Chemometric tools to comprehend a recovery process for the bioactive ingredients from purple basil (Ocimum basilicum L.): Box-Behnken design-based optimization and principal component analysis

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2025-04-15 Epub Date: 2025-01-17 DOI:10.1016/j.jpba.2025.116676
İrem Toprakçı, Ebru Kurtulbaş, Selin Şahin
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Abstract

Medicinal and aromatic plants are alternative products to synthetics because of their antioxidant, antimicrobial, anti-inflammatory and antidiabetic effects. The objective of this study is to investigate the automated solvent extraction (ASE) process parameters for the extraction of bioactive-rich substances from purple basil (Ocimum basilicum L.). Process optimization in relation to total phenolic content (TPC), total flavonoid content (TFC), and total anthocyanin content (TAC) was performed through a chemometric approach. The ASE system was designed, modelled and optimized by 3-factor and 3-level Box-Behnken design of Response Surface method (RSM). Antioxidant activity of the samples were measured by 2 different free radical scavenging activity assays (ABTS and DPPH). By using principal component analysis (PCA) to the dataset, the impact of interactions between the parameters was also evaluated according to their antioxidant activity, TPC, TFC and TAC levels. The optimal ASE conditions (0.3 g of purple basil, 19 min of immersion time and 66 % ethanol solution) provided the highest yields of TPC (98.888 mg-GAE/g-DM), TFC (27.033 mg-CE/g-DM) and TAC (11.556 mg-C3G/g-DM), which were verified by satisfactory validation findings (the error<2 %).
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紫色罗勒(Ocimum basilicum L.)生物活性成分回收过程的化学计量学工具:基于Box-Behnken设计的优化和主成分分析。
药用和芳香植物因其抗氧化、抗菌、抗炎和抗糖尿病的作用而成为合成物的替代产品。研究了自动溶剂萃取法(ASE)提取紫罗勒中富含生物活性物质的工艺参数。通过化学计量学方法对总酚含量(TPC)、总黄酮含量(TFC)和总花青素含量(TAC)进行工艺优化。采用响应面法(RSM)的3因素3层次Box-Behnken设计对ASE系统进行了设计、建模和优化。采用2种不同的自由基清除活性测定法(ABTS和DPPH)测定样品的抗氧化活性。通过主成分分析(PCA)对数据集进行分析,并根据其抗氧化活性、TPC、TFC和TAC水平来评估参数之间相互作用的影响。最佳ASE条件(0.3 g紫罗勒,19 min浸泡时间,66 %乙醇溶液)可获得TPC (98.888 mg-GAE/g- dm), TFC (27.033 mg-CE/g- dm)和TAC (11.556 mg-C3G/g- dm)的最高产率(误差)
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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