Abstract:Photothermal therapy (PTT) has been widely used for the treatment of various medical conditions due to their noninvasive and cost-effective advantages. However, the light absorption and scattering of the biosystem limit the deep tissue applications of conventional PTT probes. In this paper, we proposed the sub-10 nm NaNdF 4 nanocrystals with both incident and emission wavelengths located at the optical window. Under 800 nm laser excitation, the maximum light-to-heat conversion efficiency of these ultrasmall ph… Show more
“…The photothermal conversion efficiency reported here is of the same order of magnitude than that reported for graphene in DMF [ 37 ] and Au nanoshells or Au nanorods [ 10 ]. However, the ability of Au nanostars [ 10 ], NaNdF 4 [ 72 ], NdVO 4 in water [ 73 ], or core@shell@shell NaNdF 4 @NaYF 4 @Nd:NaYF 4 [ 74 ] to generate heat is still higher compared to the Ho, Tm doped KLuW nanocrystals reported here ( Table 1 ).…”
Section: Resultsmentioning
confidence: 89%
“…Double Beam Fluorescence Thermometry 808 102 [10] Au nanorods Double Beam Fluorescence Thermometry 808 95 [10] NaNdF4 Thermal Relaxation 800 85 [72] NaNdF4@NaYF4@ Nd:NaYF4 Thermal Relaxation 808 72.7 [74] NdVO4 in water Thermal Relaxation 808 72.1 [73] Au nanoshells Double Beam Fluorescence Thermometry 808 68 [10] Graphene in DMF Integrating Sphere 808 67 [37] Au nanorods Double Beam Fluorescence Thermometry 808 63 [10] Au nanorods Thermal Relaxation 815 61 [71] Au/AuS nanoshells Thermal Relaxation 815 59 [71] Graphene Oxide in water Integrating Sphere 808 58 [37] Ho [29] Au/SiO2 nanoshells Thermal Relaxation 815 34 [71] FePt nanoparticles Pconverted to heat/Pexcitation 800 30 [70] Cu9S5 Thermal Relaxation 980 25.7 [22] Au nanoshells Thermal Relaxation 808 25 [75] 3.6. Ho, Tm:KLuW Nanocrystals as Self-Assessed Photothermal Agents Ho, Tm:KLuW nanocrystals exhibit the ability to self-determine the temperature achieved by the system when releasing heat by using luminescence thermometry, generating self-assessed photothermal agents.…”
The incorporation of oleic acid and oleylamine, acting as organic surfactant coatings for a novel solvothermal synthesis procedure, resulted in the formation of monoclinic KLu(WO4)2 nanocrystals. The formation of this crystalline phase was confirmed structurally from X-ray powder diffraction patterns and Raman vibrational modes, and thermally by differential thermal analysis. The transmission electron microscopy images confirm the nanodimensional size (~12 nm and ~16 nm for microwave-assisted and conventional autoclave solvothermal synthesis) of the particles and no agglomeration, contrary to the traditional modified sol-gel Pechini methodology. Upon doping with holmium (III) and thulium (III) lanthanide ions, these nanocrystals can generate simultaneously photoluminescence and heat, acting as nanothermometers and as photothermal agents in the third biological window, i.e., self-assessed photothermal agents, upon excitation with 808 nm near infrared, lying in the first biological window. The emissions of these nanocrystals, regardless of the solvothermal synthetic methodology applied to synthesize them, are located at 1.45 μm, 1.8 μm and 1.96 μm, attributed to the 3H4 ® 3F4 and 3F4 ® 3H6 electronic transition of Tm3+ and 5I7 ® 5I8 electronic transition of Ho3+, respectively. The self-assessing properties of these nanocrystals are studied as a function of their size and shape and compared to the ones prepared by the modified sol-gel Pechini methodology, revealing that the small nanocrystals obtained by the hydrothermal methods have the ability to generate heat more efficiently, but their capacity to sense temperature is not as good as that of the nanoparticles prepared by the modified sol-gel Pechnini method, revealing that the synthesis method influences the performance of these self-assessed photothermal agents. The self-assessing ability of these nanocrystals in the third biological window is proven via an ex-vivo experiment, achieving thermal knowledge and heat generation at a maximum penetration depth of 2 mm.
“…The photothermal conversion efficiency reported here is of the same order of magnitude than that reported for graphene in DMF [ 37 ] and Au nanoshells or Au nanorods [ 10 ]. However, the ability of Au nanostars [ 10 ], NaNdF 4 [ 72 ], NdVO 4 in water [ 73 ], or core@shell@shell NaNdF 4 @NaYF 4 @Nd:NaYF 4 [ 74 ] to generate heat is still higher compared to the Ho, Tm doped KLuW nanocrystals reported here ( Table 1 ).…”
Section: Resultsmentioning
confidence: 89%
“…Double Beam Fluorescence Thermometry 808 102 [10] Au nanorods Double Beam Fluorescence Thermometry 808 95 [10] NaNdF4 Thermal Relaxation 800 85 [72] NaNdF4@NaYF4@ Nd:NaYF4 Thermal Relaxation 808 72.7 [74] NdVO4 in water Thermal Relaxation 808 72.1 [73] Au nanoshells Double Beam Fluorescence Thermometry 808 68 [10] Graphene in DMF Integrating Sphere 808 67 [37] Au nanorods Double Beam Fluorescence Thermometry 808 63 [10] Au nanorods Thermal Relaxation 815 61 [71] Au/AuS nanoshells Thermal Relaxation 815 59 [71] Graphene Oxide in water Integrating Sphere 808 58 [37] Ho [29] Au/SiO2 nanoshells Thermal Relaxation 815 34 [71] FePt nanoparticles Pconverted to heat/Pexcitation 800 30 [70] Cu9S5 Thermal Relaxation 980 25.7 [22] Au nanoshells Thermal Relaxation 808 25 [75] 3.6. Ho, Tm:KLuW Nanocrystals as Self-Assessed Photothermal Agents Ho, Tm:KLuW nanocrystals exhibit the ability to self-determine the temperature achieved by the system when releasing heat by using luminescence thermometry, generating self-assessed photothermal agents.…”
The incorporation of oleic acid and oleylamine, acting as organic surfactant coatings for a novel solvothermal synthesis procedure, resulted in the formation of monoclinic KLu(WO4)2 nanocrystals. The formation of this crystalline phase was confirmed structurally from X-ray powder diffraction patterns and Raman vibrational modes, and thermally by differential thermal analysis. The transmission electron microscopy images confirm the nanodimensional size (~12 nm and ~16 nm for microwave-assisted and conventional autoclave solvothermal synthesis) of the particles and no agglomeration, contrary to the traditional modified sol-gel Pechini methodology. Upon doping with holmium (III) and thulium (III) lanthanide ions, these nanocrystals can generate simultaneously photoluminescence and heat, acting as nanothermometers and as photothermal agents in the third biological window, i.e., self-assessed photothermal agents, upon excitation with 808 nm near infrared, lying in the first biological window. The emissions of these nanocrystals, regardless of the solvothermal synthetic methodology applied to synthesize them, are located at 1.45 μm, 1.8 μm and 1.96 μm, attributed to the 3H4 ® 3F4 and 3F4 ® 3H6 electronic transition of Tm3+ and 5I7 ® 5I8 electronic transition of Ho3+, respectively. The self-assessing properties of these nanocrystals are studied as a function of their size and shape and compared to the ones prepared by the modified sol-gel Pechini methodology, revealing that the small nanocrystals obtained by the hydrothermal methods have the ability to generate heat more efficiently, but their capacity to sense temperature is not as good as that of the nanoparticles prepared by the modified sol-gel Pechnini method, revealing that the synthesis method influences the performance of these self-assessed photothermal agents. The self-assessing ability of these nanocrystals in the third biological window is proven via an ex-vivo experiment, achieving thermal knowledge and heat generation at a maximum penetration depth of 2 mm.
“…Thus, we choose Er 3+ as one of the doped rare earth ions and the green emissions can be used as the detected signal in the visible range for thermometry. However, the green emissions have obvious absorption and limited penetration depth in biological tissues [17,18]. Therefore, the selected emissions shall be located in biological windows when the object is located in biological tissues [18].…”
Section: Introductionmentioning
confidence: 99%
“…However, the green emissions have obvious absorption and limited penetration depth in biological tissues [17,18]. Therefore, the selected emissions shall be located in biological windows when the object is located in biological tissues [18]. Under 980 nm laser excitation, Tm 3+ can emit red (650 nm) and near-infrared emissions (692 and 800 nm) [19], which can be used as the detected signal in the first biological window (650-1000 nm).…”
Accurate and reliable non-contact temperature sensors are imperative for industrial production and scientific research. Here, Er3+/Tm3+/Yb3+ co-doped NaYF4 phosphors were studied as an optical thermometry material. The typical hydrothermal method was used to synthesize hexagonal Er3+/Tm3+/Yb3+ co-doped NaYF4 phosphors and the morphology was approximately rod-like. The up-conversion emissions of the samples were located at 475, 520, 550, 650, 692 and 800 nm. Thermo-responsive emissions from the samples were monitored to evaluate the relative sensing sensitivity. The thermal coupled energy level- and non-thermal coupled energy level-based luminescence intensity ratio thermometry of the sample demonstrated that these two methods can be used to test temperature. Two green emissions (520 and 550 nm), radiated from 2H11/2/4S3/2 levels, were monitored, and the maximum relative sensing sensitivities reached to 0.013 K−1 at 297 K. The emissions located in the first biological window (650, 692 and 800 nm) were monitored and the maximum relative sensing sensitivities reached to 0.027 (R692/650) and 0.028 K−1 (R692/800) at 297 K, respectively. These results indicate that Er3+/Tm3+/Yb3+ co-doped NaYF4 phosphors have potential applications for temperature determination in the visible and the first biological window ranges.
“…However, by using these approaches, upconversion emissions with certain colors were obtained, which might be suitable exclusively for speci c applications. For instance, near infrared (NIR) photons exhibit deep penetration in biological tissues 8 , red light falling in the spectral biological window I (BW-I) is promising for visible imaging 9 , green light is most sensitive to human eyes, and blue and UV light are expected to trigger easily photochemical reactions 10 . Despite of these potential applications, a luminescent material capable of emitting different colors, i.e.…”
Real-time color-tunable upconversion luminescence of lanthanide ions has recently attracted increasing attention. To date, at least two different excitation wavelengths are required to obtain tunable upconversion colors containing the three-primary-color components (Red-Green-Blue). In this work, for the first time, we demonstrate that it is possible achieving tunable three-primary-color upconversion luminescence using a single excitation wavelength, on the basis of the photon-order dependent uponversion nature. A core-shell-shell nanocrystal was synthesized, with rational designed compositions of Er/Yb and Tm/Yb in the core and the outermost shell, respectively, responsible for the green/red and blue emissions. By increasing the power density of the 980 nm continuous-wave excitation laser, the color of the emitted luminescence of the core-shell-shell nanocrystal evolved as green → red → blue, corresponding to 2 → 3 → 4-photons involved in the upconversion process.
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