Optimized LC-MS/MS quantification method for the detection of piperacillin and application to the development of charged liposaccharides as oral penetration enhancers

被引:8
作者
Violette, Aude [1 ]
Cortes, Diego A. Faria [1 ]
Bergeon, Julie A. [1 ]
Falconer, Robert A. [2 ]
Toth, Istvan [1 ]
机构
[1] Univ Queensland, Sch Mol & Microbial Sci, Brisbane, Qld, Australia
[2] Univ Bradford, Sch Life Sci, Inst Canc Therapeut, Bradford BD7 1DP, W Yorkshire, England
基金
澳大利亚研究理事会;
关键词
piperacillin; charged liposaccharide; penetration enhancer; LC-MS/MS; Caco-2; permeability;
D O I
10.1016/j.ijpharm.2007.09.039
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Piperacillin, a potent beta-lactam antibiotic, is effective in a large variety of Gram+ and Gram- bacterial infections but its administration is limited to the parenteral route as it is not absorbed when given orally. In an attempt to overcome this problem, we have synthesized a novel series of charged liposaccharide complexes of piperacillin comprising a sugar moiety derived from D-glucose conjugated to a lipoamino acid residue with varying side-chain length (cationic entity) and the piperacillin anion. A complete multiple reaction monitoring LC-MS/MS method was developed to detect and characterize the synthesized complexes. The same method was then successfully applied to assess the in vitro apparent permeability values of the charged liposaccharide complexes in Caco-2 monolayers. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:152 / 157
页数:6
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