Relevant bibliographies by topics / Development of analytical methods

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Development of analytical methods'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 May 2024

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Journal articles on the topic "Development of analytical methods"

1

Basel, Chris L. "Analytical methods development." Journal of Chemical Education 64, no. 6 (June 1987): 528. http://dx.doi.org/10.1021/ed064p528.

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Burgess, Chris. "Development and validation of analytical methods." Analytica Chimica Acta 338, no. 1-2 (February 1997): 163. http://dx.doi.org/10.1016/s0003-2670(97)85322-6.

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Helaskar, Chandrashekhar Bhagvatrao, and S. R. Kulkarni. "Analytical method development and validation for Aluminium." International Journal of Research and Development in Pharmacy & Life Sciences 7, no. 4 (August 2018): 3034–38. http://dx.doi.org/10.21276/ijrdpl.2278-0238.2018.7(4).3034-3038.

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Putta, Prapulla. "Analytical Methods Development and Validation of Naproxen and Sumatriptan by RP HPLC." International Journal of Trend in Scientific Research and Development Volume-3, Issue-4 (June 30, 2019): 325–27. http://dx.doi.org/10.31142/ijtsrd23582.

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MIYAKE, Shiro. "Development of Analytical Methods Using Immunological Reactions." BUNSEKI KAGAKU 69, no. 6 (June 5, 2020): 237–45. http://dx.doi.org/10.2116/bunsekikagaku.69.237.

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Nakai, K., H. Abe, N. Matsuda, M. Kobayasiy, H. Ikeda, S. Sekiguchi, and E. Tsuchida. "Development of Analytical Methods to Evaluate Sfh." Biomaterials, Artificial Cells and Immobilization Biotechnology 20, no. 2-4 (January 1992): 447–51. http://dx.doi.org/10.3109/10731199209119667.

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SHIMIZU, Youji. "Development of Analytical Methods of Fluid Erosion." Proceedings of the Space Engineering Conference 2004.13 (2005): 11–16. http://dx.doi.org/10.1299/jsmesec.2004.13.11.

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Vogt, Frederick G., and Alireza S. Kord. "Development of Quality-By-Design Analytical Methods." Journal of Pharmaceutical Sciences 100, no. 3 (March 2011): 797–812. http://dx.doi.org/10.1002/jps.22325.

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KANEKO, Emiko. "Development of Visual Analytical Methods for Trace Determination." Analytical Sciences 20, no. 2 (2004): 247–54. http://dx.doi.org/10.2116/analsci.20.247.

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Tsong, Yi, Xiaoyu Dong, and Meiyu Shen. "Development of statistical methods for analytical similarity assessment." Journal of Biopharmaceutical Statistics 27, no. 2 (December 15, 2016): 197–205. http://dx.doi.org/10.1080/10543406.2016.1272606.

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Dissertations / Theses on the topic "Development of analytical methods"

1

Ho, Yee Man. "Development of sample pretreatment methods for complex analytical matrices." HKBU Institutional Repository, 2013. http://repository.hkbu.edu.hk/etd_ra/1510.

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Kunati, Sandeep Reddy. "DEVELOPMENT OF BIOANALYTICAL METHODS FOR QUANTITATIVE MEASUREMENT OF ANTICANCER AGENTS." Cleveland State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=csu1523439107242919.

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BRANZ, LORENZO. "STUDY AND DEVELOPMENT OF ANALYTICAL AND ANALYTICAL-NUMERICAL METHODS FOR THE STUDY OF ELECTRICAL MACHINES." Doctoral thesis, Università degli Studi di Trieste, 2016. http://hdl.handle.net/11368/2908058.

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L’attività di ricerca si è focalizzata sulla determinazione di metodi analitici e analitico-numerici per la soluzione di alcuni problemi “aperti” di interesse nella progettazione e l'analisi di macchine elettriche. La tesi include una gamma piuttosto ampia di argomenti, ma è stata sviluppata seguendo una singola linea di indagine unitaria, che consiste nel tentativo di cercare e, dove possibile, definire e implementare, metodi matematici sufficientemente veloci ma accurati per eseguire calcoli su macchine elettriche in modo da evitare l'uso massiccio di tecniche basate su analisi agli elementi finiti. Queste infatti sono note per essere precise ed affidabili, ma allo stesso tempo richiedono ingenti risorse computazionali e sono quindi poco adatte quando è necessario esplorare un gran numero di varianti di progetto, come nel caso di programmi di ottimizzazione progettuale basati su algoritmi genetici. I metodi agli elementi finiti non sono stati esclusi, naturalmente, ma piuttosto utilizzati come “benchmark” per valutare la validità delle tecniche di calcolo alternative proposte, ove non fosse possibile effettuare un confronto diretto con dati sperimentali. I tipi di macchine elettriche a cui si sono applicati i metodi di calcolo sviluppati in questa tesi sono diversi e vanno dai motori a magneti permanenti superficiali con cave statoriche a motori a magneti permanenti superficiali con statore slotless ,dalle macchine sincrone a riluttanza alle macchine sincrone a rotore avvolto, per finire con motori a induzione a gabbia di scoiattolo. Tutti questi tipi di macchine sono sempre più importanti nelle applicazioni odierne, sia nel settore industriale che per i sistemi di trazione. Per affrontare lo studio di queste macchine si sono di volta in volta sviluppati approcci di calcolo analitico diversi, anche in funzione degli obiettivi da raggiungere. Esempi di questi approcci analitici impiegati sono i seguenti: la teoria della “winding function” applicata al calcolo della coppia di macchine a magneti superficiali; la teoria della “permeance function” applicata al calcolo delle macchine con eccentricità di rotore ; l'approccio mediante circuito equivalente magnetico o reti di riluttanze in combinazione a tecniche basate sulle mappe conformi per lo studio dei motori sincroni a riluttanza; la soluzione delle equazioni di Laplace e di Poisson per determinare il campo magnetico nelle macchine a magneti permanenti superficiali slotless e a gabbia di scoiattolo. Inoltre, l'applicazione degli algoritmi di calcolo proposti è illustrata mediante opportuni casi di studio ed i risultati ottenuti sono sempre convalidati mediante confronto con tecniche di calcolo alternative (in particolare l’analisi agli elementi finiti)
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Jeyapalan, Senthuran. "Development and application of chiral analytical methods for metabolic profiling." Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/58275.

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Metabonomics utilises high resolution analytical platforms to generate spectroscopic profiles that are rich in latent biological information. At present, the two principal analytical platforms used routinely in metabonomic studies are nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS). While these analytical methods in their current state of development in the field of metabonomics give broad coverage across multiple chemical classes, none report sufficiently well, if at all, on the absolute configuration of chiral molecules. As a consequence of the stereospecificity present in biological systems, a very large number of biologically active molecules exhibit chirality. Therefore, an important aspect of the metabolome remains largely unexplored by current metabonomic analytical platforms. Current enantioselective methods exist, but these are largely unsuitable for multi-analyte measurements. The work in this thesis addresses the need for appropriate chiral analytical methods for metabolic profiling. The aim was to develop a practical, fit-for-purpose chiral analytical method that will report simultaneously on numerous endogenous metabolites by untargeted or widely targeted analysis, and importantly, could be aligned with existing analytical workflows. Initial evaluation of an NMR spectroscopic approach using chiral solvating agents concluded that additional spectral complexity and interaction-induced internal reference compound chemical shift instability would prohibit efficient chiral profiling in a metabonomics workflow. An existing targeted MS-based assay for enantioselective separation of amino acids was selected for optimisation and further development. Focused analyses were performed to characterise its performance in the differentiation of individual pairs of enantiomers, and subsequently expanded, first to cover the panel of proteinogenic amino acids, and secondly to other detectable metabolites. Each stage of assay optimisation incorporated an evaluation in a representative set of samples and was able to provide highly relevant biological information that would not be accessible using current achiral metabonomic methods. Further work to expand the number of detectable metabolites and quantitative nature of the assay are discussed.
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Brown, Jared R. "Analytical Methods Development for High-Throughput Photochemisty With Led Arrays." Thesis, Virginia Tech, 2007. http://hdl.handle.net/10919/32709.

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This thesis describes the design, construction, and evaluation of a series of LED array photolysis systems for high throughput photochemistry. Three generations of array systems of increasing sophistication are evaluated using calorimetric measurements and potassium tris(oxalato)ferrate(III) chemical actinometry. The results are analyzed using descriptive statistics and analysis of variance (ANOVA). The LEDs in the third generation array were shown to be statistically equivalent, with respect to light output, according to physical and chemical actinometry experiments. The third generation LED array was compared with a traditional 1000 W Xe arc lamp source in terms of cost, light intensity, and light stability. Two constant current drivers were evaluated with respect to LED array performance. The optimized third generation LED array was evaluated as the photolysis source for photochemical hydrogen production experiments using the supramolecular catalyst [{(bpy)2Ru(dpp)}2RhCl2](PF6)5.
Master of Science
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Pingeon, Marine. "Development and validation of analytical methods for therapeutic drug monitoring." Doctoral thesis, Universita degli studi di Salerno, 2019. http://elea.unisa.it:8080/xmlui/handle/10556/4509.

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2017 - 2018
The U.S. Food and Drug Administration defines as Precision or Personalized Medicine (PM) an innovative therapeutic approach that tailors therapy and prevention on patients based on inter-individual variabilities in molecular or environmental features and in lifestyles. The major goals of PM are to maximize treatment efficacy and to reduce cost, toxicities and therapy failure rates by early identification of patients who might benefit or not of a specific treatment. In this scenario, therapeutic drug monitoring (TDM) is an important laboratory tool for PM because of the possibility to measure several drugs and bioactive molecules in human biological matrices. TDM is based on the hypothesis that in the majority of drugs, there is a relationship between administered dose and circulating concentration of unbound fraction - and between this concentration and observed pharmacological effects. TDM is recommended for drugs with significant inter-individual pharmacokinetic variability and an established relationship between blood concentrations and clinical efficacy and/or toxicity. Moreover, TDM is also advisable in special populations such as pregnant women and children. To date, liquid chromatography and immunometric assay are still considered the standard for molecule measurement in biological fluids; however, in recent years, LC tandem mass spectrometry (LC-MS) is gaining popularity because of the possibility of in-depth and multiplexed analysis with high selectivity and specificity. During this Ph.D. program, we developed several high performance LC (HPLC)- and LC-MS/MS-based approaches for TDM of different drugs measured in various types of body fluids and validated according to EMA and FDA guidelines. In particular, we focused on: 1) TDM of hydroxychloroquine (HCQ) blood concentration, a drug with a wide therapeutic window. Our method was validated on a cohort of patients with Systemic Lupus Erythematosus treated with HCQ and blood concentrations were correlated to several clinical parameters, such quality of life. Moreover, TDM of HCQ was also used to monitor treatment adherence in those subjects. 2) TDM of a commonly used chemotherapeutic agent, the 5-fluorouracil (5-FU), which is known to have a narrow therapeutic window and a high toxicity 3) TDM of a new kinase inhibitor, Ruxolitinib, approved for the treatment of myeloproliferative hematologic disorders. 4) TDM of several drugs, such as caffeine and phenobarbital, in newborns who are at particular risk of uncorrected drug dosage. Due to the need to carry out analyses on very-small volume samples, we validated an analytical method using micro-sampling techniques such as the dried blood spot (DBS) sampling combined with LC-MS/MS analysis. [edited by author]
XVII n.s. (XXXI ciclo)
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Lindholm, Johan. "Development and Validation of HPLC Methods for Analytical and Preparative Purposes." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4442.

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Emery, Sophie. "Development of analytical methods for the stability assessment of parenteral nutrition." Thesis, Cardiff University, 2018. http://orca.cf.ac.uk/112136/.

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Parenteral nutrition (PN) provides intravenous nutritional support to patients with reduced gastrointestinal function. A PN bag comprises the basic building blocks of the food groups: lipids, glucose, amino acids, vitamins, electrolytes and trace elements. Recently there has been an increase in demand for extended storage periods for PN bags, to ease management of an increasing home care market. Prior to a PN formulation being deemed safe for a patient, a laboratory simulation is carried out on the proposed admixture under the requested storage and administration conditions. Currently only the physical stability is assessed; physical testing provides no information on the quantity of each component remaining in the bag after storage. Consequently, there is a need for assessing the chemical stability of PN to indicate the quantity of each component that remains in the PN bag. A commonly used amino acid product, Aminoven® 25, contains 16 amino acids; this work aimed to develop a HPLC assay capable of quantifying the amino acids in an aqueous PN bag containing Aminoven® 25. Fluorescence detection was used as it is a highly selective method of detection, which was preferable due to the number of components in PN. To detect the amino acids, as they don’t naturally fluoresce, derivatization was carried out using ortho-phthalaldehyde to form a fluorescing derivative. The developed assay resulted in validation of thirteen of the amino acids in Aminoven® 25. In addition, the method was shown to be unaffected by the iv presence of aqueous PN components, so this method is suitable for quantifying thirteen amino acids in aqueous PN containing Aminoven® 25. This assay can be used for assessing the stability during stability testing and confirming the quantity of amino acids after compounding for quality control release.
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Cevenini, Luca <1981&gt. "Development of muliplexed analytical methods based on bioluminescent whole-cell biosensors." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2010. http://amsdottorato.unibo.it/2910/1/Cevenini_Luca_Tesi.pdf.

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The subject of this Ph.D. research thesis is the development and application of multiplexed analytical methods based on bioluminescent whole-cell biosensors. One of the main goals of analytical chemistry is multianalyte testing in which two or more analytes are measured simultaneously in a single assay. The advantages of multianalyte testing are work simplification, high throughput, and reduction in the overall cost per test. The availability of multiplexed portable analytical systems is of particular interest for on-field analysis of clinical, environmental or food samples as well as for the drug discovery process. To allow highly sensitive and selective analysis, these devices should combine biospecific molecular recognition with ultrasensitive detection systems. To address the current need for rapid, highly sensitive and inexpensive devices for obtaining more data from each sample,genetically engineered whole-cell biosensors as biospecific recognition element were combined with ultrasensitive bioluminescence detection techniques. Genetically engineered cell-based sensing systems were obtained by introducing into bacterial, yeast or mammalian cells a vector expressing a reporter protein whose expression is controlled by regulatory proteins and promoter sequences. The regulatory protein is able to recognize the presence of the analyte (e.g., compounds with hormone-like activity, heavy metals…) and to consequently activate the expression of the reporter protein that can be readily measured and directly related to the analyte bioavailable concentration in the sample. Bioluminescence represents the ideal detection principle for miniaturized analytical devices and multiplexed assays thanks to high detectability in small sample volumes allowing an accurate signal localization and quantification. In the first chapter of this dissertation is discussed the obtainment of improved bioluminescent proteins emitting at different wavelenghts, in term of increased thermostability, enhanced emission decay kinetic and spectral resolution. The second chapter is mainly focused on the use of these proteins in the development of whole-cell based assay with improved analytical performance. In particular since the main drawback of whole-cell biosensors is the high variability of their analyte specific response mainly caused by variations in cell viability due to aspecific effects of the sample’s matrix, an additional bioluminescent reporter has been introduced to correct the analytical response thus increasing the robustness of the bioassays. The feasibility of using a combination of two or more bioluminescent proteins for obtaining biosensors with internal signal correction or for the simultaneous detection of multiple analytes has been demonstrated by developing a dual reporter yeast based biosensor for androgenic activity measurement and a triple reporter mammalian cell-based biosensor for the simultaneous monitoring of two CYP450 enzymes activation, involved in cholesterol degradation, with the use of two spectrally resolved intracellular luciferases and a secreted luciferase as a control for cells viability. In the third chapter is presented the development of a portable multianalyte detection system. In order to develop a portable system that can be used also outside the laboratory environment even by non skilled personnel, cells have been immobilized into a new biocompatible and transparent polymeric matrix within a modified clear bottom black 384 -well microtiter plate to obtain a bioluminescent cell array. The cell array was placed in contact with a portable charge-coupled device (CCD) light sensor able to localize and quantify the luminescent signal produced by different bioluminescent whole-cell biosensors. This multiplexed biosensing platform containing whole-cell biosensors was successfully used to measure the overall toxicity of a given sample as well as to obtain dose response curves for heavy metals and to detect hormonal activity in clinical samples (PCT/IB2010/050625: “Portable device based on immobilized cells for the detection of analytes.” Michelini E, Roda A, Dolci LS, Mezzanotte L, Cevenini L , 2010). At the end of the dissertation some future development steps are also discussed in order to develop a point of care (POCT) device that combine portability, minimum sample pre-treatment and highly sensitive multiplexed assays in a short assay time. In this POCT perspective, field-flow fractionation (FFF) techniques, in particular gravitational variant (GrFFF) that exploit the earth gravitational field to structure the separation, have been investigated for cells fractionation, characterization and isolation. Thanks to the simplicity of its equipment, amenable to miniaturization, the GrFFF techniques appears to be particularly suited for its implementation in POCT devices and may be used as pre-analytical integrated module to be applied directly to drive target analytes of raw samples to the modules where biospecifc recognition reactions based on ultrasensitive bioluminescence detection occurs, providing an increase in overall analytical output.
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Cevenini, Luca <1981&gt. "Development of muliplexed analytical methods based on bioluminescent whole-cell biosensors." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2010. http://amsdottorato.unibo.it/2910/.

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The subject of this Ph.D. research thesis is the development and application of multiplexed analytical methods based on bioluminescent whole-cell biosensors. One of the main goals of analytical chemistry is multianalyte testing in which two or more analytes are measured simultaneously in a single assay. The advantages of multianalyte testing are work simplification, high throughput, and reduction in the overall cost per test. The availability of multiplexed portable analytical systems is of particular interest for on-field analysis of clinical, environmental or food samples as well as for the drug discovery process. To allow highly sensitive and selective analysis, these devices should combine biospecific molecular recognition with ultrasensitive detection systems. To address the current need for rapid, highly sensitive and inexpensive devices for obtaining more data from each sample,genetically engineered whole-cell biosensors as biospecific recognition element were combined with ultrasensitive bioluminescence detection techniques. Genetically engineered cell-based sensing systems were obtained by introducing into bacterial, yeast or mammalian cells a vector expressing a reporter protein whose expression is controlled by regulatory proteins and promoter sequences. The regulatory protein is able to recognize the presence of the analyte (e.g., compounds with hormone-like activity, heavy metals…) and to consequently activate the expression of the reporter protein that can be readily measured and directly related to the analyte bioavailable concentration in the sample. Bioluminescence represents the ideal detection principle for miniaturized analytical devices and multiplexed assays thanks to high detectability in small sample volumes allowing an accurate signal localization and quantification. In the first chapter of this dissertation is discussed the obtainment of improved bioluminescent proteins emitting at different wavelenghts, in term of increased thermostability, enhanced emission decay kinetic and spectral resolution. The second chapter is mainly focused on the use of these proteins in the development of whole-cell based assay with improved analytical performance. In particular since the main drawback of whole-cell biosensors is the high variability of their analyte specific response mainly caused by variations in cell viability due to aspecific effects of the sample’s matrix, an additional bioluminescent reporter has been introduced to correct the analytical response thus increasing the robustness of the bioassays. The feasibility of using a combination of two or more bioluminescent proteins for obtaining biosensors with internal signal correction or for the simultaneous detection of multiple analytes has been demonstrated by developing a dual reporter yeast based biosensor for androgenic activity measurement and a triple reporter mammalian cell-based biosensor for the simultaneous monitoring of two CYP450 enzymes activation, involved in cholesterol degradation, with the use of two spectrally resolved intracellular luciferases and a secreted luciferase as a control for cells viability. In the third chapter is presented the development of a portable multianalyte detection system. In order to develop a portable system that can be used also outside the laboratory environment even by non skilled personnel, cells have been immobilized into a new biocompatible and transparent polymeric matrix within a modified clear bottom black 384 -well microtiter plate to obtain a bioluminescent cell array. The cell array was placed in contact with a portable charge-coupled device (CCD) light sensor able to localize and quantify the luminescent signal produced by different bioluminescent whole-cell biosensors. This multiplexed biosensing platform containing whole-cell biosensors was successfully used to measure the overall toxicity of a given sample as well as to obtain dose response curves for heavy metals and to detect hormonal activity in clinical samples (PCT/IB2010/050625: “Portable device based on immobilized cells for the detection of analytes.” Michelini E, Roda A, Dolci LS, Mezzanotte L, Cevenini L , 2010). At the end of the dissertation some future development steps are also discussed in order to develop a point of care (POCT) device that combine portability, minimum sample pre-treatment and highly sensitive multiplexed assays in a short assay time. In this POCT perspective, field-flow fractionation (FFF) techniques, in particular gravitational variant (GrFFF) that exploit the earth gravitational field to structure the separation, have been investigated for cells fractionation, characterization and isolation. Thanks to the simplicity of its equipment, amenable to miniaturization, the GrFFF techniques appears to be particularly suited for its implementation in POCT devices and may be used as pre-analytical integrated module to be applied directly to drive target analytes of raw samples to the modules where biospecifc recognition reactions based on ultrasensitive bioluminescence detection occurs, providing an increase in overall analytical output.
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Books on the topic "Development of analytical methods"

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M, Riley Christopher, and Rosanske Thomas W, eds. Development and validation of analytical methods. Tarrytown, N.Y: Pergamon, 1996.

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Clacher, Adrian Paul. Development and application of analytical methods for environmental radioactivity. Manchester: University of Manchester, 1995.

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Omar, Mei Musa Ali. Development of Analytical Methods for Acrylamide Determination in Food. Saarbrücken: LAP LAMBERT Academic Publishing, 2017.

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1940-, Krull Ira S., ed. Analytical method development and validation. New York: M. Dekker, 1997.

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Kling, Ronn. Application development with IDL: Combining analytical methods with widget programming. Warrenton, VA: Ronn Kling Consulting, 2000.

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Speziale, Charles G. Analytical methods for the development of Reynolds stress closures in turbulence. Hampton, Va: Institute for Computer Applications in Science and Engineering, 1990.

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Center, Langley Research, ed. Analytical methods for the development of Reynolds stress closures in turbulence. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1990.

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A, McClenny William, Paur Richard J, and Environmental Monitoring Systems Laboratory (Research Triangle Park, N.C.), eds. Sampling and analytical methods development for dry deposition monitoring: Project summary. Research Triangle Park, NC: U.S. Environmental Protection Agency, Environmental Monitoring Systems Laboratory, 1987.

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Renman, Lars. Development of gas chromatographic and electrochemical analytical methods for industrial hygiene applications. Lund: Univ.of Lund, 1987.

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National Research Council (U.S.). Committee to Assess the U.S. Army Corps of Engineers Methods of Analysis and Peer Review for Water Resources Project Planning. Panel on Methods and Techniques of Project Analysis., ed. Analytical methods and approaches for water resources project planning. Washington, D.C: National Academies Press, 2004.

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Book chapters on the topic "Development of analytical methods"

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Yang, Harry, and Steven J. Novick. "Analytical Methods." In Bayesian Analysis with R for Drug Development, 141–62. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: Chapman and Hall/CRC, 2019. http://dx.doi.org/10.1201/9781315100388-8.

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Kapetanovic, Izet M., and Alexander V. Lyubimov. "Analytical Chemistry Methods: Developments and Validation." In Preclinical Development Handbook, 151–210. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470249031.ch5.

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Xu, Jian-guo, Li Yao, Lin Cheng, Chao Yan, and Wei Chen. "Development of Aptamer-Based Electrochemical Methods." In Aptamers for Analytical Applications, 247–71. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527806799.ch9.

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Mach, Phillip M., and Guido F. Verbeck. "Analytical Methods and Trends in Environmental Forensics." In Development and Environment, 285–301. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-75935-7_11.

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Brandt, Peter. "Development and validation of analytical methods." In Bericht aus dem Nationalen Referenzlabor des BVL für das Jahr 2008, 8–18. Basel: Birkhäuser Basel, 2009. http://dx.doi.org/10.1007/978-3-0346-0235-8_2.

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Hout, Sam A. "Analytical Methods Development, Validation, and Transfer." In Manufacturing of Quality Oral Drug Products, 153–70. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003224716-21.

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Gu, Huajie, Liling Hao, and Zhouping Wang. "Development of Aptamer-Based Non-labeling Methods." In Aptamers for Analytical Applications, 301–43. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527806799.ch11.

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Gopinath, Subash C. B., Thangavel Lakshmipriya, M. K. Md Arshad, and Chun Hong Voon. "Development of Aptamer-Based Colorimetric Analytical Methods." In Aptamers for Analytical Applications, 205–18. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527806799.ch6.

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Jauset-Rubio, Miriam, Mohammad S. El-Shahawi, Abdulaziz S. Bashammakh, Abdulrahman O. Alyoubi, and Ciara K. O'Sullivan. "Development of Aptamer-Based Lateral Flow Assay Methods." In Aptamers for Analytical Applications, 273–99. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527806799.ch10.

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Gardner, Erin R. "Quantitative Analytical Methods: Development and Clinical Considerations." In Cancer Drug Discovery and Development, 107–16. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-9135-4_7.

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Conference papers on the topic "Development of analytical methods"

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Ахмедов, Б., and А. Рашидов. "METHODS OF EVALUATING THE UNCERTAINTY OF ANALYTICAL MEASUREMENTS." In Status and development trends of standardization and technical regulation in the world. Tashkent state technical university, 2022. http://dx.doi.org/10.51346/tstu-conf.22.1-77-0046.

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In this article, methods for estimating uncertainties in analytical measurements, as well as sources of uncertainty, their assessment and ranking function factors definition is provided. Applying the distribution laws of uncertainty, with the result associated cumulative uncertainty estimates, such as molar mass uncertainty estimates issues have been studied.
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Brown, J. R., M. Elvington, M. T. Mongelli, D. F. Zigler, and K. J. Brewer. "Analytical methods development for supramolecular design in solar hydrogen production." In SPIE Optics + Photonics, edited by Lionel Vayssieres. SPIE, 2006. http://dx.doi.org/10.1117/12.680961.

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Ding, Dachuan. "Research on Analytical Methods of Domestic and Foreign Logistics Development." In 2020 5th International Conference on Information Science, Computer Technology and Transportation (ISCTT). IEEE, 2020. http://dx.doi.org/10.1109/isctt51595.2020.00120.

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Lira, Andressa da Nóbrega, and Romildo dos Santos Escarpini Filho. "Development of a simplified analytical viscoelastic formulation for the analysis of laminated composites." In XXXVIII Iberian-Latin American Congress on Computational Methods in Engineering. Florianopolis, Brazil: ABMEC Brazilian Association of Computational Methods in Engineering, 2017. http://dx.doi.org/10.20906/cps/cilamce2017-0837.

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Hackmann, E., and C. Lämmerzahl. "Analytical solution methods for geodesic motion." In RECENT DEVELOPMENTS ON PHYSICS IN STRONG GRAVITATIONAL FIELDS: V Leopoldo García-Colín Mexican Meeting on Mathematical and Experimental Physics. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4861945.

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Liu, Chang, Jiaquan Chen, and Yin-ping Chang. "An Analytical Vehicle Kano Model Development Integrating With QFD and TRIZ Methods." In ASME 2022 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/imece2022-95644.

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Abstract The rapid development of science and technology has resulted in ever-shortening product development cycle and varies customers’ wants and needs tremendously. To keep the pace of market developments and customers’ needs, a shorter product developing process and cycle is necessary. During the process of engineering design and development, there is always a gap between customers and engineers. This research creates a new Customer to Engineering (C2E) system by integrating the Kano model, QFD and S-Curve in TRIZ method. The C2E system is the bridge to close the gap between the customers and engineers by constructing an engineering design chain from customers’ voices all the way to the engineering system. In this paper, an optimized analytical Kano model is developed, and a new classification method is conducted. Based on the classification and balance model of vehicle performance indices, two new parameters, Kano Classification Coefficient and Customer Perception Factor are introduced. Then the Relative Important Degree and the Ultimate Customer Perception Factor are derived with the concept of QFD to further optimize Kano model and digitalize HoQ (House of Quality) diagram with geometric progression for further analyses. The corresponding relationship between Kano model and S-Curve is introduced to identify the development stage of the engineering system for the first time. Once the stage is identified, further design modifications can be applied to the engineering system according to the S-Curve analyses.
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Kelana, Nurul Maulidina, Purnawarman Musa, and Amri Dunan. "Challenge handling flood disaster by recommendation system with Analytical Hierarchy Process Methods." In 2021 2nd International Conference on ICT for Rural Development (IC-ICTRuDev). IEEE, 2021. http://dx.doi.org/10.1109/ic-ictrudev50538.2021.9656513.

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Chen, Jiahuan, and Xinming Li. "Development Of A Bi-Criterion Objective Function For Analytical Inverse Kinematic Methods." In Canadian Society for Mechanical Engineering International Congress (2021 : Charlottetown, PE). Charlottetown, P.E.I.: University of Prince Edward Island. Robertson Library, 2021. http://dx.doi.org/10.32393/csme.2021.50.

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Pyanylo, Yaroslav, Sofiya Tvardovska, and Nazariy Lopuh. "The Development of Analytical and Numerical Methods for Research of Porous Mediums." In 2023 13th International Conference on Advanced Computer Information Technologies (ACIT). IEEE, 2023. http://dx.doi.org/10.1109/acit58437.2023.10275615.

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Ghosh, Amitabha. "Development of Analytical Skills Through Cooperative Learning." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-12947.

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Learning analytical skills in the context of formulating and solving a well-posed fluid flow problem requires special considerations which are often missed by students or under-emphasized by faculty during instructional delivery of materials. This paper presents the results of a pilot study in the class Transport Phenomena to determine if cooperative learning and working in groups would assist better understanding of these topics. Cooperative learning was found to have many benefits related to comprehension and positive interdependence. But benefits derived from this approach are limited unless such methods are reinforced in several places in the curriculum. Comparative performance data is presented with and without this approach. Issues related to Bloom’s taxonomy and cognitive apprenticeship were investigated and discussed in context of the class Transport Phenomena.
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Reports on the topic "Development of analytical methods"

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Dupont, Pierre E. Development of Analytical Methods Applicable to Test Data. Fort Belvoir, VA: Defense Technical Information Center, March 1998. http://dx.doi.org/10.21236/ada339328.

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Clauss, S. A., V. Hoopes, and J. Rau. Organic analysis and analytical methods development: FY 1995 progress report. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/120865.

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Dunn, Michael E., Dorothea Wiarda, and Sedat Goluoglu. Letter Report - NCSP Analytical Methods Subtask 4: AMPX Development and Maintenance. Office of Scientific and Technical Information (OSTI), February 2011. http://dx.doi.org/10.2172/1134627.

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Dunn, Michael, Dorothea Wiarda, Sedat Goluoglu, and Don Mueller. Letter Report - NCSP Analytical Methods Subtask 4: AMPX Development and Maintenance. Office of Scientific and Technical Information (OSTI), November 2011. http://dx.doi.org/10.2172/1135833.

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Campbell, J. A., S. Clauss, K. Grant, V. Hoopes, B. Lerner, R. Lucke, G. Mong, J. Rau, K. Wahl, and R. Steele. Flammable gas safety program. Analytical methods development: FY 1994 progress report. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/10190378.

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Bryan, S. A., K. H. Pool, L. L. Burger, C. D. Carlson, N. J. Hess, J. D. Matheson, J. L. Ryan, R. D. Scheele, and J. M. Tingey. Ferrocyanide safety project: Task 3. 5 cyanide species analytical methods development. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/6850842.

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Campbell, J. A., S. Clauss, K. Grant, V. Hoopes, B. Lerner, R. Lucke, G. Mong, J. Rau, and R. Steele. Flammable gas safety program. Analytical methods development: FY 1993 progress report. Office of Scientific and Technical Information (OSTI), January 1994. http://dx.doi.org/10.2172/10122073.

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Maskarinec, M. P. Analytical Methods Development in Support of the Caustic Side Solvent Extraction System. Office of Scientific and Technical Information (OSTI), July 2001. http://dx.doi.org/10.2172/786754.

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Campbell, J. A., S. A. Clauss, and K. E. Grant. Waste Tank Organic Safety Program: Analytical methods development. Progress report, FY 1994. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/10190044.

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Beckman, Ivan. Development of alternative air filtration materials and methods of analysis. Engineer Research and Development Center (U.S.), June 2023. http://dx.doi.org/10.21079/11681/47188.

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Development of high efficiency particulate air (HEPA) filters demonstrate an effort to mitigate dangerous aerosol hazards at the point of production. The nuclear power industry installs HEPA filters as a final line of containment of hazardous particles. An exploration of analytical, experimental, computational, and machine learning models is presented in this dissertation to advance the science of air filtration technology. This dissertation studies, develops, and analyzes alternative air filtration materials and methods of analysis that optimize filtration efficiency and reduce resistance to air flow. Alternative nonwoven filter materials are considered for use in HEPA filtration. A detailed review of natural and synthetic fibers is presented to compare mechanical, thermal, and chemical properties of fibers to desirable characteristics for air filtration media. Digital replication of air filtration media enables coordination among experimental, analytical, machine learning, and computational air filtration models. The value of using synthetic data to train and evaluate computational and machine learning models is demonstrated through prediction of air filtration performance, and comparison to analytical results. This dissertation concludes with discussion on potential opportunities and future work needed in the continued effort to advance clean air technologies for the mitigation of a global health and safety challenge.
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