909157
Alkyne functionalized gelatin
degree of substitution > 80%
Sinónimos:
Alkyne-functionalized gelatin, Clickable gelatin
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About This Item
descripción
Degree of substitution: >80% by TNBS method
NMR: Conforms to structure
formulario
powder
color
white to pale yellow
temp. de almacenamiento
2-8°C
Descripción general
Due to its biodegradablity and biocompatibility, gelatin is routinely used in hydrogels for biomedical applications such as drug delivery, tissue engineering, and 3D bioprinting. Gelatin-based hydrogels are synthesized by the crosslinking of functionalized gelatins. Depending on the identity of the functional groups, several different processes can be used to synthesize crosslinked gelatin hydrogels, including radical-based (either thermal or photochemical) and click chemistry methods. Alkyne-functionalized gelatin can be used in the synthesis of hydrogel using click chemistry with either azide or thiol substrates.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
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Thiol-yne ′click′/coupling chemistry and recent applications in polymer and materials synthesis and modification.
Polymer, 55, 5517-5549 (2014)
Synthesis, properties, and biomedical applications of gelatin methacryloyl (GelMA) hydrogels.
Biomaterials, 73, 254-271 (2015)
Biomacromolecules, 16(7), 2246-2253 (2015-06-10)
In this study, we present a method for the fabrication of in situ forming gelatin and poly(ethylene glycol)-based hydrogels utilizing bioorthogonal, strain-promoted alkyne-azide cycloaddition as the cross-linking reaction. By incorporating nitrobenzyl moieties within the network structure, these hydrogels can be
Gelatin hydrogels via thiol-ene chemistry.
Monatshefte fur Chemie / Chemical Monthly, 147, 587-592 (2016)
Advanced healthcare materials, 5(5), 541-547 (2016-01-26)
Injectable gelatin hydrogels formed with bioorthogonal click chemistry (ClickGel) are cell-responsive ECM mimics for in vitro and in vivo biomaterials applications. Gelatin polymers with pendant norbornene (GelN) or tetrazine (GelT) groups can quickly and spontaneously crosslink upon mixing, allowing for
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