• Journal of Korea Foresty Energy
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• v.20 no.2
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• pp.41-45
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• 2001

Japanese Larch(Larix kaempferi) was treated with aqueous solutions(30%, 40%, 50%) of polyethylene glycols(PEG, #1000, #1500, #4000, #6000) for the dimensional stabilization. The antiswelling efficiency(ASE) was measured for the evaluation of the dimensional stabilization. The weight percent gains(WPGs) of the woods treated with 40% solutions were higher than those of the others, and the highest WPG was achieved by treatment with 40% solution of PEG #1500. The ASE decreased with increasing molecular weight of PEG. ASE of woods treated with PEG #1000 and PEG #1500 were higher than those of the others.

• Journal of Pharmaceutical Investigation
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• v.41 no.4
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• pp.217-225
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• 2011

The aim of this work was to prepare porous osmotic pump tablets for controlled delivery of Aceclofenac. Aceclofenac solid dispersion was prepared to improve the solubility by using the drug - carrier (Mannitol) ratio of 1:1. The osmotic pump tablets were prepared using the solid dispersed product of Aceclofenac. The formulation contains potassium chloride as osmotic agent, cellulose acetate as semipermeable membrane, poly ethylene glycol (PEG 4000) as pore former and sodium lauryl sulphate (SLS) as solubility enhancer. The formulations were designed by the general factors such as osmotic agent and pore former. All formulations were evaluated for various physical parameters and, the in vitro release studies were conducted as per USP. The drug release kinetic studies such as zero order, first order, and Higuchi and Korsmeyer peppas were determined and compared. All the formulations gave more controlled release compared to the marketed tablet studied. Numerical optimization techniques were applied to found out the best formulation by considering the parameter of in vitro drug release kinetics and dissolution profile standards. It was concluded that the porous osmotic pump tablets (F7) composed of Aceclofenac solid dispersion/Potassium chloride/Lactose/Sodium lauryl sulphate/Magnesium Stearate (400/40/95/10/5, mg/tab) and coating composition with Cellulose acetate/ PEG 4000 (60/40 %w/w) is the most satisfactory formulation. The porous osmotic pump tablets provide prolonged, controlled, and gastrointestinal environment-independent drug release.