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Use of Retinoids in Topical Antiaging Treatments: A Focused Review of Clinical Evidence for Conventional and Nanoformulations

Advances in therapy, 2022-12, Vol.39 (12), p.5351-5375

2022

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Nitrocellulose blister material as a source of N-nitrosamine contamination of pharmaceutical drug products

International journal of pharmaceutics, 2022-04, Vol.618, p.121687-121687, Article 121687

2022

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NDMA Formation Due to Active Ingredient Degradation and Nitrite Traces in Drug Product

Journal of pharmaceutical sciences, 2023-05, Vol.112 (5), p.1277-1286

2023

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The environmental occurrence, fate, and risks of 25 endocrine disruptors in Slovenian waters

The Science of the total environment, 2024-01, Vol.906, p.167245-167245, Article 167245

2024

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Multi-parameter risk assessment of forty-one selected substances with endocrine disruptive properties in surface waters worldwide

Chemosphere (Oxford), 2022-01, Vol.287 (Pt 2), p.132195, Article 132195

2022

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Simple HPLC-UV Method for Therapeutic Drug Monitoring of 12 Antiepileptic Drugs and Their Main Metabolites in Human Plasma

Molecules (Basel, Switzerland), 2023-11, Vol.28 (23), p.7830

2023

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A comprehensive approach for the simultaneous analysis of all main water-soluble vitamins in multivitamin preparations by a stability-indicating HPLC-DAD method

Food chemistry, 2021-02, Vol.337, p.127768-127768, Article 127768

2021

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Suitability and functional characterization of two Calu-3 cell models for prediction of drug permeability across the airway epithelial barrier

International journal of pharmaceutics, 2020-07, Vol.585, p.119484, Article 119484

2020

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The potential of nanofibers to increase solubility and dissolution rate of the poorly soluble and chemically unstable drug lovastatin

International journal of pharmaceutics, 2020-01, Vol.573, p.118809-118809, Article 118809

2020

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A robust multi-residue method for the monitoring of 25 endocrine disruptors at ultra-trace levels in surface waters by SPE-LC-MS/MS

Analytical methods, 2023-06, Vol.15 (21), p.266-2621

2023

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A robust analytical method for simultaneous quantification of 13 low-molecular-weight N-Nitrosamines in various pharmaceuticals based on solid phase extraction and liquid chromatography coupled to high-resolution mass spectrometry

European journal of pharmaceutical sciences, 2024-01, Vol.192, p.106633-106633, Article 106633

2024

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Electrospun polycaprolactone nanofibers as a potential oromucosal delivery system for poorly water-soluble drugs

European journal of pharmaceutical sciences, 2015-07, Vol.75, p.101-113

2015

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A novel LC–MS/MS method for the simultaneous quantification of topiramate and its main metabolites in human plasma

Journal of pharmaceutical and biomedical analysis, 2017-05, Vol.138, p.180-188

2017

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Development of a Multi-Residue Method for Monitoring 44 Pharmaceuticals in Slovene Surface Water by SPE-LC-MS/MS

Water, air, and soil pollution, 2018-06, Vol.229 (6), p.1-18, Article 192

2018

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Design of experiments and multivariate analysis approach to study dissolution stability of a modified-release drug product to support lean design strategies

Drug development and industrial pharmacy, 2021-09, Vol.47 (9), p.1481-1488

2021

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Stability-Indicating HPLC–UV Method for Vitamin D 3 Determination in Solutions, Nutritional Supplements and Pharmaceuticals

Journal of chromatographic science, 2016-08, Vol.54 (7), p.1180-1186

2016

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Retinoid stability and degradation kinetics in commercial cosmetic products

Journal of cosmetic dermatology, 2021-07, Vol.20 (7), p.2350-2358

2021

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The Incorporated Drug Affects the Properties of Hydrophilic Nanofibers

Nanomaterials (Basel, Switzerland), 2024-06, Vol.14 (11), p.949

2024

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An LC-MS/MS Method for Quantification of Lamotrigine and Its Main Metabolite in Dried Blood Spots

Pharmaceuticals (Basel, Switzerland), 2024-04, Vol.17 (4), p.449

2024

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The Impact of Phospholipid-Based Liquid Crystals’ Microstructure on Stability and Release Profile of Ascorbyl Palmitate and Skin Performance

Molecules (Basel, Switzerland), 2024-07, Vol.29 (13), p.3173

2024

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Vitamin B 12 in Foods, Food Supplements, and Medicines-A Review of Its Role and Properties with a Focus on Its Stability

Molecules (Basel, Switzerland), 2023-01, Vol.28 (1)

2023

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The search for novel proline analogs for viscosity reduction and stabilization of highly concentrated monoclonal antibody solutions

International journal of pharmaceutics, 2024-04, Vol.655, p.124055-124055, Article 124055

2024

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Evaluation of the Stability of Hydrocortisone Sodium Succinate in Solutions for Parenteral Use by a Validated HPLC-UV Method

Acta chimica Slovenica, 2022-12, Vol.69 (4), p.796-802

2022

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Simultaneous determination of gabapentin, pregabalin, vigabatrin, and topiramate in plasma by HPLC with fluorescence detection

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2014-07, Vol.962, p.82-88

2014

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Comprehensive Stability Study of Vitamin D3 in Aqueous Solutions and Liquid Commercial Products

Pharmaceutics, 2021-04, Vol.13 (5), p.617

2021

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Use of Retinoids in Topical Antiaging Treatments: A Focused Review of Clinical Evidence for Conventional and Nanoformulations

Nitrocellulose blister material as a source of N-nitrosamine contamination of pharmaceutical drug products

NDMA Formation Due to Active Ingredient Degradation and Nitrite Traces in Drug Product

The environmental occurrence, fate, and risks of 25 endocrine disruptors in Slovenian waters

Multi-parameter risk assessment of forty-one selected substances with endocrine disruptive properties in surface waters worldwide

Simple HPLC-UV Method for Therapeutic Drug Monitoring of 12 Antiepileptic Drugs and Their Main Metabolites in Human Plasma

A comprehensive approach for the simultaneous analysis of all main water-soluble vitamins in multivitamin preparations by a stability-indicating HPLC-DAD method

Suitability and functional characterization of two Calu-3 cell models for prediction of drug permeability across the airway epithelial barrier

The potential of nanofibers to increase solubility and dissolution rate of the poorly soluble and chemically unstable drug lovastatin

A robust multi-residue method for the monitoring of 25 endocrine disruptors at ultra-trace levels in surface waters by SPE-LC-MS/MS

A robust analytical method for simultaneous quantification of 13 low-molecular-weight N-Nitrosamines in various pharmaceuticals based on solid phase extraction and liquid chromatography coupled to high-resolution mass spectrometry

Electrospun polycaprolactone nanofibers as a potential oromucosal delivery system for poorly water-soluble drugs

A novel LC–MS/MS method for the simultaneous quantification of topiramate and its main metabolites in human plasma

Development of a Multi-Residue Method for Monitoring 44 Pharmaceuticals in Slovene Surface Water by SPE-LC-MS/MS

Design of experiments and multivariate analysis approach to study dissolution stability of a modified-release drug product to support lean design strategies

Stability-Indicating HPLC–UV Method for Vitamin D 3 Determination in Solutions, Nutritional Supplements and Pharmaceuticals

Retinoid stability and degradation kinetics in commercial cosmetic products

The Incorporated Drug Affects the Properties of Hydrophilic Nanofibers

An LC-MS/MS Method for Quantification of Lamotrigine and Its Main Metabolite in Dried Blood Spots

The Impact of Phospholipid-Based Liquid Crystals’ Microstructure on Stability and Release Profile of Ascorbyl Palmitate and Skin Performance

Vitamin B 12 in Foods, Food Supplements, and Medicines-A Review of Its Role and Properties with a Focus on Its Stability

The search for novel proline analogs for viscosity reduction and stabilization of highly concentrated monoclonal antibody solutions

Evaluation of the Stability of Hydrocortisone Sodium Succinate in Solutions for Parenteral Use by a Validated HPLC-UV Method

Simultaneous determination of gabapentin, pregabalin, vigabatrin, and topiramate in plasma by HPLC with fluorescence detection

Comprehensive Stability Study of Vitamin D3 in Aqueous Solutions and Liquid Commercial Products

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