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Drug Development and Industrial Pharmacy Volume 18, 1992 - Issue 8
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Research Article

Elaboration and Physical Study of an Oxodipine Solid Dispersion in Order to formulate Tablets

F. Guillaume Laboratorie de Pharmacie Galénique, Faculté de Phramacie, Lille
,
A. M. Guyot-Hermann Laboratorie de Pharmacie Galénique, Faculté de Phramacie, Lille
,
R. Duclos Laboratories de Pharmacie Galénique, Faculté de Phramaice, Rouen
,
P. Besançon Laboratories de Pharmacie Galénique, Faculté de Phramaice, Rouen
,
A. M. Orecchioni Laboratories de Pharmacie Galénique, Faculté de Phramaice, Rouen
,
M. Drache Laboratorie de cristallochimie et Physochimie du Solide, URA CNRS 452, Université des Sciences et Techniques de Lille, Flandres, Artois
,
P. Conflant Laboratorie de cristallochimie et Physochimie du Solide, URA CNRS 452, Université des Sciences et Techniques de Lille, Flandres, Artois
,
A. Gadefait Laboratoire Delagrange, Chilly, Mazrin
&
P. Bécourt Laboratoire Delagrange, Chilly, Mazrin
 show all
Pages 811-827 | Published online: 20 Oct 2008

Citations (8)

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Jared A. Baird & Lynne S. Taylor. (2011) Evaluation and modeling of the eutectic composition of various drug-polyethylene glycol solid dispersions. Pharmaceutical Development and Technology 16:3, pages 201-211.
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F.I. Kanaze, E. Kokkalou, I. Niopas, P. Barmpalexis, E. Georgarakis & D. Bikiaris. (2010) Dissolution rate and stability study of flavanone aglycones, naringenin and hesperetin, by drug delivery systems based on polyvinylpyrrolidone (PVP) nanodispersions. Drug Development and Industrial Pharmacy 36:3, pages 292-301.
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Giovanni Filippo Palmieri, Franco Cantalamessa, Piera Di Martino, Cinzia Nasuti & Sante Martelli. (2002) Lonidamine Solid Dispersions: In Vitro and In Vivo Evaluation. Drug Development and Industrial Pharmacy 28:10, pages 1241-1250.
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Articles from other publishers (5)

Alicia Graciela Cid, Analía Simonazzi, Santiago Daniel Palma & José María Bermúdez. (2019) Solid dispersion technology as a strategy to improve the bioavailability of poorly soluble drugs. Therapeutic Delivery 10:6, pages 363-382.
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Wei-Qin (Tony) Tong, Madhav Vasanthavada & Abu Serajuddin. 2008. Water-Insoluble Drug Formulation, Second Edition. Water-Insoluble Drug Formulation, Second Edition 499 529 .
Abu T.M. Serajuddin. (1999) Solid dispersion of poorly water‐soluble drugs: Early promises, subsequent problems, and recent breakthroughs. Journal of Pharmaceutical Sciences 88:10, pages 1058-1066.
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P Longuemard, M Jbilou, A.-M Guyot-Hermann & J.-C Guyot. (1998) Ground and native crystals: comparison of compression capacity and dissolution rate. International Journal of Pharmaceutics 170:1, pages 51-61.
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J.-M. Fachaux, A.-M. Guyot-Hermann, J.-C. Guyot, P. Conflant, M. Drache, S. Veesler & R. Boistelle. (1995) Pure Paracetamol for direct compression Part II. Study of the physicochemical and mechanical properties of sintered-like crystals of Paracetamol. Powder Technology 82:2, pages 129-133.
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