Application of matrix solid-phase dispersion–HPLC method to determine patulin in apple and apple juice concentrate

2008 ◽  
Vol 21 (7) ◽  
pp. 582-586 ◽  
Author(s):  
Ri-Na Wu ◽  
Ya-Li Dang ◽  
Le Niu ◽  
Hong Hu
Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1312
Author(s):  
Luyi Jiang ◽  
Jie Wang ◽  
Huan Zhang ◽  
Caijing Liu ◽  
Yiping Tang ◽  
...  

In this study, a green ionic-liquid based vortex-synchronized matrix solid-phase dispersion (VS-MSPD) combined with high performance liquid chromatography (HPLC) method was developed as a quantitative determination method for four anthraquinones in Cassiae Semen. Two conventional adsorbents, C18 and silica gel were investigated. The strategy included two steps: Extraction and determination. Wasted crab shells were used as an alternative adsorbent and ionic liquid was used as an alternative solvent in the first step. Factors affecting extraction efficiency were optimized: A sample/adsorbent ratio of 2:1, a grinding time of 3 min, a vortex time of 3 min, and ionic liquid ([Domim]HSO4, 250 mM) was used as eluent in the VS-MSPD procedure. As a result, the established method provided satisfactory linearity (R > 0.999), good accuracy and high reproducibility (RSD < 4.60%), and it exhibited the advantages of smaller sample amounts, shorter extraction time, less volume of elution solvent, and was much more environmental-friendly when compared with other conventional methods.


2004 ◽  
Vol 87 (4) ◽  
pp. 972-985 ◽  
Author(s):  
Xiaozhong Hu ◽  
Yu Jianxin ◽  
Yan Zhigang ◽  
Ni Lansun ◽  
Lin Yanfei ◽  
...  

Abstract A multiresidue method is described for the analysis of 106 multiclass pesticides (organochlorine, organophosphate, carbamate, pyrethroid, and triazine classes) in apple juice in a single injection. The determination procedure was based on matrix solid-phase dispersion of juice on diatomaceous earth in a glass column and subsequent extraction with a mixture of hexane–dichloromethane (1 + 1) at a flow rate of 5 mL/min. The analytes were determined by capillary gas chromatography with mass spectrometric detection and confirmed by their retention times and ion ratios. The coefficients of variation for analysis of samples fortified over the range of 0.01–0.2 mg/kg were 1.62 to 18.4%, and the recoveries for all analytes were between 70 and 110%.


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