<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>29(Suppl 1)</volume><submitter>Hirasawa T</submitter><pubmed_abstract>&lt;h4>Significance&lt;/h4>We developed a high-speed optical-resolution photoacoustic microscopy (OR-PAM) system using a high-repetition-rate supercontinuum (SC) light source and a two-axes Galvano scanner. The OR-PAM system enabled real-time imaging of optical absorbers inside biological tissues with excellent excitation wavelength tunability.&lt;h4>Aim&lt;/h4>In the near-infrared (NIR) wavelength range, high-speed OR-PAM faces limitations due to the lack of wavelength-tunable light sources. Our study aimed to enable high-speed OR-PAM imaging of various optical absorbers, including NIR contrast agents, and validate the performance of high-speed OR-PAM in the detection of circulating tumor cells (CTCs).&lt;h4>Approach&lt;/h4>A high-repetition nanosecond pulsed SC light source was used for OR-PAM. The excitation wavelength was adjusted by bandpass filtering of broadband light pulses produced by an SC light source. Phantom and &lt;i>in vivo&lt;/i> experiments were performed to detect tumor cells stained with an NIR contrast agent within flowing blood samples.&lt;h4>Results&lt;/h4>The newly developed high-speed OR-PAM successfully detected stained cells both in the phantom and &lt;i>in vivo&lt;/i>. The phantom experiment confirmed the correlation between the tumor cell detection rate and tumor cell concentration in the blood sample.&lt;h4>Conclusions&lt;/h4>The high-speed OR-PAM effectively detected stained tumor cells. Combining high-speed OR-PAM with molecular probes that stain tumor cells &lt;i>in vivo&lt;/i> enables &lt;i>in vivo&lt;/i> CTC detection.</pubmed_abstract><journal>Journal of biomedical optics</journal><pagination>S11527</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924425</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Photoacoustic microscopy for real-time monitoring of near-infrared optical absorbers inside biological tissue.</pubmed_title><pmcid>PMC10924425</pmcid><pubmed_authors>Ishikawa T</pubmed_authors><pubmed_authors>Ito K</pubmed_authors><pubmed_authors>Tachi K</pubmed_authors><pubmed_authors>Hirasawa T</pubmed_authors><pubmed_authors>Ishihara M</pubmed_authors><pubmed_authors>Miyashita M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Photoacoustic microscopy for real-time monitoring of near-infrared optical absorbers inside biological tissue.</name><description>&lt;h4>Significance&lt;/h4>We developed a high-speed optical-resolution photoacoustic microscopy (OR-PAM) system using a high-repetition-rate supercontinuum (SC) light source and a two-axes Galvano scanner. The OR-PAM system enabled real-time imaging of optical absorbers inside biological tissues with excellent excitation wavelength tunability.&lt;h4>Aim&lt;/h4>In the near-infrared (NIR) wavelength range, high-speed OR-PAM faces limitations due to the lack of wavelength-tunable light sources. Our study aimed to enable high-speed OR-PAM imaging of various optical absorbers, including NIR contrast agents, and validate the performance of high-speed OR-PAM in the detection of circulating tumor cells (CTCs).&lt;h4>Approach&lt;/h4>A high-repetition nanosecond pulsed SC light source was used for OR-PAM. The excitation wavelength was adjusted by bandpass filtering of broadband light pulses produced by an SC light source. Phantom and &lt;i>in vivo&lt;/i> experiments were performed to detect tumor cells stained with an NIR contrast agent within flowing blood samples.&lt;h4>Results&lt;/h4>The newly developed high-speed OR-PAM successfully detected stained cells both in the phantom and &lt;i>in vivo&lt;/i>. The phantom experiment confirmed the correlation between the tumor cell detection rate and tumor cell concentration in the blood sample.&lt;h4>Conclusions&lt;/h4>The high-speed OR-PAM effectively detected stained tumor cells. Combining high-speed OR-PAM with molecular probes that stain tumor cells &lt;i>in vivo&lt;/i> enables &lt;i>in vivo&lt;/i> CTC detection.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-04T12:58:40.454Z</modification><creation>2025-04-04T12:58:40.454Z</creation></dates><accession>S-EPMC10924425</accession><cross_references><pubmed>38464883</pubmed><doi>10.1117/1.JBO.29.S1.S11527</doi></cross_references></HashMap>