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478

M

ASTOVSKA

ET AL

.

J

OURNAL OF

AOAC I

NTERNATIONAL

V

OL

. 98, N

O

. 2, 2015

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preparation and extraction) in comparison with currently

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complete. In addition, acceptable methods had to demonstrate

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of reference materials), and practical considerations, such as

availability of equipment.

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method was studied within the presented collaborative study, for

which the analytes were narrowed down to include only PAHs

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see

Table 1 for the

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Table 1. PAHs included in the collaborative study

Name

Abbreviation

1,7-Dimethylphenanthrene

1,7-DMP

1-Methylnaphthalene

1-MN

1-Methylphenanthrene

1-MP

2,6-Dimethylnaphthalene

2,6-DMN

3-Methylchrysene

3-MC

Anthracene

Ant

Benz[

a

]anthracene

BaA

Benzo[

a

] pyrene

BaP

Benzo[

b

@ÀXRUDQWKHQH

BbF

Benzo[

g,h,i

]perylene

BghiP

Benzo[

k

@ÀXRUDQWKHQH

BkF

Chrysene

Chr

Dibenz[

a,h

]anthracene

DBahA

)OXRUDQWKHQH

Flt

)OXRUHQH

Fln

Indeno[1,2,3-

cd

]pyrene

IcdP

Naphthalene

Naph

Phenanthrene

Phe

Pyrene

Pyr

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0XVVHO

Oyster

Low

Mid

High

Low

Mid

High

Low

Mid

High

PAH

Level 1

Level 2

Level 4

Level 1

Level 3

Level 4

Level 2

Level 3

Level 5

1,7-DMP

a

20

20

20

40

40

40

80

80

80

1-MN

20

75

200

20

100

200

75

100

250

1-MP

10

25

125

10

50

125

25

50

200

2,6-DMN

15

40

175

15

75

175

40

75

225

3-MC

10

30

145

10

90

145

30

90

225

Ant

5

10

40

5

15

40

10

15

60

BaA

5

15

60

5

25

60

15

25

100

BaP

2

5

25

2

10

25

5

10

50

BbF

5

10

75

5

30

75

10

30

100

BghiP

2

5

20

2

10

20

5

10

25

BkF

2

8

40

2

20

40

8

20

75

Chr

15

50

175

15

100

175

50

100

250

DBahA

2

5

15

2

10

15

5

10

20

Fln

5

15

50

5

25

50

15

25

75

Flt

10

25

100

10

50

100

25

50

150

IcdP

2

5

20

2

10

20

5

10

25

Naph

25

80

160

25

125

160

80

125

225

Phe

15

50

175

15

100

175

50

100

250

Pyr

15

40

125

15

75

125

40

75

200

a

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