4.8 Article

Peptide Hydrogel as an Intraocular Drug Delivery System for Inhibition of Postoperative Scarring Formation

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 2, Issue 9, Pages 2663-2671

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/am100484c

Keywords

peptide hydrogel; drug delivery system; inhibition of scarring formation

Funding

  1. Ministry of Science and Technology of China [2009CB930300]
  2. Trans(New)-Century Training Programme Foundation for the Talents from the Ministry of Education of China
  3. Natural Science Foundation of Hubei Province, China [2009CDA024]
  4. Wuhan University of China [20082030201000010]

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A biocompatible hydrogel self-assembled from a peptide comprised of a peptide backbone containing Arg-Gly-Asp (RGD) sequence and a hydrophobic N-fluorenyl-9-methoxycarbonyl (FMOC) tail was designed and prepared to load antiproliferative model drug (5-fluorouracil, 5-Fu). After administrating this 5-Fu-loaded peptide hydrogel in the filtering surgery of rabbit eyes, because of the sustained release of 5-Fu from the hydrogel to inhibit the scleral flap fibrosis efficiently, the pathology and immunohistochemistry demonstrate that the filtration fistula is patent without postoperative scarring formation, resulting in the significantly low intraocular pressure (IOP) of the rabbit eyes within postoperative 28 days. In a comparison with the conventional 5-Fu exposure, the strategy demonstrated here presents several advantages including providing convenience and preventing the toxicity of 5-Fu to the surrounding ocular tissues efficiently, suggesting a feasibility of this peptide hydrogel as a potential implanted drug delivery system for the inhibition of postoperative scarring formation.

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