General Considerations of Design and Development of Dosage Forms: Pre-formulation Review
暂无分享,去创建一个
[1] H. K. Stulzer,et al. Differential scanning calorimetry as a screening technique in compatibility studies of acyclovir extended release formulations , 2009, Pharmaceutical Chemistry Journal.
[2] Mark Gibson,et al. Pharmaceutical Preformulation and Formulation: A Practical Guide from Candidate Drug Selection to Commercial Dosage Form , 2001 .
[3] Derek Geldart,et al. The use of bulk density measurements as flowability indicators , 1999 .
[4] C. Washington. Particle size analysis in pharmaceutics and other industries : theory and practice , 1992 .
[5] W. Higuchi,et al. Theoretical model studies of drug absorption and transport in the gastrointestinal tract.i. , 1970, Journal of pharmaceutical sciences.
[6] P York,et al. Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates. , 2007, Advanced drug delivery reviews.
[7] F. Lombardo,et al. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. , 2001, Advanced drug delivery reviews.
[8] J. Crison,et al. A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability , 1995, Pharmaceutical Research.
[9] A. Noyes,et al. The rate of solution of solid substances in their own solutions , 1897 .
[10] S. H. Fox. The Theory and Practice of Industrial Pharmacy , 1970 .
[11] J. Dressman,et al. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. , 1997, Advanced drug delivery reviews.
[12] J. Carstensen,et al. Advanced Pharmaceutical Solids , 2000 .
[13] Maribel Rios,et al. Developments in powder flow testing , 2006 .
[14] G. Amidon,et al. Physicochemical model for dose-dependent drug absorption. , 1984, Journal of pharmaceutical sciences.
[15] Sunisha Kulkarni,et al. PREFORMULATION- A FOUNDATION FOR FORMULATION DEVELOPMENT , 2015 .
[16] K. C. James,et al. Solubility and Related Properties , 1986 .
[17] P. Sinko. Martin's Physical Pharmacy and Pharmaceutical Sciences , 2005 .
[18] S. Patil,et al. Formulation And Evaluation Of Anti-Ulcer Floating Tablet Using Swellable Polymers , 2014 .
[19] N. K. Freeman. Infrared spectrometry. , 1956, Advances in biological and medical physics.
[20] J. Carstensen,et al. Limits to the concept of solid-state stability. , 1987, Journal of pharmaceutical sciences.
[21] J. Carstensen,et al. The state of water in drug decomposition in the moist solid state: Description and modelling , 1992 .
[22] Gita Chaurasia. A REVIEW ON PHARMACEUTICAL PREFORMULATION STUDIES IN FORMULATION AND DEVELOPMENT OF NEW DRUG MOLECULES , 2016 .
[23] Louis Pasteur,et al. COMPATIBILITY STUDIES OF INDAPAMIDE/PHARMACEUTICAL EXCIPIENTS USED IN TABLET PREFORMULATION , 2012 .
[24] R L Carr,et al. EVALUATING FLOW PROPERTIES OF SOLIDS , 1965 .
[25] J. Haleblian,et al. Characterization of habits and crystalline modification of solids and their pharmaceutical applications. , 1975, Journal of pharmaceutical sciences.
[26] D. Mishra. A VALIDATED STABILITY INDICATING ASSAY METHOD OF ZIDOVUDINE BY UV-VISIBLE SPECTROPHOTOMETER , 2015 .
[27] Sarfaraz K. Niazi. Handbook of Preformulation: Chemical, Biological, and Botanical Drugs , 2006 .
[28] G. S. Banker,et al. Modern Pharmaceutics, Fourth Edition , 2002 .
[29] K. Seddon. Pseudopolymorph: A Polemic , 2004 .
[30] J. Mullin. Crystal size and size distribution : the role of test sieving , 1993 .
[31] Stanley A. Kaplan,et al. Biopharmaceutical Considerations in Drug Formulation Design and Evaluation , 1972 .
[32] K. Morris. STRUCTURAL ASPECTS OF HYDRATES AND SOLVATES , 1999 .