Heller J, Trescony P V
J Pharm Sci. 1979 Jul;68(7):919-21. doi: 10.1002/jps.2600680740.
A novel, closed-loop drug delivery system was developed where the presence or absence of an external compound controls drug delivery from a bioerodible polymer. In the described delivery system, hydrocortisone was incorporated into a n-hexyl half-ester of a methyl vinyl ehter-maleic anhydride copolymer, and the polymer-drug mixture was fabricated into disks. These disks were then coated with a hydrogel containing immobilized urease. In a medium of constant pH and in the absence of external urea, the hydrocortisone release was that normally expected for that polymer at the given pH. With external urea, ammonium bicarbonate and ammonium hydroxide were generated within the hydrogel, which accelerated polymer erosion and drug release. The drug delivery rate increase was proportional to the amount of external urea and was reversible; that is, when external urea was removed, the drug release rate gradually returned to its original value.
开发了一种新型闭环给药系统,其中外部化合物的存在与否控制着药物从生物可蚀性聚合物中的释放。在所描述的给药系统中,氢化可的松被掺入甲基乙烯基醚-马来酸酐共聚物的正己基半酯中,并且将聚合物-药物混合物制成圆盘。然后用含有固定化脲酶的水凝胶涂覆这些圆盘。在恒定pH的介质中且不存在外部尿素的情况下,氢化可的松的释放是该聚合物在给定pH下的正常预期释放。有外部尿素时,水凝胶内会生成碳酸氢铵和氢氧化铵,这加速了聚合物的侵蚀和药物释放。药物释放速率的增加与外部尿素的量成正比且是可逆的;也就是说,当去除外部尿素时,药物释放速率逐渐恢复到其原始值。