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INGENIERÍA 68

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In Vivo Predictive Dissolution and Biopharmaceutic-Based In Silico Model to Explain Bioequivalence Results of Valsartan, a Biopharmaceutics Classification System Class IV Drug See

Effect of thickener on disintegration, dissolution and permeability of common drug products for elderly patients See

Investigation to Explain Bioequivalence Failure in Pravastatin Immediate-Release Products See

Impact on intestinal permeability of pediatric hyperosmolar formulations after dilution: Studies with rat perfusion method See

New mathematical model from dynamic dissolution rate tests See

Determination of intestinal permeability using in situ perfusion model in rats: Challenges and advantages to BCS classification applied to digoxin See

AnInVivoPredictive Dissolution Methodology (iPD Methodology) with a BCS Class IIb Drug Can Predict the In Vivo Bioequivalence Results: Etoricoxib Products See

Comparison of segmental-dependent permeability in human and in situ perfusion model in rat See

In vitro prediction of in vivo absorption of ibuprofen from suspensions through rational choice of dissolution conditions See

Effect of Common Excipients on Intestinal Drug Absorption in Wistar Rats See

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INGENIERÍA 68

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