2018
DOI: 10.1039/c7cc08648b
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A facile one-pot synthesis of acrylated hyaluronic acid

Abstract: The synthesis of acrylated hyaluronic acid (HA-A) normally requires 2 to 3 steps of modification, needs laborious purification and also increases the risks of HA degradation. Here, we report that the conjugation of acrylate groups to hyaluronic acid can be successfully achieved via a new facile one-pot approach. Two types of new HA-A hydrogels (via chemical or UV crosslinking) were developed and applied for 3D cell encapsulation.

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Cited by 22 publications
(4 citation statements)
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“…Hyaluronic acid methacryloyl (HAMA) synthesis refers to an established protocol. 30 In short, 2.0 g of hyaluronic acid was dissolved in reverse osmosis water (150 mL) and stirred for 24 h at room temperature to dissolve completely. Subsequently, 100 mL of N,Ndimethylformamide was added dropwise to hyaluronic acid solution to obtain a water/N,N-dimethylformamide ratio of 3/2 (v/v).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Hyaluronic acid methacryloyl (HAMA) synthesis refers to an established protocol. 30 In short, 2.0 g of hyaluronic acid was dissolved in reverse osmosis water (150 mL) and stirred for 24 h at room temperature to dissolve completely. Subsequently, 100 mL of N,Ndimethylformamide was added dropwise to hyaluronic acid solution to obtain a water/N,N-dimethylformamide ratio of 3/2 (v/v).…”
Section: Methodsmentioning
confidence: 99%
“…Hyaluronic acid methacryloyl (HAMA) synthesis refers to an established protocol . In short, 2.0 g of hyaluronic acid was dissolved in reverse osmosis water (150 mL) and stirred for 24 h at room temperature to dissolve completely.…”
Section: Methodsmentioning
confidence: 99%
“…Initially, we prepared the non-thermoresponsive naturally derived materials. For that, CHTMA, GELMA, LAMMA, and HAMA were synthesized by coupling of chitosan (CHT), gelatin (GEL), laminarin (LAM), and hyaluronic acid (HA), respectively, with methacrylic acid, methacrylic anhydride, or glycidyl methacrylate on the basis of previous procedures. , CHTMA, GELMA, LAMMA, and HAMA were obtained as white solids with a degree of substitution (DS) of 33%, 52%, 18%, and 11% or 29%, respectively. The insertion of methacrylate moieties onto the polymer backbones was confirmed and quantified by 1 H NMR or UV–vis spectroscopy analysis (Figures S1–S5).…”
mentioning
confidence: 99%
“…We also evaluated the temperature-responsive performance of methacrylated gelatin (GELMA) in this system. These polymers were chosen as simple and widely known platforms with described cytocompatibility (Figure ).…”
mentioning
confidence: 99%