The use of immunoliposomes for specific delivery of antimicrobial agents to oral bacteria immobilized on polystyrene

被引:28
作者
Robinson, AM
Creeth, JE
Jones, MN [1 ]
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
[2] Unilever Res, Port Sunlight Lab, Wirral, Merseyside, England
关键词
immunoliposomes; liposome targeting; liposome drug delivery; Triclosan (TM); chlorhexidine; bactericide; bacterial biofilms; oral bacteria;
D O I
10.1163/156856200744408
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Antibacterial immunoliposomes have been prepared using covalently bound antibody, raised to the cell surface of the bacterium Streptococcus oralis (S. oralis), and incorporating the bactericides chlorhexidine and Triclosan(TM). A regrowth assay, in which the ability of a bacterial biofilm immobilised on polystyrene to grow after exposure to a test solution, was undertaken to study the action of the antibacterial immunoliposomes. The antibacterial anti-oralis immunoliposomes show enhanced growth inhibition of S, oralis, compared to free bactericide, using low bactericide concentrations. For short exposure times to the biofilms, antibacterial anti-oralis immunoliposomes can show several times enhanced growth inhibition of S, oralis compared to free bactericide. Antibacterial anti-oralis immunoliposomes inhibit the growth of S. oralis more than that of other oral bacteria. The extent of growth inhibition by antibacterial anti-oralis immunoliposomes is linearly related to the number of immunoliposomes targeted to the biofilm surface.
引用
收藏
页码:1381 / 1393
页数:13
相关论文
共 23 条
[1]   LIPOSOMES AS DELIVERY SYSTEMS IN THE PREVENTION AND TREATMENT OF INFECTIOUS-DISEASES [J].
BERGERS, JJ ;
TENHAGEN, TLM ;
VANETTEN, EWM ;
BAKKERWOUDENBERG, IAJM .
PHARMACY WORLD & SCIENCE, 1995, 17 (01) :1-11
[2]   A SIMPLE THEORETICAL TREATMENT OF A COMPETITIVE ENZYME-LINKED-IMMUNOSORBENT-ASSAY (ELISA) AND ITS APPLICATION TO THE DETECTION OF HUMAN BLOOD-GROUP ANTIGENS [J].
CHAPMAN, V ;
FLETCHER, SM ;
JONES, MN .
JOURNAL OF IMMUNOLOGICAL METHODS, 1990, 131 (01) :91-98
[3]  
DEMUTH DR, 1990, J BIOL CHEM, V265, P7120
[4]   CLONING AND EXPRESSION OF A STREPTOCOCCUS-SANGUIS SURFACE-ANTIGEN THAT INTERACTS WITH A HUMAN SALIVARY AGGLUTININ [J].
DEMUTH, DR ;
DAVIS, CA ;
CORNER, AM ;
LAMONT, RJ ;
LEBOY, PS ;
MALAMUD, D .
INFECTION AND IMMUNITY, 1988, 56 (09) :2484-2490
[5]  
Douglas C W, 1994, Adv Dent Res, V8, P254
[6]   A NEW REAGENT WHICH MAY BE USED TO INTRODUCE SULFHYDRYL-GROUPS INTO PROTEINS, AND ITS USE IN THE PREPARATION OF CONJUGATES FOR IMMUNOASSAY [J].
DUNCAN, RJS ;
WESTON, PD ;
WRIGGLESWORTH, R .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :68-73
[7]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[8]   THE CONTROL OF PROTEIN SURFACE CONCENTRATION ON PROTEOLIPOSOMES [J].
FRANCIS, SE ;
HUTCHINSON, FJ ;
LYLE, IG ;
JONES, MN .
COLLOIDS AND SURFACES, 1992, 62 (1-2) :177-184
[9]   THE IDEALITY OF PHOSPHATIDYLINOSITOL PHOSPHATIDYLCHOLINE MIXTURES IN MULTILAMELLAR LIPOSOMES [J].
HAMMOND, K ;
LYLE, IG ;
JONES, MN .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1984, 99 (01) :294-296
[10]   TARGETED LIPOSOMES - A METHOD FOR PREPARATION AND ANALYSIS [J].
JANSONS, VK ;
MALLETT, PL .
ANALYTICAL BIOCHEMISTRY, 1981, 111 (01) :54-59