The characteristics of betamethasone-loaded chitosan microparticles by spray-drying method

被引:42
作者
Huang, YC
Yeh, MK
Cheng, SN
Chiang, CH [1 ]
机构
[1] Natl Def Univ, Natl Def Med Ctr, Sch Pharm, Taipei, Taiwan
[2] Natl Def Univ, Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[3] Natl Def Univ, Natl Def Med Ctr, Tri Serv Gen Hosp, Dept Pediat & Med Res, Taipei, Taiwan
关键词
betamethasone; chitosan; Pluronic F68; gelatin; microparticles; spray drying method;
D O I
10.1080/0265204021000058456
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Betamethasone (BTM)-loaded microparticles prepared by a spray drying method using chitosan (CTS) as raw material, type-A gelatin and ethylene oxide-propylene oxide block copolymer (Pluronic F68) as modifiers. The BTM-loaded in varied chitosan/Pluronic F68/gelatin microparticle formulations was investigated. By properly choosing excipient type and concentration a high degree of control was achieved over the physical properties of the BTM-loaded microparticles. Microparticle characteristics (zeta potential, tap density, particle size and yield), loading efficiencies, microparticle morphology and in-vitro release properties were examined. Surface morphological characteristics and surface charges of prepared microparticles were observed by using scanning electron microscopy (SEM) and microelectrophoresis. A SEM micrograph shows that the particle sizes of the varied chitosan composed microparticles ranged from 1.1-4.7 mu m and the external surfaces appear smooth. The BTM-loaded microparticles entrapped in the chitosan/Pluronic F68/gelatin microparticles with trapping efficiencies up to 93%, collected yield rate 44%, and mean particle size varied between 1-3 mu m, positive surface charge (20-40 mv), and tap densities (0.04-0.40 g/cm 3 ) were obtained. The collected BTM yield and size of particle was increased with increasing BTM-loaded amount but both zeta potential and tap density of the particles decreased with increasing BTM-loaded amount. The in vitro release of BTM showed a dose-dependent burst followed by a slower release phase that was proportional to the drug concentration in the concentration range between 5-30%w/w. The in vitro drug release from the chitosan/Pluronic F68/gelatin 1/0.1/0.4 microspheres had a prolong release pattern. These formulation factors were correlated to particulate characteristics for optimizing BTM microspheres in pulmonary delivery.
引用
收藏
页码:459 / 472
页数:14
相关论文
共 29 条
[1]   Targeting to macrophages:: role of physicochemical properties of particulate carriers-liposomes and microspheres-on the phagocytosis by macrophages [J].
Ahsan, FL ;
Rivas, IP ;
Khan, MA ;
Suárez, AIT .
JOURNAL OF CONTROLLED RELEASE, 2002, 79 (1-3) :29-40
[2]  
Bain DF, 1999, J MICROENCAPSUL, V16, P369
[3]  
Bain DF, 1999, J MICROENCAPSUL, V16, P453
[4]   Large porous particles for sustained protection from carbachol-induced bronchoconstriction in guinea pigs [J].
Ben-Jebria, A ;
Chen, DH ;
Eskew, ML ;
Vanbever, R ;
Langer, R ;
Edwards, DA .
PHARMACEUTICAL RESEARCH, 1999, 16 (04) :555-561
[5]  
CARLVO P, 1997, PHARM RES, V14, P1431
[6]   Sustained-release butorphanol microparticles [J].
Chang, HC ;
Li, LC .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (08) :829-835
[7]   Use of solid corrugated particles to enhance powder aerosol performance [J].
Chew, NYK ;
Chan, HK .
PHARMACEUTICAL RESEARCH, 2001, 18 (11) :1570-1577
[8]   The spray drying of acetazolamide as method to modify crystal properties and to improve compression behaviour [J].
Di Martino, P ;
Scoppa, M ;
Joiris, E ;
Palmieri, GF ;
Andres, C ;
Pourcelot, Y ;
Martelli, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 213 (1-2) :209-221
[9]  
EWARDS DA, 1997, SCIENCE, V276, P1868
[10]   Chitosan microspheres with hydrocortisone and hydrocortisone-hydroxypropyl-β-cyclodextrin inclusion complex [J].
Filipovic-Grcic, J ;
Voinovich, D ;
Moneghini, M ;
Becirevic-Lacan, M ;
Magarotto, L ;
Jalsenjak, I .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 9 (04) :373-379