Colding H, Andersen G E
Antimicrob Agents Chemother. 1978 Apr;13(4):555-8. doi: 10.1128/AAC.13.4.555.
The stability and interaction at 29 degrees C of ampicillin, carbenicillin, gentamicin, and polymyxin B were examined in a common electrolyte solution, invertose darrow, and in two synthetic l-amino acid solutions, one commercial (vamin with fructose; Vitrum) and the other a neonatal preparation modified for use in newborn infants. The concentration of amino acids was measured before and after the addition of these antibiotics. The concentration of antibiotics was measured over a 24-h period with a microbiological method. The concentration of ampicillin in invertose darrow fell 52%, and in vamin with fructose it fell 69%, whereas in the neonatal preparation the fall was only 22%. The concentration of carbenicillin in vamin with fructose fell 37%, and in the neonatal preparation it fell 31%. The combination of ampicillin or carbenicillin with gentamicin or polymyxin B did not influence the activity of the penicillins. The concentration of gentamicin and polymyxin B was unchanged in all solutions over a 24-h period. With the exception of cystine, the concentration of all amino acids remained constant after 24 h in the neonatal preparation with and without the different combinations of antibiotics. For cystine there was a fall of 20 to 30%.
在一种常见电解质溶液(转化糖电解质溶液)、一种商品用合成左旋氨基酸溶液(含果糖的凡命;维特鲁姆公司)以及另一种专为新生儿改良的制剂中,检测了氨苄西林、羧苄西林、庆大霉素和多粘菌素B在29摄氏度时的稳定性及相互作用。在添加这些抗生素前后测定氨基酸浓度。采用微生物学方法在24小时内测定抗生素浓度。在转化糖电解质溶液中,氨苄西林浓度下降了52%,在含果糖的凡命中下降了69%,而在新生儿制剂中仅下降了22%。在含果糖的凡命中,羧苄西林浓度下降了37%,在新生儿制剂中下降了31%。氨苄西林或羧苄西林与庆大霉素或多粘菌素B联合使用不影响青霉素的活性。在24小时内,所有溶液中庆大霉素和多粘菌素B的浓度均无变化。在含不同抗生素组合和不含抗生素的新生儿制剂中,24小时后除胱氨酸外,所有氨基酸浓度均保持恒定。胱氨酸浓度下降了20%至30%。