Transdermal drug carriers: Basic properties, optimization and transfer efficiency in the case of epicutaneously applied peptides
阅读量：
127
摘要：
In order to get across the intact mammalian skin, drug carriers must pass through a series of very fine pores with a diameter of typically less than 50 nm, under the influence of a suitable transdermal gradient. Well-known agent carriers, such as liposomes, fail to do this owing to their large (minimum) size. Special, composite carrying bodies called Transfersomes
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DOI：
10.1016/0168-3659(95)00056-E
被引量：
年份：
1995
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