ORIGINAL_ARTICLE
Plant cells technology as an effective biotechnological approach for high scale production of pharmaceutical natural compounds; A meta-analysis study
Natural-based drugs are the important bioactive substances that have been used for prevention and treatment of diseases. Natural products should be prepared in commercial scale from relevant medicinal plants. Hence, large amounts of the plants have been needed for extraction and isolation of compounds of natural origin. Plant cells technology is the best strategy for the production of the plant-derived drugs, which have difficulty in high scale preparation. This study was conducted for types, frequencies and efficacies of production methods for natural-based drugs in plant cell technology as alternative method to whole herb. Pharmaceutical and biomedical databases including PubMed/Medline, Scopus, Web of Science, Embase, ProQuest and Google Scholar were searched in this study. Moreover, keywords words were ''secondary metabolite production'', ''pharmaceutical natural compounds'', ''high scale production'', ''cell suspension'', ''immobilized plant cell'', “hairy root”, ''elicitor'', ''substrate'', ''plant cell'', ''callus'', ''medicinal plants'', ''isolation and purification''. The correlations have been investigated by random effect model in an Excel program. Findings of this meta-analysis study showed all production methods had high efficacies and percentages of high scale production from 90 to 100%, which were comparable with conventional direct extractions. In addition to, median efficacy values for cell suspension, callus, hairy root and immobilized plant cell methods in production of selected drugs (atropine, paclitaxel, vincristine, camptothecin and colchicine) with 1124, 257, 797 and 969 events were 92.49 (CI95%: 89.78-95.86), 91.98 (CI95%: 89.13-95.25), 95.69 (CI95%: 92.84-98.68) and 93.86% (CI95%: 91.12-96.35), respectively. The plant cell technology for production of secondary metabolites has various advantages including high accuracy, repeatability and productivity, that is a best strategy for production of natural-based drugs.
http://pbr.mazums.ac.ir/article-1-234-en.pdf
2019-04-23
1
9
10.18502/pbr.v5i2.1579
Plant cell
hairy root
callus
immobilized cell
meta-analysis
Ali
Davoodi
adavoodi.pharm@gmail.com
1
Department of Pharmacognosy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran
AUTHOR
https://orcid.org/0000-0001-9456-4687
Elnaz
Khoshvishkaie
E_Kh.vishkaie@yahoo.com
2
Pharmaceutical Cares Department, Ayatollah Khamenei Hospital, Mazandaran University of Medical Sciences, Abbas Abad, Iran
AUTHOR
https://orcid.org/0000-0002-3546-9876
Mohammad
Azadbakht
azadbakt110@gmail.com
3
Department of Pharmacognosy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran
AUTHOR
https://orcid.org/0000-0001-4568-9425
ORIGINAL_ARTICLE
Edible films based on chitosan-flaxseed mucilage: in vitro antimicrobial and antioxidant properties and their application on survival of food-borne pathogenic bacteria in raw minced trout fillets
Various natural oils/extracts and their constituents incorporated into biopolymer-based edible films as a promising technology with the knowledge that these compounds have been able to reduce microbial growth and chemical changes of packed foodstuffs. The objective of this study was to evaluate the effect of incorporation of Ziziphora clinopodioides essential oil (ZEO; 0, 0.25 and 0.5%) and sesame oil (SO; 0, 0.5 and 0.75%) into chitosan-flaxseed mucilage (CH-FM) film against Listeria monocytogenes, Salmonella typhimurium, Staphylococcus aureus and Escherichia coli O157:H7 in vitro condition and raw minced trout fillets during refrigerated condition. The in vitro antibacterial and antioxidant properties of CH-FM films were evaluated using agar disk diffusion method and free radical scavenging activity assay, respectively. The most important constituents of ZEO were found to be carvacrol (65.22%), thymol (19.51%), ɣ-terpinene (4.63%) and p-cymene (4.86%). The lowest and highest antimicrobial effect against S. aureus, L. monocytogenes, E. coli O157:H7 and S. typhimurium were found for CH-FM films enriched with SO 0.5% (0.98-1.24 mm) and ZEO 0.5% + SO 0.75% (5.01-6.25 mm), respectively. The antioxidant property of CH-FM based films were found to be ranged 5.45% ± 0.04-37% ± 0.45. In treated trout fillets, the counts of L. monocytogenes, S. aureus, E. coli O157:H7 and S. typhimurium were 1.54-4.18, 0.34-3.35, 0.29-1.45 and 0.19-1.27 log CFU/g significantly lower than control groups after two weeks of refrigerated storage, respectively. The designated films had good antibacterial effect against some food borne pathogenic bacteria including L. monocytogenes, S. aureus, S. typhimurium and E. coli O157:H7 in raw rainbow trout fillets.
http://pbr.mazums.ac.ir/article-1-238-en.pdf
2019-09-28
10
16
10.18502/pbr.v5i2.1580
Chitosan
flaxseed mucilage
Ziziphora linopodioides essential oil
sesame oil
rainbow trout fillet
Negin
Karami
neginkarami87@gmail.com
1
Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, University of Tehran
AUTHOR
https://orcid.org/0000-0003-0329-0018
Abolfazl
Kamkar
a.kamkar@ut.ac.ir
2
Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, University of Tehran
AUTHOR
https://orcid.org/0000-0003-4001-2922
Yasser
Shahbazi
y.shahbazi@razi.ac.ir
3
Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, Razi University
AUTHOR
https://orcid.org/0000-0003-3306-2390
Ali
Misaghi
a.misaghi@ut.ac.ir
4
Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, University of Tehran
AUTHOR
https://orcid.org/0000-0002-0279-7784
ORIGINAL_ARTICLE
Floating microspheres encapsulating carvedilol for the effective management of hypertension
Carvedilol (CVD) is an antihypertensive agent with a short half-life, pH-dependent solubility, and narrow absorption window. The purpose of this research was to prepare a floating-drug delivery-system of carvedilol to increase its half-life. The present study investigates the preparation of carvedilol-floating microspheres, evaluates the floating-drug delivery-system (FDDS) (by scanning electron microscope), it’s in vitro stability, and in vivo profile. Floating microspheres were prepared by solvent-evaporation (oil-in-water emulsion) technique using hydroxypropyl methylcellulose (HPMC) and ethyl cellulose (EC) as the rate controlling polymers. The surface morphology of the prepared microspheres w:as char:acterized by scanning electron microscopy. In this study, the particle size analysis, drug entrapment efficiency, surface morphology, buoyancy percentage, and release studies were performed. The microspheres were found to be spherical and porous. The results showed that the mean/mean (SD) values of tapped density, Carr's compressibility index, angle of repose, percentage yield, in vitro buoyancy, %entrapment efficiency of CVD-loaded floating microspheres were 0.42 (0.012), 12.5 (1.895), 23.5 (1.856), 80.2 %, 79.0 %, and 85.81(1.40), respectively. The developed floating-microsphere of CVD released the drug for 24 h and based on in vivo studies, the drug-loaded floating microspheres help in maintaining the mean (SD) systolic blood pressure within the range of 120 (0.32) to 120 (1.02) mmHg and diastolic pressure within 91 (0.71) to 92 (0.79) mmHg. Thus, floating microsphere of CVD offers a suitable and practical approach for prolonged release of the drug over an extended period, and thus improves the oral bioavailability and efficacy of the drug as well as the patient’s compliance.
http://pbr.mazums.ac.ir/article-1-212-en.pdf
2019-09-28
17
24
10.18502/pbr.v5i2.1581
Floating microspheres
carvedilol
controlled release
gastric emptying time
in vitro release
Sapna
Patel
1
Sagar Institute of Pharmaceutical Sciences, Sagar (M.P), India
AUTHOR
https://orcid.org/0000-0002-0018-3121
Naina
Dubey
2
Sagar Institute of Pharmaceutical Sciences, Sagar (M.P), India
AUTHOR
https://orcid.org/0000-0001-5921-8694
Asmita
Gajbhiye
3
Department of Pharmaceutical Sciences, Dr H. S. Gour University, Sagar (M.P), India
AUTHOR
https://orcid.org/0000-0001-7180-379X
Shailendra
Patil
shailpatil27@rediffmail.com
4
SVN Institute of Pharmaceutical Sciences, Swami Vivekanand University, Sagar (M.P), India
AUTHOR
https://orcid.org/0000-0003-2986-8578
ORIGINAL_ARTICLE
Amlodipine and valsartan improving effect on the survival rate and deleterious pathological changes in streptozotocin-induced diabetic rats treated with metformin
Diabetes mellitus (DM) and hypertension usually co-exist, and when this happens, the prognosis would be worse than each disease alone. Given this, we evaluated the possible effects of valsartan and amlodipine administration on metformin-treated diabetic rats models induced by streptozotocin. Male Wistar rats (200–350 g) were fasted overnight. Then, we induced DM by administrating a single dose of 40 mg/kg streptozotocin (IP), which was confirmed after 48 h. Animals with blood sugar ≥ 200 mg/dl were considered diabetic and divided into four diabetic groups of untreated diabetic animals (Group B), diabetic animals treated with metformin (Group C), diabetic animals treated with metformin plus amlodipine (Group D), and diabetic rats treated with metformin plus valsartan (Group E). There was also a group A, consisting of normal rats with no drug treatment. After six weeks of treatment, we sacrificed the animals under chloroform anesthesia, and their blood samples were collected for hematological and biochemical analyses. The mortality rate in untreated diabetic rats was 100% before 6 weeks, but anti-diabetic treatment (metformin) significantly (P < 0.05) improved the survival rate and controlled their blood glucose level. The addition of antihypertensive drugs (amlodipine and valsartan) enhanced this curative effect. The various treated groups showed ameliorations in pathologic changes and biochemical indices, as well as, evidence of organ protection, compared with the untreated diabetic group. The study showed that adding an antihypertensive drug (amlodipine or valsartan) to metformin regimen improved outcomes in diabetic rats compared to using metformin alone.
http://pbr.mazums.ac.ir/article-1-246-en.pdf
2019-09-28
25
31
10.18502/pbr.v5i2.1582
Type 2 diabetes
biguanides
hypertension
calcium channel blockers
angiotensin II receptor blockers
Israel Olapeju
Bolanle
olapeju.bolanle@uniben.edu
1
Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Benin, Benin City, Nigeria
AUTHOR
https://orcid.org/0000-0002-4638-6522
Eric Kelly Inanemo
Omogbai
omog@uniben.edu
2
Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Benin, Benin City, Nigeria
AUTHOR
https://orcid.org/0000-0002-4638-6522
Enitome
Bafor
enitome.bafor@uniben.edu
3
Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Benin, Benin City, Nigeria
AUTHOR
https://orcid.org/0000-0002-5213-3177
ORIGINAL_ARTICLE
Effects of ethanol extract of the resin exudate of boswellia dalzielii hutch on pain in mice
This study aimed to determine the analgesic properties and the acute toxicity of Ethanol Extract of the Resin Exudate of Boswellia dalzielii (EERBD) in mice animal model. We used the writhing or acetic acid abdominal constriction, tail-immersion, and hot plate tests to assess the analgesic effect of EERBD at three doses (100, 200, and 400 mg/kg). To study the acute toxicity of EERBD, 24 female mice were divided into four groups (n=6) and were orally treated with EERBD at the doses of 0, 2000, 4000, and 5000 mg/kg, as per OECD (Organization for Economic Co-operation and Development) guidelines No. 420.
In the acetic acid-induced writhing reflex model, the EERBD ministration decreased the mean total number of writhes at the two doses (100 and 400 mg/kg), which were found highly significant (P<0.001) compared to control group. In the tail immersion model, the EERBD administration at the dose of 400 mg/kg significantly increased the pain reaction time (P<0.001 as compared to control) at 30 min, but another tested sample had no significant latency. In the hot-plate model, the drug extract created significant (P<0.001) increase in the latency period compared to the control group at oral doses of 100 and 400 mg/kg when compared to initial time and control group (4.5 ± 1.29 s) with protective effect from 4.25 ± 1.50 s after 30 min. Administration of EERBD at the dose of 200 mg/kg showed no significant analgesic activity based on writing, tail immersion, and hot-plate tests. The extract did not show toxicity signs or death at dose of less than 5000 mg/kg per oral. The results suggest that EERBD contain bioactive substances with analgesics effects; hence, it might be a better alternative to conventional drug therapy for pain management.
http://pbr.mazums.ac.ir/article-1-243-en.pdf
2019-09-28
32
37
10.18502/pbr.v5i2.1583
Writing
hot plate
tail immersion
acute toxicity
resins
Boswellia dalzielii
Jeweldai
Vedekoi
jeweldai2014@yahoo.fr
1
Department of Biological Sciences, Faculty of Science, University of Ngaoundéré, Ngaoundéré, Cameroon
AUTHOR
Sokeng
Dongmo Selestin
2
Department of Biological Sciences, Faculty of Science, University of Ngaoundéré, Ngaoundéré, Cameroon
AUTHOR
Koubé
Juliette
3
Departments of Animal Biology and Physiology, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon
AUTHOR
Kamtchouing
Pierre
4
Departments of pharmaceutical sciences, University of Douala, Douala, Cameroon
AUTHOR
ORIGINAL_ARTICLE
Computer-aided rational design of acyclovir analogs to inhibit purine nucleoside phosphorylase
Purine nucleoside phosphorylase (PNP) is one of the major enzymes in the purine salvage pathway. It is responsible for the elevation of deoxyguanosine, and thus considered as the potent target in T-cell lymphoma. The present study examined acyclovir, reported as a low-affinity PNP inhibitor, for the rational design of new acyclovir derivatives by incorporating halogens, hydroxyl, and bulky amino groups. The molecular actions of designed derivatives were investigated by employing density functional theory, molecular docking, and binding energy calculations. The results revealed that the newly designed compounds were highly stable and showed more affinity to PNP than the parent compound, acyclovir. The quantum mechanics and molecular docking studies suggested that modification of side chains with bulky polar groups provided better binding affinities than substitutions with halogens. The resultant derivatives have strong polar interactions like His257 and Tyr88. Furthermore, the designed derivatives were within the ideal range of ADMET (absorption, distribution, metabolism, elimination, and toxicity) analysis. Considering that, these findings recommend further validation of designed acyclovir derivatives in wet lab confirmatory analysis with the emphasis on the further improvements in the treatment of T-cell-mediated diseases.
http://pbr.mazums.ac.ir/article-1-252-en.pdf
2019-09-28
38
48
10.18502/pbr.v5i2.1584
Purine nucleoside phosphorylase
halogen
acyclovir
analogs
T-cell lymphoma
molecular docking simulation
Nusrat Jahan
Selsi
nusratjahan.selsi@gmail.com
1
Department of Pharmacy, University of Science and Technology Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0003-4752-3581
Lira
Barua
lira_barua@yahoo.com
2
Department of Chemistry, University of Chittagong, Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0002-0318-359X
Debpriya
Bhattacharjee
priyodeb143@gmail.com
3
Department of Pharmacy, University of Science and Technology Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0002-2945-0019
Gulamur
Rahman
pharmacisttanbir@gmail.com
4
Department of Pharmacy, University of Science and Technology Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0001-6563-3018
Syeda Sakiatuz
Zannat
syedaszannat@gmail.com
5
Department of Physics, Astronomy and Mathematics, Faculty of Science and Technology University of Central Lancashire, Lancashire, United Kingdom
AUTHOR
https://orcid.org/0000-0002-7001-768X
Najia Absar
Munia
najiaabsar98@gmail.com
6
Department of Pharmacy, BGC Trust University Bangladesh, Chandanaish, Bangladesh
AUTHOR
https://orcid.org/0000-0003-1983-4868
Rubaiyat
Fahad
rubaiyatfahad@gmail.com
7
Department of Pharmacy, University of Science and Technology Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0003-4499-4329
Tanjiba Harun
Bipasha
tanjiba.harun668@gmail.com
8
Department of Pharmacy, University of Science and Technology Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0001-5881-972X
Azizur
Rahman
jaber6449@gmail.com
9
Department of Pharmacy, Southern University Bangladesh, Chittagong, Bangladesh
AUTHOR
https://orcid.org/0000-0002-8252-3192
Raju
Dash
rajudash.bgctub@gamil.com
10
Department of Anatomy, Dongguk University Graduate School of Medicine, Gyeongju, Korea
AUTHOR
https://orcid.org/0000-0003-4128-5308
CASE_STUDY
A Case report of hemodynamic instability, cardiac arrest, and acute severe dyspnea subsequent to inhalation of crystal methamphetamine
Misuse of stimulants similar to amphetamine is a universal problem. These stimulants cause many complications in their abusers. However, myocardial infarction is rarely reported as a complication of amphetamine abuse. Herein, we report a man aged 42 years presented at the Emergency Department with the chief complaint of acute dyspnea following ice inhalation without history of dyspnea. Within the first hour and a half of admission, the patient was treated by nasal oxygen and bronchodilator aminophylline. However, he did not respond to the initial treatment and lost his consciousness; showed ventricular fibrillation, cardiac arrest, and hemodynamic instability. So, cardiopulmonary resuscitation was immediately initiated for him. The patient was intubated, mechanically ventilated. Also, the synchronized electrical shock was delivered 5 times (200-360 J) along with amiodarone (300 mg intravenously [IV] stat, then 1 mg/min IV infusion for 6 hours and next 0.5 mg/min for 18 hours) to treat the ventricular fibrillation. The arrhythmia was subsequently controlled, and his normal sinus rhythm was resumed. Two hours later, condition of the patient improved, and he was extubated. After two days, when the patient got stable, the echocardiography was performed, which was completely normal.
http://pbr.mazums.ac.ir/article-1-226-en.pdf
2019-09-28
49
52
10.18502/pbr.v5i2.1585
Crystal methamphetamine
severe dyspnea
cardiac arrest
ventricular fibrillation
hemodynamic instability
Farhad
Gholami
hosseinish20@gmail.com
1
Department of Internal Medicine, Faculty of Medicine, Mazandaran University of Medical Sciences
AUTHOR
https://orcid.org/0000-0002-1115-5003
Seyed Hamzeh
Hosseini
hosseinish20@gmail.com
2
Psychiatry and Behavioral Sciences Research Center, Addiction Institute, Mazandaran University of Medical Sciences, Sari, Iran
AUTHOR
https://orcid.org/0000-0001-7655-8869
Amirhossein
Ahmadi
amirhossein_pharma@yahoo.com
3
Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran
AUTHOR
https://orcid.org/0000-0002-9737-3633
Maryam
Nabati
dr.mr.nabati@gmail.com
4
Department of Cardiology, Cardiovascular Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
AUTHOR
https://orcid.org/0000-0002-2700-4074