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Structured-light-sheet imaging in an integrated optofluidic platform

Paie, Petra (författare)
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.;CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Calisesi, Gianmaria (författare)
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Candeo, Alessia (författare)
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.;CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
visa fler...
Comi, Andrea (författare)
CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Sala, Federico (författare)
CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Ceccarelli, Francesco (författare)
CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
De Luigi, Ada (författare)
Ist Ric Farmacol Mario Negri IRCCS, Via Mario Negri 2, I-20156 Milan, Italy.
Veglianese, Pietro (författare)
Ist Ric Farmacol Mario Negri IRCCS, Via Mario Negri 2, I-20156 Milan, Italy.
Mühlberger, Korbinian (författare)
KTH,Laserfysik
Fokine, Michael, 1970- (författare)
KTH,Tillämpad fysik
Valentini, Gianluca (författare)
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.;CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Osellame, Roberto (författare)
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.;CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Neil, Mark (författare)
Imperial Coll London, Phys Dept, Prince Consort Rd, London SW7 2BB, England.
Bassi, Andrea (författare)
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.;CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
Bragheri, Francesca (författare)
CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy.
visa färre...
Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy;CNR, Ist Foton & Nanotecnol, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy. Politecn Milan, Dipartimento Fis, Piazza Leonardo Da Vinci 32, I-20133 Milan, Italy. (creator_code:org_t)
Royal Society of Chemistry (RSC), 2023
2023
Engelska.
Ingår i: Lab on a Chip. - : Royal Society of Chemistry (RSC). - 1473-0197 .- 1473-0189. ; 24:1, s. 34-46
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Heterogeneity investigation at the single-cell level reveals morphological and phenotypic characteristics in cell populations. In clinical research, heterogeneity has important implications in the correct detection and interpretation of prognostic markers and in the analysis of patient-derived material. Among single-cell analysis, imaging flow cytometry allows combining information retrieved by single cell images with the throughput of fluidic platforms. Nevertheless, these techniques might fail in a comprehensive heterogeneity evaluation because of limited image resolution and bidimensional analysis. Light sheet fluorescence microscopy opened new ways to study in 3D the complexity of cellular functionality in samples ranging from single-cells to micro-tissues, with remarkably fast acquisition and low photo-toxicity. In addition, structured illumination microscopy has been applied to single-cell studies enhancing the resolution of imaging beyond the conventional diffraction limit. The combination of these techniques in a microfluidic environment, which permits automatic sample delivery and translation, would allow exhaustive investigation of cellular heterogeneity with high throughput image acquisition at high resolution. Here we propose an integrated optofluidic platform capable of performing structured light sheet imaging flow cytometry (SLS-IFC). The system encompasses a multicolor directional coupler equipped with a thermo-optic phase shifter, cylindrical lenses and a microfluidic network to generate and shift a patterned light sheet within a microchannel. The absence of moving parts allows a stable alignment and an automated fluorescence signal acquisition during the sample flow. The platform enables 3D imaging of an entire cell in about 1 s with a resolution enhancement capable of revealing sub-cellular features and sub-diffraction limit details. The combination of structured illumination and light sheet fluorescence microscopy in a microfluidic integrated platform enables high throughput super-resolution imaging.

Ämnesord

TEKNIK OCH TEKNOLOGIER  -- Medicinteknik -- Medicinsk bildbehandling (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Medical Engineering -- Medical Image Processing (hsv//eng)

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