In vitro stability and compatibility of daunorubicin, cytarabine, and etoposide.

Cancer treatment reports Pub Date : 1987-12-01
L E Seargeant, N L Kobrinsky, C J Sus, D R Nazeravich
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Abstract

The continuous infusion of cytarabine, daunorubicin, and etoposide offers several theoretical advantages over bolus infusion in the treatment of acute nonlymphocytic leukemia. To date, this approach has been limited by the need for three separate iv lines. The in vitro stability and compatibility of these three agents were therefore evaluated. Solutions of 200 mg of cytarabine, 25 mg of daunorubicin, and 300 mg of etoposide per 750 ml of 5% dextrose and 0.45% saline were prepared alone and in combination. The solutions were evaluated visually, spectrophotometrically, and by high-pressure liquid chromatography (HPLC) twice daily for 72 hours. Precipitates or color changes were not noted. Changes in the patterns of the spectral scans and chromatographs were not observed. Concentrations of the drugs as assessed by HPLC were stable over the 72-hour period of observation for both individual and combined drug preparations. In conclusion, cytarabine, daunorubicin, and etoposide are stable and compatible in vitro for at least 72 hours. These drugs can therefore be administered together by continuous infusion using a single iv line.

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柔红霉素、阿糖胞苷和依托泊苷的体外稳定性和相容性。
阿糖胞苷、柔红霉素和依托泊苷的持续输注在治疗急性非淋巴细胞白血病方面提供了几个理论上的优势。迄今为止,这种方法由于需要三条单独的静脉注射线而受到限制。因此,评估了这三种药物的体外稳定性和相容性。分别配制200 mg阿糖胞苷、25 mg柔红霉素和300 mg依托泊苷/ 750 ml 5%葡萄糖和0.45%生理盐水的溶液。用目测法、分光光度法和高压液相色谱法(HPLC)对溶液进行评价,每天2次,持续72小时。没有发现沉淀物或颜色变化。没有观察到光谱扫描和色谱仪模式的变化。在72小时的观察期内,通过高效液相色谱法测定的药物浓度在单独和联合药物制剂中都是稳定的。总之,阿糖胞苷、柔红霉素和依托泊苷在体外至少72小时内是稳定和相容的。因此,这些药物可以通过单一静脉滴注连续输注一起给药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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