Fluorescent nanodiamond is a new nanomaterial that possesses several useful properties, including good biocompatibility, excellent photostability and facile surface functionalizability. Moreover, when excited by a laser, defect centres within the nanodiamond emit photons that are capable of penetrating tissue, making them well suited for biological imaging applications. Here, we show that bright fluorescent nanodiamonds can be produced in large quantities by irradiating synthetic diamond nanocrystallites with helium ions. The fluorescence is sufficiently bright and stable to allow three-dimensional tracking of a single particle within the cell by means of either one- or two-photon-excited fluorescence microscopy. The excellent photophysical characteristics are maintained for particles as small as 25 nm, suggesting that fluorescent nanodiamond is an ideal probe for long-term tracking and imaging in vivo, with good temporal and spatial resolution.
The quasi-skutterudite superconductor Sr3Rh4Sn13 features a pronounced anomaly in electrical resistivity at T * ∼138 K. We show that the anomaly is caused by a second-order structural transition, which can be tuned to 0 K by applying physical pressure and chemical pressure via the substitution of Ca for Sr. A broad superconducting dome is centred around the structural quantum critical point. Detailed analysis of the tuning parameter dependence of T * as well as insights from lattice dynamics calculations strongly support the existence of a structural quantum critical point at ambient pressure when the fraction of Ca is 0.9 (i.e., xc = 0.9). This establishes (CaxSr1−x)3Rh4Sn13 series as an important system for exploring the physics of structural quantum criticality without the need of applying high pressures.Quantum criticality associated with a second-order phase transition at zero temperature has been a fruitful concept in the search for superconductivity. Particularly clear examples include the heavy fermion [1, 2] and iron-based systems [3][4][5][6], where superconductivity is stabilized in the vicinity of an antiferromagnetic quantum critical point (QCP). In addition to magnetic instabilities, structural instabilities also have an intricate influence on superconductivity. However, clean systems with continuous structural transition tunable by external parameters are relatively rare, and for the few cases studied in recent years, the structural order is found in the vicinity of magnetic order [7], making the notion of structural quantum criticality and its influence on the superconductivity less advanced than the magnetic counterpart.Superconducting stannides [8,9], including A 3 T 4 Sn 13 systems where A=La,Sr,Ca and T=Ir,Rh, have recently been reexamined using a wide range of probes [10][11][12][13][14][15][16][17][18][19][20][21][22]. Sr 3 Rh 4 Sn 13 , a member of this stoichiometry family, is a strong-coupling superconductor with a critical temperature T c ≈4.7 K. The superconducting gap function ∆ is nodeless, with 2∆/k B
Cell therapy is a promising strategy for the treatment of human diseases. While the first use of cells for therapeutic purposes can be traced to the 19th century, there has been a lack of general and reliable methods to study the biodistribution and associated pharmacokinetics of transplanted cells in various animal models for preclinical evaluation. Here, we present a new platform using albumin-conjugated fluorescent nanodiamonds (FNDs) as biocompatible and photostable labels for quantitative tracking of human placenta choriodecidual membrane-derived mesenchymal stem cells (pcMSCs) in miniature pigs by magnetic modulation. With this background-free detection technique and time-gated fluorescence imaging, we have been able to precisely determine the numbers as well as positions of the transplanted FND-labeled pcMSCs in organs and tissues of the miniature pigs after intravenous administration. The method is applicable to single-cell imaging and quantitative tracking of human stem/progenitor cells in rodents and other animal models as well.
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