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在尼日利亚销售的青蒿素类抗疟药物的质量

Quality of artemisinin-based antimalarial drugs marketed in Nigeria.

作者信息

Izevbekhai Oisaemi, Adeagbo Babatunde, Olagunju Adeniyi, Bolaji Oluseye

机构信息

Department of Pharmaceutical Chemistry, Obafemi Awolowo University, Ile-Ife, Nigeria.

出版信息

Trans R Soc Trop Med Hyg. 2017 Feb 1;111(2):90-96. doi: 10.1093/trstmh/trx019.

Abstract

BACKGROUND

Artemisinin combination therapy is first-line therapy for treatment of malaria, which is one of the most significant public health problems in Nigeria. With the increasing level of use of these drugs coupled with the emergence of resistance, there is a need for regular post-market surveillance.

METHOD

Twenty different brands of artesunate-containing antimalarial drugs and 10 brands of artemether-lumefantrine were multi-sourced in the south western part of Nigeria and were subjected to identification, weight uniformity test, and assay using United State pharmacopoeia and International Pharmacopoeia monographs. In vitro-dissolution test of the artemether tablets was also investigated.

RESULTS

All 10 brands (100%) of the artemether-lumefantrine tablets met the assay requirement for artemether and 8 (80%) met the assay requirement for lumefantrine, but only 4 brands (40%) met the requirement for artemether dissolution. One of these brands failed the weight uniformity test. Of the 20 brands of artesunate-containing brands included in this study, 15 (75%) met the standard assay requirement for artesunate and two failed the weight uniformity test.

CONCLUSIONS

There is evidence of the presence of substandard artemisinin products in the Nigerian market.

摘要

背景

青蒿素联合疗法是治疗疟疾的一线疗法,疟疾是尼日利亚最严重的公共卫生问题之一。随着这些药物使用水平的提高以及耐药性的出现,需要进行定期的上市后监测。

方法

在尼日利亚西南部多渠道采购了20种不同品牌的含青蒿琥酯抗疟药物和10种品牌的蒿甲醚-本芴醇,并按照美国药典和国际药典专论进行鉴别、重量均匀度测试和含量测定。还对蒿甲醚片进行了体外溶出度测试。

结果

所有10种品牌(100%)的蒿甲醚-本芴醇片均符合蒿甲醚的含量测定要求,8种(80%)符合本芴醇的含量测定要求,但只有4种品牌(40%)符合蒿甲醚溶出度要求。其中一个品牌重量均匀度测试不合格。在本研究纳入的20种含青蒿琥酯品牌中,15种(75%)符合青蒿琥酯的标准含量测定要求,两种重量均匀度测试不合格。

结论

有证据表明尼日利亚市场存在不合格的青蒿素产品。

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