2017
DOI: 10.6028/nist.sp.1200-24
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Sucrose density gradient centrifugation for efficient separation of engineered nanoparticles from a model organism, Caenorhabditis elegans

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Cited by 3 publications
(2 citation statements)
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“…Then, 100.00 µL of chilled bacterial culture was slowly aspirated on top of each solution. The gradient solutions in microcentrifuge tubes were centrifuged at 4 • C and 170.00× g for the first 5 min, and then 1250.00× g for another 5 min as described previously [48]. After centrifugation, 100.00 µL from each layer of solutions was collected and placed in a 96-well plate.…”
Section: Density Gradient Centrifugation Separationmentioning
confidence: 99%
“…Then, 100.00 µL of chilled bacterial culture was slowly aspirated on top of each solution. The gradient solutions in microcentrifuge tubes were centrifuged at 4 • C and 170.00× g for the first 5 min, and then 1250.00× g for another 5 min as described previously [48]. After centrifugation, 100.00 µL from each layer of solutions was collected and placed in a 96-well plate.…”
Section: Density Gradient Centrifugation Separationmentioning
confidence: 99%
“…In this direction, there is a field to be exploited because there are no standardized procedures to separate or extract CNMs from the biological matrices, especially from the nematode cuticle. However, one protocol was developed to remove non-ingested gold nanoparticles from the C. elegans cuticle and medium surrounding before bioaccumulation studies (Johnson et al, 2017b), this approach could be the basis for this additional research.…”
Section: Caenorhabditis Elegansmentioning
confidence: 99%