Validated RP-HPLC Method for Simultaneous Determination of Tocopherols and Tocotrienols in Whole Grain Barley Using Matrix Solid-Phase Dispersion

2014 ◽  
Vol 8 (2) ◽  
pp. 392-400 ◽  
Author(s):  
Emmanouil D. Tsochatzis ◽  
Roxani Tzimou-Tsitouridou
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.


2017 ◽  
Vol 233 ◽  
pp. 11-19 ◽  
Author(s):  
Gabriel Barros de Oliveira ◽  
Carolyne Menezes de Castro Gomes Vieira ◽  
Ricardo Mathias Orlando ◽  
Adriana Ferreira Faria

2020 ◽  
Vol 32 (3) ◽  
pp. 203-209
Author(s):  
Yun-feng Liu ◽  
Jia-ling Zhang ◽  
Xue-fei Nie ◽  
Ping Zhang ◽  
Xiao-qing Yan ◽  
...  

A convenient method was developed for simultaneous determination of 11 preservatives in cosmetics and pharmaceuticals. Matrix solid-phase dispersion had been optimized as the sample pretreatment technology, using Florisil as a dispersant, anhydrous sodium sulfate as a dehydrant, formic acid as an additive, and n-hexane and ethyl acetate as eluents successively, and followed by gas chromatography–flame ionization detection on a TR-5 capillary column. Experimental results showed that 11 preservatives were baseline separated within 22 min. Good linearities were observed in the concentration range of 0.53–250 μg/mL for all analytes, and there were also minor differences. All correlation coefficients (r) were more than 0.995. The average recoveries at 3 levels of spiked samples ranged from 80% to 124% with 0.9–12% intra-day RSD and 1.8–12% inter-day RSD. The limits of detection were less than 0.18 μg/mL for all analytes. Besides, there was no obvious matrix effect on the analytes. The conclusion was that the developed method was simple, cheap, accurate, precise, and environment-friendly, in addition to existing little matrix effects. It could be recommended to determine 11 preservatives individually or in any their combinations to not only in liquid and gel cosmetics but also in liquid medicine and ointment.


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