Anderson J M
Ann N Y Acad Sci. 1985;446:67-75. doi: 10.1111/j.1749-6632.1985.tb18391.x.
Preliminary efforts directed toward the synthesis and characterization of steroid-polyamino acid conjugates indicate that the preparation of these systems is feasible. Studies have indicated that the steroids may be released from the macromolecule resulting in long-term controlled release systems. Table 4 lists several of the variables that are important in controlling biocompatibility, biodegradation, and drug release characteristics. The biocompatibility, biodegradation, and drug release characteristics are all important in the design and preparation of a drug-polyamino acid delivery system. The variables listed in Table 4 may interact and interrelate to varying degrees when considering each of these factors independently. Although perhaps preliminary, efforts to date indicate that steroids bound to polyglutamic acid or polyglutamic acid derivatives are biocompatible, capable of undergoing biodegradation, and can release drugs at appropriate rates for extended periods of time.
针对甾体-聚氨基酸缀合物的合成与表征所做的初步研究表明,制备这些体系是可行的。研究表明,甾体可能从大分子中释放出来,从而形成长期控释体系。表4列出了在控制生物相容性、生物降解和药物释放特性方面重要的几个变量。生物相容性、生物降解和药物释放特性在药物-聚氨基酸递送系统的设计和制备中都很重要。在独立考虑这些因素中的每一个时,表4中列出的变量可能会在不同程度上相互作用和相互关联。尽管可能还处于初步阶段,但迄今为止的研究表明,与聚谷氨酸或聚谷氨酸衍生物结合的甾体具有生物相容性,能够进行生物降解,并且可以在较长时间内以适当的速率释放药物。