Leo E, Pecquet S, Rojas J, Couvreur P, Fattal E
University of Paris-Sud, School of Pharmacy, URA CNRS 1218, Châtenay-Malabry, France.
J Microencapsul. 1998 Jul-Aug;15(4):421-30. doi: 10.3109/02652049809006869.
The milk model protein, beta lactoglobulin (BLG), was encapsulated into microspheres prepared by a multiple emulsion/solvent evaporation method. The effect of the pH of the outer aqueous phase on protein encapsulation and release as well as on microsphere morphology has been investigated. At all tested pH values, the encapsulation efficiency was shown to decrease with increasing the initial amount of BLG. This was correlated with the reduced stability of the primary emulsion as the initial BLG increased. In addition, reducing the solubility of BLG in the external aqueous phase by decreasing the pH to the isoelectric point of BLG (pI 5.2) resulted in an improved protein encapsulation. Moreover, it was shown that combining pH modification and optimal stability of the first emulsion yielded microspheres with a high encapsulation efficiency. However, release kinetic studies revealed that a significant burst release was observed with microspheres loaded with large amounts of BLG, especially when prepared in a medium at pH 5.2. This burst effect was attributed to morphology changes in the microsphere surface which was characterized by the presence of pores or channels able to accelerate the release of BLG. These pores were assumed to result from the presence of large amounts of protein molecules on the microsphere surface, that aggregate during microsphere formation at pH 5.2. Indeed, single adsorption experiments have shown that BLG had a higher affinity for the particle surface when the pH was close to the pI. Thus, reducing the solubility of a protein in the external aqueous phase allows the product of microspheres with a better encapsulation efficiency, although this benefit is provided by a strong adsorption of the protein on microsphere surface.
乳类模型蛋白β-乳球蛋白(BLG)被包裹于通过复乳/溶剂蒸发法制备的微球中。研究了外水相pH值对蛋白质包封与释放以及微球形态的影响。在所有测试的pH值下,包封效率均随BLG初始量的增加而降低。这与随着初始BLG增加,初级乳液稳定性降低相关。此外,通过将pH值降低至BLG的等电点(pI 5.2)来降低BLG在外水相中的溶解度,可提高蛋白质包封率。而且,结果表明,将pH调节与第一乳液的最佳稳定性相结合可得到具有高包封效率的微球。然而,释放动力学研究表明,装载大量BLG的微球会出现显著的突释现象,尤其是在pH 5.2的介质中制备时。这种突释效应归因于微球表面的形态变化,其特征是存在能够加速BLG释放的孔隙或通道。这些孔隙被认为是由于微球表面存在大量蛋白质分子所致,这些蛋白质分子在pH 5.2的微球形成过程中发生聚集。事实上,单吸附实验表明,当pH接近pI时,BLG对颗粒表面具有更高的亲和力。因此,降低蛋白质在外水相中的溶解度可得到具有更好包封效率的微球产品,尽管这种益处是由蛋白质在微球表面的强烈吸附所提供的。