Preparation of polymeric nanoparticles by photo-crosslinking of an acryloylated polyaspartamide in w/o microemulsion

被引:17
作者
Craparo, EF
Cavallaro, G
Bondi, ML
Giammona, G
机构
[1] Univ Palermo, Dipartimento Chim & Tecnol Farmaceut, I-90123 Palermo, Italy
[2] CNR, Sez Palermo, ISMN, I-90146 Palermo, Italy
关键词
acryloylated polyaspartamide; inverse microemulsion; irradiation; nanoparticles; PHG; photo-crosslinking;
D O I
10.1002/macp.200400128
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Biodegradable polymeric nanoparticles have been prepared by UV irradiation of an acryloylated water soluble polymer by an inverse microemulsion. The starting polymer was a alpha,beta-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA) partially functionalized with glycidyl methacrylate (GMA) in order to introduce reactive vinyl groups in the side chain. The PHEA-GMA copolymer obtained (PHG) was crosslinked by UV irradiation of the inverse microemulsion prepared by mixing an aqueous solution of PHG with propylene carbonate (PC)/ethyl acetate (EtOAc) in the presence of sorbitan trioleate (SPAN 85) as surfactant. Nanoparticles obtained were characterized by FTIR spectrophotometry, transmission electron microscopy, size distribution analysis and zeta potential measurements. Nanoparticles investigated revealed spherical and homogeneous shading, the particle size having a mean diameter of 88 +/- 13 nm (PDI = 0.21) and a negative surface charge in several aqueous media. Moreover, in vitro chemical and enzymatic hydrolysis studies evidenced the partial biodegradability of PHG nanoparticles, which is more evident after incubation with enzymes such as esterases. PHG nanoparticles were loaded during UV irradiation process with Cytarbine, chosen as a model drug, and Cyt-loaded PHG nanoparticles were able to release it in a simulated physiological fluid (phosphate buffer at pH 7.4) and in blood plasma.
引用
收藏
页码:1955 / 1964
页数:10
相关论文
共 18 条
[1]   PREPARATION OF AQUEOUS POLYMERIC NANODISPERSIONS BY A REVERSIBLE SALTING-OUT PROCESS - INFLUENCE OF PROCESS PARAMETERS ON PARTICLE-SIZE [J].
ALLEMANN, E ;
GURNY, R ;
DOELKER, E .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 87 (1-3) :247-253
[2]  
BINDSCHAEDLER C, 1988, Patent No. 4968350
[3]  
COUVREUR P, 1995, EUR J PHARM BIOPHARM, V41, P2
[4]   FEASIBILITY OF MANUFACTURING A SOLID DOSAGE FORM USING A LIQUID NONVOLATILE DRUG CARRIER - A PHYSICOCHEMICAL CHARACTERIZATION [J].
DAHL, TC ;
BURKE, G .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1990, 16 (12) :1881-1891
[5]  
Fessi H., 1988, Method of formation of colloidal nanoparticles, Patent No. [FR 2,608,988 Al, 2608988]
[6]   New biodegradable hydrogels based on a photocrosslinkable modified polyaspartamide: synthesis and characterization [J].
Giammona, G ;
Pitarresi, G ;
Cavallaro, G ;
Buscemi, S ;
Saiano, F .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1428 (01) :29-38
[7]   Glycidyl methacrylate derivatization of alpha,beta-poly(N-hydroxyethyl)-DL-aspartamide and alpha,beta-polyasparthydrazide [J].
Giammona, G ;
Tomarchio, V ;
Pitarresi, G ;
Cavallaro, G .
POLYMER, 1997, 38 (13) :3315-3323
[8]   REACTION OF ALPHA, BETA-POLY(N-HYDROXYETHYL)-DL-ASPARTAMIDE WITH DERIVATIVES OF CARBOXYLIC-ACIDS [J].
GIAMMONA, G ;
CARLISI, B ;
PALAZZO, S .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1987, 25 (10) :2813-2818
[9]   New biodegradable hydrogels based on a photo-cross-linkable polyaspartamide and poly(ethylene glycol) derivatives. Release studies of an anticancer drug [J].
Giammona, G ;
Pitarresi, G ;
Craparo, EF ;
Cavallaro, G ;
Buscemi, S .
COLLOID AND POLYMER SCIENCE, 2001, 279 (08) :771-783
[10]  
GUINTANARGUERRE.D, 1996, INT J PHARM, V143, P133