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DOI: 10.3791/54722-v
Yuanpei Li1,2, Gaurav Bharadwaj1, Joyce S. Lee3
1Department of Biochemistry & Molecular Medicine,University of California, Davis, 2UC Davis Comprehensive Cancer Center,University of California, Davis, 3Department of Internal Medicine, Division of Hematology and Oncology,University of California, Davis
Please note that some of the translations on this page are AI generated. Click here for the English version.
为了将癌症药物以高特异性和减少副作用输送到肿瘤部位,需要基于纳米颗粒的新方法。在这里,我们描述了二硫键交联胶束,它们可以通过过氧化氢介导的氧化轻松制备,并且能够在还原性肿瘤环境中有效解离以释放有效载荷。
该程序的总体目标是提供一种简单有效的方案,用于合成用于靶向药物递送的载药二硫键交联胶束。这种方法可以帮助回答纳米医学领域的问题。比如如何有效地生产稳定的纳米制剂。
这项技术的主要优点是它使我们能够轻松地大规模合成二硫键交联胶束,这对于患者的临床研究非常可取。要开始此程序,将 2 克单甲基封端的聚乙二醇单胺添加到圆底烧瓶中。加入 10 毫升无水 DMF 使其溶解。
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