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PEG liposomalization of paclitaxel improved its in vivo disposition and anti-tumor efficacy

International journal of pharmaceutics, 2011-06, Vol.412 (1), p.132-141

2011

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Gastrointestinal Transit and Drug Absorption

Biological and Pharmaceutical Bulletin, 2002, Vol.25(2), pp.149-164

2002

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Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs

Journal of controlled release, 2006-03, Vol.111 (1), p.56-64

2006

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The relationship between in vivo nasal drug clearance and in vitro nasal mucociliary clearance: Application to the prediction of nasal drug absorption

European journal of pharmaceutical sciences, 2018-05, Vol.117, p.21-26

2018

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In Vitro Evaluation of the Ciliary Beat Frequency of the Rat Nasal Epithelium Using a High-Speed Digital Imaging System

Biological and Pharmaceutical Bulletin, 2013/06/01, Vol.36(6), pp.966-973

2013

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Development of Safe and Potent Oil-in-Water Emulsion of Paclitaxel to Treat Peritoneal Dissemination

Journal of pharmaceutical sciences, 2017-04, Vol.106 (4), p.1143-1148

2017

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Formulation and Evaluation of Paclitaxel-Loaded Polymeric Nanoparticles Composed of Polyethylene Glycol and Polylactic Acid Block Copolymer

Biological and Pharmaceutical Bulletin, 2012/08/01, Vol.35(8), pp.1306-1313

2012

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In vivo anti-tumor effect of PEG liposomal doxorubicin (DOX) in DOX-resistant tumor-bearing mice: Involvement of cytotoxic effect on vascular endothelial cells

Journal of controlled release, 2009-01, Vol.133 (1), p.4-10

2009

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Establishment of new preparation method for solid dispersion formulation of tacrolimus

International journal of pharmaceutics, 2003-11, Vol.267 (1), p.79-91

2003

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A novel approach to overcome multidrug resistance: Utilization of P-gp mediated efflux of paclitaxel to attack neighboring vascular endothelial cells in tumors

European journal of pharmaceutical sciences, 2014-10, Vol.62, p.274-280

2014

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Determinants for in vivo anti-tumor effects of PEG liposomal doxorubicin: Importance of vascular permeability within tumors

International journal of pharmaceutics, 2008-07, Vol.359 (1), p.234-240

2008

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Nanoparticle-Based Passive Drug Targeting to Tumors: Considerations and Implications for Optimization

Biological and Pharmaceutical Bulletin, 2013/05/01, Vol.36(5), pp.698-702

2013

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Interaction of Polyphenols with Proteins: Binding of (−)-Epigallocatechin Gallate to Serum Albumin, Estimated by Induced Circular Dichroism

Chemical and Pharmaceutical Bulletin, 2009/02/01, Vol.57(2), pp.224-228

2009

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Skin permeation of propranolol from polymeric film containing terpene enhancers for transdermal use

International journal of pharmaceutics, 2005-01, Vol.289 (1), p.167-178

2005

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Interaction of Polyphenolic Metabolites with Human Serum Albumin: A Circular Dichroism Study

Chemical and Pharmaceutical Bulletin, 2009/09/01, Vol.57(9), pp.1019-1023

2009

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In vitro–in vivo correlation for wet-milled tablet of poorly water-soluble cilostazol

Journal of controlled release, 2008-08, Vol.130 (1), p.29-37

2008

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Development of Transdermal Therapeutic Formulation of CNS5161, a Novel N-Methyl-D-aspartate Receptor Antagonist, by Utilizing Pressure-Sensitive Adhesives I

Biological and Pharmaceutical Bulletin, 2012/03/01, Vol.35(3), pp.321-328

2012

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Development of transdermal therapeutic formulation of CNS5161, a novel NMDA receptor antagonist, by utilizing pressure-sensitive adhesives II: Improved transdermal absorption and evaluation of efficacy and safety

European journal of pharmaceutical sciences, 2014-02, Vol.52, p.86-94

2014

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In Vitro Evaluation of Nasal Mucociliary Clearance Using Excised Rat Nasal Septum

Biological and Pharmaceutical Bulletin, 2012/06/01, Vol.35(6), pp.889-894

2012

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Quantitative Evaluation of PEPT1 Contribution to Oral Absorption of Cephalexin in Rats

Pharmaceutical research, 2009-01, Vol.26 (1), p.40-50

2009

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Evaluation of in vivo dissolution behavior and GI transit of griseofulvin, a BCS class II drug

International journal of pharmaceutics, 2008-03, Vol.352 (1), p.36-43

2008

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Sex differences in pharmacokinetics of cilostazol in rats

Xenobiotica, 2011-10, Vol.41 (10), p.903-913

2011

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Novel oral formulation safely improving intestinal absorption of poorly absorbable drugs: Utilization of polyamines and bile acids

Journal of controlled release, 2006-03, Vol.111 (1), p.27-34

2006

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Effect of adrenergic stimulation on drug absorption via passive diffusion in Caco-2 cells

International journal of pharmaceutics, 2009-02, Vol.368 (1-2), p.31-36

2009

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Prediction of oral absorption of griseofulvin, a BCS class II drug, based on GITA model: Utilization of a more suitable medium for in-vitro dissolution study

Journal of controlled release, 2007-06, Vol.119 (2), p.222-228

2007

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PEG liposomalization of paclitaxel improved its in vivo disposition and anti-tumor efficacy

Gastrointestinal Transit and Drug Absorption

Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs

The relationship between in vivo nasal drug clearance and in vitro nasal mucociliary clearance: Application to the prediction of nasal drug absorption

In Vitro Evaluation of the Ciliary Beat Frequency of the Rat Nasal Epithelium Using a High-Speed Digital Imaging System

Development of Safe and Potent Oil-in-Water Emulsion of Paclitaxel to Treat Peritoneal Dissemination

Formulation and Evaluation of Paclitaxel-Loaded Polymeric Nanoparticles Composed of Polyethylene Glycol and Polylactic Acid Block Copolymer

In vivo anti-tumor effect of PEG liposomal doxorubicin (DOX) in DOX-resistant tumor-bearing mice: Involvement of cytotoxic effect on vascular endothelial cells

Establishment of new preparation method for solid dispersion formulation of tacrolimus

A novel approach to overcome multidrug resistance: Utilization of P-gp mediated efflux of paclitaxel to attack neighboring vascular endothelial cells in tumors

Determinants for in vivo anti-tumor effects of PEG liposomal doxorubicin: Importance of vascular permeability within tumors

Nanoparticle-Based Passive Drug Targeting to Tumors: Considerations and Implications for Optimization

Interaction of Polyphenols with Proteins: Binding of (−)-Epigallocatechin Gallate to Serum Albumin, Estimated by Induced Circular Dichroism

Skin permeation of propranolol from polymeric film containing terpene enhancers for transdermal use

Interaction of Polyphenolic Metabolites with Human Serum Albumin: A Circular Dichroism Study

In vitro–in vivo correlation for wet-milled tablet of poorly water-soluble cilostazol

Development of Transdermal Therapeutic Formulation of CNS5161, a Novel N-Methyl-D-aspartate Receptor Antagonist, by Utilizing Pressure-Sensitive Adhesives I

Development of transdermal therapeutic formulation of CNS5161, a novel NMDA receptor antagonist, by utilizing pressure-sensitive adhesives II: Improved transdermal absorption and evaluation of efficacy and safety

In Vitro Evaluation of Nasal Mucociliary Clearance Using Excised Rat Nasal Septum

Quantitative Evaluation of PEPT1 Contribution to Oral Absorption of Cephalexin in Rats

Evaluation of in vivo dissolution behavior and GI transit of griseofulvin, a BCS class II drug

Sex differences in pharmacokinetics of cilostazol in rats

Novel oral formulation safely improving intestinal absorption of poorly absorbable drugs: Utilization of polyamines and bile acids

Effect of adrenergic stimulation on drug absorption via passive diffusion in Caco-2 cells

Prediction of oral absorption of griseofulvin, a BCS class II drug, based on GITA model: Utilization of a more suitable medium for in-vitro dissolution study

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