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使用重新包装机器在剂量给药辅助器具中重新包装的氯氮平片的稳定性。

Stability of clozapine tablets repackaged in dose administration aids using repackaging machines.

作者信息

Emonet Marion, Citterio-Quentin Antony, Bourgeois Sandrine, Godard Vanessa, Boidin Clément, Barratier Cynthia, Boisramé Jonathan

机构信息

Pharmacy Department, The Vinatier Hospital, Bron, France.

Biochemistry and Pharmaco-toxicology Laboratory, University Hospital of Lyon, Lyon, France.

出版信息

Eur J Hosp Pharm. 2024 Dec 30. doi: 10.1136/ejhpharm-2023-004036.

Abstract

BACKGROUND

The use of dose administration aids in automated ward dispensing devices requires the repackaging of medications, which may impact their stability compared with the original manufacturer's packaging.

OBJECTIVES

This study aimed to assess the physical and chemical stability of clozapine tablets for up to 84 days after repackaging.

METHODS

A total of 900 tablets of clozapine 100 mg (Viatris) were repackaged and stored under five different conditions to conduct physical and chemical stability tests on days 0, 28, 56 and 84. The results were compared with control tablets in their original packaging. Visual inspections of tablet appearance were performed. Physical tests included assessments of mass uniformity, friability and resistance to crushing, following the standards of the European Pharmacopoeia 11th edition. The chemical stability was determined using ultra-high performance liquid chromatography with tandem-mass spectrometry detection (UHPLC-MS/MS) to measure clozapine concentration, N-desmethyl-clozapine, and monitor clozapine degradation to detect formation of any degradation products other than N-desmethyl-clozapine.

RESULTS

Visual examination showed changes in the appearance of tablets only in those stored under UV light. Mass uniformity met standards for all tablets over 84 days. None passed the friability test due to tablet cracking after tumbling. A gradual deterioration in tablet hardness was observed with the resistance to crushing test. In terms of chemical stability, N-desmethyl-clozapine was undetected in any of the tablets stored under all conditions, and the mean concentration of clozapine remained within the target range over 84 days.

CONCLUSION

N-desmethyl-clozapine was not detected and clozapine concentrations remained stable under all storage conditions. The tablets were compliant with the mass uniformity test in each condition. However, the tablets were cracked in the friability test and gradual deterioration in tablet hardness was observed. In the light of these results, the Vinatier Hospital pharmacy has chosen to establish a shelf life for clozapine tablets of 84 days.

摘要

背景

在自动病房配药设备中使用剂量给药辅助工具需要对药物进行重新包装,与原制造商的包装相比,这可能会影响药物的稳定性。

目的

本研究旨在评估氯氮平片重新包装后长达84天的物理和化学稳定性。

方法

总共900片100毫克氯氮平片(威朗制药)被重新包装,并在五种不同条件下储存,在第0、28、56和84天进行物理和化学稳定性测试。将结果与原装包装的对照片剂进行比较。对片剂外观进行目视检查。物理测试包括按照欧洲药典第11版的标准评估质量均匀性、脆碎度和抗压碎性。使用超高效液相色谱-串联质谱检测(UHPLC-MS/MS)测定化学稳定性,以测量氯氮平浓度、N-去甲基氯氮平,并监测氯氮平降解以检测除N-去甲基氯氮平以外的任何降解产物的形成。

结果

目视检查显示,仅在紫外线照射下储存的片剂外观有变化。84天内所有片剂的质量均匀性均符合标准。由于翻滚后片剂破裂,没有一片通过脆碎度测试。通过抗压碎性测试观察到片剂硬度逐渐下降。在化学稳定性方面,在所有条件下储存的任何片剂中均未检测到N-去甲基氯氮平,并且氯氮平的平均浓度在84天内保持在目标范围内。

结论

在所有储存条件下均未检测到N-去甲基氯氮平,并且氯氮平浓度保持稳定。片剂在每种条件下均符合质量均匀性测试。然而,片剂在脆碎度测试中出现破裂,并且观察到片剂硬度逐渐下降。鉴于这些结果,维纳蒂尔医院药房选择将氯氮平片的保质期定为84天。

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