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Pharmaceutical Research|March 24, 2005
pH-dependent dissolution in vitro and absorption in vivo of weakly basic drugs: development of a canine modelRong Zhou, Paul Moench, Christopher Heran, et al.Pharmaceutical Research|March 24, 2005
A randomly coiled, high-molecular-weight polypeptide exhibits increased paracellular diffusion in vitro and in situ relative to the highly ordered alpha-helix conformerNazila Salamat-Miller, Montakarn Chittchang, Ashim K Mitra, et al.Pharmaceutical Research|February 1, 1992
Cutaneous metabolism of nitroglycerin in vitro. I. Homogenized versus intact skinN Higo, R S Hinz, D T Lau, et al.Pharmaceutical Research|February 1, 1992
Biodegradable pseudolatexes: the chemical stability of poly(D,L-lactide) and poly(epsilon-caprolactone) nanoparticles in aqueous mediaM D Coffin, J W McGinityPharmaceutical Research|February 1, 1992
Development of extended-release solid dispersions of nonsteroidal antiinflammatory drugs with aqueous polymeric dispersions: optimization of drug release via a curve-fitting techniqueC Ho, G C HwangPharmaceutical Research|February 1, 1992
Bioavailability of leuprolide acetate following nasal and inhalation delivery to rats and healthy humansA Adjei, D Sundberg, J Miller, et al.Pharmaceutical Research|June 8, 2004
Correction of permeability with pore radius of tight junctions in Caco-2 monolayers improves the prediction of the dose fraction of hydrophilic drugs absorbed by humansRyoichi Saitoh, Kiyohiko Sugano, Noriyuki Takata, et al.Pharmaceutical Research|June 8, 2004
Urinary excretion: does it accurately reflect relative differences in bioavailability/systemic exposure when renal clearance is nonlinear?Gary A Thompson, Roger D ToothakerPharmaceutical Research|June 8, 2004
Uptake of melatonin into the cerebrospinal fluid after nasal and intravenous delivery: studies in rats and comparison with a human studyMascha P van den Berg, Paul Merkus, Stefan G Romeijn, et al.Pharmaceutical Research|June 8, 2004
Predicting P-glycoprotein effects on oral absorption: correlation of transport in Caco-2 with drug pharmacokinetics in wild-type and mdr1a(-/-) mice in vivoAndrew Collett, Jolanta Tanianis-Hughes, David Hallifax, et al.Pageof 960