In vivo subsurface morphological and functional cellular and subcellular imaging of the gastrointest

来源 :World Journal of Gastroenterology | 被引量 : 0次 | 上传用户:wjjcj
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AIM: To evaluate a newly developed hand-held confocal probe for in vivo microscopic imaging of the complete gastrointestinal tract in rodents. METHODS: A novel rigid confocal probe (diameter 7 mm) was designed with optical features similar to the flexible endomicroscopy system for use in humans using a 488 nm single line laser for fluorophore excitation. Light emission was detected at 505 to 750 nm. The field of view was 475μm×475 urn. Optical slice thickness was 7μm with a lateral resolution of 0.7μm. Subsurface serial images at different depths (surface to 250μm) were generated in real time at 1024×1024 pixels (0.8 frames/s) by placing the probe onto the tissue in gentle, stable contact. Tissue specimens were sampled for histopathological correlation. RESULTS: The esophagus, stomach, small and large intestine and meso, liver, pancreas and gall bladder were visualised in vivo at high resolution in n = 48 mice. Real time microscopic imaging with the confocal minimicroscopy probe was easy to achieve. The different staining protocols (fluorescein, acriflavine, FITC-labelled dextran and L. esculentum lectin) each highlighted specific aspects of the tissue, and in vivo imaging correlated excellently with conventional histology. In vivo blood flow monitoring added a functional quality to morphologic imaging. allowing the visualisation of the complete GI tract at high resolution even of subsurface tissue structures. The new confocal probe design evaluated in this study is compatible with laparoscopy and significantly expands the field of possible applications to intra-abdominal organs. It allows immediate testing of new in vivo staining and application options and therefore permits rapid transfer from animal studies to clinical use in patients. AIM: To evaluate a newly developed hand-held confocal probe for in vivo microscopic imaging of the complete gastrointestinal tract in rodents. METHODS: A novel rigid confocal probe (diameter 7 mm) was designed with optical features similar to the flexible endomicroscopy system for use in humans using a 488 nm single line laser for fluorophore excitation. Light emission was detected at 505 to 750 nm. The field of view was 475 μm × 475 urn. Optical slice thickness was 7 μm with a lateral resolution of 0.7 μm. Subsurface serial images at Different depths (surface to 250 μm) were generated in real time at 1024 × 1024 pixels (0.8 frames / s) by placing the probe onto the tissue in gentle, stable contact. Tissues were sampled for histopathological correlation. RESULTS: The esophagus, stomach , small and large intestine and meso, liver, pancreas and gall bladder were visualized in vivo at high resolution in n = 48 mice. Real time microscopic imaging with the confocal minimicroscopy probe The different staining protocols (fluorescein, acriflavine, FITC-labeled dextran and L. esculentum lectin) each highlighted specific aspects of the tissue, and in vivo imaging correlated excellently with conventional histology. In vivo blood flow monitoring added a functional allows the visualization of the complete GI tract at high resolution even of subsurface tissue structures. The new confocal probe design evaluated in this study is compatible with laparoscopy and significantly expand the field of possible applications to intra-abdominal organs. It allows immediate testing of new in vivo staining and application options and therefore permits rapid rapid transfer from animal studies to clinical use in patients.
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