Surface modification of corneal prosthesis with nano-hydroxyapatite to enhance in vivo biointegration.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
15 04 2020
Historique:
received: 21 05 2019
revised: 15 01 2020
accepted: 16 01 2020
pubmed: 25 1 2020
medline: 15 4 2021
entrez: 25 1 2020
Statut: ppublish

Résumé

The majority of clinical corneal prostheses (KPros) adopt a core-skirt configuration. This configuration is favored owing to the optic core (generally a cylindrical, acrylic-based material, such as PMMA), that not only provides a clear window for the patients' vision, but also confers resistance to biodegradability. The surrounding skirt (typically a biological material, such as corneal tissue) allows for host tissue integration. However, due to poor biointegration between the dissimilar core and skirt materials, it results in a weak adhesion at the interface, giving rise to clinical complications, such as bacterial infections in the tissue-PMMA interface and device extrusion. Here, we physically immobilized nano-hydroxyapatite (nHAp) on a PMMA cylinder via a dip-coating technique, to create a bioactive surface that improved biointegration in vivo. We established that the nHAp coating was safe and stable in the rabbit cornea over five weeks. More importantly, we found that apoptotic, wound healing and inflammatory responses to nHAp-coated PMMA were substantially milder than to non-coated PMMA. More mature collagen, similar to the non-operated cornea, was maintained in the corneal stroma adjacent to the nHAp-coated implant edge. However, around the non-coated cylinder, an abundant new and loose connective tissue formed, similar to bone tissue response to bioinert scaffolds. As a result of superior biointegration, tissue adhesion with nHAp-coated PMMA cylinders was also significantly enhanced compared to non-coated cylinders. This study set a precedent for the future application of the nHAp coating on clinical KPros. STATEMENT OF SIGNIFICANCE: Currently, all clinical corneal prostheses utilize as-manufactured, non-surface modified PMMA optic cylinder. The bioinert cylinder, however, has poor biointegration and adhesion with the surrounding biological tissue, which can give rise to postoperative complications, such as microbial invasion in the tissue-PMMA loose interface and PMMA optic cylinder extrusion. In the current study, we showed that surface modification of the PMMA cylinder with bioactive nano-hydroxyapatite (nHAp) significantly enhanced its biointegration with corneal stromal tissue in vivo. The superior biointegration of the nHAp-coated PMMA was signified by a more attenuated corneal wound healing, inflammatory and fibrotic response, and better tissue apposition, as well as a significantly improved corneal stromal tissue adhesion when compared to the non-coated PMMA.

Identifiants

pubmed: 31978623
pii: S1742-7061(20)30037-4
doi: 10.1016/j.actbio.2020.01.023
pii:
doi:

Substances chimiques

Hydroxyapatites 0
Polymethyl Methacrylate 9011-14-7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

299-312

Informations de copyright

Copyright © 2020 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Andri K Riau (AK)

Tissue Engineering and Stem Cell Group, Singapore Eye Research Institute, Singapore; School of Materials Science and Engineering, Nanyang Technological University, Singapore.

Nyein C Lwin (NC)

Tissue Engineering and Stem Cell Group, Singapore Eye Research Institute, Singapore.

Larisa Gelfand (L)

Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA, United States.

Huanlong Hu (H)

School of Mechanical and Aerospace Engineering, Nanyang Technological University, Singapore.

Bo Liedberg (B)

School of Materials Science and Engineering, Nanyang Technological University, Singapore; Center for Biomimetic Sensor Science, Nanyang Technological University, Singapore.

James Chodosh (J)

Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA, United States.

Subbu S Venkatraman (SS)

School of Materials Science and Engineering, Nanyang Technological University, Singapore. Electronic address: subbu@nus.edu.sg.

Jodhbir S Mehta (JS)

Tissue Engineering and Stem Cell Group, Singapore Eye Research Institute, Singapore; School of Materials Science and Engineering, Nanyang Technological University, Singapore; Ophthalmology and Visual Sciences Academic Clinical Program, Duke-NUS Medical School, Singapore; Singapore National Eye Center, Singapore. Electronic address: jodmehta@gmail.com.

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Classifications MeSH