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

An injectable thiol-acrylate poly(ethylene glycol) hydrogel for sustained release of methylprednisolone sodium succinate.
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DOI:
10.1016/j.biomaterials.2010.08.106
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发表时间:
2011-01
期刊:
影响因子:
14
通讯作者:
Langer, Robert
Langer, Robert
中科院分区:
工程技术1区
文献类型:
--
作者:
Pritchard, Christopher D.;O'Shea, Timothy M.;Siegwart, Daniel J.;Calo, Eliezer;Anderson, Daniel G.;Reynolds, Francis M.;Thomas, John A.;Slotkin, Jonathan R.;Woodard, Eric J.;Langer, Robert

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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 6.9 nm resulted in sustained release of methylprednisolone sodium succinate with a loading efficiency of 2 mg/mL. Functionalization with 50 µg/mL of an oligolysine peptide resulted in attachment of freshly isolated murine 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.
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