Prediction of in vivo performance of ibuprofen immediate-release products using different dissolution models
暂无分享,去创建一个
L. Emara | N. Taha | F. Abdelfattah | A. Abdou | N. Mursi
[1] L. Emara,et al. Preparation, characterization and in-Vitro/in-Vivo evaluation of meloxicam extruded pellets with enhanced bioavailability and stability , 2020, Drug development and industrial pharmacy.
[2] L. Emara,et al. A novel combination of Soluplus®/Poloxamer for Meloxicam solid dispersions via hot melt extrusion for rapid onset of action. Part 2: comparative bioavailability and IVIVC , 2020, Drug development and industrial pharmacy.
[3] L. Emara,et al. COMPARATIVE IN VITRO DISSOLUTION STUDY ON METFORMIN MARKET PRODUCTS USING DIFFERENT DISSOLUTION APPARATUSES , 2019, International Journal of Pharmacy and Pharmaceutical Sciences.
[4] José Raúl Medina,et al. Comparison of the USP Apparatus 2 and 4 for testing the in vitro release performance of ibuprofen generic suspensions , 2017 .
[5] Sook-Joung Lee,et al. Pharmacokinetic and pharmacodynamic evaluation according to absorption differences in three formulations of ibuprofen , 2017, Drug design, development and therapy.
[6] Geoffrey N. Grove,et al. Characterization and Simulation of Hydrodynamics in the Paddle, Basket and Flow-Through Dissolution Testing Apparatuses - A Review , 2017 .
[7] Kevin G Reuter,et al. USP Apparatus 4: a Valuable In Vitro Tool to Enable Formulation Development of Long-Acting Parenteral (LAP) Nanosuspension Formulations of Poorly Water-Soluble Compounds , 2017, AAPS PharmSciTech.
[8] R. Fassihi,et al. Mechanistic Approach to Understanding the Influence of USP Apparatus I and II on Dissolution Kinetics of Tablets with Different Operating Release Mechanisms , 2016, AAPS PharmSciTech.
[9] Y. Goda,et al. Effects of Pump Pulsation on Hydrodynamic Properties and Dissolution Profiles in Flow-Through Dissolution Systems (USP 4) , 2016, Pharmaceutical Research.
[10] G. Bredael,et al. A Strategy for Quality Control Dissolution Method Development for Immediate-Release Solid Oral Dosage Forms , 2015 .
[11] L. Emara,et al. IN-VITRO DISSOLUTION STUDY OF MELOXICAM IMMEDIATE RELEASE PRODUCTS USING FLOW THROUGH CELL (USP APPARATUS 4) UNDER DIFFERENT OPERATIONAL CONDITIONS , 2014 .
[12] D. Aggarwal,et al. Establishing Prospective IVIVC for Generic Pharmaceuticals: Methodologies Assessment , 2014 .
[13] F. M. Abdelfattah,et al. IN VITRO EVALUATION OF IBUPROFEN HOT-MELT EXTRUDED PELLETS EMPLOYING DIFFERENT DESIGNS OF THE FLOW THROUGH CELL , 2014 .
[14] W. Schlindwein,et al. Comparison of in vitro dissolution tests for commercially available aspirin tablets , 2013 .
[15] A. Bose,et al. Convolution and validation of in vitro–in vivo correlation of water-insoluble sustained-release drug (domperidone) by first-order pharmacokinetic one-compartmental model fitting equation , 2013, European Journal of Drug Metabolism and Pharmacokinetics.
[16] B. K. Reddy,et al. Biopharmaceutics Classification System: A Regulatory Approach , 2011 .
[17] T. Bączek,et al. The influence of averaging procedure on the accuracy of IVIVC predictions: immediate release dosage form case study. , 2010, Journal of pharmaceutical sciences.
[18] K. Rainsford. Ibuprofen: pharmacology, efficacy and safety , 2009, Inflammopharmacology.
[19] M. Viana,et al. Comparison of Three Dissolution Apparatuses for Testing Calcium Phosphate Pellets used as Ibuprofen Delivery Systems , 2009, AAPS PharmSciTech.
[20] L. Emara,et al. Investigation of the Effect of Different Flow-Through Cell Designs on the Release of Diclofenac Sodium SR Tablets , 2009 .
[21] S. Tamilvanan,et al. In vitro and in vivo evaluation of single-unit commercial conventional tablet and sustained-release capsules compared with multiple-unit polystyrene microparticle dosage forms of ibuprofen , 2006, AAPS PharmSciTech.
[22] Limin Zhang,et al. Differences in In Vitro Dissolution Rates Using Single-Point and Multi-Point Sampling , 2007 .
[23] Raimar Löbenberg,et al. Biorelevant dissolution media as a predictive tool for glyburide a class II drug. , 2006, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[24] P. Costa,et al. Modeling and comparison of dissolution profiles. , 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[25] L H Emara,et al. In Vitro-In Vivo Correlation and Comparative Bioavailablity of Vincamine in Prolonged-Release Preparations , 2000, Drug development and industrial pharmacy.
[26] Yi Tsong,et al. fDA Guidance for Industry 1 Dissolution Testing of Immediate Release Solid Oral Dosage Forms , 1997 .
[27] J. W. Moore,et al. Mathematical comparison of dissolution profiles , 1996 .
[28] K. Florey,et al. Analytical profiles of drug substances and excipients , 1992 .