IN-VITRO INTERACTIONS OF NEOMYCIN SULFATE, BACITRACIN, AND POLYMYXIN-B SULFATE

被引:17
作者
BOOTH, JH [1 ]
BENRIMOJ, SI [1 ]
NIMMO, GR [1 ]
机构
[1] PRINCESS ALEXANDRA HOSP,DEPT MICROBIOL,BRISBANE,QLD,AUSTRALIA
关键词
D O I
10.1111/j.1365-4362.1994.tb02872.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background. Neomycin sulfate, bacitracin, and polymyxin B sulfate have been combined in topical preparations to provide a complementary antimicrobial spectrum for the prevention of minor wound infections. The advisability of the inclusion of neomycin sulfate has been questioned since it may cause contact sensitization. Methods. To assess the value of neomycin, microdilution checkerboard titrations were used to determine the in vitro interactions between two-antibiotic and three-antibiotic combinations against reference strains of bacteria commonly associated with wound infections. Using Fractional Inhibitory Concentration (FIC) indices (< 0.5 indicates synergism with two-drug combinations), the combination of neomycin/bacitracin was synergistic for both S. aureus and Ps. aeruginosa; neomycin/polymyxin B was synergistic for E. faecalis, and the bacitracin/polymyxin B combination was synergistic against Ps. aeruginosa. A three-drug combination of neomycin/bacitracin/polymyxin B had FIC values of < 1 for all organisms, indicating synergy and substantiating the clinical role of neomycin sulfate in current topical formulations. Results. Neomycin has the lowest safety profile of the drugs in this combination. A replacement agent should ideally have similar or superior synergistic capabilities with the remaining drugs and contribute to the therapeutic efficacy of the preparation. Additionally, because of the strongly synergistic tendencies displayed by the three-drug combination, it may be possible to reduce the antibiotic concentrations present in current formulations. Conclusion. By developing this concept, there is potential for the formulation of topical preparations to be based on a sound theoretical and clinical rationale.
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页码:517 / 520
页数:4
相关论文
共 18 条
[1]  
Anderson V, 1976, Int J Dermatol, V15, P1
[2]  
Beale A.S., 1983, ANTIBIOTICS ASSESSME, P299
[3]   CRITERIA FOR ANALYZING INTERACTIONS BETWEEN BIOLOGICALLY-ACTIVE AGENTS [J].
BERENBAUM, MC .
ADVANCES IN CANCER RESEARCH, 1981, 35 :269-335
[4]   SYNERGY WITH DOUBLE AND TRIPLE ANTIBIOTIC COMBINATIONS COMPARED [J].
BERENBAUM, MC ;
YU, VL ;
FELEGIE, TP .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1983, 12 (06) :555-563
[5]   SYNERGISM OF THE ANTI-MICROBIAL AGENTS MICONAZOLE, BACITRACIN AND POLYMYXIN-B [J].
CORNELISSEN, F ;
VANDENBOSSCHE, H .
CHEMOTHERAPY, 1983, 29 (06) :419-427
[6]  
ELIOPOULOS G M, 1988, Clinical Microbiology Reviews, V1, P139
[7]   THE SYNERGISM BETWEEN CETRIMIDE AND ANTIBIOTICS AGAINST PSEUDOMONAS-AERUGINOSA [J].
ELNIMA, EI .
ZENTRALBLATT FUR BAKTERIOLOGIE MIKROBIOLOGIE UND HYGIENE SERIES A-MEDICAL MICROBIOLOGY INFECTIOUS DISEASES VIROLOGY PARASITOLOGY, 1984, 258 (01) :120-127
[8]  
Krogstad D. J., 1980, ANTIBIOTICS LABORATO, P298
[9]  
LECHEVALIER HA, 1975, 25 YEARS NEOMYCIN, P359
[10]  
NEUMAN M, 1985, USEFUL HARMFUL INTER