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枸橼酸芬太尼在玻璃和塑料容器以及患者自控给药系统中的稳定性。

Stability of fentanyl citrate in glass and plastic containers and in a patient-controlled delivery system.

作者信息

Kowalski S R, Gourlay G K

机构信息

Adelaide Childrens Hospital, South Australia.

出版信息

Am J Hosp Pharm. 1990 Jul;47(7):1584-7.

PMID:2368752
Abstract

This study determined the stability of fentanyl citrate stored in glass or polyvinyl chloride containers and the concentrations of fentanyl citrate delivered by the Janssen on-demand analgesic computer (ODAC) system. Solutions containing 500 micrograms of fentanyl citrate (10 mL) were added to 100-mL three glass containers each of 5% dextrose injection or 0.9% sodium chloride injection and to three 100-mL polyvinyl chloride containers of 5% dextrose injection or 0.9% sodium chloride injection. All containers were stored under usual light conditions and at room temperature. Samples were taken immediately and at 0.25, 0.5, 1, 6, 12, 24, 36, and 48 hours. To determine the concentration of fentanyl delivered via the ODAC system, fentanyl citrate injection 2500 micrograms (50 mL) was added to a 500-mL polyvinyl chloride bag containing 5% dextrose injection. The solution was connected to the ODAC system, and samples of bolus demand doses were collected at various times during a 30-hour period. All the samples were assayed by a stability-indicating gas-liquid chromatographic method. For both glass and plastic containers, the mean +/- S.D. recovery of fentanyl after 48 hours was 98.6 +/- 2.3% when the drug was diluted in 5% dextrose injection and 97 +/- 1.5% when the drug was diluted in 0.9% sodium chloride injection. There was no significant difference between the amount of fentanyl recovered from glass containers and the amount recovered from polyvinyl chloride containers. Nor was there any significant difference between the amount of fentanyl recovered from solutions containing 5% dextrose injection and the amount recovered from solutions containing 0.9% sodium chloride injection.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究测定了枸橼酸芬太尼储存在玻璃或聚氯乙烯容器中的稳定性,以及扬森按需镇痛计算机(ODAC)系统输送的枸橼酸芬太尼浓度。将含有500微克枸橼酸芬太尼(10毫升)的溶液分别加入到三个100毫升装有5%葡萄糖注射液或0.9%氯化钠注射液的玻璃容器中,以及三个100毫升装有5%葡萄糖注射液或0.9%氯化钠注射液的聚氯乙烯容器中。所有容器均在通常光照条件和室温下储存。立即以及在0.25、0.5、1、6、12、24、36和48小时时取样。为了测定通过ODAC系统输送的芬太尼浓度,将2500微克(50毫升)枸橼酸芬太尼注射液加入到一个装有5%葡萄糖注射液的500毫升聚氯乙烯袋中。将该溶液连接到ODAC系统,并在30小时内的不同时间收集推注按需剂量的样品。所有样品均采用稳定性指示气液色谱法进行测定。对于玻璃和塑料容器,当药物在5%葡萄糖注射液中稀释时,48小时后芬太尼的平均±标准差回收率为98.6±2.3%,当药物在0.9%氯化钠注射液中稀释时为97±1.5%。从玻璃容器中回收的芬太尼量与从聚氯乙烯容器中回收的量之间无显著差异。从含有5%葡萄糖注射液的溶液中回收的芬太尼量与从含有0.9%氯化钠注射液的溶液中回收的量之间也无显著差异。(摘要截短于250字)

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