Search Results - "Tomono, Kazuo"
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Novel pharmaceutical cocrystal consisting of paracetamol and trimethylglycine, a new promising cocrystal former
Published in International journal of pharmaceutics (01-10-2014)“…[Display omitted] Paracetamol (APAP), a frequently used antipyretic drug, has poor compression moldability. In this study, we identified a novel cocrystal…”
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Determination and prediction of solubilities of active pharmaceutical ingredients in selected organic solvents
Published in Fluid phase equilibria (01-11-2015)“…•This study investigates measurements of solubilities of APIs.•Solubilities of APIs in different organic solvents were measured.•Solubilities of famotidine…”
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3
Comparison of the relative stability of pharmaceutical cocrystals consisting of paracetamol and dicarboxylic acids
Published in Drug development and industrial pharmacy (03-04-2018)“…Objective: The aim of this study is to evaluate the relative stability of pharmaceutical cocrystals consisting of paracetamol (APAP) and oxalic acid (OXA) or…”
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Pharmaceutical evaluation of steroidal ointments by ATR-IR chemical imaging: Distribution of active and inactive pharmaceutical ingredients
Published in International journal of pharmaceutics (15-04-2012)“…We recently used micro attenuated total reflection infrared (ATR-IR) spectroscopy to conduct imaging analysis of ointments and evaluate the distributions of…”
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5
Involvement of a proton-coupled organic cation antiporter in the blood-brain barrier transport of amantadine
Published in Biopharmaceutics & drug disposition (01-09-2016)“…The blood‐to‐brain transport of amantadine, a weak N‐methyl‐d‐aspartate (NMDA) antagonist, has been shown previously to participate in the cationic…”
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Comparative pharmaceutical evaluation of brand and generic clobetasone butyrate ointments
Published in International journal of pharmaceutics (10-03-2014)“…In the present study, we performed comprehensive pharmaceutical evaluation among an original clobetasone butyrate (CLB) ointment product and three generic…”
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Measurement and correlation of solubilities of the poorly water-soluble pharmaceutical compound etodolac by addition of co-solvents
Published in Fluid phase equilibria (15-11-2013)“…•This study investigates solubilities of etodolac and enhancements of them by adding co-solvents.•Six cyclodextrins (CDs): α, β, γ-CD, 2-HP-β-CD, 2-HE-β-CD,…”
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Homogeneous Nanoparticles To Enhance the Efficiency of a Hydrophobic Drug, Antihyperlipidemic Probucol, Characterized by Solid-State NMR
Published in Molecular pharmaceutics (01-02-2010)“…A low absorption in the gastrointestinal tract of hydrophobic pharmaceutical compounds in use today considerably limits their bioavailability, and therefore…”
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Pharmaceutical evaluation of atorvastatin calcium tablets available on the Internet: A preliminary investigation of substandard medicines in Japan
Published in Journal of drug delivery science and technology (01-02-2016)“…Substandard medicine is a type of substandard/spurious/falsely labeled/falsified/counterfeit (SSFFC) drug as defined by the WHO that has permeated the…”
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Effects of slow-releasing colistin microspheres on endotoxin-induced sepsis
Published in Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy (01-08-2013)“…Abstract Lipopolysaccharide (LPS) is a major contributing factor to endotoxic shock. Colistin specifically binds to LPS. However, it has the disadvantages that…”
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11
Studies on Uniformity of the Active Ingredients in Acetaminophen Suppositories Re-solidified after Melting under High Temperature Conditions
Published in Chemical & pharmaceutical bulletin (01-04-2015)“…The target of the present pharmaceutical study was the antipyretic analgesic, acetaminophen; its suppository form is usually split when used in pediatric…”
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Effect of terpenes on the skin permeation of lomerizine dihydrochloride
Published in Journal of pharmacy & pharmaceutical sciences (01-01-2013)“…Lomerizine dihydrochloride (LOM) is a Ca2+ channel blocker used as an antimigraine drug, which is currently administered orally in Japan. We therefore…”
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Formulation and in Vitro Evaluation of Pentazocine Transdermal Delivery System
Published in Biological & Pharmaceutical Bulletin (01-07-2008)“…The aim of this study was to prepare a pentazocine (PTZ) matrix-type transdermal drug delivery system (TDDS) using acrylic pressure-sensitive adhesives. Among…”
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Solubilities of Salicylic Acid in Pure Solvents and Binary Mixtures Containing Cosolvent
Published in Journal of chemical and engineering data (12-02-2009)“…The solubility of salicylic acid in water, methanol, ethanol, ethyl acetate, polyethylene glycol (PEG) 300, and 1,4-dioxane and in various binary solvent…”
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Effect of Particle Size on Skin Permeation and Retention of Piroxicam in Aqueous Suspension
Published in Chemical & Pharmaceutical Bulletin (01-08-2010)“…The effects of particle size on the skin permeation and retention of piroxicam (PXC) in an aqueous suspension were investigated. PXC particles of about 23 nm,…”
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Antagonism of NMDA receptors by butanesulfonyl-homospermine guanidine and neuroprotective effects in in vitro and in vivo
Published in Neuroscience letters (11-01-2012)“…► Polyamine derivative, BsHSPMG inhibited strongly NMDA receptor currents. ► BsHSPMG acts deeply into the channel pore of NMDA receptors containing the…”
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Involvement of an influx transporter in the blood-brain barrier transport of naloxone
Published in Biopharmaceutics & drug disposition (01-05-2010)“…Naloxone, a potent and specific opioid antagonist, has been shown in previous studies to have an influx clearance across the rat blood–brain barrier (BBB) two…”
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Nanoparticle Processing in the Solid State Dramatically Increases the Cell Membrane Permeation of a Cholesterol-Lowering Drug, Probucol
Published in Molecular pharmaceutics (01-06-2009)“…High cholesterol levels (or hypercholesterolemia) are linked with many diseases, particularly with the risk of coronary heart diseases. Probucol is commonly…”
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Determination and correlation of solubilities of famotidine in water + co-solvent mixed solvents
Published in Fluid phase equilibria (15-03-2011)“…This study aims to measure the solubilities of poorly water-soluble drugs and to enhance their solubilities by adding co-solvents. The solubilities were…”
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Characterization of multicomponent crystal formed between indomethacin and lidocaine
Published in Drug development and industrial pharmacy (01-07-2009)“…Purpose: Crystalline complex was formed between indomethacin (IDM) and lidocaine (LDC) at molar ratio 2:1 from ethanol solution. The purpose of this study was…”
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