Effects of formulation variables and characterization of guaifenesin wax microspheres for controlled release

被引:2
作者
Mani, N
Park, MO
Jun, HW [1 ]
机构
[1] Univ Georgia, Coll Pharm, Dept Pharmaceut & Biomed Sci, Athens, GA 30602 USA
[2] Forest Labs Inc, Commack, NY USA
[3] Biopolymed Inc, Seoul, South Korea
关键词
guaifenesin; wax microspheres; formulation variables; poloxamer; crystal properties;
D O I
10.1081/PDT-200049658
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Sustained-release wax microspheres of guaifenesin, a highly water-soluble drug, were prepared by the hydrophobic congealable disperse method using a salting-out procedure. The effects of formulation variables on the loading efficiency, particle properties, and in-vitro drug release from the microspheres were determined. The type of dispersant, the amount of wetting agent, and initial stirring time used affected the loading efficiency, while the volume of external phase and emulsification speed affected the particle size of the microspheres to a greater extent. The crystal properties of the drug in the wax matrix and the morphology of the microspheres were studied by differential scanning calorimetry (DSC), powder x-ray diffraction (XRD), and scanning electron microscopy (SEM). The DSC thermograrns of the microspheres showed that the drug lost its crystallinity during the microencapsulation process, which was further confirmed by the XRD data. The electron micrographs of the drug-loaded microspheres showed well-formed spherical particles with a rough exterior.
引用
收藏
页码:71 / 83
页数:13
相关论文
共 22 条
[1]
DEVELOPMENT AND EVALUATION OF SUSTAINED-RELEASE IBUPROFEN-WAX MICROSPHERES .1. EFFECT OF FORMULATION VARIABLES ON PHYSICAL CHARACTERISTICS [J].
ADEYEYE, CM ;
PRICE, JC .
PHARMACEUTICAL RESEARCH, 1991, 8 (11) :1377-1383
[2]
Blume RW, 2002, Guaifenesin sustained release formulation and tablets, Patent No. [US 6,372,252 B1, 6372252, 6,372,252 B1]
[3]
MICROENCAPSULATION OF DRUGS WITH AQUEOUS COLLOIDAL POLYMER DISPERSIONS [J].
BODMEIER, R ;
WANG, JJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1993, 82 (02) :191-194
[4]
PROCESS AND FORMULATION VARIABLES IN THE PREPARATION OF WAX MICROPARTICLES BY A MELT DISPERSION TECHNIQUE .2. W/O/W MULTIPLE EMULSION TECHNIQUE FOR WATER-SOLUBLE DRUGS [J].
BODMEIER, R ;
WANG, J ;
BHAGWATWAR, H .
JOURNAL OF MICROENCAPSULATION, 1992, 9 (01) :99-107
[5]
SOLID-STATE NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY - THEORY AND PHARMACEUTICAL APPLICATIONS [J].
BUGAY, DE .
PHARMACEUTICAL RESEARCH, 1993, 10 (03) :317-327
[6]
Collett JH, 1994, HDB PHARM EXCIPIENTS, P352
[7]
X-ray powder diffractometric method for quantitation of crystalline drug in microparticulate systems. I. Microspheres [J].
Dash, AK ;
Khin-Khin, A ;
Suryanarayanan, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (04) :983-990
[8]
IBUPROFEN-LOADED ETHYLCELLULOSE MICROSPHERES - ANALYSIS OF THE MATRIX STRUCTURE BY THERMAL-ANALYSIS [J].
DUBERNET, C ;
ROULAND, JC ;
BENOIT, JP .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1991, 80 (11) :1029-1033
[9]
MICROENCAPSULATION USING POLY (L-LACTIC ACID) .2. PREPARATIVE VARIABLES AFFECTING MICROCAPSULE PROPERTIES [J].
JALIL, R ;
NIXON, JR .
JOURNAL OF MICROENCAPSULATION, 1990, 7 (01) :25-39
[10]
Stereospecific formulation and characterization of sustained release ibuprofen microspheres [J].
Janjikhel, RK ;
Adeyeye, CM .
JOURNAL OF MICROENCAPSULATION, 1997, 14 (04) :409-426