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Drug Development and Industrial Pharmacy Volume 20, 1994 - Issue 13
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Research Article

Effect of Formulation and Process Variables on the Dissolution Profile of Naproxen Sodium from Tablets

P. Bansal Division of Pharmaceutics and Industrial Pharmacy, Arnold L Marie Schwartz College of Pharmacy Long Island University, Brooklyn, NY, 11201; Zenith Laboratories, Northvale, NJ, 07647
,
K. Haribhakti Division of Pharmaceutics and Industrial Pharmacy, Arnold L Marie Schwartz College of Pharmacy Long Island University, Brooklyn, NY, 11201; Zenith Laboratories, Northvale, NJ, 07647
,
V. Subramanian Division of Pharmaceutics and Industrial Pharmacy, Arnold L Marie Schwartz College of Pharmacy Long Island University, Brooklyn, NY, 11201; Zenith Laboratories, Northvale, NJ, 07647
&
F. Plakogiannis Division of Pharmaceutics and Industrial Pharmacy, Arnold L Marie Schwartz College of Pharmacy Long Island University, Brooklyn, NY, 11201; Zenith Laboratories, Northvale, NJ, 07647
Pages 2151-2156 | Published online: 20 Oct 2008

Citations (12)

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Read on this site (4)

Jorge Quiroz, John Strong & Lanju Zhang. (2016) Risk management for moisture related effects in dry manufacturing processes: a statistical approach. Pharmaceutical Development and Technology 21:2, pages 147-151.
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Kalyana Pingali, Rafael Mendez, Daniel Lewis, Bozena Michniak-Kohn, Alberto Cuitiño & Fernando Muzzio. (2011) Evaluation of strain-induced hydrophobicity of pharmaceutical blends and its effect on drug release rate under multiple compression conditions. Drug Development and Industrial Pharmacy 37:4, pages 428-435.
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Xudong Yuan & A. C. Capomacchia. (2005) The Binary Eutectic of NSAIDs and Two-Phase Liquid System for Enhanced Membrane Permeation. Pharmaceutical Development and Technology 10:1, pages 1-10.
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Yu-E Zhang, Ruy Tchao & Joseph B. Schwartz. (2001) Effect of Processing Methods and Heat Treatment on the Formation of Wax Matrix Tablets for Sustained Drug Release. Pharmaceutical Development and Technology 6:2, pages 131-144.
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Articles from other publishers (8)

Maha Al-Ali, P. R. Selvakannan & Rajarathinam Parthasarathy. (2018) Influences of novel microwave drying on dissolution of new formulated naproxen sodium. RSC Advances 8:29, pages 16214-16222.
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David Bär, Heiko Debus, Christian Grune, Stephan Tosch, Wolfgang Fischer, Karsten Mäder & Peter Imming. (2017) Improving the drug release of Naproxen Sodium tablets by preparing granules and tablets with a preferred mixing ratio of hydrates. European Journal of Pharmaceutics and Biopharmaceutics 121, pages 90-96.
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Dhara Raijada, Anette Müllertz, Claus Cornett, Tommy Munk, Jørn Sonnergaard & Jukka Rantanen. (2014) Miniaturized Approach for Excipient Selection During the Development of Oral Solid Dosage Form. Journal of Pharmaceutical Sciences 103:3, pages 900-908.
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Shayne Cox GadA.K. Tiwary, Bharti Sapra & Subheet Jain. 2010. Pharmaceutical Sciences Encyclopedia. Pharmaceutical Sciences Encyclopedia.
S. Sotthivirat, J.W. Lubach, J.L. Haslam, E.J. Munson & V.J. Stella. (2007) Characterization of Prednisolone in Controlled Porosity Osmotic Pump Pellets using Solid-State NMR Spectroscopy. Journal of Pharmaceutical Sciences 96:5, pages 1008-1017.
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Young-soo Kim & Ronald W. Rousseau. (2004) Characterization and Solid-State Transformations of the Pseudopolymorphic Forms of Sodium Naproxen. Crystal Growth & Design 4:6, pages 1211-1216.
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Piera Di Martino, Christine Barth?l?my, Giovanni F Palmieri & Sante Martelli. (2001) Physical characterization of naproxen sodium hydrate and anhydrate forms. European Journal of Pharmaceutical Sciences 14:4, pages 293-300.
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George Lukas. (2016) Critical Manufacturing Parameters Influencing Dissolution. Drug Information Journal 30:4, pages 1091-1104.
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