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Beckman 8000 gamma counter

Manufactured by Beckman Coulter

The Beckman 8000 gamma counter is a laboratory instrument designed for the measurement of radioactivity. It is capable of detecting and quantifying gamma radiation emitted by radioactive samples.

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9 protocols using beckman 8000 gamma counter

1

Biodistribution and Clearance of CuNCs

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Biodistribution and clearance studies were performed using female wild type C57BL/6 mice (Charles River Laboratory, Wilmington, MA), as previously reported.26 (link) Typically, 64Cu-CuNCs or 64Cu-CuNCs-FC131 (approximately 740 kBq/100 μL saline (APP pharmaceuticals, Schaumburg, IL)) was injected into mice anesthetized with inhaled isoflurane through tail vein. At 1, 4, 24 and 48 h post injection, mice were euthanatized by cervical dislocation (n = 4 / time point) and organs of interest were collected, weighed, and counted in a Beckman 8000 gamma counter (Beckman, Fullterton, CA). To measure the clearance of the two nanoclusters, a group of mice (n=4) was housed in a metabolism study cage to collect urine and feces at 4, 24, and 48 h post injection. Standards for each nanocluster were prepared and counted with the biodistribution samples together to calculate percentage of the injected dose per gram of tissue (%ID g−1).
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2

In Vivo PET Imaging of Tumor Uptake of 64Cu-Doped Gold Nanoparticles

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The U87MG tumor-bearing mice were anesthetized with isoflurane and were injected with 100 μL 7.4 MBq (200 μCi) 64Cu-doped AuNCs intravenously. All PET scans were performed on an Inveon small-animal PET scanner (Siemens, Erlangen, Germany) at indicated time point post injection. The images were collected for 10 min. For each PET scan, 3-dimensional volumes of interest (VOIs) were drawn over the tumor and muscle on decay-corrected whole-body coronal images and analyzed by Inveon Research Workplace (Siemens). At the endpoint of experiment, the mice were sacrificed and interested organs were harvested, weighted and the radioactivity was measured in a Beckman 8000 gamma counter (Beckman, Brea, CA). Standards were prepared and the organ uptake was calculated as percent of injected dose/gram of tissue (%ID/g).
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3

Biodistribution of Radiolabeled Nanoparticles

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All animal experiments were carried out in compliance with IACUC guidelines of the Washington University. Biodistribution studies were performed using female wild type C57BL/6 mice (Charles River Laboratories, Wilmington, MA). All the mice were anesthetized with inhaled isoflurane and adminstrated with about 370 kBq of 64Cu-Cu@CuOx-ECL1i or 64Cu-Cu@CuOx-ECL1i-Gem in 100 μL saline (APP pharmaceuticals, Schaumburg, IL) via the tail vein. At 1, 4, and 24 h post injection, the mice were re-anesthetized and euthanatized by cervical dislocation (n = 4/time point). Major Organs of interest from mice were harvested and weighed to acquire the weight of the organs. Then the organs were counted in a Beckman 8000 gamma counter (Beckman, Fullterton, CA) to obtain the radioactivity in these organs. The 64Cu-Cu@CuOx-ECL1i or 64Cu-Cu@CuOx-ECL1i-Gem standards were prepared and counted along with the samples to calculate percentage of the injected dose per gram of tissue (%ID/g). A nonlinear regression analysis was used to calculate the mean blood half-lives of the two nanoparticles (Prism, version 7.03, Graphpad).
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4

Biodistribution and Blood Kinetics of 64Cu-Labeled AuNCs

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All animal studies were performed in compliance with guidelines set forth by the NIH Office of Laboratory Animal Welfare and approved by the Washington University Animal Studies Committee. Normal female Balb/c mice (Charles River Laboratory, Wilmington, MA) were used for the biodistribution studies. About 370 kBq of 64CuAuNCs or 64CuAuNCs-AMD3100 in 100 μL saline (APP pharmaceuticals, Schaumburg, IL) was injected via the tail vein. The mice were anesthetized with inhaled isoflurane and re-anesthetized before euthanasia by cervical dislocation at each time point (1 h, 4 h, and 24 h post injection, n = 4/group). Organs of interest were collected, weighed, and counted in a Beckman 8000 gamma counter (Beckman, Fullterton, CA). Standards were prepared and measured along with the samples to calculate percentage of the injected dose per gram of tissue (%ID/g). The mean blood half-lives of the two nanoclusters were calculated based on the blood retention data using a nonlinear regression analysis (Prism, version 6.04, Graphpad).
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5

Biodistribution of Gold Nanoparticles in Mice

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EMT6 tumor-bearing BALB/c mice were anesthetized with inhaled isoflurane before 185–370 kBq of 198Au-incorporated nanospheres (314 kBq, 5.27 μg/mouse), nanodisks (185 kBq, 27.8 μg/mouse), nanorods (326 kBq, 4.22 μg/mouse), or nanocages (225 kBq, 17.9 μg/mouse) (suspended in 100 μL saline) was injected via the tail vein. After re-anesthetization, the mice were euthanized by cervical dislocation 1, 6, or 24 h after injection (n = 4 animals per time point). Organs of interest were collected, weighed, and counted in a well Beckman 8000 gamma counter (Beckman, Brea, CA). Standards were prepared and measured along with the samples to calculate percentage of the injected dose per gram of tissue (% ID/g).
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6

Quantification of 64Cu-AuNCs in Tissues

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Following the 24 h PET scans, animals were sacrificed, and all organs of interest were collected, weighed, and counted in a Beckman 8000 gamma counter (Beckman, Fullerton, CA). The count rate (counts per minute, CPM) from each sample of tissue was corrected by automatic background subtraction and decay corrected (compensated for the decay of 64Cu radioactivity over time). The corrected CPM from each tissue sample was normalized both to the mass of the tissue sample (in grams, g) and to the injected dose (ID). Thus, the relative concentration of 64Cu-AuNCs in each tissue sample was calculated as %ID/g.
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7

Biodistribution of 64Cu-Labeled AuNCs in Mice

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All animal studies were performed in compliance with guidelines set forth by the NIH Office of Laboratory Animal Welfare and approved by the Washington University Animal Studies Committee. Biodistribution studies were performed in male C57BL/6 mice weighing 20 to 25 g (n = 4, Charles River Laboratory, Wilmington, Massachusetts) with 0.37 MBq (0.057 pmol) of 64Cu-AuNCs-PEG-MSH or 64Cu-AuNCs-PEG in 100 μL of saline (APP Pharmaceuticals, Schaumburg, Illinios) injected via the tail vein. The mice were anesthetized with inhaled isoflurane during tracer injection and reanesthetized before euthanasia by cervical dislocation at each time point. Organs of interest were collected, weighed, and counted with a Beckman 8000 gamma counter (Beckman, Brea, California). Standards were prepared and measured along with the samples to calculate the percentage of the injected dose per gram of tissue (%ID/g).10 (link),22 (link)
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8

Biodistribution of CCR2 and CXCR4 PET Tracers

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The CCR2 specific PET tracer of 64Cu-DOTA-ECL1i and CXCR4 targeted PET tracer of 64Cu-AMD3100 were synthesized following our previous reports31 (link)–34 . For biodistribution studies, about 370 KBq of 64Cu-DOTA-ECL1i or 64Cu-AMD3100 in 100 μL saline (APP pharmaceuticals, Schaumburg, IL) were injected into the mice via tail vein (n= 4/group). The mice were anesthetized with inhaled isoflurane during injection and re-anesthetized before euthanasia by cervical dislocation at 1 hour post injection (n = 4/group). Organs of interest were collected, weighed, and counted in a Beckman 8000 gamma counter (Beckman, Fullerton, CA). Standards were prepared and measured along with the samples to calculate the percentage of the injected dose per gram of tissue (%ID/gram).
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9

Tissue Biodistribution of PET Tracer

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At 3 h post injection of PET tracer, the mice were anesthetized with inhaled isoflurane prior to euthanasia by cervical dislocation. Organs of interest were collected, weighed, and counted in Beckman 8000 gamma counter (Beckman, Fullterton, CA). Standards of each tracer were prepared and counted with the biodistribution samples together to calculate the percentage of the injected dose per gram of tissue (%ID/g).
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