2016
DOI: 10.1021/acs.biomac.6b00979
|View full text |Cite
|
Sign up to set email alerts
|

Temperature-Responsive Nanofibrillar Hydrogels for Cell Encapsulation

Abstract: Natural extracellular matrices often have a filamentous nature, however, only a limited number of artificial extracellular matrices have been designed from nanofibrillar building blocks. Here we report the preparation of temperature-responsive nanofibrillar hydrogels from rod-shaped cellulose nanocrystals (CNCs) functionalized with a copolymer of N-isopropylacrylamide and N,N'-dimethylaminoethyl methacrylate. The composition of the copolymer was tuned to achieve gelation of the suspension of copolymer-function… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
56
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
6

Relationship

4
2

Authors

Journals

citations
Cited by 68 publications
(56 citation statements)
references
References 57 publications
(75 reference statements)
0
56
0
Order By: Relevance
“…Nanofibrillar CNC microgels offer structural integrity,c atalyst retention, and enhanced transportation of molecules to the microgel interior. [26] These features underline the potential of Ch-CNC microgels in catalysis.T he combination of these properties paves the way for the design and generation of multifunctional responsive materials with avariety of applications from natural resources.…”
Section: Angewandte Chemiementioning
confidence: 85%
See 1 more Smart Citation
“…Nanofibrillar CNC microgels offer structural integrity,c atalyst retention, and enhanced transportation of molecules to the microgel interior. [26] These features underline the potential of Ch-CNC microgels in catalysis.T he combination of these properties paves the way for the design and generation of multifunctional responsive materials with avariety of applications from natural resources.…”
Section: Angewandte Chemiementioning
confidence: 85%
“…[26] These features underline the potential of Ch-CNC microgels in catalysis.T he combination of these properties paves the way for the design and generation of multifunctional responsive materials with avariety of applications from natural resources. Themicrogel morphology (predetermined by the CNC organization in the precursor droplets) resulted in the isotropic or anisotropic swelling of microgels with ac oncentric or planar bipolar CNC organization, respectively.T he catalytic performance of the Ch-CNC microgels stemmed from the nucleophilic hydroxy groups on the CNC surface.F urthermore,o wing to the negative charge and reducing properties of the CNC component, the Ch-CNC microgels sequestered and reduced Ag + ions to plasmonic Ag NPs.T he resulting hybrid microgels showed catalytic performance in ar eduction reaction.…”
mentioning
confidence: 85%
“…There is a growing interest in using CNCs in nanomedicine, due to their biocompatibility, as well as their asymmetric (rod‐like) shape facilitating prolonged blood circulation time and possible cellular uptake . Furthermore, the hydroxyl groups on the CNCs surface are amenable for attachment of polymer molecules or imaging and therapeutic agents .…”
Section: Resultsmentioning
confidence: 99%
“…enhancing the quality of imaging of biological species by suppressing background PL signal, due to, e.g., autofluorescence in the 400-550 nm spectral range. [66] There is a growing interest in using CNCs in nanomedicine, due to their biocompatibility, [67][68][69] as well as their asymmetric (rod-like) shape facilitating prolonged blood circulation time and possible cellular uptake. [70][71][72] Furthermore, the hydroxyl groups on the CNCs surface are amenable for attachment of polymer molecules [68,73] or imaging and therapeutic agents.…”
Section: Cpl Emission Of the Hybrid C-dot/cnc Nps Can Open A Way Formentioning
confidence: 99%
“…The CNCs were surface‐functionalized with PNIPAM using reversible addition‐fragmentation chain‐transfer polymerization . The grafting density of the polymer was 0.09±0.04 polymer chains/nm 2 , that is, the same as the grafting density of the chain transfer agent (evaluated using inductively coupled plasma atomic emission spectroscopy).…”
Section: Figurementioning
confidence: 99%