Suppr超能文献

一种用于定量测定玫瑰茄喷雾干燥提取物、口服粉剂和含片中山奈酚含量的稳定性指示高效液相色谱-紫外检测法。

A stability-indicating HPLC-UV method for the quantification of anthocyanin in Roselle () spray-dried extract, oral powder, and lozenges.

作者信息

Khan Nasir Hayat, Abdulbaqi Ibrahim M, Darwis Yusrida, Aminu Nafiu, Chan Siok-Yee

机构信息

School of Pharmaceutical Sciences, University Sains Malaysia, Minden 11800, Penang, Malaysia.

Product & Process Innovation Department, Qarshi Brands (Pvt) Ltd, Plot # 56/2-4, Hattar Industrial Estate-22610, District Haripur, Province KPK, Pakistan.

出版信息

Heliyon. 2022 Mar 25;8(3):e09177. doi: 10.1016/j.heliyon.2022.e09177. eCollection 2022 Mar.

Abstract

(H.S.) plant and its calyces have received much attention from researchers because of their potential medicinal and nutritional values. Calyces are the major source of anthocyanin in this plant. Therefore, a well-developed, efficient, and accurate analytical method is needed to assure proper standardization and control the quality of H.S. plant herbal and nutraceutical products. The objective of this work is to develop a simple, rapid, stability-indicating HPLC-UV method for the quantitative determination of anthocyanin in spray-dried aqueous extract (SDE), oral powder, and compressible lozenges formulations using Delphinidin-3-O-sambubioside (Dp3S) as a marker compound. The chromatographic conditions were optimized using Eclipse plus® C18 column. The mobile phase comprised water acidified with 0.2% formic acid (FA) and acetonitrile (ACN) (90:10, v/v) using a gradient system at a flow rate of 0.8 mL/min. The detection wavelength was 525 nm. The column was maintained at 45 °C, and the injection volume was 15 μL. The developed method was validated according to the international conference of harmonization (ICH) guidelines for linearity, detection and quantitation limits, accuracy, precision, specificity, and robustness. Forced degradation studies under acid, base, oxidation, heat, and U.V light, were performed on the pure compound, extract, and the H.S. developed formulations. Significant degradation of the compound was observed under all tested conditions except U.V. light, where degradation was minimum. There was no interference from impurities, degradation products, or excipients at the retention time of Dp3S 3.2 min indicating the specificity of the method. The developed method was statistically confirmed to be accurate, precise, and reproducible. This simple, rapid, and specific method can be employed efficiently to determine anthocyanin in H.S. plant extract and nutraceutical products.

摘要

(H.S.)植物及其花萼因其潜在的药用和营养价值而受到研究人员的广泛关注。花萼是该植物中花青素的主要来源。因此,需要一种完善、高效且准确的分析方法,以确保H.S.植物草药和营养产品的标准化及质量控制。本研究的目的是建立一种简单、快速、能指示稳定性的高效液相色谱 - 紫外(HPLC - UV)方法,以矢车菊素 - 3 - O - 接骨木二糖苷(Dp3S)为标记化合物,定量测定喷雾干燥水提取物(SDE)、口服粉末和可压缩含片制剂中的花青素。使用Eclipse plus® C18柱对色谱条件进行了优化。流动相由用0.2%甲酸(FA)酸化的水和乙腈(ACN)(90:10,v/v)组成,采用梯度洗脱系统,流速为0.8 mL/min。检测波长为525 nm。柱温保持在45℃,进样量为15 μL。所建立的方法根据国际协调会议(ICH)指南进行了线性、检测限和定量限、准确度、精密度、专属性和稳健性的验证。对纯化合物、提取物和所开发的H.S.制剂进行了酸、碱、氧化、加热和紫外光下的强制降解研究。除紫外光下降解最小外,在所有测试条件下均观察到化合物的显著降解。在Dp3S保留时间3.2 min处,杂质、降解产物或辅料均无干扰,表明该方法具有专属性。经统计学验证,所建立的方法准确、精密且可重现。这种简单、快速且特异的方法可有效地用于测定H.S.植物提取物和营养产品中的花青素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67f9/8971634/0683f7b3db20/ga1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验