药品
药物输送
有效载荷(计算)
结合
白蛋白
前药
体内
药理学
毒品携带者
人血清白蛋白
共轭体系
靶向给药
聚合物
血清白蛋白
化学
牛血清白蛋白
医学
材料科学
计算机科学
纳米技术
内科学
生物
数学
数学分析
网络数据包
生物技术
计算机网络
作者
Anton A. A. Smith,Kaja Zuwala,Oliver Pilgram,Karen Singers Eiskjær Johansen,Martin Tolstrup,Frederik Dagnæs-Hansen,Alexander N. Zelikin
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2016-09-15
卷期号:5 (10): 1089-1094
被引量:26
标识
DOI:10.1021/acsmacrolett.6b00544
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI