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1 ergy transfer from an electronically excited photosensitizer.
2 by the productive coupling of a protein to a photosensitizer.
3 illuminated 1 d later for activation of the photosensitizer.
4 component of natural waters and an important photosensitizer.
5 epends on the PDT dose and the nature of the photosensitizer.
6 xic reactive oxygen species generated by the photosensitizer.
7 d to light and Pc 4, a mitochondria-targeted photosensitizer.
8 cognized as an efficient genetically encoded photosensitizer.
9 bpy)(3)]Cl(2) (bpy = 2,2'-bipyridine) as the photosensitizer.
10 upon attachment to the high molecular weight photosensitizer.
11 solution containing 2-acetonaphthone as the photosensitizer.
12 and, uniquely, a bacteriochlorophyll-derived photosensitizer.
13 emical transformation without the need for a photosensitizer.
14 y for treating local cancers using light and photosensitizer.
15 ed-state deactivation precludes their use as photosensitizers.
16 tionic heteroleptic iridium(III) polypyridyl photosensitizers.
17 astatic melanoma-are all recognized clinical photosensitizers.
18 n aqueous solution with a core of pi-stacked photosensitizers.
19 in vitro and in vivo relative to unmodified photosensitizers.
20 pramolecular systems that incorporate QDs as photosensitizers.
21 ceptor and electron donors, depending on the photosensitizers.
22 via optogenetics and induce microstrokes via photosensitizers.
23 riggering to facilitate on-demand release of photosensitizers.
24 ased materials for use as light emitters and photosensitizers.
25 c therapy efficacy and the safety profile of photosensitizers.
26 e to differentially localized singlet oxygen photosensitizers.
27 in some cases exceeding that of the leading photosensitizers.
28 te reactive T lymphocytes and identified the photosensitizer 2-Se-Cl, which accumulates in stimulated
29 CDs (a-CD) yet undoped g-CD display limited photosensitizer ability due to low extraction of photoge
30 ee homologous series of rigid-rod-like donor-photosensitizer-acceptor triads with p-xylene bridges.
31 target cells by light-directed activation of photosensitizers accumulated selectively in tumor tissue
34 otosensitizer construct was found to prevent photosensitizer aggregation, boost the generation of cyt
37 f catalytic amounts of [Ru(II)(bpy)3](2+) as photosensitizer and a sacrificial electron acceptor (Na2
38 Dissolved organic matter (DOM) can act as a photosensitizer and an inhibitor in the phototransformat
40 ed in systems with water-soluble CdSe QDs as photosensitizer and ascorbic acid as a sacrificial elect
41 water when paired with Ru(bpy)(3)(2+) as the photosensitizer and ascorbic acid as the sacrificial don
45 -driven conditions using [Ru(bpy)3](2+) as a photosensitizer and persulfate as a sacrificial electron
46 fast phase is the result of EngT between the photosensitizer and the Cu-site, rather than simple exci
47 trategy allows for tuning the ratios between photosensitizer and the switch molecule, enabling maximu
48 xafluorophosphate [Ir(ppy)2(dtbbpy)][PF6] as photosensitizer and triethanolamine (TEOA) as sacrificia
49 egies to interface solar fuel catalysts with photosensitizers and construct light-harvesting antennae
50 , 11) behaved as both singlet oxygen ((1)O2) photosensitizers and fluorescent molecules upon irradiat
51 e synthesized, characterized, and applied as photosensitizers and potential nano-PDT agents against p
52 ne (AQ) acceptor flanked by two Ru(bpy)3(2+) photosensitizers and two peripheral triarylamine (TAA) d
53 mediate the co-assembly of zinc porphyrins (photosensitizer) and iridium oxide hydrosol clusters (ca
54 m, composed of a nickel catalyst, an iridium photosensitizer, and an amine electron donor, is capable
55 (+) (L = macrocyclic ligand), [Ru(bpy)3](2+) photosensitizer, and an equimolar mixture of sodium asco
57 tion, the meticulous participation of light, photosensitizer, and oxygen greatly hinders the broad ap
58 dified nucleosides, a commercially available photosensitizer, and visible light irradiation constitut
59 the protein lysozyme and one of two possible photosensitizers: anthraquinone-2,6-disulphonate and fla
61 apies involving the use of light sources and photosensitizers are currently being developed, which ma
62 which use light-activated molecules known as photosensitizers, are highly selective against many mali
63 ry to ensure tumor-selective delivery of the photosensitizers, as well as, the photoactivating light
65 notherapy (PIT), that uses a target-specific photosensitizer based on a near-infrared (NIR) phthalocy
66 nd metal-free octasubstituted phthalocyanine photosensitizers bearing [(triethylammonio)ethyl]sulfany
68 ay, which expands the capabilities of cerium photosensitizers beyond our previous results that demons
69 ther, our study discovered eEF1A1 as a novel photosensitizer binding protein, which may play an essen
70 a promising way towards enhanced control of photosensitizer biodistribution and tumor-selective deli
72 ished the oxidative quenching of the excited photosensitizer by Ni4 P2 as the initiating step of HER
73 ylethene photochromic switch and a porphyrin photosensitizer by selective irradiation at distinct wav
74 address the issue of low cellular uptake of photosensitizers by cancer cells in photodynamic therapy
75 uld be turned over with catalytic amounts of photosensitizers by coupling salt metathesis and reducti
77 he molybdenum-iron protein labeled with a Ru-photosensitizer can support the light-driven, six-electr
79 light exposure following administration of a photosensitizer, can be a valuable treatment modality bu
80 ed a ROS-producing hybrid nanoparticle-based photosensitizer capable of maintaining high levels of RO
81 FF conjugates and a proof-of-concept for new photosensitizer carriers based on peptide conjugates.
82 f bacteria inactivation, we conjugated a PDT photosensitizer, cationic or neutral porphyrin, to a CAM
83 njection of liposomes containing TTX and the photosensitizer caused an initial nerve block lasting 13
84 on at remote ambient conditions including IC photosensitizer chemistry indicate less than 0.3% contri
86 according to the quantity and quality of its photosensitizers, chiefly chromophoric dissolved organic
92 ental parameters that include dark toxicity, photosensitizer concentration, light dose, and oxygenati
93 ical properties such as absorbed light dose, photosensitizer concentration, tissue oxygen concentrati
94 eveloped a CD44-targeted monoclonal antibody photosensitizer conjugate for combined fluorescent detec
97 sin receptor kinase C (TrkC) targeted ligand-photosensitizer construct, IYIY-diiodo-boron-dipyrrometh
99 CDOM may act both as sorbent for AAs and as photosensitizer, creating microenvironments with high co
103 low silica nanoparticles, is used to carry a photosensitizer drug and deliver it to breast tumors, du
105 dresses the challenge of the accumulation of photosensitizer drugs in tumors in photodynamic therapy.
106 ic therapy, which is based on the ability of photosensitizer drugs to cause Ca(2+)-dependent cytotoxi
107 ising treatment strategy where activation of photosensitizer drugs with specific wavelengths of light
108 The oxidative stress induced by iridium photosensitizers during photoactivation can increase the
109 or ligand, has been found to be a potent UVA photosensitizer, effective at nanomolar concentrations.
111 e-response studies with simultaneous SOL and photosensitizer fluorescence measurements under various
112 edure that relies on tumor localization of a photosensitizer followed by light activation to generate
113 ) involves the intravenous administration of photosensitizers followed by illumination of the tumor w
114 molecular-like properties are employed as a photosensitizer for hydrogen generation in a photoelectr
116 work, DBP-UiO, as an exceptionally effective photosensitizer for PDT of resistant head and neck cance
117 lorin e(6) conjugate may be a more efficient photosensitizer for PDT than the commercial currently us
118 evaluate the potential of this conjugate as photosensitizer for photodynamic therapy (PDT) of cancer
119 a porphyrin of type copper chlorophyll as a photosensitizer for PSSC that achieved a power conversio
120 nosized light-harvesters that are attractive photosensitizers for biological systems as they are wate
122 d 27 extracts that potentially contained new photosensitizers for chemical dereplication using an in-
123 pand the options for designing NIR-absorbing photosensitizers for future clinical cancer treatments.
124 evaluated for their collective potential as photosensitizers for metal-organic photodynamic therapy.
125 ) dyes, recently proposed as heavy atom free photosensitizers for O(2)((1)Delta(g)) generation, were
127 n of light-sensitive/photocaged molecules or photosensitizers for photocontrolled-delivery and photod
129 selenorhodamine core for their potential as photosensitizers for photodynamic therapy (PDT) in P-gly
130 rocycle were synthesized and investigated as photosensitizers for photodynamic therapy of tumors.
132 ty and aqueous solubility make CDs versatile photosensitizers for redox enzymes with great scope for
134 s study, we evaluated 24 chalcogenorhodamine photosensitizers for their ability to selectively deplet
136 light inactivation rates of MS2 coliphage in photosensitizer-free water were measured (kobs) under di
139 inglet oxygen and releasing the pheophorbide photosensitizer has been increased by the fluorination o
140 mbining molecularly targeted drugs and novel photosensitizers has the potential to improve further th
143 r moiety (distyryl-BODIPY) is connected to a photosensitizer (i.e., diiodo-distyryl-BODIPY) to form a
144 purpurine-5 has been shown to be a promising photosensitizer in antimicrobial photodynamic therapy (a
145 rOH) to a covalently linked [Ru(bpy)(3)](2+) photosensitizer in aqueous media has been systematically
146 where under visible light irradiation the Ir photosensitizer in conjunction with triethanolamine are
147 nding stability as a visible-light-absorbing photosensitizer in hydrogen-evolving homogeneous photoca
148 rom this study underscore the role of DOM as photosensitizer in limiting the persistence of pesticide
149 ains containing a covalently attached Ru(II) photosensitizer in order to circumvent the dependency on
150 r is established as one of the most relevant photosensitizers in aquatic environments, producing sing
152 tum dots (CQDs) are established as excellent photosensitizers in combination with a molecular catalys
153 traction (SPME-GC-MS), and photobleaching of photosensitizers in milk (riboflavin, protoporphyrin IX
156 therapy application, was tested as efficient photosensitizers in the photo-oxidations of 1,5-dihydrox
158 d to full-spectrum sunlight, the presence of photosensitizers increased k(obs) of HAdV2, PRD1 and MS2
159 ffects (AKIE) were almost identical for both photosensitizers, increased from 0.9958+/-0.0013 for 4-O
161 te quenching of four different model triplet photosensitizers induced by a suite of DOM from various
162 of the HeLa cells indicated that the studied photosensitizers induced damage primarily to the lysosom
163 imidazole-2-carboxaldehyde (IC) can act as a photosensitizer, initiating aerosol growth in the presen
166 rated to provide the synthetically versatile photosensitizer [Ir(ppy)2(dtbbpy)]PF6 in >1 g quantities
168 labile by encapsulation of a NIR-triggerable photosensitizer; irradiation at 730 nm led to peroxidati
169 I and II PDT agent to a predominantly type I photosensitizer, irrespective of the oxygen content.
170 ith improved stability and a modified Ru(II) photosensitizer is able to catalyze the light-driven hyd
172 fficient generation of singlet oxygen by the photosensitizer is observed when the diarylethene unit i
174 FeP variant labeled on its surface with a Ru-photosensitizer is shown to photocatalytically reduce pr
180 ilic chitosan nanocarriers tethered with the photosensitizer meso-tetraphenylporphyrin were synthesiz
181 tions, including variable (3)O(2), using the photosensitizer meta-tetra(hydroxyphenyl)chlorin (mTHPC)
183 ve cell ablation using a genetically encoded photosensitizer, miniSOG (mini singlet oxygen generator)
184 this problem, we report the development of a photosensitizer-MnO2 nanosystem for highly efficient PDT
186 nfold in the lipophilic environment, and the photosensitizer moiety can thus be inserted into the cel
191 p activity promotes the efficient removal of photosensitizer not sequestered in mitochondria and prot
192 atic carbonyl compounds) acting as potential photosensitizers of atmospheric relevant processes are e
193 ere found to have the highest potential as a photosensitizer on the basis of the quantum yield of ele
196 hroughput assessment of photodynamic therapy photosensitizer (PDT) efficacy on Escherichia coli.
198 emented tumors, following an affinity of the photosensitizer Photofrin for collagen-containing vascul
199 ug, Pc-(L-CA4)2, composed of the fluorescent photosensitizer phthalocyanine (Pc), an SO-labile aminoa
201 receptor (AhR) agonist, acts as a nanomolar photosensitizer potentiating UVA-induced oxidative stres
202 ons by selectively enhancing accumulation of photosensitizer PpIX together with TNF-alpha in tumors.
204 arbon monoxide dehydrogenase (CODH) and a Ru photosensitizer produces CO at a rate of 250 mumol of CO
205 the importance of the cellular membrane and photosensitizer properties in modulating the contributio
206 s FAP-TAPs provides a new spectral range for photosensitizer proteins that could be useful for imagin
207 atable polymeric nanodrug by conjugating the photosensitizer protoporphyrin IX (PpIX) and polyethylen
210 nactivation (CALI) using genetically-encoded photosensitizers provides an opportunity to determine ho
211 i-dimensional shape and lipophilicity of the photosensitizer (PS) affect cellular uptake, subcellular
212 When coupled with fluorescein (Fl) as the photosensitizer (PS) and triethylamine (TEA) as the sacr
215 randomly received the following: 1) PDT; 2) photosensitizer (PS); or 3) scaling and root planing (SR
216 ation of bacteria (PIB) uses light activated photosensitizers (PS) to generate reactive oxygen specie
217 ed a number of free and apidaecin-conjugated photosensitizers (PSs) differing in structure and charge
218 ',2''-terpyridine) have been investigated as photosensitizers (PSs) for photodynamic therapy (PDT).
220 field are the physicochemical properties of photosensitizers (PSs), optimal drug release profiles, a
221 hosphate (ZnP) nanoparticles loaded with the photosensitizer pyrolipid (ZnP@pyro) can kill tumor cell
222 ticles carry oxaliplatin in the core and the photosensitizer pyropheophorbide-lipid conjugate (pyroli
225 act with O2 without the need for an external photosensitizer, resulting in selective and reversible f
229 ore-shell silver-silica nanoparticles with a photosensitizer, Rose Bengal, tethered to their surface.
231 ment photosensitizer-trap molecule where the photosensitizer segment consists of a Br-substituted bor
232 S restores the sensitizing properties of the photosensitizer segment resulting in approximately 40-fo
233 capability of Mn(2+) -assisted assembly of a photosensitizer (sinoporphyrin sodium, DVDMS) is demonst
234 ently integrates the photochromic switch and photosensitizer, SO-PCN has demonstrated reversible cont
235 The presence of all four components, light, photosensitizer, sodium persulfate, and catalyst, are re
239 e bengal, and nitrite) and two model natural photosensitizers (Suwannee River natural organic matter
242 tely 1 mum size were loaded with OVA and the photosensitizer tetraphenyl chlorine disulphonate (TPCS2
244 derivatives 16b and 18b were more effective photosensitizers than amide derivatives 15b and 17b.
245 (IY-IY) that targets the TrkC receptor and a photosensitizer that acts as an agent for photodynamic t
247 rization of a dormant singlet oxygen ((1)O2) photosensitizer that is activated upon its reaction with
248 s administration of a photosensitive drug or photosensitizer that localizes at the tumor tissue follo
249 leotide (FMN), we have developed a promising photosensitizer that overcomes many of the problems that
250 ogenic dye, forming an 'on-demand' activated photosensitizer that produces singlet oxygen and fluores
252 ion and trigger MHCI presentation by using a photosensitizer that, upon light activation, would facil
253 Currently, there are only a small number of photosensitizers that are in the clinic and many of thes
255 troducing porphyrins in SCPNs leads to novel photosensitizers that can produce singlet oxygen ((1)O2)
257 A novel addition to the family of endogenous photosensitizers, the precise mechanism(s) through which
258 we show that RAFIs act like membrane-binding photosensitizers: their antiviral effect is dependent on
259 ient light-induced electron injection from a photosensitizer to a metal oxide, but other times not co
260 has required covalent attachment of a Ru(II) photosensitizer to a nonnative cysteine near the heme (R
261 og 6-thioguanine (6-TG), which acts as a UVA photosensitizer to generate reactive oxygen species (ROS
262 ructural optimization, photostabilizers, and photosensitizers to achieve suitable persistence), the p
263 Early pioneering studies used ruthenium photosensitizers to induce EleT in azurin and this exper
264 ated by the well-established capacity of PDT photosensitizers to serve as tumour-selective fluorescen
267 of laboratory studies, potentially acting as photosensitizers triggering secondary organic aerosol gr
270 position with consequences to tumor hypoxia, photosensitizer uptake, and PDT response were measured.
274 values obtained for the clinically approved photosensitizers verteporfin, temoporfin, protoporphyrin
275 s better than that of clinically established photosensitizers verteporfin, temoporfin, S3AlOHPc, or p
276 ht-activatable prodrug of PTX by conjugating photosensitizer via singlet oxygen-cleavable aminoacryla
279 such localised retinal bacteria, instead the photosensitizer was shown to be distributed throughout t
280 -Cl-aniline by excited triplet states of the photosensitizers was associated with inverse and normal
281 each high payloads close to 1:1, rendering a photosensitizer water-soluble and providing adjustable d
283 er (RET) mechanism to construct a novel dyad photosensitizer which is able to dramatically boost NIR
286 d via introduction of protoporphyrin (PPD, a photosensitizer) which has great doping affinity with po
287 e to the location and the orientation of the photosensitizer, which are very difficult to define in s
288 ond, the Au nanoparticles act as a plasmonic photosensitizer, which enables the solar-to-hydrogen con
291 was developed by conjugating a red-emissive photosensitizer with aggregation-induced emission (AIE)
292 etramethylpyridinium porphyrin (ZnTMPyP(4+)) photosensitizer with the multicopper oxidase (MCO) lacca
294 This led to the identification of 2 new photosensitizers with cyclic tetrapyrrolic structures, t
295 t studies have shown that the combination of photosensitizers with metalloenzymes can support a light
296 photocatalytic hydrogen evolution using COF photosensitizers with molecular proton reduction catalys
297 s able to controllably encapsulate cells and photosensitizer within pL-volume droplets, incubate the
298 chromophores-which should be able to act as photosensitizers within hybrid solar cells, leading to h
300 bles for improving the loading efficiency of photosensitizer (ZnO) as the semiconductor is directly c
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