mohharam valizadeh
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امروزه، نانوذرات نقره یکی از مهمترین نانومواد تجاری محسوب می شوند. تقاضا برای سنتز نانوذرات از طریق روش های زیست سازگار به دلیل کاربرد گسترده در زمینه زیست پزشکی در حال افزایش است. استفاده از گیاهان و محصولات گیاهی به عنوان منابع پایدار و تجدیدپذیر در سنتز نانوذرات از سایر روش های سنتز بیولوژیکی سودمندتر است. در این مطالعه بیوسنتز نانوذرات نقره با استفاده از عصاره آبی گیاه پنیرباد بعنوان عامل کاهنده گزارش می شود. پارامتر های موثر بر بیوسنتز نانوذرات شامل حجم عصاره، غلظت نمک نیترات نقره، اثر pH و زمان واکنش توسط تکنیک اسپکتروسکوپی فرابنفش_ مریی بررسی و بهینه سازی شدند. تغییر رنگ محلول از زرد روشن به قهوه ای تیره در دمای اتاق به دلیل کاهیدگی یون های نقره مشاهده شد. اندازه و مورفولوژی نانوذرات به وسیله میکروسکوپ الکترون عبوری تعیین گردید که ذراتی با ساختار کروی و اندازه متوسط در حدود 35-24 نانومتر را نشان می دهد.
کلید واژگان: بیوسنتز, نانوذرات نقره, گیاه پنیرباد, اسپکتروفتومتریToday, nanosilver is one of the most commercialized nanomaterials. The demand for synthesis of Nanosilver through biocompatible routs due to wide biomedical application has increased. Use of plants and plant products as sustainable and renewable resources in the synthesis of nanoparticles is more advantageous over other biological routes. In this study, biosynthesis of silver nanoparticles (AgNPs) using aqueous extract of Withania somnifera as reducing agent is reported. Effect of parameters such as AgNO3 concentration, aqueous extract, pH and formation time were investigated and optimized by UV-visible spectroscopy in the synthesis of nanoparticles. At room temperature, the solution color started to change from pale yellow to dark brown due to the reduction of silver ion. The transmission electron microscopy (TEM) was applied for size and morphological analysis of nanoparticles. TEM result shows a spherical structure with an average size ranging from 24-35 nm for silver nanoparticles.
Keywords: Biosynthesis, silver nanoparticles, Withania somnifera, spectrophotometry -
ObjectiveOxygen free radicals may be implicated in the pathogenesis of ischemia reperfusion damage. The beneficial effects of antioxidant nutrients, as well as complex plant extracts, on cerebral ischemia-reperfusion injuries are well known. This study was conducted to determine the effects of the hydro-alcoholic root extract of Withania coagulans on CA1 hippocampus oxidative damages following global cerebral ischemia/reperfusion in rat.Materials And MethodsMale Wistar rats were randomly divided in five groups: control, sham operated, Ischemia/ Reperfiusion (IR), and Withania Coagulans Extract (WCE) 500 and 1000mg/kg I/R groups. Ischemia was induced by ligation of bilateral common carotid arteries for 30 min after 30 days of WCE administration. Three days after, the animals were sacrificed, their brains were fixed for histological analysis (NISSL and TUNEL staining) and some samples were prepared for measurement of malondialdehyde (MDA) level and superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) activity in hippocampus.ResultsWCE showed neuroprotective activity by significant decrease in MDA level and increase in the SOD, CAT and GPx activity in pretreated groups as compared to I/R groups (pConclusionWCE showed potent neuroprotective activity against oxidative stress-induced injuries caused by global cerebral ischemia/ reperfusion in rats probably by radical scavenging and antioxidant activities.Keywords: Withania coagulans, Antioxidant enzymes, Hippocampus, Ischemia, Rat
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BackgroundBenign prostate hyperplasia (BPH) is a common urological disorder in elderly men. Phytotherapy is frequently used to alleviate the symptoms of this condition.ObjectivesThe present study investigated the effect of Withania coagulans extract (WCE), which is known to have antioxidant, anti-inflammatory, antihyperglycemic, and anti-cancer properties, on testosterone-induced BPH in rats.Materials And MethodsForty Wistar rats were divided into five groups (each n = 8): the control group, the untreated BPH group, and three WCE-treated groups (WCE250, 500, and 1000). BPH was induced with 3 mg/kg subcutaneous injections of testosterone propionate for four weeks. WCE was concomitantly administrated by oral gavage. At the end of the induction schedule, the animals were sacrificed and their prostate glands were dissected, weighed, and fixed for histological examination (H&E and proliferating cell nuclear antigen [PCNA] staining). Half of each sample was prepared for measurement of malondialdehyde (MDA) and total antioxidant capacity (TAC) levels in the prostate.ResultsThe present study revealed that BPH caused elevation of MDA levels, suppression of TAC levels, and increased PCNA expression in the prostate gland. Interestingly, in a dose-dependent manner, WCE caused decreased MDA levels and increased TAC levels in the prostate gland, compared to the untreated BPH group. Histopathological examinations showed a reduction in PCNA expression in the prostate epithelium of the WCE animals.ConclusionsW. coagulans inhibits the development of BPH can be useful for the treatment of this condition.Keywords: Benign Prostatic Hyperplasia, Proliferating Cell Nuclear Antigen, Rats, Withania coagulans
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