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Confined crystallization of fenofibrate in nanoporous silica.

Confined crystallization of fenofibrate in nanoporous silica.

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(19) F NMR Spectroscopy as a Highly Sensitive Method for the Direct Monitoring of Confined Crystallization within Nanoporous Materials.Core-Shell Composite Hydrogels for Controlled Nanocrystal Formation and Release of Hydrophobic Active Pharmaceutical Ingredients.

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P2860

Confined crystallization of fenofibrate in nanoporous silica.

http://www.wikidata.org/entity/Q31037436

description

2015 nî lūn-bûn

@nan

2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Confined crystallization of fenofibrate in nanoporous silica.

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Confined crystallization of fenofibrate in nanoporous silica.

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Confined crystallization of fenofibrate in nanoporous silica.

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Confined crystallization of fenofibrate in nanoporous silica.

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Confined crystallization of fenofibrate in nanoporous silica.

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Confined crystallization of fenofibrate in nanoporous silica.

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Confined crystallization of fenofibrate in nanoporous silica.

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P2093

A S Myerson

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L M Dwyer

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M O'Mahony

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R G Griffin

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V K Michaelis

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P2860

Manipulating the crystalline state of pharmaceuticals by nanoconfinement.

Preparation and characterization of fenofibrate-loaded nanostructured lipid carriers for oral bioavailability enhancement

Formation of Organic Molecular Nanocrystals under Rigid Confinement with Analysis by Solid State NMR.

Amorphous pharmaceutical solids: preparation, characterization and stabilization.

Solution-based particle formation of pharmaceutical powders by supercritical or compressed fluid CO2 and cryogenic spray-freezing technologies.

Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs.

Solid state amorphization of pharmaceuticals.

Nanocrystal technology, drug delivery and clinical applications.

Nanocrystals: industrially feasible multifunctional formulation technology for poorly soluble actives.

Application of mesoporous silicon dioxide and silicate in oral amorphous drug delivery systems.

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7922-7929

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scholarly article

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10.1039/C5CE01148E

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41

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17

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4711376

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