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Rapid high throughput assay for fluorimetric detection of doxorubicin-Application of nucleic acid-dye bioprobe

机译:快速高通量荧光检测阿霉素的方法-核酸染料生物探针的应用

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A double stranded DNA based fluorescence bioprobe for anticancer agent (doxoruhicin) detection is described.This method provides a new way for sensitive DNA/drug interaction study by a homogeneous assay.The probe employs the long-wavelength intercalating fluorophore TOTO-3~R (TT3).The anticancer agent,doxorubicin,which interacts with the DNA-TT3 complex,was indirectly measured by the decrease in the fluorescence intensity.Various oligonucleotides with different sequences were examined.Doxorubicin has preference for the oligonucleotide 5AGCACG3'.Enhanced fluorescence observed for the TT3 intercalation with this oligonucleotide makes the DNA-dye complex a suitable bioprobe for doxorubicin detection by competitive assay.A home-built CCD camera setup was applied along with 384 well plate assay format for high throughput fluorescence imaging.The detection limit can be as low as 25 ng mL_1 with an upper limit of 100 mu g mL-1.The recovery test with spiked serum sample shows that this method can be a potential routine method for therapeutic drug monitoring (TDM).
机译:描述了一种基于双链DNA的荧光生物探针用于抗癌药(多柔比星)检测,该方法通过均相测定为灵敏的DNA /药物相互作用研究提供了一种新方法。 TT3)。通过荧光强度的降低间接测量了与DNA-TT3复合物相互作用的抗癌药阿霉素,检查了具有不同序列的各种寡核苷酸。阿霉素优先于5AGCACG3'寡核苷酸。 TT3插入该寡核苷酸使DNA-染料复合物成为通过竞争性测定法检测阿霉素的合适生物探针。使用自制的CCD相机设置和384孔板测定形式进行高通量荧光成像。低至25 ng mL_1,上限为100μg mL-1。加标血清样品的回收率测试表明,该方法可能是治疗药物监测(TDM)的潜在常规方法。

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