Academic literature on the topic 'Spectrophotometric detection with diode matrix (DAD)'

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Journal articles on the topic "Spectrophotometric detection with diode matrix (DAD)"

1

Petukhova, Svetlana Andreyevna, Daniil Nikolayevich Olennikov, and Vera Mikhaylovna Mirovich. "TRITERPENE COMPOUNDS OF THE ABOVE GROUND ORGANS OF THE BUPLEURUM SCORZONERIFOLIUM WILLD. OF THE BAIKAL REGION FLORA." chemistry of plant raw material, no. 4 (December 27, 2019): 215–22. http://dx.doi.org/10.14258/jcprm.2019045354.

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Representatives of the genus Bupleurum L. in the composition of biologically active substances accumulate triterpene compounds (derivatives of α-amyrin and β-amyrin). Triterpene glycosides isolated from plants of the genus Bupleurum are called saikosaponinov, buplevrozidy, skorzonerozidy. Plants of the genus Bupleurum in the underground organs accumulate triterpene compounds in an amount of from 1 to 7%. Triterpene compounds of plants of the genus Bupleurum possess a hepatoprotective, antiviral, cytostatic effect. We have studied the triterpene compounds of the aerial organs of Bupleurum scorzonerifolium Willd. The material for the study was collected on the territory of the Irkutsk region (Russia). Isolation of triterpene compounds was performed with 70% ethyl alcohol. The compounds were identified by liquid chromatography with mass spectrometry and diode-matrix detection (UPLC-DAD-ESI-MS/MS). According to the results of the analysis, the content of 5 triterpene compounds was established: saikosaponinov A, B2, C, D, F. The isolated compounds are structurally derived from oleanan, in which glycosidation is observed at the C-3 position with α-L-rhinose, β-D-glucose and β-D-fucose. The spectrophotometric method determined the quantitative content of the amount of triterpene compounds in the above-ground organs of B. scorzonerifolium at different phases of the vegetation of the plant, by organs (in flowers, leaves, stalks), and also depending on the place of growth. It has been established that the maximum amount of the amount of triterpene compounds accumulates in the aboveground organs of B. scorzonerifolium during the flowering phase – 1.54±0.05%; the highest content of this group of compounds is noted in flowers – 1.70±0.06%; most of all, this group of compounds is collected by samples collected in the Ust-Horde Buryat District (1.96±0.06%). The aboveground organs of B. scorzonerifolium can be used as a source of triterpene compounds, the highest content of which is noted in the flowering phase. The study of triterpene compounds in the aboveground organs of B. scorzonerifolium was carried out for the first time.
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2

Veizerová, L., J. Piešťanský, K. Maráková, et al. "Comparison of column-coupled electrophoresis with liquid chromatography methods in food analysis of quinine." Acta Facultatis Pharmaceuticae Universitatis Comenianae 59, no. 1 (2012): 67–80. http://dx.doi.org/10.2478/v10219-012-0011-y.

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Comparison of column-coupled electrophoresis with liquid chromatography methods in food analysis of quinineComparison of column-coupled electrophoresis with liquid chromatography methods in food analysis of quinine (QUI) is presented in this work. The capillary isotachophoresis (CITP) on-line coupled with capillary zone electrophoresis (CZE) and hyphenated with fibre-based spectrophotometric diode array detection (DAD) was compared with, (i) high performance liquid chromatography (HPLC) method with DAD detection, and (ii) HPLC method with fluorescence detection (FD). These methods were compared through their performance parameters and determined concentrations of QUI in beverages. The concentrations of QUI in two selected bitter drinks determined by the CITP-CZE-DAD method were in a good accordance with the HPLC-DAD and HPLC-FD methods. In addition, the electrophoretic method, as well as the chromatographic methods, was able to separate potential QUI related impurities from the QUI peak. The CITP-CZE-DAD method provided excellent performance parameters that were comparable (precision, accuracy, LOD, robustness) or even better (separation efficiency) than those ones provided by the chromatographic methods. Moreover, the effectivity of the electrophoresis method was higher when considering cost of analysis (equipment, consumption of separation systems), environmental aspects (organicvs. aqueous solvents), on-line sample pretreatment (CITP preconcentration and sample clean-up suitable also for the more complex matrices). Considering these findings, CITP-CZE-DAD was approved as a routine automatized method for the highly reliable quality food control.
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3

Vaclavik, Lukas, Frantisek Benes, Marie Fenclova, et al. "Quantitation of Cannabinoids in Cannabis Dried Plant Materials, Concentrates, and Oils Using Liquid Chromatography–Diode Array Detection Technique with Optional Mass Spectrometric Detection: Single-Laboratory Validation Study, First Action 2018.11." Journal of AOAC International 102, no. 6 (2019): 1822–33. http://dx.doi.org/10.5740/jaoacint.18-0426.

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This paper describes a single-laboratory validation of a liquid chromatography–diode array detection (LC–DAD) method for quantification of 12 major cannabinoids in Cannabis dried plant materials, concentrates, and oils. The method met Standard Method Performance Requirements for quantitative analysis of cannabinoids in Cannabis concentrates and Cannabis dried plant materials. The LOQs were in the range 0.003–0.10% (w/w), depending on the analyte and matrix. Spike recoveries were between 96.7 and 101.3% with relative SDs (RSDs) ≤2.3%. Precision expressed as repeatability and intermediate precision was within 0.3–4.8 and 1.1–5.1%, respectively. The chromatographic separation conditions used in this versatile method are compatible with both DAD–UV and MS detection. During method validation, high-resolution quadrupole time-of-flight MS was employed as a secondary detector (connected in series to the LC–DAD instrument) to provide high confidence identification of target analytes and as a tool for monitoring other cannabinoids for which reference standards were not available. The obtained results demonstrate applicability of the method to quantitative analysis of important cannabinoids in dried plants, concentrates, and oils. Limited data were generated for a food matrix (Cannabis-containing cookies) using this method with LC coupled to a compact single quadrupole mass spectrometer.
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4

Vaclavik, Lukas, Frantisek Benes, Marie Fenclova, et al. "Quantitation of Cannabinoids in Cannabis Dried Plant Materials, Concentrates, and Oils Using Liquid Chromatography–Diode Array Detection Technique with Optional Mass Spectrometric Detection: Single-Laboratory Validation Study, First Action 2018.11." Journal of AOAC INTERNATIONAL 102, no. 6 (2019): 1822–33. http://dx.doi.org/10.1093/jaoac/102.6.1822.

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Abstract This paper describes a single-laboratory validation of a liquid chromatography–diode array detection (LC–DAD) method for quantification of 12 major cannabinoids in Cannabis dried plant materials, concentrates, and oils. The method met Standard Method Performance Requirements for quantitative analysis of cannabinoids in Cannabis concentrates and Cannabis dried plant materials. The LOQs were in the range 0.003–0.10% (w/w), depending on the analyte and matrix. Spike recoveries were between 96.7 and 101.3% with relative SDs (RSDs) ≤2.3%. Precision expressed as repeatability and intermediate precision was within 0.3–4.8 and 1.1–5.1%, respectively. The chromatographic separation conditions used in this versatile method are compatible with both DAD–UV and MS detection. During method validation, high-resolution quadrupole time-of-flight MS was employed as a secondary detector (connected in series to the LC–DAD instrument) to provide high confidence identification of target analytes and as a tool for monitoring other cannabinoids for which reference standards were not available. The obtained results demonstrate applicability of the method to quantitative analysis of important cannabinoids in dried plants, concentrates, and oils. Limited data were generated for a food matrix (Cannabis-containing cookies) using this method with LC coupled to a compact single quadrupole mass spectrometer.
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5

Loper, Bobby L., and Kim A. Anderson. "Determination of Pyrethrin and Pyrethroid Pesticides in Urine and Water Matrixes by Liquid Chromatography with Diode Array Detection." Journal of AOAC INTERNATIONAL 86, no. 6 (2003): 1236–40. http://dx.doi.org/10.1093/jaoac/86.6.1236.

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Abstract The following pyrethrin and pyrethroid pesticides were determined in urine and water matrixes by liquid chromatography with diode array detection (LC–DAD): pyrethrin I, pyrethrin II, tetramethrin, baythroid, bifenthrin, fenvalerate, phenothrin, allethrin, resmethrin, cis-permethrin, and trans-permethrin. In addition, 3-phenoxybenzyl alcohol, a metabolite of various pyrethroids, was also successfully determined by the analytical method. The matrix extraction was simple, inexpensive, and fast, using only sodium chloride and acetonitrile. The acetonitrile extract was filtered and analyzed by LC–DAD. The method detection limits for the pyrethrin pesticides in 5 mL urine were determined to range from 0.002 to 0.04 μg/mL, depending on the individual pyrethrin. Recoveries from spiked tap water ranged from 77 to 96%;recoveries from urine ranged from 80 to 117%. This method is especially well-suited to clinical investigations, in which rapid analysis of forensic samples is often required.
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6

Michiu, Delia, Maria-Ioana Socaciu, Melinda Fogarasi, et al. "Implementation of an Analytical Method for Spectrophotometric Evaluation of Total Phenolic Content in Essential Oils." Molecules 27, no. 4 (2022): 1345. http://dx.doi.org/10.3390/molecules27041345.

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Over the past decade, there has been growing interest in polyphenols’ research since these compounds, as antioxidants, have several health benefits, such as preventing neurodegenerative diseases, inflammation, cancer, cardiovascular diseases, and type 2 diabetes. This study implements an analytical method to assess the total phenolic content (TPC) in essential oils using Folin–Ciocalteu’s phenol reagent and quantifies the individual phenolic compounds by liquid chromatography. Thus, the research design and methodology included: (1) extraction of essential oil from dried thyme leaves by hydrodistillation; (2) spectrophotometric measurement of TPC by Folin–Ciocalteu method; and (3) identification and quantification of individual phenolic compounds by high-performance liquid chromatography-diode array detection/electrospray ionization mass spectrometry (HPLC-DAD-ESI-MS). Results revealed a TPC of 22.62 ± 0.482 mg GAE/100 µL and a polyphenolic profile characterized by phenolic acids (52.1%), flavonoids (16.1%), and other polyphenols (31.8%). Thymol, salvianolic acid A, and rosmarinic acid were the major compounds of thyme essential oil. The proposed analytical procedure has an acceptable level of repeatability, reproducibility, linearity, LOD (limit of detection), and LOQ (limit of quantification).
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7

Ghinea, Ioana Otilia, Maria Daniela Ionica Mihaila, Giorgiana-Valentina Blaga (Costea), et al. "HPLC-DAD Polyphenolic Profiling and Antioxidant Activities of Sorghum bicolor during Germination." Agronomy 11, no. 3 (2021): 417. http://dx.doi.org/10.3390/agronomy11030417.

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The purpose of this study was to assess the suitability of the Romanian Albanus hybrid of Sorghum bicolor as a potential functional food ingredient. Ultrasound-assisted extraction in different solvents, together with spectrophotometric and chromatographic methods, was used to monitor the variation in total phenolic and flavonoid content and the antioxidant activity of raw sorghum grains before and during short germination periods (24, 36 and 48 h). The High-Performance Liquid Chromatography with Diode-Array Detection (HPLC-DAD) investigation of the extracts revealed that the ungerminated sorghum grains extracted with methanol had the highest diversity of phenolic compounds, while the total phenolic content (TPC) was the highest after 36 h of germination in both extract types: 1853 mg GAE/100 g for the methanolic extract and 1726 mg GAE/100 g for the ethanolic extract. The findings of this study showed that the TPC of sorghum extracts is strongly correlated with their antioxidant activity and, overall, that the studied extracts presented a good radical scavenger activity, which supports the benefits of alimentary uses of Sorghum bicolor grains.
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8

Vasyliev, Georgii S., Victoria I. Vorobyova, and Olga V. Linyucheva. "Evaluation of Reducing Ability and Antioxidant Activity of Fruit Pomace Extracts by Spectrophotometric and Electrochemical Methods." Journal of Analytical Methods in Chemistry 2020 (December 14, 2020): 1–16. http://dx.doi.org/10.1155/2020/8869436.

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The component profiles of apricot, grape, and black currant pomace extracts have been analyzed using HPLC coupled to diode-array detection and tandem mass spectrometry (HPLC-DAD-MS). The predominant components in grape, apricot, and black currant pomace extracts were phenolic acids and flavonols. The redox behavior of apricot, black currant, and grape pomace water extracts was evaluated by means of cyclic voltammetry. Also, individual substances mainly present in the extracts were analyzed. The results of electrochemical testing were compared to traditional chemical techniques of potassium ferricyanide reduction (FRAP) and phosphomolybdenum assay, and fair agreement was established. The 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging assays were applied in order to estimate antioxidant activity. The reducing power of the grape extract was found to be higher than that of the apricot and black currant extracts in both potassium ferricyanide reduction (FRAP) and phosphomolybdenum methods.
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9

Vidal, Òscar, Xavier Castilla, Núria Aliaga-Alcalde, et al. "Determination of Curcuminoids by Liquid Chromatography with Diode Array Detection: Application to the Characterization of Turmeric and Curry Samples." Current Analytical Chemistry 16, no. 2 (2020): 95–105. http://dx.doi.org/10.2174/1573411014666180629125729.

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Background: A simple, rapid and efficient method for the determination of curcumin and other polyphenols in turmeric and curry samples was here developed. The method relied on sample extraction with methanol and extract analysis by liquid chromatography with diode array detection (HPLC-DAD). Methods: The separation of components was carried out in reversed-phase mode using an elution gradient based on 0.1% (v/v) formic acid aqueous solution and acetonitrile as the components of the mobile phase. Chromatograms were recorded at 420 nm for specific monitoring of curcumin and related compounds. Results: Extraction and separation conditions were optimized by experimental design and multicriteria response functions. Figures of merit were established under the selected experimental conditions. In general, repeatability of peak areas were better than 0.4%, detection limits were below 0.006 mg L-1 and quantitative recoveries expressed as a percentage were about 100 ± 2. The method was applied to quantify curcuminoids in commercial samples. It was found that apart from curcumin, demethoxycurcumin and bisdemethoxycurcumin, other related molecules also occurred in the samples. In this regard, a tentative elucidation of possible unknown curcuminoids was attempted by liquid chromatography coupled to mass spectrometry. Conclusion: Differences in the compositional profiles among samples were encountered to be relevant, so that the resulting HPLC-DAD data was exploited for chemometric characterization of turmeric and curry samples. Samples were successfully discriminated according to matrix types, species varieties and origins.
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Capitán-Vallvey, Luis Fermin, Ramon Checa-Moreno, and Natalia Navas. "Rapid Ultraviolet Spectrophotometric and Liquid Chromatographic Methods for the Determination of Natamycin in Lactoserum Matrix." Journal of AOAC INTERNATIONAL 83, no. 4 (2000): 802–8. http://dx.doi.org/10.1093/jaoac/83.4.802.

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Abstract Two rapid and simple methods were developed for the determination of natamycin in lactoserum matrix by ultraviolet (UV) spectrophotometry and liquid chromatography (LC) with diode-array detection. The methods involve protein precipitation with methanol, followed by centrifugation. No cleanup is necessary. The applicable concentrations of natamycin in lactoserum range from 2 to 500 mg/L for samples analyzed by both methods. The detection and quantitation limits are 0.07 and 0.23 mg/L, respectively, for the UV spectrophotometric method and 0.1 and 0.32 mg/L, respectively, for the LC method. The methods were applied satisfactorily to the determination of natamycin in various commercial lactosera. Both methods were validated independently by standard additions and Youden methodologies, which verified their accuracy. Once the 2 proposed methods were validated independently, the validation of one method was carried out with the other.
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