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胺碘酮在聚氯乙烯输液袋和输液器上的吸附作用。

Sorption of amiodarone to polyvinyl chloride infusion bags and administration sets.

作者信息

Weir S J, Myers V A, Bengtson K D, Ueda C T

出版信息

Am J Hosp Pharm. 1985 Dec;42(12):2679-83.

PMID:4083289
Abstract

The loss of amiodarone from i.v. admixtures to flexible polyvinyl chloride (PVC) infusion bags and i.v. administration sets was studied. Admixtures containing amiodarone hydrochloride 600 micrograms/mL and either 5% dextrose injection or 0.9% sodium chloride injection were stored at room temperature in glass bottles (both with and without contact of the drug solution with the rubber bottle closure), in flexible PVC bags, or in rigid PVC bottles. After 120 hours, the contents of each flexible PVC bag were emptied and replaced by methanol, which was allowed to remain in the bag for an additional 120 hours and was then analyzed for amiodarone content. To determine availability of amiodarone after infusion through a 1.8-m PVC i.v. administration set, solutions stored in glass containers were run through the set at 0.5 mL/min for 90 minutes. Samples of drug solutions were collected at appropriate intervals and analyzed by a stability-indicating high-performance liquid chromatography (HPLC) assay. Admixtures containing 0.9% sodium chloride injection were not stable; visual incompatibility was evident after 24 hours of storage in glass bottles, and no further testing was performed. In admixtures containing 5% dextrose injection that were stored in 50-mL flexible PVC bags, 60% of the initial amiodarone concentration remained after 120 hours; approximately half of the lost drug was recovered with the methanol. In effluent collected from the PVC administration set, 82% of the initial amiodarone concentration remained. Amiodarone concentrations did not decrease appreciably, after storage in glass or rigid PVC bottles, indicating that drug loss was probably affected by the plasticizer, di-2-ethylhexyl phthalate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了静脉内混合液中的胺碘酮在软质聚氯乙烯(PVC)输液袋和静脉给药装置中的损失情况。含有600微克/毫升盐酸胺碘酮以及5%葡萄糖注射液或0.9%氯化钠注射液的混合液,在室温下分别储存在玻璃瓶中(有和没有药物溶液与橡胶瓶塞接触两种情况)、软质PVC袋中或硬质PVC瓶中。120小时后,将每个软质PVC袋中的内容物排空,并用甲醇替换,让甲醇在袋中再保留120小时,然后分析其胺碘酮含量。为了确定通过1.8米长的PVC静脉给药装置输注后胺碘酮的可用性,将储存在玻璃容器中的溶液以0.5毫升/分钟的流速通过该装置90分钟。在适当的时间间隔收集药物溶液样本,并通过稳定性指示高效液相色谱(HPLC)分析法进行分析。含有0.9%氯化钠注射液的混合液不稳定;在玻璃瓶中储存24小时后出现明显的视觉不相容性,未进行进一步测试。在储存在50毫升软质PVC袋中的含有5%葡萄糖注射液的混合液中,120小时后初始胺碘酮浓度的60%仍然存在;大约一半损失的药物可通过甲醇回收。从PVC给药装置收集的流出液中,初始胺碘酮浓度的82%仍然存在。胺碘酮浓度在储存在玻璃或硬质PVC瓶中后没有明显下降,表明药物损失可能受增塑剂邻苯二甲酸二(2-乙基己基)酯的影响。(摘要截短为250字)

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