Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis

Patricia Marcianes,1 Sofia Negro,1,2 Luis García-García,3 Consuelo Montejo,4 Emilia Barcia,1,2 Ana Fernández-Carballido1,2 1Department of Pharmaceutics, School of Pharmacy, University Complutense of Madrid, Madrid, Spain; 2Institute of Pharmaceutical Technology, Uni...

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Autores principales: Marcianes P, Negro S, García-García L, Montejo C, Barcia E, Fernández-Carballido A
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Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:da8a6987a11445bebf783069b7dd41272021-12-02T00:31:21ZSurface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis1178-2013https://doaj.org/article/da8a6987a11445bebf783069b7dd41272017-03-01T00:00:00Zhttps://www.dovepress.com/surface-modified-gatifloxacin-nanoparticles-with-potential-for-treatin-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Patricia Marcianes,1 Sofia Negro,1,2 Luis García-García,3 Consuelo Montejo,4 Emilia Barcia,1,2 Ana Fernández-Carballido1,2 1Department of Pharmaceutics, School of Pharmacy, University Complutense of Madrid, Madrid, Spain; 2Institute of Pharmaceutical Technology, University Complutense of Madrid, Madrid, Spain; 3Multidisciplinary Institute of Cerebral Cartography, University Complutense of Madrid, Madrid, Spain; 4Department of Pharmaceutical and Health Sciences, School of Pharmacy, University CEU-San Pablo, Spain Abstract: A new nanocarrier is developed for the passage of gatifloxacin through the blood–brain barrier to treat central nervous system tuberculosis. Gatifloxacin nanoparticles were prepared by nanoprecipitation using poly(lactic-co-glycolic acid) (PLGA) 502 and polysorbate 80 or Labrafil as surface modifiers. The evaluation of in vivo blood–brain barrier transport was carried out in male Wistar rats using rhodamine-loaded PLGA nanoparticles prepared with and without the surface modifiers. At 30 and 60 minutes after administration, nanoparticle biodistribution into the brain (hippocampus and cortex), lungs, and liver was studied. The results obtained from the cerebral cortex and hippocampus showed that functionalization of rhodamine nanoparticles significantly increased their passage into the central nervous system. At 60 minutes, rhodamine concentrations decreased in both the lungs and the liver but were still high in the cerebral cortex. To distinguish the effect between the surfactants, gatifloxacin-loaded PLGA nanoparticles were prepared. The best results corresponded to the formulation prepared with polysorbate 80 with regard to encapsulation efficiency (28.2%), particle size (176.5 nm), and ζ-potential (-20.1 mV), thereby resulting in a promising drug delivery system to treat cerebral tuberculosis. Keywords: polysorbate 80, Labrafil, gatifloxacin, nanoparticles, targeting, blood–brain barrier, brain deliveryMarcianes PNegro SGarcía-García LMontejo CBarcia EFernández-Carballido ADove Medical PressarticlePolysorbate 80LabrafilGatifloxacinNanoparticlesTargetingBlood-Brain BarrierBrain deliveryMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 1959-1968 (2017)
institution DOAJ
collection DOAJ
language EN
topic Polysorbate 80
Labrafil
Gatifloxacin
Nanoparticles
Targeting
Blood-Brain Barrier
Brain delivery
Medicine (General)
R5-920
spellingShingle Polysorbate 80
Labrafil
Gatifloxacin
Nanoparticles
Targeting
Blood-Brain Barrier
Brain delivery
Medicine (General)
R5-920
Marcianes P
Negro S
García-García L
Montejo C
Barcia E
Fernández-Carballido A
Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
description Patricia Marcianes,1 Sofia Negro,1,2 Luis García-García,3 Consuelo Montejo,4 Emilia Barcia,1,2 Ana Fernández-Carballido1,2 1Department of Pharmaceutics, School of Pharmacy, University Complutense of Madrid, Madrid, Spain; 2Institute of Pharmaceutical Technology, University Complutense of Madrid, Madrid, Spain; 3Multidisciplinary Institute of Cerebral Cartography, University Complutense of Madrid, Madrid, Spain; 4Department of Pharmaceutical and Health Sciences, School of Pharmacy, University CEU-San Pablo, Spain Abstract: A new nanocarrier is developed for the passage of gatifloxacin through the blood–brain barrier to treat central nervous system tuberculosis. Gatifloxacin nanoparticles were prepared by nanoprecipitation using poly(lactic-co-glycolic acid) (PLGA) 502 and polysorbate 80 or Labrafil as surface modifiers. The evaluation of in vivo blood–brain barrier transport was carried out in male Wistar rats using rhodamine-loaded PLGA nanoparticles prepared with and without the surface modifiers. At 30 and 60 minutes after administration, nanoparticle biodistribution into the brain (hippocampus and cortex), lungs, and liver was studied. The results obtained from the cerebral cortex and hippocampus showed that functionalization of rhodamine nanoparticles significantly increased their passage into the central nervous system. At 60 minutes, rhodamine concentrations decreased in both the lungs and the liver but were still high in the cerebral cortex. To distinguish the effect between the surfactants, gatifloxacin-loaded PLGA nanoparticles were prepared. The best results corresponded to the formulation prepared with polysorbate 80 with regard to encapsulation efficiency (28.2%), particle size (176.5 nm), and ζ-potential (-20.1 mV), thereby resulting in a promising drug delivery system to treat cerebral tuberculosis. Keywords: polysorbate 80, Labrafil, gatifloxacin, nanoparticles, targeting, blood–brain barrier, brain delivery
format article
author Marcianes P
Negro S
García-García L
Montejo C
Barcia E
Fernández-Carballido A
author_facet Marcianes P
Negro S
García-García L
Montejo C
Barcia E
Fernández-Carballido A
author_sort Marcianes P
title Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
title_short Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
title_full Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
title_fullStr Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
title_full_unstemmed Surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
title_sort surface-modified gatifloxacin nanoparticles with potential for treating central nervous system tuberculosis
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/da8a6987a11445bebf783069b7dd4127
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