2013
DOI: 10.1016/j.carbpol.2013.04.008
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Rapidly in situ forming chitosan/ε-polylysine hydrogels for adhesive sealants and hemostatic materials

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Cited by 117 publications
(62 citation statements)
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“…Since it can happen by simply blending the starting materials under mild conditions without any by-products, Michael addition is a better choice for in situ formation of biocompatible hydrogels [90,91]. Nie et al [40] developed a novel polysaccharides/polypeptide hydrogel for application as adhesive sealant and hemostatic material by fast in situ crosslinking thiol functionalized chitosan (CSS) with maleimide group modified ε-polylysine (EPLM) via Michael addition under mild conditions (Figure 6). Due to similarity with the natural extracellular matrix, the CSS/EPLM hydrogel showed no cytotoxicity.…”
Section: Cs-based Composite Hemostatic Materialsmentioning
confidence: 99%
“…Since it can happen by simply blending the starting materials under mild conditions without any by-products, Michael addition is a better choice for in situ formation of biocompatible hydrogels [90,91]. Nie et al [40] developed a novel polysaccharides/polypeptide hydrogel for application as adhesive sealant and hemostatic material by fast in situ crosslinking thiol functionalized chitosan (CSS) with maleimide group modified ε-polylysine (EPLM) via Michael addition under mild conditions (Figure 6). Due to similarity with the natural extracellular matrix, the CSS/EPLM hydrogel showed no cytotoxicity.…”
Section: Cs-based Composite Hemostatic Materialsmentioning
confidence: 99%
“…reported the formation of a composite hydrogel based on thiol containing chitosan (Figure 3a, v) and maleimide containing ε-polylysine [56]. The Michael addition reaction between thiol and maleimide groups led to the in situ formation of a crosslinked hydrogel upon simply mixing of the two components.…”
Section: Sealants Based On Natural Biopolymersmentioning
confidence: 99%
“…For this purpose, a thiol-maleimide reaction was chosen because it is rapid (i.e.,~1000 times faster than an aminedirected reaction), controllable, and specific at biological pH values (~7.4) [29]. Furthermore, the frequency of free cysteine (thiol) occurrence is usually very low in proteins [24][25][26][27][28][29][30][31][32][33], and thus, loaded proteins are unlikely to react with the maleimide groups of PEG. To explore the practical advantages of our hydrogel made using thioether linkages (HSA-SH/PEG-MAL hydrogel, Fig.…”
Section: Preparation and Characterization Of Hsa-sh/peg-mal Hydrogelmentioning
confidence: 99%
“…HSA-SH/PEG-MAL hydrogel was prepared as previously described method with slight modification [25,26]. Human serum albumin (HSA, 40 mg) was dissolved in 0.2 mL of PBS (pH 8.0, 10 mM) and mixed with predetermined equivalents of 2-iminothiolane (2-IT = Traut's reagent; 9-24 M equivalents (eq.)…”
Section: Fabrication Of Hsa-sh/peg-mal Hydrogelmentioning
confidence: 99%