0000000001130033

AUTHOR

J. F. Stoltz

showing 3 related works from this author

Analysis of fluorescent MRI contrast agent behavior in the liver and thoracic aorta of mice.

2004

To characterize the behavior of magnetofluorescent products injected in mice intravenously.The magnetic resonance imaging (MRI) products were labelled with fluorescent molecules to examine the biodistribution process in vivo and observe them at the cellular level by means of confocal microscopy. Three-dimensional (3D) sequences of images were obtained by spectral analysis of sample preparations in a multiphoton confocal microscope and analyzed by the factor analysis of medical image sequence algorithm, which provides factor curves. Factor images are the result of image-processing methods that utilize information from emission spectra. Preparations are also screened in the counting mode to p…

[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingContrast MediaAorta ThoracicMiceMESH : Image CytometryMESH: Microscopy ConfocalMESH : FemaleMESH : Fluorescent DyesMESH: AnimalsMESH : Algorithms[ SDV.IB.IMA ] Life Sciences [q-bio]/Bioengineering/Imaginghealth care economics and organizationsImage CytometryMice Inbred BALB CMicroscopy ConfocalMESH: Fluorescent DyesMESH: Staining and LabelingLiverMESH : MeglumineFemaleMESH : Organometallic CompoundsAlgorithmsMESH: Aorta ThoraciceducationMESH: Mice Inbred BALB CMESH: AlgorithmsMESH: MeglumineMESH : Staining and LabelingMeglumineMESH: Contrast MediaMESH : MiceOrganometallic CompoundsAnimalsMESH : Microscopy ConfocalMESH: MiceMESH : Mice Inbred BALB CFluorescent DyesMESH : Aorta ThoracicMESH : Contrast MediaStaining and LabelingMESH : LiverMESH: Organometallic CompoundsMESH : Xanthenes[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingXanthenesMESH: XanthenesMESH : AnimalsMESH: FemaleMESH: Image CytometryMESH: Liver
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Flow cytometry and spectral imaging multiphoton microscopy analysis of CD36 expression with quantum dots 605 of untreated and 7-ketocholesterol-treat…

2006

To evaluate CD36 expression with quantum dots 605 (QDs 605) on untreated and 7-ketocholesterol (7KC)-treated monocytic U937 cells by flow cytometry (FCM) and confocal and multiphoton laser scanning microscopy (CLSM).Cells were analyzed by CLSM, following flow cytometric quantification of CD36 expression and 7KC uptake. Image sequences were obtained by spectral analysis in monophoton and multiphoton CLSM and analyzed by the factor analysis of medical image sequences (FAMIS) algorithm to differentiate emission spectra. In CLSM analysis, cell deposits were screened in ultraviolet excitation modes to optimize the possibilities of QDs 605 and have the benefit of nuclei counterstaining by DAPI.FC…

CD36 AntigensMESH: PhotonsMESH : Flow CytometryMESH: AlgorithmsMESH: Flow CytometryMESH: U937 CellsMESH : Quantum DotsMESH: MonocytesMonocytesMESH : Microscopy Fluorescence MultiphotonMESH : PhotonsQuantum DotsMESH : Cells Cultured[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyHumans[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyKetocholesterols[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular BiologyCells CulturedMESH : AlgorithmsMESH : KetocholesterolsPhotonsMESH: HumansMESH: Antigens CD36MESH : HumansMESH: KetocholesterolsU937 CellsMESH: Quantum DotsFlow CytometryMESH : Antigens CD36Microscopy Fluorescence MultiphotonMESH : MonocytesMESH : U937 CellsMESH: Microscopy Fluorescence MultiphotonAlgorithmsMESH: Cells Cultured
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FRET multiphoton spectral imaging microscopy of 7-ketocholesterol and Nile Red in U937 monocytic cells loaded with 7-ketocholesterol.

2004

To show the effect of 7-ketocholesterol (7KC) on cellular lipid content by means of flow cytometry and the interaction of 7KC with Nile Red (NR) via ultraviolet fluorescence resonance energy transfer (FRET) excitation of NR on U937 monocytic cells by means of 2-photon excitation confocal laser scanning microscopy (CLSM).Untreated and 7KC-treated U937 cells were stained with NR and analyzed by flow cytometry and CLSM. 3D sequences of images were obtained by spectral analysis in a 2-photon excitation CLSM and analyzed by the factor analysis of medical image sequences (FAMIS) algorithm, which provides factor curves and images. Factor images are the result of the FAMIS image processing method, …

MESH: Cell DeathMESH: Fluorescence Resonance Energy TransferMESH: Mitochondria[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingMESH : Flow CytometryMESH: Flow CytometryMESH: U937 CellsMESH: MonocytesMonocytesMembrane PotentialsMESH : Staining and LabelingMESH : Microscopy Fluorescence MultiphotonOxazinesFluorescence Resonance Energy TransferImage Processing Computer-AssistedHumansMESH: Membrane PotentialsMESH: Microscopy ConfocalMESH : Membrane PotentialsMESH : Fluorescent DyesMESH : Microscopy ConfocalKetocholesterols[ SDV.IB.IMA ] Life Sciences [q-bio]/Bioengineering/ImagingFluorescent DyesMESH : KetocholesterolsMicroscopy ConfocalMESH: HumansMESH : OxazinesCell DeathStaining and LabelingMESH : HumansMESH: KetocholesterolsU937 CellsFlow CytometryMESH: Fluorescent DyesMESH: Image Processing Computer-AssistedMitochondriaMESH: Staining and Labeling[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingMicroscopy Fluorescence MultiphotonMESH : MonocytesMESH : Fluorescence Resonance Energy TransferMESH : Cell DeathMESH : U937 CellsMESH: Microscopy Fluorescence MultiphotonMESH : MitochondriaMESH: OxazinesMESH : Image Processing Computer-Assisted
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