化工儀器網(wǎng)
資料下載
Injectable hydrogels with in situ-forming hydrophobic domains: oligo(D,L-lactide) modified poly(olig
閱讀：216 發(fā)布時(shí)間：2015-5-25| 提 供 商 | 美國布魯克海文儀器公司 | 資料大小 | 2MB |
|---|---|---|---|
| 資料圖片 | 下載次數(shù) | 231次 | |
| 資料類型 | PDF 文件 | 瀏覽次數(shù) | 216次 |
| 免費(fèi)下載 | 點(diǎn)擊下載 |
Injectable, in situ-gelling nanostructured hydrogels have been prepared from hydrazide and aldehydefunctionalized
polymer precursors based on a copolymer of oligo(ethylene glycol) methacrylate (OEGMA)
and an oligo(lactic acid) macromonomer (OLA) with varying lactic acid chain lengths. The resulting
hydrogels contain a mix of chemical (hydrazone bond formation between hydrazide and aldehyde groups)
and physical (hydrophobic interactions between OLA chains) cross-links which form competitively as a
function of the OLA chain length and density. An increase in the OLA chain length and density results in
the formation of more physical cross-links and fewer chemical cross-links. Tuning the relative prevalence
of physical and chemical cross-link formation facilitated largely independent tuning of gel mechanics
relative to gel swelling and degradation. Small-angle neutron scattering of these OLA-containing
hydrogels reveals a microstructure consisting of associative hydrophobic domains, based on an increased
scattering intensity and decreased blob size relative to that observed for POEGMA hydrogels prepared
without the OLA co-monomer. The presence of hydrophobic OLA domains increases the uptake and
slows the release of bovine serum albumin, a protein well-known to associate with hydrophobic domains.
Coupled with the observed cytocompatibility of the reactive precursor polymers used to prepare the
hydrogels, we anticipate significant potential applications of these hydrogels for the prolonged release of
hydrophobic cargoes.