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Research Article

Ontrolled-Release Theophylline Tablet Formulations Containing Acrylic Resins. I. Dissolution Properties of Tablets

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Pages 57-68 | Published online: 20 Oct 2008

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Read on this site (16)

Ahmed Abd El-Bary, Howida Kamal Ibrahim, Balqees Saeed Haza’a & Ibrahim Al Sharabi. (2019) Formulation of sustained release bioadhesive minitablets containing solid dispersion of levofloxacin for once daily ocular use. Pharmaceutical Development and Technology 24:7, pages 824-838.
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Poj Kulvanich, Phuriwat Leesawat & Vipaluk Patomchaiviwat. (2002) Release Characteristics of the Matrices Prepared from Co-spray-Dried Powders of Theophylline and Ethylcellulose. Drug Development and Industrial Pharmacy 28:6, pages 727-739.
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N. V. Mulye & S. J. Turco. (1994) Matrix Type Tablet Formulation for Controlled Release of Highly Water Soluble Drugs. Drug Development and Industrial Pharmacy 20:17, pages 2633-2643.
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Mark D. Schulze & James W. McGinity. (1993) Indices of Tableting Performance for Acrylic Resin Polymers with Plastic and Brittle Drugs. Drug Development and Industrial Pharmacy 19:12, pages 1393-1411.
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J. A. K. Lauwo, D. K. Agrawal & I. V. Emenike. (1990) Some Pharmaceutical Studies on Sustained Release Coprbcipitates of Ampicillin Trihydrat with Acrylic Resin (Eudragit)(R)-RS). Drug Development and Industrial Pharmacy 16:8, pages 1375-1389.
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Rajesh Patel & Ravindra C. Vasavada. (1990) Effect of Ph on Enhancement of in Vitro Percutaneous Transport of Isoproterenol Hcl by Azone. Drug Development and Industrial Pharmacy 16:8, pages 1365-1374.
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Biswanath Sa, A. K. Bandyopadhyay & B. K. Gupta. (1990) Development and In-Vitro Evaluation of Ethyl Cellulose Micropellets as a Controlled Release Dosage Form for Theophylline. Drug Development and Industrial Pharmacy 16:7, pages 1153-1169.
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Mark D. Schulze, Robert O. Williams & James W. McGinity. (1990) Compaction Properties of Acrylic Resin Polymers with Plastic and Brittle Drugs. Drug Development and Industrial Pharmacy 16:5, pages 741-754.
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Hirofumi Takeuchi, Tetsurou Handa & Yoshiaki Kawashima. (1989) Controlled Release Theophylline Tablet with Acrylic Polymers Prepared by Spray-Drying Technique in Aqueous System. Drug Development and Industrial Pharmacy 15:12, pages 1999-2016.
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Yilmaz Capan. (1989) Influence of technological factors on formulation of sustained release tablets. Drug Development and Industrial Pharmacy 15:6-7, pages 927-956.
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Martin J. D'Souza. (1988) Controlled Release of Cyclosporine from Microspheres. Drug Development and Industrial Pharmacy 14:10, pages 1351-1357.
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Claud G. Cameron & James W. McGinit. (1987) Controlled-Release Theophylline Tablet Formulations Containing Acrylic Resins, II. Combination Resin Formulations. Drug Development and Industrial Pharmacy 13:8, pages 1409-1427.
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Claud G. Cameron & James W. Mcginity. (1987) Controlled-Release Theophylline Tablet Formulations Containing Acrylic Resins, III. Influence of Filler Excipient.. Drug Development and Industrial Pharmacy 13:2, pages 303-318.
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E. Ciranni Signoretti, A. Dell'utri & C. De Sena. (1987) Dissolution Characteristics of Pharmaceutical Equivalents. Drug Development and Industrial Pharmacy 13:15, pages 2719-2730.
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R. Baweja. (1986) Dissolution Profiling of Six Modified-Release Oral Solid Dosage Forms. Drug Development and Industrial Pharmacy 12:14, pages 2431-2442.
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Articles from other publishers (10)

R. Ali. (2017) Ammonio methacrylate copolymer as a carrier for water-insoluble drug, preparation and characterization of an oral controlled-release matrix tablet. Journal of Drug Delivery Science and Technology 41, pages 7-12.
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Brigitte Skalsky & Hans-Ulrich Petereit. 2016. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms 207 246 .
IkoniJ. Ogaji & StephenW. Hoag. (2014) Novel extraction and application of okra gum as a film coating agent using theophylline as a model drug. Journal of Advanced Pharmaceutical Technology & Research 5:2, pages 70.
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Ahmed Abd Elbary, Ahmed A. Aboelwafa & Ibrahim M. Al Sharabi. (2011) Once Daily, High-Dose Mesalazine Controlled-Release Tablet for Colonic Delivery: Optimization of Formulation Variables Using Box–Behnken Design. AAPS PharmSciTech 12:4, pages 1454-1464.
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Wendy Dulin. 2010. Oral Controlled Release Formulation Design and Drug Delivery. Oral Controlled Release Formulation Design and Drug Delivery 205 223 .
M. Vlachou, N. H. Choulis, M. Efentakis & A. G. Andreopoulos. (2016) The Effect of Modification of Acrylic Resins on Controlled Release and Bioadhesion. Journal of Biomaterials Applications 10:3, pages 217-229.
Crossref
H. Al-Hmoud, M. Efentakis & N.H. Choulis. (1991) A controlled release matrix using a mixture of hydrophilic and hydrophobic polymers. International Journal of Pharmaceutics 68:1-3, pages R1-R3.
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A. Li Wan Po, L.P. Wong & C.A. Gilligan. (1990) Characterisation of commercially available theophylline sustained- or controlled-release systems: in-vitro drug release profiles. International Journal of Pharmaceutics 66:1-3, pages 111-130.
Crossref
Michelle R. Jenquin, Stephen M. Liebowitz, Rafael E. Sarabia & James W. McGinity. (1990) Physical and Chemical Factors Influencing the Release of Drugs from Acrylic Resin Films. Journal of Pharmaceutical Sciences 79:9, pages 811-816.
Crossref
Y. Kawashima, T. Handa, A. Kasai, H. Takenaka, S.Y. Lin & Y. Ando. (1985) Novel Method for the Preparation of Controlled-Release Theophylline Granules Coated with a Polyelectrolyte Complex of Sodium Polyphosphate-Chitosan. Journal of Pharmaceutical Sciences 74:3, pages 264-268.
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