> Details

Churilov, Leonid; Korzhikov-Vlakh, Viktor; Sinitsyna, Ekaterina; Polyakov, Dmitry; Darashkevich, Oleg; Poida, Mikhail; Platonova, Galina; Vinogradova, Tatiana; Utekhin, Vladimir; Zabolotnykh, Natalia; Zinserling, Vsevolod; Yablonsky, Peter; Urtti, Arto; Tennikova, Tatiana

Enhanced Delivery of 4-Thioureidoiminomethylpyridinium Perchlorate in Tuberculosis Models with IgG Functionalized Poly(Lactic Acid)-Based Particles

Reference
management

Bookmarks

Remove from
bookmarks

Share this on Whatsapp

Close

Bookmarks



You can manage bookmarks using lists, please log in to your user account for this.
  • Media type: E-Article
  • Title: Enhanced Delivery of 4-Thioureidoiminomethylpyridinium Perchlorate in Tuberculosis Models with IgG Functionalized Poly(Lactic Acid)-Based Particles
  • Contributor: Churilov, Leonid; Korzhikov-Vlakh, Viktor; Sinitsyna, Ekaterina; Polyakov, Dmitry; Darashkevich, Oleg; Poida, Mikhail; Platonova, Galina; Vinogradova, Tatiana; Utekhin, Vladimir; Zabolotnykh, Natalia; Zinserling, Vsevolod; Yablonsky, Peter; Urtti, Arto; Tennikova, Tatiana
  • Published: MDPI AG, 2018
  • Published in: Pharmaceutics, 11 (2018) 1, Seite 2
  • Language: English
  • DOI: 10.3390/pharmaceutics11010002
  • ISSN: 1999-4923
  • Origination:
  • Footnote:
  • Description: The compound 4-thioureidoiminomethylpyridinium perchlorate (perchlozone©) is a novel anti-tuberculosis drug that is active in multiple drug resistance cases, but the compound is hepatotoxic. To decrease the systemic load and to achieve targeting, we encapsulated the drug into poly(lactic acid)-based micro- (1100 nm) and nanoparticles (170 nm) that were modified with single-chain camel immunoglobulin G (IgG) for targeting. Both micro- and nanoparticles formed stable suspensions in saline solution at particle concentrations of 10–50 mg/mL. The formulations were injected intraperitoneally and intravenously into the mice with experimental tuberculosis. The survival of control animals was compared to that of mice which were treated with daily oral drug solution, single intraperitoneal administration of drug-loaded particles, and those treated both intravenously and intraperitoneally by drug-loaded particles modified with polyclonal camel IgGs. The distribution of particles in the organs of mice was analyzed with immunofluorescence and liquid chromatography/mass spectrometry. Morphological changes related to tuberculosis and drug toxicity were registered. Phagocytic macrophages internalized particles and transported them to the foci of tuberculosis in inner organs. Nanoparticle-based drug formulations, especially those with IgG, resulted in better survival and lower degree of lung manifestations than the other modes of treatment.
  • Access State: Open Access