Author/Authors :
Aslani, Abolfazl Department of Pharmaceutics - School of Pharmacy and Novel Drug Delivery Systems Research Center - Isfahan University of Medical Sciences , Fathi, Azam Department of Pharmaceutics - School of Pharmacy and Novel Drug Delivery Systems Research Center - Isfahan University of Medical Sciences
Abstract :
Dispersible tablet is a new form of tablet which any dose of it is dispersed in a
small amount of water to create a uniform suspension. The advantage of this
formulation is its better and faster effect, no need to swallow, more stability
compared to suspension, better taste and greater acceptance by the patients
especially kids and elders. This study aimed to design and formulize
dispersible tablets including Co- Amoxiclav 228 and 312 mg for enhancement
of stability and easier usage and consumption. Co amoxiclav dispersible pill
was made by dry granulation method using superdisintegrants ingredients
such as crospovidone, croscarmellose sodium and sodium starch glycolate and
effervescent materials such as citric acid and sodium bicarbonate. The mixed
powder was tested in terms of compressibility, particle size distribution and
powders flowability. Some tests were performed for determination of assay,
content uniformity, hardness and friability of tablet, weight variation, wetting
time, water absorption ratio and disintegration of tablets. Prepared granules
had good flowability, compressibility and the hardness and friaibility of tablets
were in an acceptable range in most formulations. Formulations made by
effervescent bases E3 and E4 had disintegration time of 25 and 35 seconds and
S1, S4 and S5 formulations made from superdisintegrants materials showed the
disintegration time of 260, 262 and 275 seconds. E4 formulation containing
amoxicillin trihydrate, potassium clavulanate, citric acid, sodium bicarbonate,
manitol, aspartame and PEG 6000 had 25 sec disintegration time and 40 N
hardness.
Keywords :
Co-amoxiclav , Dispersible tablet , Effervescent method , Dry granulation method