Synthesis and luminescence properties of Pr ion-doped Ba Y(PO ) phosphors.

Barium yttrium phosphate (BYP) phosphor doped with trivalent praseodymium ions (BaY (PO ) :Pr (x = 0, 0.01, 0.05, 0.

Fabrication and Characterization of Gliclazide Nanocrystals.

The main aim of the present investigation was to enhance the solubility of poorly soluble Gliclazide by nanocrystallization. In present investigation gliclazide nanocrystals were prepared by sonoprecipitation using Pluronic F68, Poly Vinyl Alcohol (PVA), Poly ethylene Glycol 6000 (PEG), Poly Vinyl Pyrrolidine (PVP K30) and Sodium Lauryl Sulphate (SLS) as stabilizers. Fourier Transform Infrared Spectroscopic study (FTIR), Differential Scanning Calorimetry (DSC) and X ray diffraction (XRD) studies were conducted to study the drug interactions.

Preparation and evaluation of a novel oral delivery system for low molecular weight heparin.

Objective: The objective of the present work was to prepare and evaluate a novel oral formulation for systemic delivery of low molecular weight heparin (LMWH). The formulation consisted of Eudragit S 100-coated positively charged liposomes encapsulating LMWH and a penetration enhancer.

Materials And Methods: Positively charged liposomes were first prepared by the thin film hydration method using lipid (soy phosphotidylcholine and cholesterol) and stearyl amine (SA) in the optimum ratio of 16:1, along with cetylpyridinium chloride (CPC) as a penetration enhancer.

Anti-proliferative and Apoptotic Effects of Basella rubra (L.) Against 1, 2-Dimethyl Hydrazine-induced Colon Carcinogenesis in Rats.

Colorectal cancer is a very prevalent diagnosed cancer. The current study was performed in order to examine the role of BRAE (Basella rubra aqueous extract) in regulating aberrant crypt foci (ACF) formation, cell proliferation and inhibition of apoptosis in a colon carcinogenesis model in male Wistar rats. Rats were randomly allocated into six groups.

Colon specific drug delivery of tramadol HCl for chronotherapeutics of arthritis.

Objective: The objective of present work is to develop and evaluate a matrix system for Chronotherapeutic delivery of centrally acting of opioid analgesic (tramadol HCl) to treat nocturnal symptoms of arthritis using almond gum as carrier.

Materials And Methods: Matrix tablets of tramadol HCl were prepared by using 30, 40, 50, 60 and 70% w/w of tablet of gum badam as carrier by wet granulation technique. These tablets were compression coated with eudragit S100 to prevent drug release in stomach.

Saccharification of pretreated sawdust by Aspergillus niger cellulase.

The efficiency of two methods of pretreatment (NaOH and HO) on lignocelluloses-saw dust, wheat straw, sugarcane bagasse and rice bran-was compared in the present study. Alkali treatment of lignocelluloses relatively removed more hemicelluloses and lignin leaving behind cellulose content in the residues than peroxide treatment. Crude cellulase of Aspergillus niger, produced on the pretreated sawdust with highest cellulose content, was further tested for the release of soluble and reducing sugars during the saccharification process of same pretreated saw dust.

Mucoadhesive buccal films of glibenclamide: Development and evaluation.

Background: Glibenclamide is an oral hypoglycemic drug completely metabolized in the liver, the principal metabolite being very weakly active, buccal delivery may be useful for the treatment of diabetes more effectively. The aim of the present study was to design formulations and systematically evaluate in vitro and ex vivo performances of buccal films of glibenclamide so that the required therapeutic plasma concentrations can possibly be achieved more rapidly using the different grades of hydroxypropyl methyl cellulose (HPMC) as the base matrix.

Materials And Methods: Mucoadhesive buccal films of glibenclamide were prepared by solvent casting technique using different grades of HPMC with different ratios.