2018
DOI: 10.3791/57491
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Simple and Effective Administration and Visualization of Microparticles in the Circulatory System of Small Fishes Using Kidney Injection

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Cited by 6 publications
(15 citation statements)
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“…Fluorescent PMs-PEG were fabricated as described in detail previously ( Borvinskaya et al, 2018b ). Conjugate of the fluorescent dye fluorescein isothiocyanate with albumin (#FD20S; Sigma-Aldrich, USA; Ex 494 nm, Em 512 nm) was microencapsulated in order to contrast PMs-PEG in fish organs during fluorescent microscopy without the need for additional labeling of microcapsules after histological fixation of tissues.…”
Section: Methodsmentioning
confidence: 99%
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“…Fluorescent PMs-PEG were fabricated as described in detail previously ( Borvinskaya et al, 2018b ). Conjugate of the fluorescent dye fluorescein isothiocyanate with albumin (#FD20S; Sigma-Aldrich, USA; Ex 494 nm, Em 512 nm) was microencapsulated in order to contrast PMs-PEG in fish organs during fluorescent microscopy without the need for additional labeling of microcapsules after histological fixation of tissues.…”
Section: Methodsmentioning
confidence: 99%
“…To deliver the microcapsules into the fish bloodstream, we injected the microcapsules directly into the fish kidney, as described in detail elsewhere ( Borvinskaya et al, 2018b ). Due to the small size of D. rerio , it is difficult to administer PMs-PEG directly into the fish blood vessels; therefore, injection into vascular-rich tissues to deliver microcapsules into the circulatory system was performed as an alternative.…”
Section: Methodsmentioning
confidence: 99%
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“…Fluorescent dyes were encapsulated at room temperature using the layer-by-layer adsorption of oppositely charged polyelectrolytes, as described previously [19]. The conjugates FITC-albumin and SNARF-1-dextran were co-precipitated in porous CaCO 3 microcores by mixing 2 mL of 4 mg/mL conjugate solution with 0.615 mL of 1 M CaCl 2 and 1 M Na 2 CO 3 solutions.…”
Section: Methodsmentioning
confidence: 99%
“…Microcapsules and autofluorescence of E. verrucosus were visualized under the Mikmed-2 fluorescence microscope (LOMO, Saint Petersburg, Russia), with either the EOS 1200 camera (Canon, Taiwan) or the QE Pro spectrometer (Ocean Optics, Largo, FL, USA; acquisition range 350–1100 nm, INTSMA-200 optical slit, integration time 1–5 s) attached. The spectrometer was connected to the microscope, as described previously [19]. The animals were restrained under the 10× microscope objective using a thermostatic cell containing circulating Baikal water with a temperature of 5–8 °C, according to previous recommendations [20].…”
Section: Methodsmentioning
confidence: 99%