4.8 Article

An injectable thiol-acrylate poly(ethylene glycol) hydrogel for sustained release of methylprednisolone sodium succinate

期刊

BIOMATERIALS
卷 32, 期 2, 页码 587-597

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2010.08.106

关键词

Cell adhesion; Controlled drug release; Hydrogel; Peptide; Polyethylene oxide; Spinal surgery

资金

  1. MIT/CIMIT
  2. General Sir John Monash Award
  3. Armed Forces Institute of Regenerative Medicine
  4. NATIONAL CANCER INSTITUTE [P30CA014051] Funding Source: NIH RePORTER

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Clinically available injectable hydrogels face technical challenges associated with swelling after injection and toxicity from unreacted constituents that impede their performance as surgical biomaterials To overcome these challenges we developed a system where chemical gelation was controlled by a conjugate Michael addition between thiol and acrylate in aqueous media with 97% monomer conversion and 6 wt % sol fraction The hydrogel exhibited syneresis on equilibration reducing to 59 7% of its initial volume It had mechanical properties similar to soft human tissue with an elastic modulus of 189 8 kPa Furthermore a mesh size of 69 nm resulted in sustained release of methylprednisolone sodium succinate with a loading efficiency of 2 mg/mL Functionalization with 50 mu g/mL of an oligolysine peptide resulted in attachment of freshly Isolated munne mesenchymal stem cells The rational design of the physical chemical and biological properties of the hydrogel makes It a potentially promising candidate for injectable applications (C) 2010 Elsevier Ltd All rights reserved

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