Emulsification/internal gelation as a method for preparation of diclofenac sodium-sodium alginate microparticles

被引:54
作者
Ahmed, Mahmoud M. [1 ]
El-Rasoul, Saleh Abd [1 ]
Auda, Sayed H. [1 ]
Ibrahim, Mohamed A. [1 ]
机构
[1] Al Azhar Univ, Dept Pharmaceut & Ind Pharm, Fac Pharm, Assiut Branch, Assiut, Egypt
关键词
Sodium alginate; Internal gelation; Diclofinac sodium; Box-Behnken design; Microparticles; INTERNAL GELATION; NANOPARTICLES; MICROSPHERES;
D O I
10.1016/j.jsps.2011.08.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Emulsification/internal gelation has been suggested as an alternative to extrusion/external gelation in the encapsulation of several compounds including non-steroidal anti-inflammatory drugs such as diclofenac sodium. The objective of the present study was a trial to formulate diclofenac sodium as controlled release microparticles that might be administered once or twice daily. This could be achieved via emulsification/internal gelation technique applying Box-Behnken design to choose these formulae. Box-Behnken design determined fifteen formulae containing specified amounts of the independent variables, which included stirring speed in rpm (X1), drug: polymer ratio (X2) and the surfactant span 80% (X3). The dependent variables studied were cumulative percent release after two hours (Y1), four hours (Y2) and eight hours (Y3). The prepared microparticles were characterized for their production yield, sizes, shapes and morphology, entrapment efficiency and Diclofenac sodium in vitro release as well. The results showed that the production yield of the prepared diclofenac sodium microparticles was found to be between 79.55% and 97.41%. The formulated microparticles exhibited acceptable drug content values that lie in the range 66.20-96.36%. Also, the data obtained revealed that increasing the mixing speed (X1) generally resulted in decreased microparticle size. In addition, scanning electron microscope images of the microparticles illustrated that the formula contains lower span concentration (1%) in combination with lower stirring speed (200 rpm) which showed wrinkled, but smooth surfaces. However, by increasing surfactant concentration, microspheres' surfaces become smoother and slightly porous. Kinetic treatment of the in vitro release from drug-loaded microparticles indicated that the zero order is the drug release mechanism for the most formulae. (C) 2011 King Saud University. Production and hosting by Elsevier B. V. All rights reserved.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 19 条
[1]   Controlling of systemic absorption of gliclazide through incorporation into alginate beads [J].
Al-Kassas, Raida S. ;
Al-Gohary, Omaimah M. N. ;
Al-Faadhel, Monirah M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 341 (1-2) :230-237
[2]   Preparation and characterization of biodegradable paclitaxel loaded alginate microparticles for pulmonary delivery [J].
Alipour, Shohreh ;
Montaseri, Hashem ;
Tafaghodi, Mohsen .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 81 (02) :521-529
[3]  
Baker R.W., 1974, Controlled Release of Biologically active Agents, P15
[4]   Production of alginate microspheres by internal gelation using an emulsification method [J].
Chan, LW ;
Lee, HY ;
Heng, PWS .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 242 (1-2) :259-262
[5]   Effect of preparation conditions on the nutrient release properties of alginate-whey protein granular minicrospheres [J].
Chen, Lingyun ;
Subirade, Muriel .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 65 (03) :354-362
[6]   Preparation of alginate beads for floating drug delivery system:: effects of CO2 gas-forming agents [J].
Choi, BY ;
Park, HJ ;
Hwang, SJ ;
Park, JB .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 239 (1-2) :81-91
[7]   Increase of the duration of the anticonvulsive activity of a novel NMDA receptor antagonist using poly(butylcyanoacrylate) nanoparticles as a parenteral controlled release system [J].
Friese, A ;
Seiller, E ;
Quack, G ;
Lorenz, B ;
Kreuter, J .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2000, 49 (02) :103-109
[8]   Development and characterization of CyA-loaded poly(lactic acid)poly(ethylene glycol)PEG micro- and nanoparticles. Comparison with conventional PLA particulate carriers [J].
Gref, R ;
Quellec, P ;
Sanchez, A ;
Calvo, P ;
Dellacherie, E ;
Alonso, MJ .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2001, 51 (02) :111-118
[9]  
Guan H., 2001, CHEM ENG J, V168, P94
[10]   DISSOLUTION RATES OF FINELY DIVIDED DRUG POWDERS .2. MICRONIZED METHYLPREDNISOLONE [J].
HIGUCHI, WI ;
HIESTAND, EN ;
ROWE, EL .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1963, 52 (02) :162-&