Mucoadhesive PLGA Nanospheres and Nanocapsules for Lactoferrin Controlled Ocular Delivery

Background: the present work describes the preparation, characterization and optimization of eight types of PLGA-based nanosystems (nanospheres and nanocapsules) as innovative mucoadhesive drug delivery systems of lactoferrin, in order to achieve a preclinical consistent base as an alternative pharm...

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Main Authors: Rubén Varela-Fernández (Author), Xurxo García-Otero (Author), Victoria Díaz-Tomé (Author), Uxía Regueiro (Author), Maite López-López (Author), Miguel González-Barcia (Author), María Isabel Lema (Author), Francisco Javier Otero-Espinar (Author)
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Published: MDPI AG, 2022-04-01T00:00:00Z.
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001 doaj_ed0ce7ca83ee4f29a961f2bc4f94c639
042 |a dc 
100 1 0 |a Rubén Varela-Fernández  |e author 
700 1 0 |a Xurxo García-Otero  |e author 
700 1 0 |a Victoria Díaz-Tomé  |e author 
700 1 0 |a Uxía Regueiro  |e author 
700 1 0 |a Maite López-López  |e author 
700 1 0 |a Miguel González-Barcia  |e author 
700 1 0 |a María Isabel Lema  |e author 
700 1 0 |a Francisco Javier Otero-Espinar  |e author 
245 0 0 |a Mucoadhesive PLGA Nanospheres and Nanocapsules for Lactoferrin Controlled Ocular Delivery 
260 |b MDPI AG,   |c 2022-04-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14040799 
500 |a 1999-4923 
520 |a Background: the present work describes the preparation, characterization and optimization of eight types of PLGA-based nanosystems (nanospheres and nanocapsules) as innovative mucoadhesive drug delivery systems of lactoferrin, in order to achieve a preclinical consistent base as an alternative pharmacological treatment to different ocular syndromes and diseases. Methods: All different nanoparticles were prepared via two modified nanoprecipitation techniques, using a three-component mixture of drug/polymer/surfactant (Lf/PLGA/Poloxamer), as a way to overcome the inherent limitations of conventional PLGA NPs. These modified polymeric nanocarriers, intended for topical ophthalmic administration, were subjected to in vitro characterization, surface modification and in vitro and in vivo assessments. Results: An appropriate size range, uniform size distribution and negative ζ potential values were obtained for all types of formulations. Lactoferrin could be effectively included into all types of nanoparticles with appropriate encapsulation efficiency and loading capacity values. A greater, extended, and controlled delivery of Lf from the polymeric matrix was observed through the in vitro release studies. No instability or cytotoxicity was proved for all the formulations by means of organotypic models. Additionally, mucoadhesive in vitro and in vivo experiments show a significant increase in the residence time of the nanoparticles in the eye surface. Conclusions: all types of prepared PLGA nanoparticles might be a potential alternative for the topical ophthalmic administration of lactoferrin. 
546 |a EN 
690 |a nanoparticles 
690 |a PLGA 
690 |a lactoferrin 
690 |a topical ophthalmic administration 
690 |a nanoprecipitation 
690 |a protein nanocarriers 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 4, p 799 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/4/799 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/ed0ce7ca83ee4f29a961f2bc4f94c639  |z Connect to this object online.