Incorporation of hydrophobic porphyrins into liposomes:: characterization and structural requirements

被引:60
作者
Postigo, F
Mora, M
De Madariaga, MA
Nonell, S
Sagristá, ML
机构
[1] Univ Barcelona, Fac Quim, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
[2] Univ Ramon Llull, Inst Quim Sarria, Grp Engn Mol, Barcelona 08017, Spain
关键词
liposomes; porphyrins; characterization; interaction; singlet oxygen;
D O I
10.1016/j.ijpharm.2004.03.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability of photosensitisers to give reactive oxygenated products is considered decisive for photodynamic applications, but the hydrophobic nature of many porphyrins makes necessary to obtain suitable pharmaceutical formulations. This paper reports the structural photosensitiser features that allow the preparation of stable liposomal formulations. Metallated and non-metallated TPPs and TPyPs and different lipid/porphyrin ratios were considered in order to procure liposomal preparations containing porphyrin concentrations adequate to necessary doses. The results show that the incorporation of porphyrins into liposomes can be related with their ability to form aggregates in a watery media. Thus, ZnTPP, which structural properties avoid the formation of aggregates, was efficiently incorporated into stable liposomes. Moreover, the efficient generation of singlet oxygen by ZnTPP liposomal suspensions has been shown. Because of this, the synthesis of hydrophobic porphyrin derived structures or other sensitisers, which do not aggregate in a watery media and with Q-bands shifted to higher; values than ZnTPP, will be efficiently incorporated into liposomes and useful for clinical applications. (C)2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 254
页数:16
相关论文
共 43 条
[1]   Polymer bound pyrrole compounds, IX. Photophysical and singlet molecular oxygen photosensitizing properties of mesoporphyrin IX covalently bound to a low molecular weight polyethylene glycol [J].
Abos, P ;
Artigas, C ;
Bertolotti, S ;
Braslavsky, SE ;
Fors, P ;
Lang, K ;
Nonell, S ;
Rodriguez, FJ ;
Sese, ML ;
Trull, FR .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1997, 41 (1-2) :53-59
[2]   Aggregation of tetraaryl-substituted porphyrins in homogeneous solution [J].
Akins, DL ;
Zhu, HR ;
Guo, C .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (13) :5420-5425
[3]   THE EFFECT OF IRRADIANCE ON VIRUS STERILIZATION AND PHOTODYNAMIC DAMAGE IN RED-BLOOD-CELLS SENSITIZED BY PHTHALOCYANINES [J].
BENHUR, E ;
GEACINTOV, NE ;
STUDAMIRE, B ;
KENNEY, ME ;
HOROWITZ, B .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1995, 61 (02) :190-195
[4]   Virus inactivation in blood [J].
BenHur, E ;
Horowitz, B .
AIDS, 1996, 10 (11) :1183-1190
[5]   Gd-meso-tetraphenylporphyrins: synthesis, encapsulation into liposomes and characterization of the resulting preparations [J].
Berezin, DB ;
Bonnett, R ;
de Madariaga, MA ;
Molina, S ;
Mora, M ;
Sagrista, ML ;
Valles, MA .
PHOTOCHEMOTHERAPY: PHOTODYNAMIC THERAPY AND OTHER MODALITIES III, PROCEEDINGS OF, 1997, 3191 :359-367
[7]  
Bonnett R., 2000, Chemical Aspects of Photodynamic Therapy, P115
[8]   Structure and biodistribution relationships of photodynamic sensitizers [J].
Boyle, RW ;
Dolphin, D .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 64 (03) :469-485
[9]  
BROCKHORST K, 1994, J MAG RES IMAGING, V4, P151
[10]   Photodynamic therapy [J].
Dougherty, TJ ;
Gomer, CJ ;
Henderson, BW ;
Jori, G ;
Kessel, D ;
Korbelik, M ;
Moan, J ;
Peng, Q .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (12) :889-905