Abstract
In this work, INU, a natural polysaccharide, has been chemically modified in order to obtain new photocrosslinkable derivatives. To reach this goal, INU has been derivatized with MA thus obtaining four samples (INU-MA derivatives) as a function of the temperature and time of reaction. An aqueous solution of the derivative INU-MA1 was irradiated by using a UV lamp with an emission range from 250 to 364 nm and without using photoinitiators. The obtained hydrogel showed a remarkable water affinity but it underwent a partial degradation in simulated gastric fluid. To overcome this drawback, INU-MA 1 was derivatized with SA thus obtaining the INU-MA1-SA derivative designed to produce a hydrogel showing a low swelling and an increased chemical stability in acidic medium. Ibuprofen, as a model drug, was loaded by soaking into INU-MA1 and INU-MA1-SA hydrogeis and its release from these matrices was evaluated in simulated gastrointestinal fluids. INU-MA1 hydrogel showed the ability to quickly release the entrapped drug thus indicating its potential as a matrix for an oral formulation. INU-MA1-SA hydrogel showed a pH-responsive drug delivery. Therefore it is a a promising candidate for controlled drug release in the intestinal tract. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
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Tripodo, G., Pitarresi, G., Palumbo, F. S., Craparo, E. F., & Giammona, G. (2005). UV-photocrosslinking of inulin derivatives to produce hydrogels for drug delivery application. Macromolecular Bioscience, 5(11), 1074–1084. https://doi.org/10.1002/mabi.200500134
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