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应对静脉补钙短缺问题:评估氯化钙在0.9%氯化钠溶液和5%葡萄糖溶液聚氯乙烯袋中的稳定性

Managing the Intravenous Calcium Shortage: Evaluation of Calcium Chloride Stability in 0.9% Sodium Chloride and Dextrose 5% Water Polyvinyl Chloride Bags.

作者信息

Kiser Tyree H, Barber Gerard R, Robinson Aubrey

机构信息

Department of Clinical Pharmacy, University of Colorado Anschutz Medical Campus, Aurora, Colorado.

Department of Pharmacy, University of Colorado Hospital, Aurora, Colorado.

出版信息

Hosp Pharm. 2012 Jan 1;47(1):27-30. doi: 10.1310/hpj4701-27.

DOI:10.1310/hpj4701-27
PMID:32180591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7075352/
Abstract

BACKGROUND

Intravenous calcium chloride (CaCl) is commonly used by inpatient practitioners for a myriad of indications from electrolyte abnormalities to advanced cardiac life support. Currently, a paucity of data is available regarding the stability of CaCl after preparation of intravenous admixtures.

PURPOSE

This study evaluated the physical and chemical stability of CaCl 10% diluted in 0.9% sodium chloride or dextrose 5% water polyvinyl chloride bags.

METHOD

CaCl 10% solution (1000 mg) was diluted with 0.9% sodium chloride or dextrose 5% water 100 mL for injection to a final concentration of 10 mg/mL. CaCl 10% solution (2000 mg) was diluted with 0.9% sodium chloride or dextrose 5% water 150 mL for injection to a final concentration of 13.3 mg/mL. Each of the preparations were stored at room temperature (23-25°C) and exposed to fluorescent light. Samples of each preparation were analyzed on days 0, 2, 3, 5, and 7. Sterility and physical stability were assessed. Chemical stability of CaCl was evaluated by indirect potentiometry.

RESULTS

CaCl 10 mg/mL and 13.3 mg/mL solutions in polyvinyl chloride bags were physically stable during the entire 7-day study period. CaCl retained >90% of the original concentration at 7 days after preparation in 0.9% sodium chloride and dextrose 5% water.

CONCLUSION

CaCl diluted to 10 mg/mL or 13.3 mg/mL with 0.9% sodium chloride or dextrose 5% water for injection is both physically and chemically stable for a period of 7 days with ≤10% degradation under conditions of room temperature with fluorescent lighting.

摘要

背景

住院医生常用静脉注射氯化钙(CaCl)来治疗多种病症,从电解质异常到高级心脏生命支持。目前,关于静脉混合液配制后氯化钙的稳定性数据匮乏。

目的

本研究评估了10%氯化钙在0.9%氯化钠或5%葡萄糖水溶液聚氯乙烯袋中的物理和化学稳定性。

方法

将10%氯化钙溶液(1000毫克)用100毫升0.9%氯化钠或5%葡萄糖注射液稀释至最终浓度为10毫克/毫升。将10%氯化钙溶液(2000毫克)用150毫升0.9%氯化钠或5%葡萄糖注射液稀释至最终浓度为13.3毫克/毫升。每种制剂均在室温(23 - 25°C)下储存并暴露于荧光灯下。在第0、2、3、5和7天对每种制剂的样品进行分析。评估无菌性和物理稳定性。通过间接电位滴定法评估氯化钙的化学稳定性。

结果

在整个7天的研究期间,聚氯乙烯袋中10毫克/毫升和13.3毫克/毫升的氯化钙溶液物理稳定。在0.9%氯化钠和5%葡萄糖水溶液中配制后7天,氯化钙保留了>90%的原始浓度。

结论

用0.9%氯化钠或5%葡萄糖注射液稀释至10毫克/毫升或13.3毫克/毫升的氯化钙在室温及荧光照明条件下,7天内物理和化学均稳定,降解≤10%。

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Surg Today. 2007;37(9):778-81. doi: 10.1007/s00595-006-3426-z. Epub 2007 Aug 27.
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Physical compatibility and chemical stability of amikacin sulfate in combination with non-antibiotic drugs in large-volume parenteral solutions - part IV.硫酸阿米卡星与大容量注射剂中其他非抗生素药物的物理相容性和化学稳定性 - 第四部分。
Curr Ther Res Clin Exp. 1976 Oct;20(4):417-91.