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Phosphorescent quantum dots/doxorubicin nanohybrids based on photoinduced electron transfer for detection of DNA

机译:基于光致电子转移的磷光量子点/阿霉素纳米杂合物用于DNA检测

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摘要

MPA-capped Mn-doped ZnS QDs/DXR nanohybrids (MPA: 3-mercaptopropionic acid; QDs: quantum dots; DXR: cetyltrimethyl ammonium bromide) were constructed via photoinduced electron transfer(PIET) and then used as a room-temperature phosphorescence (RTP) probe for detection of DNA. DXR as a quencher will quench the RTP of Mn-doped ZnS QDs via PIET, thereby forming Mn-doped ZnS QDs/DXR nanohybrids and storing RTP. With the addition of DNA, it will be inserted into DXR and thus DXR will be competitively desorbed from the surface of Mn-doped ZnS QDs, thereby releasing the RTP of Mn-doped ZnS QDs. Based on this, a new method for DNA detection was built. The sensor for DNA has a detection limit of 0.039 mgL~(-1) and a linear range from 0.1 to 14 mg L~(-1). The present QDs-based RTP method does not need deoxidants or other inducers as required by conventional RTP detection methods, and avoids interference from autofluorescence and the scattering light of the matrix that are encountered in spectrofluorometry. Therefore, this method can be used to detect the DNA content in body fluid.
机译:通过光致电子转移(PIET)构建MPA掺杂的Mn掺杂的ZnS QDs / DXR纳米杂化物(MPA:3-巯基丙酸; QDs:量子点; DXR:十六烷基三甲基溴化铵),然后用作室温磷光(RTP) )用于检测DNA的探针。 DXR作为淬灭剂将通过PIET淬灭Mn掺杂的ZnS QDs的RTP,从而形成Mn掺杂的ZnS QDs / DXR纳米杂化物并存储RTP。随着DNA的添加,它将被插入DXR,因此DXR将从Mn掺杂的ZnS QDs的表面竞争性解吸,从而释放Mn掺杂的ZnS QDs的RTP。在此基础上,建立了一种新的DNA检测方法。 DNA传感器的检出限为0.039 mgL〜(-1),线性范围为0.1至14 mg L〜(-1)。当前基于QDs的RTP方法不需要常规RTP检测方法所需的脱氧剂或其他诱导剂,并且避免了自发荧光的干扰以及分光荧光法中遇到的基质散射光。因此,该方法可用于检测体液中的DNA含量。

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