In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates

Baranyai, Zsuzsa and Krátky, Martin and Vosátka, Rudolf and Szabó, Eleonóra and Senoner, Zsuzsanna and Dávid, Sándor and Stolaríkova, Jirina and Vinsová, Jarmila and Bősze, Szilvia (2017) In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 133. pp. 152-173. ISSN 0223-5234

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Abstract

Tuberculosis is caused by Mycobacterium tuberculosis, an intracellular pathogen that can survive in host cells, mainly in macrophages. An increase of multidrug-resistant tuberculosis qualifies this infectious disease as a major public health problem worldwide. The cellular uptake of the antimycobacterial agents by infected host cells is limited. Our approach is to enhance the cellular uptake of the antituberculars by target cell-directed delivery using drug-peptide conjugates to achieve an increased intracellular efficacy. In this study, salicylanilide derivatives (2-hydroxy-N-phenylbenzamides) with remarkable antimycobacterial activity were conjugated to macrophage receptor specific tuftsin based peptide carriers through oxime bond directly or by insertion of a GFLG tetrapeptide spacer. We have found that the in vitro antimycobacterial activity of the salicylanilides against M. tuberculosis H37Rv is preserved in the conjugates. While the free drug was ineffective on infected macrophage model, the conjugates were active against the intracellular bacteria. The fluorescently labelled peptide carriers that were modified with different fatty acid side chains showed outstanding cellular uptake rate to the macrophage model cells. The conjugation of the salicylanilides to tuftsin based carriers reduced or abolished the in vitro cytostatic activity of the free drugs with the exception of the palmitoylated conjugates. The conjugates degraded in the presence of rat liver lysosomal homogenate leading to the formation of an oxime bondlinked salicylanilide-amino acid fragment as the smallest active metabolite.

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