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Research Article

Evaluation of the Functional Equivalence of Crospovidone NF from Different Sources. II. Standard Performance Test

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Pages 419-430 | Received 25 Jul 2000, Accepted 10 Feb 2001, Published online: 31 Jul 2001

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Ali Al-khattawi & Afzal R Mohammed. (2013) Compressed orally disintegrating tablets: excipients evolution and formulation strategies. Expert Opinion on Drug Delivery 10:5, pages 651-663.
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M. Maghsoodi & A.S. Tajalli Bakhsh. (2011) Evaluation of physico-mechanical properties of drug-excipients agglomerates obtained by crystallization. Pharmaceutical Development and Technology 16:3, pages 243-249.
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Na Zhao & L.L. Augsburger. (2006) The Influence of Product Brand-to-Brand Variability on Superdisintegrant Performance A Case Study with Croscarmellose Sodium. Pharmaceutical Development and Technology 11:2, pages 179-185.
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Umang Shah & Larry Augsburger. (2002) Multiple Sources of Sodium Starch Glycolate, NF: Evaluation of Functional Equivalence and Development of Standard Performance Tests. Pharmaceutical Development and Technology 7:3, pages 345-359.
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Articles from other publishers (17)

Arash Yavari, Mostafa Saffary, Ali Nokhodchi & Seyed Kazem Sadjady. (2022) Evaluation of Manufacturer-to-Manufacturer Variability of Croscarmellose Sodium: Influence on the Dissolution of Sitagliptin Tablets (Water-Soluble Drug) and Escitalopram Tablets (Sparingly Soluble Drug). AAPS PharmSciTech 23:6.
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Alberto Berardi, Pauline H.M. Janssen & Bastiaan H.J. DickhoffPhDPhD. (2022) Technical insight into potential functional-related characteristics (FRCs) of sodium starch glycolate, croscarmellose sodium and crospovidone. Journal of Drug Delivery Science and Technology 70, pages 103261.
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Kristina E. Steffens & Karl G. Wagner. (2021) Immediate-Release Formulations Produced via Twin-Screw Melt Granulation: Systematic Evaluation of the Addition of Disintegrants. AAPS PharmSciTech 22:5.
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Jan Lenz, Heike Bunjes, Arno Kwade & Michael Juhnke. (2021) An improved method for the simultaneous determination of water uptake and swelling of tablets. International Journal of Pharmaceutics 595, pages 120229.
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Farouk Kamel El-Baz, Sami Ibrahim Ali, Mona Basha, Ahmed Alaa Kassem, Rehab Nabil Shamma, Rania Elgohary & Abeer Salama. (2020) Design and evaluation of bioenhanced oral tablets of Dunaliella salina microalgae for treatment of liver fibrosis. Journal of Drug Delivery Science and Technology 59, pages 101845.
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P. Zarmpi, T. Flanagan, E. Meehan, J. Mann, J. Østergaard & N. Fotaki. (2020) Biopharmaceutical implications of excipient variability on drug dissolution from immediate release products. European Journal of Pharmaceutics and Biopharmaceutics 154, pages 195-209.
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Panagiota Zarmpi, Talia Flanagan, Elizabeth Meehan, James Mann & Nikoletta Fotaki. (2020) Biopharmaceutical Understanding of Excipient Variability on Drug Apparent Solubility Based on Drug Physicochemical Properties. Case Study: Superdisintegrants. The AAPS Journal 22:2.
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Vivek Dave, Renu Bala Yadav, Richa Ahuja & Sachdev Yadav. (2017) Formulation design and optimization of novel fast dissolving tablet of chlorpheniramine maleate by using lyophilization techniques. Bulletin of Faculty of Pharmacy, Cairo University 55:1, pages 31-39.
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P. Zarmpi, T. Flanagan, E. Meehan, J. Mann & N. Fotaki. (2017) Biopharmaceutical aspects and implications of excipient variability in drug product performance. European Journal of Pharmaceutics and Biopharmaceutics 111, pages 1-15.
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Ramana Susarla, Afolawemi Afolabi, Darshan Patel, Ecevit Bilgili & Rajesh N. Davé. (2015) Novel use of superdisintegrants as viscosity enhancing agents in biocompatible polymer films containing griseofulvin nanoparticles. Powder Technology 285, pages 25-33.
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Vivek S. Dave, Suprit D. Saoji, Nishikant A. Raut & Rahul V. Haware. (2015) Excipient Variability and Its Impact on Dosage Form Functionality. Journal of Pharmaceutical Sciences 104:3, pages 906-915.
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Chandrasekhar Garapati, Himanshu Gupta, Jwala Renukuntla & Sai HS. Boddu. 2015. Excipient Applications in Formulation Design and Drug Delivery. Excipient Applications in Formulation Design and Drug Delivery 201 236 .
Sayaka Nakanishi, Makiko Fujii, Yuka Sugamura, Ayako Suzuki, Yusuke Shibata, Naoya Koizumi & Yoshiteru Watanabe. (2011) Evaluation of the physicochemical characteristics of crospovidone that influence solid dispersion preparation. International Journal of Pharmaceutics 413:1-2, pages 119-125.
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Y. Gonnissen, J.P. Remon & C. Vervaet. (2008) Effect of maltodextrin and superdisintegrant in directly compressible powder mixtures prepared via co-spray drying. European Journal of Pharmaceutics and Biopharmaceutics 68:2, pages 277-282.
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Na Zhao & Larry L. Augsburger. (2005) Functionality comparison of 3 classes of superdisintegrants in promoting aspirin tablet disintegration and dissolution. AAPS PharmSciTech 6:4, pages E634-E640.
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Na Zhao & Larry L. Augsburger. (2005) The influence of swelling capacity of superdisintegrants in different pH media on the dissolution of hydrochlorothiazide from directly compressed tablets. AAPS PharmSciTech 6:1, pages E120-E126.
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Santhi Ganesan, Joseph Felo, Mario Saldana, Victor F Kalasinsky, Michael R Lewin-Smith & Joseph F TomashefskiJrJr. (2003) Embolized Crospovidone (poly[N-vinyl-2-pyrrolidone]) in the Lungs of Intravenous Drug Users. Modern Pathology 16:4, pages 286-292.
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