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Graphene Oxide Based Nanocarrier Combined with a pH-Sensitive Tracer: A Vehicle for Concurrent pH Sensing and pH-Responsive Oligonucleotide Delivery

机译:基于氧化石墨烯的纳米载体与pH敏感示踪剂结合:同时进行pH敏感和响应pH的寡核苷酸的载体。

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We chemically tuned the oxidation status of graphene oxide (GO) and constructed a GO-based nanoplatform combined with a pH-sensitive fluorescence tracer that is designed for both pH sensing and pH-responsive drug delivery. A series of GOs oxidized to distinct degrees were examined to optimize the adsorption of the model drug, poly dT(30). We determined that highly oxidized GO was a superior drug-carrier candidate in vitro when compared to GOs oxidized to lesser degrees. In the cell experiment, the synthesized pH-sensitive rhodamine dye was first applied to monitor cellular pH; under acidic conditions, protonated rhodamine fluoresces at 588 mm (lambda(ex) = 561 nm). When the nanocarrier was introduced into cells, a rhodamine-triggered competition reaction occurred, and this led to the release of the oligonucleotides and the quenching of rhodamine fluorescence by GO. Our results indicate high drug loading (FAM-dT(30)/GO = 25/50 mu g/mL) and rapid cellular uptake (<0.5 h) of the nanocarrier which can potentially be used for targeted RNAi delivery to the acidic milieu of tumors.
机译:我们化学调节了氧化石墨烯(GO)的氧化状态,并构建了基于GO的纳米平台,结合了pH敏感的荧光示踪剂,该荧光示踪剂设计用于pH敏感和pH敏感的药物递送。检查了一系列氧化为不同程度的GO,以优化模型药物poly dT(30)的吸附。我们确定,与氧化程度较低的GO相比,高氧化的GO在体外是优良的药物载体候选者。在细胞实验中,首先将合成的对pH敏感的罗丹明染料用于监测细胞的pH;在酸性条件下,质子化的若丹明在588 mm处发出荧光(λ(ex)= 561 nm)。当将纳米载体引入细胞中时,发生了若丹明引发的竞争反应,这导致寡核苷酸的释放和通过GO猝灭若丹明荧光。我们的结果表明,纳米载体的高载药量(FAM-dT(30)/ GO = 25/50μg / mL)和快速细胞摄取(<0.5 h),可潜在地用于靶向RNAi传递至酸性环境。肿瘤。

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