评估daptomycin在基于icodextrin的腹膜透析溶液中的稳定性
Hiroyuki Suzuki1,2, Kasumi Kudo2,3, Takashi Uno2
1Division of Clinical Pharmaceutics, Faculty of Pharmaceutical Sciences, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
概括
在icodextrin腹腔透析 (PD) 溶液中的达普托米辛 (DAP) 在室温下72小时,在37°C下12小时保持稳定,有助于腹腔炎治疗. 这种稳定性对于有效的门诊管理至关重要.
科学领域:
- 药理动力学和药物稳定性
- 腹膜透析解决方案 腹膜透析解决方案
- 抗菌疗法是一种抗菌疗法.
背景情况:
- 腹膜透析 (PD) 溶液中的抗菌稳定性对于成功治疗腹膜炎至关重要.
- 这项研究评估了daptomycin (DAP) 在基于icodextrin的PD溶液中的稳定性.
研究的目的:
- 为了评估NICOPELIQ®腹腔透析溶液中达普托米辛 (DAP) 的稳定性.
- 为了确定DAP度,并识别随着时间的推移发生的任何结构变化.
主要方法:
- 达普托米辛 (350毫克) 被添加到尼科佩利克® PD溶液 (1,260毫升) 中.
- 样本从0到336小时收集.
- 使用HPLC量化了DAP度;使用LC-MS/MS进行了未识别的峰值的结构分析.
主要成果:
- 达普托米辛在室温下72小时,在37°C下12小时保持了90%以上的初始度.
- 检测到未识别的峰值,并确定为无水达普托米.
结论:
- 在测试条件下,daptomycin在基于icodextrin的PD溶液中表现出足够的稳定性.
- 这些发现支持使用达普素在PD患者的外周膜炎的门诊治疗.
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