Determination of Chlorogenic Acid in Solid-Lipid Nanoparticles: Validation by UV-spectroscopy

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY Current Pharmaceutical Analysis Pub Date : 2024-07-23 DOI:10.2174/0115734129303063240711073707
Tarapati Rana, Anju Goyal, Tapan Behl
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Abstract

Objective: The objective of the research was the development and validation of a simple, sensitive, accurate, robust, and precise UV-spectroscopic method for the quantitative determination of chlorogenic acid loaded in solid-lipid nanoparticles as per the guidelines of the International Conference on Harmonization. Methods: The solid-lipid nanoparticles of chlorogenic acid were prepared using the hot melt emulsification method and the high-speed homogenizer method. Glyceryl monostearate was used as a solid lipid, and Tween 80 was used as a surfactant for the preparation of chlorogenic acid-loaded solid lipid nanoparticles. The method was validated in terms of linearity, accuracy, precision, robustness, ruggedness, limit of detection, and limit of quantification. Results: The chlorogenic acid exhibited absorption maxima at the wavelength of 330 nm. The regression equation from the calibration curve was y=0.006x + 0.0193 with a correlation coefficient of 0.9989. The percentage recovery was found to be 99.92, 99.80, and 99.86, respectively (within the acceptable limit of 98-102%), which validated the accuracy of the method. Furthermore, the method exhibited precision, robustness, and ruggedness, as illustrated by a relative standard deviation (RSD) of less than 2%. The limit of detection and limit of quantification were found to be 6.97 and 21.13 μg/ml, respectively. Conclusion: It was concluded that the proposed spectrophotometer analytical method for the determination of Chlorogenic acid was found reliable, accurate, consistent, precise, accurate, and robust. Therefore, the proposed analytical technique could be an integral part of further evaluation and characterization of Chlorogenic acid-solid lipid nanoparticles.
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固体脂质纳米颗粒中绿原酸的测定:紫外光谱法验证
研究目的研究目的是根据国际协调会议的指导原则,建立并验证一种简单、灵敏、准确、稳健、精确的紫外光谱法,用于定量测定固体脂质纳米颗粒中的绿原酸。方法:采用热熔乳化法和高速均质机法制备绿原酸固脂纳米颗粒。以单硬脂酸甘油酯为固体脂质,以吐温 80 为表面活性剂制备绿原酸固体脂质纳米粒子。从线性、准确度、精密度、稳健性、耐用性、检出限和定量限等方面对该方法进行了验证。结果表明绿原酸在 330 nm 波长处有最大吸收。校准曲线的回归方程为 y=0.006x + 0.0193,相关系数为 0.9989。回收率分别为 99.92、99.80 和 99.86(在 98-102% 的可接受范围内),验证了该方法的准确性。此外,该方法的相对标准偏差(RSD)小于 2%,表明该方法具有精密度、稳健性和耐用性。检测限和定量限分别为 6.97 和 21.13 μg/ml。结论所提出的绿原酸分光光度计分析方法可靠、准确、一致、精密、精确且稳健。因此,所提出的分析技术可以作为进一步评估和表征绿原酸固体脂质纳米颗粒的一个组成部分。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
85
审稿时长
3 months
期刊介绍: Aims & Scope Current Pharmaceutical Analysis publishes expert reviews and original research articles on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis.
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