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A new chapter in pharmaceutical manufacturing: 3D-printed drug products

Advanced drug delivery reviews, 2017-01, Vol.108, p.39-50

2017

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Biological Synthesis of Silver Nanoparticles and Prospects in Plant Disease Management

Molecules (Basel, Switzerland), 2022-07, Vol.27 (15), p.4754

2022

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A meta-analysis of the efficacy of whole-body computed tomography imaging in the management of trauma and injury

Injury, 2017-08, Vol.48 (8), p.1784-1793

2017

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Understanding Pharmaceutical Quality by Design

The AAPS journal, 2014-07, Vol.16 (4), p.771-783

2014

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Data integrity issues in pharmaceutical industry: Common observations, challenges and mitigations strategies

International journal of pharmaceutics, 2023-01, Vol.631, p.122503-122503, Article 122503

2023

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Influence of psychostimulants and opioids on epigenetic modification of class III histone deacetylase (HDAC)-sirtuins in glial cells

Scientific reports, 2021-10, Vol.11 (1), p.21335-16, Article 21335

2021

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Selective laser sintering 3D printing - an overview of the technology and pharmaceutical applications

Drug development and industrial pharmacy, 2020-06, Vol.46 (6), p.869-877

2020

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Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing

International journal of pharmaceutics, 2019-10, Vol.570, p.118651, Article 118651

2019

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Non-destructive methods of characterization of risperidone solid lipid nanoparticles

European journal of pharmaceutics and biopharmaceutics, 2010-09, Vol.76 (1), p.127-137

2010

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Damage control resuscitation in patients with severe traumatic hemorrhage: A practice management guideline from the Eastern Association for the Surgery of Trauma

The journal of trauma and acute care surgery, 2017-03, Vol.82 (3), p.605-617

2017

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Predicting hydrophilic drug encapsulation inside unilamellar liposomes

International journal of pharmaceutics, 2012-02, Vol.423 (2), p.410-418

2012

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A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale

International journal of pharmaceutics, 2012-02, Vol.423 (2), p.543-553

2012

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Comparative Evaluation of Flow for Pharmaceutical Powders and Granules

AAPS PharmSciTech, 2008-03, Vol.9 (1), p.250-258

2008

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HIV-1 Tat and cocaine impact astrocytic energy reservoir influence on miRNA epigenetic regulation

Genomics (San Diego, Calif.), 2021-11, Vol.113 (6), p.3461-3475

2021

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Fractionated charge variants of biosimilars: A review of separation methods, structural and functional analysis

Analytica chimica acta, 2021-04, Vol.1152, p.238189-238189, Article 238189

2021

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Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development

International journal of pharmaceutics, 2011-02, Vol.405 (1), p.63-78

2011

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Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy

AAPS PharmSciTech, 2023-02, Vol.24 (2), p.60-60, Article 60

2023

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Local Identifiability Analysis, Parameter Subset Selection and Verification for a Minimal Brain PBPK Model

Bulletin of mathematical biology, 2024-02, Vol.86 (2), p.12-12, Article 12

2024

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Very-Rapidly Dissolving Printlets of Isoniazid Manufactured by SLS 3D Printing: In Vitro and In Vivo Characterization

Molecular pharmaceutics, 2022-08, Vol.19 (8), p.2937-2949

2022

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Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis

International journal of pharmaceutics, 2012-02, Vol.423 (2), p.341-350

2012

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A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes

International journal of pharmaceutics, 2012-04, Vol.426 (1-2), p.211-218

2012

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Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations

International journal of pharmaceutics, 2016-04, Vol.502 (1-2), p.138-150

2016

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Defining Patient Centric Pharmaceutical Drug Product Design

The AAPS journal, 2016-09, Vol.18 (5), p.1047-1055

2016

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Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate

Journal of pharmaceutical and biomedical analysis, 2012-03, Vol.62, p.61-67

2012

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Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett–Burman design

International journal of pharmaceutics, 2010-04, Vol.389 (1), p.186-194

2010

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A new chapter in pharmaceutical manufacturing: 3D-printed drug products

Biological Synthesis of Silver Nanoparticles and Prospects in Plant Disease Management

A meta-analysis of the efficacy of whole-body computed tomography imaging in the management of trauma and injury

Understanding Pharmaceutical Quality by Design

Data integrity issues in pharmaceutical industry: Common observations, challenges and mitigations strategies

Influence of psychostimulants and opioids on epigenetic modification of class III histone deacetylase (HDAC)-sirtuins in glial cells

Selective laser sintering 3D printing - an overview of the technology and pharmaceutical applications

Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing

Non-destructive methods of characterization of risperidone solid lipid nanoparticles

Damage control resuscitation in patients with severe traumatic hemorrhage: A practice management guideline from the Eastern Association for the Surgery of Trauma

Predicting hydrophilic drug encapsulation inside unilamellar liposomes

A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale

Comparative Evaluation of Flow for Pharmaceutical Powders and Granules

HIV-1 Tat and cocaine impact astrocytic energy reservoir influence on miRNA epigenetic regulation

Fractionated charge variants of biosimilars: A review of separation methods, structural and functional analysis

Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development

Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy

Local Identifiability Analysis, Parameter Subset Selection and Verification for a Minimal Brain PBPK Model

Very-Rapidly Dissolving Printlets of Isoniazid Manufactured by SLS 3D Printing: In Vitro and In Vivo Characterization

Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis

A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes

Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations

Defining Patient Centric Pharmaceutical Drug Product Design

Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate

Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett–Burman design

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