Vitamin B1 in Whole Blood and Vitamin B6 in Whole Blood/Plasma - HPLC

Order No.: 52052, for 100 tests
Parameters:
Vitamin B1 (TPP, thiamine pyrophosphate), Vitamin B6 (PLP, pyridoxal 5’-phosphate)

Each parameter safeguarded by a specific internal standard
No post-column derivatisation required
One sample preparation and one run for both parameters

CE-IVD validated product ready for IVDR within timeframes and transition periods specified by the IVDR 2017/746

Vitamin B1 (TPP, thiamine pyrophosphate)

Vitamin B6 (PLP, pyridoxal 5’-phosphate)

Clinical relevance

Vitamin B1 (thiamine) plays an important role in deriving energy from carbohydrates and fats. The active form is thiamine pyrophosphate (TPP), a coenzyme for some enzymatic reactions in carbohydrate metabolism and for pyruvate decarboxylase. TPP is also significantly involved in the oxidative degradation of glucose. The determination of the TPP concentration is more significant than measurements of total thiamine, as by this method only the physiologically active form is taken into account.

Vitamin B6 comprises pyridoxine, pyridoxamine and pyridoxal, as well as their phosphate derivatives. It is ingested with food and transferred via several enzymatic conversions into its active form, pyridoxal-5’-phosphate (PLP). PLP is involved in nearly one hundred different enzymatic reactions, among other things, as co-factor in amino acid metabolism, and in the formation of haemoglobin or neurotransmitters in the brain.

 

Product advantages

  • Specific internal standard for each parameter
  • No post-column derivatisation required
  • One sample preparation and one run for both parameters

 

This Chromsystems kit facilitates the combined analysis of vitamin B1 in whole blood and vitamin B6 in whole blood or plasma. The sample preparation can be processed from different matrices, so that both whole blood samples and plasma samples can easily be measured in the same run. Vitamin molecules are already derivatised during sample preparation, which renders the common post-column derivatisation unnecessary. The separation takes place with a binary gradient. The internal standard for each of the two parameters and special quality controls ensure precise and reliable quantification.

This method is also available with simplified sample preparation in pre-mixed tubes.

There is also a method using UHPLC as well as automated sample preparation for HPLC and UHPLC methods available for laboratories with a higher sample throughput.

More Information
Method of Analysis HPLC
Number of Tests 100
Please note The freely available information on this website, in particular on the sample preparation, are not sufficient to work with our products. Please read instructions and warning notices on products and/or instruction manuals.
Lower Limit of Quantitation

TPP 2.0 μg/l (whole blood)
PLP 4.5 μg/l (whole blood), 0.5 μg/l (plasma)

Upper Limit of Quantification

PLP 500 μg/l
TPP 750 μg/l

Intraassay

CV ≤ 2.3 %

Interassay

CV ≤ 5.2 %

Recovery ≤ 102 %
Specimen Whole Blood/Plasma
Sample Preparation
  • In a light protected vial mix 200 μl whole blood or plasma with 100 μl Internal Standard and 300 μl Precipitation Reagent, mix for 30 sec (vortex).
  • Centrifuge for 5 min at 14000 x g.
  • In a new light protected vial mix 250 μl Neutralisation Reagent and 100 μl Derivatisation Mix with 250 μl supernatant obtained above, mix briefly.
  • Incubate for 25 min at 60°C (waterbath).
  • Cool sample for 10 min at +2 to +8°C, then centrifuge for 2 min at 14000 x g.
  • Transfer supernatant into a light protected autosampler vial, inject 25-50 μl into the HPLC system.
Run Time 7–9 min
Injection Volume 25–50 μl
Flow Rate 1.5–2.3 ml/min
Column Temperature ambient (~25°C)
Gradient binary
Wavelength

Start EX 320 nm, EM 415 nm,

after approx. 3.8 min switch to EX 367 nm, EM 435 nm

Additional Info Every common HPLC system with binary pump and programmable fluorescence detector is suitable.
Parameters Vitamin B1 (TPP, thiamine pyrophosphate), Vitamin B6 (PLP, pyridoxal 5’-phosphate)
The following components are included in the kit:
The following products are not included in the kit but are required for the application of the method:
As a customer please login or register to gain full access.

Vitamin B1 (TPP, thiamine pyrophosphate)

Vitamin B6 (PLP, pyridoxal 5’-phosphate)

Clinical relevance

Vitamin B1 (thiamine) plays an important role in deriving energy from carbohydrates and fats. The active form is thiamine pyrophosphate (TPP), a coenzyme for some enzymatic reactions in carbohydrate metabolism and for pyruvate decarboxylase. TPP is also significantly involved in the oxidative degradation of glucose. The determination of the TPP concentration is more significant than measurements of total thiamine, as by this method only the physiologically active form is taken into account.

Vitamin B6 comprises pyridoxine, pyridoxamine and pyridoxal, as well as their phosphate derivatives. It is ingested with food and transferred via several enzymatic conversions into its active form, pyridoxal-5’-phosphate (PLP). PLP is involved in nearly one hundred different enzymatic reactions, among other things, as co-factor in amino acid metabolism, and in the formation of haemoglobin or neurotransmitters in the brain.

 

Product advantages

  • Specific internal standard for each parameter
  • No post-column derivatisation required
  • One sample preparation and one run for both parameters

 

This Chromsystems kit facilitates the combined analysis of vitamin B1 in whole blood and vitamin B6 in whole blood or plasma. The sample preparation can be processed from different matrices, so that both whole blood samples and plasma samples can easily be measured in the same run. Vitamin molecules are already derivatised during sample preparation, which renders the common post-column derivatisation unnecessary. The separation takes place with a binary gradient. The internal standard for each of the two parameters and special quality controls ensure precise and reliable quantification.

This method is also available with simplified sample preparation in pre-mixed tubes.

There is also a method using UHPLC as well as automated sample preparation for HPLC and UHPLC methods available for laboratories with a higher sample throughput.

More Information
Method of Analysis HPLC
Number of Tests 100
Please note The freely available information on this website, in particular on the sample preparation, are not sufficient to work with our products. Please read instructions and warning notices on products and/or instruction manuals.
Lower Limit of Quantitation

TPP 2.0 μg/l (whole blood)
PLP 4.5 μg/l (whole blood), 0.5 μg/l (plasma)

Upper Limit of Quantification

PLP 500 μg/l
TPP 750 μg/l

Intraassay

CV ≤ 2.3 %

Interassay

CV ≤ 5.2 %

Recovery ≤ 102 %
Specimen Whole Blood/Plasma
Sample Preparation
  • In a light protected vial mix 200 μl whole blood or plasma with 100 μl Internal Standard and 300 μl Precipitation Reagent, mix for 30 sec (vortex).
  • Centrifuge for 5 min at 14000 x g.
  • In a new light protected vial mix 250 μl Neutralisation Reagent and 100 μl Derivatisation Mix with 250 μl supernatant obtained above, mix briefly.
  • Incubate for 25 min at 60°C (waterbath).
  • Cool sample for 10 min at +2 to +8°C, then centrifuge for 2 min at 14000 x g.
  • Transfer supernatant into a light protected autosampler vial, inject 25-50 μl into the HPLC system.
Run Time 7–9 min
Injection Volume 25–50 μl
Flow Rate 1.5–2.3 ml/min
Column Temperature ambient (~25°C)
Gradient binary
Wavelength

Start EX 320 nm, EM 415 nm,

after approx. 3.8 min switch to EX 367 nm, EM 435 nm

Additional Info Every common HPLC system with binary pump and programmable fluorescence detector is suitable.
Parameters Vitamin B1 (TPP, thiamine pyrophosphate), Vitamin B6 (PLP, pyridoxal 5’-phosphate)
The following components are included in the kit:
The following products are not included in the kit but are required for the application of the method:
As a customer please login or register to gain full access.