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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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3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models

International journal of pharmaceutics, 2021-01, Vol.592, p.120059-120059, Article 120059

2021

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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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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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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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Development of stable amorphous solid dispersion and quantification of crystalline fraction of lopinavir by spectroscopic-chemometric methods

International journal of pharmaceutics, 2021-06, Vol.602, p.120657-120657, Article 120657

2021

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Effect of patients in-use and accelerated stability conditions on quality attributes and pharmacokinetic profile of four FDA approved extended-release anti-epileptic-drug products

International journal of pharmaceutics, 2024-10, p.124840, Article 124840

2024

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Ultra-long acting prodrug of dolutegravir and delivery system – Physicochemical, pharmacokinetic and formulation characterizations

International journal of pharmaceutics, 2021-09, Vol.607, p.120889-120889, Article 120889

2021

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Isolated cerebellar involvement in X-linked adrenoleukodystrophy

Annals of the Indian Academy of Neurology, 2020-11, Vol.23 (6), p.827-828

Mansoor, C

2020

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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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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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Development and validation of in vitro–in vivo correlation (IVIVC) for estradiol transdermal drug delivery systems

Journal of controlled release, 2015-07, Vol.210, p.58-66

2015

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Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments

International journal of pharmaceutics, 2015-09, Vol.493 (1-2), p.412-425

2015

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Development and Validation of Matrix of Chemistry, Manufacturing, and Control (MoCMC) System for Intramammary Drug Products (IMM)

Pharmaceutical research, 2024-05, Vol.41 (5), p.1007-1020

2024

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Percutaneous Achilles tendon tenotomy in clubfoot with a blade or a needle: a single-centre randomized controlled noninferiority trial

The bone & joint journal, 2024-08, Vol.106-B (8), p.871-878

2024

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In-use stability assessment of FDA approved metformin immediate release and extended release products for N-Nitrosodimethylamine and dissolution quality attributes

International journal of pharmaceutics, 2022-07, Vol.623, p.121923-121923, Article 121923

2022

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Vitamin C and E supplementation blunts increases in total lean body mass in elderly men after strength training

Scandinavian journal of medicine & science in sports, 2016-07, Vol.26 (7), p.755-763

2016

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

3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models

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

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

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

Development of stable amorphous solid dispersion and quantification of crystalline fraction of lopinavir by spectroscopic-chemometric methods

Effect of patients in-use and accelerated stability conditions on quality attributes and pharmacokinetic profile of four FDA approved extended-release anti-epileptic-drug products

Ultra-long acting prodrug of dolutegravir and delivery system – Physicochemical, pharmacokinetic and formulation characterizations

Isolated cerebellar involvement in X-linked adrenoleukodystrophy

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

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

Development and validation of in vitro–in vivo correlation (IVIVC) for estradiol transdermal drug delivery systems

Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments

Development and Validation of Matrix of Chemistry, Manufacturing, and Control (MoCMC) System for Intramammary Drug Products (IMM)

Percutaneous Achilles tendon tenotomy in clubfoot with a blade or a needle: a single-centre randomized controlled noninferiority trial

In-use stability assessment of FDA approved metformin immediate release and extended release products for N-Nitrosodimethylamine and dissolution quality attributes

Vitamin C and E supplementation blunts increases in total lean body mass in elderly men after strength training

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