Suppr超能文献

赤道几内亚抗疟药物质量评估:一项随访研究。

Assessing the quality of antimalarial drugs in Equatorial Guinea: a follow-up study.

作者信息

Kaur Harparkash, Paris Laura, Mba Eyono Jeremías N, Nguema Avue Restituto Mba, Phiri Wonder P, Smith Jordan M, Guerra Carlos A, Riloha Rivas Matilde, García Guillermo A

机构信息

Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, London, UK

Health Protection Surveillance Centre (HPSC) 25-27 Middle Gardiner Street, Dublin, Ireland.

出版信息

BMJ Glob Health. 2025 Jul 27;10(7):e018597. doi: 10.1136/bmjgh-2024-018597.

Abstract

INTRODUCTION

Poor-quality antimalarial medications, including falsified and substandard formulations, pose significant public health risks, contributing to ineffective treatment and potential drug resistance. Our research conducted in 2013 on Bioko Island, Equatorial Guinea (EG), found 9.6% (n=61) of the artemisinin-containing antimalarials (ACAs) purchased were of poor quality. This study aimed to update the quality of all sold antimalarials and extend to include regions on the mainland.

METHODS

A total of 637 samples, 564 ACAs and 73 non-ACAs, were purchased from 424 outlets on Bioko Island and mainland EG using a mystery client sampling approach. Samples were analysed for content using high-performance liquid chromatography with diode-array detection and classified as acceptable, substandard or falsified based on pharmacopoeia tolerance limits. Additionally, bioavailability was assessed through dissolution testing for a select number of samples.

RESULTS

Overall, 40.5% of the samples were of acceptable quality, 31.2% were substandard and 28.3% were falsified. Regional differences showed a higher prevalence of falsified samples in Bata, Mangomo, Evinayong and Ebebiyín cities on the mainland (30.9%) compared with Bioko Island (25.6%). Artemether/lumefantrine, the first-line treatment for malaria in EG, showed 25.7% were of acceptable quality, 48.2% substandard and 26.1% falsified. Artemisinin monotherapy tablets had the highest rate of falsification (56.8%). For non-ACAs, 13.3% of sulfadoxine/pyrimethamine tablets were of acceptable quality, 48.9% substandard and 37.8% falsified. All quinine syrups were falsified, and most quinine tablets (87.5%) and injections (75.0%) were substandard.

CONCLUSION

The prevalence of substandard and falsified antimalarials in EG has alarmingly increased from 9% in 2013 to 59.5% in 2018, highlighting the urgent need for enhanced regulatory measures. Immediate actions should include strengthening drug quality surveillance, particularly in private sector pharmacies, and implementing low-cost medicine screening methods for early detection of poor-quality medications. Ensuring the quality of antimalarials is critical to maintaining the efficacy of malaria control programmes and preventing the development of drug resistance.

摘要

引言

质量不佳的抗疟药物,包括伪造和不合格制剂,构成重大公共卫生风险,导致治疗无效并可能产生耐药性。我们2013年在赤道几内亚(EG)的比奥科岛开展的研究发现,所购买的含青蒿素抗疟药(ACA)中有9.6%(n = 61)质量不佳。本研究旨在更新所有在售抗疟药的质量情况,并将范围扩大至大陆地区。

方法

采用神秘顾客抽样方法,从比奥科岛和赤道几内亚大陆的424个销售点购买了总共637份样品,其中564份为ACA,73份为非ACA。使用带二极管阵列检测的高效液相色谱法对样品进行含量分析,并根据药典耐受限度将其分类为可接受、不合格或伪造。此外,通过对选定数量的样品进行溶出度测试来评估生物利用度。

结果

总体而言,40.5%的样品质量可接受,31.2%不合格,28.3%为伪造。地区差异显示,大陆的巴塔、曼戈莫、埃维纳永及埃贝比因市伪造样品的比例较高(30.9%),高于比奥科岛(25.6%)。蒿甲醚/本芴醇是赤道几内亚疟疾的一线治疗药物,结果显示25.7%质量可接受,48.2%不合格,26.1%为伪造。青蒿素单一疗法片剂的伪造率最高(56.8%)。对于非ACA,13.3%的磺胺多辛/乙胺嘧啶片质量可接受,48.9%不合格,37.8%为伪造。所有奎宁糖浆均为伪造,大多数奎宁片(87.5%)和注射剂(75.0%)不合格。

结论

赤道几内亚不合格和伪造抗疟药的比例从2013年的9%惊人地增至2018年的59.5%,凸显了加强监管措施的迫切需要。立即采取的行动应包括加强药品质量监测,尤其是在私营药店,并实施低成本药品筛查方法以早期发现质量不佳的药物。确保抗疟药的质量对于维持疟疾控制项目的有效性和防止耐药性的产生至关重要。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验