Spatially constrained skin electroporation with sodium thiosulfate and urea creates transdermal microconduits

被引:24
作者
Ilic, L
Gowrishankar, TR
Vaughan, TE
Herndon, TO
Weaver, JC
机构
[1] MIT, Harvard MIT Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] MIT, Lincoln Labs, Lexington, MA 02173 USA
关键词
transdermal drug delivery; human skin; stratum corneum (SC); microconduit (MC); electroporation; sodium thiosulfate (STS); urea;
D O I
10.1016/S0168-3659(99)00120-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlled transport of molecules through the skin's main barrier, the stratum corneum (SC), is a long standing goal of transdermal drug delivery. Traditional, needle-based injection provides delivery of almost any water soluble compound, by creating a single large aqueous pathway in the form of the hollow core of a needle, through which drug is delivered by pressure-driven flow. We extend previous work to show that SC-spanning microconduits (here with diameters of about 200 mu m) can be created in vivo by skin electroporation and low-toxicity, keratolytic molecules (here sodium thiosulfate and urea). A single microconduit in isolated SC can support volumetric flow of the order of 0.01 ml s(-1) by a pressure difference of only 0.01 atm (about 10(2) Pa), demonstrating that the SC barrier has been essentially eliminated within this microscopic area. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:185 / 202
页数:18
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