Sentence examples for tablet integrity from inspiring English sources

The tablet integrity of donepezil HCl (Fig. 1a) at 40 °C 25% RH exhibited efferescence, whereas the tablets at room temp remained unchanged (Fig. 1b).

This material is able to produce a very fast rupture of the tablet integrity after wetting, with consequent disintegration of the tablet into fine particles.

Tablets are invariably formed by uniaxial compression in rigid dies and the tablet mechanical integrity is highly dependent on its ability to withstand the physical dimensional changes resulting from the elastic relaxation due to the release of the elastic strains incurred during the tablet formation.

Furthermore, BaSO4 showed to increase the integrity of tablet matrix by reducing eroding properties.

P3 and P6 amount of coating polymer was too less which could not maintain integrity of tablet for long and time resulting in complete drug release within short period of time.

Unlike clay items today, which are usually fired in an oven and glazed to help preserve their integrity, the tablets had simply been left in the sun to dry, and they contained salt deposits from the Iraqi soil.

An accelerated thermal stability study at 40 °C and 25% relative humidity showed that the integrity of the effervescent tablets containing rivastigmine tartrate were superior to that of donepezil HCl tablets.

Tablets containing 10% w/w of xanthan gum and 10% w/w of guar gum of total tablet weight were able to keep their integrity and showed a good control on atenolol release.

Important tablet properties, such as coating uniformity and mechanical integrity, that can be predicted based on its surface properties manifest the inevitable link between a tablet's surface property (e.g. Gloss, average surface roughness) and its efficacy.

"They gave him the job knowing that he had a reputation for integrity," said Robert Mickens, the Rome correspondent for The Tablet newspaper.

From the results of in vitro drug release studies, the cumulative mean percent of FLB released from compression coated tablets containing varying amounts of GG (20 mg, 40 mg, 60 mg, 80 mg and 100 mg), with incorporation of 80 mg of polymer in the total tablet weight (F4), was found to be satisfactory to formulate a tablet with good integrity and satisfactory in vitro drug release.