max為8.162 mg/L,達(dá)峰時(shí)間tmax為1 min。結(jié)論 明確了冰片-羥丙基-β-環(huán)糊精包合物經(jīng)鼻腔給藥后在兔體內(nèi)的藥動(dòng)學(xué)特征,為進(jìn)一步制劑研究提供了參考。;Objective To study the pharmacokinetics in rabbits blood after intranasal administration of borneol-hydroxypropyl-β- cyclodextrin inclusion. Methods After intranasal administration, GC method was used to determine contents of borneol in plasma, and the pharmacokinetic parameters were calculated by the software of DAS 2.1.1. Results Pharmacokinetics of borneol- hydroxypropyl-β-cyclodextrin inclusion in rabbits fitted with the two compartment model, and Cmax was 8.162 mg/L, tmax was 1 min. Conclusion Pharmacokinetic characters of borneol in rabbits are confirmed which can provide reference for further study of preparation."/>