ライフサイエンスコーパス: photosensitizer

1 esoporous carbon nitride (mpg-CN(x) ) as the photosensitizer.

2 ansfer kinetics rather than as a traditional photosensitizer.

3 emical transformation without the need for a photosensitizer.

4 and, uniquely, a bacteriochlorophyll-derived photosensitizer.

5 uced electron transfer (PET) with DCA as the photosensitizer.

6 y for treating local cancers using light and photosensitizer.

7 ergy transfer from an electronically excited photosensitizer.

8 by the productive coupling of a protein to a photosensitizer.

9 illuminated 1 d later for activation of the photosensitizer.

10 component of natural waters and an important photosensitizer.

11 epends on the PDT dose and the nature of the photosensitizer.

12 t irradiation using [Ru(bpy)(3) ](2+) as the photosensitizer.

13 ith ultrasound also triggered the release of photosensitizer.

14 he unique photophysical behavior of cagelike photosensitizer.

15 hus obviating the necessity of any exogenous photosensitizer.

16 the intrinsic excited-state lifetime of the photosensitizer.

17 nge of potential applications for iron-based photosensitizers.

18 molecules such as lipids, carbohydrates and photosensitizers.

19 ed-state deactivation precludes their use as photosensitizers.

20 in vitro and in vivo relative to unmodified photosensitizers.

21 riggering to facilitate on-demand release of photosensitizers.

22 ased materials for use as light emitters and photosensitizers.

23 c therapy efficacy and the safety profile of photosensitizers.

24 e to differentially localized singlet oxygen photosensitizers.

25 in some cases exceeding that of the leading photosensitizers.

26 tionic heteroleptic iridium(III) polypyridyl photosensitizers.

27 enhance PDT via the controllable release of photosensitizers.

28 in the presence and absence of various model photosensitizers.

29 should be considered in the design of novel photosensitizers.

30 ability enhance their performance as triplet photosensitizers.

31 te reactive T lymphocytes and identified the photosensitizer 2-Se-Cl, which accumulates in stimulated

32 -electron oxidation by excited triplet-state photosensitizers ((3)sens*), and thus, are good potentia

33 DNBS) group as a glutathione (GSH)-activated photosensitizer, a chemo-prodrug based on combretastatin

34 CDs (a-CD) yet undoped g-CD display limited photosensitizer ability due to low extraction of photoge

35 ing the pai-pai stacking interactions of the photosensitizers, ablating of the tumors without relapse

36 ct photochemistry, where naturally occurring photosensitizers absorb sunlight and produce a range of

37 ee homologous series of rigid-rod-like donor-photosensitizer-acceptor triads with p-xylene bridges.

38 target cells by light-directed activation of photosensitizers accumulated selectively in tumor tissue

39 Improvements in the tumour specificity of photosensitizers, achieved through targeting or localize

40 nce, independence of oxygen, small size, and photosensitizer activity.

41 otosensitizer construct was found to prevent photosensitizer aggregation, boost the generation of cyt

42 lative to that of the acceptor moiety of the photosensitizer alone in the NIR range.

43 of functional linkers, a palladium-porphyrin photosensitizer and a bispyridine-derived molecular moto

44 Copper Cysteamine (Cu-Cy) is a new photosensitizer and a novel radiosensitizer that can be

45 crystalline semiconductor is employed as the photosensitizer and a redox mediator efficiently transfe

46 Dissolved organic matter (DOM) can act as a photosensitizer and an inhibitor in the phototransformat

47 ed in systems with water-soluble CdSe QDs as photosensitizer and ascorbic acid as a sacrificial elect

48 bpy=2,2'-bipyridine] connecting ligand as a photosensitizer and Co(dmgH)(2) (PPA)Cl (PPA-Co, dmgH=di

49 -Ru-Co-OTf MOL with a [Ru(DBB)(bpy)(2) ](2+) photosensitizer and Hf(12) SBU capped with triflate as s

50 , silver nanorod (Ag NR) was identified as a photosensitizer and its effect was studied in three diff

51 At equivalent dose of drug, photosensitizer and light irradiation, combination thera

52 hamber, with aerosol-phase humic acid as the photosensitizer and limonene as the VOC.

53 ent enzymes(4,5), catalyses reduction of the photosensitizer and substrate protochlorophyllide to for

54 trategy allows for tuning the ratios between photosensitizer and the switch molecule, enabling maximu

55 demonstrating their potential use as triplet photosensitizers and as metal ion sensors.

56 ch does not require employment of exogeneous photosensitizers and external oxidants, allows for effic

57 acile composites will be broadly deployed as photosensitizers and light emitters for numerous synthet

58 namic treatment, bacteria are incubated with photosensitizers and then oxidized to death by generatin

59 ne (AQ) acceptor flanked by two Ru(bpy)3(2+) photosensitizers and two peripheral triarylamine (TAA) d

60 quipped onto nanoparticles (NPs) loaded with photosensitizers and Zileuton (a leukotriene inhibitor)

61 In the presence of UV light, a photosensitizer, and a hydrogen donor, this "polyMOC" ma

62 m, composed of a nickel catalyst, an iridium photosensitizer, and an amine electron donor, is capable

63 (+) (L = macrocyclic ligand), [Ru(bpy)3](2+) photosensitizer, and an equimolar mixture of sodium asco

64 tive and eco-friendly starting materials and photosensitizer, and energy efficiency are the salient f

65 tion, the meticulous participation of light, photosensitizer, and oxygen greatly hinders the broad ap

66 gn of a redox stimuli activatable metal-free photosensitizer (aPS), also functioning as a pre-photose

67 onistic interactions between chemo-drugs and photosensitizers are frequently reported, and drugs dose

68 which use light-activated molecules known as photosensitizers, are highly selective against many mali

69 osensitizer (aPS), also functioning as a pre-photosensitizer as it is converted to a PS by the mutual

70 cribes ETT's functionalization with curcumin photosensitizer, as well as its evaluation in PDI agains

71 -carboxylates using rose bengal as a triplet photosensitizer at ambient temperature.

72 Activation of the new photosensitizer at low concentrations (0.1-1 muM) by com

73 Light-activated, photosensitizer-based therapies have been established as

74 nd metal-free octasubstituted phthalocyanine photosensitizers bearing [(triethylammonio)ethyl]sulfany

75 Tumor uptake of the photosensitizer (benzoporphyrin derivative monoacid ring

76 ay, which expands the capabilities of cerium photosensitizers beyond our previous results that demons

77 ther, our study discovered eEF1A1 as a novel photosensitizer binding protein, which may play an essen

78 -BPS, that contains both a brominated BODIPY photosensitizer (BPS) and an ethacrynic acid (EA) GST-pi

79 s in intrinsic properties of the catalyst or photosensitizer, but to hydrogen-bonding interactions be

80 ished the oxidative quenching of the excited photosensitizer by Ni4 P2 as the initiating step of HER

81 address the issue of low cellular uptake of photosensitizers by cancer cells in photodynamic therapy

82 uld be turned over with catalytic amounts of photosensitizers by coupling salt metathesis and reducti

83 ew paradigm for the construction of adaptive photosensitizers by using a supramolecular method.

84 ets converted by cells of the tissue in to a photosensitizer called protoporphyrin IX (PPIX).

85 Upon illumination, the RNA photosensitizer can controllably generate reactive oxyge

86 Humic substances (HS) acting as photosensitizers can generate a variety of reactive spec

87 r photoredox processes involving these FeNHC photosensitizers can only be determined from the ultrafa

88 light exposure following administration of a photosensitizer, can be a valuable treatment modality bu

89 ed a ROS-producing hybrid nanoparticle-based photosensitizer capable of maintaining high levels of RO

90 m cells and bacteriophage bio-nanowires as a photosensitizer carrier, as well as integration with imm

91 FF conjugates and a proof-of-concept for new photosensitizer carriers based on peptide conjugates.

92 orous silica nanoparticles (MSNs) containing photosensitizer (Ce6) through a Cathepsin B-cleavable pe

93 on at remote ambient conditions including IC photosensitizer chemistry indicate less than 0.3% contri

94 se experiments, the results suggest that the photosensitizer chemistry of HULIS in ambient atmospheri

95 cent studies have shown the potential of the photosensitizer chemistry of humic acid, as a proxy for

96 according to the quantity and quality of its photosensitizers, chiefly chromophoric dissolved organic

97 In our design, MnO2 nanosheets adsorb photosensitizer chlorin e6 (Ce6), protect it from self-d

98 ith biocompatible Zn(2+) and encapsulate the photosensitizer chlorin e6 (Ce6).

99 With azine-linked N2-COF photosensitizer, chloro(pyridine)cobaloxime co-catalyst,

100 ical properties such as absorbed light dose, photosensitizer concentration, tissue oxygen concentrati

101 eveloped a CD44-targeted monoclonal antibody photosensitizer conjugate for combined fluorescent detec

102 Here we report a type of hybrid photosensitizers consisting of plasmonic silver nanopart

103 PEGylation of the photosensitizer construct was found to prevent photosens

104 sin receptor kinase C (TrkC) targeted ligand-photosensitizer construct, IYIY-diiodo-boron-dipyrrometh

105 To overcome those issues, we have designed a photosensitizer-containing ETT to be used in photodynami

106 As a new type of radiosensitizers and photosensitizers, Cu-Cy nanoparticles have a good potent

107 gand-field excited state of the Fe(II)-based photosensitizer, definitively establishing that Fe(II) p

108 on-based metal complexes as high-performance photosensitizers demands long-lived electronically excit

109 nvestigation provides a blueprint for future photosensitizer development featuring early transition m

110 Our results indicate that the hybrid photosensitizers display low cytotoxicity without light

111 ic therapy, which is based on the ability of photosensitizer drugs to cause Ca(2+)-dependent cytotoxi

112 The oxidative stress induced by iridium photosensitizers during photoactivation can increase the

113 or ligand, has been found to be a potent UVA photosensitizer, effective at nanomolar concentrations.

114 The presence of model natural photosensitizers either reduced or did not affect photoi

115 Photosensitizers exert their therapeutic effect by produ

116 , whereas, after visible light exposure, the photosensitizers exhibited IC(50) values around 11.1-23.

117 the iron(III) N-heterocyclic carbene (FeNHC) photosensitizer [Fe(phtmeimb)(2)](+) (phtmeimb = phenylt

118 organoiridium-albumin is a strong candidate photosensitizer for anticancer photodynamic therapy.

119 velopment of TLD1433, the first Ru(II)-based photosensitizer for PDT to enter a human clinical trial.

120 ng to unprecedented performance as a triplet photosensitizer for PDT.

121 used as a natural food coloring agent and a photosensitizer for photodynamic therapy because of its

122 ptide are suitable vehicles to encapsulate a photosensitizer for photodynamic therapy.

123 s the design of a colloidal quantum dot (QD) photosensitizer for the Pd-photocatalyzed Heck coupling

124 ry optimizations, makes these compounds poor photosensitizers for (1)O(2) or other reactive oxygen sp

125 nosized light-harvesters that are attractive photosensitizers for biological systems as they are wate

126 Ideal photosensitizers for cancer treatment should both have g

127 pand the options for designing NIR-absorbing photosensitizers for future clinical cancer treatments.

128 view is to present an overview of conjugated photosensitizers for imaging and therapy.

129 capable of absorbing sunlight and serving as photosensitizers for metolachlor degradation.

130 r efforts to develop rhenium-oxo corroles as photosensitizers for oxygen sensing and photodynamic the

131 Application of the complexes as photosensitizers for photocatalytic generation of hydrog

132 n of light-sensitive/photocaged molecules or photosensitizers for photocontrolled-delivery and photod

133 eatment of lesioned tissues, and delivery of photosensitizers for photodynamic cancer therapy.

134 Nanocarriers are employed to deliver photosensitizers for photodynamic therapy (PDT) through

135 ty and aqueous solubility make CDs versatile photosensitizers for redox enzymes with great scope for

136 terials for the development of biocompatible photosensitizers for solar-driven catalysis and hydrogen

137 They are mostly known as efficient photosensitizers for the generation of singlet oxygen vi

138 te that the designed alkyl CPs are efficient photosensitizers for the photodynamic therapy of ras-dri

139 s study, we evaluated 24 chalcogenorhodamine photosensitizers for their ability to selectively deplet

140 particles are often used in conjunction with photosensitizers (for singlet oxygen generation or dye-s

141 The combination of UV-B with photosensitizers fructosazine, glucosamine caramel and r

142 r-soluble pillar[5]arene (WP5) and an AIEgen photosensitizer (G).

143 The presence of the synthetic photosensitizers generally enhanced photoinactivation of

144 nd consequences of the reactions between the photosensitizer-generated singlet oxygen and substrate m

145 hotochemical reaction of sulfite (SO(3)(2-)) photosensitizer generates strongly reducing hydrated ele

146 here a genetically encoded RNA aptamer based photosensitizer (GRAP).

147 t organic frameworks (COFs) as heterogeneous photosensitizers has gathered significant momentum by vi

148 mbining molecularly targeted drugs and novel photosensitizers has the potential to improve further th

149 Using temoporfin as the photosensitizer, here we combine field-induced droplet i

150 particular, with the Ru-dye as visible light photosensitizer, hierarchical Ni(OH)(2) nanosheet arrays

151 The origin of the photosensitizer, however, remains unclear.

152 r moiety (distyryl-BODIPY) is connected to a photosensitizer (i.e., diiodo-distyryl-BODIPY) to form a

153 iator (electron acceptor) to the C-Dots (the photosensitizer, i.e., electron donor) in aqueous soluti

154 i) the red-shifted absorbance of polynuclear photosensitizers, (ii) the more favorable driving force

155 y of the selective activation of our dormant photosensitizer in cellular nuclei, causing cancer cell

156 stem that integrates a cobalt catalyst and a photosensitizer in close proximity for hydrogen producti

157 where under visible light irradiation the Ir photosensitizer in conjunction with triethanolamine are

158 ll amounts of a porphyrin-phospholipid (PoP) photosensitizer in the bilayer.

159 solar fuel, CH(4), photocatalytically with a photosensitizer in the presence of water.

160 r is established as one of the most relevant photosensitizers in aquatic environments, producing sing

161 The efficacy of photosensitizers in cancer phototherapy is often limited

162 The proximity of Ni4 P2 to multiple photosensitizers in Ni4 P2 @MOF allows for facile multi-

163 etal complexes are of increasing interest as photosensitizers in photodynamic therapy (PDT) and, more

164 Iridium corroles thus may hold promise as photosensitizers in photodynamic therapy (PDT).

165 he potential advantages of using polynuclear photosensitizers in phototriggered redox catalysis react

166 Transition-metal complexes are used as photosensitizers, in light-emitting diodes, for biosensi

167 oo demanding for common precious metal-based photosensitizers, including the widely employed fac-[Ir(

168 h shells and the trapping ability of CM, the photosensitizer indocyanine green (ICG) is successfully

169 At higher doses, however, these photosensitizers induce "dark toxicity" through light-in

170 lecule, resulting in a constitutively active photosensitizer inside the cell.

171 Assembling photosensitizers into nanostructures can improve photody

172 rated to provide the synthetically versatile photosensitizer [Ir(ppy)2(dtbbpy)]PF6 in >1 g quantities

173 Three iridium photosensitizers, [Ir(dCF(3)ppy)(2)(N-N)](+), where N-N

174 labile by encapsulation of a NIR-triggerable photosensitizer; irradiation at 730 nm led to peroxidati

175 I and II PDT agent to a predominantly type I photosensitizer, irrespective of the oxygen content.

176 The photosensitizer is also a potent stimulator of P-glycopr

177 h (1)O(2) at expected rates when an external photosensitizer is included and show the expected change

178 A genetically encodable, protein-encased photosensitizer is one way to achieve this goal.

179 reduction without sacrifice reagent or extra photosensitizer is still challenging.

180 Whereas the administration of photosensitizers is a key component of photodynamic ther

181 Intersystem crossing (ISC) of triplet photosensitizers is a vital process for fundamental phot

182 earth-abundant 'early' transition metals in photosensitizers is clearly advantageous, a detailed und

183 erated transgenic parasites that express the photosensitizer KillerRed, which leads to parasite killi

184 epithelium can be damaged by light acting on photosensitizers like N-retinylidene-N-retinylethanolami

185 otodynamic therapy (PDT) owing to their high photosensitizer loadings, facile diffusion of reactive o

186 ed here operates at low 1 mol % catalyst and photosensitizer loadings.

187 The high selectivity of this novel photosensitizer may have broad applications and provide

188 de was previously selected to solubilize the photosensitizer meta-tetra(hydroxyphenyl)chlorin.

189 The most popular triplet photosensitizers, metal complexes and organic chromophor

190 We used three synthetic photosensitizers (methylene blue, rose bengal, and nitri

191 n-activating peptide (Mito-FAP) to deliver a photosensitizer MG-2I dye exclusively to this organelle.

192 this problem, we report the development of a photosensitizer-MnO2 nanosystem for highly efficient PDT

193 This solvation-controlled photosensitizer model has possible applications as a the

194 namic therapy (PDT), a treatment that uses a photosensitizer, molecular oxygen, and light to kill tar

195 Damage to DNA bound to a photosensitizer molecule frequently proceeds by one-elec

196 Upon illumination, photosensitizer molecules produce reactive oxygen specie

197 articles can strongly interact with adjacent photosensitizer molecules, resulting in a significant al

198 al for the performance of miniSOG as (1)O(2) photosensitizer, namely the photo-induced transformation

199 The model photosensitizers, namely 9,10-anthraquinone-1,5-disulfon

200 system, with [Ir(ppy)(2)(dtbbpy)]PF(6) as a photosensitizer, NiBr(2).glyme as a precatalyst, and 1,8

201 y indirect photolysis in the presence of the photosensitizers nitrate, nitrite, and humic acid.

202 p activity promotes the efficient removal of photosensitizer not sequestered in mitochondria and prot

203 Thus, our dual biorthogonal, activatable photosensitizers open new venues to combat current limit

204 rg-Bachmann reaction that does not require a photosensitizer or any metal reagents.

205 Notably, this method requires no exogenous photosensitizers or external oxidants.

206 oom temperature without the aid of exogenous photosensitizers or oxidants.

207 rove the design and development of efficient photosensitizers over commonly used heterogeneous cataly

208 uble conjugate, consisting of a chlorin-e(6) photosensitizer part, a 4-arylaminoquinazoline moiety wi

209 ODIPY-tetrazine probes only become efficient photosensitizers (Phi(Delta) ~0.50) through an intracell

210 Recently several photosensitizer-photochromic-switch dyads were reported

211 Higher nuclearity photosensitizers produced dehalogenation yields greater

212 Under red-light illumination, the photosensitizer produces singlet oxygen which oxidizes p

213 the importance of the cellular membrane and photosensitizer properties in modulating the contributio

214 s FAP-TAPs provides a new spectral range for photosensitizer proteins that could be useful for imagin

215 atable polymeric nanodrug by conjugating the photosensitizer protoporphyrin IX (PpIX) and polyethylen

216 of a hydrophobic drug simvastatin (SV) and a photosensitizer protoporphyrin IX (PpIX) due to the n-n

217 Hence, vaccine particles with Ag and photosensitizers proved an effective vehicle or adjuvant

218 nactivation (CALI) using genetically-encoded photosensitizers provides an opportunity to determine ho

219 range is limited by the distribution of the photosensitizer (PS) and the illuminated area.

220 ysicochemical factors include light sources, photosensitizer (PS) carriers, microwaves, electric fiel

221 namic therapy where the design of the active photosensitizer (PS) is very crucial.

222 By mixing in solution a triplet photosensitizer (PS) with the photoCORM and shining red

223 with two-photon absorption compound (T1) and photosensitizer (PS), The F127 micelles are liquid at ro

224 However, most of the available photosensitizers (PS) are highly hydrophobic, which limi

225 Photostability is considered a key asset for photosensitizers (PS) used in medical applications as we

226 Currently, photosensitizers (PSs) that are microenvironment respons

227 Photosensitizers (PSs) with stimuli-responsive reversibl

228 field are the physicochemical properties of photosensitizers (PSs), optimal drug release profiles, a

229 Despite the clinical success of approved photosensitizers (PSs), their application is sometimes l

230 hosphate (ZnP) nanoparticles loaded with the photosensitizer pyrolipid (ZnP@pyro) can kill tumor cell

231 ticles carry oxaliplatin in the core and the photosensitizer pyropheophorbide-lipid conjugate (pyroli

232 clodextrin systems comprise third generation photosensitizers, recent developments for their utilizat

233 act with O2 without the need for an external photosensitizer, resulting in selective and reversible f

234 -induced luminescence excited the conjugated photosensitizers, resulting in a PDT effect.

235 licate nanoscintillators are conjugated with photosensitizer rose bengal and arginylglycylaspartic ac

236 The photosensitizers rose bengal (RB) and acridine orange (A

237 ore-shell silver-silica nanoparticles with a photosensitizer, Rose Bengal, tethered to their surface.

238 acts as a substitute for the precious metal photosensitizer [Ru(bpy)3](2+).

239 to the control system using unsubstituted Ru photosensitizer (RuBPY) and ReDAC (TON(CO) = 28 +/- 4 an

240 ment photosensitizer-trap molecule where the photosensitizer segment consists of a Br-substituted bor

241 S restores the sensitizing properties of the photosensitizer segment resulting in approximately 40-fo

242 capability of Mn(2+) -assisted assembly of a photosensitizer (sinoporphyrin sodium, DVDMS) is demonst

243 ently integrates the photochromic switch and photosensitizer, SO-PCN has demonstrated reversible cont

244 Other, more abundant photosensitizer species, such as humic-like substances (

245 emature leakage and non-selective release of photosensitizers still exist.

246 Photosensitizers such as the small cationic molecule EtN

247 e bengal, and nitrite) and two model natural photosensitizers (Suwannee River natural organic matter

248 eractions to a Re bipyridine catalyst and Ru photosensitizer system (ReDAC/RuDAC) by the addition of

249 This targeted and activated photosensitizer (TAPs) approach enables protein inactiva

250 tely 1 mum size were loaded with OVA and the photosensitizer tetraphenyl chlorine disulphonate (TPCS2

251 fective solution is to construct an adaptive photosensitizer that can be activated to generate reacti

252 r-cysteamine nanoparticles are a new type of photosensitizer that can generate cytotoxic singlet oxyg

253 Dissolved organic matter (DOM) is a natural photosensitizer that contributes to the inactivation of

254 rization of a dormant singlet oxygen ((1)O2) photosensitizer that is activated upon its reaction with

255 leotide (FMN), we have developed a promising photosensitizer that overcomes many of the problems that

256 ogenic dye, forming an 'on-demand' activated photosensitizer that produces singlet oxygen and fluores

257 The first mitochondrion-anchoring photosensitizer that specifically generates singlet oxyg

258 ion and trigger MHCI presentation by using a photosensitizer that, upon light activation, would facil

259 a soluble amine base without any additional photosensitizer, the reaction enables the etherification

260 A novel addition to the family of endogenous photosensitizers, the precise mechanism(s) through which

261 ient light-induced electron injection from a photosensitizer to a metal oxide, but other times not co

262 fects membrane biophysics, we used a chlorin photosensitizer to oxidize vesicles of various lipid com

263 ated by the well-established capacity of PDT photosensitizers to serve as tumour-selective fluorescen

264 ransfer process promoted by an iridium-based photosensitizer, to build a complex molecular architectu

265 The compound is based on a two segment photosensitizer-trap molecule where the photosensitizer

266 of laboratory studies, potentially acting as photosensitizers triggering secondary organic aerosol gr

267 experimental conditions including different photosensitizer types, dosage controls, and different il

268 photoinduced electron transfer (PET) with a photosensitizer, undergo intramolecular cyclization to y

269 supplied from the photochemically reduced Ru photosensitizer unit.

270 peutic agents including nanotechnology-based photosensitizers used in PDT.

271 Photosensitizers used in such hybrid systems are typical

272 Photosensitizers used to date have been either exogenous

273 elopment of new supramolecular heterogeneous photosensitizers using host-guest chemistry.

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 A photosensitizer was incorporated into these polymers to

278 such localised retinal bacteria, instead the photosensitizer was shown to be distributed throughout t

279 phage, a virus indicator, the most efficient photosensitizer was the wastewater DOM isolated from the

280 -Cl-aniline by excited triplet states of the photosensitizers was associated with inverse and normal

281 , wavelength, concentration of the reagents, photosensitizer) was carried out, and the scope and limi

282 each high payloads close to 1:1, rendering a photosensitizer water-soluble and providing adjustable d

283 To control the distance between Dox and the photosensitizer, we developed a novel pH-sensitive poly

284 Inspired by protein photosensitizers, we propose here a genetically encoded

285 ear (Q1) ruthenium(II) 2,2'-bipyridine based photosensitizers were synthesized, characterized, and in

286 ness of copper-cysteamine nanoparticles as a photosensitizer when activated by radiation and suggests

287 crease in singlet oxygen generation from the photosensitizer when Dox was in close physical proximity

288 otoinduced dynamics of the [Fe(bmip)(2)](2+) photosensitizer, where bmip = 2,6-bis(3-methyl-imidazole

289 er (RET) mechanism to construct a novel dyad photosensitizer which is able to dramatically boost NIR

290 Photodynamic therapy that uses photosensitizers which only become toxic upon light-irra

291 e to the location and the orientation of the photosensitizer, which are very difficult to define in s

292 ted a novel sensor system based on a type II photosensitizer, which combines the advantages of enzyma

293 do-4-methyl-benzenechloride, complex 1, as a photosensitizer, which works under visible light.

294 Such photoreactions are triggered by triplet photosensitizers, which absorb visible-light photons and

295 constitute a new family of luminophores and photosensitizers, which is complementary to precious met

296 was developed by conjugating a red-emissive photosensitizer with aggregation-induced emission (AIE)

297 d catalyst and an organic dye can be used as photosensitizers with 0.5 mol % loading.

298 photocatalytic hydrogen evolution using COF photosensitizers with molecular proton reduction catalys

299 Replacing current benchmark rare-element photosensitizers with ones based on abundant and low-cos

300 sture-stable, visible light-absorbing Zr(IV) photosensitizer, Zr((Mes)PDP(Ph))(2), where [(Mes)PDP(Ph