Published March 2016 | Version Accepted Version
Journal Article Open

Seeing Through the Surface: Non-invasive Characterization of Biomaterial-Tissue Interactions Using Photoacoustic Microscopy

  • 1. ROR icon Harvard University
  • 2. ROR icon Brigham and Women's Hospital
  • 3. ROR icon Massachusetts Institute of Technology
  • 4. ROR icon Washington University in St. Louis
  • 5. ROR icon Georgia Institute of Technology

Abstract

At the intersection of life sciences, materials science, engineering, and medicine, regenerative medicine stands out as a rapidly progressing field that aims at retaining, restoring, or augmenting tissue/organ functions to promote the human welfare. While the field has witnessed tremendous advancements over the past few decades, it still faces many challenges. For example, it has been difficult to visualize, monitor, and assess the functions of the engineered tissue/organ constructs, particularly when three-dimensional scaffolds are involved. Conventional approaches based on histology are invasive and therefore only convey end-point assays. The development of volumetric imaging techniques such as confocal and ultrasonic imaging has enabled direct observation of intact constructs without the need of sectioning. However, the capability of these techniques is often limited in terms of penetration depth and contrast. In comparison, the recently developed photoacoustic microscopy (PAM) has allowed us to address these issues by integrating optical and ultrasonic imaging to greatly reduce the effect of tissue scattering of photons with one-way ultrasound detection while retaining the high optical absorption contrast. PAM has been successfully applied to a number of studies, such as observation of cell distribution, monitoring of vascularization, and interrogation of biomaterial degradation. In this review article, we highlight recent progress in non-invasive and volumetric characterization of biomaterial–tissue interactions using PAM. We also discuss challenges ahead and envision future directions.

Additional Information

© 2015 Biomedical Engineering Society. Received 20 August 2015; accepted 8 October 2015; published online 15 October 2015. This work was supported in part by startup funds from the Georgia Institute of Technology and NIH Grants DP1 OD000798 (NIH Director's Pioneer Award) and R01 AR060820. The authors would like to thank Dr. Yu Wang and Dr. Li Li for their assistance in OR-PAM–FCM and OR-PAM–OCT imaging of melanoma cell-scaffold interactions. Conflict of Interest: L. V. Wang has a financial interest in Endra, Inc., and Microphotoacoustics, Inc., which, however, did not support this work; all other authors declare no conflict of interest.

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Accepted Version - nihms731069.pdf

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Additional details

Identifiers

PMCID
PMC4792739
Eprint ID
68492
DOI
10.1007/s10439-015-1485-2
Resolver ID
CaltechAUTHORS:20160617-143506465

Related works

Funding

NIH
DP1 OD000798
NIH
R01 AR060820
Georgia Institute of Technology

Dates

Created
2016-06-18
Created from EPrint's datestamp field
Updated
2021-11-11
Created from EPrint's last_modified field