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采用高效液相色谱法测定 Withaferin-A 并对 Ashwagandhadi lehyam 制剂进行标准化。

Estimation of Withaferin-A by HPLC and standardization of the Ashwagandhadi lehyam formulation.

作者信息

Meena Ajay Kumar, Rekha P, Perumal Ayyam, Gokul M, Swathi K N, Ilavarasan R

机构信息

Captain Srinivasa Murthy Regional Ayurveda Drug Development Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Government of India, Arumbakkam, Chennai, 106, India.

出版信息

Heliyon. 2021 Feb 2;7(2):e06116. doi: 10.1016/j.heliyon.2021.e06116. eCollection 2021 Feb.

Abstract

Standardization is an important measurement for ensuring the quality control of herbal drugs. It has become essential to develop reliable, specific and sensitive quality control methods. Ashwagandhadi lehyam is an important Ayurvedic formulation containing L., as one of the prime ingredient of formulation. The present study was undertaken to develop standardization parameters for Ashwagandhadi lehyam. Evaluation of various standardization parameters like organoleptic characters, Physico-chemical evaluation, HPTLC finger print profiling along with dominant bioactive markers and estimation of bioactive markers Withaferin-A by HPLC. The R value of Withaferin-A 0.35 and Withanolide-A 0.45 is in formulation and reference standards were found comparable under UV light at 254 nm and 540 nm. The HPLC chromatogram of Ashwagandhadi lehyam and standard Withaferin-A showed at Rt of 5.015 and 5.050 min. The percentage of Withaferin-A was 0.092% present in Ashwagandhadi lehyam formulation. Bioactive markers are characteristic to the ingredients or botanicals to identify the presence of ingredients in formulation easily. The presence of bioactive markers is possible and its verification through the HPTLC fingerprint profile and quantification of biomarker by HPLC are the best ways to identify evaluate the quality of the finished formulation in the course of development of a standardization protocol for quality control of Ayurvedic formulation.

摘要

标准化是确保草药质量控制的一项重要措施。开发可靠、特异且灵敏的质量控制方法已变得至关重要。阿育吠陀草药膏是一种重要的阿育吠陀配方制剂,其中包含印度人参(Withania somnifera),它是该配方的主要成分之一。本研究旨在制定阿育吠陀草药膏的标准化参数。对各种标准化参数进行评估,如感官特性、理化评估、高效薄层色谱指纹图谱分析以及主要生物活性标志物的鉴定,并通过高效液相色谱法测定生物活性标志物——睡茄内酯-A。在254nm和540nm紫外光下,制剂中睡茄内酯-A的Rf值为0.35,睡茄烷醇内酯-A的Rf值为0.45,且在制剂和对照品中结果相当。阿育吠陀草药膏和标准品睡茄内酯-A的高效液相色谱图显示,其保留时间分别为5.015分钟和5.050分钟。阿育吠陀草药膏制剂中睡茄内酯-A的含量为0.092%。生物活性标志物是成分或植物药的特征,有助于轻松鉴定制剂中成分的存在。生物活性标志物的存在是可能的,通过高效薄层色谱指纹图谱进行验证以及通过高效液相色谱法对生物标志物进行定量,是在制定阿育吠陀配方制剂质量控制标准化方案过程中鉴定和评估成品制剂质量的最佳方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb7a/7889947/9d00a4f64930/gr1.jpg

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