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在玻璃和塑料瓶以及塑料注射器中的 Oral Mix SF®中,10mg/mL 替莫唑胺混悬剂的临时制剂的稳定性。

Stability of extemporaneously compounded temozolomide 10 mg/mL suspensions in Oral Mix SF® in glass and plastic bottles and plastic syringes.

机构信息

Department of Pharmacy, The Hospital for Sick Children, Toronto, Canada.

Department of Pharmacy, Akron Children's Hospital, Akron, Ohio.

出版信息

J Oncol Pharm Pract. 2021 Jan;27(1):78-87. doi: 10.1177/1078155220914349. Epub 2020 Mar 30.

Abstract

BACKGROUND

Temozolomide oral suspension is not commercially available.

OBJECTIVE

To evaluate the stability of three temozolomide 10 mg/mL suspensions prepared in Oral Mix SF® in three container types stored at 4°C and 23°C.

METHODS

Using commercial capsules, three separate batches of three different temozolomide 10 mg/mL formulations (Oral Mix SF® with PK-30; PK-30 and citric acid; and neither PK-30 nor citric acid) were made and stored in three container types (amber glass bottles, amber polyethylene terephthalate bottles, and polypropylene oral syringes). The aliquots in each container type were stored protected from light, half at 25°C and half at 4°C. On study days 0, 5, 8, 14, 21, 28, 35, 42, and 56, physical properties of samples from each container type at each temperature were assessed, and the temozolomide concentration was determined using a stability-indicating method. The beyond-use-date (time to achieve 90% of initial concentration calculated using the lower limit of the 95% confidence interval of the observed degradation rate) was calculated.

RESULTS

Samples stored at 25°C turned from white to orange within seven days. Temozolomide crystals were observed in all samples. Concentration changes due to study day and temperature (p < 0.001) were observed but not due to container (p = 0.991) or formulation (p = 0.987). The beyond-use-date of all formulations in all container types was 56 days at 4°C and 6 days at 23°C.

CONCLUSIONS

We recommend that these temozolomide 10 mg/mL formulations be stored at 4°C and be assigned a beyond-use-date of 30 days.

摘要

背景

替莫唑胺口服液尚未商品化。

目的

评估三种替莫唑胺混悬剂(Oral Mix SF®)在三种容器中的稳定性,这些混悬剂分别以三种不同的替莫唑胺 10mg/mL 配方制备(含 PK-30、含 PK-30 和柠檬酸、不含 PK-30 也不含柠檬酸),并储存在四种容器中(棕色玻璃瓶、棕色聚对苯二甲酸乙二醇酯瓶和聚丙烯口服注射器)。每个容器类型中的等分试样避光保存,一半在 25°C,一半在 4°C。在研究第 0、5、8、14、21、28、35、42 和 56 天,评估每种容器类型在每种温度下的样品的物理性质,并使用稳定性指示方法测定替莫唑胺的浓度。使用 95%置信区间下限计算初始浓度的 90%时达到的失效日期(超过使用期限)。

结果

在 25°C 储存的样品在七天内从白色变为橙色。所有样品中均观察到替莫唑胺晶体。浓度变化与研究天数和温度有关(p<0.001),但与容器(p=0.991)或配方(p=0.987)无关。所有配方在所有容器类型中的超过使用期限均为 4°C 时 56 天,23°C 时 6 天。

结论

我们建议这些 10mg/mL 替莫唑胺配方在 4°C 下储存,并设定 30 天的使用期限。

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