The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 13, 2018

Filed:

Mar. 22, 2017
Applicant:

Rhode Island Council on Postsecondary Education, Statutory Board of Education, and Rhode Island Board of Governors for Higher Education, Warwick, RI (US);

Inventors:

Fatemeh Akhlaghi, Wakerfield, RI (US);

Mwlod Ghareeb, Kingston, RI (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
B01D 15/14 (2006.01); B01D 15/22 (2006.01); B01D 15/42 (2006.01); G01N 30/00 (2006.01); G01N 30/02 (2006.01); G01N 33/94 (2006.01); G06F 19/00 (2018.01); G01N 30/04 (2006.01);
U.S. Cl.
CPC ...
G01N 33/9493 (2013.01); B01D 15/14 (2013.01); B01D 15/22 (2013.01); B01D 15/426 (2013.01); G01N 30/00 (2013.01); G06F 19/00 (2013.01); G06F 19/3456 (2013.01); G01N 2030/022 (2013.01); G01N 2030/027 (2013.01); G01N 2030/042 (2013.01); G01N 2030/045 (2013.01); G01N 2560/00 (2013.01);
Abstract

Disclosed is a method of measuring tacrolimus levels in a subject. In exemplary embodiments, the method comprises the steps of: collecting oral fluid from the subject; homogenizing the oral fluid; combining the homogenized oral fluid with a precipitating solvent; separating oral fluid components on a liquid chromatography column by gradient elution with a mixture of a solvent A and a solvent B, wherein the solvent A is about 2 mM ammonium acetate/0.1% (v/v) formic acid in water and solvent B is about 2 mM ammonium acetate/0.1% (v/v) formic acid in MeOH and wherein the amount of solvent B is increased from about 50% (v/v) to about 98% (v/v); and quantifying the amount of tacrolimus in the oral fluid by mass spectrometry.


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