World Journal of Pharmaceutical research - WJPR!
World Journal of Pharmaceutical research - WJPR!
World Journal of Pharmaceutical research - WJPR!
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Patel Sunilkumar <strong>World</strong> <strong>Journal</strong> <strong>of</strong> <strong>Pharmaceutical</strong> <strong>research</strong><br />
Formulated Power blend <strong>of</strong> Different batches were Evaluated. Showed results <strong>of</strong> Power blend<br />
have Bulk density and tapped density <strong>of</strong> F1 to F7 batches that 0.340 to 0.404 and 0.432 to<br />
0.532 Respect. Carr’s Index and hausner’s ratio have good compare to std value as according<br />
to IP <strong>of</strong> F1 to F7 batches that 11.66 to 21.48 and 1.13 to 1.27 shown table 3 Respect. Angle <strong>of</strong><br />
repose has good and Excellent as Compare standard value as According to IP <strong>of</strong> F1 to F7<br />
Batches that 12.62 0 to 22.56 0 shown table3. Ibupr<strong>of</strong>en Tablets were Prepared successfully by<br />
wet granulation Technique. In Weight variation test, the Pharmacopoeia limit for percent <strong>of</strong><br />
deviation for tablets <strong>of</strong> more than 260mg is ±5%. The average percent deviation <strong>of</strong> all tablets<br />
was found to be limit and hence all formulations passed the weight variation test. The hardness<br />
<strong>of</strong> tablets <strong>of</strong> all formulation was in range <strong>of</strong> 2.5±0.51 to 3.8±0.54 kg\cm 2 . The Thickness <strong>of</strong><br />
tablets ranged from 5.204±0.01 to 5.514±0.01.i.e. less than 1%. The Diameter <strong>of</strong> tablets<br />
ranged from 8.301±0.01 to 8.520±0.01. The Friability <strong>of</strong> tablets <strong>of</strong> all formulation was in<br />
range <strong>of</strong> 0.059±0.01 to 0.065±0.01shown table 4.All thickness shown uniform thickness. The<br />
Drug content was found to be uniform all formulation and ranged from 62.11% to 81.99%.<br />
Shown in figure1<br />
CONCLUSION<br />
Among all formulation f4 containing 40% <strong>of</strong> ehtylcellulose and 60% <strong>of</strong> Hydroxy propyl<br />
methyl cellulose showed in vitro drug release 62.11% and which is equivalent to marketed<br />
preparation hence considered as most promising formulation. Result also showed that among<br />
hydrophilic and hydrophobic matrix polymer. HPMC sustain more than EC .Combination <strong>of</strong><br />
HPMC and EC retain drug more than that individual matrix polymer. In study concluded<br />
HPMC and EC are hydrophilic and hydrophobic matrix polymer which using matrix foaming<br />
agent by wet granular technique to sustain the release <strong>of</strong> ibupr<strong>of</strong>en.<br />
ACKNOWLEDGEMENTS<br />
We are grateful to Ratmani <strong>Pharmaceutical</strong> Ltd, Mehsana for providing gift sample <strong>of</strong><br />
Ibupr<strong>of</strong>en.<br />
REFERENCES<br />
1. Dabbagh M.A and Beitmashal L.Sustained Release Formulation and In-Vitro Evaluation<br />
<strong>of</strong> Ibupr<strong>of</strong>en-Hpmc Matrix Tablets. Jundishapur J Natural Pharm Products, 2006; 1:1-7.<br />
2. Prajapati Bhupendra G., Patel Krunal R.Design and In Vitro Evaluation <strong>of</strong> Novel<br />
Nicorandil Sustained Release Matrix Tablets Based On Combination <strong>of</strong> Hydrophilic and<br />
Hydrophobic Matrix System. Int J Pharm Sci. and Res, 2010; 1(1): 2143-2156.<br />
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