Effect of osmotic pressure in the solvent extraction phase on BSA release profile from PLGA microspheres

被引:75
作者
Jiang, G
Thanoo, BC
DeLuca, PP [1 ]
机构
[1] Univ Kentucky, Coll Pharm, Fac Pharmaceut Sci, Lexington, KY 40506 USA
[2] Oakwood Labs LLC, Oakwood, OH USA
关键词
BSA; microsphere; osmotic pressure; release; solvent extraction;
D O I
10.1081/PDT-120015040
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study investigated the influence of osmotic pressure in the organic solvent extraction phase on release profile of bovine serum albumin (BSA) from poly(lactide-co-glycolide) (PLGA) microspheres. BSA-loaded PLGA microspheres with a target load of 10% were prepared by a double emulsion phase separation method. All the microsphere batches were fabricated in the same conditions except that in the organic solvent (CH2Cl2) evaporation step. Different concentrations of NaCl (0, 1.8, and 3.6%) or sucrose (20%) were used to generate a range of osmotic pressures in the extraction aqueous phase. These microspheres were characterized for incorporation efficiency, surface and internal morphology, particle size, protein stability, and in vitro release. The microspheres were spherical with particle size ranging from 16.8 to 27.8 mum. Higher osmotic pressure resulted in a denser internal structure although similar nonporous surface morphology was observed with all batches. No significant difference in encapsulation efficiency existed from batch to batch (87-94%). Sodium dodecyl sulfate-polyamide gel electrophoresis showed that BSA integrity was well retained. The release profile of the batch prepared with only water as the continuous (solvent extraction) phase exhibited a 79% burst release in the first 24 hr followed by a plateau and then a little release after 21 days. In the presence of NaCl or sucrose, the burst effect significantly decreased with increase in osmotic pressure in the extraction aqueous phase, which was then followed by sustained release for 35 days. A mass balance was made when the release terminated. Therefore, in the organic solvent extraction and evaporation step, increasing the osmotic pressure in the aqueous phase both reduced the burst release from the microspheres and unproved the subsequent sustained release profile.
引用
收藏
页码:391 / 399
页数:9
相关论文
共 31 条
[1]   Protein encapsulation and release from poly(lactide-co-glycolide) microspheres: effect of the protein and polymer properties and of the co-encapsulation of surfactants [J].
Blanco, D ;
Alonso, MJ .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1998, 45 (03) :285-294
[2]  
CONTI B, 2000, P INT S CONTR REL BI, V27, P1060
[3]   Development of 5-iodo-2′-deoxyuridine milling process to reduce initial burst release from PLGA microparticles [J].
Gèze, A ;
Venier-Julienne, MC ;
Mathieu, D ;
Filmon, R ;
Phan-Tan-Luu, R ;
Benoit, JP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 178 (02) :257-268
[4]   On the importance and mechanisms of burst release in matrix-controlled drug delivery systems [J].
Huang, X ;
Brazel, CS .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (2-3) :121-136
[5]   Drug release from PLA/PEG microparticulates [J].
Huang, YY ;
Chung, TW ;
Tzeng, TW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 156 (01) :9-15
[6]   A method using biodegradable polylactides polyethylene glycol for drug release with reduced initial burst [J].
Huang, YY ;
Chung, TW ;
Tzeng, TW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 182 (01) :93-100
[7]   Influence of formulation variables on the in-vitro release of albumin from biodegradable microparticulate systems [J].
Igartua, M ;
Hernandez, RM ;
Esquisabel, A ;
Gascon, AR ;
Calvo, MB ;
Pedraz, JL .
JOURNAL OF MICROENCAPSULATION, 1997, 14 (03) :349-356
[8]   Effect of solvent removal technique on the matrix characteristics of polylactide/glycolide microspheres for peptide delivery [J].
Jeyanthi, R ;
Thanoo, BC ;
Metha, RC ;
DeLuca, PP .
JOURNAL OF CONTROLLED RELEASE, 1996, 38 (2-3) :235-244
[9]  
Kissel T., 1996, MICROPARTICULATE SYS, P51
[10]   Preparation, characterization, and in vitro evaluation of 1-and 4-month controlled release orntide PLA and PLGA microspheres [J].
Kostanski, JW ;
Thanoo, BC ;
DeLuca, PP .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2000, 5 (04) :585-596