Advanced HPTLC Method Development for Silibinin Analysis in Nanoformulated Scaffolds: A Box-Behnken Approach.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS Phytochemical Analysis Pub Date : 2024-11-09 DOI:10.1002/pca.3474
Melvin Vincent Dsouza, Suneel Dodamani, Bhaskar Kurangi, Priya Shetti, Sachin Gudasi
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Abstract

Introduction: Silibinin (silybin), a bioactive component derived from the seeds of milk thistle (Silybum marianum), is recognized for its diverse pharmacological properties, including antioxidant, anti-inflammatory, and hepatoprotective effects. Given its therapeutic significance, accurately quantifying silybin in various formulations is essential. High-performance thin-layer chromatography (HPTLC) is a powerful analytical technique frequently used for this purpose. In this study, an HPTLC method was validated according to the International Council for Harmonization (ICH) guidelines to determine the concentration of silybin. The design of experiments (DoE), specifically the Box-Behnken design, was employed to optimize and understand the influence of critical method variables.

Methodology: The HPTLC method validation was performed using silica gel F254 HPTLC plates. The variables investigated included the composition of the mobile phase (% v/v), saturation time (minutes), and temperature in degree Celsius (°C), with the Box-Behnken design for optimization. The mobile phase consisted of chloroform, acetone, and formic acid in a 7:2:1 (v/v) ratio. Both the formulated scaffold and standard drug were applied to the plates, which were then processed in a twin chamber. After development, the plates were scanned at 288 nm using the Camag TLC Scanner IV with Vision CATS software.

Results: The validated HPTLC method demonstrated a strong linear relationship within the silybin concentration range of 2-10 μg/mL. The limit of detection (LOD) and limit of quantification (LOQ) for silybin were determined to be 0.469 and 1.423 μg/mL, respectively. Recovery studies indicated that the method provided accurate quantification, with recovery rates ranging from 97.53% to 99.82%. These results confirm the method's high accuracy, outstanding linearity, and reliability for the quantification of silybin in formulations.

Conclusion: The validated HPTLC method proved to be a reliable analytical tool for the quantification of silybin in various formulations, particularly those containing polymers. The method's strong linearity, precision, and accuracy align with the ICH guidelines, making it suitable for routine analysis in quality control laboratories. The use of the Box-Behnken design for method optimization highlights the importance of systematic experimentation in achieving robust analytical outcomes.

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用于纳米配方支架中 Silibinin 分析的先进 HPTLC 方法开发:方框-贝肯方法
简介:水飞蓟宾(水飞蓟素)是从奶蓟草(Silybum marianum)种子中提取的一种生物活性成分,它具有多种药理特性,包括抗氧化、抗炎和保肝作用。鉴于水飞蓟宾的治疗意义,准确量化各种配方中的水飞蓟宾至关重要。高效薄层色谱(HPTLC)是一种功能强大的分析技术,经常被用于这一目的。本研究根据国际协调理事会(ICH)指南对 HPTLC 方法进行了验证,以确定水飞蓟宾的浓度。实验设计(DoE),特别是方框-贝肯(Box-Behnken)设计,用于优化和了解关键方法变量的影响:采用硅胶 F254 HPTLC 板进行 HPTLC 方法验证。考察的变量包括流动相的组成(% v/v)、饱和时间(分钟)和温度(摄氏度),并采用盒-贝肯设计法进行优化。流动相由氯仿、丙酮和甲酸组成,比例为 7:2:1(v/v)。将配制好的支架和标准药物涂抹在平板上,然后在双室中进行处理。显影后,使用带有 Vision CATS 软件的 Camag TLC 扫描仪 IV 在 288 纳米波长下对平板进行扫描:结果:经过验证的 HPTLC 方法在水飞蓟宾 2-10 μg/mL 浓度范围内线性关系良好。水飞蓟宾的检出限(LOD)和定量限(LOQ)分别为 0.469 和 1.423 μg/mL。回收率研究表明,该方法定量准确,回收率在 97.53% 至 99.82% 之间。这些结果证实了该方法在配方中水飞蓟宾的定量方面具有较高的准确度、良好的线性关系和可靠性:经过验证的 HPTLC 方法是一种可靠的分析工具,可用于定量检测各种制剂,尤其是含有聚合物的制剂中的水飞蓟宾。该方法的线性度、精密度和准确度均符合 ICH 指南的要求,因此适用于质量控制实验室的常规分析。采用方框-贝肯设计法进行方法优化,突出了系统实验对获得可靠分析结果的重要性。
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来源期刊
Phytochemical Analysis
Phytochemical Analysis 生物-分析化学
CiteScore
6.00
自引率
6.10%
发文量
88
审稿时长
1.7 months
期刊介绍: Phytochemical Analysis is devoted to the publication of original articles concerning the development, improvement, validation and/or extension of application of analytical methodology in the plant sciences. The spectrum of coverage is broad, encompassing methods and techniques relevant to the detection (including bio-screening), extraction, separation, purification, identification and quantification of compounds in plant biochemistry, plant cellular and molecular biology, plant biotechnology, the food sciences, agriculture and horticulture. The Journal publishes papers describing significant novelty in the analysis of whole plants (including algae), plant cells, tissues and organs, plant-derived extracts and plant products (including those which have been partially or completely refined for use in the food, agrochemical, pharmaceutical and related industries). All forms of physical, chemical, biochemical, spectroscopic, radiometric, electrometric, chromatographic, metabolomic and chemometric investigations of plant products (monomeric species as well as polymeric molecules such as nucleic acids, proteins, lipids and carbohydrates) are included within the remit of the Journal. Papers dealing with novel methods relating to areas such as data handling/ data mining in plant sciences will also be welcomed.
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