Prothionamide Dose Optimization Using Population Pharmacokinetics for Multidrug-Resistant Tuberculosis Patients

Author:

Yun Hwi-yeol1,Chang Min Jung234ORCID,Jung Heeyoon5,Chang Vincent6,Wang Qianwen6,Strydom Natasha6ORCID,Yoon Young-Ran78ORCID,Savic Radojka M.6ORCID

Affiliation:

1. Department of Pharmacy, College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea

2. Department of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon, Republic of Korea

3. Department of Pharmaceutical Medicine and Regulatory Science, Yonsei University, Incheon, Republic of Korea

4. Graduate Program of Industrial Pharmaceutical Science, Yonsei University, Incheon, Republic of Korea

5. Department of Bio-AI Convergence, Chungnam National University, Daejeon, Republic of Korea

6. Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, USA

7. Department of Molecular Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea

8. Department of Clinical Pharmacology, Kyungpook National University Hospital, Daegu, Republic of Korea

Abstract

Prothionamide, a second-line drug for multidrug-resistant tuberculosis (MDR-TB), has been in use for a few decades. However, its pharmacokinetic (PK) profile remains unclear.

Funder

Chungnam National University

MSIT | Institute for Information and Communications Technology Promotion

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference25 articles.

1. World Health Organization. 2020. Global tuberculosis report 2020. World Health Organization, Geneva, Switzerland.

2. Treatment of Drug-Resistant Tuberculosis. An Official ATS/CDC/ERS/IDSA Clinical Practice Guideline

3. World Health Organization. 2019. Consolidated guidelines on tuberculosis. World Health Organization, Geneva, Switzerland.

4. Recent advances in the design of inhibitors of mycobacterial transcriptional regulators to boost thioamides anti-tubercular activity and circumvent acquired-resistance

5. Plasma levels of ethionamide and prothionamide in a volunteer following intravenous and oral dosages

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