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Bioengineered Human Stromal Lenticule for Recombinant Human Nerve Growth Factor Release: A Potential Biocompatible Ocular Drug Delivery System.

Authors :
Mastropasqua L
Nubile M
Acerra G
Detta N
Pelusi L
Lanzini M
Mattioli S
Santalucia M
Pietrangelo L
Allegretti M
Dua HS
Mehta JS
Pandolfi A
Mandatori D
Source :
Frontiers in bioengineering and biotechnology [Front Bioeng Biotechnol] 2022 Jun 23; Vol. 10, pp. 887414. Date of Electronic Publication: 2022 Jun 23 (Print Publication: 2022).
Publication Year :
2022

Abstract

Small incision lenticule extraction (SMILE), is a surgical procedure for the myopia correction, during which a corneal stromal lenticule is extracted. Given that we have previously demonstrated how this discarded tissue could be repurposed as a bio-scaffold for stromal engineering, this study aimed to explore its use as an ocular drug delivery system of active molecules, using neurotrophic factor Nerve Growth Factor (NGF). We employed human stromal lenticules directly collected from healthy donors undergoing SMILE. Following a sodium dodecylsulfate (SDS) treatment, decellularized lenticules were incubated with a suspension of polylactic-co-glycolic-acid (PLGA) microparticles (MPs) loaded with recombinant human NGF (rhNGF-MPs). Fluorescent MPs (Fluo-MPs) were used as control. Data demonstrated the feasibility to engineer decellularized lenticules with PLGA-MPs which remain incorporated both on the lenticules surface and in its stromal. Following their production, the in vitro release kinetic showed a sustained release for up to 1 month of rhNGF from MPs loaded to the lenticule. Interestingly, rhNGF was rapidly released in the first 24 h, but it was sustained up to the end of the experiment (1 month), with preservation of rhNGF activity (around 80%). Our results indicated that decellularized human stromal lenticules could represent a biocompatible, non-immunogenic natural scaffold potential useful for ocular drug delivery. Therefore, combining the advantages of tissue engineering and pharmaceutical approaches, this in vitro proof-of-concept study suggests the feasibility to use this scaffold to allow target release of rhNGF in vivo or other pharmaceutically active molecules that have potential to treat ocular diseases.<br />Competing Interests: Authors GA, ND, SM, and MA are employed by Dompé Farmaceutici SpA. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Mastropasqua, Nubile, Acerra, Detta, Pelusi, Lanzini, Mattioli, Santalucia, Pietrangelo, Allegretti, Dua, Mehta, Pandolfi and Mandatori.)

Details

Language :
English
ISSN :
2296-4185
Volume :
10
Database :
MEDLINE
Journal :
Frontiers in bioengineering and biotechnology
Publication Type :
Academic Journal
Accession number :
35813999
Full Text :
https://doi.org/10.3389/fbioe.2022.887414