Plasma protein adsorption of Tween 80-and poloxamer 188-stabilized solid lipid nanoparticles

被引:61
作者
Göppert, TM [1 ]
Müller, RH [1 ]
机构
[1] Free Univ Berlin, Inst Pharm, Dept Pharmaceut Biopharmaceut & Qual Management, D-12169 Berlin, Germany
关键词
plasma protein adsorption; poloxamer; 188; solid lipid nanoparticles; two-dimensional polyacrylamide gel electrophoresis; Tween; 80;
D O I
10.1080/10611860310001615956
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The plasma proteins adsorbing onto intravenously injected carriers are considered to be crucial factors determining the organ distribution. Plasma protein adsorption patterns were analyzed on solid lipid nanoparticles (SLN) stabilized with Tween 80 or stabilized with poloxamer 188. The binding patterns were determined by applying two different sample preparation methods, i.e. removal of the SLN from the plasma by (a) centrifugation and (b) gel filtration to assess, if the separation method has an effect on the patterns obtained. The Tween 80-modified SLN adsorbed the major plasma proteins known from particles with blood-brain barrier specificity. Poloxamer 188-surface modified SLN adsorbed the proteins known from model particles that exhibit prolonged circulation time in the blood. It is concluded that the biodegradable SLN stabilized with Tween 80 can potentially be used as drug carriers to the blood-brain barrier having a relatively long residence time in the blood stream. For the poloxamer 188-stabilized SLN a relatively long resistance time in the blood is predicted leading to potential accumulation in the bone marrow when looking at the distinct CII/CIII adsorption.
引用
收藏
页码:225 / 231
页数:7
相关论文
共 29 条
[1]  
BISGAIER CL, 1989, J BIOL CHEM, V264, P862
[2]   COLLOIDAL CARRIERS FOR INTRAVENOUS DRUG TARGETING - PLASMA-PROTEIN ADSORPTION PATTERNS ON SURFACE-MODIFIED LATEX-PARTICLES EVALUATED BY 2-DIMENSIONAL POLYACRYLAMIDE-GEL ELECTROPHORESIS [J].
BLUNK, T ;
HOCHSTRASSER, DF ;
SANCHEZ, JC ;
MULLER, BW ;
MULLER, RH .
ELECTROPHORESIS, 1993, 14 (12) :1382-1387
[3]  
BLUNK T, 1995, INT S CONTR REL BIOA, V22, P47
[4]  
DAVIS SS, 1981, PHARM TECHNOL, V5, P71
[5]   Plasma protein adsorption patterns on liposomes: Establishment of analytical procedure [J].
Diederichs, JE .
ELECTROPHORESIS, 1996, 17 (03) :607-611
[6]   The role of plasma proteins in brain targeting:: species dependent protein adsorption patterns on brain-specific lipid drug conjugate (LDC) nanoparticles [J].
Gessner, A ;
Olbrich, C ;
Schröder, W ;
Kayser, O ;
Müller, RH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 214 (1-2) :87-91
[7]  
Gessner A, 2000, ELECTROPHORESIS, V21, P2438, DOI 10.1002/1522-2683(20000701)21:12<2438::AID-ELPS2438>3.3.CO
[8]  
2-6
[9]   Significant transport of doxorubicin into the brain with polysorbate 80-coated nanoparticles [J].
Gulyaev, AE ;
Gelperina, SE ;
Skidan, IN ;
Antropov, AS ;
Kivman, GY ;
Kreuter, J .
PHARMACEUTICAL RESEARCH, 1999, 16 (10) :1564-1569
[10]   Plasma protein adsorption patterns on emulsions for parenteral administration:: Establishment of a protocol for two-dimensional polyacrylamide electrophoresis [J].
Harnisch, S ;
Müller, RH .
ELECTROPHORESIS, 1998, 19 (02) :349-354