The self-enhanced electrochemiluminescence (ECL) with high sensitivity could be an effective method for anticancer drug screening with cell apoptosis monitoring. Here we reported an ultrasensitive ECL cytosensor for cell apoptosis monitoring by using self-enhanced electrochemiluminescent ruthenium-silica composite nanoparticles (Ru-N-SiNPs) labeled annexin V as signal probes. The Ru-N-SiNPs were first synthesized through simple hydrolysis of a novel precursor containing luminescent and intracoreactant groups in one molecule, which presented higher emission efficiency and enhanced ECL intensity due to the shorter electron-transfer path and less energy loss. Moreover, the as-proposed ECL cytosensor was successfully used to investigate efficiency of paclitaxel toward MDA-MB-231 breast cancer cell in the range from 1 nM to 200 nM with a detection limit of 0.3 nM and a correlation coefficient of 0.9917. The improved accuracy and excellent dynamic range revealed the potential applications in biomolecules diagnostics and cells detections, especially in living and complex systems.
In this work, a novel mesoporous luminescence-functionalized metal-organic framework (Ru-PCN-777) with high stability and excellent electrochemiluminescence (ECL) performance was synthesized by immobilizing Ru(bpy)(mcpbpy) on the Zr cluster of PCN-777 via a strong coordination bond between Zr and -COO. Consequently, the Ru(bpy)(mcpbpy) could not only cover the surface of PCN-777 but also graft into the interior of PCN-777, which greatly increased the loading amount of Ru(bpy)(mcpbpy) and effectively prevented the leaching of the Ru(bpy)(mcpbpy) resulting in a stable and high ECL response. Considering the above merits, we utilized the mesoporous Ru-PCN-777 to construct an ECL immunosensor to detect mucin 1 (MUC1) based on proximity-induced intramolecular DNA strand displacement (PiDSD). The ECL signal was further enhanced by the enzyme-assisted DNA recycling amplification strategy. As expected, the immunosensor had excellent sensitivity, specificity, and responded wide linearly to the concentration of MUC1 from 100 fg/mL to 100 ng/mL with a low detection limit of 33.3 fg/mL (S/N = 3). It is the first time that mesoporous Zr-MOF was introduced into ECL system to assay biomolecules, which might expand the application of mesoporous metal-organic frameworks (MOFs) in bioanalysis. This work indicates that the use of highly stable mesoporous luminescence-functionalized MOFs to enhance the ECL intensity and stability is a feasible strategy for designing and constructing high-performance ECL materials, and therefore may shed light on new ways to develop highly sensitive and selective ECL sensors.
Despite
the widespread utilization of gold nanoparticles and graphene
for in vivo applications, complex steps for the preparation and functionalization
of these nanomaterials are commonly required. In addition, the cytotoxicity
of such materials is currently still under debate. In this work, by
taking the significant advantages of DNA in terms of biocompatibility,
nontoxicity, and controllability as building blocks for DNA nanostructures,
we describe the construction of a reconfigurable, multicolor-encoded
DNA nanostructure for multiplexed monitoring of intracellular microRNAs
(miRNAs) in living cells. The DNA nanostructure nanoprobes containing
two fluorescently quenched hairpins can be obtained by simple thermal
annealing of four ssDNA oligonucleotides. The presence of the target
miRNAs can unfold the hairpin structures and recover fluorescent emissions
at distinct wavelengths to achieve multiplexed detection of miRNAs.
Importantly, the DNA nanostructure nanoprobes exhibit significantly
improved stability over conventional DNA molecular beacon probes in
cell lysates and can steadily enter cells to realize simultaneous
detection of two types of intracellular miRNAs. The demonstration
of the self-assembled DNA nanostructures for intracellular sensing
thus offers great potential application of these nanoprobes for imaging,
drug delivery and cancer therapy in vivo.
Novel luminescence-functionalized metal-organic frameworks (MOFs) with superior electrogenerated chemiluminescence (ECL) properties were synthesized based on zinc ions as the central ions and tris(4,4'-dicarboxylicacid-2,2'-bipyridyl)ruthenium(II) dichloride ([Ru(dcbpy)3](2+)) as the ligands. For potential applications, the synthesized MOFs were used to fabricate a "signal-on" ECL immunosensor for the detection of N-terminal pro-B-type natriuretic peptide (NT-proBNP). As expected, enhanced ECL signals were obtained through a simple fabrication strategy because luminescence-functionalized MOFs not only effectively increased the loading of [Ru(dcbpy)3](2+), but also served as a loading platform in the ECL immunosensor. Furthermore, the proposed ECL immunosensor had a wide linear range from 5 pg mL(-1) to 25 ng mL(-1) and a relatively low detection limit of 1.67 pg mL(-1) (signal/noise=3). The results indicated that luminescence-functionalized MOFs provided a novel amplification strategy in the construction of ECL immunosensors and might have great prospects for application in bioanalysis.
Here, an ultrasensitive "off-on" electrochemiluminescence (ECL) biosensor was proposed for the determination of telomerase activity by using a self-enhanced ruthenium polyethylenimine (Ru-PEI) complex doped zeolitic imidazolate framework-8 (Ru-PEI@ZIF-8) with high ECL efficiency as an ECL indicator and an enzyme-assisted DNA cycle amplification strategy. The Ru-PEI@ZIF-8 nanocomposites were synthesized by self-enhanced Ru-PEI complex doping during the growth of zeolitic imidazolate framework-8 (ZIF-8), which presented high ECL efficiency and excellent stability. Furthermore, owing to the porosity of Ru-PEI@ZIF-8, the self-enhanced Ru-PEI complex in the outer layer and inner layer of self-enhanced Ru-PEI@ZIF-8 could be excited by electrons causing the utilization ratio of the self-enhanced ECL materials to be remarkably increased. To further improve the sensitivity of the proposed biosensor, the telomerase activity signal was converted into the trigger DNA signal which was further amplified by an enzyme-assisted DNA recycle-amplification strategy. The proposed ECL biosensor presented great performance for telomerase activity detection from 5 × 10 to 10 Hela cells with a detection limit of 11 cells. Moreover, this method was applied in the detection of telomerase activity from cancer cells treated with an anticancer drug, which indicated the proposed method held potential application value as an evaluation tool in anticancer drug screening.
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