Xanthan gum facilitated superabsorbent polymeric microspheres by w/o emulsion selleck compound cross-linking method which was successfully prepared and evaluated for sustained release of ciprofloxacin hydrochloride. IPN formation

was confirmed by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis. Differential scanning calorimetry (DSC) study was performed to understand the dispersion nature of drug after encapsulation. In vitro drug release study was extensively evaluated to observe the sustained drug delivery Inhibitors,research,lifescience,medical from IPN microspheres [48]. In another study an anticancer drug (5 fluorouracil) was successfully encapsulated in carbohydrate grafted IPN microspheres to increase the bioavailability. The resulting IPN microspheres were found to have an ability to release the drug for more than 12 hours [49]. 7.3. Nanoparticles Polymer based nanoparticles have been developed since the early 1980s, when progress in polymer chemistry allowed Inhibitors,research,lifescience,medical the design of biodegradable and biocompatible materials for targeting the drug into the desired

site [50]. Nanoparticles as a carrier in drug delivery have attracted much attention in the last few years and have undergone the most investigation Inhibitors,research,lifescience,medical in recent years for biomedical applications due to their wide range of applications including their size, surface Inhibitors,research,lifescience,medical area, magnetic and optical properties, and biological transport that are brought into

the perspective of drug delivery. Recently, there has been increased interest in IPN nanoparticles for utilization as the smart drug delivery system in the field of controlled drug release, to meet the demand for better control of drug administration. The idea of IPN nanoparticles as drug carriers may be employed to especially modify or to control the drug distribution Inhibitors,research,lifescience,medical at the tissue, cellular, or subcellular levels. IPN nanoparticles can be either nanospheres or nanocapsules depending on the method of preparation. Nanospheres are polymeric matrix systems in which the drug is dispersed within the polymer throughout the particle. On the contrary, nanocapsules are vesicular systems, which are formed by a drug-containing liquid core (aqueous or lipophilic) surrounded by polymeric; thus nanocapsules may be considered a reservoir system. Nanocomposites having antibacterial activity towards Escherichia coli were developed by Krishna Rao et al. The chitosan Brefeldin_A particles were prepared by desolvation followed by cross-linking with poly(ethylene glycol-dialdehyde), which was prepared with poly(ethylene glycol) in the presence of a silver nitrate solution. The developed nanocomposites were characterized using UV-visible, FTIR, XRD, SEM, and TEM to understand their physicochemical properties. It was observed that prepared nanocomposites showed good antibacterial activity towards E. coli [51].