Hostname: page-component-7bb8b95d7b-qxsvm Total loading time: 0 Render date: 2024-09-18T01:53:40.417Z Has data issue: false hasContentIssue false

Novel pH-Sensitive Hydrogels with Peg-Tethered Chains for Oral Delivery of Calcitonin

Published online by Cambridge University Press:  15 February 2011

M. Torres-Lugo
Affiliation:
School of Chemical Engineering, Purdue University, West Lafayette, IN 47907-1283, torreslu@ecn.purdue.edu
N.A. Peppas
Affiliation:
School of Chemical Engineering, Purdue University, West Lafayette, IN 47907-1283, torreslu@ecn.purdue.edu
Get access

Abstract

Major challenges in oral delivery of peptides include the need to overcome gastric and intestinal degradation. pH -Sensitive hydrogels are suitable candidates for oral drug delivery of peptides due to their ability to respond to their environment. We have developed a new type of hydrogel composed of poly(methacrylic acid) grafted with poly(ethylene glycol) which can be used as drug delivery carriers for salmon calcitonin. These hydrogels were prepared by free radical solution polymerization and were molecularly designed to contain poly(ethylene glycol) tethered chains promoting mucosal adhesion and providing calcitonin protection, as well as methacrylic acid moieties, which act as calcium binders leading to epithelial cell junction opening. Solutions of approximately 0.1 mg/ml of salmon calcitonin were used to load the protein into the gels at pH = 7 and constant ionic strength of 0.1 M. In vitro release studies were performed at pH=7 and 37 °C, while keeping an ionic strength of 0.1 M. Calcitonin release was achieved. The release behavior was explained in terms of diffusional theories.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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. Swann, P.W., Pharm. Research 16, 826834 (1998).Google Scholar
2. Putney, S.D., Burke, P.A., Nature Biotech. 16, 153157 (1998).Google Scholar
3. Lehr, C.M, Europ. J. Drug Metab. and Pharmacokin. 21, 139148 (1996).Google Scholar
4. Klier, J., Peppas, N.A., J. Controlled Release 16, 203214 (1991).Google Scholar
5. Lowman, A.M., Peppas, N.A., Macromolecules 30, 49594965 (1997).Google Scholar
6. Arvinte, T., Drake, A. F., J. Biol. Chem. 268, 64086414 (1993).Google Scholar
7. Cholewinski, M., Luckel, B., Horn, H., Pharm. Acta Helv. 71, 405419 (1996).Google Scholar