University of Liege (ULg), Department of Pharmacy, CIRM, Laboratory of Analytical Chemistry, 1 Avenue de l'Hôpital, B36, B-4000 Liège, Belgium.
J Pharm Biomed Anal. 2013 Nov;85:83-92. doi: 10.1016/j.jpba.2013.06.036. Epub 2013 Jul 12.
The poor quality of medicines is a crucial problem of public health. Therefore, it is important to have analytical tools to attend decisions of the legal authorities while combating this offense. In this context, the main objective of this study was to develop generic methods able to trace, screen and determine several antibiotics and common associated molecules by mean of liquid chromatographic techniques. For that purpose, an innovative Design Space optimization strategy was applied, targeting 16 antibiotics and 3 beta-lactamase inhibitors. The robustness of the developed method allowed using its use in an environment where operational factors such as temperature are not easy to control and eased its transfer to Ultra High Performance Liquid Chromatography. To demonstrate its ability to quantify the targeted molecules, the developed and transferred method was fully validated for two active ingredients commonly used in association, sulbactam and ceftriaxone, using the accuracy profile as decision tool. Based on this successful step, the method was then used for the quantitative determination of these two active ingredients in three pharmaceutical brands marketed in the Democratic Republic of Congo. Two out of the three pharmaceutical products did not comply with the specifications.
药品质量差是公共卫生的一个关键问题。因此,拥有分析工具来协助执法部门打击这种犯罪行为的决策非常重要。在这方面,本研究的主要目标是开发通用方法,通过液相色谱技术追踪、筛选和测定几种抗生素和常见相关分子。为此,应用了一种创新的设计空间优化策略,针对 16 种抗生素和 3 种β-内酰胺酶抑制剂。所开发方法的稳健性允许在操作因素(如温度)不易控制的环境中使用,并简化了其向超高效液相色谱的转移。为了证明其定量测定目标分子的能力,使用准确度概况作为决策工具,对开发和转移的方法进行了充分验证,用于两种常用的联合活性成分(舒巴坦和头孢曲松)的定量测定。在此成功步骤的基础上,该方法随后用于在刚果民主共和国上市的三种药品品牌中这两种活性成分的定量测定。其中两种药品不符合规格。