Abstract

As an emerging technique, ultrasound-modulated fluorescence (UMF), or ultrasound switchable fluorescence (USF) bioimaging has shown promising features to produce deep-tissue and high-resolution fluorescence imaging for biomedical research and health diagnosis. The success of UMF or USF heavily relies on the design of their contrast agents (CAs). We herein surveyed recent advances in the development of such unique CAs, including configuration, mechanism, stability, sensitivity, and selectivity. Meanwhile, UMF or USF instrumentation has emerged as developmental breakthrough technologies to existing bio-imaging techniques. The best performance of UMF or USF bio-imaging requires an interactive response between CAs and the instrument. In this review, the description of UMF or USF instrumentation are also included for clarification and better understanding. Finally, the UMF and USF's performance in bioimaging is evaluated based on signal-to-noise ratio, resolution, imaging depth and speed, using photoacoustic imaging (PAI) as a standard, a well-developed technique of hybrid bio-imaging. Unlike PAI, UMF or USF is still in its early stage. Although results demonstrated a proof-of-concept landmark being reached, significant efforts are needed to improve the performance of UMF or USF.

Highlights

  • Fluorescence imaging is a procedure widely used in biomedical laboratories for preclinical experiments and clinical stages, due to the rapid development of optical technology and the large number of fluorescent probes capable of emitting various wavelengths for targeting a variety of specific biological structures (Salzer, 2012)

  • The idea to create a new combination with known materials to fulfill the requirements of UMF or USF CAs is intriguing and encouraging

  • Numerous designs and testing had been documented for the development of USF CAs

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Summary

Introduction

Fluorescence imaging is a procedure widely used in biomedical laboratories for preclinical experiments and clinical stages, due to the rapid development of optical technology and the large number of fluorescent probes capable of emitting various wavelengths for targeting a variety of specific biological structures (Salzer, 2012). The idea to create a new combination with known materials to fulfill the requirements of UMF or USF CAs is intriguing and encouraging.

Results
Conclusion
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