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1
Stability of antibiotics and amino acids in two synthetic L-amino acid solutions commonly used for total parenteral nutrition in children.两种常用于儿童全胃肠外营养的合成L-氨基酸溶液中抗生素与氨基酸的稳定性
Antimicrob Agents Chemother. 1978 Apr;13(4):555-8. doi: 10.1128/AAC.13.4.555.
2
Stability of ampicillin, piperacillin, cefotaxime, netilmicin and amikacin in an L-amino acid solution prepared for total parenteral nutrition of newborn infants.氨苄西林、哌拉西林、头孢噻肟、奈替米星和阿米卡星在为新生儿全胃肠外营养制备的L-氨基酸溶液中的稳定性。
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Administration of gentamicin and ampicillin by continuous intravenous infusion to newborn infants during parenteral nutrition.在肠外营养期间通过持续静脉输注向新生儿给予庆大霉素和氨苄西林。
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引用本文的文献

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Continuous intravenous infusion of ampicillin and gentamicin during parenteral nutrition in 88 newborn infants.88例新生儿肠外营养期间持续静脉输注氨苄西林和庆大霉素。
Arch Dis Child. 1982 Aug;57(8):602-6. doi: 10.1136/adc.57.8.602.

本文引用的文献

1
Paper disk-agar diffusion assay of penicillin in the presence of streptomycin.在链霉素存在的情况下进行青霉素的纸碟琼脂扩散试验。
Antimicrob Agents Chemother. 1974 Nov;6(5):603-5. doi: 10.1128/AAC.6.5.603.
2
The reaction of benzylpenicillin with carbohydrates at neutral pH with a note on the immunogenicity of hapten polysaccharide conjugates.苄青霉素在中性pH条件下与碳水化合物的反应及对半抗原多糖缀合物免疫原性的注释
Immunochemistry. 1967 Sep;4(5):331-43. doi: 10.1016/0019-2791(67)90116-4.
3
Inactivation of penicillins by carbohydrate solutions at alkaline pH.在碱性pH值下,青霉素被碳水化合物溶液灭活。
N Engl J Med. 1970 Jul 16;283(3):116-9. doi: 10.1056/NEJM197007162830302.
4
Prediction of penicillin allergy by immunological tests.通过免疫学检测预测青霉素过敏。
Ann N Y Acad Sci. 1967 Sep 27;145(2):298-309. doi: 10.1111/j.1749-6632.1967.tb50227.x.
5
Stability of antibiotics in parenteral solutions.抗生素在注射剂中的稳定性。
Pediatrics. 1972 Jan;49(1):22-9.
6
A micromethod for determination of antibiotics in serum.一种测定血清中抗生素的微量方法。
Dan Med Bull. 1969 May;16(5):133-9.
7
[Inactivation of antibiotics in infusion solutions].[输液溶液中抗生素的失活]
Infection. 1973;1(3):151-6. doi: 10.1007/BF01641325.
8
Antibiotic stability in solutions used for intravenous nutrition and fluid therapy.用于静脉营养和液体治疗的溶液中抗生素的稳定性。
Pediatrics. 1973 Jun;51(6):1016-26.
9
Therapeutic implications of interaction of gentamicin and penicillins.
Lancet. 1971 Sep 11;2(7724):575-8. doi: 10.1016/s0140-6736(71)92152-0.
10
Feasibility of administering aminoglycoside antibiotics by continuous intravenous infusion.通过持续静脉输注给予氨基糖苷类抗生素的可行性。
Antimicrob Agents Chemother. 1975 Sep;8(3):328-33. doi: 10.1128/AAC.8.3.328.

两种常用于儿童全胃肠外营养的合成L-氨基酸溶液中抗生素与氨基酸的稳定性

Stability of antibiotics and amino acids in two synthetic L-amino acid solutions commonly used for total parenteral nutrition in children.

作者信息

Colding H, Andersen G E

出版信息

Antimicrob Agents Chemother. 1978 Apr;13(4):555-8. doi: 10.1128/AAC.13.4.555.

DOI:10.1128/AAC.13.4.555
PMID:27137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC352287/
Abstract

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%.

摘要

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%。