BS EN 12821:2009
Current
The latest, up-to-date edition.
Foodstuffs. Determination of vitamin D by high performance liquid chromatography. Measurement of cholecalciferol (D3) or ergocalciferol (D2)
Hardcopy , PDF
English
30-04-2009
Foreword
1 Scope
2 Normative references
3 Principle
4 Reagents
5 Apparatus
6 Procedure
7 Calculation
8 Precision
9 Test report
Annex A (informative) - Examples of suitable HPLC
systems
Annex B (informative) - Examples of suitable extraction
and saponification conditions
Annex C (normative) - Examples of suitable semi-preparative
and analytical HPLC chromatograms
Annex D (informative) - Precision data
Annex E (informative) - Additional cleanup step for the
determination of vitamin D with use of preparative
TLC, column chromatography and or SPE
Bibliography
Describes a method for the determination of vitamin D[3] (cholecalciferol) or vitamin D[2] (ergocalciferol) in foodstuffs by high performance liquid chromatography (HPLC).
Committee |
AW/275
|
DevelopmentNote |
Supersedes 97/707076 DC. (05/2005) Supersedes 07/30158610 DC. (05/2009)
|
DocumentType |
Standard
|
Pages |
28
|
PublisherName |
British Standards Institution
|
Status |
Current
|
Supersedes |
This European Standard specifies a method for the determination of vitamin D3 (cholecalciferol) or vitamin D2 (ergocalciferol) in foodstuffs by high performance liquid chromatography (HPLC). Vitamin D3 is primary in foodstuffs of animal origin, while vitamin D2 is primary in wild mushrooms. Both vitamin D3 and vitamin D2 can be present in fortified foodstuffs. This European Standard is not applicable for samples with a content of vitamin D3 and vitamin D2. Apart from the vitamin D activity from the parent forms, vitamin D3 and vitamin D2, the corresponding metabolites 25-hydroxy vitamin D and 1,25-dihydroxy vitamin D also contribute to the vitamin D activity. This European Standard does only include measurement of vitamin D3 or vitamin D2. This European Standard provides the base for the analytical methods. It is intended to serve as a frame in which the analyst can define his own analytical work in accordance to the standard procedure. This method has been validated in inter-laboratory tests on fortified and non-fortified samples such as margarine, milk, milk powder, liquid infant formula, infant formula, cooking oil, and fish oil at levels from 0,4 ?g/100 g to 14 ?g/100 g. Further information on the validation data is given in Annex D.
Standards | Relationship |
DIN EN 12821:2009-08 | Identical |
I.S. EN 12821:2009 | Identical |
NEN EN 12821 : 2009 | Identical |
UNE-EN 12821:2009 | Identical |
EN 12821:2009 | Identical |
UNI EN 12821 : 2009 | Identical |
NF EN 12821 : 2009 | Identical |
NBN EN 12821 : 2009 | Identical |
NS EN 12821 : 2009 | Identical |
SN EN 12821 : 2009 | Identical |
ISO 5725:1986 | Precision of test methods Determination of repeatability and reproducibility for a standard test method by inter-laboratory tests |
ISO 3696:1987 | Water for analytical laboratory use — Specification and test methods |
EN ISO 3696:1995 | Water for analytical laboratory use - Specification and test methods (ISO 3696:1987) |
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