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5 derivative exhibited exceptionally effective photodynamic activity on a number of tumor cell lines (H
6 ndogenous AhR ligand FICZ displays nanomolar photodynamic activity representing a molecular mechanism
8 y inducing keratinocyte cell death, and FICZ photodynamic activity was also substantiated in a murine
10 that (3)IL states of this nature are potent photodynamic agents, exhibiting the largest photocytotox
11 Cu2-XTe) nanocubes (NCs) as photothermal and photodynamic agents, leading to significant anticancer a
12 e and NIR radiate on at 4 degrees C revealed photodynamic and photothermal as mechanism of cytotoxici
13 and ultrafast experimental studies of their photodynamics and discuss the results in comparison to t
16 ermore, the trimodal therapy (photothermal-, photodynamic- and chemo-therapy) with SN-NPM demonstrate
19 port here for the first time on a reversible photodynamic bulk optode sensor based on the photoswitch
21 on chlorin as a partially approved drug for photodynamic cancer therapy, the concept is universal an
23 ding chemo-drugs, nucleotides, peptides, and photodynamic chemicals could be simply encapsulated into
24 l bridged binaphthyl units were developed as photodynamic chiral dopants for nematic liquid crystals.
27 ng intravenous PMIL administration, triggers photodynamic damage of tumour cells and microvessels, an
28 Failure to assemble such complexes provoked photodynamic damage through the generation of singlet ox
29 infrared laser irradiation induced vascular photodynamic damage, resulting in enhanced liposomal dox
30 nology such as optical coherence tomography, photodynamic diagnosis and narrow band imaging might be
32 e supports macroscopic applications, such as photodynamic diagnosis or narrow band imaging, and their
33 in urologic surgery were reviewed, including photodynamic diagnosis, near infrared fluorescence imagi
34 alization and patterning strategy based on a photodynamic disulfide exchange reaction is demonstrated
35 s for CSCR are still evolving, in particular photodynamic dynamic therapy using lower doses and reduc
36 ncreased the cellular uptake by >60% and the photodynamic effect of hydrophobic porphyrins in vitro c
37 r-soluble conjugates were screened for their photodynamic efficacy against several cancer cell lines
43 of photodynamic therapy (PDT) and microbial photodynamic inactivation (PDI) in clinical applications
44 egular cells was successfully tested via the photodynamic inactivation of a ROS stressed Gram negativ
47 n HaCaT and primary epidermal keratinocytes, photodynamic induction of apoptosis was elicited by the
48 thout light illumination yet highly enhanced photodynamic inhibition efficacy against Hela cells unde
49 and were consequently the primary targets of photodynamic injury, resulting in predominantly necrotic
51 , public awareness regarding the presence of photodynamic naphthodianthrones fagopyrins that can caus
54 azol-5(4H)-one (OHBI) to model the gas-phase photodynamics of such 2-hydroxy-substituted chromophores
55 The primary ultrafast Z-to-E isomerization photodynamics of the phytochrome-related cyanobacterioch
56 ral photochemical properties and studied the photodynamics of two model systems in more detail, obser
57 t preclinical evidence that a subtumoricidal photodynamic priming (PDP) strategy can relieve drug del
62 e has allowed identifying discrete molecular photodynamic steps, action of molecular motors, protein
66 nowhiskers (TP) as effective bio-imaging and photodynamic therapeutic (PDT) agent for RA theranostics
67 sed porphyrin (NCP) was synthesized, and the photodynamic therapeutic (PDT) application was investiga
68 hese visible photons have been combined with photodynamic therapeutic agents preclinically for increa
69 e design guideline for enhancing traditional photodynamic therapeutic efficacy integrated with a cont
70 diagnostics and analytics, photothermal and photodynamic therapies, and delivery of target molecules
72 alfa-2b (0% vs 1%), cryotherapy (0% vs 3%), photodynamic therapy (0% vs 1%), excisional biopsy and c
73 randomly assigned (1:1) to vascular-targeted photodynamic therapy (4 mg/kg padeliporfin intravenously
74 or 0.5 mg), sham injections plus verteporfin photodynamic therapy (ANCHOR), or sham injections alone
75 ts of repeated applications of antimicrobial photodynamic therapy (aPDT) adjunctive to scaling and ro
76 im of this study is to compare antimicrobial photodynamic therapy (aPDT) as an adjunctive therapy to
80 low-intensity laser (LIL); 2) antimicrobial photodynamic therapy (aPDT); or 3) toluidine blue O (TBO
82 ng for subsequent surgical excision (n = 3), photodynamic therapy (n = 1), or cryotherapy (n = 1) for
83 ffect compared with reovirus monotherapy and photodynamic therapy (p=0.042) with 100% cell death obse
85 ing pigment (methylene blue - MB) to mediate photodynamic therapy (PDT) against Streptococcus mutans
88 e recently contributed to the progression of photodynamic therapy (PDT) and microbial photodynamic in
90 , presumably through the combined effects of photodynamic therapy (PDT) and released chemotherapy dru
91 Cationic antimicrobial peptides (CAMPs) and photodynamic therapy (PDT) are attractive tools to comba
92 inical experiments addressing the effects of photodynamic therapy (PDT) as an adjunct to conventional
94 opportunities of NP imaging and therapy on a photodynamic therapy (PDT) based NP system that has been
96 we have found that addition of erlotinib to photodynamic therapy (PDT) can improve treatment respons
99 neration and exhibits significantly enhanced photodynamic therapy (PDT) efficacy on two colon cancer
105 for their potential as photosensitizers for photodynamic therapy (PDT) in P-glycoprotein (P-gp) expr
106 herapy in ancient texts and the discovery of photodynamic therapy (PDT) in the early 1900s, the landm
125 ial of this conjugate as photosensitizer for photodynamic therapy (PDT) of cancers overexpressing the
129 treatment, it allowed delivery of selective photodynamic therapy (PDT) to the cancerous tissues, wit
131 e entrapped agents that harnesses sub-lethal photodynamic therapy (PDT) using a photosensitiser that
132 3 months, additional treatment with laser or photodynamic therapy (PDT) was considered if any fluores
133 chanisms how the efficacy of photofrin based photodynamic therapy (PDT) was enhanced by miR-99a trans
134 racellular localization and cell response to photodynamic therapy (PDT) were analyzed in MCF10A norma
135 integration of fluorescence imaging (FL) and photodynamic therapy (PDT) with positron emission tomogr
137 nalysis evaluated patients who had undergone photodynamic therapy (PDT) within the preceding year (N
138 nstrate that benzoporphyrin derivative-based photodynamic therapy (PDT), a photochemical cytotoxic mo
140 f cancer and dermatological diseases through photodynamic therapy (PDT), and advanced materials for e
142 additional limitations of porphyrin-mediated photodynamic therapy (PDT), including low depths of tiss
143 ent procedures, such as laser irradiation or photodynamic therapy (PDT), may provide some additional
144 each clinical treatment tool (chemotherapy, photodynamic therapy (PDT), radiotherapy (RT)) by contro
146 ptake of photosensitizers by cancer cells in photodynamic therapy (PDT), we designed a smart plasma m
164 MRI contrasting agents, and sensitizers for photodynamic therapy (PDT); and more recently as models
165 (MARINA), or were randomized to verteporfin photodynamic therapy (PDT; n=143), 0.3-mg ranibizumab mo
166 vitreal anti-VEGF injection; (3) verteporfin photodynamic therapy (vPDT); or (4) laser photocoagulati
167 xamine the hypothesis that vascular-targeted photodynamic therapy (VTP) with WST11 and clinically rel
169 therapy and the other half treated with AWL photodynamic therapy 1 week apart and randomly allocated
170 bial and antiviral agents, anticancer drugs, photodynamic therapy agents, radiotherapy agents and bio
171 y assigned 206 patients to vascular-targeted photodynamic therapy and 207 patients to active surveill
172 e findings may help to alleviate pain during photodynamic therapy and also allow for disease modifica
173 mes were after vs before the introduction of photodynamic therapy and anti-vascular endothelial growt
175 ffectiveness and adverse effects of daylight photodynamic therapy and artificial white light (AWL) LE
177 ies based on oxygen free radicals, including photodynamic therapy and radiotherapy, have emerged as p
178 ad half of their scalp treated with daylight photodynamic therapy and the other half treated with AWL
179 Of the new non-invasive treatments, only photodynamic therapy and topical imiquimod have become e
180 mus) and the most promising absorptivity for photodynamic therapy application, was tested as efficien
182 Near-IR absorption, desired for potential photodynamic therapy applications, was not pursuable for
184 ession in cancer cells and susceptibility to photodynamic therapy based on their increased ability to
185 atoses (AKs) is as effective as conventional photodynamic therapy but has the advantage of being almo
189 -VEGF therapy increased from 60.3% to 72.7%, photodynamic therapy decreased from 12.8% to 5.3%, and t
191 imaging and synergetic photothermal therapy/photodynamic therapy derived from the porphyrin-like moi
192 osensitizers into nanostructures can improve photodynamic therapy efficacy and the safety profile of
193 re to sunlight and other patients undergoing photodynamic therapy experience similar pain, which can
194 e variety of potential applications, such as photodynamic therapy for accelerated drug screening, mag
195 therapy and artificial white light (AWL) LED photodynamic therapy for the treatment of AKs on the for
196 eporfin (VP), a light-activated drug used in photodynamic therapy for the treatment of choroidal neov
197 was 58 (28%) of 206 in the vascular-targeted photodynamic therapy group compared with 120 (58%) of 20
199 tatitis (three [2%] in the vascular-targeted photodynamic therapy group vs one [<1%] in the active su
200 rious adverse event in the vascular-targeted photodynamic therapy group was retention of urine (15 pa
206 lar endothelial growth factor or verteporfin photodynamic therapy in combination with systemic chemot
208 TERPRETATION: Padeliporfin vascular-targeted photodynamic therapy is a safe, effective treatment for
214 guided sensitizer delivery for the potential photodynamic therapy of hypoxic structures requiring cyt
218 bined with protoporphyrin IX (PpIX)-mediated photodynamic therapy on a variety of human pancreatic ca
219 gnosed as having exudative ARMD who received photodynamic therapy or anti-VEGF therapy compared with
220 atform for the high-throughput assessment of photodynamic therapy photosensitizer (PDT) efficacy on E
236 ects of reovirus combined with PpIX-mediated photodynamic therapy were analysed in methylthiazoltetra
238 in rare diseases, such as porphyrias, and in photodynamic therapy where short-term toxicity is intend
239 itization represents a promising approach in photodynamic therapy where the design of the active phot
240 photothermal therapy and porphyrin-mediated photodynamic therapy which results in complete tumor eli
244 ing oxidant production by transition metals, photodynamic therapy, activated macrophages, and platele
245 emonstrates a highly promising new agent for photodynamic therapy, and attracts attention to photosta
246 peutics and biologics, chemotherapeutics and photodynamic therapy, and chemotherapeutics and radiothe
250 cations, including therapeutic (photothermal/photodynamic therapy, chemotherapy and synergistic thera
251 as photosynthesis, vision, photolithography, photodynamic therapy, etc., is yet to become a common to
252 for phototherapeutic interventions, such as photodynamic therapy, has transformed medicine and biolo
255 interventions (argon laser photocoagulation, photodynamic therapy, intravitreal corticosteroids, and
256 iolet and visible light, and also to develop photodynamic therapy, it is important to resolve the mec
259 addition, light activation has potential in photodynamic therapy, photothermal therapy, radiotherapy
260 , which is used as an antimicrobial agent in photodynamic therapy, potentiates tellurite toxicity.
261 gated as cytotoxic agents and inhibitors, in photodynamic therapy, radiation therapy, drug/gene deliv
262 rapies were identified: electrochemotherapy, photodynamic therapy, radiotherapy, intralesional therap
263 re either ineligible for or nonresponsive to photodynamic therapy, the standard treatment at the time
264 omy, cryotherapy, laser photocoagulation, or photodynamic therapy, were excluded from the analysis.
266 mour cells with low or no PTEN expression to photodynamic therapy, which is based on the ability of p
267 l of oral infections, including their use in photodynamic therapy, will be discussed in this review.
294 on with Photodynamic Therapy; Verteporfin in Photodynamic Therapy; VEGF Inhibition Study in Ocular Ne
295 ent of Age-Related Macular Degeneration with Photodynamic Therapy; Verteporfin in Photodynamic Therap
299 eting and multi-drug strategy, chemo-/radio-/photodynamic-/ultrasound-/thermo-combined multi-modal th
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