Zhang Y P, Trissel L A
Pharmaceutical Analysis Laboratory, The University of Texas, M.D. Anderson Cancer Center, Houston,TX.
Int J Pharm Compd. 1997 Mar-Apr;1(2):132-4.
The purpose of this study was to determine that stability of aminocaproic acid 10 and 100mg/mL admixed in 5% dextrose injection and 0.9% sodiium cholride injection in polyvinyl chloride bags over periods up to seven days at 4 deg and 23 deg C. The aminocaproic acid 250-mg/mL injection was filtered and admixed in filtered 5% dextrose injection and 0.9% sodium chloride injection to yield nominal aminocaproic acid concentrations of 10 and 100 mg/mL. Evaluations were performed initially and after one, three, and seven days of storage for physical and chemical stability. The admixtures were evaluated for physical stability using visual observation in normal fluorescent room light and a high-intensity monodirectional light beam, as well as electronic measurement of turbidity and particcle content. The chemical stability was evaluated by using a stability-indicating high performance liquid chromatography (HPLC) analytical technique. Aminocaproic acid admixtures were clear and colorless. However, the admixtures in 5% dextrose injection developed a slight yellowish discoloration after 24 hours at 23 deg C. This discoloration did not indicate substantial loss of aminocaproic acid. The HPLC evalurations found that an aminocaporic acid otency of at least 98% was retained throughout seven days in all solutions at both 4 deg and 23 deg C.
本研究的目的是确定在4℃和23℃条件下,10mg/mL和100mg/mL氨甲环酸在聚氯乙烯袋中与5%葡萄糖注射液和0.9%氯化钠注射液混合,在长达7天的时间内的稳定性。将250mg/mL氨甲环酸注射液过滤后与经过滤的5%葡萄糖注射液和0.9%氯化钠注射液混合,得到氨甲环酸标称浓度为10mg/mL和100mg/mL的混合液。在储存1天、3天和7天后,对混合液的物理和化学稳定性进行初步评估和评估。使用普通荧光室内光和高强度单向光束进行目视观察,以及通过电子测量浊度和颗粒含量来评估混合液的物理稳定性。采用稳定性指示高效液相色谱(HPLC)分析技术评估化学稳定性。氨甲环酸混合液澄清无色。然而,在23℃下放置24小时后,5%葡萄糖注射液中的混合液出现轻微发黄现象。这种变色并不表明氨甲环酸有大量损失。HPLC评估发现,在4℃和23℃的所有溶液中,氨甲环酸的效价在7天内至少保持98%。