Spectrophotometric analysis of artesunate injections available in community pharmacies in Northern and Western Uganda.

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Future Science OA Pub Date : 2025-12-01 Epub Date: 2025-06-12 DOI:10.1080/20565623.2025.2511444
Ebere Emilia Ayogu, Emmanuel Aryon Ngolryeko, Joseph Obiezu Chukwujekwu Ezeonwumelu, Ibrahim Garba Wawata, Bashir Olaniyi Sadiq
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引用次数: 0

Abstract

Aim: The surge in different brands of artesunate injection in Uganda, has raised the need for this study, which aimed at quantifying the actual amount of artesunate in different brands of artesunate injections available in Northern and Western Uganda.

Materials and methods: The wavelength at maximum absorbance of pure artesunate powder was determined using Ultraviolet-visible spectrophotometer and Beer Lambert's plot was generated. This was validated and used to assay 27 brands of artesunate.

Results: In the spectrophotometric assay method used, Beer Lambert's law was obeyed within the range of 20 µg/ml-140 µg/ml with linear regression equation of y = 0.012 + 0.030 and correlation coefficient of (R2) 0.999 (n = 9). The limits of detection (sensitivity) and quantification were found to be 0.83 mg/ml and 2.09 mg/ml respectively. About 66.6% (18) and 33.3% (9) had actual artesunate content higher and lower than labeled claim respectively, while 40.7% (11) had deviations from labeled claim that were within acceptable limits.

Conclusion: Most brands of artesunate injection assayed deviated from labeled claim, regional/environmental factor impacted much on the stability of artesunate thus there is need for further screening of the quality of artesunate injection in circulation in view of the therapeutic consequences of substandard artesunate injection.

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乌干达北部和西部社区药房提供的青蒿琥酯注射剂的分光光度分析。
目的:乌干达不同品牌的青蒿琥酯注射液的激增,提高了对这项研究的需求,该研究旨在量化乌干达北部和西部不同品牌的青蒿琥酯注射液中青蒿琥酯的实际含量。材料与方法:采用紫外-可见分光光度计测定纯青蒿琥酯粉末的最大吸光度波长,并建立Beer Lambert图。该方法已被验证并用于27个牌子的青蒿琥酯的分析。结果:所采用的分光光度法在20µg/ml ~ 140µg/ml范围内符合比尔朗伯定律,线性回归方程为y = 0.012 + 0.030,相关系数为(R2) 0.999 (n = 9)。检测限(灵敏度)和定量限分别为0.83 mg/ml和2.09 mg/ml。分别有66.6%(18)和33.3%(9)药品的实际青蒿琥酯含量高于和低于说明书,40.7%(11)药品的实际青蒿琥酯含量与说明书偏差在可接受范围内。结论:大部分被检测的青蒿琥酯注射液品牌偏离标签声明,区域/环境因素对青蒿琥酯的稳定性影响较大,鉴于不合格青蒿琥酯注射液的治疗后果,有必要进一步对流通中青蒿琥酯注射液的质量进行筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Future Science OA
Future Science OA MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
5.00
自引率
4.00%
发文量
48
审稿时长
13 weeks
期刊介绍: Future Science OA is an online, open access, peer-reviewed title from the Future Science Group. The journal covers research and discussion related to advances in biotechnology, medicine and health. The journal embraces the importance of publishing all good-quality research with the potential to further the progress of research in these fields. All original research articles will be considered that are within the journal''s scope, and have been conducted with scientific rigour and research integrity. The journal also features review articles, editorials and perspectives, providing readers with a leading source of commentary and analysis. Submissions of the following article types will be considered: -Research articles -Preliminary communications -Short communications -Methodologies -Trial design articles -Trial results (including early-phase and negative studies) -Reviews -Perspectives -Commentaries
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