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:
May. 14, 2019

Filed:

May. 15, 2017
Applicant:

Instrumentation Laboratory Company, Bedford, MA (US);

Inventors:

Ethan Schonbrun, Newton, MA (US);

Gert Blankenstein, Dortmund, DE;

Josef Kerimo, Concord, MA (US);

Hansong Zeng, Lowell, MA (US);

Assignee:
Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
G01N 33/49 (2006.01); B01L 3/00 (2006.01); G01N 21/03 (2006.01); G01N 21/25 (2006.01); G01N 21/05 (2006.01); G01N 21/552 (2014.01);
U.S. Cl.
CPC ...
G01N 33/49 (2013.01); B01L 3/502 (2013.01); G01N 21/0303 (2013.01); G01N 21/05 (2013.01); G01N 21/25 (2013.01); G01N 21/552 (2013.01); B01L 2300/0654 (2013.01); B01L 2300/168 (2013.01); G01N 2201/0612 (2013.01);
Abstract

Analyte content in a cell free portion of a body fluid, such as blood, is optically determined without centrifugation or other preliminary steps for separating the cell free portion from the body fluid. A channel is configured for containing a flowing sample of the body fluid along an optical boundary. The channel is configured so that a cell free layer of the fluid naturally forms along the boundary of the channel which coincides with the optical boundary. A light source is directed onto the optical boundary at an angle selected to generate total reflection from the boundary and to generate an evanescent field across the boundary in the cell free layer of fluid. A light detector is configured to detect absorption of the light in the evanescent field. The light source and light detector are matched to the wavelength range of an absorption peak of the analyte being detected.


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