Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Combined confocal Raman and quantitative phase microscopy system for biomedical diagnosis

Combined confocal Raman and quantitative phase microscopy system for biomedical diagnosis

Thumbnail Image
Download
Name

Niles-2011-Combined confocal Raman.pdf

Size

1010.35 KB

Format

Adobe PDF

Checksum (MD5)

674145b099f08400fc3057750b47e7de

Author(s)
Kang, Jeon Woong
•
Lue, Niyom
•
Kong, Chae-Ryon
•
Barman, Ishan
•
Dingari, Narahara Chari
•
Dasari, Ramachandra Rao
•
Feld, Michael S.
•
Goldfless, Stephen Jacob
•
Niles, Jacquin
Date Issued
August 2011
Journal
Biomedical Optics Express
Publisher
Optical Society of America
Citation
Kang, Jeon Woong et al. “Combined confocal Raman and quantitative phase microscopy system for biomedical diagnosis.” Biomedical Optics Express 2 (2011): 2484. Web. 19 Oct. 2011. © 2011 Optical Society of America
Version
Final published version
Abstract
We have developed a novel multimodal microscopy system that incorporates confocal Raman, confocal reflectance, and quantitative phase microscopy (QPM) into a single imaging entity. Confocal Raman microscopy provides detailed chemical information from the sample, while confocal reflectance and quantitative phase microscopy show detailed morphology. Combining these intrinsic contrast imaging modalities makes it possible to obtain quantitative morphological and chemical information without exogenous staining. For validation and characterization, we have used this multi-modal system to investigate healthy and diseased blood samples. We first show that the thickness of a healthy red blood cell (RBC) shows good correlation with its hemoglobin distribution. Further, in malaria infected RBCs, we successfully image the distribution of hemozoin (malaria pigment) inside the cell. Our observations lead us to propose morphological screening by QPM and subsequent chemical imaging by Raman for investigating blood disorders. This new approach allows monitoring cell development and cell-drug interactions with minimal perturbation of the biological system of interest.
MIT Department
Massachusetts Institute of Technology. Department of Biological Engineering
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/66509
DOI of Published Version
https://doi.org/10.1364/BOE.2.002484
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.