McGuire T R, Narducci W A, Fox J L
Department of Pharmacy Practice, College of Pharmacy, University of Nebraska Medical Center, Omaha 68198-6045.
Am J Hosp Pharm. 1993 Jul;50(7):1410-4.
The stability of ondansetron hydrochloride, dexamethasone sodium phosphate, and lorazepam in 5% dextrose injection or 0.9% sodium chloride injection in polyvinyl chloride (PVC) minibags and glass bottles was studied. Triplicate solutions of 8 or 32 mg of ondansetron (as the hydrochloride salt) mixed with 20 mg of dexamethasone phosphate (as the sodium salt) with or without 2 mg of lorazepam were compounded in 50-mL PVC minibags and glass bottles containing either 5% dextrose injection or 0.9% sodium chloride injection and stored at 23-25 degrees C. Duplicate measurements were performed when drugs were added and at 1, 2, 4, 8, and 24 hours after addition. Samples of the 32-mg ondansetron admixtures were collected under aseptic conditions to inspect for precipitation and to count particles with a laser particle analyzer. Samples of all admixtures were evaluated for chemical stability by stability-indicating high-performance liquid chromatography. Ondansetron hydrochloride and dexamethasone were physically compatible and chemically stable for up to 24 hours under the study conditions. The concentration of lorazepam in PVC containers dropped below 90% of the original concentration within four hours. In addition, particle counts in lorazepam-containing solutions were higher when 0.9% sodium chloride injection was the diluent than when 5% dextrose injection was the diluent. In admixtures containing all drugs, ondansetron hydrochloride and dexamethasone sodium phosphate in 5% dextrose injection or 0.9% sodium chloride injection were stable for up to 24 hours when stored in PVC bags or glass bottles.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了盐酸昂丹司琼、地塞米松磷酸钠和劳拉西泮在聚氯乙烯(PVC)小袋和玻璃瓶中5%葡萄糖注射液或0.9%氯化钠注射液中的稳定性。将8毫克或32毫克昂丹司琼(盐酸盐形式)与20毫克地塞米松磷酸钠(钠盐形式)混合,有或没有2毫克劳拉西泮,配制成一式三份的溶液,置于含有5%葡萄糖注射液或0.9%氯化钠注射液的50毫升PVC小袋和玻璃瓶中,并在23 - 25摄氏度下储存。在添加药物时以及添加后1、2、4、8和24小时进行重复测量。对32毫克昂丹司琼混合液的样品进行无菌采集,以检查是否有沉淀,并使用激光颗粒分析仪计数颗粒。所有混合液的样品通过稳定性指示高效液相色谱法评估化学稳定性。在研究条件下,盐酸昂丹司琼和地塞米松在物理上相容且化学稳定长达24小时。劳拉西泮在PVC容器中的浓度在4小时内降至原始浓度的90%以下。此外,当以0.9%氯化钠注射液作为稀释剂时,含劳拉西泮溶液中的颗粒计数高于以5%葡萄糖注射液作为稀释剂时。在含有所有药物的混合液中,当储存在PVC袋或玻璃瓶中时,5%葡萄糖注射液或0.9%氯化钠注射液中的盐酸昂丹司琼和地塞米松磷酸钠稳定长达24小时。(摘要截选至250字)