journal article·2013

Investigation of the Diels–Alder reaction as a cross-linking mechanism for degradable poly(ethylene glycol) based hydrogels

Susanne Kirchhof, Ferdinand P. Brandl, Nadine Hammer, Achim M. Goepferich

Journal of Materials Chemistry B· Volume 1· Issue 37
Publisher page

Abstract

The Diels-Alder (DA) reaction was investigated as a cross-linking mechanism for poly(ethylene glycol) (PEG) based hydrogels. Two complementary macromonomers were synthesized by functionalizing star-shaped PEG with furyl and maleimide groups. Gel formation occurred in water at 37 °C; the gelation time ranged between 171 ± 25 min and 14 ± 1 min depending on the used hydrogel formulation. The complex shear modulus was dependent on the concentration, branching factor and molecular weight of the macromonomers; values between 2821 ± 1479 Pa and 37097 ± 6698 Pa were observed. Hydrogel swelling and degradation were influenced by the same parameters; the degradation time varied between a few days and several weeks. Gel dissolution was found to occur by retro-DA reaction and subsequent hydrolysis of maleimide groups. Calculations of the network mesh size revealed that the prepared hydrogels would be suitable for the controlled release of therapeutic proteins.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Hydrogels: synthesis, properties, applications · Advanced Polymer Synthesis and Characterization · Surfactants and Colloidal Systems

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (46)

Show source-provided references
1. Slaughter · Adv. Mater. · 2009 · 21 · 330710.1002/adma.200802106 ↗
2. Boateng · J. Pharm. Sci. · 2008 · 97 · 289210.1002/jps.21210 ↗
3. Hoare · Polymer · 2008 · 49 · 199310.1016/j.polymer.2008.01.027 ↗
4. Qiu · Adv. Drug Delivery Rev. · 2001 · 53 · 32110.1016/S0169-409X(01)00203-4 ↗
5. Vermonden · Chem. Rev. · 2012 · 112 · 285310.1021/cr200157d ↗
6. Lin · Pharm. Res. · 2009 · 26 · 63110.1007/s11095-008-9801-2 ↗
7. Deligkaris · Sens. Actuators, B · 2010 · 147 · 76510.1016/j.snb.2010.03.083 ↗
8. Hoffman · Adv. Drug Delivery Rev. · 2002 · 54 · 310.1016/S0169-409X(01)00239-3 ↗
9. Tessmar · Macromol. Biosci. · 2007 · 7 · 2310.1002/mabi.200600096 ↗
10. Huebsch · Nat. Mater. · 2010 · 9 · 51810.1038/nmat2732 ↗
11. Anseth · J. Controlled Release · 2002 · 78 · 19910.1016/S0168-3659(01)00500-4 ↗
12. Gilbert · Science · 2010 · 329 · 107810.1126/science.1191035 ↗
13. Mann · Cel. Mol. Bioeng. · 2010 · 3 · 4010.1007/s12195-010-0108-0 ↗
14. Brandl · Biomaterials · 2007 · 28 · 13410.1016/j.biomaterials.2006.09.017 ↗
15. Engler · Cell · 2006 · 126 · 67710.1016/j.cell.2006.06.044 ↗
16. Kloxin · Adv. Mater. · 2010 · 22 · 348410.1002/adma.200904179 ↗
17. Huisgen · Pure Appl. Chem. · 1989 · 61 · 61310.1351/pac198961040613 ↗
18. Kolb · Angew. Chem., Int. Ed. Engl. · 2001 · 40 · 200410.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5 ↗
19. Gaetke · Toxicology · 2003 · 189 · 14710.1016/S0300-483X(03)00159-8 ↗
20. Yigit · Chem.–Asian J. · 2011 · 6 · 264810.1002/asia.201100440 ↗
21. Yang · J. Polym. Sci., Part A: Polym. Chem. · 2011 · 49 · 404410.1002/pola.24847 ↗
22. Zheng · ACS Macro Lett. · 2012 · 1 · 107110.1021/mz3003775 ↗
23. Gandini · Prog. Polym. Sci. · 2013 · 38 · 110.1016/j.progpolymsci.2012.04.002 ↗
24. Nicolaou · Angew. Chem., Int. Ed. · 2002 · 41 · 166810.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z ↗
25. Tan · Macromol. Rapid Commun. · 2011 · 32 · 90510.1002/marc.201100125 ↗
26. Marref · Polym. Int. · 2013 · 62 · 8710.1002/pi.4287 ↗
27. Nimmo · Biomacromolecules · 2011 · 12 · 82410.1021/bm101446k ↗
28. Wei · Polymer · 2009 · 50 · 283610.1016/j.polymer.2009.04.032 ↗
29. Wei · J. Appl. Polym. Sci. · 2011 · 120 · 97410.1002/app.33116 ↗
30. Kozlowski · J. Controlled Release · 2001 · 72 · 21710.1016/S0168-3659(01)00277-2 ↗
31. Brandl · Adv. Eng. Mater. · 2007 · 9 · 114110.1002/adem.200700221 ↗
32. Kim · Chem. Mater. · 2008 · 20 · 585910.1021/cm801623a ↗
33. Rulíšek · J. Org. Chem. · 2005 · 70 · 629510.1021/jo050759z ↗
34. Sankaran · Macromolecules · 2010 · 43 · 553010.1021/ma100234j ↗
35. Mantovani · J. Am. Chem. Soc. · 2005 · 127 · 296610.1021/ja0430999 ↗
36. Keller · Tetrahedron Lett. · 2005 · 46 · 118110.1016/j.tetlet.2004.12.067 ↗
37. Bray · J. Appl. Polym. Sci. · 1973 · 17 · 377910.1002/app.1973.070171219 ↗
38. Elbert · J. Controlled Release · 2001 · 76 · 1110.1016/S0168-3659(01)00398-4 ↗
39. Canal · J. Biomed. Mater. Res. · 1989 · 23 · 118310.1002/jbm.820231007 ↗
40. Raeber · Biophys. J. · 2005 · 89 · 137410.1529/biophysj.104.050682 ↗
41. Metters · Biomacromolecules · 2005 · 6 · 29010.1021/bm049607o ↗
42. Lutolf · Biomacromolecules · 2003 · 4 · 71310.1021/bm025744e ↗
43. Oliva · J. Chromatogr., B: Biomed. Sci. Appl. · 2000 · 749 · 2510.1016/S0378-4347(00)00374-1 ↗
44. Armstrong · Biophys. J. · 2004 · 87 · 425910.1529/biophysj.104.047746 ↗
45. McElhanon · Langmuir · 2005 · 21 · 325910.1021/la047074z ↗
46. Koehler · Biomacromolecules · 2013 · 14 · 53810.1021/bm301789d ↗