Harnisch S, Müller R H
Department of Pharmaceutics, Biopharmaceutics and Biotechnology, The Free University of Berlin, Germany.
Electrophoresis. 1998 Feb;19(2):349-54. doi: 10.1002/elps.1150190233.
The two-dimensional polyacrylamide electrophoresis (2-D PAGE) of the plasma protein adsorption pattern previously established for polymeric nanoparticles was modified and transferred to oil in water emulsions for intravenous administration. The emulsions were incubated with citrated plasma, and separation from excess plasma was performed by centrifugation under optimized conditions: 15000 g and three washing steps with 0.05 M phosphate buffer, pH 7.4. With this sample preparation, coalescence of droplets could be avoided and an unchanged surface area maintained, in addition the phosphate buffer minimized artificial IgG adsorption. Critical factors affecting sensitivity were contamination of the sample by oil residues and the use of thiourea in the immobilized pH gradients. Changes in the protein adsorption pattern caused by altered surface properties of the emulsion (i.e. adsorbed Poloxamer 407) were detectable when applying the optimized protocol. Knowledge of the protein adsorption patterns and their correlation to in vivo behavior opens the perspective for the development of intravenous emulsions for controlled drug delivery.
先前为聚合物纳米颗粒建立的血浆蛋白吸附模式的二维聚丙烯酰胺凝胶电泳(2-D PAGE)被修改,并转移到用于静脉给药的水包油乳液中。将乳液与枸橼酸盐血浆孵育,并在优化条件下通过离心从过量血浆中分离:15000 g,用pH 7.4的0.05 M磷酸盐缓冲液进行三个洗涤步骤。通过这种样品制备,可以避免液滴聚结并保持表面积不变,此外,磷酸盐缓冲液可将人工IgG吸附降至最低。影响灵敏度的关键因素是样品被油残留污染以及在固定pH梯度中使用硫脲。应用优化方案时,可检测到由乳液表面性质改变(即吸附泊洛沙姆407)引起的蛋白质吸附模式变化。了解蛋白质吸附模式及其与体内行为的相关性为开发用于控释药物的静脉乳液开辟了前景。