Nanoparticles of Polyethylene Sebacate: A New Biodegradable Polymer

被引:63
作者
Guhagarkar, Swati A. [1 ]
Malshe, Vinod C. [2 ]
Devarajan, Padma V. [1 ]
机构
[1] Inst Chem Technol, Dept Pharmaceut Sci & Technol, Bombay 400019, Maharashtra, India
[2] Adv Agro Tech, Thana 400602, India
关键词
biodegradable polymer; emulsion solvent diffusion; nanoparticles; nanoprecipitation; silymarin; POLY(D; L-LACTIC ACID) NANOPARTICLES; DRUG-DELIVERY; NANOCAPSULES; DESIGN; BIOAVAILABILITY; FORMULATION; SILYMARIN;
D O I
10.1208/s12249-009-9284-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study demonstrates feasibility of preparation of nanoparticles using a novel polymer, polyethylene sebacate (PES), and its application in the design of drug-loaded nanocarriers. Silymarin was selected as a model hydrophobic drug for the present study. Two methods of preparation, viz., nanoprecipitation and emulsion solvent diffusion, were evaluated for preparation of nanoparticles. Effect of surfactants polyvinyl alcohol (PVA), lutrol F 68, and Tween 80 on the preparation of blank and silymarin-loaded PES nanoparticles was evaluated. Nanoprecipitation resulted in the formation of nanoparticles with all the surfactants (< 450 nm). Increase in surfactant concentration resulted in decrease in entrapment efficiency and particle size except with PVA. The type and concentration of surfactant was critical to achieve low size and adequate drug entrapment. While increase in concentration of PES resulted in larger nanoparticles, inclusion of acetone in the organic phase resulted in particles of smaller size. In case of emulsion solvent diffusion, nanoparticles were obtained only with lutrol F 68 as surfactant and high surfactant concentration. The study revealed nanoprecipitation as a more versatile method for preparation of PES nanoparticles. Scanning electron microscopy studies revealed spherical shape of nanoparticles. Freeze-dried nanoparticles exhibited ease of redispersion, with a marginal increase in size. Differential scanning calorimetry and X-ray diffraction analysis revealed amorphous nature of the drug. The study demonstrates successful design of PES nanoparticles as drug carriers.
引用
收藏
页码:935 / 942
页数:8
相关论文
共 35 条
[1]   Freeze-drying of nanoparticles: Formulation, process and storage considerations [J].
Abdelwahed, Wassim ;
Degobert, Ghania ;
Stainmesse, Serge ;
Fessi, Hatem .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (15) :1688-1713
[2]   PLGA nanoparticles in drug delivery: The state of the art [J].
Bala, I ;
Hariharan, S ;
Kumar, MNVR .
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2004, 21 (05) :387-422
[3]   Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles [J].
Bilati, U ;
Allémann, E ;
Doelker, E .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 24 (01) :67-75
[4]   Nanotechnology: Intelligent design to treat complex disease [J].
Couvreur, Patrick ;
Vauthier, Christine .
PHARMACEUTICAL RESEARCH, 2006, 23 (07) :1417-1450
[5]   Freeze-drying and lyopreservation of diblock and triblock poly(lactic acid)poly(ethylene oxide) (PLA-PEO) copolymer nanoparticles [J].
De Jaeghere, F ;
Allémann, E ;
Feijen, J ;
Kissel, T ;
Doelker, E ;
Gurny, R .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2000, 5 (04) :473-483
[6]   Polyesters based on diacid monomers [J].
Edlund, U ;
Albertsson, AC .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (04) :585-609
[7]   Increasing bioavailability of silymarin using a buccal liposomal delivery system: Preparation and experimental design investigation [J].
El-Samaligy, MS ;
Afifi, NN ;
Mahmoud, EA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 308 (1-2) :140-148
[8]   NANOCAPSULE FORMATION BY INTERFACIAL POLYMER DEPOSITION FOLLOWING SOLVENT DISPLACEMENT [J].
FESSI, H ;
PUISIEUX, F ;
DEVISSAGUET, JP ;
AMMOURY, N ;
BENITA, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 55 (01) :R1-R4
[9]   Physicochemical parameters associated with nanoparticle formation in the salting-out, emulsification-diffusion, and nanoprecipitation methods [J].
Galindo-Rodriguez, S ;
Allémann, E ;
Fessi, H ;
Doelker, E .
PHARMACEUTICAL RESEARCH, 2004, 21 (08) :1428-1439
[10]   The choice of a suitable oligosaccharide to prevent aggregation of PEGylated nanoparticles during freeze thawing and freeze drying [J].
Hinrichs, WLJ ;
Manceñido, FA ;
Sanders, NN ;
Braeckmans, K ;
De Smedt, SC ;
Demeester, J ;
Frijlink, HW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 311 (1-2) :237-244