Formulation of Silver Nanoparticle of Cassia angustifoliaby Using Green Synthesis Method and Screening for In-Vitro Anti-Inflammatory Activity

Priyanka Annaso. Patil, Shubdha Dalvi, Vishwajit D. Dhaygude, Sanmati D. Shete
{"title":"Formulation of Silver Nanoparticle of Cassia angustifoliaby Using Green Synthesis Method and Screening for In-Vitro Anti-Inflammatory Activity","authors":"Priyanka Annaso. Patil, Shubdha Dalvi, Vishwajit D. Dhaygude, Sanmati D. Shete","doi":"10.35652/igjps.2022.12022","DOIUrl":null,"url":null,"abstract":"The main objectives in developing nanoparticles as a delivery system are to manage particle size, surface characteristics, and the release of pharmacologically active substancesto achieve the drug's site-specific action at the appropriate rate and dose. They can help boost medication stability and have helpful controlled release features, for example.Nowadays researchers are movingtowards the green chemistry approach which is an alternative routethat is eco-friendly, cheap and fast; in that plant extracts and microorganisms are used in the reduction of the metal salt which is fast gaining demand in the field of nanobiotechnology. In this study, silver nitrate was reduced to its “nanosilver form”through a one-step synthesis protocol using an extract of Cassia Angustifolia.Three different batches namely batch A, B, C of varying temperature and another three batches namely D,E,F of varying pH were synthesized. The prepared nanoparticles were optimized and characterized by practical yield determination, drug entrapment efficiency, particle size determination and measurement of zeta potential. The synthesized nanoparticles were screened for in vitro anti-inflammatory activity.Result found that the percentage practical yield of synthesized nanoparticles waswithin the range of 6.41-52.61%. The drug entrapment efficiency was found to be 99.875%. AgNPs inhibited protein denaturation and showed 75.52% inhibition at 500μg ml-1 whereas standard drug Aspirin exhibited 65.03% protein denaturation.©2022iGlobal Research and PublishingFoundation. All rights reserved.","PeriodicalId":13366,"journal":{"name":"Indo Global Journal of Pharmaceutical Sciences","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indo Global Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35652/igjps.2022.12022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

The main objectives in developing nanoparticles as a delivery system are to manage particle size, surface characteristics, and the release of pharmacologically active substancesto achieve the drug's site-specific action at the appropriate rate and dose. They can help boost medication stability and have helpful controlled release features, for example.Nowadays researchers are movingtowards the green chemistry approach which is an alternative routethat is eco-friendly, cheap and fast; in that plant extracts and microorganisms are used in the reduction of the metal salt which is fast gaining demand in the field of nanobiotechnology. In this study, silver nitrate was reduced to its “nanosilver form”through a one-step synthesis protocol using an extract of Cassia Angustifolia.Three different batches namely batch A, B, C of varying temperature and another three batches namely D,E,F of varying pH were synthesized. The prepared nanoparticles were optimized and characterized by practical yield determination, drug entrapment efficiency, particle size determination and measurement of zeta potential. The synthesized nanoparticles were screened for in vitro anti-inflammatory activity.Result found that the percentage practical yield of synthesized nanoparticles waswithin the range of 6.41-52.61%. The drug entrapment efficiency was found to be 99.875%. AgNPs inhibited protein denaturation and showed 75.52% inhibition at 500μg ml-1 whereas standard drug Aspirin exhibited 65.03% protein denaturation.©2022iGlobal Research and PublishingFoundation. All rights reserved.
绿色合成法制备消炎决明子纳米银颗粒及体外抗炎活性筛选
开发纳米颗粒作为递送系统的主要目标是管理颗粒大小,表面特性和药理活性物质的释放,以适当的速率和剂量实现药物的位点特异性作用。例如,它们可以帮助提高药物稳定性,并具有有益的控制释放功能。如今,研究人员正朝着绿色化学的方向发展,这是一种环保、廉价和快速的替代途径;其中,植物提取物和微生物被用于金属盐的还原,金属盐在纳米生物技术领域的需求迅速增加。本研究以决明子提取物为原料,通过一步合成工艺将硝酸银还原为“纳米银形态”。合成了A、B、C三个不同温度的批次和D、E、F三个不同pH的批次。对制备的纳米颗粒进行了优化,并通过实际产率测定、药物包封效率测定、粒径测定和zeta电位测定对其进行了表征。对合成的纳米颗粒进行体外抗炎活性筛选。结果表明,合成的纳米颗粒的实际产率在6.41 ~ 52.61%之间。药物包封效率为99.875%。AgNPs抑制蛋白质变性,500μg ml-1时的抑制率为75.52%,而标准药物阿司匹林的蛋白质变性率为65.03%。©2022全球研究与出版基金会。版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信