Conjugates of Ciprofloxacin and Levofloxacin with Cell-Penetrating Peptide Exhibit Antifungal Activity and Mammalian Cytotoxicity

• Published in: International journal of molecular sciences Vol. 21; no. 13; p. 4696
• Main Authors: Ptaszyńska, Natalia, Gucwa, Katarzyna, Olkiewicz, Katarzyna, Heldt, Mateusz, Serocki, Marcin, Stupak, Anna, Martynow, Dorota, Dębowski, Dawid, Gitlin-Domagalska, Agata, Lica, Jan, Łęgowska, Anna, Milewski, Sławomir, Rolka, Krzysztof
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 30.06.2020; MDPI AG
• Subjects: Animals; Anti-Infective Agents - chemical synthesis; Anti-Infective Agents - pharmacology; antimicrobial agents; Antineoplastic Agents - chemical synthesis; bacteriostatic and mycostatic agents; Candida - drug effects; Candida - metabolism; cell-penetrating peptide (CPP); Cell-Penetrating Peptides; Ciprofloxacin; ciprofloxacin bioconjugates; Drug Resistance, Bacterial; HEK293 Cells; Hep G2 Cells; HL-60 Cells; Humans; Levofloxacin; levofloxacin bioconjugates; Microbial Sensitivity Tests; Recombinant Fusion Proteins; Swine; transportan 10 (TP10-NH2); antimicrobial agents; redox-resistant and redox-sensitive linkers; bacteriostatic and mycostatic agents; cell-penetrating peptide (CPP); ciprofloxacin bioconjugates; levofloxacin bioconjugates; transportan 10 (TP10-NH2)
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms21134696

Seven conjugates composed of well-known fluoroquinolone antibacterial agents, ciprofloxacin (CIP) or levofloxacin (LVX), and a cell-penetrating peptide transportan 10 (TP10-NH ) were synthesised. The drugs were covalently bound to the peptide via an amide bond, methylenecarbonyl moiety, or a disulfide bridge. Conjugation of fluoroquinolones to TP10-NH resulted in congeners demonstrating antifungal in vitro activity against human pathogenic yeasts of the genus (MICs in the 6.25 - 100 µM range), whereas the components were poorly active. The antibacterial in vitro activity of most of the conjugates was lower than the activity of CIP or LVX, but the antibacterial effect of CIP-S-S-TP10-NH was similar to the mother fluoroquinolone. Additionally, for two representative CIP and LVX conjugates, a rapid bactericidal effect was shown. Compared to fluoroquinolones, TP10-NH and the majority of its conjugates generated a relatively low level of reactive oxygen species (ROS) in human embryonic kidney cells (HEK293) and human myeloid leukemia cells (HL-60). The conjugates exhibited cytotoxicity against three cell lines, HEK293, HepG2 (human liver cancer cell line), and LLC-PK1 (old male pig kidney cells), with IC values in the 10 - 100 µM range and hemolytic activity. The mammalian toxicity was due to the intrinsic cytoplasmic membrane disruption activity of TP10-NH since fluoroquinolones themselves were not cytotoxic. Nevertheless, the selectivity index values of the conjugates, both for the bacteria and human pathogenic yeasts, remained favourable.