细辛脑羟丙基-β-环糊精溶液剂鼻腔给药脑内释药可行性  被引量:7

Feasibility of Brain Release of Asarone Hydroxypropyl-β-Cyclodextrin Solution Agent by Intranasal Administration

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作  者:王光明[1] 潘艳[2] 孔秋玲[2] 田军[2] 

机构地区:[1]广东食品药品职业学院,广州510520 [2]广州中医药大学中药学院,广州510006

出  处:《中国实验方剂学杂志》2012年第3期16-18,共3页Chinese Journal of Experimental Traditional Medical Formulae

基  金:广东省中医药管理局项目(2008198)

摘  要:目的:探讨细辛脑羟丙基-β-环糊精溶液剂鼻腔给药脑内释药的可行性。方法:采用家兔静脉注射细辛脑羟丙基-β-环糊精溶液剂与家兔鼻腔灌流细辛脑羟丙基-β-环糊精溶液剂相比较,探求细辛脑鼻腔给药后药物在脑内释放的可行性通路。结果:鼻腔灌流方式血液中细辛脑质量浓度与嗅脑、大脑、筛鼻甲内的细辛脑的量,均高于静脉给药方式。结论:细辛脑羟丙基-β-环糊精溶液剂经过筛鼻甲进入脑部这一通路过程中,药物的吸收量方面,静脉给药要小于鼻腔灌流,故细辛脑鼻腔给药脑内释药具有实践之可行性。Objective: To investigate feasibility of brain release of asarone hydroxypropyl-β-cyclodextrin solution agent by intranasal administration.Method:Compared injection and nasal administration perfusion in rabbit of asarone hydroxypropyl-β-cyclodextrin solution agent,feasibility pathway of drug release in brain was investigated after intranasal administration.Result:The content of asarone in blood,olfactory brain,brain and ethmoidal concha had higher quantity by nasal perfusion group than that by intravenous injection group.Conclusion: In pathway process of asarone hydroxypropyl-β-cyclodextrin solution agent enter brain by ethmoidal concha,the content of asarone was higher by nasal perfusion than injection,so it had practical feasibility of brain release by intranasal administration of asarone.

关 键 词:细辛脑 环糊精 鼻腔给药 

分 类 号:R283.6[医药卫生—中药学]

 

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