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1.
Opt Lett ; 46(19): 4968-4971, 2021 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-34598245

RESUMO

In this Letter, we report a high-efficiency, miniaturized, ultra-fast coherent beam, combined with 3D-printed micro-optics directly on the tip of a multicore fiber bundle. The highly compact device footprint (180 µm in diameter) facilitates its incorporation into a minimally invasive ultra-thin nonlinear endoscope to perform two-photon imaging.


Assuntos
Endoscópios , Endoscopia , Endoscopia Gastrointestinal , Óptica e Fotônica , Fótons , Impressão Tridimensional
2.
Elife ; 92020 10 13.
Artigo em Inglês | MEDLINE | ID: mdl-33048047

RESUMO

Imaging neuronal activity with high and homogeneous spatial resolution across the field-of-view (FOV) and limited invasiveness in deep brain regions is fundamental for the progress of neuroscience, yet is a major technical challenge. We achieved this goal by correcting optical aberrations in gradient index lens-based ultrathin (≤500 µm) microendoscopes using aspheric microlenses generated through 3D-microprinting. Corrected microendoscopes had extended FOV (eFOV) with homogeneous spatial resolution for two-photon fluorescence imaging and required no modification of the optical set-up. Synthetic calcium imaging data showed that, compared to uncorrected endoscopes, eFOV-microendoscopes led to improved signal-to-noise ratio and more precise evaluation of correlated neuronal activity. We experimentally validated these predictions in awake head-fixed mice. Moreover, using eFOV-microendoscopes we demonstrated cell-specific encoding of behavioral state-dependent information in distributed functional subnetworks in a primary somatosensory thalamic nucleus. eFOV-microendoscopes are, therefore, small-cross-section ready-to-use tools for deep two-photon functional imaging with unprecedentedly high and homogeneous spatial resolution.


Assuntos
Microscopia de Fluorescência por Excitação Multifotônica/métodos , Tálamo/diagnóstico por imagem , Animais , Comportamento Animal , Endoscópios , Feminino , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Microscopia de Fluorescência por Excitação Multifotônica/instrumentação , Neurônios/fisiologia , Tálamo/fisiologia
3.
J Biophotonics ; 12(9): e201900028, 2019 09.
Artigo em Inglês | MEDLINE | ID: mdl-31081280

RESUMO

Stimulated Raman scattering (SRS) microscopy is a label-free method generating images based on chemical contrast within samples, and has already shown its great potential for high-sensitivity and fast imaging of biological specimens. The capability of SRS to collect molecular vibrational signatures in bio-samples, coupled with the availability of powerful statistical analysis methods, allows quantitative chemical imaging of live cells with sub-cellular resolution. This application has substantially driven the development of new SRS microscopy platforms. Indeed, in recent years, there has been a constant effort on devising configurations able to rapidly collect Raman spectra from samples over a wide vibrational spectral range, as needed for quantitative analysis by using chemometric methods. In this paper, an SRS microscope which exploits spectral shaping by a narrowband and rapidly tunable acousto-optical tunable filter (AOTF) is presented. This microscope enables spectral scanning from the Raman fingerprint region to the Carbon-Hydrogen (CH)-stretch region without any modification of the optical setup. Moreover, it features also a high enough spectral resolution to allow resolving Raman peaks in the crowded fingerprint region. Finally, application of the developed SRS microscope to broadband hyperspectral imaging of biological samples over a large spectral range from 800 to 3600 cm-1 , is demonstrated.


Assuntos
Microscopia Óptica não Linear/métodos , Análise Espectral Raman/métodos , Carbono/química , Linhagem Celular Tumoral , Células Hep G2 , Humanos , Hidrogênio/química , Oscilometria , Polimetil Metacrilato/química , Poliestirenos/química , Vibração
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