necessary to establish an analytical method to monitor the concentration of hapepunine.
To the best of our knowledge, the pharmacokinetics of hapepunine had not been reported. In this paper, an ultra-performance liquid chromatography–tandemmass
Authors:Yonggang Li, Xiaohong Liu, Rui Zhang, DerGer ZomPa, Ping Luo, Lin Tang, Xiao Liu, Yan Zhou, and Sheng Wen
spectrometry (MS) [ 18 , 19 ], or coupled to tandemmassspectrometry (MS/MS) [ 6 , 18 , 20 – 23 ], had become the best choice for the determination of CAP because of its advantages of high selectivity and sensitivity, timesaving, and the accuracy of
/sample. The injection volume was 10 μL.
Electrospray ionization–tandemmassspectrometry (ESI–MS/MS) detection was achieved on an Agilent 6410 triple quadrupole tandem mass spectrometer. The positive ionization mode was used, and the ions were
Authors:T. H. Kim, G. H. Jung, E. H. Lee, H. R. Park, J. K. Lee, and H. G. Kim
. Therefore, we attempted to develop and validate a sensitive and specific analytical method for the simultaneous determination of ZnPT and PT in shampoos using liquid chromatography–tandemmassspectrometry (LC–MS/MS).
Authors:Ruijie Chen, Mengrou Lu, Xiaoting Tu, Wei Sun, Weijian Ye, Jianshe Ma, Congcong Wen, Xianqin Wang, and Peiwu Geng
There is no effective bioanalytical method available to quantify panasenoside in biological samples to date. Compared to liquid chromatography tandemmassspectrometry (LC–MS/MS), ultra-performance liquid chromatography (UPLC)–MS/MS is more sensitive and
Authors:Yonggang Li, Ziliang Chen, Sheng Wen, Xiaolin Hou, Rui Zhang, and Meihu Ma
]. LC coupled to an ultraviolet (UV) source or diode array [ 16 , 18 , 19 ], fluorescence [ 20 ], a time-of-flight (TOF) analyzer [ 21 ], or biosensor [ 22 ] has been used to detect antibiotics. Meanwhile, LC coupled to tandemmassspectrometry (LC
Authors:Genquan Yan, Lu Yu, Xu Chen, Triet Tran, Lam Nguyen, Zhijun Wang, and Ling Wang
humans, they both used [ 14 C]-labeled apremilast rather than normal tablets [ 15 ]. Liu’s method has been used to study the drug interactions with apremilast by liquid chromatography-tandemmassspectrometry [ 16, 17 ]. However, no study has reported
Authors:SeonJu Park, Nanyoung Kim, Jun Hyung Park, Sang-Won Lee, Jae-Hyoung Song, Hyun-Jeong Ko, Han-Jung Chae, Hyung-Ryong Kim, and Seung Hyun Kim
quadrupole MS stands out as a fast, sensitive, and accurate quantification method for complex systems, such as natural product extracts [ 10 , 11 ].
The goal of the present study was to develop and validate a method coupling HPLC with tandemmass
Authors:X. Wang, Y. Wu, Q. Wu, Y. Qian, W. Yue, and Q. Liang
The rhizome of Sparganium stoloniferum Buch.-Ham has been used as a traditional Chinese folk medicine for thousands of years. Phenolic compounds are the main bioactive ingredients of the plant. In order to determine the content of phenolic compounds from different major cultivations, a reliable method has been developed using ultra-high performance liquid chromatography coupled with a triple quadrupole electrospray tandem mass spectrometry. Seven compounds, including rutin, kaempferol, p-hydroxybenzaldehyde, formononetin, ferulic acid, vanillic acid, and p-coumaric acid, were simultaneously measured in 10 min. The established approach was fully validated in terms of linearity, sensitivity, precision, repeatability as well as recovery, and successfully applied to determine seven phenolic compounds of Rhizoma Sparganii. This study may be helpful in the quality control of Rhizoma Sparganii and can offer technical support for the pharmacological and clinical study of related drugs.
Authors:Shiming Song, Zhaojie Chen, Jie Wei, Yuhao Lei, Cheng Deng, Huihua Tan, and Xuesheng Li
A sensitive and effective method based on a modified QuECHERS (quick, easy, cheap, effective, rugged, and safe) method for the determination of polyoxin B in cucumber and soil using liquid chromatography tandem–mass spectrometry (LC–MS/MS) was developed and validated. Samples were extracted using 1% formic acid in ultrapure water and purified via reversed-dispersive solid phase extraction (r-dSPE) using C18. Recovery of polyoxin B ranged from 83.0% to 112.1% with relative standard deviation (RSD) (n = 5) of 3.0–5.2%. The limit of quantification (LOQ) and the limit of detection (LOD) were 0.01 and 0.003 mg/kg for cucumber and soil, respectively. The method was subsequently applied for real sample analysis. The dissipation experiments showed that half-lives of polyoxin B in cucumber and soil were 2.5–5.0 days. The terminal residues of polyoxin B at preharvest intervals (PHIs) of 3 days and 5 days in cucumber were less than 0.05 mg/kg. We therefore suggest that the developed method can be extrapolated to other agricultural crops or food for routine analysis. It also can be used to determine the PHIs. Moreover, these results will aid in establishing the maximum residue limit (MRL) for cucumber in China.