氟沙匹坦、地塞米松、昂丹司琼和格拉司琼在临床应用中的稳定性研究

A. M. Gil, María Amparo Martínez Gómez, E. Colomer, B. P. Oltra, M. Martí
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引用次数: 3

摘要

5HT3受体拮抗剂、NK-1受体拮抗剂和地塞米松的联合使用已被归类为接受高度和中度致呕吐性化疗(如顺铂和蒽环类药物)的患者的最新技术。在相同的静脉输注溶液中使用fosaprepitant,地塞米松和昂丹司琼(FDO)或格拉司琼(FDG)的特殊混合物,将改善与减少给药时间和静脉制剂给药次数相关的门诊程序管理。所有这些都将提高患者的安全性和舒适度。为了保证患者的安全和治疗效果,需要了解这两种三元混合物在常规临床使用浓度和不同储存条件下的物理化学稳定性。在这项研究中,评估了氟萨吡坦(150毫克)、地塞米松(8毫克)和昂丹司琼(8毫克)或格兰司琼(3毫克)在50,100和250毫升0.9 g/dl NaCl中室温/冷藏和避光/暴露的理化稳定性。根据国际协调会议的指导方针,建立并验证了一种高效液相色谱法同时评价混合药物的化学稳定性。通过目测、pH测定和重量测定等方法对其进行了物理稳定性研究,以控制蒸发。本文所显示的结果是临床实践中在不同储存条件下使用的这两种三元混合物的物理化学稳定性的第一个证据。FDG在100和250 ml 0.9 g/dl NaCl中的三元混合物在室温、冷藏、避光条件下可保持15天的物理化学稳定性;50ml的混合物在6天内物理化学稳定。FDO在50、100和250 ml 0.9 g/dl NaCl中的三元混合物在温度和光照条件下均具有15 d的物理化学稳定性。
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Stability Studies of Ternary Mixtures Containing Fosaprepitant,Dexamethasone, Ondansetron and Granisetron Used in Clinical Practice
The use of a combination of 5HT3 receptor antagonist, a NK-1 receptor antagonist and dexamethasone has been classified to be state of the art in patients receiving highly as well as moderately emetogenic chemotherapy like cisplatin and anthracyclines. The administration of the ad-hoc admixture of fosaprepitant, dexamethasone and ondansetron (FDO) or granisetron (FDG) in the same IV infusion solution will improve the management of ambulatory procedures related to reducing administration time and number of administered intravenous preparations. All this would improve patient safety and comfort. In order to guarantee security of patients and efficacy of treatment, information about physico-chemical stability of both ternary mixtures at concentrations used in routine clinical practice and at different conditions of storage is needed. In this study, physico-chemical stability of ternary mixtures of fosaprepitant (150 mg), dexamethasone (8 mg) and ondansetron (8 mg) or granisetron (3 mg) in 50,100 and 250 ml of 0.9 g/dl NaCl at room temperature/refrigerated and protective from/exposed to light has been evaluated. An HPLC method has been developed and validated according to International Conference on Harmonization guidelines to evaluate chemical stability of drugs in mixtures simultaneously. Physical stability study has been carried out by visual inspection, pH measure and gravimetry to control evaporation. The results shown in this paper represent the first evidence of the physico-chemical stability of both ternary mixtures used in clinical practice at different conditions of storage. The ternary mixtures of FDG in 100 and 250 ml of 0.9 g/dl NaCl are physico-chemical stable for 15 days at room temperature and refrigerated and exposed to and protected from light; mixtures in 50 ml are physico-chemical stable for 6 days. The ternary mixtures of FDO in 50, 100 and 250 ml of 0.9 g/dl NaCl are physico-chemical stable for 15 days at both conditions of temperature and light.
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