Results 161 to 170 of about 3,607 (204)
Pheophorbide-a, a chlorine based photosensitizer known to be selectively accumulated in cancer cells, was conjugated with anticancer drugs, doxorubicin and paclitaxel in the purpose of selective cancer diagnosis and therapy. Pheophorbide-a was conjugated
Hyo-Eun Yoon +2 more
exaly +2 more sources
Pheophorbide a identified in an Eupatorium perfoliatum extract is a novel lymphatic vascular activator [PDF]
The lymphatic vascular system is crucial for maintaining tissue fluid homeostasis and immune surveillance. Promoting lymphatic function represents a new strategy to treat several diseases including lymphedema, chronic inflammation and impaired wound ...
Jihye Kim +2 more
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Background Our previous study has shown a prolonged retention and accumulation of Zn-pheophorbide a, a water-soluble derivative of chlorophyll a, in tumor tissue (Szczygiel et al. [19]).
Monika A Jakubowska +2 more
exaly +2 more sources
Pheophorbide-a conjugates with cancer-targeting moieties for targeted photodynamic cancer therapy
Pheophorbide-a, a non-selective photosensitizer, was conjugated with cancer-targeting moieties, such as folic acid, the CRGDLASLC peptide, the cRGDfK peptide and leuprorelin, for the purpose of targeted photodynamic cancer therapy. The cellular uptake of
Hyo-Eun Yoon +2 more
exaly +2 more sources
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The synthesis of galactopyranosyl-substituted derivatives of pheophorbide
Russian Journal of Bioorganic Chemistry, 2000New pheophorbide and pyropheophorbide derivatives containing carbohydrate fragments, derivatives of galactopyranose, were synthesized. Galactopyranosylpheophorbide and galactopyranosylpyropheophorbide with free hydroxyl groups were found to be water-soluble and useful as sensitizers in photodynamic therapy of cancer.
A A, Aksenova +2 more
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Tetrahedron, 1997
Abstract A series of ortho-, meta- and para-substituted zinc porphyrin-pheophorbide dyads were synthesized directly from methyl pheophorbide-a by trans-esterification of β-keto methyl ester with hydroxymethyl substituted porphyrins. Quantitative energy transfer occurred from the excited zinc porphyrin to the pheophorbide.
Satoshi Shinoda +4 more
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Abstract A series of ortho-, meta- and para-substituted zinc porphyrin-pheophorbide dyads were synthesized directly from methyl pheophorbide-a by trans-esterification of β-keto methyl ester with hydroxymethyl substituted porphyrins. Quantitative energy transfer occurred from the excited zinc porphyrin to the pheophorbide.
Satoshi Shinoda +4 more
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Characteristics of photosensitization of Pheophorbide a in liposomal media
Science in China Series C: Life Sciences, 1999Pheophorbide a (PPa), a decomposition product of chlorophyll a, is a photosensitizer. The photosensitization mechanisms (Type I and Type 11) of PPa in simple buffer solutions and in buffer solutions containing double-layered DPPC liposomes have been studied using techniques of ESR, spin-trapping, spin-counteraction and laser flash photolysis.
H, Yang +4 more
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Derivatives of Pheophorbide‐a and Pheophorbide‐b from Photocytotoxic Piper penangense Extract
Chemistry & Biodiversity, 2011AbstractIn our screening program for new photosensitizers from Malaysian biodiversity for photodynamic therapy (PDT) of cancer, MeOH extracts of ten terrestrial plants from Cameron Highlands in Pahang, Peninsular Malaysia, were tested. In a short‐term 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyl‐2H‐tetrazolium bromide (MTT) assay, 20 μg/ml each of these ...
Fadzly Adzhar, Kamarulzaman +5 more
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Photodynamic Imaging of a Rat Pancreatic Cancer with Pheophorbide a
Photochemistry and Photobiology, 1996ABSTRACTLaser‐induced fluorescence of pheophorbide a (Ph‐a) was used for in vitro photodynamic imaging (PDI) of a rat pancreatic acinar tumor. A 400 nm excitation induced a 470 nm autofluorescence and a 678 nm dye fluorescence in tumors and their surrounding pancreas 24 h after a 9 mg kg−1 body weight Ph‐a intravenous administration.
Keller, P. +8 more
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Synthesis of boronated derivatives of pheophorbide a
Doklady Chemistry, 2008294 Photodynamic therapy (PDT) [1] and boron neutron capture therapy (BNCT) [2] are promising clinical approaches enabling a local effect on a tumor with little if any damage to the healthy tissue around it. Both methods are based on the selective accumulation of photoand radiosensitizer in cancer cells and in situ production of high-energy particles ...
V. A. Ol’shevskaya +5 more
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