info:eu-repo/semantics/article
Photodynamic ultradeformable liposomes: Design and characterization
Fecha
2007-02Registro en:
Montanari, J.; Perez, Ana Paula; Di Salvo, Florencia; Diz, Virginia Emilse; Barnadas, R.; et al.; Photodynamic ultradeformable liposomes: Design and characterization; Elsevier Science; International Journal Of Pharmaceutics; 330; 1-2; 2-2007; 183-194
0378-5173
CONICET Digital
CONICET
Autor
Montanari, J.
Perez, Ana Paula
Di Salvo, Florencia
Diz, Virginia Emilse
Barnadas, R.
Dicelio, Lelia Elina
Doctorovich, Fabio
Morilla, María José
Romero, Eder Lilia
Resumen
Hydrophobic ([tetrakis(2,4-dimetil-3-pentyloxi)-phthalocyaninate]zinc(II)) (ZnPc) and hydrophilic ([tetrakis(N,N,N-trimethylammoniumetoxi)-phthalocyaninate]zinc(II) tetraiodide) (ZnPcMet) phthalocyanines were synthesized and loaded in ultradeformable liposomes (UDL) of soybean phosphatidylcholine and sodium cholate (6:1, w/w, ratio), resulting 100 nm mean size vesicles of negative Zeta potential, with encapsulation efficiencies of 85 and 53%, enthalpy of phase transition of 5.33 and 158 J/mmol for ZnPc and ZnPcMet, respectively, indicating their deep and moderate partition into UD matrices. Matrix elasticity of UDL-phthalocyanines resulted 28-fold greater than that of non-UDL, leaking only 25% of its inner aqueous content after passage through a nanoporous barrier versus 100% leakage for non-UDL. UDL-ZnPc made ZnPc soluble in aqueous buffer while kept the monomeric state, rendering singlet oxygen quantum yield (fi delta) similar to that obtained in ethanol (0.61), whereas UDL-ZnPcMet had a four-fold higher fi delta than that of free ZnPcMet (0.21). Free phthalocyanines were non-toxic at 1 and 10 microM, both in dark or upon irradiation at 15 J/cm2 on Vero and J-774 cells (MTT assay). Only liposomal ZnPc at 10 microM was toxic for J-774 cells under both conditions. Additionally, endo-lysosomal confinement of the HPTS dye was kept after irradiation at 15 J/cm2 in the presence of UDL-phtalocyanines. This could lead to improve effects of singlet oxygen against intra-vesicular pathogen targets inside the endo-lysosomal system.