24.12.2012 Views

World Journal of Pharmaceutical research - WJPR!

World Journal of Pharmaceutical research - WJPR!

World Journal of Pharmaceutical research - WJPR!

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

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 />

www.wjpr.net<br />

1339

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!