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Formulation Optimization and in Vitro Characterization of Orally Disintegrating Films Using a Factorial Design and Mathematical Modeling for Drug Release

Chemical and Pharmaceutical Bulletin, 2017/02/01, Vol.65(2), pp.166-177

2017

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Effects of moisture content and compression pressure of various deforming granules on the physical properties of tablets

Powder technology, 2017-04, Vol.310, p.92-102

2017

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Process Analytical Technology Tools for Monitoring Pharmaceutical Unit Operations: A Control Strategy for Continuous Process Verification

Pharmaceutics, 2021-06, Vol.13 (6), p.919

2021

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Control Strategy for Excipient Variability in the Quality by Design Approach Using Statistical Analysis and Predictive Model: Effect of Microcrystalline Cellulose Variability on Design Space

Pharmaceutics, 2022-11, Vol.14 (11), p.2416

2022

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Application of the Discrete Element Method for Manufacturing Process Simulation in the Pharmaceutical Industry

Pharmaceutics, 2019-08, Vol.11 (8), p.414

2019

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Scale-Up Strategy in Quality by Design Approach for Pharmaceutical Blending Process with Discrete Element Method Simulation

Pharmaceutics, 2019-06, Vol.11 (6), p.264

2019

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Comprehensive Study of Intermediate and Critical Quality Attributes for Process Control of High-Shear Wet Granulation Using Multivariate Analysis and The Quality by Design Approach

Pharmaceutics, 2019-06, Vol.11 (6), p.252

2019

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Effects of granulation process variables on the physical properties of dosage forms by combination of experimental design and principal component analysis

Asian journal of pharmceutical sciences, 2019-05, Vol.14 (3), p.287-304

2019

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Control Strategy for Process Development of High-Shear Wet Granulation and Roller Compaction to Prepare a Combination Drug Using Integrated Quality by Design

Pharmaceutics, 2021-01, Vol.13 (1), p.80

2021

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Development of a Robust Control Strategy for Fixed-Dose Combination Bilayer Tablets with Integrated Quality by Design, Statistical, and Process Analytical Technology Approach

Pharmaceutics, 2021-09, Vol.13 (9), p.1443

2021

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Enhanced Oral Bioavailability of Resveratrol by Using Neutralized Eudragit E Solid Dispersion Prepared via Spray Drying

Antioxidants, 2021-01, Vol.10 (1), p.90

2021

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Model-Based Scale-Up Methodologies for Pharmaceutical Granulation

Pharmaceutics, 2020-05, Vol.12 (5), p.453

2020

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Development of a Resveratrol Nanosuspension Using the Antisolvent Precipitation Method without Solvent Removal, Based on a Quality by Design (QbD) Approach

Pharmaceutics, 2019-12, Vol.11 (12), p.688

2019

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Application of diethylene glycol monoethyl ether in solubilization of poorly water-soluble drugs

Journal of Pharmaceutical Investigation, 2020, 50(3), , pp.231-250

2020

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Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery

Antioxidants, 2019-11, Vol.8 (11), p.554

2019

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Pharmacokinetics of eperisone following oral administration in healthy Korean volunteers

Biopharmaceutics & drug disposition, 2021-03, Vol.42 (2-3), p.94-102

2021

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New Preclinical Development of a c-Met Inhibitor and Its Combined Anti-Tumor Effect in c-Met-Amplified NSCLC

Pharmaceutics, 2020-02, Vol.12 (2), p.121

2020

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Pharmacokinetic Study of a Soft Gelatin Capsule and a Solid-Supersaturatable SMEDDS Tablet of Dutasteride in Beagle Dogs

European journal of drug metabolism and pharmacokinetics, 2020-04, Vol.45 (2), p.235-241

2020

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Quality by design approach with multivariate analysis and artificial neural network models to understand and control excipient variability

Journal of pharmaceutical investigation, 2023-05, Vol.53 (3), p.389-406

2023

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Investigation of the effects of materials and dry granulation process on the mirabegron tablet by integrated QbD approach with multivariate analysis

Powder technology, 2021-04, Vol.382, p.23-39

2021

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Quality by Design (QbD) approach to optimize the formulation of a bilayer combination tablet (Telmiduo®) manufactured via high shear wet granulation

International journal of pharmaceutics, 2017-12, Vol.534 (1-2), p.144-158

2017

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Effects of pharmaceutical processes on the quality of ethylcellulose coated pellets: Quality by design approach

Powder technology, 2018-11, Vol.339, p.25-38

2018

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Off-label use of plastic syringes with silicone oil for intravenous infusion bags of antibodies

European journal of pharmaceutics and biopharmaceutics, 2021-09, Vol.166, p.205-215

2021

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Evaluation of subvisible particles in human immunoglobulin and lipid nanoparticles repackaged from a multi-dose vial using plastic syringes

International journal of biological macromolecules, 2023-03, Vol.232, p.123439-123439, Article 123439

2023

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A formulation development strategy for dual-release bilayer tablets: An integrated approach of quality by design and a placebo layer

International journal of pharmaceutics, 2022-04, Vol.618, p.121659-121659, Article 121659

2022

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Formulation Optimization and in Vitro Characterization of Orally Disintegrating Films Using a Factorial Design and Mathematical Modeling for Drug Release

Effects of moisture content and compression pressure of various deforming granules on the physical properties of tablets

Process Analytical Technology Tools for Monitoring Pharmaceutical Unit Operations: A Control Strategy for Continuous Process Verification

Control Strategy for Excipient Variability in the Quality by Design Approach Using Statistical Analysis and Predictive Model: Effect of Microcrystalline Cellulose Variability on Design Space

Application of the Discrete Element Method for Manufacturing Process Simulation in the Pharmaceutical Industry

Scale-Up Strategy in Quality by Design Approach for Pharmaceutical Blending Process with Discrete Element Method Simulation

Comprehensive Study of Intermediate and Critical Quality Attributes for Process Control of High-Shear Wet Granulation Using Multivariate Analysis and The Quality by Design Approach

Effects of granulation process variables on the physical properties of dosage forms by combination of experimental design and principal component analysis

Control Strategy for Process Development of High-Shear Wet Granulation and Roller Compaction to Prepare a Combination Drug Using Integrated Quality by Design

Development of a Robust Control Strategy for Fixed-Dose Combination Bilayer Tablets with Integrated Quality by Design, Statistical, and Process Analytical Technology Approach

Enhanced Oral Bioavailability of Resveratrol by Using Neutralized Eudragit E Solid Dispersion Prepared via Spray Drying

Model-Based Scale-Up Methodologies for Pharmaceutical Granulation

Development of a Resveratrol Nanosuspension Using the Antisolvent Precipitation Method without Solvent Removal, Based on a Quality by Design (QbD) Approach

Application of diethylene glycol monoethyl ether in solubilization of poorly water-soluble drugs

Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery

Pharmacokinetics of eperisone following oral administration in healthy Korean volunteers

New Preclinical Development of a c-Met Inhibitor and Its Combined Anti-Tumor Effect in c-Met-Amplified NSCLC

Pharmacokinetic Study of a Soft Gelatin Capsule and a Solid-Supersaturatable SMEDDS Tablet of Dutasteride in Beagle Dogs

Quality by design approach with multivariate analysis and artificial neural network models to understand and control excipient variability

Investigation of the effects of materials and dry granulation process on the mirabegron tablet by integrated QbD approach with multivariate analysis

Quality by Design (QbD) approach to optimize the formulation of a bilayer combination tablet (Telmiduo®) manufactured via high shear wet granulation

Effects of pharmaceutical processes on the quality of ethylcellulose coated pellets: Quality by design approach

Off-label use of plastic syringes with silicone oil for intravenous infusion bags of antibodies

Evaluation of subvisible particles in human immunoglobulin and lipid nanoparticles repackaged from a multi-dose vial using plastic syringes

A formulation development strategy for dual-release bilayer tablets: An integrated approach of quality by design and a placebo layer

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