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Aniracetam does not improve working memory in neurologically healthy pigeons

PloS one, 2019-04, Vol.14 (4), p.e0215612-e0215612

2019

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An In Silico Knockout Model for Gastrointestinal Absorption Using a Systems Pharmacology Approach - Development and Application for Ketones

PloS one, 2016-09, Vol.11 (9), p.e0163795-e0163795

2016

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Evaluation of an on-farm culture system for the detection of subclinical mastitis pathogens in dairy cattle

JDS communications, 2023-07, Vol.4 (4), p.298-302

2023

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Characterization of a Nanoparticulate Drug Delivery System Using Scanning Ion Occlusion Sensing

Pharmaceutical research, 2012-09, Vol.29 (9), p.2578-2586

2012

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Surface Energy Determined by Inverse Gas Chromatography as a Tool to Investigate Particulate Interactions in Dry Powder Inhalers

Current pharmaceutical design, 2015-01, Vol.21 (27), p.3932-3944

2015

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In vitro Dissolution Testing of Rifampicin Powder Formulations For Prediction of Plasma Concentration–Time Profiles After Inhaled Delivery

Pharmaceutical research, 2023-05, Vol.40 (5), p.1153-1163

2023

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In vitro dissolution testing of respirable size anti-tubercular drug particles using a small volume dissolution apparatus

International journal of pharmaceutics, 2019-03, Vol.559, p.235-244

2019

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Phospholipid-based pyrazinamide spray-dried inhalable powders for treating tuberculosis

International journal of pharmaceutics, 2016-06, Vol.506 (1-2), p.174-183

2016

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High dose dry powder inhalers to overcome the challenges of tuberculosis treatment

International journal of pharmaceutics, 2018-10, Vol.550 (1-2), p.398-417

2018

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Dry powder formulation of kanamycin with enhanced aerosolization efficiency for drug-resistant tuberculosis

International journal of pharmaceutics, 2017-08, Vol.528 (1-2), p.107-117

2017

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Pharmacokinetics of rifampicin after repeated intra-tracheal administration of amorphous and crystalline powder formulations to Sprague Dawley rats

European journal of pharmaceutics and biopharmaceutics, 2021-05, Vol.162, p.1-11

2021

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A STELLA simulation model for in vitro dissolution testing of respirable size particles

Scientific reports, 2019-12, Vol.9 (1), p.18522-14, Article 18522

2019

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Studies on the safety and the tissue distribution of inhaled high-dose amorphous and crystalline rifampicin in a rat model

International journal of pharmaceutics, 2021-03, Vol.597, p.120345-120345, Article 120345

2021

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Cell‐based, animal and H1 receptor binding studies relative to the sedative effects of ketotifen and norketotifen atropisomers

Journal of pharmacy and pharmacology, 2020-04, Vol.72 (4), p.507-518

2020

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Preparation of biodegradable insulin nanocapsules from biocompatible microemulsions

Pharmaceutical research, 2000-06, Vol.17 (6), p.684-689

2000

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Co-spray drying of hygroscopic kanamycin with the hydrophobic drug rifampicin to improve the aerosolization of kanamycin powder for treating respiratory infections

International journal of pharmaceutics, 2018-04, Vol.541 (1-2), p.26-36

2018

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Manipulation of spray-drying conditions to develop dry powder particles with surfaces enriched in hydrophobic material to achieve high aerosolization of a hygroscopic drug

International journal of pharmaceutics, 2018-05, Vol.543 (1-2), p.318-327

2018

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Simultaneous determination of methotrexate and its polyglutamate metabolites in Caco-2 cells by liquid chromatography–tandem mass spectrometry

Journal of pharmaceutical and biomedical analysis, 2009-09, Vol.50 (2), p.262-266

2009

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The Population Pharmacokinetics of d-β-hydroxybutyrate Following Administration of (R)-3-Hydroxybutyl (R)-3-Hydroxybutyrate

The AAPS journal, 2016-05, Vol.18 (3), p.678-688

2016

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Crystalline adduct of moxifloxacin with trans-cinnamic acid to reduce the aqueous solubility and dissolution rate for improved residence time in the lungs

European journal of pharmaceutical sciences, 2019-08, Vol.136, p.104961-104961, Article 104961

2019

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Modeling the interaction of polymeric nanoparticles functionalized with cell penetrating peptides at the nano-bio interface

Colloids and surfaces, B, Biointerfaces, 2022-09, Vol.217, p.112626-112626, Article 112626

2022

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The respiratory delivery of high dose dry powders

International journal of pharmaceutics, 2018-10, Vol.550 (1-2), p.486-487

2018

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Oral Delivery of Mycobacterium bovis BCG in a Lipid Formulation Induces Resistance to Pulmonary Tuberculosis in Mice

Infection and Immunity, 2003-01, Vol.71 (1), p.101-108

2003

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Carrier-free combination dry powder inhaler formulation of ethionamide and moxifloxacin for treating drug-resistant tuberculosis

Drug development and industrial pharmacy, 2019-08, Vol.45 (8), p.1321-1331

2019

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Determination of moisture content in relation to thermal behaviour and plasticization of Eudragit RLPO

International journal of pharmaceutics, 2012-01, Vol.422 (1), p.68-74

2012

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Aniracetam does not improve working memory in neurologically healthy pigeons

An In Silico Knockout Model for Gastrointestinal Absorption Using a Systems Pharmacology Approach - Development and Application for Ketones

Evaluation of an on-farm culture system for the detection of subclinical mastitis pathogens in dairy cattle

Characterization of a Nanoparticulate Drug Delivery System Using Scanning Ion Occlusion Sensing

Surface Energy Determined by Inverse Gas Chromatography as a Tool to Investigate Particulate Interactions in Dry Powder Inhalers

In vitro Dissolution Testing of Rifampicin Powder Formulations For Prediction of Plasma Concentration–Time Profiles After Inhaled Delivery

In vitro dissolution testing of respirable size anti-tubercular drug particles using a small volume dissolution apparatus

Phospholipid-based pyrazinamide spray-dried inhalable powders for treating tuberculosis

High dose dry powder inhalers to overcome the challenges of tuberculosis treatment

Dry powder formulation of kanamycin with enhanced aerosolization efficiency for drug-resistant tuberculosis

Pharmacokinetics of rifampicin after repeated intra-tracheal administration of amorphous and crystalline powder formulations to Sprague Dawley rats

A STELLA simulation model for in vitro dissolution testing of respirable size particles

Studies on the safety and the tissue distribution of inhaled high-dose amorphous and crystalline rifampicin in a rat model

Cell‐based, animal and H1 receptor binding studies relative to the sedative effects of ketotifen and norketotifen atropisomers

Preparation of biodegradable insulin nanocapsules from biocompatible microemulsions

Co-spray drying of hygroscopic kanamycin with the hydrophobic drug rifampicin to improve the aerosolization of kanamycin powder for treating respiratory infections

Manipulation of spray-drying conditions to develop dry powder particles with surfaces enriched in hydrophobic material to achieve high aerosolization of a hygroscopic drug

Simultaneous determination of methotrexate and its polyglutamate metabolites in Caco-2 cells by liquid chromatography–tandem mass spectrometry

The Population Pharmacokinetics of d-β-hydroxybutyrate Following Administration of (R)-3-Hydroxybutyl (R)-3-Hydroxybutyrate

Crystalline adduct of moxifloxacin with trans-cinnamic acid to reduce the aqueous solubility and dissolution rate for improved residence time in the lungs

Modeling the interaction of polymeric nanoparticles functionalized with cell penetrating peptides at the nano-bio interface

The respiratory delivery of high dose dry powders

Oral Delivery of Mycobacterium bovis BCG in a Lipid Formulation Induces Resistance to Pulmonary Tuberculosis in Mice

Carrier-free combination dry powder inhaler formulation of ethionamide and moxifloxacin for treating drug-resistant tuberculosis

Determination of moisture content in relation to thermal behaviour and plasticization of Eudragit RLPO

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