Generated: April 30, 2017
|Title:||Method of treating skin diseases|
|Abstract:||A group of hydro-monobenzoporphyrins "green porphyrins" (Gp) having absorption maxima in the range of 670-780 nanometers is useful in treating disorders or conditions which are subject to hematoporphyrin derivative (HPD) treatment in the presence of light, or in treating virus, cells and tissues generally to destroy unwanted targets. The use of the Gp of the invention permits the irradiation for therapy to use wavelengths other than those absorbed by blood. The Gp of the invention may also be conjugated to ligands specific for receptor or to specific immunoglobulins or fragments thereof to target specific tissues or cells for the radiation treatment. Use of these materials permits lower levels of drug to be used, thus preventing side reactions which might destroy normal tissues.|
|Inventor(s):||Levy; Julia G. (Vancouver, CA), Dolphin; David (Vancouver, CA), Chow; Jack J. (Vancouver, CA), Sternberg; Ethan (Vancouver, CA)|
|Assignee:||The University of British Columbia (Vancouver, CA)|
|Filing Date:||Jan 25, 1994|
|Claims:||1. A method for treating skin diseases in an animal which comprises topically treating an animal in need of such treatment with an effective amount of a hydro-monobenzoporphyrin (Gp) having a light absorption maximum between 670-780 nm; |
wherein the Gp is selected from the group consisting of ##STR17## and mixtures thereof and the metalated and labeled forms thereof, wherein each R.sup.1 and R.sup.2 independently selected from the group consisting of carbalkoxy (2-6C), alkyl (1-6C) sulfonyl, aryl (6-10C) sulfonyl, aryl (6-10C); cyano; and --CONR.sup.5 CO-- wherein R.sup.5 is aryl (6-10C) or alkyl (1-6C);
each R.sup.3 is independently carboxyalkyl (2-6C) or a salt, amide, ester or acylhydrazone thereof, or is alkyl (1-6C); and
R.sup.4 is CHCH.sub.2, CH.sub.2 OR.sup.4', --CHO, --COOR.sup.4', CH(OR.sup.4')CH.sub.3, CH(OR.sup.4')CH.sub.2 OR.sup.4', --CH(SR.sup.4')CH.sub.3, --CH(NR.sup.4'.sub.2)CH.sub.3, --CH(CN)CH.sub.3, --CH(COOR.sup.4')CH.sub.3, --CH(halo)CH.sub.3, or --CH(halo)CH.sub.2 (halo), wherein R.sup.4' is H or alkyl (1-6C) optionally substituted with a hydrophilic substituent; or
wherein R.sup.4 is an organic group of <12C resulting from direct or indirect derivatization of vinyl; or
wherein R.sup.4 consists of 1-3 tetrapyrrole-type nuclei of the formula --L--P wherein --L-- is selected from the group consisting of ##STR18## and P is selected from the group consisting of Gp which is of the formula 1-6 but lacking R.sup.4 and conjugated through the position shown as occupied by R.sup.4 to L, and a porphyrin of the formula: ##STR19## wherein each R is independently H or lower alkyl (1-4C); wherein two of the bonds shown as unoccupied on adjacent rings are joined to R.sup.3 and one of the remaining bonds shown as unoccupied is joined to R.sup.4 and the other to L;
with the proviso that if R.sup.4 is CHCH.sub.2, both R.sup.3 cannot be carbalkoxyethyl;
and irradiating the animal with light absorbed by said Gp.
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