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  • Hindawi Limited  (5)
  • Zhang, Yan  (5)
  • 1
    In: Journal of Food Quality, Hindawi Limited, Vol. 2021 ( 2021-9-4), p. 1-9
    Abstract: Eugenol compounds are widely used in the circulation and transportation of fresh aquatic products because of their good anesthetic effects. However, some studies have shown that eugenol compounds are potential carcinogens. Therefore, in order to ensure the edible safety of aquatic products, eugenol compounds in aquatic products need to be screened quickly. A method for determination of six eugenol residues in aquatic products was established by multiplug filtration cleanup (m-PFC), combined with gas chromatography-Orbitrap mass spectrometry (Orbitrap GC-MS). Samples were ultrasonically extracted with acetonitrile, and the extracts were frozen at −18°C for 1 h, then purified with the m-PFC column, and detected by Orbitrap GC-MS in full scan mode. The results showed the linear relationships for six eugenols were good in the range of 0.001–0.1 μg/mL, and the correlation coefficients (R2) were above 0.9950. The limits of detection (LODs) were 2–10 μg/kg, and the limits of quantitation (LOQs) were 5–20 μg/kg. The average recoveries at the spiked levels of 5–200 μg/kg were in the range of 76.4%–105.1%, with relative standard deviations (RSDs) of 1.2%–7.5%. Eighty aquatic products were detected by this method, of which only eugenol was detected in 12 samples, and eugenol and isoeugenol were detected in two samples at the same time. The other eugenol compounds were not detected in any sample. The detection rate of positive samples was 17.5%. The method is simple, accurate, and suitable for the rapid screening of eugenol compounds in aquatic products.
    Type of Medium: Online Resource
    ISSN: 1745-4557 , 0146-9428
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2021
    detail.hit.zdb_id: 2175284-9
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  • 2
    In: Journal of Food Quality, Hindawi Limited, Vol. 2021 ( 2021-9-23), p. 1-12
    Abstract: In this experiment, inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) was used to determine the content of 30 elements in rice from six places of production and to explore the relationship between the multielement content in rice and the producing area. The contents of Ca, P, S, Zn, Cu, Fe, Mn, K, Mg, Na, Ge, Sb, Ba, Ti, V, Se, As, Sr, Mo, Ni, Co, Cr, Al, Li, Cs, Pb, Cd, B, In, and Sn in rice were determined by ICP-MS/MS in the SQ and MS/MS mode. By passing H2, O2, He, and NH3/He reaction gas into the ICP-MS/MS, respectively, the interference was eliminated by means of in situ mass spectrometry and mass transfer. The detection limit of each element was 0.0000662–0.144 mg/kg, and the limit of quantification was in the range of 0.000221–0.479 mg/kg, the linear correlation coefficient was greater or equal to 0.9987 (R2 ≥ 0.9987), and the detection results had low detection limit and great linear regression. Recovery of the method was in the range of 80.6% to 110.5% with spike levels of 0.10–100.00 mg/kg, and relative standard deviations were lower than 10%. For the multielement content of rice from different producing areas, the principal component factor analysis can get six principal component factors, 87.878% cumulative contribution rate, and the distribution of the principal component scores of each element and different producing areas. Based on the multielement content and cluster analysis, the samples were accurately divided into two major categories and six subcategories according to the places of production, which proved that there was a significant correlation between the multielement content in rice and the place of production, so that the place of rice origin can be traced.
    Type of Medium: Online Resource
    ISSN: 1745-4557 , 0146-9428
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2021
    detail.hit.zdb_id: 2175284-9
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  • 3
    In: International Journal of Analytical Chemistry, Hindawi Limited, Vol. 2022 ( 2022-9-27), p. 1-8
    Abstract: A new method was developed for the identification and determination of L-ergothioneine in cosmetics based on ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The pretreatment method, chromatographic column, chromatographic conditions, and mass spectrometric conditions of cosmetic samples were optimized. Methanol was chosen as the extraction solvent, 85% acetonitrile with 0.1% FA was selected as the mobile phase, and the Waters CORTECS UPLC hydrophilic interaction liquid chromatography (HILIC) column was chosen for the separation. The sample was extracted with methanol and filtered, then separated by HILIC and detected by triple-quadrupole mass spectrometry. The quantitation was done under the matrix calibration curve using the external standard method. The results showed good linear relationships in the range of 5–200 ng/mL, and the correlation coefficient was greater than 0.999 in cosmetic samples. The limit of detection was in the range of 25–50 μg/kg and the limit of quantitation was in the range of 50–100 μg/kg. The recoveries of the method spiked ranged from 85.3% to 96.2% and the relative standard deviation (RSD) was in the range of 0.84%–2.08% (n = 6). The method is simple, quick, and accurate for the determination of L-ergothioneine in cosmetics, and has great practical value.
    Type of Medium: Online Resource
    ISSN: 1687-8779 , 1687-8760
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2022
    detail.hit.zdb_id: 2494714-3
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  • 4
    In: Journal of Food Quality, Hindawi Limited, Vol. 2020 ( 2020-09-24), p. 1-10
    Abstract: A ultrahigh performance liquid chromatography coupled with quadrupole-time of flight mass spectrometry (UPLC-Q-TOF/MS) method was developed for simultaneous determination of 8 endogenous alkaloid compounds in Boletus . Boletus samples were extracted by 50% (V/V) methanol-water solution, then separated by CORTECS UPLC HILIC column using a binary solvent system by gradient elution. The analytes were determined by Q-TOF/MS in TOF MS and information dependent acquisition (IDA)-MS/MS mode. The results showed that mass accuracy error of the 8 endogenous alkaloids were lower than 5.0 × 10 −6 , good linear relationship was got in range of 0.2–500  μ g/L, and correlation coefficient was higher than 0.9990. The limit of detection was in the range of 0.002–0.100 mg/kg and the limit of quantification was in the range of 0.004–0.200 mg/kg. Recovery of the method was in range of 80.1%–101.5% with spike levels of 0.004–2.00 mg/kg, relative standard deviations were lower than 10%. The method was simple, specific, and reliable. It could be used for the rapid screening and quantitative analysis of 8 endogenous alkaloids in Boletus .
    Type of Medium: Online Resource
    ISSN: 0146-9428 , 1745-4557
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2020
    detail.hit.zdb_id: 2175284-9
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  • 5
    Online Resource
    Online Resource
    Hindawi Limited ; 2015
    In:  International Journal of Antennas and Propagation Vol. 2015 ( 2015), p. 1-7
    In: International Journal of Antennas and Propagation, Hindawi Limited, Vol. 2015 ( 2015), p. 1-7
    Abstract: An open slot antenna with extended bandwidth for WLAN and UWB applications is proposed. The radiating structure is composed of a rectangular microstrip patch antenna exciting an L-shaped slot etched on the ground plane. The feed position is optimized to get better impedance match for the higher range of the UWB spectrum, while a step in the slot, realized in the ground plane, is employed to extend the lower limit of the bandwidth so as to cover the 2.4 GHz WLAN frequency band. Using these design solutions the antenna bandwidth is successfully extended to 140% so as to cover both the WLAN and the UWB spectrum.
    Type of Medium: Online Resource
    ISSN: 1687-5869 , 1687-5877
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2015
    detail.hit.zdb_id: 2397585-4
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