Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Dynamic fluorescence molecular tomography (DFMT) is a promising molecular imaging technique that offers the potential to monitor fast kinetic behaviors within small animals in three dimensions. Early monitoring of liver disease requires the ability to distinguish and analyze normal and injured liver tissues. However, the inherent ill-posed nature of the problem and energy signal interference between the normal and injured liver regions limit the practical application of liver injury monitoring. In this study, we propose a novel strategy based on time and energy, leveraging the temporal correlation in fluorescence molecular imaging (FMI) sequences and the metabolic differences between normal and injured liver tissue. Additionally, considering fluorescence signal distribution disparity between the injured and normal regions, we designed a universal Golden Ratio Primal-Dual Algorithm (GRPDA) to reconstruct both the normal and injured liver regions. Numerical simulation and experiment results demonstrate that the proposed strategy can effectively avoid signal interference between liver and liver injury energy and lead to significant improvements in morphology recovery and positioning accuracy compared to existing approaches. Our research presents a new perspective on distinguishing normal and injured liver tissues for early liver injury monitoring.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581805PMC
http://dx.doi.org/10.1364/BOE.498092DOI Listing

Publication Analysis

Top Keywords

normal injured
20
injured liver
20
liver injury
16
injury monitoring
12
fluorescence molecular
12
liver
11
dynamic fluorescence
8
molecular tomography
8
molecular imaging
8
liver tissues
8

Similar Publications

Background: Superficial digital flexor tendon (SDFT) injuries cause progressive loss of its mechanical properties. Two-dimensional shear wave elastography (2D-SWE) provides information about tissue stiffness.

Objective: To determine the feasibility, repeatability, and reproducibility of 2D-SWE of healthy and pathological forelimb SDFT.

View Article and Find Full Text PDF

BackgroundTo investigate the clinical utility of shear wave elastography (SWE) in the diagnosis and prognostic evaluation of acute anterior talofibular ligament (ATFL) injuries.MethodsThis prospective cohort study enrolled 46 patients with unilateral acute ATFL injuries and 32 age and gender-matched healthy volunteers. All patients underwent B-mode ultrasonography and SWE within 48 h post-injury and at 3 month post-rehabilitation.

View Article and Find Full Text PDF

This three-part study investigated alternative pre-processing techniques to better understand the differences in patterns of ground reaction force (GRF) and load rate (LR) among runners with running-related injury (RRI). 534 runners were assessed on an instrumented treadmill with 3D kinematic data capture. Participants were classified as "injured" or "uninjured" and "rearfoot" (RF) or "non-rearfoot" (non-RF) strikers.

View Article and Find Full Text PDF

In this letter, we put forward the light sheet fluorescence microscopy (LSFM) as a cutting-edge tool for 3D imaging of whole skeletal muscle, focusing on satellite cells (SCs). SCs represent the resident adult muscle stem cells, normally lying quiescent between the sarcolemma of the myofiber and the surrounding basal lamina. They typically express Pax-7 and, when activated following damage, they sequentially express specific myogenic regulatory factors including the myogenic determination factor, MyoD, thus starting differentiation towards multinucleated myofibers to repair injured tissue.

View Article and Find Full Text PDF

The efficacy of surfactant replacement therapy (SRT) depends on the effective delivery of active ingredients─therapeutic lung surfactant (LS), specifically polymer lung surfactant (PLS) nanoparticles in this study─to their target site, the alveoli, in the lungs. This study examines how PLS concentration affects the spreading and distribution of PLS solutions in mouse lungs. A constant volumetric dose (∼80 μL, 4 mL/kg body weight) of PLS solutions at three polymer concentrations (0.

View Article and Find Full Text PDF