以柚皮苷为模板的磁性分子印迹聚合物用于从洋葱皮中选择性提取槲皮素

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Vinitha Udhayabanu Govindarajan, Vaishnavi Renganathan, Meenakshi Sundaram Muthuraman
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引用次数: 0

摘要

以柚皮苷为模板分子,丙烯酰胺为功能单体,经超声波辐照聚合而成的磁性分子印迹聚合物(MMIP)吸附了柚皮苷。结果出人意料,选择性研究显示,合成的 MMIP 对槲皮素的亲和力高于柚皮素。鉴于这种高选择性,我们对槲皮素和柚皮苷进行了吸附等温线和动力学研究。吸附等温线表明吸附剂上存在多层吸附。动力学研究表明,与假二阶动力学模型的吻合度较高。在 50 mg/L 浓度下,槲皮素的最大吸附容量为 7.2 mg/g,在相同浓度下,柚皮苷的最大吸附容量为 4.9 mg/g。此外,通过将 MMIP 与 HPLC-UV 联用,对槲皮素进行了定量,方法验证显示了槲皮素的检出限(LOD)和定量限(LOQ)。此外,利用 MMIP 对富含槲皮素等酚类化合物的农用工业废洋葱皮进行固相萃取,以纯化槲皮素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Naringin-templated magnetic molecularly imprinted polymers for selective quercetin extraction from onion peel
A Magnetic Molecularly Imprinted Polymer (MMIP) was developed using naringin as template molecule, acrylamide as functional monomer and polymerized by ultrasound irradiation for the adsorption of naringin. In an unexpected turn of results, the selectivity study unveiled that the synthesized MMIP exhibited a higher affinity for quercetin over naringin. Given this high selectivity, adsorption isotherm and kinetic studies were conducted for both quercetin and naringin. The adsorption isotherm indicated multilayer adsorption of the adsorbate on the adsorbent. The kinetic study showed better agreement with the pseudo-second-order kinetic model. The maximum adsorption capacity of 7.2 mg/g was achieved for quercetin at 50 mg/L and 4.9 mg/g was attained for naringin at the same concentration. Furthermore, quercetin quantification was performed by coupling MMIP with HPLC-UV, with method validation revealing the limits of detection (LOD) and quantification (LOQ) for quercetin. Additionally, agro-industrial waste onion peel, enriched with phenolic compounds such as quercetin, was subjected to solid-phase extraction using MMIP for the purification of quercetin.
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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