Rösler A, Vandermeulen G W, Klok H A
Max-Planck-Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.
Adv Drug Deliv Rev. 2001 Dec 3;53(1):95-108. doi: 10.1016/s0169-409x(01)00222-8.
Amphiphilic block copolymers are well established as building blocks for the preparation of micellar drug carriers. Over the past decade, the effectiveness of such self-assembled drug delivery devices has been demonstrated numerous times. This review will discuss two approaches that can be used to further improve the effectiveness of amphiphilic block copolymer-based drug delivery systems. The first approach involves the chemical modification of the block copolymer building blocks. Several examples will be discussed of amphiphilic block copolymers modified with crosslinkable groups in order to increase the stability of the micellar drug carriers, or of block copolymers containing specific ligands that could ultimately allow targeted drug delivery. The second approach to improve the performance of micellar drug carriers is the addition of auxiliary agents. To illustrate this approach, the feasibility of channel proteins and metal (nano)particles to improve temporal control over the drug release process is discussed.
两亲性嵌段共聚物作为制备胶束药物载体的构建单元已得到广泛认可。在过去十年中,这种自组装药物递送装置的有效性已被多次证明。本综述将讨论两种可用于进一步提高两亲性嵌段共聚物基药物递送系统有效性的方法。第一种方法涉及对嵌段共聚物构建单元进行化学修饰。将讨论几个例子,包括用可交联基团修饰的两亲性嵌段共聚物,以提高胶束药物载体的稳定性,或含有特定配体的嵌段共聚物,最终实现靶向药物递送。提高胶束药物载体性能的第二种方法是添加辅助剂。为说明这种方法,讨论了通道蛋白和金属(纳米)颗粒改善药物释放过程时间控制的可行性。