MOESM2 of The Study of Enhanced High-Intensity Focused Ultrasound Therapy by Sonodynamic N2O Microbubbles
Additional file 2: Figure S2. Determination of optimal LIFU irradiation time. (The data were shown as mean ± SD, n = 5 per group, *p < 0.05). To Select the optimal time for ultrasound, MDA-MB-231 cells were seeded in a 96-well plate at a density of 5000 cells per well for 24 h. And then use the s...
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description | Additional file 2: Figure S2. Determination of optimal LIFU irradiation time. (The data were shown as mean ± SD, n = 5 per group, *p < 0.05). To Select the optimal time for ultrasound, MDA-MB-231 cells were seeded in a 96-well plate at a density of 5000 cells per well for 24 h. And then use the strength of 2 W/cm2 ultrasonic processing cells, respectively for the 50 s, 100 s, 150 s and 200 s. After the indicated treatments, CCK8 solution (10 μL) was added in each well. Then, the MDA-MB-231 cells were cultured at 37 °C, 5% CO2 cell incubation box to save. At 3 h, 6 h, 9 h and 12 h, cell viabilities were determined by CCK-8 assay. The optical density of each well was measured at 450 nm with a Bio-Tek microplate reader. Cell viability of the control group was defined as 100%. The test results show (Figure S1) that the cells viability in 50 s and 100 s groups were more than 95% at 3 h, 6 h, 9 h and 12 h after treatment, and the difference in cell viability between the two groups is not statistically significant (p > 0.05). The cell viability decreased in 150 s and 200 s groups (p < 0.01), and the survival rate was 74% in 150 s group and 55% in 200 s group. Combined with the oxygen free radicals generated condition, 100 s was selected as the optimal time of ultrasound. |
doi_str_mv | 10.6084/m9.figshare.11376984 |
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Determination of optimal LIFU irradiation time. (The data were shown as mean ± SD, n = 5 per group, *p < 0.05). To Select the optimal time for ultrasound, MDA-MB-231 cells were seeded in a 96-well plate at a density of 5000 cells per well for 24 h. And then use the strength of 2 W/cm2 ultrasonic processing cells, respectively for the 50 s, 100 s, 150 s and 200 s. After the indicated treatments, CCK8 solution (10 μL) was added in each well. Then, the MDA-MB-231 cells were cultured at 37 °C, 5% CO2 cell incubation box to save. At 3 h, 6 h, 9 h and 12 h, cell viabilities were determined by CCK-8 assay. The optical density of each well was measured at 450 nm with a Bio-Tek microplate reader. Cell viability of the control group was defined as 100%. The test results show (Figure S1) that the cells viability in 50 s and 100 s groups were more than 95% at 3 h, 6 h, 9 h and 12 h after treatment, and the difference in cell viability between the two groups is not statistically significant (p > 0.05). The cell viability decreased in 150 s and 200 s groups (p < 0.01), and the survival rate was 74% in 150 s group and 55% in 200 s group. Combined with the oxygen free radicals generated condition, 100 s was selected as the optimal time of ultrasound.</description><identifier>DOI: 10.6084/m9.figshare.11376984</identifier><language>eng</language><publisher>figshare</publisher><subject>Biochemistry ; Biological Sciences not elsewhere classified ; Cancer ; Cell Biology ; Chemical Sciences not elsewhere classified ; Developmental Biology ; FOS: Biological sciences ; Hematology ; Physiology ; Space Science</subject><creationdate>2019</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1892</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.11376984$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Zhong, Xiaowen</creatorcontrib><creatorcontrib>Zhang, Mei</creatorcontrib><creatorcontrib>Tian, Zedan</creatorcontrib><creatorcontrib>Wang, Qi</creatorcontrib><creatorcontrib>Wang, Zhigang</creatorcontrib><title>MOESM2 of The Study of Enhanced High-Intensity Focused Ultrasound Therapy by Sonodynamic N2O Microbubbles</title><description>Additional file 2: Figure S2. Determination of optimal LIFU irradiation time. (The data were shown as mean ± SD, n = 5 per group, *p < 0.05). To Select the optimal time for ultrasound, MDA-MB-231 cells were seeded in a 96-well plate at a density of 5000 cells per well for 24 h. And then use the strength of 2 W/cm2 ultrasonic processing cells, respectively for the 50 s, 100 s, 150 s and 200 s. After the indicated treatments, CCK8 solution (10 μL) was added in each well. Then, the MDA-MB-231 cells were cultured at 37 °C, 5% CO2 cell incubation box to save. At 3 h, 6 h, 9 h and 12 h, cell viabilities were determined by CCK-8 assay. The optical density of each well was measured at 450 nm with a Bio-Tek microplate reader. Cell viability of the control group was defined as 100%. The test results show (Figure S1) that the cells viability in 50 s and 100 s groups were more than 95% at 3 h, 6 h, 9 h and 12 h after treatment, and the difference in cell viability between the two groups is not statistically significant (p > 0.05). The cell viability decreased in 150 s and 200 s groups (p < 0.01), and the survival rate was 74% in 150 s group and 55% in 200 s group. Combined with the oxygen free radicals generated condition, 100 s was selected as the optimal time of ultrasound.</description><subject>Biochemistry</subject><subject>Biological Sciences not elsewhere classified</subject><subject>Cancer</subject><subject>Cell Biology</subject><subject>Chemical Sciences not elsewhere classified</subject><subject>Developmental Biology</subject><subject>FOS: Biological sciences</subject><subject>Hematology</subject><subject>Physiology</subject><subject>Space Science</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2019</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNqdjrEOgjAURbs4GPUPHN4PiKBEYTYQHNABnZtHW6AJtKQtQ_9eSeQHnG7OTU5yCNlHYXAJk_g4pEEjW9uhEUEUna-XNInXRJbPrCpPoBt4dQIqN3E_Q6Y6VExwKGTbHe7KCWWl85BrNtnv_e6dQasnxWfP4Oih9lBppblXOEgGj9MTSsmMrqe67oXdklWDvRW7325InGevW3Hg6JBJJ-ho5IDG0yikczEdUroU06X4_Kf2AVlQVIc</recordid><startdate>20191217</startdate><enddate>20191217</enddate><creator>Zhong, Xiaowen</creator><creator>Zhang, Mei</creator><creator>Tian, Zedan</creator><creator>Wang, Qi</creator><creator>Wang, Zhigang</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20191217</creationdate><title>MOESM2 of The Study of Enhanced High-Intensity Focused Ultrasound Therapy by Sonodynamic N2O Microbubbles</title><author>Zhong, Xiaowen ; Zhang, Mei ; Tian, Zedan ; Wang, Qi ; Wang, Zhigang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_113769843</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biochemistry</topic><topic>Biological Sciences not elsewhere classified</topic><topic>Cancer</topic><topic>Cell Biology</topic><topic>Chemical Sciences not elsewhere classified</topic><topic>Developmental Biology</topic><topic>FOS: Biological sciences</topic><topic>Hematology</topic><topic>Physiology</topic><topic>Space Science</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhong, Xiaowen</creatorcontrib><creatorcontrib>Zhang, Mei</creatorcontrib><creatorcontrib>Tian, Zedan</creatorcontrib><creatorcontrib>Wang, Qi</creatorcontrib><creatorcontrib>Wang, Zhigang</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Zhong, Xiaowen</au><au>Zhang, Mei</au><au>Tian, Zedan</au><au>Wang, Qi</au><au>Wang, Zhigang</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>MOESM2 of The Study of Enhanced High-Intensity Focused Ultrasound Therapy by Sonodynamic N2O Microbubbles</title><date>2019-12-17</date><risdate>2019</risdate><abstract>Additional file 2: Figure S2. Determination of optimal LIFU irradiation time. (The data were shown as mean ± SD, n = 5 per group, *p < 0.05). To Select the optimal time for ultrasound, MDA-MB-231 cells were seeded in a 96-well plate at a density of 5000 cells per well for 24 h. And then use the strength of 2 W/cm2 ultrasonic processing cells, respectively for the 50 s, 100 s, 150 s and 200 s. After the indicated treatments, CCK8 solution (10 μL) was added in each well. Then, the MDA-MB-231 cells were cultured at 37 °C, 5% CO2 cell incubation box to save. At 3 h, 6 h, 9 h and 12 h, cell viabilities were determined by CCK-8 assay. The optical density of each well was measured at 450 nm with a Bio-Tek microplate reader. Cell viability of the control group was defined as 100%. The test results show (Figure S1) that the cells viability in 50 s and 100 s groups were more than 95% at 3 h, 6 h, 9 h and 12 h after treatment, and the difference in cell viability between the two groups is not statistically significant (p > 0.05). The cell viability decreased in 150 s and 200 s groups (p < 0.01), and the survival rate was 74% in 150 s group and 55% in 200 s group. Combined with the oxygen free radicals generated condition, 100 s was selected as the optimal time of ultrasound.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.11376984</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry Biological Sciences not elsewhere classified Cancer Cell Biology Chemical Sciences not elsewhere classified Developmental Biology FOS: Biological sciences Hematology Physiology Space Science |
title | MOESM2 of The Study of Enhanced High-Intensity Focused Ultrasound Therapy by Sonodynamic N2O Microbubbles |
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