Quantitation of glycated hemoglobin in single red blood cells by transient absorption microscopy and phasor analysis (Conference Presentation)

Pu-Ting Dong; Haonan Lin; Ji-Xin Cheng

doi:10.1117/12.2511195

4 March 2019 Quantitation of glycated hemoglobin in single red blood cells by transient absorption microscopy and phasor analysis (Conference Presentation)

Pu-Ting Dong, Haonan Lin, Ji-Xin Cheng

Author Affiliations +

Proceedings Volume 10882, Multiphoton Microscopy in the Biomedical Sciences XIX; 1088225 (2019) https://doi.org/10.1117/12.2511195
Event: SPIE BiOS, 2019, San Francisco, California, United States

Abstract

Type 2 diabetes is an increasingly prevalent disease, with more than 400 million people worldwide diagnosed in 2016. As a stable and accurate biomarker, glycated hemoglobin (HbA1c) is clinically used to diagnose type 2 diabetes with a threshold of 6.5% HbA1c among total hemoglobin (Hb). Current methods such as boronate affinity chromatography or enzymatic assay involve complex processing of large-volume blood samples, which inhibits real-time measurement in clinic. Moreover, these methods cannot measure the HbA1c fraction at single red blood cell level, thus unable to separate the contribution by diabetes from other factors such as diseases related to lifetime of red blood cells. Here, we demonstrate a transient absorption imaging approach that is able to differentiate HbA1c from Hb based on the excited state dynamics measurement. HbA1c fraction inside a single red blood cell is derived quantitatively through phasor analysis. HbA1c fraction distribution for diabetic blood is found apparently different from that for healthy blood. A mathematical model is developed to derive the long-term glucose concentration in the blood. Our technology provides a new way to study heme modification and to derive clinically important information avoid of glucose fluctuation in the bloodstream.

Conference Presentation

Citation Download Citation

Pu-Ting Dong, Haonan Lin, and Ji-Xin Cheng "Quantitation of glycated hemoglobin in single red blood cells by transient absorption microscopy and phasor analysis (Conference Presentation)", Proc. SPIE 10882, Multiphoton Microscopy in the Biomedical Sciences XIX, 1088225 (4 March 2019); https://doi.org/10.1117/12.2511195

ACCESS THE FULL ARTICLE

INSTITUTIONAL
Select your institution to access the SPIE Digital Library.

SELECT YOUR INSTITUTION

PERSONAL
Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.

PERSONAL SIGN IN

No SPIE Account? Create one

PURCHASE THIS CONTENT

SUBSCRIBE TO DIGITAL LIBRARY

50 downloads per 1-year subscription

Members: $195

Non-members: $335 ADD TO CART

25 downloads per 1 - year subscription

Members: $145

Non-members: $250 ADD TO CART

PURCHASE SINGLE ARTICLE

Includes PDF, HTML & Video, when available

Members: $17.00

Non-members: $21.00 ADD TO CART

PROCEEDINGS
PRESENTATION

WATCH
PRESENTATION SAVE TO MY LIBRARY

GET CITATION

KEYWORDS

Blood

Absorption

Microscopy

Glucose

Chromatography

Diagnostics

Mathematical modeling

Keywords/Phrases

Search In:

Publication Years