Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-23T16:28:43.955Z Has data issue: false hasContentIssue false

Thermal Gelation and Stability of Pectin Grafted with PEPE

Published online by Cambridge University Press:  12 April 2012

Harshal D. Santan
Affiliation:
Center for Biomaterial Development and Berlin-Brandenburg Center for Regenerative Therapies, Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstraße 55, 14513 Teltow, Germany Institute of Chemistry, University of Potsdam, 14476 Potsdam-Golm, Germany
Axel T. Neffe
Affiliation:
Center for Biomaterial Development and Berlin-Brandenburg Center for Regenerative Therapies, Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstraße 55, 14513 Teltow, Germany Institute of Chemistry, University of Potsdam, 14476 Potsdam-Golm, Germany
Stefan Kamlage
Affiliation:
Center for Biomaterial Development and Berlin-Brandenburg Center for Regenerative Therapies, Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstraße 55, 14513 Teltow, Germany
Andreas Lendlein
Affiliation:
Center for Biomaterial Development and Berlin-Brandenburg Center for Regenerative Therapies, Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstraße 55, 14513 Teltow, Germany Institute of Chemistry, University of Potsdam, 14476 Potsdam-Golm, Germany
Get access

Abstract

Stimuli-sensitive materials can change properties upon exposure to an external stimulus. Thermoreversible gelation upon heating is one example for such a stimuli sensitivity. Here, it is of significance to tailor the transition temperature and to achieve large changes of G’ and the viscosity. Grafting of the thermosensitive poly(ethylene glycol-b-propylene glycol-b-ethylene glycol)s (PEPEs) to pectin was performed in order to investigate if tailoring of the sol-gel-transition temperature can be achieved by adjusting the grafting ratio. PEPEs were aminated and grafted to the polysaccharide via EDC coupling as shown by FTIR. The sol-gel transition of the pectin, PEPE, and the grafted system (PGP) was investigated by rheology. The gelation temperature (Tgel) of the system could be adjusted by varying the grafting density of PEPE onto pectin as well as by the concentration of the thermosensitive polymer in aqueous solution. A concentration of 15 – 20 wt% of the grafted system in water led to gelation temperatures in the range of 25 – 33 °C and the critical micelle concentration (CMC) and critical micelle temperature (CMT) of the grafted systems were determined by UV spectroscopy. The viscosity and the G’ increased by four orders of magnitudes at Tgel, which is comparable to PEPEs alone, but could be reached at lower PEPE concentrations. In the future, a thorough mechanistic investigation of the gelation process would be of interest.

Type
Research Article
Copyright
Copyright © Materials Research Society 2012

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Schild, H. G, Progress Polym. Sci. 1992, 17, 163.Google Scholar
2. Fusco, S., Borzacchiello, A., Netti, P. A., J. Bioactive Compatible Polym. 2006, 21, 149.Google Scholar
3. Alexandridis, P., Holzwarth, J.F., Hatton, T.A, Macromolecules, 1994, 27, 2414.Google Scholar
4. Ma, W.D., Xu, H., Wang, C., Nie, S.F., Pan, W.S., Int. J. Pharm. 2008, 350, 247.Google Scholar
5. Piluso, S., Hiebl, B., Gorb, S.N., Kovalev, A., Lendlein, A., Neffe, A.T., Int. J. Artif. Organs 2011, 34, 192.Google Scholar
6. Lendlein, A., Wischke, C., Exp. Rev. Med. Devices 2011, 8, 533.Google Scholar
7. Tronci, G., Neffe, A.T., Pierce, B.F., Lendlein, A., J. Mater. Chem. 2010, 20, 8875 Google Scholar
8. Neffe, A.T., Zaupa, A., Pierce, B.F., Hofmann, D., Lendlein, A., Macromol. Rapid Comm. 2010, 31, 1534.Google Scholar
9. Mohnen, D., Curr. Op. Plant Biol. 2008, 11, 266.Google Scholar
10. Hsu, S.H., Leu, Y.L., Hu, J.W., Fang, J.Y., Chem. Pharm. Bull. 2009, 57, 453.Google Scholar
11. Bubnis, W.A., Ill, C.M.O., Anal. Biochem. 1992, 207, 120.Google Scholar
12. Censi, R., Fieten, P.J., di Martino, P., Hennink, W.E., Vermonden, T., Macromolecules, 2010, 43, 5771.Google Scholar