Authentication and Quality Evaluation of Herbal Crude Drugs from Indian Markets

IF 1.2 4区 综合性期刊 Q3 MULTIDISCIPLINARY SCIENCES
Talat Anjum, V. Narsimhaji, Shevita Pandita,  Yashoda,  Shiddhamallayya, Sanjay K. Singh, N. Srikant
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Abstract

Medicinal plants or chemical substances derived from plants are the source of therapeutic ingredients considered important drugs currently in use in the world. In India, the AYUSH system has been included in mainstream healthcare and all these traditional systems of medicine rely on herbal crude drugs. Trading in dried raw plant drugs with no traceability to their origin is quite common in Indian markets. The safety, potency and efficacy of herbal drugs depend upon the use of standardized crude raw drugs. Present study serves as baseline information for herbal drug regulatory authorities to have strict guidelines on the sale of crude drugs and also the need for implementation of Good Agricultural and Collection Practices (GACP). In the present study, 295 market samples of 102 crude drugs were studied for quality standards and genuineness. It was found that 17% of the crude market samples were adulterated and 83% were botanically correct species, as these complied with diagnostic macro-microscopical characters of authentic crude drugs. However, the qualitative analysis indicated that the foreign matter, total ash, acid insoluble ash, and water soluble extractive values of these market samples deviated from authentic samples by 5% to > 15%, indicating thereby that samples collected from market may differ in collection time, storage practices like drying process, storage, time /season of collection and geography which may affect its pharmaceutical quality.

Abstract Image

印度市场草药原药的鉴定和质量评估
药用植物或从植物中提取的化学物质是治疗成分的来源,被视为目前世界上使用的重要药物。在印度,AYUSH 系统已被纳入主流医疗保健,所有这些传统医学系统都依赖于草药原药。在印度市场上,无法追溯来源的干燥植物原药交易相当普遍。草药的安全性、效力和疗效取决于标准化原生药物的使用。本研究为草药监管部门提供了基准信息,以便对粗制药物的销售制定严格的指导方针,同时也说明了实施良好农业和采集规范(GACP)的必要性。在本研究中,对 102 种原药的 295 个市场样本进行了质量标准和真实性研究。结果发现,17% 的市场粗制样品掺假,83% 的样品是植物学上正确的品种,因为这些样品符合真实粗制药物的宏观显微诊断特征。然而,定性分析表明,这些市场样品的异物、总灰分、酸不溶性灰分和水溶性萃取值与正宗样品的偏差在 5%至 15%之间,这表明从市场采集的样品可能在采集时间、储存方法(如干燥过程、储存)、采集时间/季节和地理位置等方面存在差异,从而影响其药品质量。
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来源期刊
National Academy Science Letters
National Academy Science Letters 综合性期刊-综合性期刊
CiteScore
2.20
自引率
0.00%
发文量
86
审稿时长
12 months
期刊介绍: The National Academy Science Letters is published by the National Academy of Sciences, India, since 1978. The publication of this unique journal was started with a view to give quick and wide publicity to the innovations in all fields of science
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