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

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Marion Emonet, Antony Citterio-Quentin, Sandrine Bourgeois, Vanessa Godard, Clément Boidin, Cynthia Barratier, Jonathan Boisramé
{"title":"Stability of clozapine tablets repackaged in dose administration aids using repackaging machines.","authors":"Marion Emonet, Antony Citterio-Quentin, Sandrine Bourgeois, Vanessa Godard, Clément Boidin, Cynthia Barratier, Jonathan Boisramé","doi":"10.1136/ejhpharm-2023-004036","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Objectives: </strong>This study aimed to assess the physical and chemical stability of clozapine tablets for up to 84 days after repackaging.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":12050,"journal":{"name":"European journal of hospital pharmacy : science and practice","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2024-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of hospital pharmacy : science and practice","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1136/ejhpharm-2023-004036","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

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.

使用重新包装机将氯氮平片剂重新包装在给药辅助工具中的稳定性。
背景:在自动病房配药设备中使用给药辅助装置需要对药物进行重新包装,这可能会影响药物与原包装相比的稳定性:本研究旨在评估氯氮平片在重新包装后长达 84 天内的物理和化学稳定性:方法:将总共 900 片氯氮平 100 毫克片剂(Viatris)重新包装并储存在五种不同的条件下,分别在第 0 天、第 28 天、第 56 天和第 84 天进行物理和化学稳定性测试。测试结果与原包装的对照药片进行了比较。对药片外观进行目测。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、易碎性和抗压性。化学稳定性采用超高效液相色谱-串联质谱检测法(UHPLC-MS/MS)进行测定,以测量氯氮平浓度、N-去甲基氯氮平浓度,并监测氯氮平降解情况,以检测除 N-去甲基氯氮平以外的任何降解产物的形成:目测结果表明,只有在紫外线照射下储存的药片外观才会发生变化。在 84 天内,所有药片的质量均匀性均符合标准。由于片剂在翻滚后开裂,因此没有通过易碎性测试。在抗粉碎性测试中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片剂中均未检测到 N-去甲基氯氮平,84 天内氯氮平的平均浓度仍在目标范围内:结论:在所有储存条件下均未检测出 N-去甲基氯氮平,氯氮平的浓度保持稳定。药片在各种条件下都符合质量均匀性测试的要求。不过,在易碎性测试中,片剂出现了裂纹,片剂硬度也逐渐下降。鉴于上述结果,Vinatier 医院药房决定将氯氮平片剂的保质期定为 84 天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.40
自引率
5.90%
发文量
104
审稿时长
6-12 weeks
期刊介绍: European Journal of Hospital Pharmacy (EJHP) offers a high quality, peer-reviewed platform for the publication of practical and innovative research which aims to strengthen the profile and professional status of hospital pharmacists. EJHP is committed to being the leading journal on all aspects of hospital pharmacy, thereby advancing the science, practice and profession of hospital pharmacy. The journal aims to become a major source for education and inspiration to improve practice and the standard of patient care in hospitals and related institutions worldwide. EJHP is the only official journal of the European Association of Hospital Pharmacists.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信