Analytical Chemistry · 2019 · 467 citations · 34 references
EngineeringBioengineeringBiotechnologyBiosensorsElectroanalytical MethodsSensorsBiosensor DesignElectrochemical BiosensorsElectrochemical SensorsNanomaterial-based BiosensorsNanosensorsNucleic Acid BiosensorsBiosensor InterfacesCancer Biomarker BiosensorsCancer Biomarker DetectionElectrochemical NanobiosensorsMetal-organic Framework SensorsMetal-organic FrameworksMultifunctional NanomaterialsNanomaterial-enabled Biosensors
Simultaneous detection of multiple tumor biomarkers is urgently needed for early and accurate cancer diagnosis, yet achieving this with homogeneous electrochemical biosensors remains challenging. We present a novel homogeneous electrochemical biosensor that uses functionalized metal–organic frameworks to detect multiple tumor biomarkers simultaneously. The sensor employs UIO‑66‑NH₂ MOFs loaded with electroactive dyes and capped by dsDNA; two variants (MB@UIO and TMB@UIO) release dyes upon miRNA hybridization, enabling detection of let‑7a and miRNA‑21. The biosensor achieves simultaneous detection of let‑7a and miRNA‑21 with limits of 3.6 fM and 8.2 fM, shows stronger signals in the presence of targets, and works in serum samples, offering enhanced diagnostic information.
Simultaneous detection of multiple tumor biomarkers is in great demand for early and accurate cancer diagnosis. A homogeneous electrochemical biosensor has been proven to possess high sensitivity, but achieving simultaneous detection of multiple tumor biomarkers is still a challenge. Herein, we develop a novel homogeneous electrochemical biosensor for simultaneous detection of multiple tumor biomarkers based on the functionalized metal–organic frameworks (MOFs). The functionalized MOFs were prepared by using porous UIO-66-NH2 as nanocontainer to load electroactive dyes and dsDNA as a gatekeeper to cap MOFs. In this context, two functionalized MOFs (MB@UIO and TMB@UIO) were fabricated and applied to simultaneous detection of let-7a and miRNA-21, used as the proof-of-concept analytes. The recognition and hybridization of PX with target miRNAs impel the generation of RNA–DNA complexes, which separated from MOFs and allowed the electroactive dyes to be released. In comparison with the case when target miRNAs are absent, two stronger signals are recorded, and dependent on target miRNA concentrations. Thus, simultaneous detection of let-7a and minRNA-21 is achieved, with detection limits down to 3.6 and 8.2 fM, respectively, comparable or lower than those of reported strategies that concentrated on single miRNA detection. Moreover, the proposed biosensor has also been successfully applied for simultaneous detection of target miRNAs spiked in serum samples. Therefore, the proposed strategy was expected to provide more information for early and accurate cancer diagnosis and was an useful application in disease diagnosis and clinical biomedicine.
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Ahmedin Jemal, Freddie Bray, Jacques Ferlay et al. · CA A Cancer Journal for Clinicians · 2011 · 55K citations · Full text
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