2013
DOI: 10.1002/anie.201304822
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Semiconducting Polymer Dots Doped with Europium Complexes Showing Ultranarrow Emission and Long Luminescence Lifetime for Time‐Gated Cellular Imaging

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Cited by 93 publications
(58 citation statements)
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“…With the development of fluorescence lifetime imaging microscopy and relevant techniques, optical multiplexing can employ nanomaterials with distinct fluorescence lifetime in a single color emission channel, which enables one‐color emissive nanomaterials to generate more populations and hence greatly extends its capability . Moreover, fluorescence lifetime lying in the microsecond region is superior for practical applications, because shorter lifetime on the order of nanoseconds cannot be easily separated from background noise by time‐gated technique, and longer lifetime on the order of milliseconds is less favorable for high‐throughput analysis . Therefore, it is highly desirable to prepare nanomaterials to simultaneously match all these four criteria for fluorescence‐lifetime optical multiplexing, including a single color emission with narrow band widths, tunable fluorescence lifetime in a wide time‐domain range, fluorescence lifetime on the order of microseconds, and high‐brightness luminescence.…”
Section: Introductionmentioning
confidence: 99%
“…With the development of fluorescence lifetime imaging microscopy and relevant techniques, optical multiplexing can employ nanomaterials with distinct fluorescence lifetime in a single color emission channel, which enables one‐color emissive nanomaterials to generate more populations and hence greatly extends its capability . Moreover, fluorescence lifetime lying in the microsecond region is superior for practical applications, because shorter lifetime on the order of nanoseconds cannot be easily separated from background noise by time‐gated technique, and longer lifetime on the order of milliseconds is less favorable for high‐throughput analysis . Therefore, it is highly desirable to prepare nanomaterials to simultaneously match all these four criteria for fluorescence‐lifetime optical multiplexing, including a single color emission with narrow band widths, tunable fluorescence lifetime in a wide time‐domain range, fluorescence lifetime on the order of microseconds, and high‐brightness luminescence.…”
Section: Introductionmentioning
confidence: 99%
“…First, Pdots show low non-specific binding, which has been demonstrated in our previous work with flow cytometry. [18] Second, the size (typically 10 – 30 nm in diameter) of Pdots ensures that they will carry enough metal atoms for the purposes of mass cytometry. Third, the small size of metal-loaded Pdots will be completely converted into mass signals in the ICP torch, which will increase sensitivity.…”
mentioning
confidence: 99%
“…Furthermore, we can adjust the fluorescence color by using different Pdots synthesized with carboxyl-functional groups. [18b,19] Also, by changing the lanthanide salt, different Ln atoms can be coordinated into Pdots. Combining these two features, we potentially can create a series of dual-functionality probes for both flow and mass cytometry.…”
mentioning
confidence: 99%
“…47 In comparison with semiconductor QDs, carbon-based fluorescent nanomaterials possess excellent biocompatibility, low cytotoxicity and chemical inertness, availability of multifunctional surface groups for covalent linkage of diverse bioactive molecules, making them promising candidates for imaging application. 64 These features have rendered them extremely useful for a number of applications including cellular imaging, targeted photodynamic therapy and in vivo tumor targeting. Nobel metal nanoclusters.…”
Section: Fluorescent Nanomaterialsmentioning
confidence: 99%