INTERACTION OF AMINOGLYCOSIDE ANTIBIOTICS WITH PHOSPHOLIPID LIPOSOMES STUDIES BY MICRO-ELECTROPHORESIS

被引:37
作者
ALEXANDER, AM [1 ]
GONDA, I [1 ]
HARPUR, ES [1 ]
KAYES, JB [1 ]
机构
[1] UNIV ASTON,DEPT PHARM,BIRMINGHAM B4 7ET,W MIDLANDS,ENGLAND
关键词
D O I
10.7164/antibiotics.32.504
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microelectrophoresis was found to be a rapid method for studying the interaction between aminoglycoside antibiotics and liposomes prepared from acid phospholipids. The ability to cause charge reversai of liposomes prepared from phosphatidyl inositol was ranked in the order neomycin > gentamicin tobramycin amikacin kanamycin ribostamycin streptomycin dihydrostreptomycin Ca2+. Similar results were obtained with liposomes prepared from a mixture (8:2) of phosphatidyl choline and phosphatidic acid, but no effect was detectable with neutral liposomes made from phosphatidyl choline only. The results support the view that the attraction between positively charged nitrogen groups on the antibiotics and the negatively charged groups of acidic phospholipids are predominantly responsible for the interaction. Extension of the studies to ionic strengths and calcium concentrations similar to those found in vivo showed a reduction, but nou: elimination, of the observed effects. © 1979, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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页码:504 / 510
页数:7
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