Antitubercular nanocarrier monotherapy: Study of In Vivo efficacy and pharmacokinetics for rifampicin

Jiří Trousil*, Oto Pavliš, Pavla Kubíčková, Miša Škorič, Věra Marešová, Ewa Pavlova, Kenneth D. Knudsen, You Shan Dai, Matthew Zimmerman, Véronique Dartois, Jia You Fang, Martin Hrubý

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

31 Scopus citations

Abstract

Tuberculosis represents a major global health problem for which improved approaches are needed to shorten the course of treatment and to combat the emergence of resistant strains. The development of effective and safe nanobead-based interventions can be particularly relevant for increasing the concentrations of antitubercular agents within the infected site and reducing the concentrations in the general circulation, thereby avoiding off-target toxic effects. In this work, rifampicin, a first-line antitubercular agent, was encapsulated into biocompatible and biodegradable polyester-based nanoparticles. In a well-established BALB/c mouse model of pulmonary tuberculosis, the nanoparticles provided improved pharmacokinetics and pharmacodynamics. The nanoparticles were well tolerated and much more efficient than an equivalent amount of free rifampicin.

Original languageEnglish
Pages (from-to)312-323
Number of pages12
JournalJournal of Controlled Release
Volume321
DOIs
StatePublished - 10 05 2020

Bibliographical note

Publisher Copyright:
© 2020 Elsevier B.V.

Keywords

  • BALB/c mice
  • Drug delivery system
  • Histopathology
  • Nanoparticles
  • Pharmacokinetics
  • Rifampicin
  • Tuberculosis

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