Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Elizabeth Waterfield"'
Autor:
Alice J. Canaan, Anna M. Richter, Ashok K. Jain, Elizabeth Waterfield, Beth Anne Allison, Julia G. Levy
Publikováno v:
Photochemistry and Photobiology. 57:1000-1006
Biodistribution studies were carried out on 14C-labeled benzoporphyrin derivative monoacid ring A (BPD), which had been formulated as a unilamellar liposome or taken from a stock solution in dimethyl sulfoxide diluted into phosphate-buffered saline i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eceac67bdc6ee7588a30b263659fc03
https://doi.org/10.1111/j.1751-1097.1993.tb02962.x
https://doi.org/10.1111/j.1751-1097.1993.tb02962.x
Autor:
Julia G. Levy, Alice J. Canaan, Ashok K. Jain, Elizabeth Waterfield, Ethan Sternberg, Anna M. Richter
Publikováno v:
Biochemical Pharmacology. 43:2349-2358
Benzoporphyrin derivative, monoacid ring A (BPD-MA), currently in clinical trials as a photosensitizer for photodynamic therapy for cancer, consists of two regioisomers (A1 and A2) present in equal proportions. The contribution of the regioisomers to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76911c3de4a02e059c9ccc74e5ccc317
https://doi.org/10.1016/0006-2952(92)90313-8
https://doi.org/10.1016/0006-2952(92)90313-8
In vitro EVALUATION OF PHOTOTOXIC PROPERTIES OF FOUR STRUCTURALLY RELATED BENZOPORPHYRIN DERIVATIVES
Autor:
Ethan Sternberg, David Dolphin, Julia G. Levy, Elizabeth Waterfield, Ashok K. Jain, Anna M. Richter
Publikováno v:
Photochemistry and Photobiology. 52:495-500
Four structural analogs of benzoporphyrin derivative (BPD) have been studied and compared for photosensitizing activity in vitro. All analogs have an identical reduced tetrapyrrol porphyrin ring, and differ by the position of a cyclohexadiene ring (f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b364aaf5a073a8a276277d68461a1b7
https://doi.org/10.1111/j.1751-1097.1990.tb01791.x
https://doi.org/10.1111/j.1751-1097.1990.tb01791.x
Publikováno v:
International journal of immunopharmacology. 17(1)
The porphyrin photosensitizer, Photofrin® porfimer sodium (Photofrin®), has been widely studied for its capacity to evoke destruction of malignant tissues. In addition to its photosensitizing properties, Photofrin® may exert myelostimulatory effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea2f4fce1a8dba2cbd5282d5b5e80fca
https://pubmed.ncbi.nlm.nih.gov/7782151
https://pubmed.ncbi.nlm.nih.gov/7782151
Autor:
Claire Smits, Martin Renke, Robert D. Bower, Julia G. Levy, Elizabeth Waterfield, Michele D. Gervais, Michael S. Stonefield
Publikováno v:
Photochemistry and photobiology. 60(4)
Benzoporphyrin derivative monoacid ring A (BPD-MA) is a chlorin-like photosensitizer currently in clinical trials for cancer and psoriasis. It has maximal absorption peaks at both 630 and 690 nm and can be activated at both these wavelengths. In vitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d8388450625e9f7b3288dfcb6436bbb
https://pubmed.ncbi.nlm.nih.gov/7991665
https://pubmed.ncbi.nlm.nih.gov/7991665
Autor:
Vincent Salvatori, Levy Julia G, Claire Smits, Luciann Hruza, Anna M. Richter, Harvey Lui, Elizabeth Waterfield, R. Rox Anderson
Publikováno v:
SPIE Proceedings.
Benzoporohyrin derivative monoacid ring A (BPD) is a lipophilic photosensitizer with a maximum absorption peak at 690 nm. When liposomally formulated, it distributes in human plasma almost exclusively to the lipoprotein fraction. In experimental anim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d45eb593f730e82dc4f44fd832c69c22
https://doi.org/10.1117/12.168659
https://doi.org/10.1117/12.168659
Autor:
Julia G. Levy, Elizabeth Waterfield, Lily Xie, Martin Renke, Robert A. Sorrenti, David W. C. Hunt
Publikováno v:
Immunopharmacology and immunotoxicology. 16(1)
Porphyrins are a group of organic compounds involved in a wide spectrum of fundamental biological processes. Non-metallic, naturally occurring and synthetic porphyrin derivatives may produce cytotoxic effects in malignant or normal tissues exposed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d384b4b78025fd5526d4ec22dd9aa46
https://pubmed.ncbi.nlm.nih.gov/8169323
https://pubmed.ncbi.nlm.nih.gov/8169323
Publikováno v:
Photochemistry and photobiology. 54(5)
The influence of lipoprotein association on in vitro tumor cell killing and in vivo tumor photosensitization with benzoporphyrin derivative (BPD) has been investigated in M-1 tumor bearing mice. The association of benzoporphyrin mono acid ring A with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7379a53cc4e8939f8e84f0e3ee716c5a
https://pubmed.ncbi.nlm.nih.gov/1798748
https://pubmed.ncbi.nlm.nih.gov/1798748
Publikováno v:
Advances in Photochemotherapy.
Benzoporphyrin derivative (BPD), synthesized from protoporphyrin and involving the formation of Diels-Alder adducts, contains four components, mono and di-acid derivatives of either ring A or ring B fused porphyrins. These compounds have been isolate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c5debe2a4e1b65a6e764c87a59bc2f0
https://doi.org/10.1117/12.960196
https://doi.org/10.1117/12.960196