Development of Peptide Targeted PLGA-PEGylated Nanoparticles Loading Licochalcone-A for Ocular Inflammation

Licochalcone-A is a natural compound with anti-inflammatory properties. However, it possesses low water solubility, making its application for the treatment of ocular inflammation difficult. To overcome this drawback, biodegradable nanoparticles incorporating Licochalcone-A have been developed. Addi...

Full description

Saved in:
Bibliographic Details
Main Authors: Ruth Galindo (Author), Elena Sánchez-López (Author), María José Gómara (Author), Marta Espina (Author), Miren Ettcheto (Author), Amanda Cano (Author), Isabel Haro (Author), Antoni Camins (Author), María Luisa García (Author)
Format: Book
Published: MDPI AG, 2022-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_a08804d3ddd04c66a72a43f28a2502c7
042 |a dc 
100 1 0 |a Ruth Galindo  |e author 
700 1 0 |a Elena Sánchez-López  |e author 
700 1 0 |a María José Gómara  |e author 
700 1 0 |a Marta Espina  |e author 
700 1 0 |a Miren Ettcheto  |e author 
700 1 0 |a Amanda Cano  |e author 
700 1 0 |a Isabel Haro  |e author 
700 1 0 |a Antoni Camins  |e author 
700 1 0 |a María Luisa García  |e author 
245 0 0 |a Development of Peptide Targeted PLGA-PEGylated Nanoparticles Loading Licochalcone-A for Ocular Inflammation 
260 |b MDPI AG,   |c 2022-01-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14020285 
500 |a 1999-4923 
520 |a Licochalcone-A is a natural compound with anti-inflammatory properties. However, it possesses low water solubility, making its application for the treatment of ocular inflammation difficult. To overcome this drawback, biodegradable nanoparticles incorporating Licochalcone-A have been developed. Additionally, to avoid fast clearance and increase cellular internalization into the ocular tissues, PLGA nanoparticles have been functionalized using PEG and cell penetrating peptides (Tet-1 and B6). To optimize the formulations, a factorial design was carried out and short-term stability of the nanoparticles was studied. Moreover, morphology was also observed by transmission electron microcopy and in vitro drug release was carried out. Ocular tolerance of the formulations was ensured in vitro and in vivo and anti-inflammatory therapeutic efficacy was also assessed. Surface functionalized nanoparticles loading Licochalcone-A were developed with an average size below 200 nm, a positive surface charge, and a monodisperse population. The formulations were non-irritant and showed a prolonged Licochalcone-A release. Despite the fact that both Licochalcone-A Tet-1 and B6 functionalized nanoparticles demonstrated to be suitable for the treatment of ocular inflammation, B6 targeted nanoparticles provided greater therapeutic efficacy in in vivo assays. 
546 |a EN 
690 |a Licochalcone-A 
690 |a nanoparticles 
690 |a ocular inflammation 
690 |a cell-penetrating peptides 
690 |a PLGA 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 2, p 285 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/2/285 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/a08804d3ddd04c66a72a43f28a2502c7  |z Connect to this object online.