Pre-formulation of liposomes against Helicobacter pylori:: Characterization and interaction with the bacteria

被引:31
作者
Bardonnet, Pierre-Louis [2 ,3 ]
Faivre, Vincent [1 ]
Boullanger, Paul [4 ]
Piffaretti, Jean-Claude [5 ]
Falson, Francoise [3 ]
机构
[1] Univ Paris Sud, Lab Physicochim Syst Polyphases, IFR 141, CNRS,UMR 8612, F-92296 Chatenay Malabry, France
[2] Pharmapeptides Parc Affaires Int, Archamps, France
[3] Univ Lyon 1, ISPB, F-69365 Lyon, France
[4] Univ Lyon 1, ICBMS, F-69622 Villeurbanne, France
[5] Ist Cantonale Microbiol, Bellinzona, Switzerland
关键词
liposome; Helicobacter pyloric; glycolipid; tageting; BabA2;
D O I
10.1016/j.ejpb.2008.01.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This paper deals with the formulation of targeted liposome against Helicobacler pylori. We describe the characterization of liposomes loaded with antimicrobial agents (ampicillin and metronidazole) and the quantification of the interactions between such formulations and bacteria. If the encapsulation rate of ampicillin seems not strongly affected by the change of phospholipidic composition, the encapsulation of metronidazole drastically decreased in epikuron 170 liposomes compared to DPPC ones. Furthermore, as observed with X-ray diffraction measurements, the presence of metronidazole results in the disorganisation of the phospholipid bilayers. Concerning the liposome-bacteria interactions, it has been observed that the incorporation of fucosyled glycolipids in the vesicle membrane leads to liposomes that Lire able to interact with the bacteria either in their spiral or in their coccoid forms. Since coccoid forms are occasionally found in vivo, their recognition by the liposomes we have formulated seems promising in the fight against Helicobacter pylori. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:908 / 922
页数:15
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