Amorolfine hydrochloride ethosomes showed a slow release rate.
盐酸阿莫罗芬醇质体释放速度较慢。
Results: Amorolfine hydrochloride ethosomes showed a slow release rate.
结果：盐酸阿莫罗芬乙醇脂质体体外释放速度较慢；
METHODS: Tanshinone ethosomes were prepared by thin-film ultrasonic method.
方法采用薄膜超声法制备脂质传递体。
OBJECTIVE To investigate the penetration characteristics of finasteride ethosomes as a transdermal vehicle.
目的考察醇质体作为非那甾胺经皮给药载体的渗透特性。
OBJECTIVE To prepare ethosomes and investigate the feasibility of ethosome as transdermal carries of colchicines.
目的制备秋水仙碱醇质体并考察醇质体作为秋水仙碱经皮给药载体的可行性。
Conclusion: the ethosomes loading 2me2 exhibited a better transdermal potential, which were worth studying further.
结论：2 -甲氧基雌二醇醇质体具有较好的透皮吸收的潜力，值得进一步开发研究。
Objective: to investigate the effect of different matrixes on the in vitro release of scutellarin ethosomes gel, and to select the suitable matrixes.
目的：考察不同基质对灯盏乙素醇质体凝胶剂体外释放的影响，筛选出适合灯盏乙素醇质体的凝胶基质。
The percentage of amorolfine in ethosomes permeated from isolated skin was increased by 1.7 and 3 times as that of hydroalcoholic solution and liposomes, respectively.
乙醇脂质体透过皮肤进入接受液中的药物量分别为乙醇溶液及脂质体的1.7和3倍，乙醇脂质体可有效增加探针药物的透皮量和穿透深度。
METHODS Taking encapsulated ratio and average diameter as evaluation index to optimize the best matching of soybean phospholipid, drug and absolute alcohol in ethosomes.
方法：以包封率和平均粒径为评价指标，采用星点设计-效应面法优化醇质体处方中大豆磷脂、药物和无水乙醇的最佳配比。
METHODS Taking encapsulated ratio and average diameter as evaluation index to optimize the best matching of soybean phospholipid, drug and absolute alcohol in ethosomes.
方法：以包封率和平均粒径为评价指标，采用星点设计-效应面法优化醇质体处方中大豆磷脂、药物和无水乙醇的最佳配比。
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