Hostname: page-component-78c5997874-xbtfd Total loading time: 0 Render date: 2024-11-02T21:53:09.515Z Has data issue: false hasContentIssue false
  • English
  • Français

Temperature- and pH- Sensitive Hydrogels for Controlled Release of Antithrombotic Agents

Published online by Cambridge University Press:  15 February 2011

Christopher S. Brazel  and
Nicholas A. Peppas
Christopher S. Brazel
Affiliation:
School of Chemical Engineering, Purdue University, West Lafayette, IN 47907–1283.
Nicholas A. Peppas
Affiliation:
School of Chemical Engineering, Purdue University, West Lafayette, IN 47907–1283.
Get access

Abstract

Polymeric hydrogels capable of reversible swelling with changes in environmental temperature and pH were synthesized and studied as matrix systems capable of controlled release of antithrombotic drugs to the site of a blood clot. Monomers N-isopropylacrylamide (NIPAAm) and methacrylic acid (MAA) were chosen for the temperature- and pHdependent swelling characteristics of their polymers, respectively. Equilibrium swelling studies were performed as functions of pH and of temperature, and kinetic swelling studies were performed on the thermally responsive gels as a function of time after the gel was subjected to a step-change in temperature. Experimental results indicate that P(NIPAAmco- MAA) hydrogels can be synthesized so that they are either pH- or temperaturesensitive, depending upon the composition of the network. The pure PNIPAAm gels showed a lower critical solubility temperature (LCST) of around 32°C, below which the gel was in its swollen state, and above which the gel collapsed. As the amount of methacrylic acid in the gels was increased, the degree of swelling in deionized water decreased and the temperature sensitivity was lost. The hydrogels containing MAA displayed a transition in swelling behavior between pH 4 and 6. The mesh sizes of the hydrogel networks were calculated from the results of the swelling studies by Flory-Rehner theory. A kinetic experiment on the temperature-sensitive pure PNIPAAm hydrogel showed that the polymer network collapsed rapidly upon temperature changes across the LCST.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 331: Symposium T – Biomaterials for Drug and Cell Delivery , 1993 , 211
Copyright
Copyright © Materials Research Society 1994

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

1. Garcia, J., Estrada, M.P., in Therapeutic Proteins: Pharmacokinetics and Pharmacodynamics, edited by Kung, A.H.C., Baughman, R.A. and Larrick, J.W. (W.H.Freeman and Company, New York, 1993) pp. 283–293.Google Scholar
2. Heskins, M., Guillet, J.E., J Macromol Sci - Chem, A 2, 1441 (1968).Google Scholar
3. Hoffman, A.S., in Polymers in Medicine III, edited by Migliaresi, C., (Elsevier Science Publishers, The Netherlands, 1988) p. 161.Google Scholar
4. Gutowska, A., Bae, Y.H., Feijen, J., Kim, S.W., J Controlled Release, 22, 95. (1992).Google Scholar
5. Barton, A.F.M.. CRC Handbook of Polymer-Solvent Interaction Parameters, 1 st ed. (CRC Press, Ann Arbor, 1990), pp. 566,578–579.Google Scholar
6. Bae, Y.H., Okano, T., Kim, S.W., J Polym Sci: Part B: Polym Physics, 28, 923 (1990).Google Scholar