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药物的稳定性与配伍性:以某些头孢菌素为例

Stability and Compatibility Aspects of Drugs: The Case of Selected Cephalosporins.

作者信息

Tomczak Szymon, Gostyńska Aleksandra, Nadolna Malwina, Reisner Karolina, Orlando Marta, Jelińska Anna, Stawny Maciej

机构信息

Department and Chair of Pharmaceutical Chemistry, Poznan University of Medical Sciences, 6 Grunwaldzka, 60-780 Poznań, Poland.

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale F. Stagno D'Alcontres 31, I-98166 Messina, Italy.

出版信息

Antibiotics (Basel). 2021 May 9;10(5):549. doi: 10.3390/antibiotics10050549.

Abstract

Intravenous drug incompatibilities are a common cause of medical errors, contributing to ineffective therapy and even life-threatening events. The co-administration of drugs must always be supported by studies confirming compatibility and thus guarantee the therapy's safety. Particular attention should be paid to the possible incompatibilities or degradation of intravenous cephalosporins in different infusion regimens since the administration of drugs with inadequate quality may cause treatment failure. Therefore, an appropriate stability test should be performed. The study aimed to present various aspects of the stability and compatibility of five cephalosporins: cefepime (CFE), cefuroxime (CFU), ceftriaxone (CFX), ceftazidime (CFZ), and cefazoline (CFL). The degradation studies in parenteral infusion fluids and PN admixtures were conducted for CFE and CFU. The interactions between CFX or CFZ and PN admixtures, as well as the compatibility of CFL with five commercial parenteral nutrition (PN) admixtures, were investigated. The content of CFX and CFZ in PN admixture after 24 h was >90%. CFL administered simultaneously with PN admixture by the same infusion set using Y-site was compatible only with Nutriflex Lipid Special. CFE and CFU were stable in all tested infusion fluids for a minimum of 48 h and decomposed in PN admixtures during storage.

摘要

静脉药物配伍禁忌是医疗差错的常见原因,会导致治疗无效甚至危及生命的事件。药物的联合使用必须始终有证实其配伍性的研究支持,从而确保治疗的安全性。由于使用质量不佳的药物可能导致治疗失败,因此应特别注意不同输注方案中静脉用头孢菌素可能存在的配伍禁忌或降解情况。因此,应进行适当的稳定性测试。该研究旨在呈现五种头孢菌素(头孢吡肟(CFE)、头孢呋辛(CFU)、头孢曲松(CFX)、头孢他啶(CFZ)和头孢唑林(CFL))稳定性和配伍性的各个方面。对CFE和CFU进行了在肠外输液和肠外营养(PN)混合液中的降解研究。研究了CFX或CFZ与PN混合液之间的相互作用,以及CFL与五种市售肠外营养(PN)混合液的配伍性。24小时后PN混合液中CFX和CFZ的含量>90%。通过Y型接口同一输液器与PN混合液同时给药时,CFL仅与Nutriflex Lipid Special配伍。CFE和CFU在所有测试的输液中至少稳定48小时,在储存期间在PN混合液中分解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc4/8151819/b2a35267587c/antibiotics-10-00549-g001.jpg

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