Abstract
Temperature is a fundamental quantity that can regulate various biological phenomena and thus important in clinical biology as well as sport and health sciences. This chapter reviews how the body temperature is regulated in the organisms (mainly in mammals including humans), and how the body temperature of not only the surface but also the deep tissues. As an emerging technique, the luminescence nanothermometry that works in the over-thousand-nanometer (OTN) near-infrared (NIR) wavelength range, which allows us to look the biological tissues transparently, is being developed to visualize and reveal the mechanisms of dynamic time-dependent changes in body temperature distribution in deep tissues. The data and knowledge collected with the new techniques will provide insights into body temperature control in biology and its management in biomedical and engineering fields.
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References
T.D. Brock, H. Freeze, Thermus aquaticus gen. g. and sp. n., a nonsporulating extreme thermophile. J. Bact. 98, 289 (1969)
A. Chien, D.B. Edgar, J.M. Trela, Deoxyribonucleic acid polymerase from the extreme thermophile thermus aquaticus. J. Bact. 127, 1550 (1976)
K.S. Lundberg, D.D. Shoemaker, M.W. Adams et al., High-fidelity amplification using a thermostable DNA polymerase isolated from pyrococcus furiosus. Gene 108, 1 (1991). https://doi.org/10.1016/0378-1119(91)90480-y
R.K. Saiki, S. Scharf, F. Faloona et al., Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science 230, 1350 (1985). https://doi.org/10.1126/science.2999980
R.K. Saiki, D.H. Gelfand, S. Stoffel et al., Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239, 487 (1988). https://doi.org/10.1126/science.239.4839.487
T.W. Schulte, M.V. Blagosklonny, C. Ingui et al., Disruption of the Raf-1-Hsp90 molecular complex results in destabilization of Raf-1 and loss of Raf-1-Ras association. J. Biol. Chem. 270, 24585 (1995). https://doi.org/10.1074/jbc.270.41.24585
D.S. Cissel, M.A. Beaven, Disruption of Raf-1/heat shock protein 90 complex and Raf signaling by Dexamethasone in mast cells. J. Biol. Chem. 275, 7066 (2000). https://doi.org/10.1074/jbc.275.10.7066
N. Gomez, T. Erazo, J.M. Lizcano, ERK5 and cell proliferation: nuclear localization is what matters. Front. Cell Dev. Biol. 4, 105 (2016). https://doi.org/10.3389/fcell.2016.00105
I.M. Verma, J.K. Stevenson, E.M. Schwarz et al., Rel/NF-kappa B/I Kappa B family: intimate tales of association and dissociation. Genes Dev. 9, 2723 (1995). https://doi.org/10.1101/gad.9.22.2723
V. Krajka-Kuźniak, J. Paluszczak, W. Baer-Dubowska, The Nrf2-ARE signaling pathway: an update on its regulation and possible role in cancer prevention and treatment. Pharmacol. Rep. 69, 393 (2017). https://doi.org/10.1016/j.pharep.2016.12.011
T. Shimizu, A. Lengalova, V. MartÃnek et al., Heme: emergent roles of heme in signal transduction, functional regulation and as catalytic centres. Chem. Soc. Rev. 48, 5624 (2019). https://doi.org/10.1039/c9cs00268e
M.L. Begasse, M. Leaver, F. Vazquez, et al., Temperature Dependence of cell division timing accounts for a shift in the thermal limits of C. Elegans and C. Briggsae. Cell Rep. 10, 647 (2015). https://doi.org/10.1016/j.celrep.2015.01.006
D. Patel, K.A. Franklin, Temperature-regulation of plant architecture. Plant Signal Behav. 4, 577 (2009). https://doi.org/10.4161/psb.4.7.8849
D.A. Warner, R. Shine, The adaptive significance of temperature-dependent sex determination in a reptile. Nature 451, 566 (2008). https://doi.org/10.1038/nature06519
A. Bahat, I. Tur-Kaspa, A. Gakamsky et al., Thermotaxis of mammalian sperm cells: a potential navigation mechanism in the female genital tract. Nat. Med. 9, 149 (2003). https://doi.org/10.1038/nm0203-149
K. Okabe, N. Inada, C. Gota et al., Intracellular temperature mapping with a fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy. Nat. Commun. 3, 705 (2012). https://doi.org/10.1038/ncomms1714
P.A. Mackowiak, S.S. Wasserman, M.M. Levine, A Critical appraisal of 98.6 degrees F, the upper limit of the normal body temperature, and other legacies of Carl Reinhold August Wunderlich. JAMA 268, 1578 (1992). https://doi.org/10.1001/jama.1992.03490120092034
G.S. Kelly, Body temperature variability (Part 1): a review of the history of body temperature and its variability due to site selection, biological rhythms, fitness, and aging. Altern. Med. Rev. 11, 278 (2006)
G.S. Kelly, Body temperature variability (Part 2): masking influences of body temperature variability and a review of body temperature variability in disease. Altern. Med. Rev. 12, 49 (2007)
K. Kanosue, L.I. Crawshaw, K. Nagashima et al., Concepts to utilize in describing thermoregulation and neurophysiological evidence for how the system works. Eur. J. Appl. Physiol. 109, 5 (2010). https://doi.org/10.1007/s00421-009-1256-6
S. Kobayashi, Temperature-sensitive neurons in the hypothalamus: a new hypothesis that they act as thermostats, not as transducers. Prog. Neurobiol. 32, 103 (1989). https://doi.org/10.1016/0301-0082(89)90012-9
J.A. Boulant, Role of the preoptic-anterior hypothalamus in thermoregulation and fever. Clin. Infect. Dis. 31(Suppl 5), S157 (2000). https://doi.org/10.1086/317521
G. Mory, F. Bouillaud, M. Combes-George et al., Noradrenaline controls the concentration of the uncoupling protein in brown adipose tissue. FEBS Lett. 166, 393 (1984). https://doi.org/10.1016/0014-5793(84)80120-9
Z.B. Andrews, S. Diano, T.L. Horvath, Mitochondrial uncoupling proteins in the CNS: in support of function and survival. Nat. Rev. Neurosci. 6, 829 (2005). https://doi.org/10.1038/nrn1767
M.J. Gaudry, M. Jastroch, Molecular evolution of uncoupling proteins and implications for brain function. Neurosci. Lett. 696, 140 (2019). https://doi.org/10.1016/j.neulet.2018.12.027
R.S. Seymour, Biophysics and physiology of temperature regulation in thermogenic flowers. Biosci. Rep. 21, 223 (2001). https://doi.org/10.1023/A:1013608627084
A. Tissières, H.K. Mitchell, U.M. Tracy, Protein synthesis in salivary glands of drosophila melanogaster: relation to chromosome puffs. J. Mol. Biol. 84, 389 (1974). https://doi.org/10.1016/0022-2836(74)90447-1
M.J. Caterina, M.A. Schumacher, M. Tominaga et al., The Capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature 389, 816 (1997). https://doi.org/10.1038/39807
R. Inoue, T. Hanano, J. Shi et al., Transient receptor potential protein as a novel non-voltage-gated Ca2+ entry channel involved in diverse pathophysiological functions. J. Pharmacol. Sci. 91, 271 (2003). https://doi.org/10.1254/jphs.91.271
G.M. Story, The emerging role of TRP channels in mechanisms of temperature and pain sensation. Curr. Neuropharmacol. 4, 183 (2006). https://doi.org/10.2174/157015906778019482
K. Uchida, K. Dezaki, T. Yoneshiro et al., Involvement of thermosensitive TRP channels in energy metabolism. J. Physiol. Sci. 67, 549 (2017). https://doi.org/10.1007/s12576-017-0552-x
D.J. Cosens, A. Manning, Abnormal electroretinogram from a drosophila mutant. Nature 224, 285 (1969). https://doi.org/10.1038/224285a0
T. Sugiura, M. Tominaga, H. Katsuya et al., Bradykinin lowers the threshold temperature for heat activation of vanilloid receptor 1. J. Neurophysiol. 88, 544 (2002). https://doi.org/10.1152/jn.2002.88.1.544
N.R. Gavva, A.W. Bannon, S. Surapaneni et al., The vanilloid receptor TRPV1 Is tonically activated in vivo and involved in body temperature regulation. J. Neurosci. 27, 3366 (2007). https://doi.org/10.1523/JNEUROSCI.4833-06.2007
R. Sharif-Naeini, S. Ciura, C.W. Bourque, TRPV1 gene required for thermosensory transduction and anticipatory secretion from vasopressin neurons during hyperthermia. Neuron 58, 179 (2008). https://doi.org/10.1016/j.neuron.2008.02.013
A.D. Güler, H. Lee, T. Iida, Heat-evoked activation of the ion channel, TRPV4. J. Neurosci. 22, 6408 (2002). https://doi.org/10.1523/JNEUROSCI.22-15-06408.2002
H. Lee, T. Iida, A. Mizuno et al., Altered thermal selection behavior in mice lacking transient receptor potential vanilloid 4. J. Neurosci. 25, 1304 (2005). https://doi.org/10.1523/JNEUROSCI.4745.04.2005
A.S.M. El-Radhi, Why is the evidence not affecting the practice of fever management? Arch. Dis. Child. 93, 918 (2008). https://doi.org/10.1136/adc.2008.139949
M. Richardson, E. Purssell, Who’s afraid of fever? Arch. Dis. Child. 100, 818 (2015). https://doi.org/10.1136/archdischild-2014-307483
E.A. Dennis, Diversity of group types, regulation, and function of phospholipase A2. J. Biol. Chem. 269, 13057 (1994)
C.C. Leslie, Properties and regulation of cytosolic phospholipase A2. J. Biol. Chem. 272, 16709 (1997). https://doi.org/10.1074/jbc.272.27.16709
K. Matsumura, C. Cao, M. Ozaki et al., Brain endothelial cells express cyclooxygenase-2 during lipopolysaccharide-induced fever: light and electron microscopic immunocytochemical studies. J. Neurosci. 18, 6279 (1998). https://doi.org/10.1523/JNEUROSCI.18-16-06279.1998
H.E. de Vries. K.H. Hoogendoorn, J.van Dijk, et al., Eicosanoid production by rat cerebral endothelial cells: Stimulation by lipopolysaccharide, interleukin-1 and interleukin-6. J. Neuroimmunol. 59, 1 (1995). https://doi.org/10.1016/0165-5728(95)00009-q
R. Hanada, A. Leibbrandt, T. Hanada et al., Central control of fever and female body temperature by RANKL/RANK. Nature 462, 505 (2009). https://doi.org/10.1038/nature08596
F. Ushikubi, E. Segi, Y. Sugimoto et al., Impaired febrile response in mice lacking the prostaglandin E receptor subtype EP3. Nature 395, 281 (1998). https://doi.org/10.1038/26233
K. Nakamura, K. Matsumura, T. Kaneko et al., The rostral raphe pallidus nucleus mediates pyrogenic transmission from the preoptic area. J. Neurosci. 22, 4600 (2002). https://doi.org/10.1523/JNEUROSCI.22-11-04600.2002
M. Lazarus, K. Yoshida, R. Coppari et al., EP3 prostaglandin receptors in the median preoptic nucleus are critical for fever responses. Nat. Neurosci. 10, 1131 (2007). https://doi.org/10.1038/nn1949
S. Conolly, J.E. Arrowsmith, A.A. Klein, Deep hypothermic circulatory arrest. Continuing Educ Anaesth Crit Care Pain 10, 138 (2010). https://doi.org/10.1093/bjaceaccp/mkq024
M. Saxena, P.J.D. Andrews, A. Cheng, et al., Modest cooling therapies (35 to 37.5 ºC) for traumatic brain injury. Cochrane Database Syst. Rev. 2014, CD006811 (2014). https://doi.org/10.1002/14651858.CD006811.pub3
S.R. Lewis, D.J. Evans, A.R. Butler, et al., Hypothermia for Traumatic Brain Injury. Cochrane Database Syst. Rev. 2017 CD001048, (2017). https://doi.org/10.1002/14651858.CD001048.pub5
S.E. Jacobs, M. Berg, R. Hunt, et al. Cooling for newborns with hypoxic ischaemic encephalopathy. Cochrane Database Syst. Rev. 2013, CD003311 (2013). https://doi.org/10.1002/14651858.CD003311.pub3
A. Ascensão, M. Leite, A.N. Rebelo et al., Effects of cold water immersion on the recovery of physical performance and muscle damage following a one-off soccer match. J. Sports Sci. 29, 217 (2011). https://doi.org/10.1080/02640414.2010.526132
T.A.H. Järvinen, T.L.N. Järvinen, M. Kääriäinen et al., Muscle Injuries: optimising recovery. Best Pract. Res. Clin. Rheumatil. 21, 317 (2007). https://doi.org/10.1016/j.berh.2006.12.004
L.A. Roberts, T. Raastad, J.F. Markworth et al., Post-exercise cold water immersion attenuates acute anabolic signalling and long-term adaptations in muscle to strength training. J. Physiol. 593, 4285 (2015). https://doi.org/10.1113/JP270570
L. Guan, G. Xu, Damage effect of high-intensity focused ultrasound on breast cancer tissues and their vascularities. World J. Surg. Oncol. 14, 153 (2016). https://doi.org/10.1186/s12957-016-0908-3
J.Y. Park, P. Choi, H.K. Kim et al., Increase in apoptotic effect of Panax ginseng by microwave processing in human prostate cancer cells: in vitro and in vivo studies. J. Ginseng Res. 40, 62 (2016). https://doi.org/10.1016/j.jgr.2015.04.007
G. Baffou, R. Quidant, Thermo-plasmonics: using metallic nanostructures as nano-sources of heat. Laser Photonics Rev. 7, 171 (2013). https://doi.org/10.1002/lpor.201200003
I. Krylov, R. Akasov, V. Rocheva et al., Local overheating of biotissue labeled with upconversion nanoparticles under Yb3+ resonance excitation. Front. Phys. 8, 295 (2020). https://doi.org/10.3389/fchem.2020.00295
L. Ding, F. Ren, Z. Liu et al., Size-dependent photothermal conversion and photoluminescence of theranostic NaNdF4 nanoparticles under excitation of different-wavelength lasers. Bioconjugate Chem. 31, 340 (2020). https://doi.org/10.1021/acs.bioconjchem.9b00700
E. Carrasco, B. del Rosal, F. Sanz-RodrÃguez et al., Intratumoral thermal reading during photo-thermal therapy by multifunctional fluorescent nanoparticles. Adv. Funct. Mater. 25, 615 (2015). https://doi.org/10.1002/adfm.201403653
J.T. Robinson, K. Welsher, S.M. Tabakman et al., High performance in vivo Near-IR (>1 μm) imaging and photothermal cancer therapy with carbon nanotubes. Nano Res. 3, 779 (2010). https://doi.org/10.1007/s12274-010-0045-1
A.L. Antaris, J.T. Robinson, O.K. Yaghi et al., Ultra-low doses of chirality sorted (6,5) carbon nanotubes for simultaneous tumor imaging and photothermal therapy. ACS Nano 7, 3644 (2013). https://doi.org/10.1021/nn4006472
C. Liang, S. Diao, C. Wang et al., Tumor metastasis inhibition by imaging-guided photothermal therapy with single-walled carbon nanotubes. Adv. Mater. 26, 5646 (2014). https://doi.org/10.1002/adma.201401825
M. Sund-Levander, C. Forsberg, L.K. Wahren, Normal oral, rectal, tympanic and axillary body temperature in adult men and women: a systematic literature review. Scand. J. Caring Sci. 16, 122 (2002). https://doi.org/10.1046/j.1471-6712.2002.00069.x
I. Sage, Thermochromic liquid crystals. Liq. Cryst. 38, 1551 (2011). https://doi.org/10.1080/02678292.2011.631302
P. Kiekkas, N. Stefanopoulos, N. Bakalis et al., Agreement of infrared temporal artery thermometry with other thermometry methods in adults: systematic review. J. Clin. Nurs. 25, 894 (2016). https://doi.org/10.1111/jocn.13117
C. Zhen, Z. Xia, L. Long et al., Accuracy of infrared ear thermometry in children: a meta-analysis and systematic review. Clin. Pediatr. (Phila) 53, 1158 (2014). https://doi.org/10.1177/0009922814536774
J.P. Feist, A.L. Heyes, Europium-doped yttria-stabilized zirconia for high-temperature phosphor thermometry. Proc. Inst. Mechanic. Eng. 214 Part L, 7 (2000). https://doi.org/10.1177/146442070021400102
H. Zhou, M. Sharma, O. Berezin et al., Nanothermometry: from microscopy to thermal treatments. Chem. Phys. Chem. 17, 27 (2016). https://doi.org/10.1002/cphc.201500753
T. Bai, N. Gu, Micro/nanoscale thermometry for cellular thermal sensing. Small 12, 4590 (2016). https://doi.org/10.1002/smll.201600665
A.M. Stark, S. Way, The use of thermovision in the detection of early breast cancer. Cancer 33, 1664 (1974). https://doi.org/10.1002/1097-0142(197406)33:6%3c1664::AID-CNCR2820330629%3e3.0.CO;2-7
D. Jaque, L.M. Maestro, B. del Rosal et al., Nanoparticles for photothermal therapies. Nanoscale 6, 9494 (2014). https://doi.org/10.1039/C4NR00708E
D. Jaque, F. Vetrone, Luminescence nanothermometry. Nanoscale 4, 4301 (2012). https://doi.org/10.1039/C2NR30764B
K. Nigoghossian, S. Ouellet, J. Plain et al., Upconversion nanoparticle-decorated gold nanoshells for near-infrared induced heating and thermometry. J. Mater. Chem. B 5, 7109 (2017). https://doi.org/10.1039/c7tb01621b
Y. Zhang, S. Xu, X. Li et al., Temperature sensing, excitation power dependent fluorescence branching ratios, and photothermal conversion in NaYF4:Er3+/Yb3+ @NaYF4:Tm3+/Yb3+ core-shell particles. Opt. Mater. Exp. 8, 368 (2018). https://doi.org/10.1364/OME.8.000368
B. del Rosal, E. Ximendes, U. Rocha et al., In vivo luminescence nanothermometry: from materials to applications. Adv. Opt. Mater. 5, 1600508 (2017). https://doi.org/10.1002/adom.201600508
E. Hemmer, P. Acosta-Mora, J. Méndez-Ramos et al., Optical nanoprobes for biomedical applications: shining a light on upconverting and near-infrared emitting nanoparticles for imaging, thermal sensing, and photodynamic therapy. J. Mater. Chem. B 5, 4365 (2017). https://doi.org/10.1039/C7TB00403F
C.D.S. Brites, P.P. Lima, N.J.O. Silva et al., Thermometry at the nanoscale. Nanoscale 4, 4799 (2012). https://doi.org/10.1039/c2nr30663h
C.D.S. Brites, S. Balabhadra, L.D. Carlos, Lanthanide-based thermometers: at the cutting-edge of luminescence thermometry. Adv. Opt. Mater. 7, 1801239 (2019). https://doi.org/10.1002/adom.201801239
K. Okabe, R. Sakaguchi, B, Shi, et al., Intracellular thermometry with fluorescent sensors for thermal biology. Eur. J. Physiol. 470, 717 (2018). https://doi.org/10.1007/s00424-018-2113-4
V.A. Vlaskin, N. Janssen, J. van Rijssel et al., Tunable Dual Emission in Doped Semiconductor Nanocrystals. Nano Lett. 10, 3670 (2010). https://doi.org/10.1021/nl102135k
N. Inada, N. Fukuda, T. Hayashi et al., Temperature imaging using a cationic linear fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy. Nat. Protoc. 14, 1293 (2019). https://doi.org/10.1038/s41596-019-0145-7
J.S. Donner, S.A. Thompson, M.A. Kreuzer et al., Mapping intracellular temperature using green fluorescent protein. Nano Lett. 12, 2107 (2012). https://doi.org/10.1021/nl300389y
S. Kiyonaka, T. Kajimoto, R. Sakaguchim et al., Genetically encoded fluorescent thermosensors visualize subcellular thermoregulation in living cells. Nat. Methods 10, 1232 (2013). https://doi.org/10.1038/nmeth.2690
M. Nakano, Y. Arai, I. Kotera et al., Genetically encoded ratiometric fluorescent thermometer with wide range and rapid response. PLoS ONE 12, e0172344 (2017). https://doi.org/10.1371/journal.pone.0172344
D. Chrétien, P. Bénit, H.H. Ha et al., Mitochondria are physiologically maintained at close to 50 °C. PLoS Biol. 16, e2003992 (2018). https://doi.org/10.1371/journal.pbio.2003992
M.C. Rajagopal, J.W. Brown, D. Gelda et al., Transient heat release during induced mitochondrial proton uncoupling. Commun. Biol. 2, 279 (2019). https://doi.org/10.1038/s42003-019-0535-y
E. Hemmer, N. Venkatachalam, H. Hyodo et al., Upconverting and NIR emitting rare earth based nanostructures for NIR-bioimaging. Nanoscale 5, 11339 (2013). https://doi.org/10.1039/c3nr02286b
S. Arai, Ferdinandus, S. Takeoka, et al., Micro-thermography in millimeter-scale animals by using orally-dosed fluorescent nanoparticle thermosensors. Analyst 140, 7534 (2015). https://doi.org/10.1039/C5AN01287B
J.S. Donner, S.A. Thompson, C. Alonso-Ortega et al., Imaging of plasmonic heating in a living organism. ACS Nano 7, 8666 (2013). https://doi.org/10.1021/nn403659n
L. Huo, J. Zhou, R. Wu et al., Dual-functional β-NaYF4: Yb3+, Er3+ nanoparticles for bioimaging and temperature sensing. Opt. Mater. Exp. 6, 1056 (2016). https://doi.org/10.1364/OME.6.001056
K. Soga, M. Kamimura, K. Okubo et al., Near-infrared biomedical imaging for transparency. J. Imag. Soc. Jpn 58, 602 (2019). https://doi.org/10.11370/isj.58.602
F. Vetrone, R. Naccache, A. Zamarrón et al., Temperature sensing using fluorescent nanothermometers. ACS Nano 4, 3254 (2010). https://doi.org/10.1021/nn100244a
M. Kamimura, T. Matsumoto, S. Suyari et al., Ratiometric near-infrared fluorescence nanothermometry in the OTN-NIR (NIR II/III) biological window based on rare-earth doped β-NaYF4 nanoparticles. J. Mater. Chem. B 5, 1917 (2017). https://doi.org/10.1039/C7TB00070G
L. Wortmann, S. Suyari, T. Ube et al., Tuning the thermal sensitivity of β-NaYF4: Yb3+, Ho3+, Er3+ nanothermometers for optimal temperature sensing in OTN-NIR (NIR II/III) biological window. J. Lumin. 198, 236 (2018). https://doi.org/10.1016/j.jlumin.2018.01.049
S. Sekiyama, M. Umezawa, S. Kuraoka et al., Temperature sensing of deep abdominal region in mice by using over-1000 nm near-infrared luminescence of rare-earth-doped NaYF4 nanothermometer. Sci. Rep. 8, 16979 (2018). https://doi.org/10.1038/s41598-018-35354-y
E.C. Ximendes, A.F. Pereira, U. Rocha et al., Thulium doped LaF3 for nanothermometry operating over 1000Â nm. Nanoscale 11, 8864 (2019). https://doi.org/10.1039/c9nr00082h
E.C. Ximendes, U. Rocha, T.O. Sales et al., In vivo subcutaneous thermal video recording by supersensitive infrared nanothermometers. Adv. Funct. Mater. 27, 1702249 (2017). https://doi.org/10.1002/adfm.201702249
A. Skripka, A. Morinvil, M. Matulionyte et al., Advancing neodymium single-band nanothermometry. Nanoscale 11, 11322 (2019). https://doi.org/10.1039/c9nr02801c
E.C. Ximendes, W.Q. Santos, U. Rocha et al., Unveiling in vivo subcutaneous thermal dynamics by infrared luminescent nanothermometers. Nano Lett. 16, 1695 (2016). https://doi.org/10.1021/acs.nanolett.5b04611
F. Xu, Z. Ba, Y. Zheng et al., Rare-earth-doped optical nanothermometer in visible and near-infrared regions. J. Mater. Sci. 53, 15107 (2018). https://doi.org/10.1007/s10853-018-2702-9
P. Cortelletti, A. Skripka, C. Facciotti et al., Tuning the sensitivity of lanthanide-activated NIR nanothermometers in the biological windows. Nanoscale 10, 2568 (2018). https://doi.org/10.1039/c7nr06141b
A. Skripka, A. Benayas, R. Marin et al., Double rare-earth nanothermometer in aqueous media: opening the third optical transparency window to temperature sensing. Nanoscale 9, 3079 (2017). https://doi.org/10.1039/c6nr08472a
T. Chihara, M. Umezawa, K. Miyata et al., Biological deep temperature imaging with fluorescence lifetime of rare-earth-doped ceramics particles in the second NIR biological window. Sci. Rep. 9, 12806 (2019). https://doi.org/10.1038/s41598-019-49291-x
E. Thimsen, B. Sadtler, M.Y. Berezin, Shortwave-infrared (SWIR) emitters for biological imaging: a review of challenges and opportunities. Nanophotonics 6, 1043 (2017). https://doi.org/10.1515/nanoph-2017-0039
B. del Rosal, E. Carrasco, F. Ren et al., Infrared-emitting QDs for thermal therapy with real-time subcutaneous temperature feedback. Adv. Funct. Mater. 26, 6060 (2016). https://doi.org/10.1002/adfm.201601953
H.D.A. Santos, E.C. Ximendes, M. del C. Iglesias-de la Cruz, et al., In vivo early tumor detection and diagnosis by infrared luminescence transient nanothermometry. Adv. Funct. Mater. 28, 1803924 (2018). https://doi.org/10.1002/adfm.201803924
B. del Rosal, D. Ruiz, I. Chaves-Coira et al., In vivo contactless brain nanothermometry. Adv. Funct. Mater. 28, 1806088 (2018). https://doi.org/10.1002/adfm.201806088
E.N. Cerón, D.H. Ortgies, B. del Rosal et al., Hybrid nanostructures for high-sensitivity luminescence nanothermometry in the second biological window. Adv. Mater. 27, 4781 (2015). https://doi.org/10.1002/adma.201501014
D. Ruiz, B. del Rosal, M. Acebrón et al., Ag/Ag2S nanocrystals for high sensitivity near-infrared luminescence nanothermometry. Adv. Funct. Mater. 27, 1604629 (2017). https://doi.org/10.1002/adfm.201604629
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Umezawa, M., Nigoghossian, K. (2021). Nanothermometry for Deep Tissues by Using Near-Infrared Fluorophores. In: Soga, K., Umezawa, M., Okubo, K. (eds) Transparency in Biology. Springer, Singapore. https://doi.org/10.1007/978-981-15-9627-8_7
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