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Per Fagerholm

Researcher at Linköping University

Publications -  194
Citations -  7396

Per Fagerholm is an academic researcher from Linköping University. The author has contributed to research in topics: Cornea & Photorefractive keratectomy. The author has an hindex of 44, co-authored 190 publications receiving 6678 citations. Previous affiliations of Per Fagerholm include Massachusetts Eye and Ear Infirmary & Karolinska Institutet.

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PEG-stabilized carbodiimide crosslinked collagen-chitosan hydrogels for corneal tissue engineering.

TL;DR: Optimum hybrid hydrogel demonstrated significantly enhanced mechanical strength and elasticity by 100 and 20%, respectively, compared to its non-hybrid counterpart and had excellent biocompatibility and when implanted into pig corneas for 12 months, allowed seamless host-graft integration with successful regeneration of host corneal epithelium, stroma, and nerves.
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A Biosynthetic Alternative to Human Donor Tissue for Inducing Corneal Regeneration: 24-Month Follow-Up of a Phase 1 Clinical Study

TL;DR: A phase 1 clinical study in which biosynthetic mimics of corneal extracellular matrix were implanted to replace the pathologic anterior cornea of 10 patients who had significant vision loss, with the aim of facilitating endogenous tissue regeneration without the use of human donor tissue.
Journal Article

[Age-related cataract].

Anders Petersson, +1 more
- 23 Aug 2006 - 
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Stable corneal regeneration four years after implantation of a cell-free recombinant human collagen scaffold

TL;DR: Cell-free implants, comprising carbodiimide crosslinked recombinant human collagen (RHC) can achieve stable regeneration and therefore, represent a potentially safe alternative to donor organ transplantation.
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Recombinant human collagen for tissue engineered corneal substitutes.

TL;DR: Transparent, robust hydrogels are fabricated as corneal substitutes from concentrated recombinant human type I and type III collagen solutions crosslinked with 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide and N-hydroxysuccinimide to eliminate the risk of pathogen transfer or xenogeneic immuno- responses posed by animal collagens.