Boyce S T, Warden G D, Holder I A
Research Department, Shriners Burns Institute, Cincinnati, Ohio 45229, USA.
Antimicrob Agents Chemother. 1995 Jun;39(6):1324-8. doi: 10.1128/AAC.39.6.1324.
Cultured skin grafts are destroyed more easily than split-thickness skin grafts by common burn wound organisms, including gram-negative and gram-positive bacteria and fungi. To increase the survival and engraftment of cultured skin grafts, formulations of antimicrobial agents were tested for cytotoxicity to cultured human keratinocytes and fibroblasts and for activity against common organisms from burn wounds. On the basis of previous studies, a base formulation containing neomycin (40 micrograms/ml), polymyxin B (700 U/ml), and mupirocin (40 micrograms/ml) was prepared, to which ciprofloxacin (20 micrograms/ml) or norfloxacin (20 micrograms/ml) and amphotericin B (0.25 microgram/ml) or nystatin (100 U/ml) were added. Toxicity to cultured human cells was determined by the growth response of cell cultures (n = 6) to each drug combination over 4 days. Activity against clinical isolates (n = 40) of Staphylococcus aureus, Pseudomonas aeruginosa, other gram-negative bacteria, and Candida spp. was determined by the wet disc assay. Analysis of variance testing showed no significant differences in the growth of keratinocytes or fibroblasts under control or experimental conditions. Medium without antimicrobial agents was not effective against any of the 40 microbial strains tested. The base formulation was effective against all bacterial strains tested but against none of the fungi, while all experimental formulations were effective against all microbial strains tested. These findings suggest that neomycin, mupirocin, and polymyxin B may be combined with a quinolone and an antimycotic agent to provide broad antimicrobial activity for a formulation for topical use with cultured skin on burns. However, the formulations described here are strictly experimental and are not recommended for clinical use without further evaluation.
与中厚皮片相比,培养的皮肤移植物更容易被常见的烧伤创面微生物破坏,这些微生物包括革兰氏阴性菌、革兰氏阳性菌和真菌。为了提高培养的皮肤移植物的存活率和植入率,对抗菌剂配方进行了测试,以检测其对培养的人角质形成细胞和成纤维细胞的细胞毒性以及对烧伤创面常见微生物的活性。根据先前的研究,制备了一种基础配方,其中含有新霉素(40微克/毫升)、多粘菌素B(700单位/毫升)和莫匹罗星(40微克/毫升),并添加环丙沙星(20微克/毫升)或诺氟沙星(20微克/毫升)以及两性霉素B(0.25微克/毫升)或制霉菌素(100单位/毫升)。通过细胞培养物(n = 6)在4天内对每种药物组合的生长反应来确定对培养的人细胞的毒性。通过湿盘试验确定对金黄色葡萄球菌、铜绿假单胞菌、其他革兰氏阴性菌和念珠菌属临床分离株(n = 40)的活性。方差分析测试表明,在对照或实验条件下,角质形成细胞或成纤维细胞的生长没有显著差异。不含抗菌剂的培养基对所测试的40种微生物菌株均无效。基础配方对所有测试的细菌菌株有效,但对所有真菌均无效,而所有实验配方对所有测试的微生物菌株均有效。这些发现表明,新霉素、莫匹罗星和多粘菌素B可与喹诺酮类和抗真菌剂联合使用,为烧伤培养皮肤的局部使用配方提供广泛的抗菌活性。然而,这里描述的配方严格来说是实验性的,未经进一步评估不建议临床使用。