Metal substituted non-centrosimmetrical phthalocyanine analogues, their preparation and use in photodynamic therapy and in vivo diagnostic
View Patent ↗Phthalocyanine analogues having an active group able to link the phthalocyanine t carriers molecules and phthalocyanine to carriers molecules and phthalocyanine analogues as phthalocyanine-carrier conjugates showing enhanced photodynamic properties, red shifted absorption characteristic, all useful for photodynamic therapy, are described. Photosensitizers themselves or the photosensitizers-carriers conjugates are useful compounds either for treatment of various infectious diseases, the in vivo eradication of micro-organisms as well as diseases characterized by cellular hyperproliferation, in particular tumours psoriasis, actinic keratosis, atheromas, endoarterial hyperplasia and prostate hyperplasia. The above compounds can be also useful for blood and blood derivatives sterilization and in vivo/vitro diagnostics.
1. A metal substituted non-centrosymmetrical phthalocyanine of formula (I):
wherein:
n is 1, 2 or 4;
M is selected from the group consisting of Zn, Si(OR 7 ) 2 and AlOR 7 wherein R 7 is selected from the group consisting of H and C 1-15 alkyl;
R is selected from the groups consisting of: —COOH, —SH, —OH, —NH 2 , —CO—CH 2 —Br, —SO 2 Cl, maleimide, hydrazide, phenol, imidate, biotine, possibly bound to the phthalocyanine nucleus through a suitable linker and
when n=2 and the two groups R 1 are in the positions 9,10,16,17,23,24, said two groups R 1 can form a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms chosen from N, O, S; or
R 1 is represented by the group (X) p R 2 , wherein:
X is selected from the group consisting of O, S, —NR 5 and —CH 2 — and R 2 is
where:
Y is selected from the group consisting of C 1-10 alkyl and phenyl, possibly substituted, or it forms with the Z group, to which it is bound, a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms selected from the group consisting of N, O and S;
Z is selected from the group consisting of —N, —CH 2 N and —CONHCH 2 CH 2 N;
R 3 and R 4 , equal or different from one another, are selected from the group consisting of C 1-15 alkyl and phenyl, or form with the Z group, to which they are bound, a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms selected from the group consisting of N, O and S;
R 5 and R 6 , equal or different from one another, are selected from the group consisting of H and C 1-15 alkyl;
m, n, p, w, t and u, independently from one another, are 0 or 1;and
v is an integer comprised between 1 and 3;
with the proviso that:
R is in the position 1 or 2,
R 1 is in the positions: 8(11), 15(18), 22(25), or 9(10), 16(17), 23(24) when n=1,
R 1 is in the positions: 8,11,15,18,22,25 or 9,10,16,17,23,24 when n=2.
2. Metal phthalocyanine according to claim 1 wherein M is Zn.
3. Metal phthalocyanine according to claim 1 wherein the group (X) p R 2 is selected from the group consisting of:
4. The metal phthalocyanine according to claim 1 represented by:
2-[(4-hydroxycarbonyl)phenoxy]-{[9,10][16,17][23,24]-tribenzo}zinc(II)phthalo cyanine;
2-[(4-hydroxycarbonyl)phenoxy]-9(10),16(17),23(24)-tri[2-(morfolin-1-yl) ethoxy]zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-2(3),9(10),16(17),23(24)-tri[2 -(piperidin-1-yl) ethoxy]zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-1(4),8(11),15(18),22(25)-tri[2 -(morfolin-1-yl) ethoxy]zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-9(10),16(17),23(24)-tri[3-(dimethylamino) phenoxy]zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-8(11),15(18),22(25)-tri[3-(dimethylamino) phenoxy] zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-9(10),16(17),23(24)-tri[3-(trimethylammonium) -phenoxy]zinc(II)phthalocyanine triiodide;
2-[(4-hydroxycarbonyl)phenoxy]-8(11),15(18),22(25)-tri[3-(trimethylammonium) -phenoxy]zinc(II)phthalocyanine triiodide;
2-[(4-aminobenzamidyl)-phenoxy]-8(11),15(18),22(25)-tri[3-(trimethylammonium) phenoxy]zinc(II)phthalocyanine triiodide;
N,N′-dimethyl-N-2-(4-oxybenzoxy)-8(11),15(18),22(25)-tri[3-(trimethylammonium) phenoxy]zinc(II)phthalocyanine N′-biotinyl-1,2-diaminoethane triiodide;
2-[(4-bromomethylcarbonyl)-phenoxy]-8(11),15(18),22(25)-tri[3-(trimethylammonium) phenoxy]zinc(II)phthalocyanine triiodide;
2-[(4-maleimidomethyl)-phenoxy]-8(11),15(18),22(25)-tri[3-(trimethylammonium) -phenoxy]zinc(II)phthalocyanine triiodide;
2-[(4-hydrazidomethyl)-phenoxy]-8(11),15(18),22(25)-tri[3-(trimethylammonium) -phenoxy]zinc(II)phthalocyanine triiodide;
2-[(4-hydroxycarbonyl)phenoxy]-9,10,16,17,23,24-esa[3-(dimethylamino) phenoxy]zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-9,10,16,17,23,24-esa[3-(trimethylammonium) -phenoxy]zinc(II)phthalocyanine esaiodide;
2-[(4-sulphonate)phenoxy]-9,10,16,17,23,24-esa[3-(dimethylamino) phenoxy]zinc(II)phthalocyanine;
2-[(4-sulphonate)phenoxy]-9,10,16,17,23,24-esa[3-(trimethylammonium) phenoxy]zinc(II)phthalocyanine esaiodide;
2-[(4-hydroxycarbonyl)phenoxy]-9,10,16,17,23,24-esa[2-(N,N-diethylamino) ethylthio]zinc(II)phthalocyanine;
2-[(4-hydroxycarbonyl)phenoxy]-9,10,16,17,23,24-esa[2-(N,N,N-triethylammonium) ethylthio]zinc(II)phthalocyanine esaiodide; and
N,N′-dimethyl-N-2-(4-oxybenzoxyl)-9,10,16,17,23,24-esa[3-(trimethylammonium) phenoxy]zinc(II)phthalocyanine N′-biotinyl-1,2-diaminoethane esaiodide.
5. A pharmaceutical composition for use in photodynamic therapy, comprising the meta phthalocyanine according to claim 1 , optionally in combination with one or more pharmaceutically acceptable diluents and excipients.
6. The pharmaceutical composition according to claim 5 for the treatment of infectious diseases of viral, fungal and bacterial origin, of diseases characterised by cellular hyperproliferation and of dermatological diseases.
7. The pharmaceutical composition according to claim 5 in the form of a liposome or microvesicle preparation, dispersion, ointment, solution for parenteral injection, or topical dermatological preparation.
8. A sterilizing agent for blood and blood derivatives comprising a metal substituted non-centrosymmetrical phthalocyanine of formula (I):
wherein:
n is 1,2 or 4;
M is selected from the group consisting of Zn, Si(OR 7 ) 2 and AlOR 7 wherein R 7 is selected from the group consisting of H and C 1-15 alkyl;
R is selected from the groups consisting of: —COOH, —SH, —OH, —NH 2 , —CO—CH 2 —Br, —SO 2 Cl, maleimide, hydrazide, phenol, imidate, biotine, possibly bound to the phthalocyanine nucleus through a suitable linker and
when n=2 and the two groups R 1 are in the positions 9,10,16,17,23,24, said two groups R 1 can form a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms chosen from N, O, S; or
R 1 is represented by the group (X) p R 2 , wherein:
X is selected from the group consisting of O, S, —NR 5 and —CH 2 — and R 2 is
where:
Y is selected from the group consisting of C 1-10 alkyl and phenyl, possibly substituted, or it forms with the Z group, to which it is bound, a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms selected from the group consisting of N, O and S;
Z is selected from the group consisting of —N, —CH 2 N and —CONHCH 2 CH 2 N;
R 3 and R 4 , equal or different from one another, are selected from the group consisting of C 1-15 alkyl and phenyl, or form with the Z group, to which they are bound, a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms selected from the group consisting of N, O and S;
R 5 and R 6 , equal or different from one another, are selected from the group consisting of H and C 1-15 alkyl;
m, n, p, w, t and u, independently from one another, are 0 or 1; and
v is an integer comprised between 1 and 3;
with the proviso that:
R is in the position 1 or 2,
R1 is in the positions: 8(11), 15(18), 22(25), or 9(10), 16(17), 23(24) when n=1,
R1 is in the positions: 8,11,15,18,22,25 or 9,10,16,17,23,24 when n=2.
9. A diagnostic agent comprising a metal substituted non-centrosymmetrical phthalocyanine of formula (I):
wherein:
n is 1, 2 or 4;
M is selected from the group consisting of Zn, Si(OR 7 ) 2 and AlOR 7 wherein R 7 is selected from the group consisting of H and C 1-15 alkyl;
R is selected from the groups consisting of: —COOH, —SH, —OH, —NH 2 , —CO—CH 2 —Br, —SO 2 Cl, maleimide, hydrazide, phenol, imidate, biotine, possibly bound to the phthalocyanine nucleus through a suitable linker and
when n=2 and the two groups R 1 are in the positions 9,10,16,17,23,24, said two groups R 1 can form a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms chosen from N, O, S; or
R 1 is represented by the group (X) p R 2 , wherein:
X is selected from the group consisting of O, S, —NR 5 and —CH 2 —and R 2 is
where:
Y is selected from the group consisting of C 1-10 alkyl and phenyl, possibly substituted, or it forms with the Z group, to which it is bound, a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms selected from the group consisting of N, O and S;
Z is selected from the group consisting of —N, —CH 2 N and —CONHCH 2 CH 2 N;
R 3 and R 4 , equal or different from one another, are selected from the group consisting of C 1-15 alkyl and phenyl, or form with the Z group, to which they are bound, a saturated or unsaturated heterocycle, possibly substituted, which may contain up to two heteroatoms selected from the group consisting of N, O and S;
R 5 and R 6 , equal or different from one another, are selected from the group consisting of H and C 1-15 alkyl;
m, n, p, w, t and u, independently from one another, are 0 or 1;and
v is an integer comprised between 1 and 3;
with the proviso that:
R is in the position 1 or 2,
R1 is in the positions: 8(11), 15(18), 22(25), or 9(10), 16(17), 23(24) when n=1,
R1 is in the positions: 8,11,15,18,22,25 or 9,10,16,17,23,24 when n=2.
10. A method of treating infectious diseases of fungal origin caused by Candida albicans , comprising administering to a patient in need of such treatment an effective amount of a metal phthalocyanine according to claim 1 .
11. A method of localizing areas pathologically affected by infectious diseases of fungal origin caused by Candida albicans , comprising administering to a patient an effective amount of a metal phthalocyanine according to claim 1 .