HPLC
HPLC
HPLC
analysis system
N-Methyl carbamate pesticides
analysis system
CH3 O O O
H3C CH3
CH3NH C O CH3NH C O CH3 O
H3C S C CH N O C NH CH3
O CH CHCH2CH3 (CH3 ) 2N C O N
3
CH3 N
N(CH3 ) 2
O CH3
Aldicarb Bendiocarb Fenobucarb Pirimicarb
O O O O O
O C NHCH3 CH3NH C O CH3NH C O CH3 CH3NH C O CH3NH C O
CH2SCH2CH3 CH CH3
CH3 CH3
CH3
Carbaryl(NAC) Ethiofencarb Isoprocarb Metholcarb(MTMC) Xylylcarb(MPMC)
O O O
CH3 CH3
CH3N C O N C CH3NH C O CH3NH C O O
O SCH3 SCH3
S OCH(CH3 ) 2 O CH3 CH3NH C O
CH3NH C O N C SCH3
CH3 CH3N C O N C CH3 CH3
CH3
Methomyl O Propoxur(PHC) Carbofuran Macbal(XMC)
Thiodicarb
Principle of carbamate pesticides analysis
O
0.05N NaOH
R O C NHCH3 CH3NH2 + R OH + H2CO3
Heating
N-Methyl carbamete Methylamine
Precolumn Carbamatepak CO
PU AS FP
Column
Cooling
Backpressure
coil
LG 0.25I.D. x 1m
coil
0.25 I.D. x 1m
RO
DG 80℃
Reaction coil
0.5 I.D. x 2m
Backpressure Backpressure
Linefilter
capillary capillary
PU PU
Measurement conditions specified in
official method
Column: Octadecylsilyl silica gel (3.9 mm I.D. x 150 mmL)
Column temperature: 40 degree C
Mobile phase: A: H2O, B: CH3OH, C: THF
Flow rate: 0.6 ml/min
Reagents 1: 50 mMNaOH aq.
Reagent flow rate 1: 0.5 ml/min
Reagents 2: 50 mM Na2B4O7・10H2O / 0.4 mg
OPA in 5 ml CH3OH /2-mercaptoethanol (1000/5/1)
Reagent flow rate 2: 0.5 ml/min
Gradient conditions
Reaction temperature: 80 to 100 °C
Detection : Ex; 340 nm, Em; 455 nm, Gain; x100 A B C
0min 88% 12% 0%
0.1min 90% 0% 10%
20.0min 70% 0% 30%
29.9min 70% 0% 30%
30.0min 88% 12% 0%
1cycle 40min
Chromatogram of carbamete pesticides
(official method)
Concentration of each additive component : 10 ppb
Injection volume : 50 µl
Extraction pre-treatment of carbamate
pesticides in food (official method)
Sample 20g
(H2O 30mL, 2.0h)
Acetone 200mL
Homogenize 5 mL
Filtration (Diatomaceous earth)
Filtrate Residue
Acetone 50mL
Stirring, Filtration
Filtrate
evaporate
0.3mL fractionation Dichloromethane 100 mL
5% NaCl aq. 200 mL
5% NaCl aq. 200 mL
Dichloromethane layer Water
Dichloromethane 100 mL
Boiling
Dichloromethane layer
7
1.5E+05
10
5 11
3
2
1.0E+05 4
5.0E+04
8
0.0E+00
1. Oxamyl 7. Ethiofencar
2. Methiocarb sulfoxide 8. Pirimicarb
3. Methiocarb sulfone 9. Isoprocarb(MIPC)
4. Aldicarb 10.Fenobcarb(BPMC)
5. Bendiocarb 11.Methiocarb
6. Carbaryl
JASCO Measurement conditions
for the separation of 18 kinds of components
Column: CarbamatePak (4.0 mm I.D. x 150 mmL)
Column temperature: 40 °C
Mobile phase: A: H2O, B: CH3OH, C: THF
Flow rate: 1.0 ml/min
Reagents 1: 50 mMNaOH aq.
Reagent flow rate 1: 0.5 ml/min Gradient conditions
Reagents 2: 50 mM Na2B4O7・10H2O / 0.4 mg OPA
A B C
in 5 ml CH3OH /2-mercaptoethanol (1000/5/0.5)
Reagent flow rate 2: 0.5 ml/min 0min 88% 12% 0%
Reaction temperature: 80 °C 0.2min 88% 12% 0%
Detection: Ex; 339 nm, Em; 455 nm, Gain; x100 3.0min 90% 0% 10%
20.0min 85% 0% 15%
35.0min 70% 0% 30%
40.0min 70% 0% 30%
40.1min 88% 12% 0%
1cycle 50min
Chromatogram of 18 kinds of components of
carbamate pesticide (standard samples)
uV
2.0E+04
10 ppb
2
1.6E+04
17
16
13
18
8
3
12
14
10
4
15
6
11
5
1
1.2E+04
7
8.0E+03
2
100 ppb
16
6.0E+04
13
17
12
14
3
18
4
10
15
11
6
9
5
4.0E+04
1
2.0E+04
7
0.0E+00
10.0 20.0 30.0 40.0 [min]
Oxamyl 0.54 20 37
Methiocarb sulfoxide 0.36 50 137
Methiocarb sulfone 0.32 50 152
Aldicarb 0.56 20 35
Bendiocarb 0.36 20 56
Carbaryl 0.26 100 396
Ethiofencarb 0.26 100 374
Isoprocarb 0.22 500 2190
Fenobucarb 0.36 300 836
Methiocarb 0.42 50 118
* Injection volume
Compoments Retention time (min) Peak height(µV) Peak area (mV sec)
Oxamyl 7.053 0.0049 0.069 30266 209 0.69 334369 2703 0.78
Methiocarb sulfoxide 12.030 0.0078 0.065 13909 162 1.17 167168 1797 1.08
Methiocarb sulfone 13.481 0.0103 0.076 6063 272 4.49 70661 2618 3.71
Aldicar 15.691 0.0124 0.079 20345 134 0.66 259049 4301 1.66
Bendiocarb 18.667 0.0122 0.065 15682 172 1.10 204956 4937 2.41
Carbaryl 19.892 0.0121 0.061 18425 131 0.71 226471 5722 2.53
Ethiofencarb 20.524 0.0120 0.059 14743 212 1.44 182936 6307 3.45
Isoprocarb 21.795 0.0161 0.074 18081 317 1.76 226641 6834 3.02
Fenobucarb 24.356 0.0192 0.079 13120 215 1.64 172654 2573 1.49
Methiocarb 25.003 0.0237 0.095 6712 154 2.30 90581 1729 1.91
Procedure
Sample
Comparing with conventional pre-treatment
method based on solvent extraction, using GPC
for pre-treatment of residual pesticides makes Solvent extraction
possible to save a lot of time.
It is used for removing fat (Triglyceride etc.) and GPC Clean-up
pigments (chlorophyl etc.)
Preparative
HPLC, GC
GPC Chromatogram of standard samples and
brown rice uV
2
3.0E+5
1
3
2.0E+5
4 Calibration solution 1
1.0E+5 5
0.0
6
6.0E+5
Calibration solution
4.0E+5 7 of target components 2
2.0E+5
0.0
4.0E+5
0.0
10.0 20.0 30.0 40.0
[min]
7
0.0
4.0E+4 5
4
6 7
0.0