Hecq J-D, Godet M, Gillet P, Jamart J, Galanti L
Int J Pharm Compd. 2014 Jan-Feb;18(1):78-82.
The aim of this study was to investigate the long-term stability of morphine hydrochloride in 0.9% NaCI infusion polyolefin bags and polypropylene syringes after storage at 5 degrees C + 3 degrees C and to evaluate the influence of initial freezing and microwave thawing on this stability. Ten polyolefin bags and five polypropylene syringes containing 100 mL of 1 mg/mL of morphine hydrochloride solution in 0.9% NaCI were prepared under aseptic conditions. Five polyolefin bags were frozen at -20 degrees C for 90 days before storage. Immediately after the preparation and after thawing, 2 mL of each bag were withdrawn for the initial concentration measurements. All polyolefin bags and polypropylene syringes were then refrigerated at 5 degrees C + 3 degrees C for 58 days during which the morphine concentrations were measured periodically by high-performance liquid chromatography using a reversed-phase column, naloxone as internal standard, a mobile phase consisting of 5% acetonitrile and 95% of KH2PO4 buffer (pH 3.50), and detection with diode array detector at 254 nm. Visual and microscopic observations and spectrophotometric and pH measurements were also performed. Solutions were considered stable if the concentration remained superior to 90% of the initial concentration. The degradation products peaks were not quantitatively significant and were resolved from the native drug. Polyolefin bag and polypropylene syringe solutions were stable when stored at 5 degrees C + 3 degrees C during these 58 days. No color change or precipitation in the solutions was observed. The physical stability was confirmed by visual, microscopic, and spectrophotometric inspection. There was no significant change in pH during storage. Freezing and microwave thawing didn't influence the infusion stability. Morphine hydrochloride infusions may be prepared in advance by centralized intravenous additive service, frozen in polyolefin bags, and microwave thawed before storage under refrigeration until 58 days either in polyolefin bags or polypropylene syringes. Such treatment could improve safety and management.
本研究的目的是调查盐酸吗啡在0.9%氯化钠输液聚烯烃袋和聚丙烯注射器中于5℃±3℃储存后的长期稳定性,并评估初始冷冻和微波解冻对该稳定性的影响。在无菌条件下制备了10个聚烯烃袋和5个聚丙烯注射器,每个容器中含有100 mL 0.9%氯化钠中1 mg/mL的盐酸吗啡溶液。5个聚烯烃袋在储存前于-20℃冷冻90天。制备后及解冻后立即从每个袋子中取出2 mL进行初始浓度测量。然后将所有聚烯烃袋和聚丙烯注射器在5℃±3℃冷藏58天,在此期间通过高效液相色谱法定期测量吗啡浓度,使用反相柱、纳洛酮作为内标、由5%乙腈和95%磷酸二氢钾缓冲液(pH 3.50)组成的流动相,并在254 nm处用二极管阵列检测器进行检测。还进行了视觉和显微镜观察以及分光光度法和pH测量。如果浓度保持高于初始浓度的90%,则认为溶液稳定。降解产物峰在定量方面不显著,并且与原药分离。在这58天期间,聚烯烃袋和聚丙烯注射器溶液在5℃±3℃储存时是稳定的。溶液中未观察到颜色变化或沉淀。通过视觉、显微镜和分光光度检查证实了物理稳定性。储存期间pH没有显著变化。冷冻和微波解冻不影响输液稳定性。盐酸吗啡输液可由集中静脉加药服务预先制备,在聚烯烃袋中冷冻,并在冷藏储存前微波解冻,在聚烯烃袋或聚丙烯注射器中可保存至58天。这种处理可以提高安全性和管理水平。