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分子印迹聚合物在β-受体阻滞剂药物分析中的应用进展:作为生物和环境分析中一种选择性分离方法

An Update on the Use of Molecularly Imprinted Polymers in Beta-Blocker Drug Analysis as a Selective Separation Method in Biological and Environmental Analysis.

机构信息

Pharmaceutical Analysis and Medicinal Chemistry Department, Faculty of Pharmacy, Universitas Padjadjaran, Jalan Raya Bandung Sumedang KM 21 Jatinangor, Bandung 45363, Indonesia.

Drug Development Study Center, Faculty of Pharmacy, Universitas Padjadjaran, Jalan Raya Bandung Sumedang KM 21 Jatinangor, Bandung 45363, Indonesia.

出版信息

Molecules. 2022 Apr 30;27(9):2880. doi: 10.3390/molecules27092880.

Abstract

Beta-blockers are antihypertensive drugs and can be abused by athletes in some sport competitions; it is therefore necessary to monitor beta-blocker levels in biological samples. In addition, beta-blocker levels in environmental samples need to be monitored to determine whether there are contaminants from the activities of the pharmaceutical industry. Several extraction methods have been developed to separate beta-blocker drugs in a sample, one of which is molecularly imprinted polymer solid-phase extraction (MIP-SPE). MIPs have some advantages, including good selectivity, high affinity, ease of synthesis, and low cost. This review provides an overview of the polymerization methods for synthesizing MIPs of beta-blocker groups. The methods that are still widely used to synthesize MIPs for beta-blockers are the bulk polymerization method and the precipitation polymerization method. MIPs for beta-blockers still need further development, especially since many types of beta-blockers have not been used as templates in the MIP synthesis process and modification of the MIP sorbent is required, to obtain high throughput analysis.

摘要

β受体阻滞剂是一种降压药物,在某些运动竞赛中可能被运动员滥用,因此有必要监测生物样本中的β受体阻滞剂水平。此外,还需要监测环境样本中的β受体阻滞剂水平,以确定是否存在来自制药行业活动的污染物。已经开发了几种提取方法来分离样品中的β受体阻滞剂药物,其中之一是分子印迹聚合物固相萃取(MIP-SPE)。MIP 具有一些优点,包括良好的选择性、高亲和力、易于合成和低成本。本文综述了合成β受体阻滞剂 MIP 的聚合方法。目前仍广泛用于合成β受体阻滞剂 MIP 的方法是本体聚合方法和沉淀聚合方法。β受体阻滞剂的 MIP 仍需要进一步发展,特别是因为许多类型的β受体阻滞剂尚未在 MIP 合成过程中用作模板,并且需要对 MIP 吸附剂进行修饰,以获得高通量分析。

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