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Ivis lumina xr series 3

Manufactured by PerkinElmer
Sourced in United States

The IVIS Lumina XR Series III is a high-performance in vivo imaging system designed for preclinical research. It utilizes bioluminescent and fluorescent imaging techniques to visualize and quantify biological processes within small animal models.

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4 protocols using ivis lumina xr series 3

1

In Vivo Biodistribution of Rg5-BSA Nanoparticles

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The in vivo biological distribution of DiR-labeled Rg5-BSA NPs and FA-Rg5-BSA NPs over time was investigated by a near-infrared fluorescence imaging system in MCF-7 tumor-bearing mice.32 (link),33 (link) A 100 µL portion of free DiR and DiR-labeled nanoparticles was intraperitoneally (i.p.) injected at a dose of 0.5 mg/kg. After injection, fluorescence images were taken at different intervals (2, 8 and 24 h) using an in vivo imaging system (IVIS® Lumina XR Series III, PerkinElmer, Waltham, MA, USA).
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2

Evaluating miR365 Antagomir Tissue Toxicity

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Before analysing the PTOA therapy capacity, we evaluated the in vivo tissue toxicity of miR365 antagomir/NPs-YCWP. Mice were orally administrated with miR365 antagomir/NPs-YCWP or NgmiRNA/NPs-YCWP (106/YCWP with 100 pmol miR365antagomir or NgmiRNA) every two days for 50 days. Then liver, lung and spleen of mice were collected for hematoxylin-eosin (HE) staining.
According to NPs-YCWP construction method, Cy5 fluorescent labeled RNA to construct Cy5RNA/NPs-YCWP. Mice were orally administrated with Cy5RNA/NPs-YCWP (106 YCWP with 1nmol Cy5RNA) every 10 h for 3 times. The fluorescence signals of organs such as heart, liver, spleen, lung and kidney, brain, stomach and leg were detected by PerkinElmer (PerkinElmer IVIS Lumina XR Series III).
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3

PEG-PPMDT Nanoparticle Biodistribution

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The distribution of PEG-PPMDT NPs in vivo was studied by small animal imaging system (IVIS ® Lumina XR Series III, PerkinElmer), and Cy5.5 was used as a fluorescent marker. The tumor model was constructed as described in section 2.8.1. Cy5.5-loaded PEG-PPMDT NPs and free Cy5.5 were injected intravenously to tumor-bearing nude mice at Cy5.5 concentration of 0.4 mg/kg. The fluorescence signals of the mice were recorded by the imaging system from 1 h to 24 h after injection. The mice were dissected, and their tumors and normal organs were collected after 24 h. The fluorescence intensity of each organ was detected and quantified by ex vivo imaging.
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4

Establishment and Fluorescence Imaging of Gastric Tumor Models

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All animal experiments were performed according to the Guidelines for Use and Care of Animals at Xi’an Jiaotong University (No. 2019–293). The Department of Experimental Animals, Health Science Center, Xi’an Jiaotong University supplied male nude mice (8-week-old). To establish a subcutaneous gastric tumor model, 1 × 107 BGC-823 cells suspended in 200 μL of saline/Matrigel were inoculated subcutaneously at the left flank of the male nude mice. Furthermore, to establish an orthotopic gastric tumor model, we maintained the nude mice under anesthesia and opened the abdomen of the nude mice, and then injected 1 × 107 BGC-823 cells suspended in 100 μL of saline/Matrigel directly between the submucosa and the muscular layer of the stomach, finally sutured the wound according to the previous method (Kang et al., 2021 (link)). When the long axis of the tumor diameter arrived at 1–2 cm or palpation of abdominal nodules, MB (250 µM/100 µL) in saline containing 10% BSA was injected into tumor-bearing mice through the tail vein. In brief, isoflurane was used to anesthetize the tumor-bearing mice with the image of 0.5, 1, 2, 4, 8, 24, 48, and 72 h under NIR imaging (PerkinElmer IVIS Lumina XR Series III, United States). After finishing the real-time imaging, we euthanized mice and dissected major organs and gastric tumor tissues for fluorescence imaging. Each sample used three mice.
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