| Autor: |
Lowman, A.M., Morishita, M., Kajita, M., Nagai, T., Peppas, N.A. |
| Zdroj: |
Journal of Pharmaceutical Sciences; September 1999, Vol. 88 Issue: 9 p933-937, 5p |
| Abstrakt: |
The goal of oral insulin delivery devices is to protect the sensitive drug from proteolytic degradation in the stomach and upper portion of the small intestine. In this work, we investigate the use of pH‐responsive, poly(methacrylic‐g‐ethylene glycol) hydrogels as oral delivery vehicles for insulin. Insulin was loaded into polymeric microspheres and administered orally to healthy and diabetic Wistar rats. In the acidic environment of the stomach, the gels were unswollen due to the formation of intermolecular polymer complexes. The insulin remained in the gel and was protected from proteolytic degradation. In the basic and neutral environments of the intestine, the complexes dissociated which resulted in rapid gel swelling and insulin release. Within 2 h of administration of the insulin‐containing polymers, strong dose‐dependent hypoglycemic effects were observed in both healthy and diabetic rats. These effects lasted for up to 8 h following administration. |
| Databáze: |
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