Systemic absorption of topical lidocaine in normal volunteers, patients with post-herpetic neuralgia, and patients with acute herpes zoster

被引:66
作者
Campbell, BJ
Rowbotham, M
Davies, PS
Jacob, P
Benowitz, NL [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Div Clin Pharmacol & Expt Therapeut, San Francisco, CA 94143 USA
[6] Univ N Carolina, Sch Pharm, Dept Drug Delivery & Disposit, Chapel Hill, NC 27599 USA
关键词
lidocaine; pharmacokinetics; skin; transdermal; herpes zoster; neuralgia;
D O I
10.1002/jps.10133
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Topical lidocaine has been recently marketed as a new treatment for post-herpetic neuralgia. The aim of our study was to characterize the absorption profile of and systemic exposure to lidocaine from patch and gel formulations in normal volunteers, patients with post-herpetic neuralgia, and patients with acute herpes zoster. The bioavailability of lidocaine from the patch formulation averaged 3%, and was similar after single and repeated doses. Systemic exposure to lidocaine and monoethylglycinexylidide (MEGX), the primary active metabolite of lidocaine, after application of lidocaine gel or patches was minimal in normal volunteers, patients with post-herpetic neuralgia, and patients with acute herpes zoster. Considering the benefit versus risk of topical lidocaine, systemic absorption and toxicity of lidocaine seems not to be a significant risk. (C) 2002 Wiley-Liss, Inc. and the American Pharmaceutical Association.
引用
收藏
页码:1343 / 1350
页数:8
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