Intracellular thermometry provides important information about the physiological activity of single cells and has been implemented using diverse temperature-sensitive materials as nanoprobes. However, measuring the temperature of specific organelles or subcellular structures is challenging because it requires precise positioning of the nanoprobes. Here, it is shown that dispersed fluorescent nanodiamonds (FNDs) endocytosed in living cells can be aggregated into microspheres using optical forces and used as intracellular temperature probes. The aggregation of the FNDs and electromagnetic resonance between individual nanodiamonds in the microspheres lead to a sevenfold intensity enhancement of 546-nm laser excitation. With the assistance of a scanning optical tweezing system, the FND microspheres can be precisely patterned and positioned within the cells. By measuring the fluorescence spectra of the microspheres, the temperatures at different locations within the cells are detected. The method provides an approach to the constructing and positioning of nanoprobes in an intracellular manner, which has potential applications in high-precision and flexible single-cell analysis.
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http://dx.doi.org/10.1002/advs.202103354 | DOI Listing |
ACS Sens
December 2024
School of Mechanical Engineering, Southeast University, Nanjing 211189, People's Republic of China.
Background noise interferes with the accurate detection of early tumor biomarkers. This study introduces a method that effectively reduces background noise to enhance detection accuracy by combining a color-coded signaling approach with the unique fluorescent properties and room-temperature tunable quantum spin characteristics of fluorescent diamonds (FNDs) with nitrogen-vacancy centers. In this approach, a red signal indicates the presence of the target analyte within the spectral region, a green signal indicates its absence, and a yellow signal indicates the need for further analysis using FNDs' quantum spin properties for optical detection magnetic resonance (ODMR) to distinguish the FND signal from background noise.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Mechanical Engineering, Southeast University, Nanjing 211189, China.
Sensitive and accurate miRNA detection is important in cancer diagnosis but remains challenging owing to the essential features of miRNAs, such as their small size, high homology, and low abundance. This work proposes a novel electrochemical (EC)-enhanced quantum sensor achieving quantitative detection of miRNA-155 with simultaneous EC sensing. Specifically, fluorescent nanodiamonds/MXene nanocomposites were synthesized and modified with dual-mode signal labels, enabling miRNA-155 concentration measurement via relaxation time of nitrogen-vacancy (NV) centers and EC signals.
View Article and Find Full Text PDFACS Nano
December 2024
Department of Chemistry, Graduate School of Life, Environmental, Natural Science and Technology, Okayama University, Okayama 700-8530, Japan.
Optically accessible spin-active nanomaterials are promising as quantum nanosensors for probing biological samples. However, achieving bioimaging-level brightness and high-quality spin properties for these materials is challenging and hinders their application in quantum biosensing. Here, we demonstrate bright fluorescent nanodiamonds (NDs) containing 0.
View Article and Find Full Text PDFSci Adv
December 2024
Department of Chemistry, University of California, Berkeley, Berkeley, CA 94720, USA.
A method is presented for high-precision chemical detection that integrates quantum sensing with droplet microfluidics. Using nanodiamonds (ND) with fluorescent nitrogen-vacancy (NV) centers as quantum sensors, rapidly flowing microdroplets containing analyte molecules are analyzed. A noise-suppressed mode of optically detected magnetic resonance is enabled by pairing controllable flow with microwave control of NV electronic spins, to detect analyte-induced signals of a few hundredths of a percent of the ND fluorescence.
View Article and Find Full Text PDFNat Commun
December 2024
Department of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong, China.
Physical unclonable function labels have emerged as a promising candidate for achieving unbreakable anticounterfeiting. Despite their significant progress, two challenges for developing practical physical unclonable function systems remain, namely 1) fairly few high-dimensional encoded labels with excellent material properties, and 2) existing authentication methods with poor noise tolerance or inapplicability to unseen labels. Herein, we employ the linear polarization modulation of randomly distributed fluorescent nanodiamonds to demonstrate, for the first time, three-dimensional encoding for diamond-based labels.
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