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白蛋白-聚合物-药物缀合物:长循环、高载药量的药物递送载体。

Albumin-Polymer-Drug Conjugates: Long Circulating, High Payload Drug Delivery Vehicles.

作者信息

Smith Anton A A, Zuwala Kaja, Pilgram Oliver, Johansen Karen Singers, Tolstrup Martin, Dagnæs-Hansen Frederik, Zelikin Alexander N

机构信息

Department of Infectious Diseases, Aarhus University Hospital, DK-8000 Aarhus C, Denmark.

出版信息

ACS Macro Lett. 2016 Oct 18;5(10):1089-1094. doi: 10.1021/acsmacrolett.6b00544. Epub 2016 Sep 15.

Abstract

Albumin is an exquisite tool of nature used in biomedicine to achieve long blood residence time for drugs, but the payload it can carry is typically limited to one molecule per protein. In contrast, synthetic macromolecular prodrugs contain multiple copies of drugs per polymer chain but offer only a marginal increase in the circulation lifetime of the drugs. We combine the benefits of the two platforms and at the same time overcome their respective limitations. Specifically, we develop the synthesis of albumin-polymer-drug conjugates to obtain long circulating, high payload drug delivery vehicles. In vivo data validate that albumin endows the conjugate with a blood residence time similar to that of the protein and well exceeding that of the polymer. Therapeutic activity of the conjugates is validated using prodrugs of panobinostat, an HIV latency reversal agent, in which case the conjugates matched the drug in terms of efficacy of treatment.

摘要

白蛋白是自然界中一种精妙的工具,在生物医学中用于使药物在血液中保持较长的停留时间,但它所能携带的有效载荷通常限制为每个蛋白质一个分子。相比之下,合成高分子前药每条聚合物链包含多个药物分子拷贝,但药物的循环寿命仅略有增加。我们结合了这两种平台的优势,同时克服了它们各自的局限性。具体而言,我们开发了白蛋白 - 聚合物 - 药物缀合物的合成方法,以获得具有长循环时间、高有效载荷的药物递送载体。体内数据证实,白蛋白赋予缀合物与蛋白质相似的血液停留时间,且远超聚合物的血液停留时间。使用HIV潜伏逆转剂帕比司他的前药验证了缀合物的治疗活性,在这种情况下,缀合物在治疗效果方面与药物相当。

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