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Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications

INTRODUCTION: Untreated ocular infections can damage the unique fine structures of the eye with possible visual impairments and blindness. Ciprofloxacin (CIP) ophthalmic solution is prescribed as first-line therapy in ocular bacterial infections. Natamycin (NT) ophthalmic suspension is one of the pr...

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Autores principales: Youssef, Ahmed Adel Ali, Dudhipala, Narendar, Majumdar, Soumyajit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124492/
https://www.ncbi.nlm.nih.gov/pubmed/35611213
http://dx.doi.org/10.2147/IJN.S360740
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author Youssef, Ahmed Adel Ali
Dudhipala, Narendar
Majumdar, Soumyajit
author_facet Youssef, Ahmed Adel Ali
Dudhipala, Narendar
Majumdar, Soumyajit
author_sort Youssef, Ahmed Adel Ali
collection PubMed
description INTRODUCTION: Untreated ocular infections can damage the unique fine structures of the eye with possible visual impairments and blindness. Ciprofloxacin (CIP) ophthalmic solution is prescribed as first-line therapy in ocular bacterial infections. Natamycin (NT) ophthalmic suspension is one of the progenitors in ocular antifungal therapy. Nanostructured lipid carriers (NLCs) have been widely examined for ocular penetration enhancement and distribution to deeper ocular tissues. The objective of the current study was to prepare NLCs loaded with a combination of CIP and NT (CIP-NT-NLCs) and embed them in an in-situ gelling system (CIP-NT-NLCs-IG). This novel formulation will target the co-delivery of CIP and NT for the treatment of mixed ocular infections or as empirical treatment in case of limited access to healthcare diagnostic services. METHODS: CIP-NT-NLC and CIP-NT-NLC-IG formulations were evaluated based on physicochemical characteristics, in vitro release, and ex vivo transcorneal permeation studies and compared against commercial CIP and NT ophthalmic eye drops. RESULTS AND DISCUSSION: NLCs formulation (0.1% CIP and 0.3% NT) showed particle size, polydispersity index, and zeta potential of 196.2 ± 1.2 nm, 0.43 ± 0.06, and −28.1 ± 1.4 mV, respectively. Moreover, CIP-NT-NLCs showed entrapment efficiency of 80.9 ± 2.9 and 98.7 ± 1.9% for CIP and NT, respectively. CIP-NT-NLCs-IGformulation with 0.2% w/v gellan gum demonstrated the most favorable viscoelastic characteristics for ocular application. CIP-NT-NLCs and CIP-NT-NLCs-IG formulations exhibited a sustained release pattern for both drugs over 24 h. Moreover, CIP-NT-NLCs and CIP-NT-NLC-IG formulations showed 4.0- and 2.2-folds, and 5.0- and 2.5-folds enhancement in ex vivo transcorneal permeability of CIP and NT, respectively, compared to the control formulations. CONCLUSION: The results suggest that this dual nanoparticulate-based in-situ gelling drug delivery system can serve as a promising topical delivery platform for the treatment of ocular infections.
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spelling pubmed-91244922022-05-23 Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications Youssef, Ahmed Adel Ali Dudhipala, Narendar Majumdar, Soumyajit Int J Nanomedicine Original Research INTRODUCTION: Untreated ocular infections can damage the unique fine structures of the eye with possible visual impairments and blindness. Ciprofloxacin (CIP) ophthalmic solution is prescribed as first-line therapy in ocular bacterial infections. Natamycin (NT) ophthalmic suspension is one of the progenitors in ocular antifungal therapy. Nanostructured lipid carriers (NLCs) have been widely examined for ocular penetration enhancement and distribution to deeper ocular tissues. The objective of the current study was to prepare NLCs loaded with a combination of CIP and NT (CIP-NT-NLCs) and embed them in an in-situ gelling system (CIP-NT-NLCs-IG). This novel formulation will target the co-delivery of CIP and NT for the treatment of mixed ocular infections or as empirical treatment in case of limited access to healthcare diagnostic services. METHODS: CIP-NT-NLC and CIP-NT-NLC-IG formulations were evaluated based on physicochemical characteristics, in vitro release, and ex vivo transcorneal permeation studies and compared against commercial CIP and NT ophthalmic eye drops. RESULTS AND DISCUSSION: NLCs formulation (0.1% CIP and 0.3% NT) showed particle size, polydispersity index, and zeta potential of 196.2 ± 1.2 nm, 0.43 ± 0.06, and −28.1 ± 1.4 mV, respectively. Moreover, CIP-NT-NLCs showed entrapment efficiency of 80.9 ± 2.9 and 98.7 ± 1.9% for CIP and NT, respectively. CIP-NT-NLCs-IGformulation with 0.2% w/v gellan gum demonstrated the most favorable viscoelastic characteristics for ocular application. CIP-NT-NLCs and CIP-NT-NLCs-IG formulations exhibited a sustained release pattern for both drugs over 24 h. Moreover, CIP-NT-NLCs and CIP-NT-NLC-IG formulations showed 4.0- and 2.2-folds, and 5.0- and 2.5-folds enhancement in ex vivo transcorneal permeability of CIP and NT, respectively, compared to the control formulations. CONCLUSION: The results suggest that this dual nanoparticulate-based in-situ gelling drug delivery system can serve as a promising topical delivery platform for the treatment of ocular infections. Dove 2022-05-18 /pmc/articles/PMC9124492/ /pubmed/35611213 http://dx.doi.org/10.2147/IJN.S360740 Text en © 2022 Youssef et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Youssef, Ahmed Adel Ali
Dudhipala, Narendar
Majumdar, Soumyajit
Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications
title Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications
title_full Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications
title_fullStr Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications
title_full_unstemmed Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications
title_short Dual Drug Loaded Lipid Nanocarrier Formulations for Topical Ocular Applications
title_sort dual drug loaded lipid nanocarrier formulations for topical ocular applications
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124492/
https://www.ncbi.nlm.nih.gov/pubmed/35611213
http://dx.doi.org/10.2147/IJN.S360740
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