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Analytical Quality by Design: Achieving Robustness of an LC-CAD Method for the Analysis of Non-Volatile Fatty Acids

Pharmaceuticals (Basel, Switzerland), 2023-03, Vol.16 (4), p.478

2023

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Optimization of Extraction and HPLC–MS/MS Profiling of Phenolic Compounds from Red Grape Seed Extracts Using Conventional and Deep Eutectic Solvents

Antioxidants, 2022-08, Vol.11 (8), p.1595

2022

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An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient

Microporous and mesoporous materials, 2013-02, Vol.167, p.94-101

2013

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Robust optimization of gradient RP HPLC method for simultaneous determination of ivabradine and its eleven related substances by AQbD approach

Acta chromatographica, 2022-01, Vol.34 (1), p.1-11

2022

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Determination of critical micelle concentration of cetyltrimethylammonium bromide: Different procedures for analysis of experimental data

Hemijska industrija, 2016, Vol.70 (4), p.485-492

2016

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Demasking large dummy effects approach in revealing important interactions in Plackett-Burman experimental design

Journal of chemometrics, 2012-10, Vol.26 (10), p.518-525

2012

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Validation of a column liquid chromatographic method for the analysis of pramipexole and its five impurities

Journal of AOAC International, 2010-07, Vol.93 (4), p.1102

2010

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Optimization and validation of an RP-HPLC method for analysis of hydrocortisone acetate and lidocaine in suppositories

Journal of AOAC International, 2010-01, Vol.93 (1), p.102

2010

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Computer—Assisted Optimization and Validation of LC Analysis of Trimetazidine Dihydrochloride and Its Impurities

Journal of chromatographic science, 2008-05, Vol.46 (5), p.430-435

2008

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New methods for drug analysis in biological samples and other matrixes

Journal of AOAC International, 2011-05, Vol.94 (3), p.665

2011

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Compounding of a topical drug with prospective natural surfactant-stabilized pharmaceutical bases: Physicochemical and in vitro/ in vivo characterization – A ketoprofen case study

European journal of pharmaceutics and biopharmaceutics, 2012, Vol.80 (1), p.164-175

2012

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A Contribution to the Glimepiride Dissociation Constant Determination

Journal of chemical and engineering data, 2010-03, Vol.55 (3), p.1368-1371

2010

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A comprehensive study on retention of selected model substances in β-cyclodextrin-modified high performance liquid chromatography

Journal of Chromatography A, 2021-05, Vol.1645, p.462120, Article 462120

2021

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LC Determination of Lercanidipine and Its Impurities Using Drylab Software and Experimental Design Procedures

Chromatographia, 2008-03, Vol.67 (5-6), p.449-454

2008

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Retention modelling in liquid chromatographic separation of simvastatin and six impurities using a microemulsion as eluent

Journal of separation science, 2004-09, Vol.27 (13), p.1087-1092

2004

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Optimization of an RP-HPLC Method for Drug Control Analysis

Journal of liquid chromatography & related technologies, 2003-12, Vol.26 (20), p.3401-3412

2003

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Development of Karl Fischer titration method using quality by design concept

Hemijska industrija, 2012-01, Vol.66 (5), p.659-665

2012

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Simultaneous determination of compounds in Septalen pellets by derivative spectrophotometry

Journal of the Serbian Chemical Society, 2000-06, Vol.65 (5-6), p.339-344

2000

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Simultaneous determination of compounds in Septalen® pellets by derivative spectrophotometry

Journal of the Serbian Chemical Society, 2000, Vol.65 (5-6), p.339-344

2000

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A comprehensive study on retention of selected model substances in β-cyclodextrin-modified high performance liquid chromatography

Journal of chromatography. A, 2021-05, Vol.1645, p.462120

2021

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The Second-Derivative Spectrophotometric Assay of a Multicomponent Analgetic Mixture

Spectroscopy letters, 2000-03, Vol.33 (2), p.173-183

2000

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Analytical Quality by Design: Achieving Robustness of an LC-CAD Method for the Analysis of Non-Volatile Fatty Acids

Optimization of Extraction and HPLC–MS/MS Profiling of Phenolic Compounds from Red Grape Seed Extracts Using Conventional and Deep Eutectic Solvents

An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient

Robust optimization of gradient RP HPLC method for simultaneous determination of ivabradine and its eleven related substances by AQbD approach

Determination of critical micelle concentration of cetyltrimethylammonium bromide: Different procedures for analysis of experimental data

Demasking large dummy effects approach in revealing important interactions in Plackett-Burman experimental design

Validation of a column liquid chromatographic method for the analysis of pramipexole and its five impurities

Optimization and validation of an RP-HPLC method for analysis of hydrocortisone acetate and lidocaine in suppositories

Computer—Assisted Optimization and Validation of LC Analysis of Trimetazidine Dihydrochloride and Its Impurities

New methods for drug analysis in biological samples and other matrixes

Compounding of a topical drug with prospective natural surfactant-stabilized pharmaceutical bases: Physicochemical and in vitro/ in vivo characterization – A ketoprofen case study

A Contribution to the Glimepiride Dissociation Constant Determination

A comprehensive study on retention of selected model substances in β-cyclodextrin-modified high performance liquid chromatography

LC Determination of Lercanidipine and Its Impurities Using Drylab Software and Experimental Design Procedures

Retention modelling in liquid chromatographic separation of simvastatin and six impurities using a microemulsion as eluent

Optimization of an RP-HPLC Method for Drug Control Analysis

Development of Karl Fischer titration method using quality by design concept

Simultaneous determination of compounds in Septalen pellets by derivative spectrophotometry

Simultaneous determination of compounds in Septalen® pellets by derivative spectrophotometry

A comprehensive study on retention of selected model substances in β-cyclodextrin-modified high performance liquid chromatography

The Second-Derivative Spectrophotometric Assay of a Multicomponent Analgetic Mixture

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