Modeling and comparison of dissolution profiles.

By P. Costa, J. M. Lobo. European Journal of Pharmaceutical Sciences, 2001

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Meticulous Overview on the Controlled Release Fertilizers (2014, background): “where a refers to a constant incorporating structural and geometric characteristics of the given active substance, n is the release exponent indicative of the releasemechanism, and t is fractional release of active substance [M t /M ∞ ] described in (6) above [40].”
Applied Concepts in PBPK Modeling: How to Build a PBPK/PD Model (2016, neutral): “As an alternative to a direct correlation between in vitro and in vivo concentrations, it is possible to include dissolution functions in the GI compartments of PBPK models to account for the disintegration and dissolution processes in the GI tract.(40) The inclusion of such dissolution profiles in ”
DDSolver: An Add-In Program for Modeling and Comparison of Drug Dissolution Profiles (2010, background): “f1 0 1⁄4 Pn t1⁄41 Rt Tt j j= Pn t1⁄41 Rt þ Tt ð Þ=2 100 DD_f1cp (13)”
Biological Activities and Application of Marine Polysaccharides (2017, methodology): “Langmuir, Freundlich and Temkin equilibrium sorption isotherms [30] were used for the mathematical description of the adsorption equilibrium of Cr(VI) ions on CH or CHM adsorbents.”
Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability (2014, background): “[6] Costa P, Sousa Lobo JM.”