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1                                              NIR and XRF spectra, combined with partial least squares
2                                              NIR band energy and intensity sensitively depend on the
3                                              NIR spectra were employed in raw form and preprocessed b
4                                              NIR wavelengths 890, 940nm (associated with fat) and 970
5                                              NIR-II fluorophores can provide noninvasive assessment o
6                                              NIR-II fluorophores draw from a broad spectrum of materi
7 length differences in the range of 70-100nm, NIR spectra in the wavenumber range of 4000-7500cm(-1) a
8 sulting in improved cell killing after a 2nd NIR-PIT session.
9                           Besides the Yb(3+) NIR emission, the hybrid composite shows organic chromop
10 or was significantly lower in group 3 and 5 (NIR-PIT groups) than in group 1, 2, and 4 (no NIR-PIT) y
11 t RFI in the d-tumor was highest in group 5 (NIR-PIT+additional APC) compared to the other groups.
12  environment (pH~5) and/or applying an 808nm NIR laser radiation.
13          In a tandem solar cell comprising a NIR BODIPY subcell and a matching "green" absorber subce
14 as designed to mimic the full process from a NIR measurement perspective, thereby facilitating a more
15 however, APCs administered immediately after NIR-PIT penetrated deeper into tissue resulting in impro
16 ased vascular permeability immediately after NIR-PIT.
17                           Cell killing after NIR-PIT was primarily on the surface, however, APCs admi
18 nticancer drug) and IR780 iodide (IR780) (an NIR-absorbing dye) into nanoparticles made of a eutectic
19                    After irradiating with an NIR laser, a good anti-tumor effect was observed owing t
20 es that dual noninvasive bioluminescence and NIR fluorescence imaging of cancer xenograft models repr
21  UV excitation at 325nm for quantum dots and NIR excitation at 980nm for upconverting nanoparticles,
22  of the fundus examination and of SW-FAF and NIR-FAF imaging were normal in both eyes, whereas NIR-RE
23 ngth (SW) fundus autofluorescence (FAF), and NIR reflectance (REF).
24 ween blue- and red-sensitive, and green- and NIR-responsive.
25 s(-1) ), low risk of release of Gd ions, and NIR-triggered drug release.
26                             Solution NMR and NIR spectroscopy suggest Np(IV) U(V) but single-crystal
27 ctivity, are characterized in the UV-vis and NIR wavelength ranges, at 1073 K.
28 ging instrument spanning the UV, visible and NIR regions (19 wavelengths ranging from 375 to 970nm).
29 ible effects were seen with long visible and NIR wavelength.
30 developing highly efficient UV, visible, and NIR light responsive photocatalysts.
31                       To find an appropriate NIR-absorbing BHJ is essential for highly efficient, org
32 tial use of [a]phenanthrene-fused BODIPYs as NIR bioimaging probes.
33 s use in optoelectronic applications such as NIR optical switches and photovoltaic devices.
34 iangle dissection at VR in 100% of cases, at NIR-C in 98.15%, and in 96.15% at IOC.Mean time to obtai
35 rightness in mammalian cells among available NIR FPs.
36 en present strategies to engineer BphP-based NIR fluorescent proteins and review their properties and
37 the first example of a lanthanide(III)-based NIR-emitting probe that can be targeted to a specific ty
38 ively, these results indicate that LbL-based NIR-II probes can serve as a promising theranostic platf
39 nsitizer which is able to dramatically boost NIR photon utility and enhance singlet oxygen generation
40 ges, and by the presence of hyper-AF on both NIR-AF and SW-AF images.
41 sequent burst release of Dox was achieved by NIR triggered collapse of HGNPs.
42 change in organic composition, as assayed by NIR, except for a decrease in the soluble sugar and an i
43 up to 127-times higher than that obtained by NIR fluorescence imaging.
44      The degree of drug release triggered by NIR laser light could be adjusted by varying the laser i
45 the release of a payload can be triggered by NIR light and the release rate can be modulated by a mag
46               Near-infrared cholangiography (NIR-C) provides real-time, radiation-free biliary anatom
47                                 By contrast, NIR stimulated cells when exposed to dermal tissue oxyge
48 t is believed that the remotely-controllable NIR-responsive lignin-AuNPs liquid marble can be used in
49 se control at 207 nm by using a conventional NIR pulse shaper.
50  regression models were applied to correlate NIR spectra with aforementioned fatty acids and lipid cl
51 ation of NIR-PIT is the inability to deliver NIR light to a tumor located deep inside the body.
52 w method to expand the options for designing NIR-absorbing photosensitizers for future clinical cance
53 ul implementation into photovoltaic devices, NIR optical switches and smart windows.
54  Before and after Calot triangle dissection, NIR-C was obtained by turning the camera to NIR mode.
55 d Class III structures that display distinct NIR transitions at 6500 and 4000 cm(-1).
56 l approach toward spectroscopically distinct NIR dyes for which the degree of electronic coupling cor
57           We aimed to prospectively evaluate NIR-C, VR-AR, and x-ray intraoperative cholangiography (
58                           Here, we evaluated NIR FPs of the iRFP protein family, which were reported
59  and iRFPs, the chimeric luciferases exhibit NIR bioluminescence with maxima at 670 nm and 720 nm, re
60 ll, operated in conjunction with an external NIR laser diode, is developed as a power delivery system
61 lution and tissue penetration depth, but few NIR-IIb probes exist.
62                            However, very few NIR-IIb fluorescent probes exist currently.
63                                To fluoresce, NIR FPs utilize an enzymatic derivative of heme, the lin
64 re 0.61, 0.79, 0.53, 0.77, 0.54 and 0.60 for NIR and 0.96, 0.93, 0.80, 0.79, 0.76 and 0.90 for XRF, r
65 ienopyrazine (TPz) building block allows for NIR photon absorption in dye-sensitized solar cells (DSC
66 irst time the promise of A-D-A type dyes for NIR OLEDs applications thereby paving the way for furthe
67 h a UV- and IR-translucent window (glass for NIR and CaF2 window for MIR).
68 as a biocompatible phase-change material for NIR-triggered drug release.
69 concept study provides a new methodology for NIR photocatalysis and would potentially guide future co
70 oparticle (UCNP)-based siRNA nanocarrier for NIR-controlled gene silencing.
71 hest value achieved so far by a "metal-free" NIR-OLED not intentionally benefitting from triplet-trip
72 ty were found using a PLS model derived from NIR (near infrared) spectra obtained in DRIFTS (diffuse
73 is a Stokes emission ( 1.30 eV) derived from NIR excitation ( 1.40 eV) on samples previously exposed
74                                           FT-NIR and ATR FT-MIR spectroscopy, coupled with spectral p
75 e of haddock (n=90), in comparison with a FT-NIR benchtop spectrometer.
76 ed using Fourier transform near infrared (FT-NIR) transmission spectroscopy in the range of 5435cm(-1
77 to damaging Abeta oligomers, thus furthering NIR light therapy as a viable treatment for AD.
78  Thus, the work demonstrated that a handheld NIR device can be a simple, cost-effective, and reliable
79 tudy evaluates the reliability of a handheld NIR device in distinguishing fillets and patties of Atla
80                                        Here, NIR-II fluorescent probes, including down-conversion nan
81                            More importantly, NIR-controlled spatiotemporal knockdown of GFP expressio
82 ow-bangap PTB7-Th and small-bandgap ATT-2 in NIR region, the proof-of-concept STOPVs show the highest
83 , representing the brightest organic dyes in NIR-II region reported so far.
84                               Near infrared (NIR) and X-ray fluorescence (XRF) spectroscopy were inve
85 arrays, functionalized with a near infrared (NIR) fluorophore-conjugated immunoassay to Carbohydrate
86 ion by simply controlling the near infrared (NIR) irradiation.
87 tion from ultraviolet (UV) to near infrared (NIR) is one of the key factors to ensure high photocurre
88 t of a treatment of mice with near infrared (NIR) light on synaptic vulnerability to Abeta oligomers.
89 ocarrier for targeted, pH-and near infrared (NIR) radiation dual-stimuli triggered drug delivery.
90 nous fluorescence, UV-Vis and near infrared (NIR) spectroscopy coupled with chemometric methods to di
91 s to explore the potential of near infrared (NIR) spectroscopy to quantify volatile compounds in Vinh
92  amylose content in rice with near infrared (NIR) spectroscopy, associated with a suitable multivaria
93 using optical illumination at near infrared (NIR) wavelengths, to which the skin is highly transparen
94 y nonlinear excitation at the near infrared (NIR) window.
95 ad of using tandem devices or near infrared (NIR)-absorbing Sn-containing perovskites.
96 taneously possess substantial near-infrared (NIR) absorptivity and long-lived, high-yield triplet exc
97                    Metal-free near-infrared (NIR) active unsymmetrical squaraine dyes, RSQ1 and RSQ2,
98        Fourier transform (FT) near-infrared (NIR) and attenuated total reflection (ATR) FT mid-infrar
99 oherence tomography (SD-OCT), near-infrared (NIR) and short-wavelength (SW) fundus autofluorescence (
100 on reflectance at visible and near-infrared (NIR) bands with high spatial and temporal resolutions, a
101                             A near-infrared (NIR) calibration was developed using an efficient offlin
102  (LP) and MeHg(+) -responsive near-infrared (NIR) cyanine dye (hCy7) for MeHg(+) detection within liv
103 ogies are demonstrated on two near-infrared (NIR) data sets.
104  if we loaded the hydrophobic near-infrared (NIR) dye IR780 into the liposome phospholipid bilayer, t
105 ly, by using a profluorescent near-infrared (NIR) dye, we characterize the nature of NTR activity loc
106 (MCs) that possess attractive near-infrared (NIR) emission and are highly photostable.
107 ise ratios, luminophores with near-infrared (NIR) emission are particularly important for in vivo use
108 vely low brightness and short-near-infrared (NIR) emission.
109                               Near-infrared (NIR) emitters that can also be excited with NIR radiatio
110  = 266 nm) with an overlapped near-infrared (NIR) energy addition pulse (lambda = 1064 nm).
111  (CQ) conjugate-based turn-on near-infrared (NIR) fluorescence probe for specific detection of beta-a
112  donor-acceptor-donor (D-A-D) near-infrared (NIR) fluorescent compounds were synthesized through a ra
113  were composed with green and near-infrared (NIR) fluorescent dyes tethered to Schaap's dioxetane.
114                               Near-infrared (NIR) fluorescent dyes with favorable photophysical prope
115 eporters for luciferase and a near-infrared (NIR) fluorescent protein (iRFP670), with the latter fuse
116                     Monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as pr
117             Several series of near-infrared (NIR) fluorescent proteins (FPs) were recently engineered
118 rate, CNIR800, that carries a near-infrared (NIR) fluorochrome IRDye 800CW, with a quencher connected
119 orm by quantitatively imaging near-infrared (NIR) Forster resonance energy transfer (FRET) both in vi
120 olecules in an intense 800-nm near-infrared (NIR) laser field.
121 oreceptors absorb far-red and near-infrared (NIR) light and regulate light responses in plants, fungi
122  release system responsive to near-infrared (NIR) light is developed for intracellular drug delivery.
123 ly to UV irradiation, but not near-infrared (NIR) light that offers a deeper tissue penetration depth
124 further activated with 808-nm near-infrared (NIR) light to generate heat for photothermal therapy (PP
125 ow gold nanoshells (HGNs) and near-infrared (NIR) light.
126                   A series of near-infrared (NIR) organic emissive materials were synthesized and the
127 ting polymer based far-red to near-infrared (NIR) Pdot nanoprobe for the ratiometric detection of hyp
128 o overcome this limitation, a near-infrared (NIR) photothermal activation method is presented for con
129 ibody (mAb) conjugated with a near-infrared (NIR) phthalocyanine dye IRDye 700DX.
130 o strongly influenced modeled near-infrared (NIR) reflectance, explaining why both modeled and observ
131 ilon > 10(5) M(-1) cm(-1)) in near-infrared (NIR) region and exhibit similar optical and electrochemi
132 in the deep-tissue-penetrable near-infrared (NIR) region has been the major hurdle that has hindered
133      Strong absorbance in the near-infrared (NIR) region is observed for 1-7 with the lowest-energy a
134 eed to be harvested in UV-vis-near-infrared (NIR) region to generate high photocurrent, which leads t
135 range from the visible to the near-infrared (NIR) regions.
136  in vivo imaging due to their near-infrared (NIR) spectra and use of available in mammalian cells bil
137 electronic transitions in the near-infrared (NIR) spectral region.
138 ectral imaging (HSI) combines Near-infrared (NIR) spectroscopy and digital imaging to give informatio
139                               Near-infrared (NIR) spectroscopy was evaluated as a rapid method for th
140 red with those obtained using near-infrared (NIR) spectroscopy.
141 the near-ultraviolet (NUV) to near-infrared (NIR) spectrum along with favorable excited-state propert
142 tor) oligomer emitting in the near-infrared (NIR) thanks to delocalisation of the BODIPY low-lying lo
143 ed a strong absorption in the near-infrared (NIR) window and enhanced the transverse relaxation (T2 )
144           In this system, the near-infrared (NIR)-absorbing PDA acts as a platform for the assembly o
145 visible spectrum, including a near-infrared (NIR)-emitting cyanine dye.
146 ced (DLR) sensors make use of near-infrared (NIR)-emitting Egyptian blue as a reference material and
147 nthesis of highly luminescent near-infrared (NIR)-emitting gold nanoclusters (AuNCs) using bovine ser
148 rolled drug delivery/release, near-infrared (NIR)-excited deep PDT, and radiosensitization, respectiv
149 ne-based anions paired with a near-infrared (NIR)-selective heptamethine cation.
150 ging from ultraviolet (UV) to near-infrared (NIR).
151  compared to red (660 nm) and near-infrared (NIR, 810 nm).
152 ic (PA) imaging in the second near-infrared (NIR-II) window (1000-1350 nm).
153 ful and versatile arsenal for intraoperative NIR imaging in real time.
154 c8 luciferase fused with iRFP670 and iRFP720 NIR fluorescent proteins.
155  under UV, visible, and near-infrared light (NIR) irradiation, which can be attributed to the vacancy
156 on energy via chemical defects and emit long-NIR afterglow luminescence at 780 nm with a half-life of
157 ible electrochemical doping creating midgap (NIR absorbing) polaronic states.
158                                    Moreover, NIR experiments were performed in order to compare spect
159 linear tetrapyrroles, BphPs exhibit the most NIR-shifted spectra that reside within the NIR tissue tr
160 acy, open up the possibility for multiplexed NIR-fluorescence enhancement microarrays, for early canc
161                                          New NIR spectroscopy combined with multivariate analysis for
162 ld potentially guide future conceptually new NIR responsive system designs.
163 otostable, renal clearable, and nontoxic new NIR probe (CyG) for precise quantification of albumin in
164 orophore scaffolds in the development of new NIR probes for bioimaging.
165 esults show the feasibility of using the new NIR handheld spectrometer to determine quality parameter
166  with multiple MLCT bands in the 800-1100 nm NIR region and a red-shifted Soret band (lambdamax, 443
167 e near-infrared region between 1500-1700 nm (NIR-IIb window) affords high spatial resolution, deep-ti
168 e near-infrared window between 1500-1700 nm (NIR-IIb window) offers superior spatial resolution and t
169 (AF) images at 488 nm (SW-AF) and at 787 nm (NIR-AF).
170 IR-PIT groups) than in group 1, 2, and 4 (no NIR-PIT) yet there was no significant difference in d-tu
171 s, the PEG-coated AMQDs demonstrated notable NIR-induced tumor ablation ability.
172 in electron density associated with each NUV-NIR absorption transition.
173 e anticipate that our strategy for obtaining NIR luminophores will open new doors for further explora
174         The development of a unique class of NIR dyes via modifying the rhodol scaffold with fused te
175           Here, we report the development of NIR to UV-Vis-NIR UCNPs consisting of LiYF4:Yb(3+)/Tm(3+
176 nd 4683-4335cm(-1)) shows the feasibility of NIR technology for determination of the amylose with hig
177 ased PTAs also exhibited a unique feature of NIR-induced rapid degradability.
178 S regression were used for interpretation of NIR spectral data.
179                              A limitation of NIR-PIT is the inability to deliver NIR light to a tumor
180             Ex vivo spectral measurements of NIR fluorescence through the skin showed linear response
181 up was developed and tested for measuring of NIR (760nm excitation) emission spectra in the skin.
182 minescent luminophores with a direct mode of NIR light emission that are suitable for use under physi
183 ere, we report on fluorescence properties of NIR FPs with key alterations in their BV binding sites.
184 iew provides guidelines for the selection of NIR probes and tools for noninvasive imaging, sensing, a
185  with acute vision loss and abnormalities on NIR-REF imaging, especially if multimodal imaging suppor
186                                          Our NIR probe was able to image cells transfected with beta-
187            Near-infrared photoimmunotherapy (NIR-PIT) is a new cancer treatment that combines the spe
188                                          PLS-NIR has a good predictive capability with relative root
189  conjunction with an exceptionally low-power NIR LED light irradiation (10 mW cm(-2) ), these nanopar
190                                 The proposed NIR-VISPAOCT system has potential applications in neuros
191 very system using a near-infrared-radiation (NIR) responsive hollow gold nanoparticle (HGNPs) to achi
192 nanoparticles (MNPs) with near infrared ray (NIR) biophotonic possess tremendous potential for non-in
193 eic acid probes bearing a tetrazine-reactive NIR fluorogen.
194                  The overall near infra-red (NIR) emission intensity of Yb(3+) ions is increased by a
195 lasts exposed to visible and near infra-red (NIR) light.
196 /green which inhibited proliferation and red/NIR which stimulated proliferation, all at 3 J/cm(2).
197 MMP) and lowered intracellular pH, while red/NIR had the opposite effect.
198   Blue/green reduced cellular ATP, while red/NIR increased ATP in a biphasic manner.
199 e (FAF), confocal near-infrared reflectance (NIR), and high-resolution optical coherence tomography v
200 the fastest video-rate imaging in the second NIR window with approximately 50-fold reduced exposure t
201 activity can be exploited both for selective NIR imaging of mitochondria and for mitochondrial target
202 fluorescent turn-on probes, WSP-NIR and SeSP-NIR, were devised for the detection of H2 S.
203                               The probe SeSP-NIR was applied in visualizing intracellular H2 S.
204 LP-hCy7 nanoprobe displays unique dual-shift NIR absorbance peaks and produces a normalized turn-on r
205                  This paper reports a simple NIR-to-UV upconversion nanoparticle (UCNP)-based siRNA n
206 and analytical approaches, such as spectral (NIR spectra), multi-elemental (Fe, Zn, Mn, Cu, Li, Sr) a
207 of organic salts for inexpensive, and stable NIR-selective molecular salt photovoltaics.
208   This study presents photolytically stable, NIR photoluminescent, porous silicon nanoparticles with
209 -(PM')n-M), wherein high-oscillator-strength NIR absorptivity up to 850 nm, near-unity intersystem cr
210 cceptor material ATT-2, which shows a strong NIR absorption between 600 and 940 nm with an Eg(opt) of
211 CDPGM NPs show good biocompatibility, strong NIR absorption, high relaxivity (r 1 = 14.06 mM(-1) s(-1
212                   The cations exhibit strong NIR bands at approximately 1000 nm and 2000-5000 nm, whi
213 blies of protein complexes with a sulfonated NIR-II organic dye (CH-4T) to produce a brilliant 110-fo
214 ell-based libraries of reversibly switchable NIR fluorescent proteins.
215  deep within body, it is less effective than NIR-PIT, possibly related to the relatively lower effici
216 er efficiency of short wavelength light than NIR.
217            This study provides evidence that NIR light can effectively reduce synaptic vulnerability
218                                We found that NIR FP variants with Cys in the GAF or with Cys in both
219  PCA exploratory analysis, which showed that NIR spectra would be suitable for the classification tas
220                                          The NIR polymeric NPs are small ( approximately 50 nm), show
221 Using optical scattering and absorption, the NIR-VISPAOCT system simultaneously provides surgeons wit
222  irradiation and emitted fluorescence at the NIR region with large Stokes shift, high quantum yield,
223 ivation of the subcutaneous dose from by the NIR laser.
224             The UV emission generated by the NIR-activated UCNP effectively triggers the trans-to-cis
225 l, which causes important differences in the NIR emission dynamics.
226 r moiety of the photosensitizer alone in the NIR range.
227 with direct light emission wavelength in the NIR region.
228 ow that 4a-c strongly absorb and emit in the NIR spectral region, in the range 642-701 nm.
229 The TSPNs generate a strong PA signal in the NIR-II optical window, where background signals from end
230                 TSPN as a PA contrast in the NIR-II window opens new opportunities for biomedical ima
231 ature in the mouse brain and hindlimb in the NIR-IIb window with short exposure time of 20 ms for rar
232                                 Notably, the NIR spectral domain absorptivities of M-(PM')n-M chromop
233                              Analysis of the NIR and IR spectra indicates that the polaron is delocal
234 he first demonstration of (i) the use of the NIR emission arising from a single lanthanide(III) catio
235 ian cancer mouse model demonstrated that the NIR dye DiD encapsulated BCM could preferentially accumu
236 nd PLS-DA, respectively, indicating that the NIR spectra can be used as an alternative to evaluate th
237         In addition, we demonstrate that the NIR-II molecular complexes are superior to clinically ap
238  a broad wavelength range from the UV to the NIR region (1450 nm).
239 dustrial sectors, sensing from the UV to the NIR region is of critical importance.
240  samples were correctly classified using the NIR spectra of milk dried on paper.
241 t NIR-shifted spectra that reside within the NIR tissue transparency window.
242 o have reasonable quantum yields within this NIR region (>1%), with emission wavelengths reaching 100
243  NIR-C was obtained by turning the camera to NIR mode.
244 ansion of tetrazine fluorogenic chemistry to NIR dyes, we believe highly selective proximity-induced
245 t induces rapid cell death after exposure to NIR light.
246 g, such as high brightness, ideal far-red to NIR optical window, excellent photostability, self-refer
247 effect and quick drug release in response to NIR irradiation.
248 served EVI, which is especially sensitive to NIR, captures canopy seasonal dynamics well.
249 nent, we realized the first COF-based UV- to NIR-responsive photodetector.
250 ich originates from (1) Enhancing far red-to-NIR (700~1200 nm) harvesting, up to 25%.
251 the structural effects on obvious far red-to-NIR photocatalysis enhancement, which originates from (1
252 e proteins, including use of minimally toxic NIR light, labeling without need for genetic interventio
253                Here we report that transient NIR exposure is dissipation-free and has no adverse effe
254                            Based on WR6, two NIR fluorescent turn-on probes, WSP-NIR and SeSP-NIR, we
255  efficiently released into the cytosol under NIR irradiation, resulting in enhanced anticancer activi
256 rform the following multiple functions under NIR excitation at 800 nm: 1) Light harvesting by the UCN
257 elivery of miR-21i and Dox using HGNPs under NIR after intravenous administration showed high tumor a
258 cting metal ions in biological systems under NIR light that exhibits lower phototoxicity and higher t
259 ating the TSDP onto gold nanoshells and upon NIR illumination, the increased temperature dehybridizes
260                               Moreover, upon NIR laser irradiation, the tumor is completely eliminate
261 YbLD)2Tbx] (x = 1 to 3) complexes that, upon NIR excitation at 980 nm, showed an unprecedented Yb to
262 of Sultanate of Oman and were measured using NIR spectroscopy in absorption mode in the wavelength ra
263               The current methodology, using NIR spectroscopy and chemometrics, can be seen as a prom
264 nd the season of ewe's milk production using NIR spectroscopy.
265 ging guided photothermal therapy (PTT) using NIR excitation.
266  mice was followed in vivo and ex vivo using NIR luminescence.
267 nal control of drug release was achieved via NIR laser light and plasma concentrations of the model d
268 ctaphyrin is a potent chromophore with a vis-NIR absorption profile strongly influenced by the redox
269 electrochemical oxidation, and probed by vis-NIR-IR and EPR spectroscopies.
270 sured soil, and a visible-near-infrared (vis-NIR) spectrometer to measure iron oxides and clay minera
271 on radicals are characterized by in situ vis-NIR absorption and electron paramagnetic resonance spect
272 m a broad range of methods, including UV-vis-NIR absorption and MCD spectroscopies, single-crystal X-
273 pectively, were probed extensively by UV-vis-NIR absorption, EPR, and electron nuclear double resonan
274  experiments and variable temperature UV-Vis-NIR and EPR spectroscopic data indicate that, relative t
275 eudorotaxanes were obtained using the UV-vis-NIR dilution method and the [2]pseudorotaxanes were char
276                                       UV-Vis-NIR measurements reveal that only the m-xylylene-linked
277 scanning calorimetry and (1)H NMR and UV-vis-NIR spectroscopies is presented, demonstrating this DHAP
278 heterostructure studied using XPS and UV-Vis-NIR spectroscopy.
279 , we report the development of NIR to UV-Vis-NIR UCNPs consisting of LiYF4:Yb(3+)/Tm(3+)@SiO2 individ
280 d results of electron spin resonance, UV-vis-NIR, and ultraviolet photoelectron spectroscopy.
281 c species formed were investigated by UV-vis-NIR, fluorescence and EPR spectroscopy, spectroelectroch
282 ted by spectroscopic data ((1) H-NMR, UV-vis-NIR, infra-red, (57) Fe-Mossbauer, EPR), X-ray crystallo
283 o-absorption, which were confirmed by UV/Vis-NIR diffuse reflectance spectra (DRS) and photocurrent m
284 AF imaging were normal in both eyes, whereas NIR-REF imaging showed a region of hyporeflectance tempo
285  imaging in the second near-infrared window (NIR-II) allows visualization of deep anatomical features
286  systems in the second near-infrared window (NIR-II) can probe tissue at centimetre depths and achiev
287  new design for second near-infrared window (NIR-II) molecular fluorophores based on a shielding unit
288  imaging in the second near-infrared window (NIR-II, 1,000-1,700 nm) features deep tissue penetration
289                                Compared with NIR FPs in which BV covalently binds to Cys15 or those t
290                HyP-1 is also compatible with NIR fluorescence imaging, establishing its versatility a
291 (NIR) emitters that can also be excited with NIR radiation via two-photon processes can mitigate thes
292  in the visible region upon irradiation with NIR light through a multiphoton mechanism.
293 ced by photoabsorbers after irradiation with NIR light.
294         Image quality scores were lower with NIR-C versus AR (P = 0.018) and versus IOC (P < 0.0001).
295 tional chemo-PTT therapy of ICG-EPI NPs with NIR laser irradiation synergistically induced apoptosis
296 handle and easier to initiate than PETN with NIR lasers.
297 e to obtain relevant images was shorter with NIR-C versus AR (P = 0.008) and versus IOC (P = 0.000000
298 olated from wild type (wt) mice treated with NIR light was significantly reduced and the resulting su
299  Similarly, APP transgenic mice treated with NIR showed a significant reduction of endogenous Abeta a
300 WR6, two NIR fluorescent turn-on probes, WSP-NIR and SeSP-NIR, were devised for the detection of H2 S

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