Method and kit for determining metabolites on dried blood spot samples

摘要

A method for individuating with high sensitivity and specificity ADA metabolites from dried blood spot. The method described herein can be used to extract Adenosine and Deoxyadenosine from a sample under conditions that permit concurrently extracting other metabolites, such as amino acids, free carnitine, or acylcarnitines. For example, harsh extraction conditions (such as extreme acidity and high temperature) can be avoided. The method can be used, along with other neonatal screenings, on blood samples and preferably on dried blood spots (Guthrie cards) and more preferably on Guthrie cards obtained in the II-IV day of life. The method is reliable and reproducible, easy to perform and gives a definitive response within a short time (1-2 days). One or more kit for use in the method.

主权项

1. A method for an analytical determination of Adenosine and Deoxyadenosine and a plurality of metabolites selected from the group consisting of purines, pyrimidines, amino acids, free carnitine, acylcarnitines and any combinations thereof from a dried blood sample, said method comprising:
providing a dried blood sample; extracting Adenosine and Deoxyadenosine from the dried blood sample concurrently with the plurality of metabolites selected from the group consisting of purines, pyrimidines, amino acids, acylcarnitines, free carnitine, and any combinations thereof using an extraction mixture comprising a mixture of water and C1-3 linear or branched chain monoalcohol, wherein water is present at least at 10% v/v, wherein the extracting is performed by first contacting the dried blood sample with the C1-3 linear or branched chain monoalcohol corresponding to 100-x % v/v of the final volume v/v of the extraction mixture, and second adding water to the sample corresponding to x % v/v of the final volume v/v of the extraction mixture, wherein x is the v/v water percentage and ranges from about 10% to about 90%; and determining the presence or amount of Adenosine and Deoxyadenosine concurrently with the plurality of metabolites selected from the group consisting of purines, pyrimidines, amino acids, acylcarnitines, free carnitine, and any combinations thereof using MS directly on the extract.