Thermoresponsive and Photocrosslinkable Poly(2-alkyl-2-oxazoline) Toolbox - Customizable Ultralow-Fouling Hydrogel Coatings for Blood Plasma Environments
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
633937
European Union's Horizon 2020 Research and Innovation Program under grant agreement
DIPLAB I 5119-B
Austrian Science Fund
22-30456J
Czech Science Fund
13GW0349C
BMBF - KMU-innovativ -Verbundprojekt
PubMed
37983912
DOI
10.1002/marc.202300549
Knihovny.cz E-zdroje
- Klíčová slova
- SPR/OWS, antifouling thermoresponsive hydrogel coatings, betaines, blood plasma, photocrosslinkable poly(2-oxazoline)s,
- MeSH
- alkyny MeSH
- azidy * MeSH
- benzofenony MeSH
- hydrogely * chemie MeSH
- krevní plazma MeSH
- lidé MeSH
- polymery chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- alkyny MeSH
- azidy * MeSH
- benzofenony MeSH
- hydrogely * MeSH
- polymery MeSH
This study focuses on developing surface coatings with excellent antifouling properties, crucial for applications in the medical, biological, and technical fields, for materials and devices in direct contact with living tissues and bodily fluids such as blood. This approach combines thermoresponsive poly(2-alkyl-2-oxazoline)s, known for their inherent protein-repellent characteristics, with established antifouling motifs based on betaines. The polymer framework is constructed from various monomer types, including a novel benzophenone-modified 2-oxazoline for photocrosslinking and an azide-functionalized 2-oxazoline, allowing subsequent modification with alkyne-substituted antifouling motifs through copper(I)-catalyzed azide-alkyne cycloaddition. From these polymers surface-attached networks are created on benzophenone-modified gold substrates via photocrosslinking, resulting in hydrogel coatings with several micrometers thickness when swollen with aqueous media. Given that poly(2-alkyl-2-oxazoline)s can exhibit a lower critical solution temperature in water, their temperature-dependent solubility is compared to the swelling behavior of the surface-attached hydrogels upon thermal stimulation. The antifouling performance of these hydrogel coatings in contact with human blood plasma is further evaluated by surface plasmon resonance and optical waveguide spectroscopy. All surfaces demonstrate extremely low retention of blood plasma components, even with undiluted plasma. Notably, hydrogel layers with sulfobetaine moieties allow efficient penetration by plasma components, which can then be easily removed by rinsing with buffer.
Zobrazit více v PubMed
I. Banerjee, R. C. Pangule, R. S. Kane, Adv. Mater. 2011, 23, 690,
J. B. Kristensen, R. L. Meyer, B. S. Laursen, S. Shipovskov, F. Besenbacher, C. H. Poulsen, Biotechnol. Adv. 2008, 26, 471.
B. Liu, X. Liu, S. Shi, R. Huang, R. Su, W. Qi, Z. He, Acta Biomater. 2016, 40, 100.
Y.-N. Chou, F. Sun, H.-C. Hung, P. Jain, A. Sinclair, P. Zhang, T. Bai, Y. Chang, T.-C. Wen, Q. Yu, S. Jiang, Acta Biomater. 2016, 40, 31,
S. Chen, L. Li, C. Zhao, J. Zheng, Polymer (Guildf) 2010, 51, 5283.
J. M. Harris, in Poly(Ethylene Glycol) Chemistry (Ed.: J. M. Harris), Springer Science+Business Media, New York 1992, pp. 1-14.
Q. Shao, S. Jiang, Adv. Mater. 2015, 27, 15.
X. Liu, R. Huang, R. Su, W. Qi, L. Wang, Z. He, ACS Appl. Mater. Interfaces 2014, 6, 13034,.
T. Goda, M. Tabata, M. Sanjoh, M. Uchimura, Y. Iwasaki, Y. Miyahara, Chem. Commun. 2013, 49, 8683.
F. Wang, H. Zhang, B. Yu, S. Wang, Y. Shen, H. Cong, Prog. Org. Coat. 2020, 147, 105860.
R. A. Wolf, in Proc. J. Vinyl and Additive Technology, Vol. 13, 2007, pp. 87-90.
G. Gunkel, M. Weinhart, T. Becherer, R. Haag, W. T. S. Huck, Biomacromolecules 2011, 12, 4169.
B. Liu, X. Liu, S.e Shi, R. Huang, R. Su, W. Qi, Z. He, Acta Biomater. 2016, 40, 100.
D. Kuckling, M. E. Harmon, C. W. Frank, Macromolecules 2002, 35, 6377.
P. W. Beines, I. Klosterkamp, B. Menges, U. Jonas, W. Knoll, Langmuir 2007, 23, 2231,
C. Haslinger, A. Zahoranová, S. Baudis, Monatsh. Chem. 2023, 154, 459.
L. Korchia, C. Bouilhac, V. Lapinte, C. Travelet, R. Borsali, J.-J. Robin, Polym. Chem. 2015, 6, 6029.
R. Navarro, M. Pérez Perrino, O. Prucker, J. Rühe, Langmuir 2013, 29, 10932.
K. Schuh, O. Prucker, J. Rühe, Macromolecules 2008, 41, 9284.
R. Hoogenboom, H. Schlaad, Polymers 2011, 3, 467.
R. Hoogenboom, Angew. Chem., Int. Ed. 2009, 48, 7978.
R. Hoogenboom, H. M. L. Thijs, M. J. H. C. Jochems, B. M. Van Lankvelt, M. W. M. Fijten, U. S. Schubert, Chem. Commun. 2008, 5758.
F. Diehl, S. Hageneder, S. Fossati, S. K. Auer, J. Dostalek, U. Jonas, Chem. Soc. Rev. 2022, 51, 3926.
D. Kotlarek, S. Fossati, P. Venugopalan, N. Gisbert Quilis, J. Slabý, J. Homola, M. Lequeux, F. Amiard, M. Lamy De La Chapelle, U. Jonas, J. Dostálek, Nanoscale 2020, 12, 9756,
K. Sergelen, C. Petri, U. Jonas, J. Dostalek, Biointerphases 2017, 12, 051002.
M. Toma, U. Jonas, A. Mateescu, W. Knoll, J. Dostalek, J. Phys. Chem. C 2013, 117, 11705.
N. Gisbert Quilis, M. Van Dongen, P. Venugopalan, D. Kotlarek, C. Petri, A. Moreno Cencerrado, S. Stanescu, J. L. Toca Herrera, U. Jonas, M. Möller, A. Mourran, J. Dostalek, Adv. Opt. Mater. 2019, 7, 1900342.
S. K. Auer, S. Fossati, Y. Morozov, U. Jonas, J. Dostálek, J. Phys. Chem. B 2022, 126, 3170.
S. Hageneder, V. Jungbluth, R. Soldo, C. Petri, M. Pertiller, M. Kreivi, A. Weinhäusel, U. Jonas, J. Dostalek, ACS Appl. Mater. Interfaces 2021, 13, 27645.
T. R. Dargaville, R. Forster, B. L. Farrugia, K. Kempe, L. Voorhaar, U. S. Schubert, R. Hoogenboom, Macromol. Rapid Commun. 2012, 33, 1695.
A. Gress, A. Völkel, H. Schlaad, Macromolecules 2007, 40, 7928.
N. Jung, F. Diehl, U. Jonas, Polymers 2020, 12, 1767.
L. Korchia, C. Bouilhac, V. Lapinte, C. Travelet, R. Borsali, J.-J. Robin, Polym. Chem. 2015, 6, 6029.
C. Haslinger, A. Zahoranová, S. Baudis, Monatsh. Chem. 2023, 154, 459.
O. Prucker, C. A. Naumann, J. Rühe, W. Knoll, C. W. Frank, J. Am. Chem. Soc. 1999, 121, 8766.
A. Mateescu, Y. Wang, J. Dostalek, U. Jonas, Membranes 2012, 2, 40.
M. Gianneli, R. F. Roskamp, U. Jonas, B. Loppinet, G. Fytas, W. Knoll, Soft Matter 2008, 4, 1443.
J. D. J. S. Samuel, T. Brenner, O. Prucker, M. Grumann, J. Ducree, R. Zengerle, J. Rühe, Macromol. Chem. Phys. 2010, 211, 195.
B. L. Rivas, K. E. Geckeler, in Advances in Polymer Science, Springer-Verlag, Berlin 1992, Vol. 102, pp. 171-188.
V. P. Dhende, S. Samanta, D. M. Jones, I. R. Hardin, J. Locklin, ACS Appl. Mater. Interfaces 2011, 3, 2830.
J. C. Kappel, Y.i C. Fan, K. S. Lam, J. Comb. Chem. 2008, 10, 333.
C. Petri, Synthesis and Characterization of Novel Photocrosslinkable Poly(2-Oxazoline)-Based Hydrogel Systems for the Application as Biosensor Matrix. Dissertation, University of Siegen, Siegen 2018.
M. M. Ouberai, K. Xu, M. E. Welland, Biomaterials 2014, 35, 6157.
A. Aulasevich, R. F. Roskamp, U. Jonas, B. Menges, J. Dostálek, W. Knoll, Macromol. Rapid Commun. 2009, 30, 872.
D. E. Aspnes, Thin Solid Films 1982, 89, 249.
G. E. Perlmann, L. G. Longsworth, J. Am. Chem. Soc. 1948, 70, 2719.
E. Stenberg, B. Persson, H. Roos, C. Urbaniczky, J. Colloid Interface Sci. 1991, 143, 513.
B. Sudha, R. Kamble, S. Shashikanth, J. Serb. Chem. Soc. 2008, 73, 261.
H. Witte, W. Seeliger, Justus Liebigs Ann. Chem. 1974, 1974, 996.
T.-X. Lav, P. Lemechko, E. Renard, C. Amiel, V. Langlois, G. Volet, React. Funct. Polym. 2013, 73, 1001.
G. Le Fer, C. Amiel, G. Volet, Eur. Polym. J. 2015, 71, 523.
N. M. Leonard, J. Brunckova, J. Org. Chem. 2011, 76, 9169.
L. Tauhardt, D. Pretzel, K. Kempe, M. Gottschaldt, D. Pohlers, U. S. Schubert, Polym. Chem. 2014, 5, 5751.
J. Seuring, S. Agarwal, ACS Macro Lett. 2013, 2, 597.
R. Hoogenboom, H. M. L. Thijs, M. J. H. C. Jochems, B. M. Van Lankvelt, M. W. M. Fijten, U. S. Schubert, Chem. Commun. 2008, 5758.
A. Laschewsky, Polymers 2014, 6, 1544.
R. J. Young, P. A. Lovell, Introduction to Polymers, 3rd ed., CRC Press, Boca Raton, FL 2011.
M. Namazian, S. Halvani, M. R. Noorbala, J. Mol. Struct. 2004, 711, 13.
L. Wu, J. Jasinski, S. Krishnan, J. Appl. Polym. Sci. 2012, 124, 2154.
R. R. Netz, D. Andelman, Phys. Rep. 2003, 380, 1.
N. Giovambattista, P. G. Debenedetti, P. J. Rossky, J. Phys. Chem. B 2007, 111, 9581.
R. J. Scott, L.-Y. Lian, S. H. Muharram, A. Cockayne, S. J. Wood, B. W. Bycroft, P. Williams, W. C. Chan, Bioorg. Med. Chem. Lett. 2003, 13, 2449.
S. Sakakibara, N. Inukai, Bull. Chem. Soc. Jpn. 1965, 38, 1979.
M. T. Zarka, O. Nuyken, R. Weberskirch, Chem. - Eur. J. 2003, 9, 3228.
S. M. Andreev, L. A. Pavlova, Y. A. Davidovich, S. V. Rogozhin, Russ. Chem. Bull. 1980, 29, 785.
S. Asano, J. Gavrilyuk, D. R. Burton, C. F. Barbas, ACS Med. Chem. Lett. 2014, 5, 133.
O. Norberg, L. Deng, M. Yan, O. Ramström, Bioconjugate Chem. 2009, 20, 2364.
E. W. Della, P. A. Smith, J. Org. Chem. 1999, 64, 1798.