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Featured researches published by Janice North.


Photochemotherapy: Photodynamic Therapy and Other Modalities III | 1997

Photodynamic treatment with BPD-MA (verteporfin) activated with light within different spectral ranges

Anna M. Richter; Ashok K. Jain; Alice J. Canaan; Robert D. Bower; Janice North; Guillermo O. Simkin; Julia G. Levy

Benzoporphyrin derivative monoacid ring A [BPD-MA (verteporfin) or BPD], a second generation photosensitizer tested in clinical trials in combination with red light was compared for its PDT efficiency in vitro and in vivo upon activation with light in the UVA, blue and red spectral ranges. PDT efficiency, calculated based on the BPD absorption spectrum and spectral output of the different light sources, was compared with actual PDT efficiency determined in vitro and in vivo. Results obtained in an in vitro cytotoxicity assay, in which aliquots of murine P815 cells, pre-incubated for 1 h with BPD at 5 ng/mL, were exposed simultaneously to various light doses delivered within UVA, blue and red spectral ranges showed that in this test system PDT efficiency was governed by BPD absorption and light source emission spectra. Similar results were obtained in an in vitro BPD photobleaching test. Thus in vitro, values for calculated, theoretical PDT efficiency corresponded to the actual PDT efficiency. However, in vivo factors, such as depth of tissue penetration with light and localization of the target, had an important influence on PDT efficiency. In mouse models of skin photosensitivity and the cutaneous hypersensitivity immune response (CHS) assay, because of the thinness of mouse skin, PDT efficiency approximated the theoretical PDT efficiency, although blue light was somewhat more efficient in PDT than UVA, and red light was somewhat more efficient than blue or UVA. In a pig skin photosensitivity model, red light induced the highest skin response manifested by erythema and swelling, while blue light caused erythema and minimal swelling and UVA caused only erythema. These differences could be related to the thickness of pig skin and the depth of tissue penetration characteristic of each spectral range. Fluence rate was found to be an additional factor which modifies the effect of BPD and light. In conclusion, BPD can be efficiently activated with light within the UVA, blue and red spectral ranges. Moreover, light doses, deemed safe for red light, can be utilized with light of other spectral ranges, but only after a very careful evaluation of the conditions under which they were determined and the conditions under which they will be used.


Archive | 1995

Photodynamic therapy in selective cell inactivation in blood and treating immune dysfunction diseases

Julia G. Levy; Janice North


Archive | 1993

Selective cell inactivation in blood

Janice North


Journal of Acquired Immune Deficiency Syndromes | 1994

Photodynamic inactivation of free and cell-associated HIV-1 using the photosensitizer, benzoporphyrin derivative.

Janice North; Robert W. Coombs; Julia G. Levy


International Reviews of Immunology | 1988

Characterization of Antigen-Binding Molecules from T Suppressor Hybridomas

Agnes Chan; Anthea Tench Stammers; Janice North; J. Kevin Steele; N. Randall Chu; Julia G. Levy


Archive | 1995

Use of porphyrins in the treatment of multiple sclerosis

Julia G. Levy; Janice North


Archive | 1995

Therapie photodynamique dans l'inactivation cellulaire selective dans le sang et traitement de maladies induites par une dysfonction immunitaire

Simon Leong; Agnes How-Ching-Chan; Hunt David William Carey; Martin Renke; Julia G. Levy; Janice North


Archive | 1995

Verwendung von porphyrine in der behandlung von multiple sklerose

Julia G. Levy; Janice North


Archive | 1995

Verwendung von porphyrine in der behandlung von multiple sklerose Use of porphyrins in the treatment of multiple sclerosis

Julia G. Levy; Janice North


Archive | 1995

Photodynamische therapie zur selektive zell-inaktivierung von blut und zur behandlung von immundisfunktionen erkrankungen

Hunt David William Carey; Agnes How-Ching-Chan; Simon Leong; Julia G. Levy; Janice North; Martin Renke

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Julia G. Levy

University of British Columbia

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Martin Renke

University of British Columbia

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Simon Leong

University of British Columbia

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Agnes Chan

University of British Columbia

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Alice J. Canaan

University of British Columbia

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Anna M. Richter

University of British Columbia

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Anthea Tench Stammers

University of British Columbia

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Ashok K. Jain

University of British Columbia

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Guillermo O. Simkin

University of British Columbia

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N. Randall Chu

University of British Columbia

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