Green coffee. Determination of loss in mass at 105°C

2003 ◽  
Keyword(s):  
1975 ◽  
Vol 58 (2) ◽  
pp. 258-262 ◽  
Author(s):  
Colette P Levi

Abstract A method for the semiquantitative determination of ochratoxin A in green coffee has been studied collaboratively by 11 laboratories. The average recovery for the 7 samples spiked at 3 levels of ochratoxin A was 69.1%, ranging from 60.5 to 85.6%. This is comparable to other visual thin layer chromatographic methods of mycotoxin detection. The method has been adopted as official first action for the determination of ochratoxin A in green coffee beans.


1969 ◽  
Vol 52 (6) ◽  
pp. 1300-1303
Author(s):  
Colette P Levi

Abstract Nine laboratories collaboratively studied a method for the detection of aflatoxin B1 in green coffee beans. The method investigated incorporates a Florisil column cleanup step, followed by visual estimation of aflatoxin. The method is recommended for adoption as official first action for semiquantitative determination of aflatoxin B1. Further study is required on the Florisil cleanup step.


2016 ◽  
Vol 8 (35) ◽  
pp. 6537-6544 ◽  
Author(s):  
I. G. David ◽  
D. E. Popa ◽  
M. Buleandra ◽  
Z. Moldovan ◽  
E. E. Iorgulescu ◽  
...  

A disposable pencil graphite electrode was used for the first time for rapid voltammetric determination of chlorogenic acid in green coffee dietary supplements.


2020 ◽  
Vol 32 (1) ◽  
pp. 34-38
Author(s):  
Lenche Velkoska-Markovska ◽  
Mirjana S. Jankulovska ◽  
Biljana Petanovska-Ilievska ◽  
Kristijan Hristovski

Coffee is one of the most widely consumed beverages in the world. It contains many bioactive compounds, including chlorogenic acid which possesses various biological properties. In this study, in order to determine concentration of chlorogenic acid in green coffee, a reverse-phase rapid resolution liquid chromatography (RP-RRLC) method with diode-array detection (DAD) was developed. Successful separation was achieved on a Poroshell 120 EC-C18 (50 mm × 3 mm; 2.7 μm) column using acetonitrile–water with 1% phosphoric acid (10:90, v/v) as a mobile phase, at a flow rate of 1 mL/min, and with UV detection at 325 nm. The identification was made with comparison of the retention time of pure analytical standard with the retention time of chlorogenic acid in the analyzed samples. The developed method was validated using the following parameters: linearity, sensitivity, selectivity, precision, and accuracy. Excellent linearity over the range 12.33–143.50 μg/mL was achieved with R2 values greater than 0.99. The intra-day precision was validated with the %RSD values, which confirmed that the method for determination of chlorogenic acid was repeatable. The mean recovery rate of the method ranged between 97.87% and 106.67% with %RSD values lower than 1%. The limit of detection and limit of quantification values under the used chromatographic conditions were 0.29 and 0.96 pg, respectively. This method was successfully employed for quantitative determination of chlorogenic acid in green coffee samples.


2019 ◽  
Vol 22 (3) ◽  
pp. 314-320 ◽  
Author(s):  
Joe A. Vinson ◽  
Xi Chen ◽  
Deanne Dulik Garver

Sign in / Sign up

Export Citation Format

Share Document