Pub Date : 2025-06-12DOI: 10.1016/j.pacs.2025.100742
Yaocai Huang , Ibrahim Oraiqat , Dale Litzenberg , Madhumithra Subramanian Karthikesh , Christopher Tichacek , Glebys Gonzalez , Zhanpeng Xu , Sarah Dykstra , Borui Li , Scott Hadley , Eduardo G. Moros , Man Zhang , Paul L. Carson , Kyle C. Cuneo , Xueding Wang , Issam El Naqa , Wei Zhang
The aim of this study is to visualize the radiation dose on anatomical structures during radiation therapy (RT) by mapping radiation dose deposition and tracking anatomical structures simultaneously. A dual-modality volumetric imaging system, which combines ionizing radiation acoustic imaging (iRAI) and ultrasound (US) imaging, was developed to provide dose deposition and anatomical information in real-time during RT. The performance of the proposed system was first evaluated via experiments on tissue-mimicking phantoms driven by a custom motion stage. By using US imaging to correct the position of anatomical structures, the dose mapping accuracy of the system increased by up to 0.51 in structural similarity index measure (SSIM) and 74.60 % in Gamma passing rate (GPR) compared to standalone iRAI. A subsequent study on a rabbit model in vivo further confirmed the capability of the system in mapping of the radiation dose deposition in the target tissue as well as its change caused by the motion mainly due to the animal breath. These findings demonstrate that this first-of-its-kind dual-modality volumetric imaging system can provide volumetric dose-on-anatomy information during RT. After further validation in clinic, this technique holds potential for enhancing RT outcomes by ensuring accurate alignment between the planned radiation beams, the target, and surrounding organs at risk.
{"title":"Ionizing radiation acoustic and ultrasound dual-modality imaging for visualization of dose on anatomical structures during radiotherapy","authors":"Yaocai Huang , Ibrahim Oraiqat , Dale Litzenberg , Madhumithra Subramanian Karthikesh , Christopher Tichacek , Glebys Gonzalez , Zhanpeng Xu , Sarah Dykstra , Borui Li , Scott Hadley , Eduardo G. Moros , Man Zhang , Paul L. Carson , Kyle C. Cuneo , Xueding Wang , Issam El Naqa , Wei Zhang","doi":"10.1016/j.pacs.2025.100742","DOIUrl":"10.1016/j.pacs.2025.100742","url":null,"abstract":"<div><div>The aim of this study is to visualize the radiation dose on anatomical structures during radiation therapy (RT) by mapping radiation dose deposition and tracking anatomical structures simultaneously. A dual-modality volumetric imaging system, which combines ionizing radiation acoustic imaging (iRAI) and ultrasound (US) imaging, was developed to provide dose deposition and anatomical information in real-time during RT. The performance of the proposed system was first evaluated via experiments on tissue-mimicking phantoms driven by a custom motion stage. By using US imaging to correct the position of anatomical structures, the dose mapping accuracy of the system increased by up to 0.51 in structural similarity index measure (SSIM) and 74.60 % in Gamma passing rate (GPR) compared to standalone iRAI. A subsequent study on a rabbit model <em>in vivo</em> further confirmed the capability of the system in mapping of the radiation dose deposition in the target tissue as well as its change caused by the motion mainly due to the animal breath. These findings demonstrate that this first-of-its-kind dual-modality volumetric imaging system can provide volumetric dose-on-anatomy information during RT. After further validation in clinic, this technique holds potential for enhancing RT outcomes by ensuring accurate alignment between the planned radiation beams, the target, and surrounding organs at risk.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100742"},"PeriodicalIF":7.1,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144298120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-11DOI: 10.1016/j.pacs.2025.100741
Jianshuang Wei , Ren Zhang , Mingchen Jiang , Lulu Gao , Ximiao Yu , XiuLi Liu , Yanfeng Dai , Qingming Luo , Zhihong Zhang , Xiaoquan Yang
Non-alcoholic steatohepatitis (NASH) is a prevalent chronic liver disease characterized by significant alterations in liver microvascular structures, leading to microcirculatory dysfunction and potentially contributing to various extrahepatic complications. In this study, we propose a longitudinal investigative pipeline based on liver photoacoustic microscopy (LPAM), integrating optical-resolution photoacoustic microscopy (OR-PAM), a modular liver window (MLW), a custom 3D-printed liver imaging mount (LIM), and a dedicated vessel-sinusoid separation and analysis method. This pipeline enabled continuous monitoring and quantitative assessment of microvascular changes in a NASH mouse model over a six-week period. As NASH progressed, vessel density decreased by 64.18 %, and hepatic sinusoid vessel coverage was reduced by 77.38 %. Furthermore, hepatic sinusoidal volume, length, radius, tortuosity, and density declined by 87.29 %, 83.92 %, 21.86 %, 71.57 %, and 86.81 %, Analysis of hepatic sinusoidal branches revealed a 51.80 % decrease in the fractal dimension of composite branches and a 54.90 % increase in that of dead-end branches. These findings suggest that lipid accumulation and inflammatory responses contribute to the progressive deterioration of hepatic microvascular structures, thereby exacerbating vascular damage. LPAM offers a high-resolution, label-free imaging approach for dynamic monitoring of NASH-associated microvascular alterations. This study advances our understanding of hepatic microcirculatory changes in NASH and provides valuable insights for both basic research and clinical management.
{"title":"Quantitative longitudinal investigation of non-alcoholic steatohepatitis in mice by photoacoustic microscopy","authors":"Jianshuang Wei , Ren Zhang , Mingchen Jiang , Lulu Gao , Ximiao Yu , XiuLi Liu , Yanfeng Dai , Qingming Luo , Zhihong Zhang , Xiaoquan Yang","doi":"10.1016/j.pacs.2025.100741","DOIUrl":"10.1016/j.pacs.2025.100741","url":null,"abstract":"<div><div>Non-alcoholic steatohepatitis (NASH) is a prevalent chronic liver disease characterized by significant alterations in liver microvascular structures, leading to microcirculatory dysfunction and potentially contributing to various extrahepatic complications. In this study, we propose a longitudinal investigative pipeline based on liver photoacoustic microscopy (LPAM), integrating optical-resolution photoacoustic microscopy (OR-PAM), a modular liver window (MLW), a custom 3D-printed liver imaging mount (LIM), and a dedicated vessel-sinusoid separation and analysis method. This pipeline enabled continuous monitoring and quantitative assessment of microvascular changes in a NASH mouse model over a six-week period. As NASH progressed, vessel density decreased by 64.18 %, and hepatic sinusoid vessel coverage was reduced by 77.38 %. Furthermore, hepatic sinusoidal volume, length, radius, tortuosity, and density declined by 87.29 %, 83.92 %, 21.86 %, 71.57 %, and 86.81 %, Analysis of hepatic sinusoidal branches revealed a 51.80 % decrease in the fractal dimension of composite branches and a 54.90 % increase in that of dead-end branches. These findings suggest that lipid accumulation and inflammatory responses contribute to the progressive deterioration of hepatic microvascular structures, thereby exacerbating vascular damage. LPAM offers a high-resolution, label-free imaging approach for dynamic monitoring of NASH-associated microvascular alterations. This study advances our understanding of hepatic microcirculatory changes in NASH and provides valuable insights for both basic research and clinical management.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100741"},"PeriodicalIF":7.1,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144280283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-06DOI: 10.1016/j.pacs.2025.100738
Farzin Ghane Golmohamadi, Amna Mehmood, Hoang Trong Phan, Franz-Josef Schmitt, Jan Laufer
Pump-probe excitation of fluorophores has been shown to overcome the limitations of conventional multiwavelength imaging and linear unmixing approaches by providing fluorophore-specific contrast whilst eliminating the dominant background signal of endogenous chromophores. In this study, methods for generating pump-probe signals and images are investigated that rely on changing 1) the pump wavelength whilst keeping the probe wavelength fixed, 2) the probe wavelength whilst keeping the pump wavelength fixed, and 3) the time delay between the pump and probe pulse. Time-resolved PA signals were generated in purified solutions of genetically expressed red fluorescent proteins Katushka, mNeptune, and mCardinal in a cuvette. Spectra of the difference signal amplitude were found to correlate with the absorption and emission spectra. The difference signal plotted as a function of time delay also showed characteristic features for each protein. To demonstrate the capability of multiplexed imaging, the spatial distributions of Katushka and mNeptune were recovered from 2D difference images of a phantom. This study demonstrates that methods based on pump-probe excitation can be used to probe the photophysical properties of fluorophores. By detecting changes in these properties due to a stimulant, such as pH, the methods may find application in biosensing of the cellular microenvironment.
{"title":"Probing the photophysical properties of fluorescent proteins using photoacoustic pump-probe spectroscopy and imaging","authors":"Farzin Ghane Golmohamadi, Amna Mehmood, Hoang Trong Phan, Franz-Josef Schmitt, Jan Laufer","doi":"10.1016/j.pacs.2025.100738","DOIUrl":"10.1016/j.pacs.2025.100738","url":null,"abstract":"<div><div>Pump-probe excitation of fluorophores has been shown to overcome the limitations of conventional multiwavelength imaging and linear unmixing approaches by providing fluorophore-specific contrast whilst eliminating the dominant background signal of endogenous chromophores. In this study, methods for generating pump-probe signals and images are investigated that rely on changing 1) the pump wavelength whilst keeping the probe wavelength fixed, 2) the probe wavelength whilst keeping the pump wavelength fixed, and 3) the time delay between the pump and probe pulse. Time-resolved PA signals were generated in purified solutions of genetically expressed red fluorescent proteins Katushka, mNeptune, and mCardinal in a cuvette. Spectra of the difference signal amplitude were found to correlate with the absorption and emission spectra. The difference signal plotted as a function of time delay also showed characteristic features for each protein. To demonstrate the capability of multiplexed imaging, the spatial distributions of Katushka and mNeptune were recovered from 2D difference images of a phantom. This study demonstrates that methods based on pump-probe excitation can be used to probe the photophysical properties of fluorophores. By detecting changes in these properties due to a stimulant, such as pH, the methods may find application in biosensing of the cellular microenvironment.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100738"},"PeriodicalIF":7.1,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144280282","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-04DOI: 10.1016/j.pacs.2025.100733
Tianrui Zhao , Edward Zhang , Paul C. Beard , Wenfeng Xia
Photoacoustic endoscopy has gained intensive research interest in recent years, particularly for guiding minimally invasive procedures in several clinical disciplines including oncology, cardiology and fetal medicine. Multimode fibres hold the potential to revolutionise medical endoscopy with ultrathin size and micrometre-level resolution. Compared to conventional endomicroscopes based on multi-core fibre bundles, multimode fibres-based endoscopes offer significantly higher spatial resolution, smaller diameters, and lower costs. However, current implementations of multimode fibre imaging, whether using raster-scan or speckle compressive sensing imaging, are hindered by limitations in frame rate or signal-to-noise ratio. In this work, we developed a multifocal excitation compressive-sensing photoacoustic endomicroscopy system that combines wavefront shaping-based light focusing with compressive sensing to achieve high imaging speed without compromising image quality. The method was validated through numerical simulations and experiments with carbon fibre phantoms and red blood cells ex vivo. Our results demonstrated comparable image quality to raster-scan-based imaging, while improving the frame rate by a factor of 5, reaching 11.5 frames per second. With further enhancements in focusing performance and the use of a higher repetition rate laser, this method shows promise for achieving real-time, high-resolution endomicroscopy through ultrathin probes, making it a valuable tool for guiding minimally invasive procedures.
{"title":"MECOPE: Multifocal excitation compressive-sensing photoacoustic endomicroscopy through a multimode fibre","authors":"Tianrui Zhao , Edward Zhang , Paul C. Beard , Wenfeng Xia","doi":"10.1016/j.pacs.2025.100733","DOIUrl":"10.1016/j.pacs.2025.100733","url":null,"abstract":"<div><div>Photoacoustic endoscopy has gained intensive research interest in recent years, particularly for guiding minimally invasive procedures in several clinical disciplines including oncology, cardiology and fetal medicine. Multimode fibres hold the potential to revolutionise medical endoscopy with ultrathin size and micrometre-level resolution. Compared to conventional endomicroscopes based on multi-core fibre bundles, multimode fibres-based endoscopes offer significantly higher spatial resolution, smaller diameters, and lower costs. However, current implementations of multimode fibre imaging, whether using raster-scan or speckle compressive sensing imaging, are hindered by limitations in frame rate or signal-to-noise ratio. In this work, we developed a multifocal excitation compressive-sensing photoacoustic endomicroscopy system that combines wavefront shaping-based light focusing with compressive sensing to achieve high imaging speed without compromising image quality. The method was validated through numerical simulations and experiments with carbon fibre phantoms and red blood cells <em>ex vivo</em>. Our results demonstrated comparable image quality to raster-scan-based imaging, while improving the frame rate by a factor of 5, reaching 11.5 frames per second. With further enhancements in focusing performance and the use of a higher repetition rate laser, this method shows promise for achieving real-time, high-resolution endomicroscopy through ultrathin probes, making it a valuable tool for guiding minimally invasive procedures.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100733"},"PeriodicalIF":7.1,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144263650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-04DOI: 10.1016/j.pacs.2025.100739
Eunwoo Park , Donggyu Kim , Mingyu Ha , Donghyun Kim , Chulhong Kim
Photoacoustic microscopy (PAM), an imaging modality with emerging importance in diverse biomedical applications, provides excellent structural and functional information at the micro-scale. Technological innovations have significantly enhanced PAM’s performance, including sensitivity and contrast, making it a powerful tool. This review explores high-performance PAM, focusing on its signal-to-noise ratio, imaging speed, resolution, depth, functionality, and practicality, and commenting on the role of artificial intelligence in enhancing each feature. After providing comprehensive insights, the review concludes with future directions for developing high-performance PAM for advanced biomedical imaging and clinical applications.
{"title":"A comprehensive review of high-performance photoacoustic microscopy systems","authors":"Eunwoo Park , Donggyu Kim , Mingyu Ha , Donghyun Kim , Chulhong Kim","doi":"10.1016/j.pacs.2025.100739","DOIUrl":"10.1016/j.pacs.2025.100739","url":null,"abstract":"<div><div>Photoacoustic microscopy (PAM), an imaging modality with emerging importance in diverse biomedical applications, provides excellent structural and functional information at the micro-scale. Technological innovations have significantly enhanced PAM’s performance, including sensitivity and contrast, making it a powerful tool. This review explores high-performance PAM, focusing on its signal-to-noise ratio, imaging speed, resolution, depth, functionality, and practicality, and commenting on the role of artificial intelligence in enhancing each feature. After providing comprehensive insights, the review concludes with future directions for developing high-performance PAM for advanced biomedical imaging and clinical applications.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100739"},"PeriodicalIF":7.1,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144222615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-05-30DOI: 10.1016/j.pacs.2025.100737
Zhigang Wang , Changpeng Ai , Ting Sun , Zhiyang Wang , Wuyu Zhang , Feifan Zhou , Shengnan Wu
Sepsis-associated encephalopathy (SAE) is a common complication of sepsis, involving acute brain dysfunction. Although cerebrovascular impairment plays a critical role in SAE, sepsis-induced microvascular changes remain poorly quantified. Here, we used photoacoustic microscopy to dynamically assess blood-brain barrier permeability in septic mice, analyzing vascular structure across five parameters. Additionally, we examined pathological changes in major cortical regions and conducted behavioral tests to validate the findings. Results showed microvascular degeneration, including reduced vascular density and branching, alongside an increase in fine vessels. Motor-related cortical areas were most affected, correlating with severe motor and cognitive deficits in septic mice. This study provides the first in vivo, multi-parametric analysis of sepsis-induced cerebrovascular pathology, revealing region-specific damage. Our findings directly link microvascular dysfunction to SAE progression and highlight photoacoustic microscopy’s potential in neuroscience research.
{"title":"Photoacoustic imaging detects cerebrovascular pathological changes in sepsis","authors":"Zhigang Wang , Changpeng Ai , Ting Sun , Zhiyang Wang , Wuyu Zhang , Feifan Zhou , Shengnan Wu","doi":"10.1016/j.pacs.2025.100737","DOIUrl":"10.1016/j.pacs.2025.100737","url":null,"abstract":"<div><div>Sepsis-associated encephalopathy (SAE) is a common complication of sepsis, involving acute brain dysfunction. Although cerebrovascular impairment plays a critical role in SAE, sepsis-induced microvascular changes remain poorly quantified. Here, we used photoacoustic microscopy to dynamically assess blood-brain barrier permeability in septic mice, analyzing vascular structure across five parameters. Additionally, we examined pathological changes in major cortical regions and conducted behavioral tests to validate the findings. Results showed microvascular degeneration, including reduced vascular density and branching, alongside an increase in fine vessels. Motor-related cortical areas were most affected, correlating with severe motor and cognitive deficits in septic mice. This study provides the first <em>in vivo</em>, multi-parametric analysis of sepsis-induced cerebrovascular pathology, revealing region-specific damage. Our findings directly link microvascular dysfunction to SAE progression and highlight photoacoustic microscopy’s potential in neuroscience research.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100737"},"PeriodicalIF":7.1,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144189517","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-05-29DOI: 10.1016/j.pacs.2025.100731
Xiaoxue Wang , Jinzhuang Xu , Chenglong Zhang , Moritz Wildgruber , Wenjing Jiang , Lili Wang , Xiaopeng Ma
Photoacoustic tomography (PAT) combines the high spatial resolution of ultrasound imaging with the high contrast of optical imaging. To reduce acquisition time and lower the cost of photoacoustic imaging, sparse sampling strategy is often employed. Conventional reconstruction methods often produce artifacts when dealing with sparse data, affecting image quality and diagnostic accuracy. This paper proposes a Residual-Conditioned Sparse Transformer (RCST) network for reducing artifacts in photoacoustic images, aiming to enhance image quality under sparse sampling. By introducing residual prior information, our algorithm encodes and embeds it into local enhancement and detail recovery stages. We utilize sparse transformer blocks to identify and reduce artifacts while preserving key structures and details of the images. Experiments on multiple simulated and experimental datasets demonstrate that our method significantly suppresses artifacts and improves image quality, offering new possibilities for the application of photoacoustic imaging in biomedical research and clinical diagnostics.
{"title":"Residual-conditioned sparse transformer for photoacoustic image artifact reduction","authors":"Xiaoxue Wang , Jinzhuang Xu , Chenglong Zhang , Moritz Wildgruber , Wenjing Jiang , Lili Wang , Xiaopeng Ma","doi":"10.1016/j.pacs.2025.100731","DOIUrl":"10.1016/j.pacs.2025.100731","url":null,"abstract":"<div><div>Photoacoustic tomography (PAT) combines the high spatial resolution of ultrasound imaging with the high contrast of optical imaging. To reduce acquisition time and lower the cost of photoacoustic imaging, sparse sampling strategy is often employed. Conventional reconstruction methods often produce artifacts when dealing with sparse data, affecting image quality and diagnostic accuracy. This paper proposes a Residual-Conditioned Sparse Transformer (RCST) network for reducing artifacts in photoacoustic images, aiming to enhance image quality under sparse sampling. By introducing residual prior information, our algorithm encodes and embeds it into local enhancement and detail recovery stages. We utilize sparse transformer blocks to identify and reduce artifacts while preserving key structures and details of the images. Experiments on multiple simulated and experimental datasets demonstrate that our method significantly suppresses artifacts and improves image quality, offering new possibilities for the application of photoacoustic imaging in biomedical research and clinical diagnostics.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100731"},"PeriodicalIF":7.1,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-05-29DOI: 10.1016/j.pacs.2025.100734
Daria Voitovich , Alexey Kurnikov , Anna Orlova , Aleksej Petushkov , Liubov Shimolina , Anastasia Komarova , Marina Shirmanova , Yu-Hang Liu , Daniel Razansky , Pavel Subochev
Optical-resolution optoacoustic (photoacoustic) microscopy is a hybrid imaging modality combining focused optical excitation with ultrasound detection, thus achieving micrometer-scale spatial resolution and high-contrast angiographic imaging. Despite these important advantages, maintaining safe laser fluence levels is essential to prevent tissue damage while ensuring sufficient detection sensitivity. Here, we introduce a model that directly relates the detector’s noise-equivalent pressure (NEP) to the local laser fluence at the imaged blood vessel. The model incorporates acoustic propagation effects from an optoacoustic source to a spherically focused detector with limited aperture and bandwidth, offering a more comprehensive understanding of how fluence and ultrasonic sensitivity are interconnected. The effects of ultrasound generation propagation and detection were accounted for using analytical estimations and numerical simulations, while detector's NEP was experimentally measured with a calibrated hydrophone. The proposed model for evaluating of local laser fluence with a calibrated ultrasound detector was validated through in vitro experiments with superficially located blood layer and numerical Monte Carlo/k-Wave simulations featuring deeper vessels. In vivo experiments employing 532 nm laser excitation and wideband 1–30 MHz ultrasonic detection further demonstrated the model’s capacity for real-time adjustments of laser parameters to ensure tissue safety.
{"title":"Local laser fluence estimation in optical resolution optoacoustic angiography employing calibrated ultrasound detector","authors":"Daria Voitovich , Alexey Kurnikov , Anna Orlova , Aleksej Petushkov , Liubov Shimolina , Anastasia Komarova , Marina Shirmanova , Yu-Hang Liu , Daniel Razansky , Pavel Subochev","doi":"10.1016/j.pacs.2025.100734","DOIUrl":"10.1016/j.pacs.2025.100734","url":null,"abstract":"<div><div>Optical-resolution optoacoustic (photoacoustic) microscopy is a hybrid imaging modality combining focused optical excitation with ultrasound detection, thus achieving micrometer-scale spatial resolution and high-contrast angiographic imaging. Despite these important advantages, maintaining safe laser fluence levels is essential to prevent tissue damage while ensuring sufficient detection sensitivity. Here, we introduce a model that directly relates the detector’s noise-equivalent pressure (NEP) to the local laser fluence at the imaged blood vessel. The model incorporates acoustic propagation effects from an optoacoustic source to a spherically focused detector with limited aperture and bandwidth, offering a more comprehensive understanding of how fluence and ultrasonic sensitivity are interconnected. The effects of ultrasound generation propagation and detection were accounted for using analytical estimations and numerical simulations, while detector's NEP was experimentally measured with a calibrated hydrophone. The proposed model for evaluating of local laser fluence with a calibrated ultrasound detector was validated through in vitro experiments with superficially located blood layer and numerical Monte Carlo/k-Wave simulations featuring deeper vessels. In vivo experiments employing 532 nm laser excitation and wideband 1–30 MHz ultrasonic detection further demonstrated the model’s capacity for real-time adjustments of laser parameters to ensure tissue safety.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100734"},"PeriodicalIF":7.1,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144314645","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Photoacoustic imaging combines the advantages of optical and acoustic imaging, making it a promising tool in biomedical imaging. Photoacoustic tomography (PAT) reconstructs images by solving the inverse problem from detected photoacoustic waves to initial pressure map. The heterogeneous speed of sound (SoS) distribution in biological tissue significantly affects image quality, as uncertain SoS variations can cause image distortions. Previously reported dual-speed-of-sound (dual-SoS) imaging methods effectively address these distortions by accounting for the SoS differences between tissues and the coupling medium. However, these methods require recalculating the distribution parameters of the SoS for each frame during dynamic imaging, which is highly time-consuming and poses a significant challenge for achieving real-time dynamic dual-SoS PAT imaging. To address this issue, we propose a signal-domain dual-SoS correction method for PAT image reconstruction. In this method, two distinct SoS regions are differentiated by recognizing the photoacoustic signal features of the imaging target's contours. The signals are then corrected based on the respective SoS values, enabling signal-domain-based dual-SoS dynamic real-time PAT imaging. The proposed method was validated through numerical simulations and in-vivo experiments of human finger. The results show that, compared to the single-SoS reconstruction method, the proposed approach produces higher-quality images, achieving the resolution error by near 12 times and a 30 % increase in contrast. Furthermore, the method enables dual-SoS dynamic real-time PAT reconstruction at 10 fps, which is 187.22 % faster than existing dual-SoS reconstruction methods, highlighting its feasibility for dynamic PAT imaging of heterogeneous tissues.
{"title":"Signal-domain speed-of-sound correction for ring-array-based photoacoustic tomography","authors":"Daohuai Jiang , Hengrong Lan , Shangqing Tong , Xianzeng Zhang , Fei Gao","doi":"10.1016/j.pacs.2025.100735","DOIUrl":"10.1016/j.pacs.2025.100735","url":null,"abstract":"<div><div>Photoacoustic imaging combines the advantages of optical and acoustic imaging, making it a promising tool in biomedical imaging. Photoacoustic tomography (PAT) reconstructs images by solving the inverse problem from detected photoacoustic waves to initial pressure map. The heterogeneous speed of sound (SoS) distribution in biological tissue significantly affects image quality, as uncertain SoS variations can cause image distortions. Previously reported dual-speed-of-sound (dual-SoS) imaging methods effectively address these distortions by accounting for the SoS differences between tissues and the coupling medium. However, these methods require recalculating the distribution parameters of the SoS for each frame during dynamic imaging, which is highly time-consuming and poses a significant challenge for achieving real-time dynamic dual-SoS PAT imaging. To address this issue, we propose a signal-domain dual-SoS correction method for PAT image reconstruction. In this method, two distinct SoS regions are differentiated by recognizing the photoacoustic signal features of the imaging target's contours. The signals are then corrected based on the respective SoS values, enabling signal-domain-based dual-SoS dynamic real-time PAT imaging. The proposed method was validated through numerical simulations and in-vivo experiments of human finger. The results show that, compared to the single-SoS reconstruction method, the proposed approach produces higher-quality images, achieving the resolution error by near 12 times and a 30 % increase in contrast. Furthermore, the method enables dual-SoS dynamic real-time PAT reconstruction at 10 fps, which is 187.22 % faster than existing dual-SoS reconstruction methods, highlighting its feasibility for dynamic PAT imaging of heterogeneous tissues.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100735"},"PeriodicalIF":7.1,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144154505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-05-17DOI: 10.1016/j.pacs.2025.100730
Yizhou Tan , Min Zhang , Zhifeng Wu , Jingqin Chen , Yaguang Ren , Chengbo Liu , Ying Gu
Current consensus suggests a simultaneous occurrence of hypoxia and inflammation. For the first time, we observed a hyperoxia state during the initiation stage of gouty arthritis (GA) via optical-resolution photoacoustic microscopy. GA as a paradigm of acute sterile inflammation, has been regarded as a single process. However, our experimental results demonstrated that the onset-resolution inflammation process composed of two sub-processes with different features. In the initial sub-process, inflammation and resolution events appear in hyperoxia state (1st-5th days). In the subsequent sub-process, post-resolution events appear in hypoxia state (6th-15th days), which is related with the second wave of immune response. Furthermore, we demonstrated that the inflammatory cytokines together with hyperoxia levels in initial sub-process can be downregulated by photobiomodulation, resulting in the hypoxia levels in subsequent sub-process were inhibited. Our results unveiled the detailed progress of GA and provided potential non-invasive monitoring and treatment strategies.
{"title":"Local oxygen concentration reversal from hyperoxia to hypoxia monitored by optical-resolution photoacoustic microscopy in inflammation-resolution process","authors":"Yizhou Tan , Min Zhang , Zhifeng Wu , Jingqin Chen , Yaguang Ren , Chengbo Liu , Ying Gu","doi":"10.1016/j.pacs.2025.100730","DOIUrl":"10.1016/j.pacs.2025.100730","url":null,"abstract":"<div><div>Current consensus suggests a simultaneous occurrence of hypoxia and inflammation. For the first time, we observed a hyperoxia state during the initiation stage of gouty arthritis (GA) via optical-resolution photoacoustic microscopy. GA as a paradigm of acute sterile inflammation, has been regarded as a single process. However, our experimental results demonstrated that the onset-resolution inflammation process composed of two sub-processes with different features. In the initial sub-process, inflammation and resolution events appear in hyperoxia state (1st-5th days). In the subsequent sub-process, post-resolution events appear in hypoxia state (6th-15th days), which is related with the second wave of immune response. Furthermore, we demonstrated that the inflammatory cytokines together with hyperoxia levels in initial sub-process can be downregulated by photobiomodulation, resulting in the hypoxia levels in subsequent sub-process were inhibited. Our results unveiled the detailed progress of GA and provided potential non-invasive monitoring and treatment strategies.</div></div>","PeriodicalId":56025,"journal":{"name":"Photoacoustics","volume":"44 ","pages":"Article 100730"},"PeriodicalIF":7.1,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144168794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}