Etsuo Yonemochi
米持, 悦生, 1961-
Yonemochi, Etsuo, 1961-....
米持, 悦生
VIAF ID: 259715068 (Personal)
Permalink: http://viaf.org/viaf/259715068
Preferred Forms
- 100 0 _ ‡a Etsuo Yonemochi
- 100 1 _ ‡a Yonemochi, Etsuo, ‡d 1961-....
- 100 1 _ ‡a 米持, 悦生
- 100 1 _ ‡a 米持, 悦生 ‡d 1961-
- 100 1 _ ‡a 米持, 悦生, ‡d 1961-
4xx's: Alternate Name Forms (9)
Works
Title | Sources |
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Applicability of DPI formulations for novel neurokinin receptor antagonist | |
Application and mechanism of inhalation profile improvement of DPI formulations by mechanofusion with magnesium stearate | |
Application of eudragit RS to thermo-sensitive drug delivery systems. I. Thermo-sensitive drug release from acetaminophen matrix tablets consisting of eudragit RS/PEG 400 blend polymers | |
Applying terahertz technology for nondestructive detection of crack initiation in a film-coated layer on a swelling tablet | |
Characterization and Quality Control of Pharmaceutical Cocrystals | |
Characterization of complexes between phenethylamine enantiomers and β-cyclodextrin derivatives by capillary electrophoresis-Determination of binding constants and complex mobilities. | |
Characterization of polymorphs of a novel quinolinone derivative, TA-270 (4-hydroxy-1-methyl-3-octyloxy-7-sinapinoylamino-2(1H)-quinolinone) | |
Cocrystallization and amorphization induced by drug-excipient interaction improves the physical properties of acyclovir. | |
Component crystallization and physical collapse during freeze-drying of L-arginine-citric acid mixtures | |
Crystal Structure Determination of Dimenhydrinate after More than 60 Years: Solving Salt–Cocrystal Ambiguity via Solid-State Characterizations and Solubility Study | |
Development of a rapid process monitoring method for dry-coated tableting process by using near-infrared spectroscopy. | |
Development of fast disintegrating compressed tablets using amino acid as disintegration accelerator: evaluation of wetting and disintegration of tablet on the basis of surface free energy | |
Development of microparticles coated with poly-γ-glutamic acid to improve oral absorption of a poorly water-soluble drug | |
Differences in crystallization behavior between quenched and ground amorphous ursodeoxycholic acid | |
Do amorphous troglitazones prepared from two diastereomer-pairs have the same molecular mobility and crystallization rate at the surface? | |
Effect of physical properties of troglitazone crystal on the molecular interaction with PVP during heating | |
Effect of Polymers and Storage Relative Humidity on Amorphous Rebamipide and Its Solid Dispersion Transformation: Multiple Spectra Chemometrics of Powder X-Ray Diffraction and Near-Infrared Spectroscopy | |
The effect of structurally related impurities on crystallinity reduction of sulfamethazine by grinding. | |
Effect of sulfobutyl ether-β-cyclodextrin and propylene glycol alginate on the solubility of clozapine | |
Effect of the type of lubricant on the characteristics of orally disintegrating tablets manufactured using the phase transition of sugar alcohol | |
Effect of water-soluble carriers on dissolution characteristics of nifedipine solid dispersions | |
Effects of formulation and process factors on the crystal structure of freeze-dried Myo-inositol | |
Effects of solute miscibility on the micro- and macroscopic structural integrity of freeze-dried solids | |
Effects of sugar ester and hydroxypropyl methylcellulose on the physicochemical stability of amorphous cefditoren pivoxil in aqueous suspension | |
Effects of water content in physical mixture and heating temperature on crystallinity of troglitazone-PVP K30 solid dispersions prepared by closed melting method | |
Enhanced dissolution and skin permeation profiles of epalrestat with β-cyclodextrin derivatives using a cogrinding method. | |
Epalrestat tetra-hydro-furan monosolvate: crystal structure and phase transition | |
Estimation of initial dissolution rate of drug substance by thermal analysis: application for carbamazepine hydrate | |
Evaluation of amorphous ursodeoxycholic acid by thermal methods | |
Evaluation of rapidly disintegrating tablets containing glycine and carboxymethylcellulose | |
Evaluation of solid dispersions on a molecular level by the Raman mapping technique | |
Evaluation of the crystalline and amorphous states of drug products by nanothermal analysis and Raman imaging | |
Evaluation of the physical properties of dry surface-modified ibuprofen using a powder rheometer (FT4) and analysis of the influence of pharmaceutical additives on improvement of the powder flowability | |
Factors affecting the apparent solubility of ursodeoxycholic acid in the grinding process | |
Fluorometric Studies of Pyrene Adsorption on Porous Crystalline Cellulose | |
Fluorometric study of the molecular states of 2,5-diphenyloxazole in ground mixtures with gamma-cyclodextrin | |
Formulation design of a novel fast-disintegrating tablet | |
Freeze-drying of proteins with glass-forming oligosaccharide-derived sugar alcohols | |
Glass-state amorphous salt solids formed by freeze-drying of amines and hydroxy carboxylic acids: effect of hydrogen-bonding and electrostatic interactions | |
The importance of binder moisture content in Metformin HCL high-dose formulations prepared by moist aqueous granulation (MAG). | |
Importance of excipient wettability on tablet characteristics prepared by moisture activated dry granulation (MADG). | |
In vivo siRNA delivery system for targeting to the liver by poly-l-glutamic acid-coated lipoplex | |
Interaction of microcrystalline cellulose and water in granules prepared by a high-shear mixer | |
Investigation of the dynamic process during spray-drying to improve aerodynamic performance of inhalation particles. | |
Kiso kara manabu seizaika no saiensu. | |
Kotai iyakuhin no bussei hyoka. | |
Low-density microparticles with petaloid surface structure for pulmonary drug delivery | |
Mechanisms for Improved Hygroscopicity of L-Arginine Valproate Revealed by X-Ray Single Crystal Structure Analysis. | |
Microscopic molecular mobility of amorphous AG-041R measured by solid-state 13C NMR. | |
Molecular properties of propranolol hydrochloride prepared as drug-resin complexes | |
New approach to optimizing risk management of the sticking problem using scale-independent critical material attributes and the quantitative process parameter | |
A new solvate of epalerstat, a drug for diabetic neuropathy. | |
Novel approach to DPI carrier lactose with mechanofusion process with additives and evaluation by IGC. | |
Novel approach to evaluating granulation and segregation level considering the contribution of hydroxypropyl cellulose to the surface property change of granules | |
Novel, lean and environment-friendly granulation method: Green fluidized bed granulation (GFBG) | |
Optimization of primary drying condition for pharmaceutical lyophilization using a novel simulation program with a predictive model for dry layer resistance | |
Physicochemical and crystal structure analysis of pranlukast pseudo-polymorphs II: Solvate and cocrystal | |
Physicochemical properties of amorphous clarithromycin obtained by grinding and spray drying | |
Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass | |
Potential of synchrotron X-ray powder diffractometry for detection and quantification of small amounts of crystalline drug substances in pharmaceutical tablets | |
Practical approach for measuring heat capacity of pharmaceutical crystals/glasses by modulated-temperature differential scanning calorimetry | |
Quantitative determination of amorphous nicardipine hydrochloride in long acting formula (NIC-LA) using light anhydrous silicic acid | |
Quantitative relationship between solubility, initial dissolution rate and heat of solution of chiral drugs. | |
Reevaluation of solubility of tolbutamide and polymorphic transformation from Form I to unknown crystal form. | |
Refarensu butsuri kagaku. | |
Relationship between crystallization tendencies during cooling from melt and isothermal storage: toward a general understanding of physical stability of pharmaceutical glasses | |
Sequential intravenous injection of anionic polymer and cationic lipoplex of siRNA could effectively deliver siRNA to the liver | |
siRNA delivery to lung-metastasized tumor by systemic injection with cationic liposomes | |
Solid-state 13C NMR study of indomethacin polymorphism | |
Solid-state fluorescence study of naphthalene adsorption on porous material. | |
Solid states fluorescence study of p-dimethylaminobenzonitrile by co-grinding with cyclodextrins | |
Solubility Improvement of Benexate through Salt Formation Using Artificial Sweetener. | |
Stabilization of protein structure in freeze-dried amorphous organic acid buffer salts. | |
Study of the pseudo-crystalline transformation from form i to form II of thiamine hydrochloride (vitamin B(1)) | |
Studying the morphology of lyophilized protein solids using X-ray micro-CT: effect of post-freeze annealing and controlled nucleation | |
Swelling kinetics of spray-dried chitosan acetate assessed by magnetic resonance imaging and their relation to drug release kinetics of chitosan matrix tablets | |
Synthesis and Characterization of Cholesteryl Conjugated Lysozyme (CHLysozyme) | |
Triboelectrification of active pharmaceutical ingredients: week acids and their salts | |
Tumor delivery of liposomal doxorubicin prepared with poly-L-glutamic acid as a drug-trapping agent. | |
Uniformity and physical states of troglitazone in solid dispersions determined by electron probe microanalysis and microthermal analysis | |
Water sorption and near IR spectroscopy to study the differences between microcrystalline cellulose and silicified microcrystalline cellulose before and after wet granulation | |
Zoledronic acid enhances antitumor efficacy of liposomal doxorubicin | |
レファレンス物理化学 | |
固体医薬品の物性評価 = Pharmaceutical Profiling | |
基礎から学ぶ製剤化のサイエンス |