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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 PolliInternational Journal of Pharmaceutics|June 9, 2026
Ritonavir release from spherical amorphous solid dispersions: prediction and observationShuaiqian Men, Daniel Treffer, James E PolliMolecular Pharmaceutics|January 24, 2026
Prediction of Solvent Penetration Rate-Limited Release of Drug from Amorphous Solid Dispersion Discs of Various GeometriesShuaiqian Men, Yuly Chiang Yu, James E PolliDrug Metabolism and Disposition: the Biological Fate of Chemicals|November 9, 2022
Phenobarbital in Nuclear Receptor Activation: An UpdateShuaiqian Men, Hongbing WangNature Machine Intelligence|October 22, 2021
A Versatile Deep Learning Architecture for Classification and Label-Free Prediction of Hyperspectral ImagesBryce Manifold, Shuaiqian Men, Ruoqian Hu, et al.The AAPS Journal|November 17, 2022
A Simple One-Parameter Percent Dissolved Versus Time Dissolution Equation that Accommodates Sink and Non-sink Conditions via Drug Solubility and Dissolution VolumeJames E PolliThe AAPS Journal|May 27, 2008
In vitro studies are sometimes better than conventional human pharmacokinetic in vivo studies in assessing bioequivalence of immediate-release solid oral dosage formsJames E PolliThe Journal of Physical Chemistry. B|September 22, 2022
Quantitative Imaging of Intracellular Density with Ratiometric Stimulated Raman Scattering MicroscopyBenjamin Figueroa, Fiona Xi Xu, Ruoqian Hu, et al.Journal of Pharmaceutical Sciences|April 2, 2011
Synthesis and in vitro characterization of drug conjugates of l-carnitine as potential prodrugs that target human Octn2Lei Diao, James E PolliMolecular Pharmaceutics|June 6, 2006
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug targetAnand Balakrishnan, James E PolliPageof 19