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Tuberculosis (TB) remains one of the leading global causes of mortality. Several methods have been established to detect anti-TB agents in human plasma and serum. However, there is a notable absence of studies analyzing TB drugs in urine. Thus, our objective was to validate a method for quantifying first-line anti-TB agents: isoniazid (INH), pyrazinamide (PZA), ethambutol (ETH), and rifampicin (RIF), along with its metabolite 25-desacetylrifampicin, and degradation products: rifampicin quinone and 3-formyl-rifampicin in 10 µL of urine. Chromatographic separation was achieved using a Kinetex Polar C18 analytical column with gradient elution (5 mM ammonium acetate and acetonitrile with 0.1% formic acid). Mass spectrometry detection was carried out using a triple-quadrupole tandem mass spectrometer operating in positive ion mode. The lower limit of quantification (LLOQ) was 0.5 µg/mL for INH, PZA, ETH, and RIF, and 0.1 µg/mL for RIF's metabolites and degradation products. The method was validated following FDA guidance criteria and successfully applied to the analysis of the studied compounds in urine of TB patients. Additionally, we conducted a stability study of the anti-TB agents under various pH and temperature conditions to mimic the urine collection process in different settings (peripheral clinics or central laboratories).
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http://dx.doi.org/10.3390/molecules29020337 | DOI Listing |
Clin Exp Med
August 2025
Department of pathology, College of Medicine, King Khalid University, Abha, Saudi Arabia.
This study examined the association between diabetes mellitus and tuberculosis (TB) in a cohort of 200TB-positive patients, stratified by gender, age, treatment regimen, and comorbidities, including diabetes, acute gastroenteritis, and hypertension, compared to TB patients without additional complications. Clinical parameters-Random Blood Sugar (RBS), C-reactive protein (CRP), and Erythrocyte Sedimentation Rate (ESR)-were assessed at baseline and after four months of anti-TB therapy. The results showed no significant changes in mean RBS or CRP levels post-treatment, but a notable reduction in mean ESR was observed.
View Article and Find Full Text PDFEur J Pharmacol
August 2025
National Clinical Research Center for Infectious Diseases, Shenzhen Third People's Hospital, Shenzhen, Guangdong, China. Electronic address:
The increasing prevalence of drug-resistant tuberculosis (TB), coupled with the lengthy and toxic nature of conventional treatments and the complicating factor of Human Immunodeficiency Virus (HIV) co-infection, underscores the urgent need for the development of effective anti-TB drugs and robust stockpiles to combat this global health crisis. In this study, the anti-tubercular activity and potential antibacterial mechanisms of tioconazole were investigated. Tioconazole exhibited remarkable antibacterial activity against Mtb H37Ra and H37Rv, with minimum inhibitory concentrations (MICs) of 4 μg/mL and 1 μg/mL respectively.
View Article and Find Full Text PDFSci Rep
August 2025
Quality assurance and enhancement directorate, College of Medicine and Health Sciences, Wachemo University, Hosaina, Ethiopia.
Tuberculosis (TB) is a curable disease that can be treated with antitubercular (anti-TB) drugs that have markedly reduced mortality due to the disease. However, the drugs may cause liver injury, which is associated with increased morbidity due to acute liver failure, disease progression, and drug resistance. There is a scarcity of evidence on the prevalence and predictors of anti-TB drug-induced liver injury (ATDILI).
View Article and Find Full Text PDFJ Med Chem
August 2025
Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana 500037, India.
The alarming rise of multidrug-resistant tuberculosis (MDR-TB) underscores the urgent need for new classes of antitubercular agents targeting novel pathways. To address this, a series of indole triazole sulfonamides were rationally designed, incorporating an indole pharmacophore hybridized with a triazole linker containing a sulfonamide group. Compound had the highest anti-TB efficacy against with a MIC of 0.
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