An updated overview with simple and practical approach for developing in vitro–in vivo correlation
- 26 April 2018
- journal article
- research article
- Published by Wiley in Drug Development Research
- Vol. 79 (3) , 97-110
Abstract
Preclinical Research & Development An in vitro–in vivo correlation (IVIVC) is as a predictive mathematical model that demonstrates a key role in the development, advancement, evaluation and optimization of extended release, modified release and immediate release pharmaceutical formulations. A validated IVIVC model can serve as a surrogate for bioequivalence studies and subsequently save time, effort and expenditure during pharmaceutical product development. This review discusses about different levels of correlations, general approaches to develop an IVIVC by mathematical modelling, validation, data analysis and various applications. In the current setting, the dearth of success associated with IVIVC is due to complexity of underlying scientific principles as well as the practice of fitting/matching in vivo plasma level‐time data with in vitro dissolution profile. Hence, a simple, straightforward practical means to predict plasma drug levels by convolution technique and percentage drug absorbed computed from in vitro dissolution profile based on deconvolution method are illustrated. The bioavailability/bioequivalence assessment and evaluation are frequently validated by the pharmacokinetic parameters such as maximum concentration, time to reach maximum concentration, and area under the curve. The implementation of a quality by design manufacturing based on in vivo bioavailability and clinically relevant dissolution specification are recommended because corresponding design safe space will guarantee that all batches from relevant products are met with sufficient quality and bioperformance. Recently, United States Food and Drug Administration and European Medicines Agency have proposed that in silico/physiologically based pharmacokinetic modelling can be used in decision making during preclinical experiments as well as to recognize the dissolution profiles that can forecast and ensure the desired clinical performance.Keywords
This publication has 51 references indexed in Scilit:
- In Vitro-In Vivo Correlation (IVIVC) and Determining Drug Concentrations in Blood from Dissolution Testing – A Simple and Practical Approach~!2009-10-30~!2010-01-04~!2010-04-29~!The Open Drug Delivery Journal, 2010
- Preparation and Evaluation of Fast-Disintegrating Effervescent Tablets of GlibenclamideDrug Development and Industrial Pharmacy, 2009
- A century of dissolution research: From Noyes and Whitney to the Biopharmaceutics Classification SystemInternational Journal of Pharmaceutics, 2006
- Once-a-Day Extended-Release Dosage form of Divalproex Sodium III: Development and Validation of a Level A in Vitro–in Vivo Correlation (IVIVC)Journal of Pharmaceutical Sciences, 2005
- Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compoundsEuropean Journal of Pharmaceutics and Biopharmaceutics, 2005
- Application of in vitro–in vivo correlations (IVIVC) in setting formulation release specificationsBiopharmaceutics & Drug Disposition, 2000
- Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tractAdvanced Drug Delivery Reviews, 1997
- Mechanisms of solute release from porous hydrophilic polymersInternational Journal of Pharmaceutics, 1983
- Some Factors Affecting the Release of a Water-Soluble Drug from a Compressed Hydrophilic MatrixJournal of Pharmaceutical Sciences, 1966
- Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matricesJournal of Pharmaceutical Sciences, 1963