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Detection of fluorine labeled herceptin using cellular (19)F MRI ex vivo.

机译:使用细胞(19)F MRI离体检测氟标记的赫赛汀。

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摘要

The aim of this study was to assess the herceptin efficacy in ex vivo cultures of MCF-7 breast carcinoma cells. Herceptin was used with perfluorooctyl bromide (PFOB) and conjugated with lipoplex, containing plasmid DNA and lipofectamine (LipA), to allow fluorine-19 magnetic resonance imaging ((19)F MRI) study. Treatments such as herceptin, herceptin/PFOB and herceptin/PFOB/lipoplex were used for ex vivo targeting of MCF-7 cells cultured in three-dimensional (3D) geometry using hollow fiber bioreactor (HFB) device. The viability of MCF-7 cells after 72h treatments decreased to 54+/-2%, 50+/-3% and 45+/-1% for herceptin, herceptin/PFOB and herceptin/PFOB/Lipoplex, respectively. The EC(50) values were 1000microg/ml, 930microg/ml and 730microg/ml, respectively. The significant correlation between the treatment concentration and efficacy was observed in MCF-7 cell cultures.
机译:这项研究的目的是评估赫赛汀在MCF-7乳腺癌细胞体外培养中的功效。赫赛汀与全氟辛基溴化物(PFOB)一起使用,并与lipoplex偶联,其中包含质粒DNA和lipofectamine(LipA),可进行氟19磁共振成像((19)F MRI)研究。使用诸如赫赛汀,赫赛汀/ PFOB和赫赛汀/ PFOB /脂质复合物的处理方法,可使用中空纤维生物反应器(HFB)装置体外培养以三维(3D)几何形状培养的MCF-7细胞。对于赫赛汀,赫赛汀/ PFOB和赫赛汀/ PFOB /脂质体,处理72h后MCF-7细胞的存活率分别降至54 +/- 2%,50 +/- 3%和45 +/- 1%。 EC(50)值分别为1000microg / ml,930microg / ml和730microg / ml。在MCF-7细胞培养物中观察到治疗浓度和功效之间的显着相关性。

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