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James Polli
James Polli
Endowed Professor of Pharmaceutical Sciences, University of Maryland
Verified email at rx.umaryland.edu - Homepage
Title
Cited by
Cited by
Year
Understanding pharmaceutical quality by design
LX Yu, G Amidon, MA Khan, SW Hoag, J Polli, GK Raju, J Woodcock
The AAPS journal 16, 771-783, 2014
12252014
Biopharmaceutics classification system: the scientific basis for biowaiver extensions
JE Polli, LX Yu, MU Mehta, GL Amidon, H Zhao, LJ Lesko, ML Chen, ...
Kluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation …, 2002
9122002
Effects of nonionic surfactants on membrane transporters in Caco-2 cell monolayers
BD Rege, JPY Kao, JE Polli
European journal of pharmaceutical sciences 16 (4-5), 237-246, 2002
6062002
Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets
JE Polli, GS Rekhi, LL Augsburger, VP Shah
Journal of pharmaceutical sciences 86 (6), 690-700, 1997
4651997
Recent advances in ligand-based drug design: relevance and utility of the conformationally sampled pharmacophore approach
C Acharya, A Coop, J E Polli, A D MacKerell
Current computer-aided drug design 7 (1), 10-22, 2011
2982011
Biowaiver monographs for immediate release solid oral dosage forms: Diclofenac sodium and diclofenac potassium
B Chuasuwan, V Binjesoh, JE Polli, H Zhang, GL Amidon, HE Junginger, ...
Journal of pharmaceutical sciences 98 (4), 1206-1219, 2009
2382009
Effect of common excipients on Caco-2 transport of low-permeability drugs
BD Rege, XY Lawrence, AS Hussain, JE Polli
Journal of pharmaceutical sciences 90 (11), 1776-1786, 2001
2352001
In Vitro Studies are Sometimes Better than Conventional Human Pharmacokinetic In Vivo Studies in Assessing Bioequivalence of Immediate-Release Solid Oral …
JE Polli
The AAPS journal 10, 289-299, 2008
2202008
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug target
A Balakrishnan, JE Polli
Molecular pharmaceutics 3 (3), 223-230, 2006
2022006
The solute carrier family 10 (SLC10): beyond bile acid transport
TC Da Silva, JE Polli, PW Swaan
Molecular aspects of medicine 34 (2-3), 252-269, 2013
1952013
Rapid identification of P-glycoprotein substrates and inhibitors
C Chang, PM Bahadduri, JE Polli, PW Swaan, S Ekins
Drug metabolism and disposition 34 (12), 1976-1984, 2006
1872006
Surfactant-mediated dissolution: contributions of solubility enhancement and relatively low micelle diffusivity
A Balakrishnan, BD Rege, GL Amidon, JE Polli
Journal of pharmaceutical sciences 93 (8), 2064-2075, 2004
1792004
The use of BDDCS in classifying the permeability of marketed drugs
LZ Benet, GL Amidon, DM Barends, H Lennernäs, JE Polli, VP Shah, ...
Pharmaceutical research 25, 483-488, 2008
1782008
Summary workshop report: biopharmaceutics classification system—implementation challenges and extension opportunities
JE Polli, XY Lawrence, JA Cook, GL Amidon, RT Borchardt, BA Burnside, ...
Journal of pharmaceutical sciences 93 (6), 1375-1381, 2004
1682004
Influence of passive permeability on apparent P-glycoprotein kinetics
KA Lentz, JW Polli, SA Wring, JE Humphreys, JE Polli
Pharmaceutical research 17, 1456-1460, 2000
1482000
Increased acyclovir oral bioavailability via a bile acid conjugate
S Tolle-Sander, KA Lentz, DY Maeda, A Coop, JE Polli
Molecular pharmaceutics 1 (1), 40-48, 2004
1442004
Lack of medication dose uniformity in commonly split tablets
J Teng, CK Song, RL Williams, JE Polli
Journal of the American Pharmaceutical Association (1996) 42 (2), 195-199, 2002
1342002
Transport of poly amidoamine dendrimers across Madin–Darby canine kidney cells
F Tajarobi, M El-Sayed, BD Rege, JE Polli, H Ghandehari
International journal of pharmaceutics 215 (1-2), 263-267, 2001
1312001
Structure–activity relationship for FDA approved drugs as inhibitors of the human sodium taurocholate cotransporting polypeptide (NTCP)
Z Dong, S Ekins, JE Polli
Molecular pharmaceutics 10 (3), 1008-1019, 2013
1262013
Prediction of dissolution–absorption relationships from a dissolution/Caco-2 system
MJ Ginski, JE Polli
International journal of pharmaceutics 177 (1), 117-125, 1999
1181999
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