An Analytical Study for Validation and Standardization of Vati.

Jagriti Sharma, Pooja Swami
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Abstract

Introduction-Traditional medicine has a long history of serving people all over the world. Today the world is looking towards the Ayurveda with great hope and faith. With these new challengesemerges in the form of queries of the modern man who would have a right to know about the drug he is consuming. To meet this new trust of inquisitiveness, standard of drugs of Indian System of Medicine is mandatory. In the process of assurance, to ascertain the prepared product is full proof and without any defects, these prepared products need to undergo several analytical parameters concerned to them and get clearance. This article is a step to standardized and validate the ayurvedic formulation through analytical study. Material and methods-The drugs selected for study are one of the mahakashaya Dasemani –Angamardha Prashaman Dasemanidescribed in Charak Samhita Sutra Sthanand Bhagottar Gutikaa Herbo-mineral formulation is from Bhaishajya Ratnavali. The various parameters studies are or organoleptic characters, physicochemical parameters of vatilike disintegration, friability, loss on drying, acid insoluble ash, water soluble ash etc. and microbial contamination.Results –All the parameters studied are within the limits and hence validate the safely and effectively use ofvati.Conclusion Analytical study of a product provides standards to judge its quality. It is useful to decide future work plan and objective parameters to know the exact status of drug by conducting the comparative study of various samples during drug preparation
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Vati验证与标准化的分析研究。
传统医学在世界各地为人们服务有着悠久的历史。今天,世界对阿育吠陀充满了希望和信心。随着这些新的挑战的出现,现代人有权利知道他正在服用的药物。为了满足这种新的好奇心,印度医学体系的药物标准是强制性的。在保证过程中,为了确定制备的产品是完全证明,没有任何缺陷,这些制备的产品需要经过几个与它们有关的分析参数并获得许可。本文是通过分析研究来规范和验证阿育吠陀配方的一步。材料和方法:所选药物为《查拉克三经》中所述的大伽沙雅-安伽玛达- Prashaman Dasemani》中的一种,而Bhagottar Gutikaa草药矿物配方来自Bhaishajya Ratnavali。各种参数的研究包括感官特性、各种崩解、脆性、干燥损失、酸不溶灰分、水溶性灰分等理化参数和微生物污染等。结果:所研究的所有参数均在限定范围内,从而验证了vati的安全有效使用。结论对产品进行分析研究,为产品质量的判断提供了依据。在药物制备过程中对各种样品进行对比研究,有助于确定今后的工作计划和客观参数,了解药物的确切状态
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