Getahun Habtamu, Belew Sileshi, Hasen Gemmechu, Tefera Guta, Mekasha Yesuneh Tefera, Suleman Sultan
Pharmaceutical Quality Assurance and Regulatory Affairs, Oromia Regional Health Bureau, Addis Ababa, Oromia, Ethiopia.
School of Pharmacy, Institute of Health Science, Jimma University, Jimma, Oromia, Ethiopia.
Front Med (Lausanne). 2024 Aug 7;11:1420146. doi: 10.3389/fmed.2024.1420146. eCollection 2024.
The problem of medicine expiration presents a notable obstacle, resulting in considerable financial losses. Nevertheless, there is currently limited data indicating that certain medications do not experience a significant decrease in effectiveness after their expiration date. Therefore, the aim of the study was to assess the physico-chemical quality of expired fluoroquinolone antibiotics.
The expired samples of fluoroquinolone antibiotics were purposively collected from public hospitals in the Jimma zone of the Oromia regional state, Ethiopia. A World Health Organization quality evaluation sampling strategy was employed. Then, simple random sampling techniques were utilized for the selection of tablets for the laboratory quality control test. The assay, identification, and dissolution were performed in accordance with the United States Pharmacopeia (USP) guidelines, as well as failure mode and effect analysis (FMEA) techniques.
The finding revealed that about 100% (7/7) expired samples passed pharmacopeia quality specifications for identity and assay tests. However, of the seven expired brands, about 14.3% (1/7) of the sample (Code-002) was unable to release its API content within the USP criteria of 30 min. The risk-based quality evaluation revealed that assay was the most critical quality attributed to ciprofloxacin tablets (RPN = 189), followed by identity (RPN = 100). Assay was also the most critical quality attribute (RPN = 378), followed by identity (RPN = 100) for Norfloxacin tablets. The risk-based desirability function approach showed that 75% (3/4) of ciprofloxacin products were of good quality, and 25% (1) were found to be of acceptable quality, while the desirability function of norfloxacin tablets was found to be excellent 1 (33.3%), good 1 (33.3%), and acceptable 1 (33.3%).
The study revealed that medications can maintain their quality beyond their labeled expiration date. By combining pharmacopeial standards with risk-based approaches like failure mode and effect analysis (FMEA), the study provides a comprehensive evaluation framework. This approach not only confirms the continued effectiveness of expired fluoroquinolone antibiotics but also underscores the potential waste reduction and cost-saving benefits. This could significantly contribute to addressing healthcare challenges in low-resource settings, promoting more efficient pharmaceutical resource utilization.
药品过期问题是一个显著障碍,会导致相当大的经济损失。然而,目前仅有有限的数据表明某些药物在过期后其有效性不会显著下降。因此,本研究的目的是评估过期氟喹诺酮类抗生素的物理化学质量。
从埃塞俄比亚奥罗米亚州吉马地区的公立医院有目的地收集过期的氟喹诺酮类抗生素样本。采用了世界卫生组织的质量评估抽样策略。然后,运用简单随机抽样技术选择片剂进行实验室质量控制测试。按照美国药典(USP)指南以及失效模式与效应分析(FMEA)技术进行含量测定、鉴别和溶出度测试。
研究发现约100%(7/7)的过期样本通过了鉴别和含量测定测试的药典质量规范。然而,在这七个过期品牌中,约14.3%(1/7)的样本(编号002)在30分钟的USP标准内无法释放其活性成分。基于风险的质量评估表明,含量测定是环丙沙星片剂最关键的质量属性(风险优先数RPN = 189),其次是鉴别(RPN = 100)。对于诺氟沙星片剂,含量测定也是最关键的质量属性(RPN = 378),其次是鉴别(RPN = 100)。基于风险的合意函数方法表明,75%(3/4)的环丙沙星产品质量良好,25%(1)质量可接受,而诺氟沙星片剂的合意函数结果为优秀1个(33.3%)、良好1个(33.3%)、可接受1个(33.3%)。
该研究表明药物在超过其标签上的有效期后仍可保持其质量。通过将药典标准与失效模式与效应分析(FMEA)等基于风险的方法相结合,该研究提供了一个全面的评估框架。这种方法不仅证实了过期氟喹诺酮类抗生素的持续有效性,还强调了潜在的减少浪费和节省成本的益处。这可能会对解决资源匮乏地区的医疗保健挑战做出重大贡献,促进更高效的药品资源利用。