Antimicrobial Photodynamic Activity of Phthalocyanine Derivatives

Table 2

Generation of quantum yield of singlet oxygen () and fluorescence () for various phthalocyanines in dimethyl sulfoxide (DMSO).

Phthalocyanine	ΦΔ		Ref.
-[1-(4-Bromophenyl)ethoxy]phthalocyaninatzinc(II)	0.67	0.10	[14]
Cu-tris(hydroxymethyl)-trihidroximetil- phthalocyanine	0.05		[6]
-[S-1-(4-Bromophenyl)ethoxy]phthalocyaninatzinc(II)	0.65	0.10	[14]
Zinc phthalocinine	0.67		[6]
-[R-1-(4-Bromophenyl)ethoxy]phthalocyaninatzinc(II)	0.76	0.12	[14]
Cu-tris(hydroxyethylaminomethyl)- phthalocyanine	0.02		[6]
4 iron phthalocyanines	0.9		[6]
Hydroxyaluminium phthalocyanine (AlPcOH)	0.41		[6]
Zn(II) phthalocyanine with fluconazole (ZnPcF)	0.14	0.19	[15]
Tris11,19,27-(1,2-diethylaminoethylthiol)-2-(captopril) phthalocyanines} Zn	0.26	0.1	[16]
Tris11,19,27-(1,2-diethylaminoethylthiol)-2-(captopril) phthalocyanines} Zn conjugated to silver nanoparticles	0.57	0.058	[16]
Octacationic Zn(II)-phthalocyanine	0.6	-	[17]
Tetracationic phthalocyanine	0.73	0.12	[18]