新型复方HYDALJSS08的研制与高效液相色谱分离,苦参干果中没食子酸的含量测定,以及已上市的复方“Kabusura Kudineer”

Q3 Pharmacology, Toxicology and Pharmaceutics
Ramkishan Jatoth, Dhanabal S.P, Duraiswamy Basavan, Venkatachalam Senthil, Thangavel Ganesh, Jubie Selvaraj, Jeyprakash M
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引用次数: 0

摘要

以悉达达为基础的多草药配方被称为“Kabusura Kudineer(已上市)”,含有15种干燥的植物原料,印度政府阿尤什部在2019冠状病毒病大流行期间高度认可使用“Kabusura Kudineer”,因为它具有增强免疫的特性。目前的研究旨在开发和记录一种分析策略,用于估计苦荞麦干果和多草药制剂(已上市,&开发)。开发的“HYDALJSS08”复方中药制剂中的活性物质之一是板栗(T. chebula干果- combretacae)。Myrobalan抑制活性的主要物质是GA。GA已被证明具有抗病毒和免疫调节活性。在2019冠状病毒病大流行期间,印度阿尤什政府部强烈推荐免疫增强剂siddhara多草药配方“Kabusura Kudineer”用于免疫增强和治疗COVID-19。TLC和FTIR对GA和样品进行了初步鉴别。采用HPLC法,色谱柱为Inertsil C18 (150*4.6 mm, 5 μm)。流动相为水:乙腈(50:50)。流速为1 ml /min,用紫外检测器在272 nm处进行GA跟踪。色谱总运行时间为8分钟,并观察GA的保留时间。GA和样品的Rf值为0.27。根据ICH指南进行验证。GA的停留时间为2.2 min,有效参数为系统精度,SD (14247.75), %RSD(0.9),回归方程y = 25511 x−947505,相关系数(R2) 0.9999。线性范围为50 ~ 150 μg/mL,检出限(loq)为1.70 μg/mL,检出限(loq)为5.16 μg/mL,方法精密度%RSD (0.8), SD(11626.7),回收率99.8,101.1%。复方“Kabusura Kudineer”的GA含量为1.39 μg/mL,开发的复方“HYDALJSS08”的GA含量为379.4 μg/mL, chebula干果的乙酸乙酯部位GA含量分别为105.59和29.17 μg/mL。所开发的高效液相色谱(HPLC)超高效液相色谱(UPLC)方法对这两种成分进行了新颖、简单、准确、快速、简便、重现性、坚固性和线性分析,并以悉达达为基础,开发了“HYDALJSS08”复方制剂“Kabusura kudineer”(已上市)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel HYDALJSS08 Polyherbal Formulation Development and Ultra-Performance Liquid Chromatographic Separation, Estimation of Gallic Acid in Terminalia chebula Dried Fruits, and a Marketed Siddha-based Polyherbal Formulation “Kabusura Kudineer”
The Siddha-based polyherbal formulation known as “Kabusura Kudineer (Marketed)” contains fifteen plants materials in dried raw form and The Ayush Ministry, Govt. of India highly endorsed for use of “Kabusura kudineer” during the pandemic of COVID-19, due to its immuno-booster properties. The current study aims to develop and document an analytical strategy for the estimation of gallic acid (GA) and methyl, ethyl acetate fraction of Terminalia chebula dried fruits and in polyherbal formulations (Marketed, & Developed). One of the active substances of Kabusura Kudineer and developed “HYDALJSS08” Polyherbal formulation is Myrobalan (T. chebula dried fruit-Combretaceae). Myrobalan restrains active principal substances are GA. GA is proven for its Anti-viral and immunomodulatory activity. During the pandemic of, COVID-19 ministry of Ayush, Govt of India highly recommended the immuno-booster Siddha-based polyherbal formulation “Kabusura Kudineer” for immune-boosting and treatment of COVID-19. TLC, and FTIR carried out the preliminary identification of GA and the sample. The HPLC method was developed on an Inertsil C18 (150*4.6 mm and 5 μm) column. The mobile phase was enhanced for water: Acetonitrile (50:50). The flow rate was 1-mL/min and was GA tracked at 272 nm in a UV detector. The total run time of the chromatogram is 8 minutes and the retention time of GA is observed. The Rf value of GA and sample was found to be 0.27. Validation was carried out according to ICH guidelines. The retention time of GA was 2.2 min, and the Valid parameter of GA is system precision, SD (14247.75), %RSD (0.9), Regression equation y = 25511 x−947505, Correlation coefficient (R2) 0.9999. The adequate Linearity concentration was found to be 50 to 150 μg/mL, LoDs (1.70 μg/mL), LoQs (5.16 μg/mL), Method precision %RSD (0.8), SD (11626.7), Recovery 99.8, and 101.1%. GA content was found in a formulation (“Kabusura Kudineer”- 1.39 μg/mL, developed “HYDALJSS08” Polyherbal formulation-379.4 μg/mL), and ethyl, methyl acetate fraction of T. chebula dried fruits was 105.59 and 29.17 μg/mL. The developed (HPLC) UPLC methods have enabled novel, simple, accurate, rapid, easy, reproducible, rugged, and linear analysis in these two fractions, and Siddha-based formulation “Kabusura kudineer” (Marketed), a developed “HYDALJSS08” Polyherbal formulation.
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来源期刊
International Journal of Pharmaceutical Quality Assurance
International Journal of Pharmaceutical Quality Assurance Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
0.80
自引率
0.00%
发文量
0
期刊介绍: INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE is a quarterly international journal publishing the finest peer-reviewed research in the field of Pharmaceutical Quality Assurance and Pharmaceutical Analysis on the basis of its originality, importance, disciplinary interest, timeliness, accessibility, elegance, and surprising conclusions. IJPQA also provides rapid, authoritative, insightful and arresting news and interpretation of topical and coming trends affecting science, scientists and the wider public.
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