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Formulation and evaluation of fast dissolving tablet of - Pelagia ...

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Harish Ch<strong>and</strong>er et al Der Pharmacia Sinica, 2011, 2(6):163-170<br />

______________________________________________________________________________<br />

content was determined from st<strong>and</strong>ard calibration curve. Dissolution rate was studied for all<br />

designed formulation.<br />

RESULTS AND DISCUSSION<br />

Eight formulations <strong>of</strong> Fast Dissolving Tablets <strong>of</strong> Ramipril were prepared with varying<br />

concentration <strong>of</strong> Sodium bicarbonate: Mannitol <strong>and</strong> also Citric acid, PVP were used as diluents<br />

(Table. no. 2). For each formulation, blend <strong>of</strong> drug <strong>and</strong> excipients were prepared <strong>and</strong> evaluated<br />

for various parameters as explained earlier. The powder blend was compressed using direct<br />

compression technique.<br />

Table no. 3- Evaluation data <strong>of</strong> Micromeritic property <strong>of</strong> bulk powder blend<br />

Different Batches FDT<br />

Micromeritic properties 1<br />

FDT<br />

2<br />

FDT<br />

3<br />

FDT<br />

4<br />

<strong>Pelagia</strong> Research Library<br />

FDT<br />

5<br />

FDT<br />

6<br />

FDT<br />

7<br />

FDT<br />

8<br />

Bulk Density (gm/cm3) 0.96 0.69 0.56 0.50 0.43 0.41 0.82 0.83<br />

Tapped Density (gm/cm3) 1.09 0.79 0.63 0.57 0.50 0.48 0.92 0.95<br />

Angle <strong>of</strong> Repose ( 0 ) 25.34 24.42 26.34 24.24 25.66 25.47 24.98 26.64<br />

Compressibility Index (%) 11.92 12.65 10.93 13.26 12.72 13.30 10.66 12.14<br />

Bulk density, was found in the range <strong>of</strong> (0.41-0.96 gm/cm3) <strong>and</strong> the tapped density between<br />

(0.48-1.09 g/cm3).The compressibility index was found between (10.66-13.30) which indicates a<br />

fairly good flowbility <strong>of</strong> the powder blend. The good flowability <strong>of</strong> the powder blend was also<br />

evidenced with angle <strong>of</strong> repose in the range <strong>of</strong> (24.24-26.64) which is below 40( 0 ) indicating<br />

good flow properties <strong>of</strong> the granules (Table no.3)<br />

Table no. 4- Evaluation data <strong>of</strong> compressed <strong>tablet</strong>s <strong>of</strong> different formulations<br />

Different Batches FDT FDT FDT FDT FDT FDT FDT FDT<br />

Evaluation data 1 2 3 4 5 6 7 8<br />

Hardness (kg/cm2) 2.3 2.8 3.2 3.8 4.1 4.2 2.5 2.7<br />

Friability (%) 0.51 0.43 0.41 0.42 0.43 0.42 0.43 0.47<br />

Weight variation(mg) 251.2 252.6 250.4 250.0 254.1 253.6 249.5 250.3<br />

Water absorption ratio 102.2 130.5 145.8 156.8 153.9 155.0 150 149.5<br />

Wetting Time (sec) 174 165 159 152 145 143 160 155<br />

Batches<br />

Table no. 5:- % Drug release <strong>of</strong> Different Batches<br />

% DRUG RELEASE<br />

TIME<br />

(min)<br />

FDT1 FDT2 FDT3 FDT4 FDT5 FDT6 FDT7 FDT8<br />

0 0 0 0 0 0 0 0 0<br />

5 52.21 53.67 55.41 60.41 57.87 55.78 58.21 60.15<br />

10 65.34 78.89 85.67 90.23 80.89 78.56 75.34 69.34<br />

15 69.98 80.65 88.56 92.31 87.56 82.34 79.7 74.5<br />

20 75.67 85.67 91.23 96.42 90.87 84.5 83.6 78.6<br />

30 78.34 88.56 95.58 99.91 97.56 95.67 93.67 86.8<br />

Tablets were prepared using direct compression technique. Since the powder material was free<br />

flowing, <strong>tablet</strong>s were obtained <strong>of</strong> uniform weight due <strong>of</strong> uniform die fill, with acceptable weight<br />

variations as per I.P. The average weight <strong>of</strong> the prepared <strong>tablet</strong> was found 249 to 254 mg. All the<br />

<strong>tablet</strong>s were exhibit in white colour, odourless, smooth surface with zero defects. A <strong>tablet</strong><br />

requires certain amount <strong>of</strong> hardness to withst<strong>and</strong> the mechanical shocks in h<strong>and</strong>ling, packaging<br />

168

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