Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University (TWIns), 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan.
Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University (TWIns), 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan.
J Control Release. 2014 Nov 10;193:2-8. doi: 10.1016/j.jconrel.2014.06.062. Epub 2014 Jul 16.
Targeting to solid tumors is the most challenging issue in the drug delivery field. To obtain the ideal pharmacodynamics of administrated drugs, drug carriers must suppress drug release and interactions with non-target tissues while circulating in the bloodstream, yet actively release the incorporated drug and interact with target cells after delivery to the tumor tissue. To handle this situation, stimuli-responsive drug carriers are extremely useful, because carriers change their physicochemical properties to control the drug release rate and interaction with cells in response to the surrounding environmental conditions or applied physical signals. The current review focuses on the strategy and availability of temperature-responsive (TR) polymeric micelles as a next-generation drug carrier. In particular, we discuss the unique properties of TR polymeric micelles, such as temperature-triggered drug release and intracellular uptake system. In addition, we explore the methodology for integrating other targeting systems into TR micelles to pursue the ideal pharmacodynamics in conjunction with thermal therapy as a future prospective of the TR system.
靶向实体瘤是药物输送领域最具挑战性的问题。为了获得给药后药物的理想药效学,药物载体必须在血液循环中循环时抑制药物释放和与非靶组织相互作用,而在递送至肿瘤组织后则积极释放所包含的药物并与靶细胞相互作用。为了应对这种情况,刺激响应性药物载体非常有用,因为载体改变其物理化学性质以控制药物释放速度并响应周围环境条件或施加的物理信号与细胞相互作用。本综述重点介绍了作为下一代药物载体的温度响应(TR)聚合物胶束的策略和可用性。特别地,我们讨论了 TR 聚合物胶束的独特性质,例如温度触发的药物释放和细胞内摄取系统。此外,我们还探索了将其他靶向系统整合到 TR 胶束中的方法,以在作为 TR 系统的未来展望的热疗中追求理想的药效学。
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