Analytical quality by design: Development and control strategy for a LC method to evaluate the cannabinoids content in cannabis olive oil extracts
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Sandra Furlanetto | Serena Orlandini | Riccardo Deidda | Hermane T. Avohou | Philippe Hubert | Benedetta Pasquini | Massimo Del Bubba | Cédric Hubert | Roberto Baronti | S. Furlanetto | P. Hubert | Riccardo Deidda | S. Orlandini | C. Hubert | B. Pasquini | M. Del Bubba | H. Avohou | Pier Luigi Davolio | R. Baronti | P. Davolio
[1] Maitane Olivares,et al. Identification and quantification of cannabinoids in Cannabis sativa L. plants by high performance liquid chromatography-mass spectrometry , 2014, Analytical and Bioanalytical Chemistry.
[2] G. T. Pollard,et al. Preparation and Distribution of Cannabis and Cannabis-Derived Dosage Formulations for Investigational and Therapeutic Use in the United States , 2016, Frontiers in Pharmacology.
[3] S. Benvenuti,et al. Development of a new extraction technique and HPLC method for the analysis of non‐psychoactive cannabinoids in fibre‐type Cannabis sativa L. (hemp) , 2017, Journal of pharmaceutical and biomedical analysis.
[4] S Furlanetto,et al. Optimization and validation of a CZE method for rufloxacin hydrochloride determination in coated tablets. , 2002, Journal of pharmaceutical and biomedical analysis.
[5] Giuseppe Cannazza,et al. A Metabolomic Approach Applied to a Liquid Chromatography Coupled to High-Resolution Tandem Mass Spectrometry Method (HPLC-ESI-HRMS/MS): Towards the Comprehensive Evaluation of the Chemical Composition of Cannabis Medicinal Extracts. , 2018, Phytochemical analysis : PCA.
[6] Benjamin Debrus,et al. Design Spaces for analytical methods , 2013 .
[7] Claudia Giuliani,et al. Extraction Method and Analysis of Cannabinoids in Cannabis Olive Oil Preparations , 2017, Planta Medica.
[8] Wieland Peschel,et al. ¹H NMR and HPLC/DAD for Cannabis sativa L. chemotype distinction, extract profiling and specification. , 2015, Talanta.
[9] R. Gotti,et al. Multivariate optimization of capillary electrophoresis methods: a critical review. , 2014, Journal of pharmaceutical and biomedical analysis.
[10] Sandra Furlanetto,et al. Application of quality by design to the development of analytical separation methods , 2012, Analytical and Bioanalytical Chemistry.
[11] M. Elsohly,et al. Phytochemistry of Cannabis sativa L. , 2017, Progress in the chemistry of organic natural products.
[12] S. Furlanetto,et al. Quality by design approach in the development of an ultra-high-performance liquid chromatography method for Bexsero meningococcal group B vaccine. , 2018, Talanta.
[13] Benjamin Debrus,et al. Software-Assisted Method Development in High Performance Liquid Chromatography , 2018 .
[14] Benjamin Debrus,et al. Innovative development and validation of an HPLC/DAD method for the qualitative and quantitative determination of major cannabinoids in cannabis plant material. , 2009, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
[15] Giuseppe Cannazza,et al. Medicinal cannabis: Principal cannabinoids concentration and their stability evaluated by a high performance liquid chromatography coupled to diode array and quadrupole time of flight mass spectrometry method. , 2016, Journal of pharmaceutical and biomedical analysis.
[16] S. Furlanetto,et al. Enantioseparation and impurity determination of ambrisentan using cyclodextrin-modified micellar electrokinetic chromatography: Visualizing the design space within quality by design framework. , 2016, Journal of chromatography. A.
[17] A. Darker,et al. TOTAL QUALITY CONTROL , 1987 .
[18] R. Verpoorte,et al. PKS activities and biosynthesis of cannabinoids and flavonoids in Cannabis sativa L. plants. , 2008, Plant & cell physiology.
[19] Serge Rudaz,et al. Implementation of a generic liquid chromatographic method development workflow: Application to the analysis of phytocannabinoids and Cannabis sativa extracts , 2018, Journal of pharmaceutical and biomedical analysis.
[20] Philippe Hubert,et al. Quantitative determination of salbutamol sulfate impurities using achiral supercritical fluid chromatography , 2017, Journal of pharmaceutical and biomedical analysis.
[21] Simona Pichini,et al. Evaluation of cannabinoids concentration and stability in standardized preparations of cannabis tea and cannabis oil by ultra-high performance liquid chromatography tandem mass spectrometry , 2017, Clinical chemistry and laboratory medicine.
[22] Serena Orlandini,et al. Risk‐based approach for method development in pharmaceutical quality control context: A critical review , 2018, Journal of pharmaceutical and biomedical analysis.
[23] S Furlanetto,et al. A comprehensive strategy in the development of a cyclodextrin-modified microemulsion electrokinetic chromatographic method for the assay of diclofenac and its impurities: Mixture-process variable experiments and quality by design. , 2016, Journal of chromatography. A.
[24] G. Guy,et al. A tale of two cannabinoids: the therapeutic rationale for combining tetrahydrocannabinol and cannabidiol. , 2006, Medical hypotheses.
[25] W. Weinmann,et al. Simultaneous quantification of delta-9-THC, THC-acid A, CBN and CBD in seized drugs using HPLC-DAD. , 2014, Forensic science international.
[26] Arno Hazekamp,et al. Cannabis Oil: chemical evaluation of an upcoming cannabis-based medicine , 2013 .
[27] S. Morimoto,et al. Phytocannabinoids in Cannabis sativa: Recent Studies on Biosynthetic Enzymes , 2007, Chemistry & biodiversity.
[28] G. di Perri,et al. Cannabinoids concentration variability in cannabis olive oil galenic preparations , 2018, The Journal of pharmacy and pharmacology.
[29] M. Schatman,et al. Cannabis in Pain Treatment: Clinical and Research Considerations. , 2016, The journal of pain : official journal of the American Pain Society.
[30] Pierre Lebrun,et al. Implementation of a generic SFC-MS method for the quality control of potentially counterfeited medicinal cannabis with synthetic cannabinoids. , 2018, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
[31] R. Gotti,et al. Chiral capillary zone electrophoresis in enantioseparation and analysis of cinacalcet impurities: Use of Quality by Design principles in method development. , 2018, Journal of chromatography. A.
[32] Ana Stajić,et al. Quality by Design in the development of hydrophilic interaction liquid chromatography method with gradient elution for the analysis of olanzapine , 2017, Journal of pharmaceutical and biomedical analysis.
[33] S Furlanetto,et al. Mixture-process variable approach to optimize a microemulsion electrokinetic chromatography method for the quality control of a nutraceutical based on coenzyme Q10. , 2012, Talanta.
[34] David B. Dunson,et al. Bayesian Data Analysis , 2010 .
[35] John J. Peterson,et al. Predictive Distributions for Constructing the ICH Q8 Design Space , 2017 .
[36] Giuseppe Cannazza,et al. Pharmaceutical and biomedical analysis of cannabinoids: A critical review , 2018, Journal of pharmaceutical and biomedical analysis.
[37] Gintaras V. Reklaitis,et al. Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture , 2017 .
[38] Hermane T. Avohou,et al. ‘Quality by Design’ approach for the analysis of impurities in pharmaceutical drug products and drug substances , 2017 .
[39] R. Carlson,et al. Design of Experiments, Principles and Applications, L. Eriksson, E. Johansson, N. Kettaneh‐ Wold, C. Wikström and S. Wold, Umetrics AB, Umeå Learnways AB, Stockholm, 2000, ISBN 91‐973730‐0‐1, xii + 329 pp. , 2001 .