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951.
952.
Jeong‐Min Choi Weijia Zheng A. M. Abd El‐Aty Seong‐Kwan Kim Da‐Hee Park Kyung‐Hee Yoo Gyu‐Hee Lee Denis A. Baranenko Ahmet Hacmüftüolu Ji Hoon Jeong Young‐Sun Kang Ho‐Chul Shin 《Biomedical chromatography : BMC》2019,33(7)
We developed an analytical method using liquid–liquid extraction (LLE) and liquid chromatography–tandem mass spectrometry (LC‐MS/MS) to detect and quantify tebufenozide (TEB) and indoxacarb (IND) residues in animal and aquatic products (chicken muscle, milk, egg, eel, flatfish, and shrimp). The target compounds were extracted using 1% acetic acid (0.1% acetic acid for egg only) in acetonitrile and purified using n‐hexane. The analytes were separated on a Gemini‐NX C18 column using (a) distilled water with 0.1% formic acid and 5 mm ammonium acetate and (b) methanol with 0.1% formic acid as the mobile phase. All six‐point matrix‐matched calibration curves showed good linearity with coefficients of determination (R2) ≥0.9864 over a concentration range of 5–50 μg/kg. Intra‐ and inter‐day accuracy was expressed as the recovery rate at three spiking levels and ranged between 73.22 and 114.93% in all matrices, with a relative standard deviation (RSD, corresponding to precision) ≤13.87%. The limits of quantification (LOQ) of all target analytes ranged from 2 to 20 μg/kg, which were substantially lower than the maximum residue limits (MRLs) specified by the regulatory agencies of different countries. All samples were collected from different markets in Seoul, Republic of Korea, and tested negative for tebufenozide and indoxacarb residues. These results show that the method developed is robust and may be a promising tool to detect trace levels of the target analytes in animal products. 相似文献
953.
Weijia Zheng A. M. Abd El‐Aty Seong‐Kwan Kim Jeong‐Min Choi Da‐Hee Park Kyung‐Hee Yoo Young‐Sun Kang Jong‐Sup Jeon Ahmet Hacmüftüolu Jae‐Han Shim Ho‐Chul Shin 《Biomedical chromatography : BMC》2019,33(5)
The present study was carried out to determine 16 antibiotics belonging to seven different groups (tetracyclines, sulfonamides, penicillins, fluoroquinolones, macrolides, lincosamides and trimethoprims) in duck meat. A solid‐phase extraction method based on Oasis HLB cartridges coupled with liquid chromatography–electrospray ionization tandem mass spectrometry was developed. Solutions of 0.1 m ethylenediaminetetraacetic acid disodium salt and 2% trifluoroacetic acid were used for the preliminary extraction of the target antibiotics from duck meat and n‐hexane was used for purification prior to solid‐phase extraction. Mobile phases composed of 0.1% trifluoroacetic acid in distilled water (solvent A) and 0.1% trifluoroacetic acid in methanol (solvent B), combined with a reversed‐phase C18 analytical column, provided the optimal separation and signal intensity. The linearity of the method was assessed using six concentrations (5, 10, 20, 30, 40, and 50 μg/kg), and the recoveries, which were calculated at three spiking concentrations (5, 10 and 20 μg/kg), were in the range 69.8–103.3% with relative standard deviations (RSDs) ≤ 6.9% for the 16 tested antibiotics. Matrix effects ranging from ?47.2 to ?13.5% were observed for all the analytes, and the limits of quantitation (LOQ), which ranged from 4.93 to 26.21 μg/kg, were much lower than the maximum residue limits (MRLs) set by various regulatory authorities. Ten samples from a market were tested, and none of the target analytes were detected. Thus, a simple and versatile protocol has been developed to detect and quantify 16 antibiotics in duck meat samples. 相似文献
954.
Choon Ki Ahn 《Nonlinear dynamics》2014,78(1):409-420
The passivity concept plays an important role in circuit theory, signal processing, and control, but no criteria have yet been established for two-dimensional (2D) digital filters. In this article, we propose a new and first criterion for 2D digital filters in the Roesser form, to ensure passivity from the interference vector to the output vector with a certain storage function. The proposed criterion also guarantees the asymptotic stability of 2D digital filters in the Roesser form without interference. This criterion is described by linear matrix inequality, making it computationally attractive. A simulation example is presented, which demonstrates the usefulness of the 2D passivity criterion. 相似文献
955.
956.
Keun Man SongJong Min Kim Bong Kyun KangChan Soo Shin Chul Gi KoBo Hyun Kong Hyung Koun ChoDae Ho Yoon Hogyoung Kim Sung Min Hwang 《Applied Surface Science》2012,258(8):3565-3570
Nonpolar a-plane GaN layers grown on r-plane sapphire substrates were examined by using a two-step growth process. The higher initial growth pressure for the nucleation layer resulted in the improved crystalline quality with lower density of both threading dislocations and basal stacking faults. This was attributed to the higher degree of initial roughening and recovery time via a growth mode transition from three-dimensional (3D) to quasi two-dimensional (2D) lateral growth. Using Hall-effect measurements, the overgrown Si doped GaN layers grown with higher initial growth pressure were found to have higher mobility. The scattering mechanism due to the dislocations was dominant especially at low temperature (<200 K) for the lower initial growth pressure, which was insignificant for the higher initial growth pressure. The temperature-dependent Hall-effect measurements for the Mg doped GaN with a higher initial growth pressure yielded the activation energy and the acceptor concentration to be 128 meV and 1.2 × 1019 cm−3, respectively, corresponding to about 3.6% of activation at room temperature. Two-step growth scheme with a higher initial growth pressure is suggested as a potential method to improve the performance of nonpolar a-plane GaN based devices. 相似文献
957.
958.
Le Thi Kim Van Tran Manh Hung Soo Hyun Kim Jin Cheol Kim MinKyun Na Hyun Ju Jung Seung Jun Kwack Kee Tae Kweon Jae Sue Choi Hyeong Kyu Lee KiHwan Bae Byung‐Sun Min 《Helvetica chimica acta》2010,93(9):1803-1807
A new stereoisomer of a tetrahydrofuranoid lignan, acerifuranoid A ( 1 ), and two new oleanane‐type triterpenoids, aceriphyllic acids J and K ( 2 and 3 ), were isolated from the roots of Aceriphyllum rossii. Their structures were elucidated on the basis of spectroscopic analyses and chemical evidence. These isolated compounds exhibited weak cytotoxic activity against various cancer cell lines with IC50>150 μM . 相似文献
959.
960.
5-ortho-Carboranylsalicylaldehyde was prepared from 5-iodosalicylaldehyde in six steps in 18% overall yield, and also from 5-iodosalicylic acid in seven steps in 45% overall yield. The reaction of 5-ortho-carboranylsalicylaldehyde with Fischer's base gave a spiropyran in 63% yield. 相似文献