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Sustained release enteric coated tablets of pantoprazole: Formulation, in vitro and in vivo evaluation Cover

Sustained release enteric coated tablets of pantoprazole: Formulation, in vitro and in vivo evaluation

Open Access
|Mar 2013

References

  1. 1. S. W. Hosking, S. C. S. Chung, M. Y. Yung, A. K. C. Li, J. J. Y. Sung, T. K. W. Ling and A. F. B. Cheng, Duodenal ulcer healing by eradication of Helicobacter pylori without anti-acid treatment: randomised controlled trial, Lancet 343 (1994) 508- 510; DOI: 10.1016/S0140-6736(94)91460-5.10.1016/S0140-6736(94)91460-5
  2. 2. J. Weil, D. Colin-Jones, M. Langman, D. Lawson, M. Murphy, M. Rawlins, M. Vessey and P. Wainwright, Prophylactic aspirin and risk of peptic ulcer bleeding, Br. Med. J. 310 (1995) 827-830.10.1136/bmj.310.6983.827
  3. 3. G. Sachs, Proton pump inhibitors and acid-related diseases, Pharmacotherapy 17 (1997) 22-37. DOI: 10.1002/j.1875-9114.1997.tb03675.x.
  4. 4. S. S. Ozturk, B. O. Palsson, B. Donohoe and J. B. Dressman, Kinetics of release from enteric- -coated tablets, Pharm. Res. 5 (1988) 550-565; DOI: 10.1023/A:1015937912504.10.1023/A:1015937912504
  5. 5. Y. B. Huang, Y. H. Tsai, W. C. Yang, J. S. Chang, P. C. Wu and K. Takayama, Once-daily propranolol extended tablet dosage form: formulation design and in vitro/in vivo investigation. Eur. J. Pharm. Biopharm. 58 (2004) 607-614; DOI: 10.1016/j.ejpb.2004.03.037.10.1016/j.ejpb.2004.03.037
  6. 6. K. R. Reddy, S. Mutalik and S. Reddy, Once-daily sustained release matrix tablets of nicorandil: Formulation and in vitro evaluation,AAPS Pharm. Sci. Tech. 4 (2003) 480-488; DOI: 10.1208/pt040461.10.1208/pt040461
  7. 7. B.Wilson, P. H. Sitarambhai, M. S. Sajeev and G. Vinothapooshan, Design and evaluation of sustained release matrix tablets of levofloxacin for effective treatment of microbial infection, Int. J. Drug Deliv. 3 (2011) 305-314.
  8. 8. Pharmacopoeia of India, Ministry of Health and Family Welfare, Government of India, Controller of Publications, New Delhi 1996, pp. A80-A84.
  9. 9. United States Pharmacopoiea 23, National Formulary 18, USP Convention, Rockville (MD) 1995, pp. 1328.
  10. 10. K. Tahara, K. Yamamoto and T. Nishihata, Application of model-independent and model analysis for the investigation of effect of drug solubility on its release rate from hydroxypropyl methylcellulose sustained release tablets, Int. J. Pharm. 133 (1996) 17-27; DOI: 10.1016/0378- -5173(95)04400-0.
  11. 11. P. Costa and J. M. S. Lobo, Modeling and comparison of dissolution profiles, Eur. J. Pharm. Sci.13 (2001) 123-133; DOI: 10.1016/S0928-0987(01)00095-1.10.1016/S0928-0987(01)00095-1
  12. 12. N. S. Parmar and J. K. Desai, A review of the current methodology for the evaluation of gastric and duodenal anti-ulcer agents, Indian. J. Pharmacol. 25 (1993) 120-135. 140
DOI: https://doi.org/10.2478/acph-2013-0002 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 131 - 140
Published on: Mar 12, 2013
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
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© 2013 Barnabas Wilson, Patel Pritesh Babubhai, M. S. Sajeev, Josephine Leno Jenita, S. R. Brahmani Priyadarshini, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.