制备盐酸尼卡地平的凝胶骨架控释贴剂。
Nicardipine hydrochloride transdermal controlled release patches with gel matrix were prepared.
结论：聚乳酸可用于制备口服盐酸尼卡地平缓释制剂。
Conclusion: PLA can be used to prepare oral nicardipine hydrochloride sustained-release.
用改良的扩散装置评价了盐酸尼卡地平（1）通过脱毛大鼠皮肤的渗透动力学以及促渗剂月桂氮酮（2）的作用。
The in vitro permeation kinetics of nicardipine hydrochloride (1) through the depilatory rat skin and the effect of laurocapram (2) using a modified diffusion cell were evaluated.
用改良的扩散装置评价了盐酸尼卡地平（1）通过脱毛大鼠皮肤的渗透动力学以及促渗剂月桂氮酮（2）的作用。
The in vitro permeation kinetics of nicardipine hydrochloride (1) through the depilatory rat skin and the effect of laurocapram (2) using a modified diffusion cell were evaluated.
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