Department of Biomedical Engineering, Boston University, Boston, MA, 02215, USA.
Department of Biomedical Engineering, Boston University, Boston, MA, 02215, USA; Howard Hughes Medical Institute, Boston University, Boston, MA, 02215, USA.
J Pharm Biomed Anal. 2021 Apr 15;197:113941. doi: 10.1016/j.jpba.2021.113941. Epub 2021 Feb 2.
Rifampicin is an antibiotic used as a first line treatment for tuberculosis, as well as in the treatment of other infectious diseases. Drug quality is essential for drug efficacy. Determining the stability and activity of Rifampicin Quinone in solution is important in its role as a standard against which to determine Rifampicin quality and in its effect on treatment and AMR development. Poor quality medicines, such as antimicrobials not only increase mortality and morbidity, but can also contribute to the development of antimicrobial resistance (AMR). One common marker of poor quality in Rifampicin samples is the presence of the degradation product Rifampicin Quinone. In this study we have found that Rifampicin Quinone in solution undergoes a chemical conversion to Rifampicin that is temperature dependent. This conversion occurs in physiologically relevant temperatures (30-50 °C) and time scales (24-120 h) and was verified using HPLC and LC-MS methods. Additionally, the conversion of Rifampicin Quinone to Rifampicin results in an increase in antimicrobial activity. We believe that ours is the first study reporting the instability of Rifampicin Quinone, and this instability in solution at these temperatures and time scales raises concerns for its use as a standard in quality testing using liquid chromatography methods and in studies of the effect of Rifampicin Quinone on AMR. Due to the use of Rifampicin Quinone as a standard in determining Rifampicin quality, the instability of Rifampicin Quinone also poses public health concerns, as the incorrect determination of medicine quality risks patient health and may promote the development of AMR.
利福平是一种抗生素,用于治疗肺结核,也用于治疗其他传染病。药物质量对于药物疗效至关重要。确定利福平醌在溶液中的稳定性和活性对于作为标准来确定利福平质量以及其对治疗和 AMR 发展的影响非常重要。质量差的药物,如抗菌药物,不仅会增加死亡率和发病率,还会导致抗菌药物耐药性(AMR)的发展。利福平样品中质量差的一个常见标志是存在降解产物利福平醌。在这项研究中,我们发现溶液中的利福平醌会发生化学转化为利福平,这是温度依赖性的。这种转化发生在生理相关的温度(30-50°C)和时间范围内(24-120 小时),并使用 HPLC 和 LC-MS 方法进行了验证。此外,利福平醌转化为利福平会导致抗菌活性增加。我们相信,这是首次报道利福平醌不稳定的研究,这种在这些温度和时间范围内的溶液不稳定性引起了人们对其在使用液相色谱法进行质量检测以及研究利福平醌对 AMR 影响中的应用的关注。由于利福平醌被用作确定利福平质量的标准,因此利福平醌的不稳定性也对公共卫生构成了关注,因为不正确地确定药物质量会影响患者健康,并可能促进 AMR 的发展。