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Journal articles on the topic 'Chromatographic analysis'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Denisov, I. S., V. V. Korotkov, and D. S. Smirnov. "Gaschromatographic monitoring of volatile pollutants of urban air: optimizing analysis and concentrating." Sanitarnyj vrač (Sanitary Doctor), no. 10 (October 1, 2020): 70–76. http://dx.doi.org/10.33920/med-08-2010-08.

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For determining 22 volatile organic compounds in the atmospheric air, the operating modes of the gas chromatographic complexes «chromatography-mass spectrometer — two-stage thermodesorber» and «gas chromatograph with 2 FID — static headspace analysis sampler» are optimized. The modes provide the values of the separation coefficients of the chromatographic peaks in the range of 1.5 ÷ 21. It has been experimentally established that the highest desorption efficiency of volatile organic compounds is registered when the sample is concentrated into Tenax TA sorption tubes.

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2

Onjia, Antonije, Tatjana Vasiljevic, Djuro Cokesa, and Mila Lausevic. "Validation of chromatographic analysis." Chemical Industry 56, no. 2 (2002): 76–79. http://dx.doi.org/10.2298/hemind0202076o.

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The parameters for the development of a chromatographic (HPLC) method and its validation are discused in the paper. Chromatographic analysis involves a multi-step procedure consisting of sample collection, pretreatment instrumental measurements and data processing. Emphasize was placed on the instrumental part of the analysis presuming that the contributions of the other variables were minor. The roles of precision, accuracy, detection limit, quantification limit, specificity, selectivity, range, linearity and robustness, as well as system suitability in the analytical application of chromatog

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3

Christie, W. W. "Lipid chromatographic analysis." TrAC Trends in Analytical Chemistry 13, no. 10 (1994): xiii. http://dx.doi.org/10.1016/0165-9936(94)85032-1.

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4

Janis, Linda J., and Fred E. Regnier. "Immunological-Chromatographic Analysis." Journal of Chromatography A 444 (July 1988): 1–11. http://dx.doi.org/10.1016/s0021-9673(01)94003-8.

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5

Lyle, S. J. "Inorganic chromatographic analysis." Endeavour 9, no. 4 (1985): 205–6. http://dx.doi.org/10.1016/0160-9327(85)90088-2.

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6

Hais, I. M. "Chromatographic adsorption analysis." Journal of Pharmaceutical and Biomedical Analysis 9, no. 9 (1991): 785–86. http://dx.doi.org/10.1016/0731-7085(91)80223-v.

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7

Worsfold, PaulJ. "Chromatographic Environmental Analysis." Analytica Chimica Acta 296, no. 2 (1994): 220. http://dx.doi.org/10.1016/0003-2670(94)80268-8.

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8

Cooke, M. "Inorganic Chromatographic Analysis." Analytica Chimica Acta 183 (1986): 328–29. http://dx.doi.org/10.1016/0003-2670(86)80117-9.

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9

Zhang, Jing, and Hongye Zhang. "Research progress on the detection of water-soluble vitamins in food using liquid chromatography." Theoretical and Natural Science 37, no. 1 (2024): 158–69. http://dx.doi.org/10.54254/2753-8818/37/20240183.

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Currently, liquid chromatography is widely used for the analysis and determination of water-soluble vitamins (WSVs) in functional foods. However, due to the diversity of sample characteristics and the requirement for purification accuracy, the chromatographic conditions and specific methods used vary. This paper reviews the chromatographic conditions of liquid chromatography techniques for detecting WSVs in food, as well as the selection of liquid chromatography methods in different application fields. The chromatographic conditions include chromatographic columns, column temperature, mobile p

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10

Custodio-Mendoza, Jorge Antonio, Patryk Pokorski, Havva Aktaş, Alicja Napiórkowska, and Marcin Andrzej Kurek. "Advances in Chromatographic Analysis of Phenolic Phytochemicals in Foods: Bridging Gaps and Exploring New Horizons." Foods 13, no. 14 (2024): 2268. http://dx.doi.org/10.3390/foods13142268.

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Chromatographic analysis of phenolic phytochemicals in foods has significantly advanced over the past decade (2014–2024), meeting increasing demands for precision and efficiency. This review covers both conventional and advanced chromatographic techniques used for detecting phenolic phytochemicals in foods. Conventional methods like High-Performance Liquid Chromatography, Ultra High-Performance Liquid Chromatography, Thin-Layer Chromatography, and Gas Chromatography are discussed, along with their benefits and limitations. Advanced techniques, including Hydrophilic Interaction Liquid Chromatog

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11

Diroh, Vina Awallina, Rio Gusraya Unaldi, Mutiara Wayu Puspasari, and Muhammad Muzhil Aslam. "NSAID Analysis Using Chromatographic and Spectrophotometric Methods." Asian Journal of Analytical Chemistry 1, no. 1 (2023): 12–17. http://dx.doi.org/10.53866/ajac.v1i1.269.

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The purpose of this review article to evaluate the content of Nonsteroidal anti-inflammatory drugs (NSAID) using chromatographic and spectrophotometric methods. This journal review uses seven analytical methods on NSAID , namely high performance liquid chromatography (HPLC), fourier transform infrared (FTIR), gas chromatography (GC), thin layer chromatography (TLC), and spectrophotometry methods. The outcomes of every method have been elaborated in this paper and all of them can be used to detect the NSAID compounds.

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12

Saha, Sourav, Sandip Mallik, Bikash Debnath, Waikhom Somraj Singh, Abu Md Ashif Ikbal, and Kuntal Manna. "Application of HPLC in Biomedical Research for Pesticide and Drug Analysis." Global Journal of Medical, Pharmaceutical, and Biomedical Update 18 (September 7, 2023): 20. http://dx.doi.org/10.25259/gjmpbu_40_2023.

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Compared to traditional liquid chromatography, high-performance liquid chromatography (HPLC) delivers better results for analyzing unknown compounds. It permits faster resolution time, better peak shapes, repeatable responses, and greater precision. A comprehensive literature search has been conducted using online academic databases such as Google Scholar, PubMed, Web of Science, and Scopus, using keywords such as HPLC, pesticide analysis, drugs analysis, chromatographic conditions, and HPLC Column type. Total 75 number of articles were collected from peer-reviewed journals. With the help of l

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13

Pytela, Oldřich, Jaroslava Hálová, and Miroslav Ludwig. "Interpretation of chromatographic characteristics of mobile phase in liquid chromatography by means of solvent parameters." Collection of Czechoslovak Chemical Communications 55, no. 11 (1990): 2629–35. http://dx.doi.org/10.1135/cccc19902629.

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The paper applies the methods of correlation analysis and analysis of latant variables (PCA, PLS, canonical correlation) to study the interrelations of general chromatographic characteristics in the adsorption and partition chromatography (ε0, P', χe, χd, χn, Iap) and interpretation posibilities of these characteristics by means of general solvent parameters. The analyzed set of chromatographical parameters has been found to be relatively heterogeneous, its dominant properties being expressible by two principal components including 75.6% of source variability. The chemometrical solvent scale w

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14

Kordzakhia, T. N., M. G. Zautashvili, L. G. Eprikashvili, et al. "New sorbents for determining the quality of alcoholic beverages by chromatographic analysis." Himia, Fizika ta Tehnologia Poverhni 15, no. 4 (2024): 500–506. http://dx.doi.org/10.15407/hftp15.04.500.

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A new universal gas-chromatographic method of identification of toxic impurities is proposed in order to improve the quality indicators of alcoholic beverages. Application of chromatographic methods in wine making is characterized by some peculiarities, which is stipulated from one hand by substance characteristics as they are and from the other by changes in chromatographic methods possibilities. The method allows to determine the quality and chemical composition of the alcoholic beverages, which to some extent determines the possibility of regulating its quality on a scientific basis. Modifi

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15

Memon, Najma, Tahira Qureshi, Muhammad Iqbal Bhanger, and Muhammad Imran Malik. "Recent Trends in Fast Liquid Chromatography for Pharmaceutical Analysis." Current Analytical Chemistry 15, no. 4 (2019): 349–72. http://dx.doi.org/10.2174/1573411014666180912125155.

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Background: Liquid chromatography is the workhorse of analytical laboratories of pharmaceutical companies for analysis of bulk drug materials, intermediates, drug products, impurities and degradation products. This efficient technique is impeded by its long and tedious analysis procedures. Continuous efforts of scientists to reduce the analysis time resulted in the development of three different approaches namely, HTLC, chromatography using monolithic columns and UHPLC. Methods: Modern column technology and advances in chromatographic stationary phase including silica-based monolithic columns

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16

Valverde, Antonio. "Chromatographic Pesticide Residue Analysis." Journal of AOAC INTERNATIONAL 83, no. 3 (2000): 679. http://dx.doi.org/10.1093/jaoac/83.3.679.

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17

McCreedy, Tom. "Chromatographic analysis of pharmaceuticals." Analytica Chimica Acta 347, no. 3 (1997): 397. http://dx.doi.org/10.1016/s0003-2670(97)81191-9.

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18

Macek, Karel. "Chromatographic analysis of pharmaceuticals." Journal of Chromatography A 545, no. 1 (1991): 219–20. http://dx.doi.org/10.1016/s0021-9673(01)88712-4.

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19

Manetto, Giulia, and Franco Tagliaro. "Chromatographic analysis of pharmaceuticals." Journal of Chromatography A 786, no. 2 (1997): 385–87. http://dx.doi.org/10.1016/s0021-9673(97)00753-x.

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20

Sparidans, Rolf W., Jan den Hartigh, Serge Cremers, and Pieter Vermeij. "Chromatographic analysis of bisphosphonates." Journal of Chromatography A 868, no. 1 (2000): 141–42. http://dx.doi.org/10.1016/s0021-9673(99)01233-9.

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21

Lee, Hyoung S., and Victor Hong. "Chromatographic analysis of anthocyanins." Journal of Chromatography A 624, no. 1-2 (1992): 221–34. http://dx.doi.org/10.1016/0021-9673(92)85681-i.

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22

Childs, JJ. "Chromatographic analysis of alkaloids." Biochemical Education 19, no. 4 (1991): 221. http://dx.doi.org/10.1016/0307-4412(91)90116-p.

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23

Barry, Eugene F. "Chromatographic analysis of pharmaceuticals." Microchemical Journal 44, no. 2 (1991): 237. http://dx.doi.org/10.1016/0026-265x(91)90103-v.

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24

Willför, S. M., A. I. Smeds, and B. R. Holmbom. "Chromatographic analysis of lignans." Journal of Chromatography A 1112, no. 1-2 (2006): 64–77. http://dx.doi.org/10.1016/j.chroma.2005.11.054.

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25

Christie, W. W. "Chromatographic analysis of phospholipids." Zeitschrift für Lebensmittel-Untersuchung und -Forschung 181, no. 3 (1985): 171–82. http://dx.doi.org/10.1007/bf02425573.

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26

Potier, P. "Chromatographic Analysis of Alkaloids." Biochimie 74, no. 6 (1992): 590. http://dx.doi.org/10.1016/0300-9084(92)90162-8.

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27

Eichman, Chad, Brian Rivera, and M. Christina Malinao. "Chromatographic Analysis for PAT." Genetic Engineering & Biotechnology News 38, no. 20 (2018): 20. http://dx.doi.org/10.1089/gen.38.20.09.

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28

Molyneux, Russell J., Dale R. Gardner, Lynn F. James, and Steven M. Colegate. "Polyhydroxy alkaloids: chromatographic analysis." Journal of Chromatography A 967, no. 1 (2002): 57–74. http://dx.doi.org/10.1016/s0021-9673(01)01558-8.

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29

Karnes, H. Thomas. "Chromatographic analysis of pharmaceuticals." Journal of Pharmaceutical Sciences 80, no. 3 (1991): 303–4. http://dx.doi.org/10.1002/jps.2600800326.

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30

Manda, Swapna* Rongali Indu Dr. P.V. Madhavi Latha B. Rama Madhuri. "A Comprehensive Review on UHPLC and UPLC: Advancements, Comparison, and Applications." International Journal of Scientific Research and Technology 1, no. 11 (2024): 87–91. https://doi.org/10.5281/zenodo.14173528.

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Ultra-High-Performance Liquid Chromatography (UHPLC) and Ultra Performance Liquid Chromatography (UPLC) are two of the most advanced liquid chromatographic techniques, offering improved separation, sensitivity, and speed over traditional High-Performance Liquid Chromatography (HPLC). While both technologies share similar principles, they differ in system configurations, column technologies, and applications. UHPLC generally refers to any liquid chromatography system capable of using sub-2 µm particles, while UPLC is a proprietary technology developed by Waters Corporation that optimizes

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31

AHUMADA FORIGUA, Diego Alejandro, and Jairo Arturo GUERRERO DALLOS. "Reduction of matrix effects in pesticide residue analysis in food by programmable temperature vaporizer." Vitae 20, no. 3 (2013): 184–1941. http://dx.doi.org/10.17533/udea.vitae.11056.

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Background: The phenomenon known as the “matrix-induced chromatographic response enhancement” commonly affects the sensibility, precision, and accuracy in pesticide residue analysis. The presence of matrix effects can be given by adsorption and/or thermal decomposition of pesticides on the gas chromatograph injection port. Objective: To reduce the matrix-induced chromatographic response enhancement on pesticide residues analysis in food through the use of several operational modes of programmable temperature vaporizer inlet. Methods: The analyses were carried out in potato (Solanum tuberosum)

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32

Verpoorte, R. "Chromatographic analysis of alkaloids (Chromatographic Science Series Vol. 53)." Journal of Chromatography A 545, no. 1 (1991): 221–22. http://dx.doi.org/10.1016/s0021-9673(01)88713-6.

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33

Nagels, Luc. "Chromatographic analysis of pharmaceuticals, chromatographic science series vol 74." TrAC Trends in Analytical Chemistry 16, no. 10 (1997): X. http://dx.doi.org/10.1016/s0165-9936(97)82183-8.

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34

Liu, Guo Bin, Ning Wang, Qing Hao Wang, et al. "Chromatographic Analysis of Oil-Based Electrical Equipment Discharge Failure." Applied Mechanics and Materials 602-605 (August 2014): 2953–57. http://dx.doi.org/10.4028/www.scientific.net/amm.602-605.2953.

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Discharge of failure was the fault type are likely to occur in transformers, bushings, transformers, and the extent of damage to the equipment is a serious and direct impact on the stable operation of the system, first introduced the principle and gas chromatographic analysis its test methods, then gas chromatography equipment discharge failure is how to judge the conduct described. Through the analysis of transformer oil chromatographic method can be found as early as possible transformers and other equipment inside the existence of latent failures, thus chromatography is to oversee and guara

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35

Isoherranen, Nina, and Stefan Soback. "Chromatographic Methods for Analysis of Aminoglycoside Antibiotics." Journal of AOAC INTERNATIONAL 82, no. 5 (1999): 1017–45. http://dx.doi.org/10.1093/jaoac/82.5.1017.

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Abstract Aminoglycosides are antimicrobial agents used frequently in treatment of human and animal diseases caused by aerobic, gram-negative bacteria. Because of the toxicity of these compounds, considerable effort has been attributed to analysis of aminoglycoside content in drug preparations, in serum and urine specimen in therapeutic drug monitoring, and in edible animal tissues in residue control. The present review emphasizes the analytical problems associated with aminoglycoside analysis. Screening methods based on microbiological and immunological procedures were briefly discussed. Gas c

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36

Gehrke, Charles W., Kenneth C. Kuo, Floyd E. Kaiser та Robert W. Zumwalt. "Analysis of Amino Acids by Gas Chromatography as the N-Trifluoroacetyl η-Butyl Esters". Journal of AOAC INTERNATIONAL 70, № 1 (1987): 160–70. http://dx.doi.org/10.1093/jaoac/70.1.160.

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Abstract This presentation describes amino acid analysis with the gas chromatographic method and experimental conditions using the N-trifluoroacetyl n-butyl ester derivatives; the study we describe here was undertaken to compare gas chromatographic (GC) and ion-exchange chromatographic (IEC) analyses of amino acids in hydrolysates of 9 diverse sample types to gain insight into effects of these 2 chromatographic methods of analysis on variation in amino acid results. Our study showed that values for samples prepared by 2 separate laboratories using the same procedure were generally in good agre

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37

P., K. Gutch, Dubey V., S. Dangi R., C. Malhotra R., and K. Jaiswal D. "Chromatographic analysis of benzylidenemalononitrile analogues of 2-chlorobenzylidenemalononitrile." Journal of Indian Chemical Society Vol. 81, Oct 2004 (2004): 874–78. https://doi.org/10.5281/zenodo.5832676.

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Synthetic Chemistry Division, Defence R & D Establishment, Jhansi Road, Gwalior-474 002, India <em>E-mail</em>: pkgutch@yahoo.com         <em>Fax:</em> 91-751-2341148 <em>Manuscript received 6 May 2003, revised 17 October 2003, accepted 3 May 2004</em> The riot control agent 2-chorobenzylidenemalononitrile (CS) and its <em>ortho</em> and<em> para </em>substituted benzylidenemalononitrile (BMN) analogues were synthesised and characterized by spectroscopic techniques (IR, NMR and mass spectrometry). These compounds were also analysed using thin layer chromatogra

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38

Kholin, Andrey Yu, Svetlana V. Kurbatova, and Margarita N. Zemtsova. "Comparative analysis of the various structures quinoline derivatives retention under RP HPLC." Butlerov Communications 63, no. 8 (2020): 31–39. http://dx.doi.org/10.37952/roi-jbc-01/20-63-8-31.

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The study results of the structure and physicochemical parameters effect of various quinoline derivatives on their retention under conditions of reversed-phase high-performance liquid chromatography are presented. It is shown that since the establishment of the relationship between the structure of a substance and its properties is still one of the most important problems of modern chemistry and materials science, chromatography is a very convenient and effective method for obtaining the information necessary for this. To establish the relationship between the structure and sorption characteri

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39

Shimada, K. "Modern chromatographic analysis of vitamins (Chromatographic Science Series, Vol. 60)." Journal of Chromatography A 633, no. 1-2 (1993): 320. http://dx.doi.org/10.1016/0021-9673(93)83171-n.

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40

Swanson, Steven P., Andrew M. Dahlem, Harold D. Rood, Louis-Marie Côte, William B. Buck, and Takumi Yoshizawa. "Gas Chromatographic Analysis of Milk for Deoxynivalenol and Its Metabolite DOM-1." Journal of AOAC INTERNATIONAL 69, no. 1 (1986): 41–43. http://dx.doi.org/10.1093/jaoac/69.1.41.

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Abstract A gas chromatographic method is described for the determination of deoxynivalenol (DON) and its metabolite DOM-1 in milk. Milk samples were extracted with ethyl acetate on a commercially available disposable extraction column, followed by hexane-acetonitrile partitioning. Final purification was accomplished on a reverse phase C-18 cartridge. The trimethylsilyl ether (TMS) derivatives of DON were prepared, chromatographed on an OV-17 column, and quantitated with an electron capture detector. Chromatography of the TMS derivatives of milk extracts was compared to that of the correspondin

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41

Tóth, Gábor, Simon Sugár, Mirjam Balbisi, et al. "Optimized Sample Preparation and Microscale Separation Methods for High-Sensitivity Analysis of Hydrophilic Peptides." Molecules 27, no. 19 (2022): 6645. http://dx.doi.org/10.3390/molecules27196645.

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The optimization of solid-phase extraction (SPE) purification and chromatographic separation is usually neglected during proteomics studies. However, the effects on detection performance are not negligible, especially when working with highly glycosylated samples. We performed a comparative study of different SPE setups, including an in-house optimized method and reversed-phase chromatographic gradients for the analysis of highly glycosylated plasma fractions as a model sample for glycopeptide analysis. The in-house-developed SPE method outperformed the graphite-based and hydrophilic interacti

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42

Swati, Pachore Anushka shinde Sandip laware. "A Review On Chromatographic Separation Techniques." International Journal of Pharmaceutical Sciences 2, no. 10 (2024): 758–66. https://doi.org/10.5281/zenodo.13935296.

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Chromatographic separation techniques are essential tools in analytical chemistry, utilized for the isolation, identification, and quantification of complex mixtures. This review provides an overview of various chromatographic methods, including gas chromatography (GC), liquid chromatography (LC), and their advanced variations such as high-performance liquid chromatography (HPLC) and supercritical fluid chromatography (SFC). Each technique’s principles, advantages, and limitations are discussed, along with their applications across diverse fields, including pharmaceuticals, environmental

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43

Gertsiuk, Modest. "Chromatography in Ukraine: Development and Achievements." Separations 9, no. 5 (2022): 114. http://dx.doi.org/10.3390/separations9050114.

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The development of chromatographic science in Ukraine is due to the widespread use of chromatography to solve practical problems. The centers of chromatographic research in Ukraine are in large cities: Kyiv, Kharkiv, Lviv, Odessa, and others. Along with the development of chromatographic research methods, analysis methods for control of food and agricultural raw materials, medicinal products, petroleum products, and determination of the environmental pollution state are created. Chromatography is used in medicine, pharmacology, biology, and other sciences.

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44

Simion Beldean-Galea, Mihail, Florina-Maria Copaciu, and Maria-Virginia Coman. "Chromatographic Analysis of Textile Dyes." Journal of AOAC INTERNATIONAL 101, no. 5 (2018): 1353–70. http://dx.doi.org/10.5740/jaoacint.18-0066.

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Abstract The textile industry uses many raw materials (natural and synthetic dyes and fibers) and different dyeing techniques that can be considered important pollutants with a negative impact on the environment (toxic working conditions, discharged wastewater, and contamination). Although synthetic dyes are intensively used, offer a wide range of colors and hues and properties of adhesion, longevity, and resistance to sunshine and chemical processes, and are cost-effective, they have begun to be restricted by many textile producers because they are nonbiodegradable and have toxic, carcinogeni

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45

KISHIKAWA, Naoya. "Derivatization Techniques for Chromatographic Analysis." Analytical Sciences 34, no. 10 (2018): 1109–10. http://dx.doi.org/10.2116/analsci.highlights1810.

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46

Vimalasiri, P. A. D. T., R. P. Burford, and J. K. Haken. "Chromatographic Analysis of Elastomeric Polyurethanes." Rubber Chemistry and Technology 60, no. 3 (1987): 555–77. http://dx.doi.org/10.5254/1.3536140.

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Abstract Both alkali and acid fusion reactions can be used to cleave polyurethane polymers successfully. Fusion reaction rates are much faster than conventional aqueous alkali or acid fusion methods. Separation of fragments could be carried out using the liquid-liquid extraction procedures described. After quantitative and qualitative analysis of fragments using GC, SEC, and HPLC, chemical structure of the polymer can be established. Although the work described uses only elastomeric polyurethanes for the development of the analytical schemes, these schemes can be used to analyze other types of

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47

Ahmad, Sayeed, MasoodShah Khan, Rabea Parveen, Kshipra Mishra, and Rajkumar Tulsawani. "Chromatographic analysis of wheatgrass extracts." Journal of Pharmacy and Bioallied Sciences 7, no. 4 (2015): 267. http://dx.doi.org/10.4103/0975-7406.168023.

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48

Stirbet, Daniela, Simona-Carmen Litescu, and Gabriel-Lucian Radu. "Chromatographic analysis of immobilized cefotaxime." Journal of the Serbian Chemical Society 79, no. 5 (2014): 579–86. http://dx.doi.org/10.2298/jsc130821008s.

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The aim of the present work was to widen the application of an in-house developed fast, flexible and sensitive high performance liquid chromatography (HPLC) method to the assessment of cefotaxime sodium from aqueous samples. The method was applied to establish the release profile of cefotaxime sodium immobilised in MCM-41 nanoparticles using pH controlled release in aqueous medium. The analytical method proved to be sensible, repeatable (RSD < 1.5 %) and reproducible (RSD < 1 %) in the concentration range studied (0.01-10 ?g?mL-1), limit of detection and limit of quantification were 0.03

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49

LIU, Yujian, Fuyou DU, Zhimin LIU, Xiaoxi SI, and Zhigang XU. "Tandem technologies in chromatographic analysis." Chinese Journal of Chromatography 36, no. 9 (2018): 842. http://dx.doi.org/10.3724/sp.j.1123.2018.04015.

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50

Iwasaka, M., and S. Ueno. "Liquid Chromatographic Analysis of Magnetophoresis." Journal of the Magnetics Society of Japan 21, no. 4_2 (1997): 741–44. http://dx.doi.org/10.3379/jmsjmag.21.741.

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