-
Je něco špatně v tomto záznamu ?
Pentapeptide-modified poly(N,N-diethylacrylamide) hydrogel scaffolds for tissue engineering
D. Horák, K. Matulka, H. Hlídková, M. Lapčíková, MJ. Beneš, J. Jaroš, A. Hampl, P. Dvořák,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21563303
DOI
10.1002/jbm.b.31832
Knihovny.cz E-zdroje
- MeSH
- akrylamidy chemie MeSH
- buněčné linie MeSH
- embryonální kmenové buňky cytologie MeSH
- hydrogely chemie MeSH
- lidé MeSH
- myši MeSH
- oligopeptidy chemie MeSH
- polymery chemie MeSH
- proliferace buněk MeSH
- tkáňové inženýrství metody MeSH
- tkáňové podpůrné struktury MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Poly(N,N-diethylacrylamide) (PDEAAm) hydrogel scaffolds were prepared by radical copolymerization of N,N-diethylacrylamide (DEAAm), N,N'-methylenebisacrylamide and methacrylic acid in the presence of (NH₄)₂SO₄ or NaCl. The hydrogels were characterized by low-vacuum scanning electron microscopy in the water-swollen state, water and cyclohexane regain, and by mercury porosimetry. The pentapeptide, YIGSR-NH₂, was immobilized on the hydrogel. Human embryonic stem cells (hESCs) were cultured with the hydrogels to test their biocompatibility. The results suggest that the PDEAAm hydrogel scaffolds are nontoxic and support hESC attachment and proliferation, and that interconnected pores of the scaffolds are important for hESC cultivation. Immobilization of YIGSR-NH₂ pentapeptide on the PDEAAm surface improved both adhesion and growth of hESCs compared with the unmodified hydrogel. The YIGSR-NH₂-modified PDEAAm hydrogels may be a useful tool for tissue-engineering purposes.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12027542
- 003
- CZ-PrNML
- 005
- 20170301074550.0
- 007
- ta
- 008
- 120817s2011 xxu f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1002/jbm.b.31832 $2 doi
- 035 __
- $a (PubMed)21563303
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Horák, Daniel $u Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, 16206 Prague 6, Czech Republic. horak@imc.cas.cz
- 245 10
- $a Pentapeptide-modified poly(N,N-diethylacrylamide) hydrogel scaffolds for tissue engineering / $c D. Horák, K. Matulka, H. Hlídková, M. Lapčíková, MJ. Beneš, J. Jaroš, A. Hampl, P. Dvořák,
- 520 9_
- $a Poly(N,N-diethylacrylamide) (PDEAAm) hydrogel scaffolds were prepared by radical copolymerization of N,N-diethylacrylamide (DEAAm), N,N'-methylenebisacrylamide and methacrylic acid in the presence of (NH₄)₂SO₄ or NaCl. The hydrogels were characterized by low-vacuum scanning electron microscopy in the water-swollen state, water and cyclohexane regain, and by mercury porosimetry. The pentapeptide, YIGSR-NH₂, was immobilized on the hydrogel. Human embryonic stem cells (hESCs) were cultured with the hydrogels to test their biocompatibility. The results suggest that the PDEAAm hydrogel scaffolds are nontoxic and support hESC attachment and proliferation, and that interconnected pores of the scaffolds are important for hESC cultivation. Immobilization of YIGSR-NH₂ pentapeptide on the PDEAAm surface improved both adhesion and growth of hESCs compared with the unmodified hydrogel. The YIGSR-NH₂-modified PDEAAm hydrogels may be a useful tool for tissue-engineering purposes.
- 650 _2
- $a akrylamidy $x chemie $7 D000178
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a proliferace buněk $7 D049109
- 650 _2
- $a embryonální kmenové buňky $x cytologie $7 D053595
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a hydrogely $x chemie $7 D020100
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a oligopeptidy $x chemie $7 D009842
- 650 _2
- $a polymery $x chemie $7 D011108
- 650 _2
- $a tkáňové inženýrství $x metody $7 D023822
- 650 _2
- $a tkáňové podpůrné struktury $7 D054457
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Matulka, Kamil
- 700 1_
- $a Hlídková, Helena
- 700 1_
- $a Lapčíková, Monika
- 700 1_
- $a Beneš, Milan J
- 700 1_
- $a Jaroš, Josef $7 xx0211297
- 700 1_
- $a Hampl, Aleš
- 700 1_
- $a Dvořák, Petr
- 773 0_
- $w MED00007497 $t Journal of biomedical materials research. Part B, Applied biomaterials $x 1552-4981 $g Roč. 98, č. 1 (2011), s. 54-67
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21563303 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m $z 0
- 990 __
- $a 20120817 $b ABA008
- 991 __
- $a 20170301074754 $b ABA008
- 999 __
- $a ok $b bmc $g 949584 $s 784888
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 98 $c 1 $d 54-67 $e 20110511 $i 1552-4981 $m Journal of biomedical materials research. Part B, Applied biomaterials $n J Biomed Mater Res $x MED00007497
- LZP __
- $a Pubmed-20120817/11/03