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Release performance of a poorly soluble drug from a novel, Eudragit®-based multi-unit erosion matrix

International journal of pharmaceutics, 2001-02, Vol.213 (1), p.7-12

2001

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Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs

International journal of pharmaceutics, 1994-05, Vol.106 (1), p.15-23

1994

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Controlled Drug Delivery by Biodegradable Poly(Ester) Devices: Different Preparative Approaches

Drug development and industrial pharmacy, 1998-01, Vol.24 (8), p.703-727

1998

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Controlled release of drugs from injectable in situ formed biodegradable PLGA microspheres: effect of various formulation variables

European journal of pharmaceutics and biopharmaceutics, 2000-09, Vol.50 (2), p.257-262

2000

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Controlled-Release Drug Delivery Systems for Prolonged Gastric Residence: An Overview

Drug development and industrial pharmacy, 1996, Vol.22 (6), p.531-539

1996

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Controlled delivery of drugs from a novel injectable in situ formed biodegradable PLGA microsphere system

Journal of microencapsulation, 2000, Vol.17 (3), p.343-362

2000

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Prediction of drug release from hydroxypropyl methylcellulose (HPMC) matrices : effect of polymer concentration

Pharmaceutical research, 1993-11, Vol.10 (11), p.1693-1695

1993

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Factors Affecting the Efficiency of a Self-Emulsifying Oral Delivery System

Drug development and industrial pharmacy, 1997, Vol.23 (8), p.809-816

1997

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Effect of novel penetration enhancers on the transdermal delivery of hydrocortisone: an in vitro species comparison

Journal of controlled release, 1997, Vol.45 (2), p.199-206

1997

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Stability of a hydrophobic drug in presence of hydrous and anhydrous lactose

European journal of pharmaceutics and biopharmaceutics, 1998-09, Vol.46 (2), p.177-182

1998

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Physical and enteric properties of soft gelatin capsules coated with eudragit ® L 30 D-55

International journal of pharmaceutics, 1995-01, Vol.113 (1), p.17-24

1995

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Compatibility Evaluation of Metered-Dose Inhaler Valve Elastomers with Tetrafluoroethane (P134a), a Non-CFC Propellant

Drug development and industrial pharmacy, 1998-01, Vol.24 (4), p.345-352

1998

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Influence of a lipophilic thermal lubricant on the processing conditions and drug release properties of chlorpheniramine maleate tablets prepared by hot-melt extrusion

Journal of drug delivery science and technology, 2004, Vol.14 (4), p.313-318

2004

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Physical-mechanical properties of film-coated soft gelatin capsules

International journal of pharmaceutics, 1996-02, Vol.127 (2), p.203-211

1996

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Effect of formulation and process variables on porosity parameters and release rates from a multi unit erosion matrix of a poorly soluble drug

Journal of controlled release, 2000-01, Vol.63 (1-2), p.201-211

2000

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Effect of buffer constituents on the determination of therapeutic proteins by capillary electrophoresis

Journal of Chromatography A, 1992-09, Vol.608 (1), p.197-204

1992

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N-Methyl-2-Pyrrolidone as a Cosolvent: Relationship of Cosolvent Effect with Solute Polarity and the Presence of Proton-Donating Groups on Model Drug Compounds

Journal of pharmaceutical sciences, 1994-09, Vol.83 (9), p.1213-1216

1994

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Assay of protein drug substances present in solution mixtures by fluorescamine derivatization and capillary electrophoresis

Journal of Chromatography A, 1992-05, Vol.598 (1), p.123-131

1992

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Degradation profile and reversed-phase LC method development of the antiinflammatory drug, Ro 24-5913

Journal of pharmaceutical and biomedical analysis, 1993-10, Vol.11 (10), p.1037-1043

1993

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Biotin uptake and transport across bovine brain microvessel endothelial cell monolayers

Pharmaceutical research, 1993-02, Vol.10 (2), p.282-288

1993

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Compaction Properties of Spheronized Binary Granular Mixtures

Drug development and industrial pharmacy, 1995, Vol.21 (7), p.753-779

1995

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In vitro release of the mTOR inhibitor rapamycin from poly(ethylene glycol)-b-poly(ε-caprolactone) micelles

Journal of controlled release, 2006-01, Vol.110 (2), p.370-377

2006

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Scaleup of immediate release oral solid dosage forms

Pharmaceutical research, 1993-02, Vol.10 (2), p.313-316

1993

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Influence of plasticizers on the mechanical properties of pellets containing Eudragit® RS 30 D

International journal of pharmaceutics, 1997-06, Vol.152 (2), p.153-163

1997

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A biodegradable injectable implant for delivering micro and macromolecules using poly (lactic-co-glycolic) acid (PLGA) copolymers

Journal of controlled release, 1993, Vol.27 (2), p.139-147

1993

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Release performance of a poorly soluble drug from a novel, Eudragit®-based multi-unit erosion matrix

Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs

Controlled Drug Delivery by Biodegradable Poly(Ester) Devices: Different Preparative Approaches

Controlled release of drugs from injectable in situ formed biodegradable PLGA microspheres: effect of various formulation variables

Controlled-Release Drug Delivery Systems for Prolonged Gastric Residence: An Overview

Controlled delivery of drugs from a novel injectable in situ formed biodegradable PLGA microsphere system

Prediction of drug release from hydroxypropyl methylcellulose (HPMC) matrices : effect of polymer concentration

Factors Affecting the Efficiency of a Self-Emulsifying Oral Delivery System

Effect of novel penetration enhancers on the transdermal delivery of hydrocortisone: an in vitro species comparison

Stability of a hydrophobic drug in presence of hydrous and anhydrous lactose

Physical and enteric properties of soft gelatin capsules coated with eudragit ® L 30 D-55

Compatibility Evaluation of Metered-Dose Inhaler Valve Elastomers with Tetrafluoroethane (P134a), a Non-CFC Propellant

Influence of a lipophilic thermal lubricant on the processing conditions and drug release properties of chlorpheniramine maleate tablets prepared by hot-melt extrusion

Physical-mechanical properties of film-coated soft gelatin capsules

Effect of formulation and process variables on porosity parameters and release rates from a multi unit erosion matrix of a poorly soluble drug

Effect of buffer constituents on the determination of therapeutic proteins by capillary electrophoresis

N-Methyl-2-Pyrrolidone as a Cosolvent: Relationship of Cosolvent Effect with Solute Polarity and the Presence of Proton-Donating Groups on Model Drug Compounds

Assay of protein drug substances present in solution mixtures by fluorescamine derivatization and capillary electrophoresis

Degradation profile and reversed-phase LC method development of the antiinflammatory drug, Ro 24-5913

Biotin uptake and transport across bovine brain microvessel endothelial cell monolayers

Compaction Properties of Spheronized Binary Granular Mixtures

In vitro release of the mTOR inhibitor rapamycin from poly(ethylene glycol)-b-poly(ε-caprolactone) micelles

Scaleup of immediate release oral solid dosage forms

Influence of plasticizers on the mechanical properties of pellets containing Eudragit® RS 30 D

A biodegradable injectable implant for delivering micro and macromolecules using poly (lactic-co-glycolic) acid (PLGA) copolymers

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