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Dissolution profiles of perindopril and indapamide in their fixed-dose formulations by a new HPLC method and different mathematical approaches

perspective, Eur. J. Pharm. Sci. 29 (2006) 288–293; DOI: 10.1016/j.ejps.2006.05.003. 11. T. O′Hara, A. Dunne, J. Butler and J. Devane, A review of methods used to compare dissolution profile data, Pharm. Sci. Technol . Today 1 (1998) 214–223; DOI: 10.1016/S1461-5347(98)00053-4. 12. P. Costa and J. M. S. Lobo, Modeling and comparison of dissolution profiles, Eur. J. Pharm. Sci. 13 (2001) 123–133; DOI: 10.1016/S0928-0987(01)00095-1. 13. N. Yuksel, A. E. Kanik and T. Baykara, Comparison of in vitro dissolution profiles by ANOVA-based, model

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Challenges relating to comparison of flavonoid glycosides dissolution profiles from Sutherlandia frutescens products

-011-9272-y. 11. S. P. Karuppiah, Analytical method development for dissolution release of finished solid oral dosage forms, Int. J. Curr. Pharm. Res. 4 (2012) 48-53. 12. J. W. Moore and H. H. Flanner, Mathematical comparison of dissolution profiles, Pharma Tech. 20 (1996) 64-74. 13. B. Zhang, W. K. Leung, Y. Zou, W. Mabusela, Q. Johnson, T. E. Michaelsen and B. S. Paulsen, Immunomodulating polysaccharides from Lessertia frutescens leaves: isolation, characterization and structure activity

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Compressibility of tableting materials and properties of tablets with glyceryl behenate

.3109/03639049809082350. 13. M. Roberts, D. Vellucci, S. Mostafa, C. Miolane and D. Marchaud, Development and evaluation of sustained-release CompritolR 888 ATO matrix mini-tablets, Drug Dev. Ind. Pharm. 38 (2012) 1068-1076; DOI: 10.3109/03639045.2011.638302. 14. P. Costa and J. M. Sousa Lobo, Modeling and comparison of dissolution profiles, Eur. J. Pharm. Sci. 13 (2001) 123-133; DOI: 10.1016/S0928-0987(01)00095-1.

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Physicochemical characterization and in vitro dissolution behaviour of celecoxib-β-cyclodextrin inclusion complexes

Physicochemical characterization and in vitro dissolution behaviour of celecoxib-β-cyclodextrin inclusion complexes

In this study, attempts were made to investigate the effects of β-cyclodextrin (β-CD) on the aqueous solubility and dissolution rate of celecoxib. Inclusion complexes were prepared by the kneading method and characterized by SEM, NMR, IR, DSC, and X-ray powder diffraction. Dissolution rate of the complexes was significantly greater than that of the corresponding physical mixtures and pure drug, indicating that the formation of inclusion complex increased the solubility of the poorly soluble drug celecoxib.

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Research Article. Kinetics and Mechanism of Drug Release from Loratadine Orodispersible Tablets Developed without Lactose

8. **** U.S. Pharmacopeial Convention - USP 38, NF 33 Edition, 2015 9. Motulsky HJ, Christopoulos A - Fitting models to biological data using linear and nonlinear regression. A practical guide to curve fitting, GraphPad Software Inc, Sandiego CA, (www.graphpad.com), 2003:134-160. 10. Young Z, Meirong H, Jianping Z et al - DDSolver: An Add-In Program for Modeling and Comparision of Drug Dissolution Profiles. The AAPS Journal, 2010;12(3):263-271.

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Kinetic Modelling of Drug Release from Pentoxifylline Matrix Tablets based on Hydrophilic, Lipophilic and Inert Polymers

References [1] Costa P, Lobo JMS. Modelling and comparison of dissolution profiles. Eur J Pharm Sci. 2001;13:123-133. [2] Kohler AN, Murphree ES. A comparison of the Akaike and Schwarz criteria for selecting model order. Appl Statist. 1998;37:187-195. [3] Ludden TM, Beal SL, Sheiner LB. Comparison of the Akaike Information Criterion, the Schwarz criterion and the F test as guides to model selection. J. Pharmacokinetic Biopharm. 1994;22:431-445. [4] Martindale, The Complete Drug Reference. 37th ed

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Piecewise function parameters as responses of the design of experiment in the development of a pulsatile release chronopharmaceutical system

Healthcare, New York 2007, pp. 1287–1297. 11. A. Maroni, L. Zema, G. Loreti, L. Palugan and A. Gazzaniga, Film coatings for oral pulsatile release, Int. J. Pharm. 457 (2013) 362–371; DOI: 10.1016/j.ijpharm.2013.03.010. 12. L. Palugan, M. Cerea, L. Zema, A. Gazzaniga and A Maroni, Coated pellets for oral colon delivery, J. Drug Del. Sci. Tech. 25 (2015) 1–15; DOI: 10.1016/j.jddst.2014.12.003 13. Y. Zhang, M. Huo, J. Zhou, A. Zou, Li W, Yao C and Xie S, DDSolver: an add-in program for modeling and comparison of drug dissolution profiles, AAPS J

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Release of selected amino acids from zinc carriers

, Modeling and comparison of dissolution profiles, Eur. J. Pharm. Sci. 13 (2001) 123–133; DOI: 10.1016/S0928-0987(01)00095-1.

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Formulation and evaluation of multiple tablets as a biphasic gastroretentive floating drug delivery system for fenoverine

. Chrom. Rel. Tech.   31 (2008) 2101-2112; DOI: 10.1080/10826070802225379. United States Pharmacopoeia 24/National Formulary 19, USO Convention, Rockville 2002. P. Costa and J.M. Sousa Lobo, Modelling and comparison of dissolution profiles, Eur. J. Pharm. Sci.   13 (2001) 123-133; DOI: 10.1016/S0928-0987(01)00095-1. W.I. Higuchi, Analysis of data on the medicament release from ointments, J. Pharm. Sci.   51 (1962) 802-804. J.W. Moore and H.H. Flanner

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Formulation And Performance Evaluation Of Betahistine Dihydrochloride Microspheres As Sustained Release Systems

variables for the preparation of fl uconazole-loaded ethyl cellulose microspheres by modifi ed multiple emulsion technique. AAPS PharmSciTech 2009;10(3):703-15. 11. Costa P, Sousa Lobo JM. Modeling and comparison of dissolution profiles. Eur J Pharm Sci 2001;13(2):123-33. 12. Dash S, Murthy PN, Nath L, et al. Kinetic modeling on drug release from controlled drug delivery systems. Acta Poloniae Pharmaceutica 2010;67 (3):217-23.

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