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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
32 nce, independence of oxygen, small size, and photosensitizer activity.
33 the preferential intercalation of riboflavin photosensitizer adjacent to (Me)C:G base pairs.
34 otosensitizer construct was found to prevent photosensitizer aggregation, boost the generation of cyt
35 lative to that of the acceptor moiety of the photosensitizer alone in the NIR range.
36           Copper Cysteamine (Cu-Cy) is a new photosensitizer and a novel radiosensitizer that can be
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
39      In conjunction with [Ru(bpy)3](2+) as a photosensitizer and ascorbate as an electron donor, MOF-
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
42 ared using a pyrazine-based linker to join a photosensitizer and catalyst moiety.
43                  At equivalent dose of drug, photosensitizer and light irradiation, combination thera
44 ivity to the photochemical treatment itself (photosensitizer and light without MH3-B1/rGel).
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
56 , CMP-L-CA4, where CMP is dithiaporphyrin, a photosensitizer, and L is an aminoacrylate linker.
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
60 e surface of particles when only traces of a photosensitizer are present in the seed aerosol.
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
64                        Activation of the new photosensitizer at low concentrations (0.1-1 muM) by com
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
67                          Tumor uptake of the photosensitizer (benzoporphyrin derivative monoacid ring
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
71  more clinically feasible dosimetry based on photosensitizer bleaching.
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
76 ets converted by cells of the tissue in to a photosensitizer called protoporphyrin IX (PPIX).
77 he molybdenum-iron protein labeled with a Ru-photosensitizer can support the light-driven, six-electr
78              Humic substances (HS) acting as photosensitizers can generate a variety of reactive spec
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
85 aboratory observations of SOA production via photosensitizer chemistry.
86 according to the quantity and quality of its photosensitizers, chiefly chromophoric dissolved organic
87        In our design, MnO2 nanosheets adsorb photosensitizer chlorin e6 (Ce6), protect it from self-d
88 ith biocompatible Zn(2+) and encapsulate the photosensitizer chlorin e6 (Ce6).
89                     With azine-linked N2-COF photosensitizer, chloro(pyridine)cobaloxime co-catalyst,
90                           In the presence of photosensitizer-collagen localization, PDT effects on co
91                                    These new photosensitizer compounds have been evaluated for their
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
95              Here we report a type of hybrid photosensitizers consisting of plasmonic silver nanopart
96                            PEGylation of the photosensitizer construct was found to prevent photosens
97 sin receptor kinase C (TrkC) targeted ligand-photosensitizer construct, IYIY-diiodo-boron-dipyrrometh
98                               The lipophilic photosensitizer could be introduced in a quantitative an
99  CDOM may act both as sorbent for AAs and as photosensitizer, creating microenvironments with high co
100        As a new type of radiosensitizers and photosensitizers, Cu-Cy nanoparticles have a good potent
101         Our results indicate that the hybrid photosensitizers display low cytotoxicity without light
102 d visible light in the presence of different photosensitizers dissolved in buffered solutions.
103 low silica nanoparticles, is used to carry a photosensitizer drug and deliver it to breast tumors, du
104                            Without light the photosensitizer drugs are minimally toxic and the photoa
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.
110                The presence of model natural photosensitizers either reduced or did not affect photoi
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
115                Using metal nanoclusters as a photosensitizer for hydrogen generation lays the foundat
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
121                                        Ideal photosensitizers for cancer treatment should both have g
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
126              Application of the complexes as photosensitizers for photocatalytic generation of hydrog
127 n of light-sensitive/photocaged molecules or photosensitizers for photocontrolled-delivery and photod
128 eatment of lesioned tissues, and delivery of photosensitizers for photodynamic cancer therapy.
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.
131                 The combination of light and photosensitizers for phototherapeutic interventions, suc
132 ty and aqueous solubility make CDs versatile photosensitizers for redox enzymes with great scope for
133           They are mostly known as efficient photosensitizers for the generation of singlet oxygen vi
134 s study, we evaluated 24 chalcogenorhodamine photosensitizers for their ability to selectively deplet
135 es these bacteriochlorins great potential as photosensitizers for treatment of cancer.
136 light inactivation rates of MS2 coliphage in photosensitizer-free water were measured (kobs) under di
137 ural extracts to search for structurally new photosensitizers from Malaysian biodiversity.
138                The presence of the synthetic photosensitizers generally enhanced photoinactivation of
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
141                     Certain cationic dyes or photosensitizers have good specificity for binding to mi
142                            The origin of the photosensitizer, however, remains unclear.
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
151                              The efficacy of photosensitizers in cancer phototherapy is often limited
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
154          The proximity of Ni4 P2 to multiple photosensitizers in Ni4 P2 @MOF allows for facile multi-
155 and could be potential candidates for use as photosensitizers in photodynamic therapy (PDT).
156 therapy application, was tested as efficient photosensitizers in the photo-oxidations of 1,5-dihydrox
157       Transition-metal complexes are used as photosensitizers, in light-emitting diodes, for biosensi
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
160              At higher doses, however, these photosensitizers induce "dark toxicity" through light-in
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
164 lecule, resulting in a constitutively active photosensitizer inside the cell.
165                                   Assembling photosensitizers into nanostructures can improve photody
166 rated to provide the synthetically versatile photosensitizer [Ir(ppy)2(dtbbpy)]PF6 in >1 g quantities
167 tibody conjugate with a phthalocyanine-based photosensitizer, IR700.
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
171                                          The photosensitizer is also a potent stimulator of P-glycopr
172 fficient generation of singlet oxygen by the photosensitizer is observed when the diarylethene unit i
173     A genetically encodable, protein-encased photosensitizer is one way to achieve this goal.
174 FeP variant labeled on its surface with a Ru-photosensitizer is shown to photocatalytically reduce pr
175  for understanding the photochemistry of the photosensitizer KillerRed.
176 let oxygen ((1)O(2)) through interactions of photosensitizer, light, and oxygen ((3)O(2)).
177 ed here operates at low 1 mol % catalyst and photosensitizer loadings.
178             Together, our findings show that photosensitizer localization to collagen increases vascu
179           The high selectivity of this novel photosensitizer may have broad applications and provide
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)
182                      We used three synthetic photosensitizers (methylene blue, rose bengal, and nitri
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
185                    This solvation-controlled photosensitizer model has possible applications as a the
186 nfold in the lipophilic environment, and the photosensitizer moiety can thus be inserted into the cel
187                     Damage to DNA bound to a photosensitizer molecule frequently proceeds by one-elec
188                           Upon illumination, photosensitizer molecules produce reactive oxygen specie
189                                    The model photosensitizers, namely 9,10-anthraquinone-1,5-disulfon
190 of magnitude greater than rates reported for photosensitizer/[Ni(P2(Ph)N2(Ph))2](BF4)2 systems.
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
194   Notably, this method requires no exogenous photosensitizers or external oxidants.
195 oom temperature without the aid of exogenous photosensitizers or oxidants.
196 hroughput assessment of photodynamic therapy photosensitizer (PDT) efficacy on Escherichia coli.
197                             Recently several photosensitizer-photochromic-switch dyads were reported
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
200           Our results showed that the tested photosensitizer possesses very interesting biological ac
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.
203 tion of boronic acids with methylene blue as photosensitizer proceeds with high efficiency.
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
208                                              Photosensitizer protoporphyrin IX (PpIX) fluorescence, i
209         Hence, vaccine particles with Ag and photosensitizers proved an effective vehicle or adjuvant
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
213 namic therapy where the design of the active photosensitizer (PS) is very crucial.
214              By mixing in solution a triplet photosensitizer (PS) with the photoCORM and shining red
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).
219                                    Rhodamine photosensitizers (PSs) substituting S or Se for O in the
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
223         Quantitative, unquenched activatable photosensitizers (QUaPS) hold potential for new feedback
224                    During the transport, the photosensitizer remains nonreactive to light, offering a
225 act with O2 without the need for an external photosensitizer, resulting in selective and reversible f
226 rmed to be activated photodynamically by the photosensitizer Rose Bengal.
227                                          The photosensitizers rose bengal (RB) and acridine orange (A
228 rom macrophages exposed to visible light and photosensitizer (rose bengal).
229 ore-shell silver-silica nanoparticles with a photosensitizer, Rose Bengal, tethered to their surface.
230  acts as a substitute for the precious metal photosensitizer [Ru(bpy)3](2+).
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
236                         Other, more abundant photosensitizer species, such as humic-like substances (
237 ) due to accumulation of naturally occurring photosensitizers such as porphyrins and flavins.
238                                              Photosensitizers such as the small cationic molecule EtN
239 e bengal, and nitrite) and two model natural photosensitizers (Suwannee River natural organic matter
240                    Here we employ two azurin photosensitizer systems, the previously reported Ru(2,2'
241                  This targeted and activated photosensitizer (TAPs) approach enables protein inactiva
242 tely 1 mum size were loaded with OVA and the photosensitizer tetraphenyl chlorine disulphonate (TPCS2
243 crobial origin was found to be a more potent photosensitizer than NOM from terrestrial sources.
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
246 sacrificial electron acceptor to oxidize the photosensitizer that in turn drives the catalysis.
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
251            The first mitochondrion-anchoring photosensitizer that specifically generates singlet oxyg
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
254             One method is to use activatable photosensitizers that can both induce cell death (via si
255 troducing porphyrins in SCPNs leads to novel photosensitizers that can produce singlet oxygen ((1)O2)
256              Mild PD stress mediated by both photosensitizers that elicits no significant morphologic
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
265 ancement of toxicity after PCI utilizing the photosensitizer TPCS2a (Amphinex(R)).
266       The compound is based on a two segment photosensitizer-trap molecule where the photosensitizer
267 of laboratory studies, potentially acting as photosensitizers triggering secondary organic aerosol gr
268              By using an inexpensive organic photosensitizer under visible-light excitation (lambda >
269 supplied from the photochemically reduced Ru photosensitizer unit.
270 position with consequences to tumor hypoxia, photosensitizer uptake, and PDT response were measured.
271 peutic agents including nanotechnology-based photosensitizers used in PDT.
272                                              Photosensitizers used in such hybrid systems are typical
273                                              Photosensitizers used to date have been either exogenous
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
277               Moreover, in the presence of a photosensitizer, visible-light energy is the only fuel s
278                   After internalization, the photosensitizer was photoactivated, significantly increa
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
282                       PEGylated chlorin e(6) photosensitizers were synthesized with tri(ethylene glyc
283 er (RET) mechanism to construct a novel dyad photosensitizer which is able to dramatically boost NIR
284                   PCI employs an amphiphilic photosensitizer which localizes in the membranes of endo
285               Photodynamic therapy that uses photosensitizers which only become toxic upon light-irra
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
289 do-4-methyl-benzenechloride, complex 1, as a photosensitizer, which works under visible light.
290                               By tethering a photosensitizer with a hydrogen-evolving catalyst, attac
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
293 d catalyst and an organic dye can be used as photosensitizers with 0.5 mol % loading.
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
299 hown to significantly outperform the control photosensitizers without adsorbing moieties.
300 bles for improving the loading efficiency of photosensitizer (ZnO) as the semiconductor is directly c

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