Table of Contents Table of Contents
Previous Page  429 / 471 Next Page
Information
Show Menu
Previous Page 429 / 471 Next Page
Page Background

© 2012 AOAC INTERNATIONAL

solution 2,

D

(

p

)(

2

), and 25.0 mL of the calibration standard stock

solution 3,

D

(

p

)(

3

). Then make up to the mark with

n

-hexane.

Dilute accordingly to the type of injector used.

Note

: This solution keeps for about 6 months if stored in the

dark at –20°C. To prevent contamination of the standard solution,

immediately distribute the solution into different vials (ready

to inject) and store at –20°C before use. Use each vial once then

discard it.

(

q

)

Commercially available calibration standard FAME

mixture solution

.—Before use, allow the ampoule to come to

room temperature (maximum 25°C) in the dark without heating.

Cut the ampoule with a glass knife and using a Pasteur pipet,

rapidly transfer the content of the ampoule into a 50 mL pre-tarred

volumetric flask, weigh, and make up to the mark with

n

-hexane.

Dilute accordingly to the type of injector used.

Note

: This solution keeps for about 6 months if stored in the

dark at –20°C. To prevent contamination of the standard solution,

immediately distribute the solution into different vials (ready to

inject) and store at –20°C before use. Use each vial once and then

discard it.

E. Preparation of Test Sample

Milk powder and infant formula

.—Mix well to ensure that

sample is homogeneous.

(

1

)

Class or group of fatty acids in 100 g fat.—

Calculate the

mass fraction of all fatty acids included in a group or in a class

of fatty acids by simple addition of individual fatty acids results

(expressed in g FA/100 g fat).

(

2

)

Performance of the transesterification

.—Record the areas

of the two internal standard peaks (methyl undecanoate and

tritridecanoin) in the analyzed samples.

The performance of transesterification, PT expressed in %, is

calculated on the recovery of the tritridecanoin as a second internal

standard as follows:

ܲ

ݐ

= ݉

௖ଵଵ

×

ܣ

௖ଵଷ

× ܴ

௖ଵଷ

× ܵ

௖ଵଷ

)ܩܣ

ܣ

௖ଵଵ

× ݉

௖ଵଷ

× 100

where m

C11

is the mass, in milligrams, of C-11:0 internal standard

added to the solution; A

C13

is the peak area of C-13:0 internal

standard in the chromatogram; R

C13

is the response factor of C13:0

relative to C11:0, calculated according to

G

(

a

)(

2

); S

C13

is the

stoichiometric factor to convert C13:0 FAME into C13:0 TAG; A

C11

is the peak area of C-11:0 internal standard in the chromatogram;

and m

C13

is the mass of liquid milk and liquid formula. Bring sample

to room temperature and shake vigorously before use.

F. Procedure

As a check on method performance, carry out two single

determinations in accordance with

F

(

a

) and (

b

).

Note

: An alternative procedure using fat-extraction tubes with

siphon or wash-bottle fittings is given in Figures

2012.13A–C

.

(

a

)

Resolution between C18:1 trans and cis

.—Inject once the

qualitative

cis/trans

FAME isomers standard mixture solution,

D

(

o

).

(

b

)

Calibrating solution for the determination of response

factor

.—Inject three times the calibrated solution,

D

(

q

).

(

c

)

Test portion

.—Into a 25 mL centrifuge tube with a screw

cap, weigh to the nearest 0.1 mg an equivalent quantity of sample

in order to have ca 50 mg fat in the tube (

Example

: For a sample

containing 26 g fat/100 g product, the corresponding sample weight

is approximately 190 mg).

Note 1

: For fatty acid analysis on fat extracted from foods, the

same amount of fat is required. For milk powder or infant formula

powder, add 2.0 mL water using a micropipet. Close the tube, and

then dissolve gently using a vortex mixer. Wait for 15 min at room

temperature.

Note 2

: For liquid milk samples and fat extracted from foods, no

pretreatment (water addition) is required.

Pipet 5 mL of internal standard solution,

D

(

j

). Add with a pipet

5 mL of 5% (w/v) methanolic sodium methoxide solution,

D

(

d

).

The transesterification time starts with the addition of the first drop.

Close the tube hermetically and shake well for 10 s using a vortex

mixer.

After 180 s, open the tube and add 2 mL hexane. After 210 s

add 10 mL disodium hydrogen citrate and sodium chloride

aqueous solution,

D

(

f

). The transesterification time stops after the

addition of the last drop. Shake gently using a vortex mixer. The

transesterification time should not exceed 240 s.

Note 3

: To respect the total reaction time (240 s), the

transesterification reaction should be carried out with a maximum

of six tubes at the same time. Rapid delivery system (dispenser)

can be used to add reagents, but not for the addition of internal

standard solution.

Centrifuge the tube at 1750 rpm (or equivalent rpm to

g

= 375 ±

25) for 5 min.

Into a 10 mL volumetric flask, pipet 200 μL of the supernatant

and make up to the mark with

n

-hexane.

Note 4

: The dilution factor is calculated for on-column and

splitless injection only. When using split injection, adapt the

dilution to obtain the desired peak responses accordingly to split

ratio used (ensure sufficient and accurate detection level for small

peaks especially). Stored in the dark at 4°C, the sample solution

after dilution is stable for 2 days.

G. Determination

(

a

)

Quantitative determination.

(

1

)

Resolution.—

Inject into the gas chromatograph 1.0 μL of the

calibrating solution,

F

(

a

). Determine peak width at half height and

distance between the left of the chromatogram and the top of peak

for C18:1

trans

Δ13/14 and oleic acid methyl ester. The resolution

criteria (R) is calculated as follows:

ܴ = 1.18(

ݐ

ோଶ

ݐ

ோଵ

)/ܹ

൫ ଵ ଶൗ ൯ଵ

+ ܹ

൫ ଵ ଶൗ ൯ଶ

where t

R1

= distance, in centimeters, between the left of the

chromatogram and the top of peak 1 (C18:1

trans

Δ13/14); t

R2

=

distance, in centimeters, between the left of the chromatogram and

the top of peak 2 (oleic acid); W

(½)1

= peak width, in centimeters, at

half height of peak 1 (C18:1

trans

Δ13/14); W

(½)2

= peak width, in

centimeters, at half height of peak 2 (oleic acid).

The resolution test is acceptable when value calculated for R is

equivalent or higher than 1.00 (±5%) (to determine with the ring test).

Note

: Example of the calculation is given in Figure

2012.13C

.

(

2

)

Calculation of response factor.—

Inject into the gas

chromatograph 1.0 μL of the calibrating solution,

F

(

b

). Determine

the area of peaks attributable to each FAME present in the

calibration standard mixture,

D

(

q

), and calculate their respective

response factors (Rf

i

) relative to the internal standard (C11:0):

ܴ݂

= ݉Ԣ

ȉ

ܣ

Ԣ

݉Ԣ

ȉ

ܣ

Ԣ

Candidates for 2016 Method of the Year

364