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AAPS Update.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1735, doi. 10.1007/s11095-008-9633-0
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- Article
In Vitro – In Vivo Correlation on Delivery of Drug Candidates to Articular Cartilage.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1641
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Plasmid CpG Depletion Improves Degree and Duration of Tumor Gene Expression After Intravenous Administration of Polyplexes.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1654, doi. 10.1007/s11095-008-9558-7
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Intravesical Treatments of Bladder Cancer: Review.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1500, doi. 10.1007/s11095-008-9566-7
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Pharmacokinetics of the CYP 3A Substrate Simvastatin following Administration of Delayed Versus Immediate Release Oral Dosage Forms.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1591, doi. 10.1007/s11095-007-9519-6
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What is a Suitable Dissolution Method for Drug Nanoparticles?
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1696
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- Article
Dissolution Enhancement by Bio-Inspired Mesocrystals: The Study of Racemic ( R , S )-(±)-Sodium Ibuprofen Dihydrate.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1563
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- Article
Solid Lipid Nanoparticles as Delivery Systems for Bromocriptine.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1521
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Intra and Inter-Molecular Interactions Dictate the Aggregation State of Irinotecan Co-Encapsulated with Floxuridine Inside Liposomes.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1702, doi. 10.1007/s11095-008-9561-z
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- Article
What is a Suitable Dissolution Method for Drug Nanoparticles?
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1696
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- Article
Optimizing Metrics for the Assessment of Bioequivalence Between Topical Drug Products.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1621, doi. 10.1007/s11095-008-9577-4
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- Article
Inhibition of Polymorphic Human Carbonyl Reductase 1 (CBR1) by the Cardioprotectant Flavonoid 7-monohydroxyethyl Rutoside (monoHER).
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1730, doi. 10.1007/s11095-008-9592-5
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Flux Across of Microneedle-treated Skin is Increased by Increasing Charge of Naltrexone and Naltrexol In Vitro.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1677, doi. 10.1007/s11095-008-9578-3
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The Asymmetry of the Unstirred Water Layer in Permeability Experiments.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1714, doi. 10.1007/s11095-008-9573-8
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Scaling Up the Spray Drying Process from Pilot to Production Scale Using an Atomized Droplet Size Criterion.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1610, doi. 10.1007/s11095-008-9565-8
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Dissolution Media Simulating Conditions in the Proximal Human Gastrointestinal Tract: An Update.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1663, doi. 10.1007/s11095-008-9569-4
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- Article
Characterization of the Mechanism of Zidovudine Uptake by Rat Conditionally Immortalized Syncytiotrophoblast Cell Line TR-TBT.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1647, doi. 10.1007/s11095-008-9564-9
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- Article
In Vitro – In Vivo Correlation on Delivery of Drug Candidates to Articular Cartilage.
- Published in:
- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1641
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- Publication type:
- Article
Cytotoxicity of Paclitaxel in Biodegradable Self-Assembled Core-Shell Poly(Lactide-Co-Glycolide Ethylene Oxide Fumarate) Nanoparticles.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1552, doi. 10.1007/s11095-007-9513-z
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- Publication type:
- Article
Dissolution Enhancement by Bio-Inspired Mesocrystals: The Study of Racemic ( R , S )-(±)-Sodium Ibuprofen Dihydrate.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1563
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- Publication type:
- Article
Microdosing Assessment to Evaluate Pharmacokinetics and Drug Metabolism in Rats Using Liquid Chromatography-Tandem Mass Spectrometry.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1572, doi. 10.1007/s11095-008-9555-x
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Evaluation of Direct Transport Pathways of Glycine Receptor Antagonists and an Angiotensin Antagonist from the Nasal Cavity to the Central Nervous System in the Rat Model.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1531, doi. 10.1007/s11095-008-9550-2
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Optimisation of the Caco-2 Permeability Assay Using Experimental Design Methodology.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1544, doi. 10.1007/s11095-008-9556-9
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Prolonging the In Vivo Residence Time of Prostaglandin E<sub>1</sub> with Biodegradable Nanoparticles.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1686, doi. 10.1007/s11095-008-9549-8
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A Comparison of the Pulmonary Bioavailability of Powder and Liquid Aerosol Formulations of Salmon Calcitonin.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1583, doi. 10.1007/s11095-008-9547-x
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The Role of Fines in the Modification of the Fluidization and Dispersion Mechanism Within Dry Powder Inhaler Formulations.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1631, doi. 10.1007/s11095-008-9538-y
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A Novel Design of Artificial Membrane for Improving the PAMPA Model.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1511, doi. 10.1007/s11095-007-9517-8
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Extrinsic Fluorescent Dyes as Tools for Protein Characterization.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1487, doi. 10.1007/s11095-007-9516-9
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- Article
Solid Lipid Nanoparticles as Delivery Systems for Bromocriptine.
- Published in:
- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1521
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- Publication type:
- Article
Angiogenic and Cell Proliferating Action of the Natural Diarylnonanoids, Malabaricone B and Malabaricone C during Healing of Indomethacin-induced Gastric Ulceration.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1601, doi. 10.1007/s11095-007-9512-0
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- Article
Potential Oral Delivery of 7-Ethyl-10-Hydroxy-Camptothecin (SN-38) using Poly(amidoamine) Dendrimers.
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- Pharmaceutical Research, 2008, v. 25, n. 7, p. 1723, doi. 10.1007/s11095-008-9572-9
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- Article