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Nanodisks: hydrophobic drug delivery vehicles.

机译:纳米盘:疏水性药物递送载体。

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摘要

Members of the class of exchangeable apolipoproteins possess the unique capacity to transform phospholipid vesicle substrates into nanoscale disk-shaped bilayers. This reaction can proceed in the presence of exogenous hydrophobic biomolecules, resulting in the formation of novel transport vehicles termed nanodisks (NDs). The objective of this study is to describe the structural organization of NDs and evaluate the utility of these complexes as hydrophobic biomolecule transport vehicles. The topics presented focus on two distinct water insoluble drugs, amphotericin B (AMB) and all trans retinoic acid (ATRA). In vitro and in vivo studies reveal that AMB-ND display potent anti-fungal and anti-protozoal activity, while ATRA-ND show promise in the treatment of cancer. The versatility conferred by the presence of a polypeptide component provides opportunities for targeted delivery of ND to cells.
机译:可交换载脂蛋白类的成员具有将磷脂囊泡底物转化为纳米级盘状双层的独特能力。该反应可以在外源疏水生物分子的存在下进行,导致形成称为纳米盘(ND)的新型运输媒介。这项研究的目的是描述NDs的结构组织,并评估这些复合物作为疏水性生物分子运输载体的效用。提出的主题集中于两种不同的水不溶性药物,两性霉素B(AMB)和所有反式维甲酸(ATRA)。体外和体内研究表明,AMB-ND显示出有效的抗真菌和原生动物活性,而ATRA-ND在治疗癌症方面显示出希望。多肽组分的存在所赋予的多功能性提供了将ND靶向递送至细胞的机会。

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