatayeva N. Role of viruses in the development of breast cancer. Infect Agent Cancer. 2013; 8:32.[DOI:10.1186/1750-9378-8-32] [PMID] ##Hachana M, Amara K, Ziadi S, Gacem RB, Korbi S, Trimeche M. Investigation of human JC and BK polyomaviruses in breast carcinomas. Breast Cancer Res Treat. 2012; 133(3):969-77. [DOI:10.1007/s10549-011-1876-5] [PMID]##James LM, Georgopoulos AP. Breast cancer, viruses, and human leukocyte antigen (HLA). Sci Rep. 2024; 14(1):16179. [DOI:10.1038/s41598-024-65707-9] [PMID] ##Del Valle L, White MK, Enam S, Piña Oviedo S, Bromer MQ, et al. Detection of JC virus DNA sequences and expression of viral T antigen and agnoprotein in esophageal carcinoma. Cancer. 2005; 103(3):516-27. [DOI:10.1002/cncr.20806] [PMID]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Gastro-retentive Drug Delivery Systems Based on Pectin: An Overview</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Controlled drug delivery systems (DDS) are designed to release therapeutic agents in a regulated manner to maintain consistent plasma drug concentrations. Among these systems, gastro-retentive DDS (GRDDS) have gained considerable attention due to their ability to prolong gastric residence time, thereby enhancing drug bioavailability and therapeutic efficacy for drugs absorbed primarily in the stomach or upper gastrointestinal tract.
Objectives: This review aimed to critically examine the role of pectin-based polymers in the development of GRDDS, with particular emphasis on formulation strategies using high- and low-methoxylated pectins.
Results: Pectin, a naturally derived polysaccharide, is widely utilized in pharmaceutical formulations owing to its biocompatibility, biodegradability, non-toxic nature, and excellent gel-forming capacity. Based on its degree of methoxylation (DM), pectin is classified into high-methoxylated and low-methoxylated forms, each exhibiting distinct physicochemical and functional properties. Low-methoxylated pectin has been extensively explored in floating DDS due to its calcium-dependent gelation behavior. In contrast, high-methoxylated pectin demonstrates strong mucoadhesive properties, making it suitable for mucoadhesive gastro-retentive formulations. Comparative studies with other natural polymers highlight the versatility of pectin in GRDDS design.
Conclusion: Pectin-based gastro-retentive formulations represent a promising and sustainable approach for controlled drug delivery. Understanding the distinct characteristics of high- and low-methoxylated pectin enables the rational design of effective GRDDS, potentially improving therapeutic outcomes and patient compliance.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>9</FPAGE>
			<TPAGE>26</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/05/12025/09/24
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/7/2
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/12/22026/02/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/11/25
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Aeman</Name>
				<MidName></MidName>
				<Family>Anis</Family>
				<NameE>Aeman</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Anis</FamilyE>
				<Organizations>
				<Organization>School of Pharmacy, Techno India University, Kolkata, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>mdanisakhter5@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Arpan</Name>
				<MidName></MidName>
				<Family>Das</Family>
				<NameE>Arpan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Das</FamilyE>
				<Organizations>
				<Organization>BCDA College of Pharmacy and Technology, Kolkata, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>arpandas13733@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Moumita</Name>
				<MidName></MidName>
				<Family>Das Kirtania</Family>
				<NameE>Moumita</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Das Kirtania</FamilyE>
				<Organizations>
				<Organization>BCDA College of Pharmacy and Technology, Kolkata, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>mmtdas@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Laboni</Name>
				<MidName></MidName>
				<Family>Das</Family>
				<NameE>Laboni</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Das</FamilyE>
				<Organizations>
				<Organization>School of Pharmacy, Techno India University, Kolkata, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>laboni.d@technoindiaeducation.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Gopa</Name>
				<MidName></MidName>
				<Family>Roy Biswas</Family>
				<NameE>Gopa</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Roy Biswas</FamilyE>
				<Organizations>
				<Organization>School of Pharmacy, Techno India University, Kolkata, India.</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>goparoy2020@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Gastro-retentive drug delivery systems (GRDDS)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Controlled drug delivery</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pectin-based polymers</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>High-methoxylated pectin</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Low-methoxylated pectin</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Floating DDS</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Mucoadhesive formulations</KeyText>
			</KEYWORD>
		</KEYWORDS>

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

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Atorvastatin Mitigates Cisplatin-induced Genotoxicity and Oxidative Stress in Human Lymphocytes: Insights From the Micronucleus Assay</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>&#160;Background: Cisplatin (Cis), an alkylating antineoplastic agent, is commonly used to treat bladder, ovarian, and testicular cancers. Prolonged use can lead to genotoxicity, potentially mediated by oxidative stress.&#160;
Objectives: This study aimed to evaluate the protective potential of atorvastatin (Atv) against Cis-induced genotoxicity in cultured human lymphocytes.
Methods: Peripheral lymphocytes were divided into four groups: control, Cis (12 &#956;M), Atv combined with Cis (50, 100, 1000 &#956;M), and Atv alone (1000 &#956;M). Micronucleus (MN) frequency was assessed as a marker of chromosomal damage, while glutathione (GSH) levels and lipid peroxidation (LPO) were measured to evaluate oxidative stress.
Results: Cis treatment significantly increased MN frequency and LPO levels and reduced GSH compared with the control group (P&#60;0.05). Co-treatment with Atv markedly ameliorated MN formation and oxidative stress markers, restoring GSH levels toward baseline. Notably, the protective effect was most pronounced at 50 &#956;M Atv, consistent with a hormetic antioxidant response. Higher concentrations (100&#8211;1000 &#956;M) did not further enhance antioxidant effects, likely due to saturation of cellular uptake or mild redox imbalance.
Conclusion: Cis induces genotoxicity in human lymphocytes primarily through oxidative stress mechanisms. Atv effectively mitigates this genotoxicity by restoring redox homeostasis and enhancing chromosomal protection, with an optimal protective effect observed at intermediate concentrations. These findings suggest that Atv may have therapeutic potential to counteract Cis-induced cellular damage and support further investigation into its adjunctive use in chemotherapy.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>27</FPAGE>
			<TPAGE>36</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/05/12025/09/242025/01/27
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1403/11/8
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/12/22026/02/142025/12/13
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/9/22
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Mohammad</Name>
				<MidName></MidName>
				<Family>Shokrzadeh</Family>
				<NameE>Mohammad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shokrzadeh</FamilyE>
				<Organizations>
				<Organization>Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mslamuk@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mona</Name>
				<MidName></MidName>
				<Family>Modanloo</Family>
				<NameE>Mona</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Modanloo</FamilyE>
				<Organizations>
				<Organization>Department of Toxicology and Pharmacology, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>dr_modanloo@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mina</Name>
				<MidName></MidName>
				<Family>Fasihbeiki</Family>
				<NameE>Mina</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Fasihbeiki</FamilyE>
				<Organizations>
				<Organization>Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mina.fasih5726@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ehsan</Name>
				<MidName></MidName>
				<Family>Zamani</Family>
				<NameE>Ehsan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Zamani</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology and Toxicology, School of Pharmacy, Guilan University of Medical Sciences, Rasht, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>shadigholampour97@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mona</Name>
				<MidName></MidName>
				<Family>Alinia</Family>
				<NameE>Mona</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Alinia</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology and Toxicology, School of Pharmacy, Guilan University of Medical Sciences, Rasht, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>monaaliniiia@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Shaki</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shaki</FamilyE>
				<Organizations>
				<Organization>Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>fshaki.tox@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Cisplatin (Cis)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Genotoxicity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Lymphocytes</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Atorvastatin (Atv)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Micronucleus (MN) test</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Oxidative stress</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Brown A, Kumar S, Tchounwou PB. Cisplatin-based chemotherapy of human cancers. J Cancer Sci Ther. 2019; 11(4):97. [PMID]##Ranjbar A, Ghaseminejhad S, Takalu H, Baiaty A, Rahimi F, Abdollahi M. Anti oxidative stress potential of cinnamon (cinnamomum zeylanicum) in operating room personnel; a before/after cross sectional clinical trial. Int J Pharmacol. 2007; 3(6):482-86. [DOI:10.3923/ijp.2007.482.486]##Cohen SM, Lippard SJ. Cisplatin: From DNA damage to cancer chemotherapy. Prog Nucleic Acid Res Mol Biol. 2001; 67:93-130. [DOI:10.1016/S0079-6603(01)67026-0] [PMID]##Makovec T. Cisplatin and beyond: Molecular mechanisms of action and drug resistance development in cancer chemotherapy. Radiol Oncol. 2019; 53(2):148-58. [DOI:10.2478/raon-2019-0018] [PMID] ##Sancho-Martínez SM, Prieto-García L, Prieto M, López-Novoa JM, López-Hernández FJ. Subcellular targets of cisplatin cytotoxicity: An integrated view. Pharmacol Ther. 2012; 136(1):35-55. [DOI:10.1016/j.pharmthera.2012.07.003] [PMID]##Dos Santos GC, Mendonça LM, Antonucci GA, Dos Santos AC, Antunes LM, Bianchi Mde L. Protective effect of bixin on cisplatin-induced genotoxicity in PC12 cells. Food Chem Toxicol. 2012; 50(2):335-40. [DOI:10.1016/j.fct.2011.10.033] [PMID]##Erbas M, Sekerci H. Importance of free radicals and occurring during food processing. GIDA J Food. 2011; 36(6):1. [Link]##Lobo V, Patil A, Phatak A, Chandra N. Free radicals, antioxidants and functional foods: Impact on human health. Pharmacogn Rev. 2010; 4(8):118-26. [DOI:10.4103/0973-7847.70902] [PMID] ##Ji LL. Oxidative stress during exercise: Implication of antioxidant nutrients. Free Radic Biol Med. 1995; 18(6):1079-86. [DOI:10.1016/0891-5849(94)00212-3] [PMID]##Akbari B, Baghaei-Yazdi N, Bahmaie M, Mahdavi Abhari F. The role of plant-derived natural antioxidants in reduction of oxidative stress. Biofactors. 2022; 48(3):611-33. [DOI:10.1002/biof.1831] [PMID]##Mansouri A, Reiner Ž, Ruscica M, Tedeschi-Reiner E, Radbakhsh S, Bagheri Ekta M, et al. Antioxidant effects of statins by modulating Nrf2 and Nrf2/HO-1 signaling in different diseases. J Clin Med. 2022; 11(5):1313. [DOI:10.3390/jcm11051313] [PMID] ##Clim A, Maranduca MA, Filip N, Tănase DM, Floria M, Pinzariu AC, et al. The Influence of Atorvastatin Treatment on Homocysteine Metabolism and Oxidative Stress in an Experimental Model of Diabetic Rats. Life. 2024; 14(11):1414. [DOI:10.3390/life14111414] [PMID] ##Voltan R, Secchiero P, Casciano F, Milani D, Zauli G, Tisato V. Redox signaling and oxidative stress: Cross talk with TNF-related apoptosis inducing ligand activity. Int J Biochem Cell Biol. 2016; 81(Pt B):364-74. [DOI:10.1016/j.biocel.2016.09.019] [PMID]##Yuan W, Fan H, Yang H, Tang L, Liu Z, Ouyang F, et al. Effect and mechanism of HMG-CoA reductase inhibitor on the improvement of elderly essential hypertension-induced vascular endothelial function impairment based on the JAK/STAT pathway. Diagn Pathol. 2023;18(1):108. [DOI:10.1186/s13000-023-01393-x] [PMID] ##Stefanis L, Burke RE, Greene LA. Apoptosis in neurodegenerative disorders. Curr Opin Neurol. 1997; 10(4):299-305. [DOI:10.1097/00019052-199708000-00004] [PMID]##Mayyas F. Short-term effect of atorvastatin on renal oxidative stress, inflammation, and fibrosis in a rat model of streptozotocin-induced diabetes. J Diabetes Metab Disord. 2024; 24(1):12. [DOI:10.1007/s40200-024-01514-3] [PMID] ##Zhang Y, Qu Y, Cai R, Gao J, Xu Q, Zhang L, et al. Atorvastatin ameliorates diabetic nephropathy through inhibiting oxidative stress and ferroptosis signaling. Eur J Pharmacol. 2024; 976:176699. [DOI:10.1016/j.ejphar.2024.176699] [PMID]##Vance DE, Vance JE. Biochemistry of lipids, lipoproteins and membranes. Edinburgh: Elsevier; 1996. [Link]##Inia JA, Stokman G, Pieterman EJ, Morrison MC, Menke AL, Verschuren L, et al. Atorvastatin attenuates diet-induced non-alcoholic steatohepatitis in APOE*3-leiden mice by reducing hepatic inflammation. Int J Mol Sci. 2023; 24(9):7818. [DOI:10.3390/ijms24097818] [PMID] ##Evazalipour M, Moayedi S, Safarzadeh Kozani P, Safarzadeh Kozani P. The protective effects of carvacrol on diphenhydramine-induced genotoxicity in human peripheral blood lymphocytes. Res J Pharmacognosy. 2021; 8(1):19-27. [Link]##Yamamoto V, Wang B, Lee AS. Suppression of head and neck cancer cell survival and cisplatin resistance by GRP78 small molecule inhibitor YUM70. Front Oncol. 2023; 12:1044699. [DOI:10.3389/fonc.2022.1044699] [PMID] ##Marullo R, Werner E, Degtyareva N, Moore B, Altavilla G, Ramalingam SS, et al. Cisplatin induces a mitochondrial-ROS response that contributes to cytotoxicity depending on mitochondrial redox status and bioenergetic functions. Plos One. 2013; 8(11):e81162. [DOI:10.1371/journal.pone.0081162] [PMID] ##Araujo-Lima CF, Christoni LSA, Justo G, Soeiro MNC, Aiub CAF, Felzenszwalb I. Atorvastatin downregulates in vitro methyl methanesulfonate and cyclophosphamide alkylation-mediated cellular and DNA injuries. Oxid Med Cell Longev. 2018; 2018:7820890. [DOI:10.1155/2018/7820890] [PMID] ##Soufi BR, Evazalipour M, Motavallian A, Chakosari MH, Zamani E. The protective effect of melatonin on diazepam-induced genotoxicity in peripheral blood lymphocytes using micronucleus assay. J Rep Pharm Sci. 2022; 11(1):92-7. [DOI:10.4103/jrptps.JRPTPS_111_20]##Ghosh S. Cisplatin: The first metal based anticancer drug. Bioorganic chemistry. 2019; 88:102925. [DOI:10.1016/j.bioorg.2019.102925] [PMID] ##Khabour OF, Alzoubi KH, Doa’a SM, Alasseiri M, Hasheesh TF. Tempol protects human lymphocytes from genotoxicity induced by cisplatin. Int J Clin Experiment Med. 2014 Apr 15;7(4):982. [PMID] ##Al-Eitan LN, Alzoubi KH, Al-Smadi LI, Khabour OF. Vitamin E protects against cisplatin-induced genotoxicity in human lymphocytes. Toxicol In Vitro. 2020; 62:104672. [DOI:10.1016/j.tiv.2019.104672] [PMID]##Siddik ZH. Mechanisms of action of cancer chemotherapeutic agents: DNA-interactive alkylating agents and antitumour platinum-based drugs. In: Alison MR, editor. The Cancer Handbook 1st Edition. Hoboken: John Wiley &#38; Sons, Ltd; 2002. [Link]##Tchounwou PB, Dasari S, Noubissi FK, Ray P, Kumar S. Advances in our understanding of the molecular mechanisms of action of cisplatin in cancer therapy. J Exp Pharmacol. 2021; 13:303-28. [DOI:10.2147/JEP.S267383] [PMID] ##Sami DH, Soliman AS, Khowailed AA, Hassanein EHM, Kamel EM, Mahmoud AM. 7-hydroxycoumarin modulates Nrf2/HO-1 and microRNA-34a/SIRT1 signaling and prevents cisplatin-induced oxidative stress, inflammation, and kidney injury in rats. Life Sci. 2022; 310:121104. [DOI:10.1016/j.lfs.2022.121104] [PMID]##Ghosh P, Roy SS, Chakraborty P, Ghosh S, Bhattacharya S. Effects of organoselenium compound 2-(5-selenocyanato-pentyl)-benzo[de]isoquinoline 1,3-dione on cisplatin induced nephrotoxicity and genotoxicity: An investigation of the influence of the compound on oxidative stress and antioxidant enzyme system. Biometals. 2013; 26(1):61-73. [DOI:10.1007/s10534-012-9594-y] [PMID]##Brahmi D, Ayed Y, Hfaiedh M, Bouaziz C, Mansour HB, Zourgui L, et al. Protective effect of cactus cladode extract against cisplatin induced oxidative stress, genotoxicity and apoptosis in balb/c mice: Combination with phytochemical composition. BMC Complement Altern Med. 2012; 12:111. [DOI:10.1186/1472-6882-12-111] [PMID] ##Hu JN, Leng J, Shen Q, Liu Y, Li XD, Wang SH, et al. Platycodin D suppresses cisplatin-induced cytotoxicity by suppressing ROS-mediated oxidative damage, apoptosis, and inflammation in HEK-293 cells. J Biochem Mol Toxicol. 2021; 35(1):e22624. [DOI:10.1002/jbt.22624] [PMID]##Hu JN, Yang JY, Jiang S, Zhang J, Liu Z, Hou JG, et al. Panax quinquefolium saponins protect against cisplatin evoked intestinal injury via ROS-mediated multiple mechanisms. Phytomedicine. 2021; 82:153446. [DOI:10.1016/j.phymed.2020.153446] [PMID]##Nazari A, Mirian M, Aghaei M, Aliomrani M. 4-Hydroxyhalcone effects on cisplatin-induced genotoxicity model. Toxicol Res. 2021; 10(1):11-7. [DOI:10.1093/toxres/tfaa091] [PMID] ##Said Salem NI, Noshy MM, Said AA. Modulatory effect of curcumin against genotoxicity and oxidative stress induced by cisplatin and methotrexate in male mice. Food Chem Toxicol. 2017; 105:370-6. [DOI:10.1016/j.fct.2017.04.007] [PMID]##Blasiak J, Trzeciak A, Malecka-Panas E, Drzewoski J, Wojewódzka M. In vitro genotoxicity of ethanol and acetaldehyde in human lymphocytes and the gastrointestinal tract mucosa cells. Toxicol In Vitro. 2000; 14(4):287-95. [DOI:10.1016/S0887-2333(00)00022-9] [PMID]##Singh M, Kaur P, Sandhir R, Kiran R. Protective effects of vitamin E against atrazine-induced genotoxicity in rats. Mutat Res. 2008; 654(2):145-9. [DOI:10.1016/j.mrgentox.2008.05.010] [PMID]##Anderson D, Yu TW, Phillips BJ, Schmezer P. The effect of various antioxidants and other modifying agents on oxygen-radical-generated DNA damage in human lymphocytes in the COMET assay. Mutat Res. 1994; 307(1):261-71. [DOI:10.1016/0027-5107(94)90300-X] [PMID]##Hosseinimehr SJ, Izakmehri M, Ghasemi A. In vitro protective effect of atorvastatin against ionizing radiation induced genotoxicity in human lymphocytes. Cell Mol Biol. 2015; 61(1):68-71. [PMID]##Shaghaghi Z, Alvandi M, Farzipour S, Dehbanpour MR, Nosrati S. A review of effects of atorvastatin in cancer therapy. Med Oncol. 2022; 40(1):27. [DOI:10.1007/s12032-022-01892-9] [PMID]##Zhang XB, Cheng HJ, Yuan YT, Chen Y, Chen YY, Chiu KY, et al. Atorvastatin attenuates intermittent hypoxia-induced myocardial oxidative stress in a mouse obstructive sleep apnea model. Aging. 2021; 13(14):18870-8. [DOI:10.18632/aging.203339] [PMID] ##Ghoreshi ZA, Kabirifar R, Khodarahmi A, Karimollah A, Moradi A. The preventive effect of atorvastatin on liver fibrosis in the bile duct ligation rats via antioxidant activity and down-regulation of Rac1 and NOX1. Iran J Basic Med Sci. 2020; 23(1):30-5. [DOI:10.22038/IJBMS.2019.33663.8047] [PMID]##Sahebkar A, Foroutan Z, Katsiki N, Jamialahmadi T, Mantzoros CS. Ferroptosis, a new pathogenetic mechanism in cardiometabolic diseases and cancer: Is there a role for statin therapy? Metabolism. 2023; 146:155659. [DOI:10.1016/j.metabol.2023.155659] [PMID]##Kadhim SS, Al-Windy SA, Al-Nami MS, Al Kuraishy HM, Al Gareeb AI. Statins improve periodontal disease-induced inflammatory changes and associated lipid peroxidation in patients with dyslipidemia: Two birds by one stone. J Int Oral Health. 2020; 12(1):66-73. [DOI:10.4103/jioh.jioh_194_19]##Najah R, Mohammad A, Ammar R. Effect of atorvastatin on oxidative stress parameters and lipid profile in type 2 diabetic patients. IIUM Med J Malaysia. 2008; 7(2):43-50. [DOI:10.31436/imjm.v7i2.783]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Antibacterial Activity and Phytochemical Analysis of Plantago lanceolata Root Petroleum Ether and Aqueous Extracts</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Plantago lanceolata L., a perennial plant of the Plantaginaceae family, is widely distributed across various regions. It is used globally for multiple purposes, including medicinal treatments, food additives, cosmetics, and industrial applications.&#160;
Objectives: This study aimed to investigate the antimicrobial activity and phytochemical profile of root extracts of P. lanceolata.&#160;
Methods: Antibacterial activity was assessed using petroleum ether and aqueous extracts of P. lanceolata roots. The antibacterial activity was assessed using disc diffusion and microtiter broth dilution assays to determine the minimum inhibitory concentration (MIC). Additionally, the minimum bactericidal concentrations (MBCs) were evaluated by culturing the samples on agar media. Gas chromatography-mass spectrometry (GC-MS) was also employed to identify the chemical constituents present in the extracts.&#160;
Results: The petroleum ether extract exhibited the strongest antimicrobial effect, producing an inhibition zone of 15.50 mm against Proteus vulgaris (PTCC 1182). The lowest MIC of 2 mg/mL was observed for both P. vulgaris and Bacillus cereus (ATCC 11778) with this extract, while minimum bactericidal concentration (MBC) values confirmed effectiveness at 3 mg/mL. Chemical analysis revealed that hexadecanoic acid ethyl ester (16.15%) and hexadecanoic acid, methyl ester (5.03%) were the predominant compounds in the petroleum ether extract. In contrast, the aqueous extract contained major artifactual components, such as 3-methoxy-2, 2-dimethyloxirane (30.78%).&#160;
Conclusion: P. lanceolata roots show promise as a natural antibacterial agent with potential applications across pharmaceutical, chemical, food, and medicinal industries. The antibacterial efficacy of the extracts is supported by the identification of active compounds through GC-MS analysis.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>37</FPAGE>
			<TPAGE>48</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/05/12025/09/242025/01/272025/06/29
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/4/8
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/12/22026/02/142025/12/132026/01/5
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/10/15
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Samaneh</Name>
				<MidName></MidName>
				<Family>Rahamouz-Haghighi</Family>
				<NameE>Samaneh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rahamouz-Haghighi</FamilyE>
				<Organizations>
				<Organization>Agricultural Research, Education and Extension Organization (AREEO), Mashhad, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>rahamouz_haghighi.s@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Disc diffusion method</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Gas chromatography-mass spectrometry (GC-MS)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Microtiter broth dilution</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Minimum inhibitory concentrations (MICs)</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Plantago lanceolata</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Ribwort plantain</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abate L, Bachheti RK, Tadesse MG, Bachheti A. Ethnobotanical uses, chemical constituents, and application of Plantago lanceolata L. J Chem. 2022; 2022:1532031. [DOI:10.1155/2022/1532031]##Pol M, Schmidtke K, Lewandowska S. Plantago lanceolata-An overview of its agronomically and healing valuable features. Open Agric. 2021; 6(1):479-88. [DOI:10.1515/opag-2021-0035]##Pandita D, Pandita A, Pandita S. Cytogenetic exploration of P. lanceolata L. Linn.: The soldier’s herb, in Jammu &#38; Kashmir (India). Int J Bioassays. 2015; 4:4241-6. [Link]##Boudjelal A, Henchiri C, Sari M, Sarri D, Hendel N, Benkhaled A, et al. Herbalists and wild medicinal plants in M&#039;Sila (North Algeria): An ethnopharmacology survey. J Ethnopharmacol. 2013; 148(2):395-402. [DOI:10.1016/j.jep.2013.03.082] [PMID]##Aziz MA, Adnan M, Khan AH, Shahat AA, Al-Said MS, Ullah R. Traditional uses of medicinal plants practiced by the indigenous communities at Mohmand Agency, FATA, Pakistan. J Ethnobiol Ethnomed. 2018; 14(1):2. [DOI:10.1186/s13002-017-0204-5] [PMID] ##Grigore A, Bubueanu C, Pirvu L, Ionita L, Toba G. Plantago lanceolata L. crops-source of valuable raw material for various industrial applications. Scient. Papers-Series A Agron. 2015; 58:207-14. [Link]##Ahmad M, Sultana S, Fazl-i-Hadi S, Ben Hadda T, Rashid S, Zafar M, et al. An ethnobotanical study of medicinal plants in high mountainous region of Chail valley (District Swat-Pakistan). J ethnobiol Ethnomed. 2014; 10:1-18. [DOI:10.1186/1746-4269-10-36] [PMID] ##Mazzutti S, Riehl CA, Ibañez E, Ferreira SR. Green-based methods to obtain bioactive extracts from Plantago major and Plantago lanceolata. J Supercrit Fluids. 2017; 119:211-20. [DOI:10.1016/j.supflu.2016.09.018]##Rahamouz-Haghighi S, Bagheri K, Mohsen-Pour N, Sharafi A. Quantitative determination of apigenin, catalpol, and gallic acid in total extracts from different parts of Plantago species by high-performance liquid chromatography. 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Antibacterial and antifungal efficacy of fatty acid methyl esters from the leaves of Sesuvium portulacastrum L. Eur Rev Med Pharmacol Sci. 2011; 15(7):775-80. [Link]##Arora S, Kumar G, Meena S. Screening and evaluation of bioactive components of Cenchrus ciliaris L. by GC-MS analysis. Int Res J Pharm. 2017; 8:69-76. [DOI:10.7897/2230-8407.08699]##Subavathy P, Thilaga RD. GC-MS analysis of bioactive compounds from whole body tissue methanolic extract of Cypraea arabica (L. 1758). World J Pharm Res. 2016; 5(3):800-6. [Link]##Manivannan P, Muralitharan G, Balaji NP. Prediction aided in vitro analysis of octa-decanoic acid from Cyanobacterium Lyngbya sp. as a proapoptotic factor in eliciting anti-inflammatory properties. Bioinformation. 2017; 13(9):301. [DOI:10.6026/97320630013301] [PMID] ##Barathikannan K, Venkatadri B, Khusro A, Al-Dhabi NA, Agastian P, Arasu MV, et al. Chemical analysis of Punica granatum fruit peel and its in vitro and in vivo biological properties. BMC Complement Altern Med. 2016; 16:1-10. [DOI:10.1186/s12906-016-1237-3] [PMID] ##Akpuaka A, Ekwenchi MM, Dashak DA, Dildar A. Biological activities of characterized isolates of n-hexane extract of Azadirachta indica A. Juss (Neem) leaves. Nat Sci. 2013; 11(5):141-7. [Link]##Mujeeb F, Bajpai P, Pathak N. Phytochemical evaluation, antimicrobial activity, and determination of bioactive components from leaves of Aegle marmelos. Biomed Res Int. 2014; 2014:497606. [DOI:10.1155/2014/497606] [PMID] ##Kumar D, Karthik M, Rajakumar R. GC-MS analysis of bioactive compounds from ethanolic leaves extract of Eichhornia crassipes (Mart) Solms. and their pharmacological activities. Pharma Innov J. 2018; 7(8):459-62. [Link]##Agoramoorthy G, Chandrasekaran M, Venkatesalu V, Hsu M. Antibacterial and antifungal activities of fatty acid methyl esters of the blind-your-eye mangrove from India. Braz J Microbiol. 2007; 38(4):739-42. [DOI:10.1590/S1517-83822007000400028]## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Characterization and Antimicrobial Activity of Biosynthesized Iron (III) Oxide Nanoparticles Stabilized by Luffa cylindrica Extract</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: The search for environmentally friendly nanomaterials with strong antimicrobial activity has generated growing interest in using plants to produce nanoparticles.
Objectives: This study aimed to biosynthesize and characterize iron (III) oxide (Fe2O3) nanoparticles stabilized by Luffa cylindrica extract and assess their antimicrobial properties.&#160;
Methods: The biosynthesized Fe2O3 nanoparticles were characterized using ultraviolet&#8211;visible (UV&#8211;Vis) spectroscopy, Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy to elucidate their optical, structural, morphological, and elemental properties.
Results: The formation of Fe2O3 nanoparticles was confirmed by standard absorbance at 370 nm and functional groups attributed to the capping and stabilization observed via FTIR. XRD patterns showed a crystalline rhombohedral phase, and SEM images indicated that the nanoparticles were uniformly dispersed with diameters of 20-50 nm. Nanoparticle efficacy was tested using the agar well diffusion method against a panel of gram-positive and gram-negative bacterial strains and fungal pathogens. The results revealed substantial dose-dependent antimicrobial activity, with greater inhibitory activity against Staphylococcus aureus, Escherichia coli, and Candida albicans, indicating potential broad-spectrum antimicrobial activity.&#160;
Conclusion: This study highlights the potential of L. cylindrica-mediated Fe2O3 nanoparticles as sustainable and effective antimicrobial agents with potential application in the biomedical, pharmaceutical, and environmental fields.&#160;</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>49</FPAGE>
			<TPAGE>60</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/05/12025/09/242025/01/272025/06/292025/08/8
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/5/17
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/12/22026/02/142025/12/132026/01/52026/01/5
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/10/15
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Azaki Gideon</Name>
				<MidName></MidName>
				<Family>Philip</Family>
				<NameE>Azaki Gideon</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Philip</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, School of Physical Sciences, Federal University of Technology, Minna, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>azakigideon@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Adamu Makanta</Name>
				<MidName></MidName>
				<Family>Salihu</Family>
				<NameE>Adamu Makanta</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Salihu</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, School of Physical Sciences, Federal University of Technology, Minna, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>a.salihu@futminna.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fadipe Labake</Name>
				<MidName></MidName>
				<Family>Ajoke</Family>
				<NameE>Fadipe Labake</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ajoke</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, School of Physical Sciences, Federal University of Technology, Minna, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>labake.fadipe@futminna.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shaba Elijah</Name>
				<MidName></MidName>
				<Family>Yanda</Family>
				<NameE>Shaba Elijah</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Yanda</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, School of Physical Sciences, Federal University of Technology, Minna, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>elijah.shaba@futminna.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Agbai Uche</Name>
				<MidName></MidName>
				<Family>Timothy</Family>
				<NameE>Agbai Uche</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Timothy</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry and Biochemistry, College of Engineering and Physical Sciences, University of New Hampshire, Durham, United States.</Organization>
				</Organizations>
				<Countries>
				<Country>United States</Country>
				</Countries>
				<EMAILS>
				<Email>ekoyanuche111@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>James</Name>
				<MidName></MidName>
				<Family>Daniel</Family>
				<NameE>James</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Daniel</FamilyE>
				<Organizations>
				<Organization>Wuhan Institute of Virology, University of Chinese Academy of Sciences, Beijing, China.</Organization>
				</Organizations>
				<Countries>
				<Country>China</Country>
				</Countries>
				<EMAILS>
				<Email>jamesonykachi084@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Suleiman</Name>
				<MidName></MidName>
				<Family>Rahmat</Family>
				<NameE>Suleiman</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rahmat</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, School of Physical Sciences, Federal University of Technology, Minna, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>suleimanrahmat67@futminna.edu.ng</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Iron oxides</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Nanoparticles</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Plant extracts</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antibacterial agents</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Biological products</KeyText>
			</KEYWORD>
		</KEYWORDS>

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

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Exploring the Ethical Dimensions of Telepharmacy in Iran: A Focus Group Discussion Study</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Telepharmacy is the use of telecommunication technology to remotely provide pharmacy services, such as medication review, drug therapy monitoring, and patient counseling. It is particularly important for individuals who are physically or geographically isolated from pharmacies, such as those living in rural areas or with disabilities. With the COVID-19 pandemic, the importance of telepharmacy has increased dramatically. However, the use of technology without considering its ethical dimensions can have negative consequences.&#160;
Objectives: This study aimed to explore the ethical dimensions of telepharmacy through focus group discussion (FGD).
Methods: In this study, 15 experienced and knowledgeable pharmacists in the field of telepharmacy were selected and engaged in focused group discussions in three five-person sessions lasting 60-90 minutes. Subsequently, the ethical concerns raised by the participants about telepharmacy services were extracted and analyzed. After data analysis, results on the ethical dimensions of telepharmacy and suggested strategies to address these issues were reported.&#160;
Results: After a thorough analysis of the participants&#8217; comments, we identified 10 general themes and their subcategories related to the ethical dimensions of telepharmacy. Throughout the discussions, we identified that the most controversial themes were broadly classified into four key ethical dimensions: patient-pharmacist relationship, privacy and data, impersonal care, and access disparities.
Conclusion: Based on focus-group data from practicing pharmacists in Iran, we identified three empirically grounded ethical priorities for clinical telepharmacy: protecting the therapeutic pharmacist&#8211;patient relationship, ensuring data privacy and security, and clarifying professional liability. We recommend standardized informed-consent templates, platform security certification, and regulatory guidance to address these priorities.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>61</FPAGE>
			<TPAGE>70</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2025/05/12025/09/242025/01/272025/06/292025/08/82025/11/10
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1404/8/19
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2025/12/22026/02/142025/12/132026/01/52026/01/52026/01/28
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1404/11/8
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Elnaz</Name>
				<MidName></MidName>
				<Family>Zoghi</Family>
				<NameE>Elnaz</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Zoghi</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pharmacy, School of Pharmacy, Tabriz University of Medical Sciences, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>elnaz.zoghii@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Saeed</Name>
				<MidName></MidName>
				<Family>Mohammad Soleymani</Family>
				<NameE>Saeed</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mohammad Soleymani</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pharmacy, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mamsoloni@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hadi</Name>
				<MidName></MidName>
				<Family>Esmaily</Family>
				<NameE>Hadi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Esmaily</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pharmacy, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>esmaily_hadi@sbmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Telepharmacy</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Telemedicine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Ethics</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pharmacy</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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	</ARTICLE>

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