20mg /mL盐酸胺碘酮口服混悬液在syspend®SF PH4(液体)中的理化稳定性

A. Adoum, Pho V. Le, S. Faisant, Pauline Legendre, M. Lester, P. Boivin
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引用次数: 1

摘要

摘要目的盐酸胺碘酮是一类抗心律失常药物,适用于室性和室上性心动过速的治疗。口服胺碘酮仅以片剂形式提供,不适合儿童使用。在syspend®SF PH4(液体)中评估了5mg /mL盐酸胺碘酮混悬液的稳定性,但口服胺碘酮通常以10 - 15mg /kg/天的负荷剂量给药,持续4-10天,然后减少到5mg /kg/天的维持剂量,因此20mg /mL浓度是更好的选择。研制了20 mg/mL盐酸胺碘酮口服混悬液的医院制剂。本研究的目的是测定20mg /mL盐酸胺碘酮口服多剂量混悬液在常温和黑暗条件下的物理化学稳定性。方法采用盐酸胺碘酮粉剂和syspend SF PH4(液体)配制三批口服混悬液。悬浮液保存在室温下并避光(琥珀玻璃小瓶)。在制备后和第1、2、5、10、15、30、60和90天立即从每个瓶子中取出样品。将样品用甲醇进一步稀释至预期浓度100 μg/mL后,采用稳定性指示的高效液相色谱法(HPLC)和紫外(UV)检测,一式三份。在分析的每一天,对90天内的理化性质(pH值、渗透压、胺碘酮浓度、宏观变化)进行评估。稳定性是通过评估在每个时间点保留的初始浓度的百分比来确定的,并定义为保留至少95%的初始浓度的盐酸胺碘酮。结果90天后,研究表明盐酸胺碘酮浓度不低于初始药物浓度的95%。没有检测到降解产物,也没有检测到理化性质的变化。结论含20mg /mL盐酸胺碘酮的syspend®SF PH4(液体)复合口服混悬液在室温下琥珀色玻璃瓶中稳定保存至少90天。
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Physicochemical stability of 20 mg/mL amiodarone hydrochloride oral suspension in SyrSpend® SF PH4 (liquid)
Abstract Objectives Amiodarone hydrochloride is a class III antiarrhythmic drug indicated for the treatment of ventricular and supraventricular tachycardias. Oral amiodarone is only available in a tablet dosage form, which is not suitable for pediatric use. The stability of amiodarone hydrochloride suspension at 5 mg/mL was assessed in SyrSpend® SF PH4 (liquid) but oral amiodarone is typically given as a loading dose of 10–15 mg/kg/day for 4–10 days and then reduced to a maintenance dose of 5 mg/kg/day, making the 20 mg/mL concentration a better option. A hospital preparation of 20 mg/mL amiodarone hydrochloride oral suspension was developed. The purpose of this study was to determine the physicochemical stability of a 20 mg/mL amiodarone hydrochloride oral multidose suspension in a commercial compounding excipient, SyrSpend® SF PH4 (liquid) at ambient temperature and under dark conditions. Methods Three batches of oral suspension were prepared using amiodarone hydrochloride powder and SyrSpend SF PH4 (liquid). The suspensions were stored at room temperature and protected from light (amber glass vials). A sample was withdrawn from each bottle immediately after preparation and at 1, 2, 5, 10, 15, 30, 60, and 90 days. After additional dilution to an expected concentration of 100 μg/mL with methanol, the samples were assayed in triplicate using a stability-indicating high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection. The physicochemical properties (pH, osmolality, amiodarone concentration, macroscopic changes) were assessed over 90 days at each day of analysis. Stability was determined by evaluating the percentage of the initial concentration remaining at each time point and defined as retention of at least 95% of the initial concentration of amiodarone hydrochloride. Results After 90 days, the study showed that amiodarone hydrochloride concentrations did not go below 95% of the initial drug concentration. Neither degradation products nor changes of physicochemical properties were detected. Conclusions Compounded oral suspensions of 20 mg/mL amiodarone hydrochloride in SyrSpend® SF PH4 (liquid) were stable for at least 90 days when stored in amber glass bottles at room temperature.
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