Switchable release of bone morphogenetic protein from thermoresponsive poly(NIPAM-co-DMAEMA)/cellulose sulfate particle coatings

Thermoresponsive coatings of poly(N-isopropylacrylamide-co-DMAEMA)/cellulose sulfate (PNIPAM-DMAEMA/CS) complexes are reported eluting bone-morphogenetic-protein-2 (BMP-2) on demand relevant for implant assisted local bone healing. PNIPAM-DMAEMA/CS dispersions contained colloid particles with hydrod...

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Bibliographic Details
Main Authors: Müller, Martin (Author) , Grab, Anna Luise (Author) , Cavalcanti-Adam, Elisabetta A. (Author)
Format: Article (Journal)
Language:English
Published: 27 November 2018
In: Polymers
Year: 2018, Volume: 10, Issue: 12
ISSN:2073-4360
DOI:10.3390/polym10121314
Online Access:Verlag, Volltext: https://doi.org/10.3390/polym10121314
Verlag, Volltext: https://www.mdpi.com/2073-4360/10/12/1314
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Author Notes:Martin Müller, Birgit Urban, Berthold Reis, Xiaoqian Yu, Anna Luise Grab, Elisabetta Ada Cavalcanti-Adam and Dirk Kuckling
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Summary:Thermoresponsive coatings of poly(N-isopropylacrylamide-co-DMAEMA)/cellulose sulfate (PNIPAM-DMAEMA/CS) complexes are reported eluting bone-morphogenetic-protein-2 (BMP-2) on demand relevant for implant assisted local bone healing. PNIPAM-DMAEMA/CS dispersions contained colloid particles with hydrodynamic radii RH = 170-288 nm at T = 25 °C shrinking to RH = 74-103 nm at T = 60 °C. Obviously, PNIPAM-DMAEMA/CS undergoes volume phase transition (VPT) analogously to pure PNIPAM, when critical VPT temperature (VPTT) is exceeded. Temperature dependent turbidity measurements revealed broad VPT and VPTT 47 °C for PNIPAM-DMAEMA/CS colloid dispersions at pH = 7.0. FTIR spectroscopy on thermoresponsive PNIPAM-DMAEMA/CS particle coatings at germanium model substrates under HEPES buffer indicated both wet-adhesiveness and VPT behavior based on diagnostic band intensity increases with temperature. From respective temperature courses empirical VPTT ≈ 42 °C for PNIPAM-DMAEMA/CS coatings at pH = 7.0 were found, which were comparable to VPTT found for respective dispersions. Finally, the PNIPAM-DMAEMA/CS coatings were loaded with BMP-2 and model protein papain (PAP). Time dependent FTIR spectroscopic measurements showed, that for T = 37 °C there was a relative protein release of ≈ 30% for PAP and ≈ 10% for BMP-2 after 24 h, which did not increase further. Heating to T = 42 °C for PAP and to 47 °C for BMP-2 further secondary protein release of ≈ 20% after 24 h was found, respectively, interesting for clinical applications. BMP-2 eluted even at 47 °C was found to be still biologically active.
Item Description:Gesehen am 27.11.2019
Physical Description:Online Resource
ISSN:2073-4360
DOI:10.3390/polym10121314