2012
DOI: 10.1002/adfm.201202433
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A Stiff Injectable Biodegradable Elastomer

Abstract: Injectable materials often have shortcomings in mechanical and drug-eluting properties that are attributable to their high water contents. A water-free, liquid four-armed PEG modified with dopamine end groups is described which changed from liquid to elastic solid by reaction with a small volume of Fe3+ solution. The elastic modulus and degradation times increased with increasing Fe3+ concentrations. Both the free base and the water-soluble form of lidocaine could be dissolved in the PEG4-dopamine and released… Show more

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Cited by 54 publications
(49 citation statements)
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“…Most of the PEG end groups (70%) were functionalized with CAA as confirmed by 1 H‐NMR (Figure S2). These conversion rates are comparable with those reported for similar multiarmed PEG polymers . Molecular weights of PEG 4 and PEG 4 ‐CAA were 1426 and 1949 Da, respectively, as determined by gel permeation chromatography (Figure S3), confirming the 1 H‐NMR results.…”
Section: Resultssupporting
confidence: 87%
See 1 more Smart Citation
“…Most of the PEG end groups (70%) were functionalized with CAA as confirmed by 1 H‐NMR (Figure S2). These conversion rates are comparable with those reported for similar multiarmed PEG polymers . Molecular weights of PEG 4 and PEG 4 ‐CAA were 1426 and 1949 Da, respectively, as determined by gel permeation chromatography (Figure S3), confirming the 1 H‐NMR results.…”
Section: Resultssupporting
confidence: 87%
“…These conversion rates are comparable with those reported for similar multiarmed PEG polymers. 27,28 Molecular weights of PEG 4 and PEG 4 -CAA were 1426 and 1949 Da, respectively, as determined by gel permeation chromatography ( Figure S3), confirming the 1 H-NMR results. Moreover, the UVvis spectrum of the PEG 4 -CAA conjugate showed two absorption maxima at 234 and 313 nm, which are indicative of the presence of CAA 29 (Figure S4).…”
Section: Resultssupporting
confidence: 77%
“…This yield is comparable with the efficiencies reported by us and by others for modification of PEG 4 with similar molecular weight. For example, our previous reports of substituting PEG 4 with dopamine showed substitution rates of about 77% …”
Section: Resultssupporting
confidence: 67%
“…Both spectra revealed a narrow, dominant peak at 280 nm, characteristic of non-oxidized dopamine groups. 23 A slight broadening of the peak, in the range of 310-370 nm was observed in the recovered PEG 4 –dopamine, confirming the oxidation process revealed by 1 H NMR spectroscopy.…”
Section: Resultssupporting
confidence: 64%