SINGLET OXYGEN GENERATION OF PORPHYRINS, CHLORINS, AND PHTHALOCYANINES
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Summary
The discrepancy between the efficiencies of sensitizers to generate singlet oxygen and their cytotoxicity was explained in terms of photodegradation, intracellular localization, and contributions from a Type I mechanism.
- Type
- article
- Published
- 1989-08-01
- Cited by
- 105
- References
- 36
- Access
- Open access
- OpenAlex
- https://openalex.org/W2528752
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:6180888
Keywords
Geography
References
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- The distribution of tetraphenylporphinesulfonate in the tumor-bearing rat.
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- DIRECT DETECTION OF SINGLET OXYGEN SENSITIZED BY HAEMATOPORPHYRIN AND RELATED COMPOUNDS
- The photochemistry of haematoporphyrin and related systems.
- TYPES I AND II SENSITIZED PHOTOOXIDATION OF AMINOACID BY PHTHALOCYANINES: A FLASH PHOTOCHEMICAL STUDY
- DRUG and LIGHT DOSE DEPENDENCE OF PHOTODYNAMIC THERAPY: A STUDY OF TUMOR and NORMAL TISSUE RESPONSE
- INTRODUCTION.: PHOTODYNAMIC THERAPY
- THE PRODUCTION OF SINGLET MOLECULAR OXYGEN BY ZINC(II) PHTHALOCYANINE IN ETHANOL AND IN UNILAMELLAR VESICLES. CHEMICAL QUENCHING AND PHOSPHORESCENCE STUDIES
- SKIN PHOTOSENSITIVITY AND PHOTODESTRUCTION OF SEVERAL POTENTIAL PHOTODYNAMIC SENSITIZERS
- PHOTOSENSITIZERS: THERAPY AND DETECTION OF MALIGNANT TUMORS
- In vitro photosensitization I. Cellular uptake and subcellular localization of mono‐L‐aspartyl chlorin e6, chloro‐aluminum sulfonated phthalocyanine, and photofrin II
- THE EFFECT OF MEDIUM POLARITY ON THE HEMATOPORPHYRIN‐SENSITIZED PHOTOOXIDATION OF l‐TRYPTOPHAN
- TYPE I AND TYPE II MECHANISMS IN THE PHOTOSENSITIZED LYSIS OF PHOSPHATIDYLCHOLINE LIPOSOMES BY HEMATOPORPHYRIN
- PHTHALOCYANINES AS PHOTOSENSITIZERS IN BIOLOGICAL SYSTEMS AND FOR THE PHOTODYNAMIC THERAPY OF TUMORS
- Lange's Handbook of Chemistry
- A TEST OF DIFFERENT PHOTOSENSITIZERS FOR PHOTODYNAMIC TREATMENT OF CANCER IN A MURINE TUMOR MODEL
- Photodynamic therapy with phthalocyanine sensitisation: quantitative studies in a transplantable rat fibrosarcoma.
Cited by
- PHTHALOCYANINES AS PHOTODYNAMIC SENSITIZERS *
- Photodynamic activity of lutetium‐texaphyrin in a mouse tumor system
- Mathematical Modeling of Oxygen Transport, Cell Killing and Cell Decision Making in Photodynamic Therapy of Cancer
- Spectral-Luminescent Properties and Electronic Structure of the Chlorin p6 Derivatives with an Extended Conjugated Bond System
- 循環器系におけるmono-L-aspartyl chlorin e6の診断と治療への応用
- Chlorins as photosensitizers in biology and medicine.
- Potential photosensitizers for photodynamic therapy. IV. Photophysical and photochemical properties of azaporphyrin and azachlorin derivatives.
- Potential photosensitizers for photodynamic therapy. III. Photophysical properties of a lipophilic chlorin and its zinc and tin chelates.
- Active immunotherapy of Walker-256 carcinosarcoma by tumor-infiltrating lymphocytes associated with photodynamic therapy
- Photodynamic Studies of Metallo 5,10,15,20‐Tetrakis(4‐methoxyphenyl) porphyrin: Photochemical Characterization and Biological Consequences in a Human Carcinoma Cell Line ¶
- PEG‐m‐THPC–mediated Photodynamic Effects on Normal Rat Tissues ¶
- Effect of administration route and estrogen manipulation on endometrial uptake of Photofrin porfimer sodium.
- Quenching of luminescence singlet oxygen by chemical dimers of porphyrins
- The Excited Triplet State Properties of Titanyl Phthalocyanine and its Sulfonated Derivatives
- Phthalocyanines bound to insoluble polystyrene. Synthesis and properties as energy-transfer photosensitizers
- Photodynamic therapy for the hypercalcemic type of the small cell carcinoma of the ovary in a mouse xenograft model.
- Deactivation ofS1 andT1 states of porphyrins and chlorins upon their interaction with molecular oxygen in solutions
- Photoinduced electron transfer from triplet states of phthalocyanines to fullerenes studied by transient absorption spectroscopies in visible and near‐IR regions
- Photodynamic therapy of locoregional breast cancer recurrences using a chlorin‐type photosensitizer
- Photobleaching of 1,3-diphenylisobenzofuran by novel phthalocyanine dye derivatives.
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