In Vivo Quantitative Vasculature Segmentation and Assessment for Photodynamic Therapy Process Monitoring Using Photoacoustic Microscopy

Vascular damage is one of the therapeutic mechanisms of photodynamic therapy (PDT). In particular, short-term PDT treatments can effectively destroy malignant lesions while minimizing damage to nonmalignant tissue. In this study, we investigate the feasibility of label-free quantitative photoacousti...

Full description

Saved in:
Bibliographic Details
Published inSensors (Basel, Switzerland) Vol. 21; no. 5; p. 1776
Main Authors Mai, Thi Thao, Yoo, Su Woong, Park, Suhyun, Kim, Jin Young, Choi, Kang-Ho, Kim, Chulhong, Kwon, Seong Young, Min, Jung-Joon, Lee, Changho
Format Journal Article
LanguageEnglish
Published Switzerland MDPI 04.03.2021
MDPI AG
Subjects
Online AccessGet full text
ISSN1424-8220
1424-8220
DOI10.3390/s21051776

Cover

More Information
Summary:Vascular damage is one of the therapeutic mechanisms of photodynamic therapy (PDT). In particular, short-term PDT treatments can effectively destroy malignant lesions while minimizing damage to nonmalignant tissue. In this study, we investigate the feasibility of label-free quantitative photoacoustic microscopy (PAM) for monitoring the vasculature changes under the effect of PDT in mouse ear melanoma tumors. In particular, quantitative vasculature evaluation was conducted based on Hessian filter segmentation. Three-dimensional morphological PAM and depth-resolved images before and after PDT treatment were acquired. In addition, five quantitative vasculature parameters, including the PA signal, vessel diameter, vessel density, perfused vessel density, and vessel complexity, were analyzed to evaluate the influence of PDT on four different areas: Two melanoma tumors, and control and normal vessel areas. The quantitative and qualitative results successfully demonstrated the potential of the proposed PAM-based quantitative approach to evaluate the effectiveness of the PDT method.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors contributed equally to this work.
ISSN:1424-8220
1424-8220
DOI:10.3390/s21051776