Label-free identification of neutropenia using deep-ultraviolet microscopy

Author(s):  
Ashkan Ojaghi ◽  
Francisco E. Robles
2021 ◽  
Author(s):  
Ashkan Ojaghi ◽  
Paloma Casteleiro Costa ◽  
Christina Caruso ◽  
wilbur lam ◽  
Francisco Robles

2020 ◽  
Vol 117 (26) ◽  
pp. 14779-14789 ◽  
Author(s):  
Ashkan Ojaghi ◽  
Gabriel Carrazana ◽  
Christina Caruso ◽  
Asad Abbas ◽  
David R. Myers ◽  
...  

Hematological analysis, via a complete blood count (CBC) and microscopy, is critical for screening, diagnosing, and monitoring blood conditions and diseases but requires complex equipment, multiple chemical reagents, laborious system calibration and procedures, and highly trained personnel for operation. Here we introduce a hematological assay based on label-free molecular imaging with deep-ultraviolet microscopy that can provide fast quantitative information of key hematological parameters to facilitate and improve hematological analysis. We demonstrate that this label-free approach yields 1) a quantitative five-part white blood cell differential, 2) quantitative red blood cell and hemoglobin characterization, 3) clear identification of platelets, and 4) detailed subcellular morphology. Analysis of tens of thousands of live cells is achieved in minutes without any sample preparation. Finally, we introduce a pseudocolorization scheme that accurately recapitulates the appearance of cells under conventional staining protocols for microscopic analysis of blood smears and bone marrow aspirates. Diagnostic efficacy is evaluated by a panel of hematologists performing a blind analysis of blood smears from healthy donors and thrombocytopenic and sickle cell disease patients. This work has significant implications toward simplifying and improving CBC and blood smear analysis, which is currently performed manually via bright-field microscopy, and toward the development of a low-cost, easy-to-use, and fast hematological analyzer as a point-of-care device and for low-resource settings.


2016 ◽  
Vol 88 (8) ◽  
pp. 4580-4580
Author(s):  
Masakazu Kikawada ◽  
Atsushi Ono ◽  
Wataru Inami ◽  
Yoshimasa Kawata

2007 ◽  
Vol 4 (7) ◽  
pp. 567-569 ◽  
Author(s):  
Benjamin J Zeskind ◽  
Caroline D Jordan ◽  
Winston Timp ◽  
Linda Trapani ◽  
Guichy Waller ◽  
...  

2020 ◽  
Vol 27 (3) ◽  
pp. 772-778 ◽  
Author(s):  
Frédéric Jamme ◽  
Bertrand Cinquin ◽  
Yann Gohon ◽  
Eva Pereiro ◽  
Matthieu Réfrégiers ◽  
...  

A lipid droplet (LD) core of a cell consists mainly of neutral lipids, triacylglycerols and/or steryl esters (SEs). The structuration of these lipids inside the core is still under debate. Lipid segregation inside LDs has been observed but is sometimes suggested to be an artefact of LD isolation and chemical fixation. LD imaging in their native state and in unaltered cellular environments appears essential to overcome these possible technical pitfalls. Here, imaging techniques for ultrastructural study of native LDs in cellulo are provided and it is shown that LDs are organized structures. Cryo soft X-ray tomography and deep-ultraviolet (DUV) transmittance imaging are showing a partitioning of SEs at the periphery of the LD core. Furthermore, DUV transmittance and tryptophan/tyrosine auto-fluorescence imaging on living cells are combined to obtain complementary information on cell chemical contents. This multimodal approach paves the way for a new label-free organelle imaging technique in living cells.


2008 ◽  
Vol 14 (S2) ◽  
pp. 740-741
Author(s):  
BJ Zeskind

Extended abstract of a paper presented at Microscopy and Microanalysis 2008 in Albuquerque, New Mexico, USA, August 3 – August 7, 2008


The Analyst ◽  
2014 ◽  
Vol 139 (11) ◽  
pp. 2663-2667 ◽  
Author(s):  
Vitalijs Zubkovs ◽  
Frédéric Jamme ◽  
Slavka Kascakova ◽  
Franck Chiappini ◽  
François Le Naour ◽  
...  

Single photon ultraviolet microscopy is complementary to two-photon microscopy for tissue diagnosis.


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