Biodegradable nanocarriers coated with polymyxin B: Evaluation of leishmanicidal and antibacterial potential.
Anti-Bacterial Agents
/ chemistry
Antiprotozoal Agents
/ chemistry
Bacteria
/ drug effects
Bacterial Infections
/ drug therapy
Drug Delivery Systems
/ instrumentation
Drug Evaluation, Preclinical
Leishmania
/ drug effects
Leishmaniasis
/ drug therapy
Macrophages
/ parasitology
Nanoparticles
/ chemistry
Polymyxin B
/ chemistry
Journal
PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
received:
22
09
2018
accepted:
13
04
2019
revised:
13
05
2019
pubmed:
3
5
2019
medline:
28
10
2019
entrez:
3
5
2019
Statut:
epublish
Résumé
Most treatments of leishmaniasis require hospitalization and present side effects or parasite resistance; innovations in drug formulation/reposition can overcome these barriers and must be pursued to increase therapeutic alternatives. Therefore, we tested polymyxin B (polB) potential to kill Leishmania amazonensis, adsorbed or not in PBCA nanoparticles (PBCAnp), which could augment polB internalization in infected macrophages. PBCAnps were fabricated by anionic polymerization and analyzed by Dynamic Light Scattering (size, ζ potential), Nanoparticle Tracking Analysis (size/concentration), vertical diffusion cell (release rate), drug incorporation (indirect method, protein determination) and in vitro cell viability. Nanoparticles coated with polB (PBCAnp-polB) presented an adequate size of 261.5 ± 25.9 nm, low PDI and ζ of 1.79 ± 0.17 mV (stable for 45 days, at least). The 50% drug release from PBCAnp-polB was 6-7 times slower than the free polB, which favors a prolonged and desired release profile. Concerning in vitro evaluations, polB alone reduced in vitro amastigote infection of macrophages (10 μg/mL) without complete parasite elimination, even at higher concentrations. This behavior limits its future application to adjuvant leishmanicidal therapy or antimicrobial coating of carriers. The nanocarrier PBCAnp also presented leishmanicidal effect and surpassed polB activity; however, no antimicrobial activity was detected. PolB maintained its activity against E. coli, Pseudomonas and Klebsiella, adding antimicrobial properties to the nanoparticles. Thus, this coated drug delivery system, described for the first time, demonstrated antileishmanial and antimicrobial properties. The bactericidal feature helps with concomitant prevention/treatment of secondary infections that worst ulcers induced by cutaneous L. amazonensis, ultimately ending in disfiguring or disabling lesions.
Identifiants
pubmed: 31042710
doi: 10.1371/journal.pntd.0007388
pii: PNTD-D-18-01414
pmc: PMC6513107
doi:
Substances chimiques
Anti-Bacterial Agents
0
Antiprotozoal Agents
0
Polymyxin B
J2VZ07J96K
Types de publication
Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0007388Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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