To improve the properties of the hydrogel networks, a new class of hydrogels based on the interpenetration of two-polymer network has been recently developed. IPN hydrogels are a subset of the general class of IPNs. IPN hydrogel offers a variety in the formulation of http://www.selleckchem.com/products/17-AAG(Geldanamycin).html physical forms including microspheres, nanoparticles, and films. One of the most Inhibitors,research,lifescience,medical outstanding achievements of IPN hydrogels in drug delivery is the Lapatinib mechanism development of smart drug delivery systems (SDDS), also called stimuli-sensitive delivery systems. The concept of SDDS is based on conversation of physicochemical property of polymer systems upon an environmental stimulus, which includes physical

(temperature, electricity, light, and mechanical stress) chemical (pH, ionic strength), or biological (enzymes) signals. Inhibitors,research,lifescience,medical Such stimuli can be either internal signals (as a result of changes

in the physiological condition of a living subject) or external signals (artificially induced). This sensitive behavior of hydrogels has sparked particular interest in their use Inhibitors,research,lifescience,medical as drug delivery vehicle capable of controlling drug release and drug targeting. In a study pH-sensitive IPN hydrogel beads of ibuprofen were formulated to minimize the release of drug in acidic medium and to control the drug release in alkaline medium (phosphate buffer) depending on the need [45]. Inhibitors,research,lifescience,medical IPN beads were prepared by ionotropic gelation process using AlCl3 as a cross-linking agent. It was observed that the drug release in acidic medium (pH 1.2) was considerably slow and complete drug release was achieved in phosphate buffer (pH 6.8) within 210 to 330min depending upon the formulation variables. It can be concluded that pH-sensitive IPN hydrogels could be used to target the drug in the desired region. Pescosolido et al. reported a novel class of hydrogels based on the interpenetration of two polysaccharide networks. In situ forming IPN hydrogels of

calcium alginate and dextran hydroxyethyl-methacrylate were developed Inhibitors,research,lifescience,medical and evaluated for protein release as well as for the Cilengitide behavior of embedded cells. It was observed that after an initial burst release bovine serum albumin was gradually released from the IPN hydrogels for up to 15 days. Encapsulation of expanded chondrocytes in the IPNs revealed that cells remained viable and were able to redifferentiate. IPN was described as a promising system as injectable in situ forming hydrogels for protein delivery and tissue engineering applications [46]. 7.2. Microspheres Microspheres are another promising class of IPN based drug delivery systems. Microspheres are free flowing small spherical powder particles made up of natural or synthetic polymers having diameter in the range of 1μm to 1000μm [47].