Trissel Lawrence A, Zhang Yanping, Douglas Kate, Kastango Eric
Clinical Pharmaceutics Research, Division of Pharmacy, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Int J Pharm Compd. 2006 Mar-Apr;10(2):156-8.
The objective of this study was to evaluate the physical and chemical stability of oxytocin 0.08 U/mL admixed in 5% dextrose injection, 0.9% sodium chloride injection, and lactated Ringer's injection bags. Triplicate test samples of oxytocin 0.08 U/mL in each infusion solution were prepared by adding the required amount of oxytocin injection to bags of the three infusion solutions. The samples were stored protected from light and evaluated at appropriate intervals for up to 90 days at room temperature (near 23 deg C). Physical stability was assessed by using an evaluation procedure that included both turbidimetric measurement and visual inspection. Chemical stability was assessed by using a stability-indicating high-performance liquid chromatographic analytical technique and was based on the determination of drug concentrations initally and at appropriate intervals over the study period. The oxytocin admixtures in 5% dextrose and 0.9% sodium chloride were clear and colorless when viewed in normal fluorescent room light and when viewed with a Tyndall beam initially and throughout 90 days. Measured turbidity was low initially and exhibited little change throughout the study. High-performance liquid chromatographic analysis revealed that little or no decomposition occurred in the samples. Oxytocin in the infusion solutions remained stable at room temperature for 90 days. The lactated Ringer's injection samples remained clear and colorless for up to 28 days. However, after that time a small amount of white fluffy microprecipitate developed in two of the three samples by the 35-day observation point. High-performance liquid chromatographic analysis revealed that oxytocin remained stable in lactated Ringer's injection for 28 days at room temperature; substantial losses of oxytocin occurred in all three samples after that time, with about 10% loss at 35 days and up to 21% loss at 60 days. Oxytocin 0.08 U/mL in 5% dextrose injection or 0.9% sodium chloride injection is physically and chemically stable for at least 90 days at room temperature. However, oxytocin in lactated Ringer's injection should be restricted to a use period no greater than 28 days at room temperature to avoid microprecipitate formation and drug loss.
本研究的目的是评估0.08 U/mL缩宫素与5%葡萄糖注射液、0.9%氯化钠注射液和乳酸林格氏注射液混合后的物理和化学稳定性。通过向三种输液袋中加入所需量的缩宫素注射液,制备了每种输液溶液中0.08 U/mL缩宫素的一式三份测试样品。样品避光保存,并在室温(接近23℃)下每隔适当时间进行评估,最长90天。通过包括比浊法测量和目视检查的评估程序来评估物理稳定性。通过使用稳定性指示高效液相色谱分析技术来评估化学稳定性,该技术基于在研究期间初始和适当时间间隔测定药物浓度。在正常荧光室内光线下以及最初和整个90天用廷德尔光束观察时,5%葡萄糖和0.9%氯化钠中的缩宫素混合液均清澈无色。最初测得的浊度较低,并且在整个研究过程中变化很小。高效液相色谱分析表明,样品中几乎没有或没有发生分解。输液溶液中的缩宫素在室温下90天内保持稳定。乳酸林格氏注射液样品在长达28天内保持清澈无色。然而,在那个时间点之后,在35天观察点时,三个样品中有两个出现了少量白色蓬松微沉淀。高效液相色谱分析表明,缩宫素在乳酸林格氏注射液中在室温下28天内保持稳定;在那个时间点之后,所有三个样品中缩宫素均大量损失,在35天时损失约10%,在60天时损失高达21%。5%葡萄糖注射液或0.9%氯化钠注射液中0.08 U/mL缩宫素在室温下物理和化学稳定性至少为90天。然而,乳酸林格氏注射液中的缩宫素在室温下的使用期限应限制在不超过28天,以避免微沉淀形成和药物损失。