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在体猪耳静脉灌流经皮吸收模型的建立与应用
引用本文:胡晋红,朱全刚,沈琦.在体猪耳静脉灌流经皮吸收模型的建立与应用[J].药学学报,2003,38(10):783-786.
作者姓名:胡晋红  朱全刚  沈琦
作者单位:第二军医大学,长海医院,药学部,上海200433
基金项目:国家自然科学基金资助项目(39970880 )
摘    要:目的建立在体猪耳静脉灌流经皮吸收模型,为经皮吸收制剂研究提供新方法。方法建立在体猪耳静脉灌流经皮吸收模型。以葡萄糖利用试验及乳酸脱氢酶活性检测评价模型的生物学活性,以酮洛芬异丙酯和水杨酸甲酯为模型药物考察系统的应用。结果葡萄糖利用及乳酸脱氢酶活性检测表明系统7 h内保持良好生物学活性。酮洛芬异丙酯经皮渗透过程中被完全代谢为酮洛芬,稳态时酮洛芬累积形成量Q与时间t回归的方程为Q=-0.024+0.120t,形成速率为0.120 μg·cm-2·h-1。水杨酸甲酯经皮渗透过程中部分被代谢为水杨酸,稳态时水杨酸甲酯累积渗透量Q与时间t回归的方程为Q=-3.809+6.129 t,渗透速率为6.129 μg·cm-2·h-1;水杨酸累积形成量Q与时间t回归的方程为Q=-1.785+0.879 t,形成速率为0.879 μg·cm-2·h-1。结论该模型操作简便、价格经济,不仅可以考察药物的经皮吸收,而且能够用于研究药物的皮肤代谢。

关 键 词:经皮吸收  皮肤代谢  幼猪  酮洛芬异丙酯  水杨酸甲酯
收稿时间:2002-10-14

Establishment and application of in situ perfused pig ear model for percutaneous absorption
HU Jin-hong,ZHU Quan-gang,SHEN Qi.Establishment and application of in situ perfused pig ear model for percutaneous absorption[J].Acta Pharmaceutica Sinica,2003,38(10):783-786.
Authors:HU Jin-hong  ZHU Quan-gang  SHEN Qi
Institution:Department of Pharmacy, Changhai Hospital, Second Military Medical University, Shanghai 200433, China. PharmCR@yaoxue.net
Abstract:AIM: To establish an in situ perfused pig ear model for percutaneous absorption. METHODS: The in situ perfused pig ear model for percutaneous absorption consisted of artificial gas, sample chamber, constant flow pump, constant temperature system, polytetrafluorethylene connective tube, porcine ear vein, porcine ear skin and special laminar flow apparatus. The perfused system viability was assessed by glucose utilization and lactate production. Ketoprofen isopropyl ester and methyl salicylate was used for validating this model. The concentrations of perfused sample were measured by HPLC. RESULTS: Glucose utilization and lactate production showed that this model was viable till 7 h. Ketoprofen isopropyl ester was completely metabolized to ketoprofen in situ in perfused pig ear model. The steady cumulative amount (Q) of ketoprofen from permeation and metabolism was linear with time (t), the equation of ketoprofen formation was Q = -0.024 + 0.120t, the rate of ketoprofen formation was 0.120 microgram.cm-2.h-1. Methyl salicylate was partially metabolized to salicylic acid. The steady cumulative amount (Q) of methyl salicylate from permeation was linear with time (t), the permeation equation of methyl salicylate was Q = -3.809 + 6.129t, the permeation rate of metyl salicylate was 6.129 micrograms.cm-2.h-1. The steady cumulative amount (Q) of salicylic acid from metabolism was also linear with time (t), the formation equation of salicylic acid was Q = -1.785 + 0.879t, the formation rate of salicylic acid was 0.879 microgram.cm-2.h-1. CONCLUSION: The in situ pig ear vein perfused model is a novel easy-handing and cost-efficient technique for percutaneous absorption and skin metabolism.
Keywords:percutaneous absorption  skin metabolism  pig  ketoprofen isopropyl ester  metyl salicylate
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