Jiang-Nan Zhang, Feng-Min Liu, Xiao-Juan Du, Xi-Le Zhao
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引用次数: 0
Abstract
miR-135a is highly expressed in patients with gestational diabetes mellitus, and its target genes are also involved in insulin signaling pathway, so it is one biomarker for gestational diabetes mellitus. Herein we designed a dual-mode DNA biosensor for reliable assay of miR-135a based on the fluorescence and colorimetric signals. Several experiments were carried out to demonstrate the assay feasibility and mechanism for this dual-mode DNA biosensor. With optimum parameters, this proposed dual-mode biosensor has been realized sensitive and quantitative assay of miR-135a. For the fluorescence and colorimetric signals, the working ranges are 0.56–61 and 8.3–74 nM, while limits of detection are 0.18 and 3.7 nM respectively. This dual-mode strategy allows two independent signals for miR-135a assay, so it can verify each other to show more accurate results with good fidelity. Furthermore, there is a good selectivity in the biosensor for target miR-135a over other nucleotide variants, as well as good anti-interference ability in complex samples. This dual-mode DNA biosensor provides a new approach for miR-135a assay and miRNA expression profiling in gestational diabetes mellitus.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.