Protein Binding of First-Line Antituberculosis Drugs

• Published in: Antimicrobial agents and chemotherapy 2018-07, Vol.62 (7)
• Main Authors: Alghamdi, Wael A, Al-Shaer, Mohammad H, Peloquin, Charles A
• Format: Article
• Language: English
• Subjects: Antitubercular Agents; Clinical Therapeutics
• ISSN: 0066-4804; 1098-6596
• DOI: 10.1128/AAC.00641-18

The 4-drug regimen of rifampin, isoniazid, pyrazinamide, and ethambutol is an inexpensive, reliable option for treating patients with drug-susceptible tuberculosis (TB). Its efficacy could be further improved by determining the free drug concentrations in plasma, knowing that only the unbound drug can freely penetrate to the tissues. Using an ultrafiltration technique, we determined the protein binding (PB) extent and variability of the first-line anti-TB drugs when given simultaneously to TB patients, representing a real-life case scenario. We used clinical samples routinely received by our laboratory. Plasma proteins were also measured. A protein-free medium was used to determine the nonspecific binding. Plasma samples from 22 patients were included, of which plasma proteins were measured for 18 patients. The median PB was determined for rifampin (88%; range, 72 to 91%), isoniazid (14%; range, 0 to 34%), pyrazinamide (1%; range, 0 to 7%), and ethambutol (12%; range, 4 to 24%). Plasma proteins were not found to be significant predictors for the PB of first-line anti-TB drugs. Rifampin PB was positively correlated with its plasma concentration ( value = 0.0051). Conversely, isoniazid PB was negatively correlated with its plasma concentration ( value = 0.0417). Age was found to have a significant effect on isoniazid PB ( value = 0.0376). No correlations were observed in pyrazinamide or ethambutol. In conclusion, we have determined variable PB of rifampin, isoniazid, pyrazinamide, and ethambutol in patient plasma samples, with median values of 88, 14, 1, and 12%, respectively. In this small study, PB of rifampin and that of isoniazid are dependent on their plasma concentrations.