We present a two-photon microendoscope capable of in vivo label-free deep-tissue high-resolution fast imaging through a very long optical fiber. First, an advanced light-pulse spectro-temporal shaping device optimally precompensates for linear and nonlinear distortions occurring during propagation within the endoscopic fiber. This enables the delivery of sub-40-fs duration infrared excitation pulses at the output of 5 meters of fiber. Second, the endoscopic fiber is a custom-made double-clad polarization-maintaining photonic crystal fiber specifically designed to optimize the imaging resolution and the intrinsic luminescence backward collection. Third, a miniaturized fiber-scanner of 2.2 mm outer diameter allows simultaneous second harmonic generation (SHG) and two-photon excited autofluorescence (TPEF) imaging at 8 frames per second. This microendoscope's transverse and axial resolutions amount respectively to 0.8 μm and 12 μm, with a field-of-view as large as 450 μm. This microendoscope's unprecedented capabilities are validated during label-free imaging, ex vivo on various fixed human tissue samples, and in vivo on an anesthetized mouse kidney demonstrating an imaging penetration depth greater than 300 μm below the surface of the organ. The results reported in this manuscript confirm that nonlinear microendoscopy can become a valuable clinical tool for real-time in situ assessment of pathological states.
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http://dx.doi.org/10.1038/srep18303 | DOI Listing |
Quant Imaging Med Surg
January 2025
Paul. C. Lauterbur Research Centers for Biomedical Imaging, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Background: Brain temperature signifies the thermal homeostasis of the tissue, and may serve as a marker for neuroprotective therapy. Currently, it remains challenging to map the human brain temperature with high spatial resolution. The thermal dependence of chemical exchange saturation transfer (CEST) effects of endogenous labile protons may provide a promising mechanism for the absolute brain temperature imaging.
View Article and Find Full Text PDFBiosens Bioelectron
January 2025
College of Mathematical Medicine, Zhejiang Normal University, Jinhua, China; Affiliated Dongyang Hospital of Wenzhou Medical University, Jinhua, China. Electronic address:
Pathological conditions in organisms often arise from various cellular or tissue abnormalities, including dysregulation of cell numbers, infections, aberrant differentiation, and tissue pathologies such as lung tumors and skin tumors. Thus, developing methods for analyzing and identifying these biological abnormalities presents a significant challenge. While traditional bioanalytical methods such as flow cytometry and magnetic resonance imaging are well-established, they suffer from inefficiencies, high costs, complexity, and potential hazards.
View Article and Find Full Text PDFLight Sci Appl
January 2025
Department of Electrical and Computer Engineering, Boston University, Boston, MA, 02215, USA.
A major challenge in neuroscience is visualizing the structure of the human brain at different scales. Traditional histology reveals micro- and meso-scale brain features but suffers from staining variability, tissue damage, and distortion, which impedes accurate 3D reconstructions. The emerging label-free serial sectioning optical coherence tomography (S-OCT) technique offers uniform 3D imaging capability across samples but has poor histological interpretability despite its sensitivity to cortical features.
View Article and Find Full Text PDFACS Photonics
January 2025
Institute of Biomedical Physics, Medical University of Innsbruck, Müllerstraße 44, 6020 Innsbruck, Austria.
Confocal Raman microscopy, a highly specific and label-free technique for the microscale study of thick samples, often presents difficulties due to weak Raman signals. Inhomogeneous samples introduce wavefront aberrations that further reduce these signals, requiring even longer acquisition times. In this study, we introduce Adaptive Optics to confocal Raman microscopy for the first time to counteract such aberrations, significantly increasing the Raman signal and image quality.
View Article and Find Full Text PDFChemistry
January 2025
Istituto di Ricerche Farmacologiche Mario Negri, Laboratory of Biochemistry and Protein Chemistry, Via Mario Negri, 2, 20156, Milano, ITALY.
The use of fluorescent labels is the most common tool to visualize cells. However, the internalization of dye molecules often modifies the cell behavior. In this paper we demonstrate that it is possible to transiently label cells using a 3D scaffold, a hydrogel, covalently functionalized with luminescent cyclometalated iridium(III) complexes.
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