Hilleman D E, McEvoy G K, Bailey R T, Reich J
Hosp Pharm. 1984 Mar;19(3):202, 207, 211-3.
The freeze-microwave thaw technique has important advantages compared with conventional piggyback delivery systems. A requirement for the implementation of this technique, however, is the documentation of antibiotic stability following freezing and microwave thawing. The purpose of this study was to assess the stability of a commonly used cephalosporin, cephapirin sodium, following freezing and conventional or microwave thawing. This data was not previously available. Cephapirin sodium was admixed with either 5% dextrose injection or 0.9% sodium chloride injection in polyvinylchloride minibags at concentrations of 10 and 40 mg/ml and then frozen for 14 days. Admixtures were then thawed conventionally or by microwave heating. Cephapirin concentrations were determined spectrophotometrically after reconstitution, immediately after thawing, and 6, 12, and 24 hours after thawing. No significant differences in admixture potency after reconstitution, immediately after thawing, or at 6, 12, and 24 hours after thawing were observed when thaw techniques were compared. All admixtures retained at least 90% of labeled content regardless of thaw technique, type of diluent, or initial concentration. In addition, all admixtures retained at least 90% potency 24 hours after thawing when compared with the actual concentration determined immediately after reconstitution. The rate of cephapirin degradation was not influenced by thaw technique, type of diluent, or initial admixture concentration. The results of this study suggest that cephapirin sodium may be added to the list of drugs capable of withstanding freeze-microwave thaw treatment.
与传统的背驮式给药系统相比,冷冻-微波解冻技术具有重要优势。然而,实施该技术的一个要求是记录冷冻和微波解冻后抗生素的稳定性。本研究的目的是评估常用头孢菌素头孢匹林钠在冷冻以及传统解冻或微波解冻后的稳定性。此前尚无该数据。将头孢匹林钠以10mg/ml和40mg/ml的浓度与5%葡萄糖注射液或0.9%氯化钠注射液在聚氯乙烯小袋中混合,然后冷冻14天。然后将混合物进行传统解冻或微波加热解冻。复溶后、解冻后立即以及解冻后6、12和24小时,通过分光光度法测定头孢匹林浓度。比较解冻技术时,未观察到复溶后、解冻后立即或解冻后6、12和24小时混合物效力的显著差异。无论解冻技术、稀释剂类型或初始浓度如何,所有混合物均保留至少90%的标示含量。此外,与复溶后立即测定的实际浓度相比,所有混合物在解冻后24小时仍保留至少90%的效力。头孢匹林的降解速率不受解冻技术、稀释剂类型或初始混合物浓度的影响。本研究结果表明,头孢匹林钠可能可列入能够耐受冷冻-微波解冻处理的药物名单。