寡肽酶在前药设计脑啡肽类似物脑靶向递送中的应用。

Q2 Pharmacology, Toxicology and Pharmaceutics
K Prokai-Tatrai, H-S Kim, L Prokai
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引用次数: 8

摘要

在代谢稳定的脑啡肽类似物DADLE的脑靶向前药方法中,利用特定的酶进行体内前药激活。脯氨酸寡肽酶(POP)在这方面可能特别有用。具有各种“间隔物”的前药的假定代谢物的体外代谢稳定性表明,与使用单一氨基酸作为间隔物时使用的其他肽酶相比,具有二肽基间隔物(特别是Xaa-Pro或Xaa-Ala)的偶联物的POP释放DADLE的速度要快得多。在大鼠脑浆液中测量的体外半衰期显示,使用甩尾模型的大鼠与中枢神经系统介导的镇痛具有良好的相关性,因此,在体内证实了依靠POP作为肽酶释放DADLE的药物前途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The utility of oligopeptidase in brain-targeting delivery of an enkephalin analogue by prodrug design.

The utility of oligopeptidase in brain-targeting delivery of an enkephalin analogue by prodrug design.

In a brain-targeting prodrug approach for a metabolically stable enkephalin analogue DADLE, specific enzymes are utilized for in vivo prodrug activation. Prolyl oligopeptidase (POP) may be especially useful in this regard. In vitro metabolic stability of the putative metabolites of prodrugs having various "spacers" has shown that POP provides significantly faster release of DADLE from conjugates having dipeptidyl spacer (specifically Xaa-Pro or Xaa-Ala) than alternative peptidases utilized when single amino acids are used as spacers. In vitro half-lives measured in rat brain homogenate showed excellent correlation with CNS-mediated analgesia using the tail-flick model in rats providing, thus, an in vivo substantiation of the prodrug approach relying on POP as the peptidase to release DADLE.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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