Photobiological and ultrastructural studies of nanoparticles of poly(lactic-co-glycolic acid)-containing bacteriochlorophyll-a as a photosensitizer useful for PDT treatment

被引:40
作者
Gomes, AJ
Lunardi, LO
Marchetti, JM
Lunardi, CN
Tedesco, AC
机构
[1] Univ Fed Uberlandia, Inst Quim, Uberlandia, MG, Brazil
[2] Fac Odontol Ribeirao Preto, Ribeirao Preto, Brazil
[3] Fac Ciencias Farmaceut Ribeirao Preto, Ribeirao Preto, Brazil
[4] Fac Filosofia Ciencias & Letras Ribeirao Preto, Ribeirao Preto, Brazil
基金
巴西圣保罗研究基金会;
关键词
bacteriochlorophyll-a; nanoparticle; photodynamic therapy; ultrastructural;
D O I
10.1080/10717540590931846
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The interaction of polymeric nanoparticles formulated from the biodegradable polymer poly(DL-lactide-co-glycolide) loaded with bacteriochlorophyll-a was studied in homogeneous solution and ill vitro in the presence of a macrophage cell line (P388-D1-ATCC). Photodynamic therapy (PDT) activity after different laser doses also was investigated. Scanning electron microscopy analysis of cell phagocyte nanoparticles showed that after 30 min of incubation most of the nanoparticles are in a clear adhesion process to the cell surface. The majority of nanoparticles became phagocytic after 2 hr of incubation time. After laser irradiation of the dye-containing system a total photodamage by nanoparticle phagocyte cells was observed and the cell survival was quantified by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide test. Our results indicate that polymeric nanoparticles work as an efficient drug delivery system for PDT drugs. This approach can be widely used for many other hydrophobic photosensitizers with higher aggregation tendency in neoplastic cell treatment.
引用
收藏
页码:159 / 164
页数:6
相关论文
共 21 条
[1]  
ASHSAN F, 2002, J CONTROL RELEASE, V79, P29
[2]   PHOTOPHYSICAL STUDIES OF BACTERIOCHLOROPHYLL-A AND BACTERIOPHEOPHYTIN-A - SINGLET OXYGEN GENERATION [J].
BORLAND, CF ;
MCGARVEY, DJ ;
TRUSCOTT, TG ;
CODGELL, RJ ;
LAND, EJ .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1987, 1 (01) :93-101
[3]  
Chen W, 1999, J MICROENCAPSUL, V16, P551
[4]   Protein delivery from poly(lactic-co-glycolic acid) biodegradable microspheres: release kinetics and stability issues [J].
Crotts, G ;
Park, TG .
JOURNAL OF MICROENCAPSULATION, 1998, 15 (06) :699-713
[5]   The effect of co-administration of adjuvants with a nanoparticle-based genetic vaccine delivery system on the resulting immune responses [J].
Cui, ZR ;
Mumper, RJ .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2003, 55 (01) :11-18
[6]   Increase of the photosensitizing efficiency of the Bacteriochlorin a by liposome-incorporation [J].
Damoiseau, X ;
Schuitmaker, HJ ;
Lagerberg, JWM ;
Hoebeke, M .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2001, 60 (01) :50-60
[7]   Influence of particle size and dissolution conditions on the degradation properties of polylactide-co-glycolide particles [J].
Dunne, M ;
Corrigan, OI ;
Ramtoola, Z .
BIOMATERIALS, 2000, 21 (16) :1659-1668
[8]   Preparation and characterization of cationic microspheres for gene delivery [J].
Esposito, E ;
Sebben, S ;
Cortesi, R ;
Menegatti, E ;
Nastruzzi, C .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 189 (01) :29-41
[9]   Encapsulation of phthalocyanines in biodegradable poly(sebacic anhydride) nanoparticles [J].
Fu, J ;
Li, X ;
Ng, DKP ;
Wu, C .
LANGMUIR, 2002, 18 (10) :3843-3847
[10]   Comparative degradation study of biodegradable microspheres of poly(DL-lactide-co-glycolide) with poly(ethyleneglycol) derivates [J].
Garcia, JT ;
Fariña, JB ;
Munguía, O ;
Llabrés, M .
JOURNAL OF MICROENCAPSULATION, 1999, 16 (01) :83-94