Impressão molecular: uma estratégia promissora na elaboração de matrizes para a liberação controlada de fármacos

E. Figueiredo, Ana Cristi Basile Dias, M. A. Arruda
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引用次数: 19

Abstract

Biomolecular interactions (antigen-antibody, enzyme-substrate and drug-receptor) have been investigated due to their selective nature. Thus, since 1940, the search for synthetic materials presenting specific binding sites has been increasing. Nowadays, they are well established in different science areas such as pharmacy, analytical chemistry, biochemistry, among others, being the referred materials called molecularly imprinted polymers-MIP. Although the largest applications of MIP are found in the separations science field, few applications of these polymers have been reported as drug delivery systems-DDS. Such applications have been promising due to the feasibility of the MIP synthesis. However, the clinical use of the MIP as DDS is still not observed, probably due to its recent application, as well as extensive tests necessary for its approval as a new pharmaceutical form. In this way, this work aims to present the most recent progresses in the use of MIP as DDS, reinforcing the most significant aspects of this application (potentialities and limitations), as well as classifying and detailing such systems.
分子印迹:一种很有前途的药物控释基质开发策略
生物分子相互作用(抗原-抗体,酶-底物和药物受体)由于其选择性而被研究。因此,自1940年以来,对具有特定结合位点的合成材料的研究一直在增加。如今,它们在药学、分析化学、生物化学等不同的科学领域得到了很好的应用,被称为分子印迹聚合物(mip)的参考材料。尽管MIP的最大应用是在分离科学领域,但这些聚合物作为药物传递系统- dds的应用很少。由于MIP合成的可行性,这些应用前景广阔。然而,仍未观察到MIP作为DDS的临床应用,这可能是由于其最近的应用,以及为批准其作为一种新药物形式所需的大量试验。通过这种方式,本工作旨在介绍MIP作为DDS使用的最新进展,加强该应用的最重要方面(潜力和局限性),以及对此类系统进行分类和详细说明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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