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Journal of Pharmaceutical Sciences|October 25, 2024
Microscope-enabled disc dissolution system: Concordance between drug and polymer dissolution from an amorphous solid dispersion disc and visual disc degradationShuaiqian Men, James E PolliJournal of Pharmaceutical Sciences|August 18, 2025
Transient pH film model for in vitro powder dissolution of weakly acidic drugs into buffer: Consideration of surface acidification and comparison to conventional film modelRoshni P Patel, James E PolliPharmaceutics|November 27, 2024
Screening of Polymers for Oral Ritonavir Amorphous Solid Dispersions by Film CastingAyse Nur Oktay, James E PolliTurkish Journal of Pharmaceutical Sciences|September 8, 2025
Comparison of In Vitro and In Vivo Dissolution of Norvir® Oral Powder: In Vivo Relevance of a too Rapid In Vitro Dissolution TestAyşe Nur Oktay, James E PolliInternational Journal of Pharmaceutics|July 15, 2022
Comparison of a single pharmaceutical surfactant versus intestinal biorelevant media for etravirine dissolution: Role and impact of micelle diffusivityAyse Nur Oktay, James E PolliInternational Journal of Pharmaceutics|November 12, 2025
Comparison of the z-factor and Polli dissolution rate coefficient for monodisperse powdersRoshni P Patel, James E PolliInternational Journal of Pharmaceutics|June 3, 2025
Impact of antioxidant addition on drug dissolution: Implications for NDSRI mitigation biowaiversRutu R Valapil, James E PolliJournal of Pharmaceutical Sciences|March 29, 2026
Transient pH film model for in vitro powder dissolution of weakly basic drugs into buffer and comparison to conventional film modelRoshni P Patel, James E PolliInternational Journal of Pharmaceutics|September 27, 2025
Formulation optimization of ritonavir tablets containing spray dried dispersion from HPMCAS-L or PVP-VA and comparative dissolution/permeation performanceAyse Nur Oktay, James E PolliPageof 18