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化妆品、药品和食品补充剂中熊果苷的亲水相互作用色谱法定量分析。

Quantification of Arbutin in Cosmetics, Drugs and Food Supplements by Hydrophilic-Interaction Chromatography.

机构信息

Department of Agriculture, Ecotrophology, and Landscape Development, Anhalt University of Applied Sciences, 06406 Bernburg, Germany.

出版信息

Molecules. 2022 Sep 2;27(17):5673. doi: 10.3390/molecules27175673.

Abstract

Arbutin, the glucoside of hydroquinone, exists in two isomers, α-arbutin and β-arbutin. The synthetic α isomer is mainly used as a skin brightening agent, while β-arbutin occurs naturally, for instance in bearberry, and is used in drugs for treatment of lower urinary tract infections and as a food supplement. Since both isomers can be harmful at high concentrations, methods for their quantification are required. Classically they have been determined by reversed-phase chromatography, but separation of both isomers is often unsatisfactory. Here we present a simple and reliable method for quantification of α- and β-arbutin based on hydrophilic-interaction chromatography. Prior to analysis, interfering compounds that would frequently be present in cosmetics and drugs, particularly biopolymers, were efficiently removed by precipitation with acetonitrile. In this paper, for separation, a Cyclobond I 2000 5 µm 250 × 4.6 mm column was employed as stationary phase and acetonitrile/water 92/8 (v/v) was used as an eluent at a flow rate of 0.8 mL min−1. For quantification, a UV detector operating at 284 nm was applied. Although analysis took less than 10 min, baseline separation of α- and β-arbutin was achieved. The response was highly linear (r > 0.999) and the method had, for both α- and β-arbutin, a LOD of 0.003% (w/w) and a LOQ of 0.009% (w/w). Moreover, the method showed excellent intra-day and inter-day repeatability with relative standard deviations in the range of 0.5% to 2.3% and 1.0% to 2.2%, respectively, with cosmetics, drugs and food supplements as samples.

摘要

熊果苷是对苯二酚的糖苷,有两种异构体,α-熊果苷和β-熊果苷。合成的 α 异构体主要用作皮肤增亮剂,而β-熊果苷则天然存在于熊果中,用于治疗下尿路感染的药物和作为食品补充剂。由于这两种异构体在高浓度下都可能有害,因此需要定量它们的方法。经典方法是通过反相色谱法,但两种异构体的分离往往不理想。在这里,我们提出了一种基于亲水相互作用色谱法的简单可靠的α-和β-熊果苷定量方法。在分析之前,通过乙腈沉淀有效地去除了化妆品和药物中经常存在的干扰化合物,特别是生物聚合物。在本文中,为了分离,采用 Cyclobond I 2000 5 µm 250 × 4.6 毫米柱作为固定相,乙腈/水 92/8(v/v)作为洗脱剂,流速为 0.8 mL min−1。用于定量的是在 284nm 处工作的 UV 检测器。虽然分析时间不到 10 分钟,但实现了 α-和β-熊果苷的基线分离。响应高度线性(r > 0.999),方法对α-和β-熊果苷的检出限分别为 0.003%(w/w)和 0.009%(w/w)。此外,该方法对化妆品、药物和食品补充剂等样品具有出色的日内和日间重复性,相对标准偏差在 0.5%至 2.3%和 1.0%至 2.2%之间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9daa/9457821/f624393d3730/molecules-27-05673-g001.jpg

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