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Drug Development and Industrial Pharmacy Volume 20, 1994 - Issue 19
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Research Article

Investigation into The Yellowing on Aging of Sabril® Tablet Cores

Ron C. George Marion Merrell Dow Inc., P.O. Box 9627, Kansas City, MO, 64134-0627
,
Robert J. Barbuch Marion Merrell Dow Inc., P.O. Box 9627, Kansas City, MO, 64134-0627
,
Edward W. Huber Marion Merrell Dow Inc., P.O. Box 9627, Kansas City, MO, 64134-0627
&
Brian T. Regg Marion Merrell Dow Inc., P.O. Box 9627, Kansas City, MO, 64134-0627
Pages 3023-3032 | Published online: 20 Oct 2008

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Brenda L. Valle, Wycliffe S. Omwancha, Steven H. Neau & Rodney J. Wigent. (2016) Use of к-carrageenan, chitosan and Carbopol 974P in extruded and spheronized pellets that are devoid of MCC. Drug Development and Industrial Pharmacy 42:11, pages 1903-1916.
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Koji Mochizuki & Kozo Takayama. (2016) Prediction of color changes in acetaminophen solution using the time–temperature superposition principle. Drug Development and Industrial Pharmacy 42:7, pages 1050-1057.
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Yongmei Wu, Mandar Dali, Abhishek Gupta & Krishnaswamy Raghavan. (2009) Understanding drug-excipient compatibility: Oxidation of compound A in a solid dosage form. Pharmaceutical Development and Technology 14:5, pages 556-564.
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Articles from other publishers (15)

Daniel Robin Thio, Paul Wan Sia Heng & Lai Wah Chan. (2022) MUPS Tableting—Comparison between Crospovidone and Microcrystalline Cellulose Core Pellets. Pharmaceutics 14:12, pages 2812.
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Faranak Ghaderi & Farnaz Monajjemzadeh. (2020) Review of the physicochemical methods applied in the investigation of the maillard reaction in pharmaceutical preparations. Journal of Drug Delivery Science and Technology 55, pages 101362.
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Ankit Sharma. 2019. Innovative Dosage Forms. Innovative Dosage Forms 91 118 .
C. Martano, F. Ferretti, S. Ghiani, F. Buonsanti, E. Bruno, L. Lattuada & C. Medana. (2018) Development and validation of a new HPLC–MS method for meglumine impurity profiling. Journal of Pharmaceutical and Biomedical Analysis 149, pages 517-524.
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A.S. Narang, R.V. Mantri & K.S. Raghavan. 2017. Developing Solid Oral Dosage Forms. Developing Solid Oral Dosage Forms 151 179 .
David Good & Yongmei Wu. 2016. Pharmaceutical Excipients. Pharmaceutical Excipients 1 49 .
Kalyan K. Saripella, Nikhil C. Loka, Rama Mallipeddi, Anuja M. Rane & Steven H. Neau. (2015) A Quality by Experimental Design Approach to Assess the Effect of Formulation and Process Variables on the Extrusion and Spheronization of Drug-Loaded Pellets Containing Polyplasdone® XL-10. AAPS PharmSciTech 17:2, pages 368-379.
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Ajit S. Narang, Divyakant Desai & Sherif Badawy. 2015. Excipient Applications in Formulation Design and Drug Delivery. Excipient Applications in Formulation Design and Drug Delivery 93 137 .
Yongmei Wu, Jaquan K. Levons, Ajit S. Narang, Krishnaswamy Raghavan & Rao V. Mantri. 2015. Excipient Applications in Formulation Design and Drug Delivery. Excipient Applications in Formulation Design and Drug Delivery 37 65 .
Melanie Köllmer, Carmen Popescu, Prashanth Manda, Leon Zhou & Richard A. Gemeinhart. (2013) Stability of Benzocaine Formulated in Commercial Oral Disintegrating Tablet Platforms. AAPS PharmSciTech 14:4, pages 1333-1340.
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Ajit S. Narang, Divyakant Desai & Sherif Badawy. (2012) Impact of Excipient Interactions on Solid Dosage Form Stability. Pharmaceutical Research 29:10, pages 2660-2683.
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Yongmei Wu, Jaquan Levons, Ajit S. Narang, Krishnaswamy Raghavan & Venkatramana M. Rao. (2011) Reactive Impurities in Excipients: Profiling, Identification and Mitigation of Drug–Excipient Incompatibility. AAPS PharmSciTech 12:4, pages 1248-1263.
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Rama Mallipeddi, Kalyan K. Saripella & Steven H. Neau. (2010) Use of coarse ethylcellulose and PEO in beads produced by extrusion–spheronization. International Journal of Pharmaceutics 385:1-2, pages 53-65.
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Ajit S. Narang, Venkatramana M. Rao & Krishnaswamy S. Raghavan. 2009. Developing Solid Oral Dosage Forms. Developing Solid Oral Dosage Forms 125 145 .
Yunhui Wu, Tsang-Lin Hwang, Kimberly Algayer, Wei Xu, Hong Wang, Adam Procopio, Laura DeBusi, Chia-Yi Yang & Bozena Matuszewska. (2003) Identification of oxidative degradates of the TRIS salt of a 5,6,7,8-tetrahydro-1,8-naphthyridine derivative by LC/MS/MS and NMR spectroscopy?interactions between the active pharmaceutical ingredient and its counterion. Journal of Pharmaceutical and Biomedical Analysis 33:5, pages 999-1015.
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