IPN nanoparticles were synthesized by using poly(oligo(ethylene glycol) methyl ether methacrylate-co-oligo(ethylene glycol) ethyl ether methacrylate)-poly(acrylic acid). Atomic force microscopic images confirmed the homogenous and monodisperse morphology of the IPN nanoparticles. The study demonstrated that the IPN nanoparticles exhibit thermogelling properties at body temperature and these IPN nanoparticles allow their

ease of injection and then slow release of protein. Histological analysis showed that following subcutaneous implantation IPN implants exerted minimal inflammation [52]. Inhibitors,research,lifescience,medical 7.4. Tablets Mandal et al. developed calcium ion cross-linked IPN matrix tablets of polyacrylamide-grafted-sodium alginate and sodium alginate for sustained release of diltiazem hydrochloride. Formulation of IPN structure was confirmed using FTIR spectroscopy. It was found that the relative magnitude of swelling capacity of IPN matrix and viscosity of the gel formed following dissolution of the polymers governs the drug release from IPN matrix [53].

The application Inhibitors,research,lifescience,medical of IPN tablets for controlled release of a water soluble antihypertensive drug (propranolol Inhibitors,research,lifescience,medical hydrochloride) was investigated by Kulkarni et al. The IPN tablets were prepared by a wet granulation/covalent cross-linking method. FTIR confirmed the cross-linking reaction and IPN formation, while XRD and SEM studies confirmed the amorphous dispersion of the drug within the IPN tablets. It was observed that the plain drug was released within 1 hr, while drug release from the resinate was prolonged

for 2.5 hrs and the IPN matrices showed drug release up to 24 hrs [54]. 8. Some Natural Polymers Used for IPN 8.1. Chitin Chitin is the natural Inhibitors,research,lifescience,medical polysaccharide composed of β (1→4)-linked http://www.selleckchem.com/products/ganetespib-sta-9090.html 2-acetamido-2-deoxy-β-D-glucose (N-acetylglucosamine) [55]. The principle derivative of chitin is chitosan. Chitin and chitosan are naturally available polymers having excellent properties such as biodegradability, biocompatibility, nontoxicity, and adsorption. Chitosan based IPN systems have gained considerable attention as Inhibitors,research,lifescience,medical a vehicle for drug delivery systems. A number of chitosan based IPN delivery systems have been developed to explore the useful features of chitosan. Mephenoxalone Rani et al. reported use of pH-sensitive IPN beads composed of chitosan-glycine-glutamic acid cross-linked with glutaraldehyde for controlled drug release. It was observed that the swelling behavior and release of drug depend on pH, degree of cross-linking, and their composition. The results of this study indicated that the IPN beads of chitosan-glycine-glutamic acid might be useful for controlled release of drug [56]. In a study Reddy et al. synthesized ghatti gum and chitosan IPN microparticles by emulsion-cross-linking method using glutaraldehyde as a cross-linker. IPN microparticles were used to deliver diclofenac sodium to the intestine.