Search Results - "Aungst, B."
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Intestinal permeation enhancers
Published in Journal of pharmaceutical sciences (01-04-2000)“…This review addresses the field of improving oral bioavailability through the use of excipients that increase intestinal membrane permeability. The critical…”
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Novel formulation strategies for improving oral bioavailability of drugs with poor membrane permeation or presystemic metabolism
Published in Journal of pharmaceutical sciences (01-10-1993)“…The oral route is most preferred for chronic drug therapy. Poor oral bioavailability has the consequences of more variable and poorly controlled plasma…”
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Possible involvement of multiple P-glycoprotein-mediated efflux systems in the transport of verapamil and other organic cations across rat intestine
Published in Pharmaceutical research (01-09-1995)“…We investigated the intestinal transport of verapamil, chlorpromazine, and propantheline, particularly their P-glycoprotein-mediated secretion. Permeation of…”
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The influence of donor and reservoir additives on Caco-2 permeability and secretory transport of HIV protease inhibitors and other lipophilic compounds
Published in Pharmaceutical research (01-10-2000)“…To optimize the conditions for determining Caco-2 permeation of HIV protease inhibitors and other lipophilic compounds, and to compare cyclic urea HIV protease…”
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P-glycoprotein, secretory transport, and other barriers to the oral delivery of anti-HIV drugs
Published in Advanced drug delivery reviews (18-10-1999)“…Orally administered anti-HIV drugs must be adequately and consistently absorbed for therapy to be successful. This review discusses the barriers to achieving…”
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Discovery of 1-[3-(Aminomethyl)phenyl]-N-[3-fluoro-2‘-(methylsulfonyl)- [1,1‘-biphenyl]-4-yl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (DPC423), a Highly Potent, Selective, and Orally Bioavailable Inhibitor of Blood Coagulation Factor Xa
Published in Journal of medicinal chemistry (15-02-2001)“…Factor Xa (fXa) plays a critical role in the coagulation cascade, serving as the point of convergence of the intrinsic and extrinsic pathways. Together with…”
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Comparison of nasal, rectal, buccal, sublingual and intramuscular insulin efficacy and the effects of a bile salt absorption promoter
Published in The Journal of pharmacology and experimental therapeutics (01-01-1988)“…The purpose of this investigation was to develop a method to quantitate insulin absorption, and to compare insulin absorption from various noninjection sites…”
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Structure/effect studies of fatty acid isomers as skin penetration enhancers and skin irritants
Published in Pharmaceutical research (01-03-1989)“…Comparisons were made of branched vs unbranched saturated fatty acids and cis vs trans unsaturated fatty acids as skin penetration enhancers and primary skin…”
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The secretory intestinal transport of some beta-lactam antibiotics and anionic compounds: a mechanism contributing to poor oral absorption
Published in The Journal of pharmacology and experimental therapeutics (01-07-1996)“…The mechanisms of intestinal permeation of several beta-lactam antibiotics and anionic compounds were studied in vitro using excised rat intestinal segments…”
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Intestinal absorption barriers and transport mechanisms, including secretory transport, for a cyclic peptide, fibrinogen antagonist
Published in Pharmaceutical research (1996)“…The intestinal absorption of DMP 728, a cyclic peptide fibrinogen antagonist, was examined with the goals of identifying the cause(s) of its low oral…”
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Intranasal absorption of oxymorphone
Published in Journal of pharmaceutical sciences (01-08-1997)“…The nasal bioavailability of oxymorphone HCI was determined. Rats were surgically prepared to isolate the nasal cavity, into which a solution of oxymorphone…”
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Amphiphilic vehicles improve the oral bioavailability of a poorly soluble HIV protease inhibitor at high doses
Published in International journal of pharmaceutics (10-10-1997)“…DMP 323 is the first clinical candidate from a novel series of HIV protease inhibitors having a cyclic urea structural backbone. In dogs dosed with…”
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Restricted intestinal absorption of some β-lactam antibiotics by an energy-dependent efflux system in rat intestine
Published in Pharmaceutical research (01-05-1997)“…The purpose of this study was to examine factors limiting the intestinal absorption of orally inactive beta-lactam antibiotics. Permeation behaviors of various…”
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Effects of structural modifications on the intestinal permeability of angiotensin II receptor antagonists and the correlation of in vitro, in situ, and in vivo absorption
Published in Pharmaceutical research (01-02-1996)“…The effects of structural modifications on the membrane permeability of angiotensin II (Ang II) receptor antagonists and the usefulness of in vitro and in situ…”
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Sustained propranolol delivery and increased oral bioavailability in dogs given a propranolol laurate salt
Published in Pharmaceutical research (01-11-1992)Get full text
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The effect of absorption enhancers on the oral absorption of the GP IIB/IIIA receptor antagonist, DMP 728, in rats and dogs
Published in Pharmaceutical research (01-12-1995)Get full text
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The de novo design and synthesis of cyclic urea inhibitors of factor Xa : Optimization of the S4 ligand
Published in Bioorganic & medicinal chemistry letters (07-02-2000)“…In this report refinements to the S4 ligand group leads to compound 19, an inhibitor of fXa with good potency in vitro and an improved pharmacokinetic profile…”
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Intranasal absorption of the platelet glycoprotein IIb/IIIa receptor antagonist, DMP 755, and the effect of anesthesia on nasal bioavailability
Published in Journal of pharmaceutical sciences (01-12-1997)“…Intranasal absorption and bioavailability of DMP 755, a peptidomimetic, platelet glycoprotein IIb/IIIa receptor antagonist, were examined in anesthetized and…”
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Region-dependent disappearance of vinblastine in rat small intestine and characterization of its P-glycoprotein-mediated efflux system
Published in European journal of pharmaceutical sciences (01-10-2000)“…This study was aimed to characterize the absorption behavior of vinblastine (VLB), a well-known substrate of P-glycoprotein (P-gp), from rat small intestine,…”
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