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首页> 外文期刊>RSC Advances >A hyaluronic acid-pentamidine bioconjugate as a macrophage mediated drug targeting delivery system for the treatment of leishmaniasis
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A hyaluronic acid-pentamidine bioconjugate as a macrophage mediated drug targeting delivery system for the treatment of leishmaniasis

机译:透明质酸-戊am生物缀合物作为巨噬细胞介导的药物靶向递送系统,用于治疗利什曼病

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摘要

Leishmaniasis is still a serious public health problem worldwide, especially in tropical areas where this infectious disease is endemic. The most severe form of the disease (i.e. visceral) can claim victims if left untreated and the few accessible drugs have several drawbacks including major side effects and parenteral administration. In this context, the investigation of new delivery modalities which might reduce the toxicity and increase the bioavailability of the drugs currently on the market represents a valid strategy to counter these problems. Herein we present the development of a macrophage mediated drug targeting delivery system by conjugating the anti-leishmanial drug pentamidine (Pent) with the biocompatible polymer hyaluronic acid (HA), the latter employed at the same time as a delivery platform and targeting scaffold. Biological assays against Leishmania major amastigote-infected macrophages and primary bone marrow derived macrophages (BMDM) confirmed the validity of our strategy as the resulting bioconjugate HA-Pent increased both the potency and the selectivity index of the drug.
机译:利什曼病在全世界仍然是一个严重的公共卫生问题,尤其是在这种传染病为地方病的热带地区。如果不及时治疗,该疾病的最严重形式(即内脏性疾病)可成为受害者,而且几种可及的药物也具有一些缺点,包括主要的副作用和肠胃外给药。在这种情况下,对可能降低毒性并增加目前市场上药物的生物利用度的新递送方式的研究代表了应对这些问题的有效策略。本文中,我们介绍了巨噬细胞介导的药物靶向递送系统的发展,方法是将抗利什曼原虫药物戊tam(Pent)与生物相容性聚合物透明质酸(HA)结合,后者同时用作递送平台和靶向支架。针对利什曼原虫感染的主要鞭毛巨噬细胞和原代骨髓衍生巨噬细胞(BMDM)的生物学分析证实了我们策略的有效性,因为所得的生物缀合物HA-Pent既提高了药物的效力,又提高了药物的选择性指数。

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