In this study we sought to formulate and evaluate sustained release matrix tablet of guaiphenesin by melt granulation technology. The sustained release tablets were prepared by melt granulation technique using rice bran wax as a drug retardant and dibasic calcium phosphate (DCP) as a channelling agent. Guaiphenesin is an expectorant and has a short plasma half-life of one hour. Because of high frequency of administration and short biological half-life, guaiphenesin was considered as model drug. Sustained release formulation that would maintain plasma levels for 12 hours is sufficient for twice daily dosing of guaiphenesin. The compatibility of drug and wax was examined by differential scanning calorimetry (DSC). The effect of waxes at different (drug: wax) concentrations on the release profile of drug from matrix formulation were studied. Drug release was studied at pH 1.2 for 2 hour and pH 6.8 for 10 hours. A significant retardation in the drug release was observed by increasing the wax concentration. The drug release study revealed that wax concentration of 30% to be optimum. Dissolution study showed 99% drug release within 12 hrs. Kinetic modelling of in vitro dissolution profiles revealed the drug release mechanism ranges from diffusion controlled or Fickian transport to anomalous type or non-Fickian transport. These results suggest that the rice bran wax has good release retardant property for highly water-soluble drug such as guaiphenesin.
The objective of the present study was to control the release of freely water soluble Tramadol hydrochloride over a prolonged period of time by embedding the drug into novel wax matrix system. The matrix granules were prepared by melt granulation technique. The need for the administration two to four times a day when larger dose are required can decrease patient compliance. Sustained release formulation that would maintain plasma levels for 24 hrs for once daily dosing of Tramadol hydrochloride was prepared. The compatibility of the drug and wax examined using Differential Scanning Calorimetry (DSC) and Fourier Transform Infrared Spectrophotometer (FTIR). The effect of wax concentration (5 to 35%) and channeling agents (Avicel PH-101 and Di-calcium phosphate) on the in vitro drug release at 24 hrs. was studied. Results of DSC confirmed drug-wax compatibility. Increasing the wax concentration resulted in a significant retardation of drug release. The drug release study revealed that the optimized formulation (F6) 30% novel wax sustained drug release for 24hrs. At the same wax concentration, drug release from tablets decreased with Di-calcium phosphate and increased with Avicel PH 101. Kinetic modeling of in vitro dissolution profiles revealed the drug release mechanism ranges from diffusion controlled or Fickian transport to anomalous type or non-Fickian transport. A hydrophobic matrix system is thus useful technique for prolonging the drug release of freely water soluble drugs such as Tramadol hydrochloride
Natural polymers are the most accepted pharmaceutical excipients of formulator’s choice. The reasons for this are their cost effectiveness, biocompatibility and availability. In this research article natural gum was extracted from the seeds of Samanea saman by using ethanol as a solvent. The physicochemical characterization like Loss on drying, Total ash and Acid insoluble ash, Swelling Index, Viscosity and qualitative evaluation of purified gum was done. The percent yield of gum was found to 6% w/w and the swelling index was found to be 18.5. Total ash value (7.5% w/w) and Acid insoluble ash value (1.4%w/w) shows purity of gum whereas 3.2% w/w loss on drying suggest low moisture content of gum. Chemical evaluation shows presence of carbohydrate. X ray diffraction graph of gum shows crystalline nature. The gum has average particle size 45.0±0.32 to 50±0.18μm, and the surface texture of the particles was found to be rough and irregular by scanning Electron Microscopy. Mucoadhesive property of gum was evaluated by Swelling index, Mucoadhesive force, Shear stress measurement. For this study polymeric tablet of gum with concentrations like 10%, 30%, 50%, 70% and 90 %w/w were formulated and the results shows best mucoadhesive and swelling property. From the above result the gum may be used in the formulation of mucoadhesive dosage form.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.