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喷他脒异硫氰酸盐在5%葡萄糖注射液和0.9%氯化钠注射液中的稳定性。

Stability of pentamidine isethionate in 5% dextrose and 0.9% sodium chloride injections.

作者信息

De N C, Alam A S, Kapoor J N

出版信息

Am J Hosp Pharm. 1986 Jun;43(6):1486-8.

PMID:3728484
Abstract

The stability of pentamidine isethionate in small-volume intravenous admixtures was studied. In an initial experiment, duplicate admixtures containing pentamidine 1 or 2 mg/mL were prepared using 100 mL each of 5% dextrose injection and 0.9% sodium chloride injection in polyvinyl chloride (PVC) bags. All solutions were kept at room temperature and were assayed at various times up to 48 hours by high-performance liquid chromatography. Solutions were also examined visually and tested for pH at each assay time. In a second experiment, single admixtures containing pentamidine 2 mg/mL were prepared in 100-mL PVC bags of both 5% dextrose injection and 0.9% sodium chloride injection. After time-zero determinations of pentamidine concentration, pH, and visual clarity, solutions were allowed to run through PVC infusion sets at 20 mL/hr. Samples were collected at the distal end of each set at various times up to five hours for analysis of pentamidine concentration, pH, and clarity. All admixtures in the initial experiment retained greater than 90% of initial concentration for the 48-hour study period. However, 5% dextrose admixtures infused through PVC administration sets showed a loss in initial concentration of about 2%, while 0.9% sodium chloride admixtures lost about 10% of initial concentration after infusion through these sets. The pH of all solutions in both experiments varied by less than 0.5 units, and no particulate matter or color change was noted in any of the admixtures. In the concentrations and diluents studied, pentamidine appears to be stable for 48 hours in PVC bags. Slight losses in the initial concentrations of these solutions after infusing them through PVC infusion sets may be caused by adsorption to the set.

摘要

研究了乙磺酸盐喷他脒在小容量静脉混合液中的稳定性。在初始实验中,分别用100 mL的5%葡萄糖注射液和0.9%氯化钠注射液在聚氯乙烯(PVC)袋中制备含1或2 mg/mL喷他脒的重复混合液。所有溶液均保持在室温下,并在长达48小时的不同时间通过高效液相色谱法进行测定。在每次测定时还对溶液进行外观检查并测试pH值。在第二个实验中,分别在100 mL的5%葡萄糖注射液和0.9%氯化钠注射液的PVC袋中制备含2 mg/mL喷他脒的单一混合液。在对喷他脒浓度、pH值和外观清晰度进行零时间测定后,使溶液以20 mL/小时的速度流经PVC输液器。在长达5小时的不同时间从每个输液器的远端收集样品,以分析喷他脒浓度、pH值和清晰度。初始实验中的所有混合液在48小时的研究期内均保持大于初始浓度的90%。然而,通过PVC给药装置输注的5%葡萄糖混合液初始浓度损失约2%,而0.9%氯化钠混合液通过这些装置输注后初始浓度损失约10%。两个实验中所有溶液的pH值变化均小于0.5个单位,并且在任何混合液中均未观察到颗粒物或颜色变化。在所研究的浓度和稀释剂中,喷他脒在PVC袋中似乎可稳定48小时。这些溶液通过PVC输液器输注后初始浓度的轻微损失可能是由于吸附到输液器上所致。

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