Dominguez-Medina Sergio, Blankenburg Jan, Olson Jana, Landes Christy F, Link Stephan
Department of Chemistry, Laboratory for Nanophotonics, Rice University, Houston, Texas 77005.
ACS Sustain Chem Eng. 2013 Jul 1;1(7):833-842. doi: 10.1021/sc400042h.
We find that citrate-stabilized gold nanoparticles aggregate and precipitate in saline solutions below the NaCl concentration of many bodily fluids and blood plasma. Our experiments indicate that this is due to complexation of the citrate anions with Na cations in solution. A dramatically enhanced colloidal stability is achieved when bovine serum albumin is adsorbed to the gold nanoparticle surface, completely preventing nanoparticle aggregation under harsh environmental conditions where the NaCl concentration is well beyond the isotonic point. Furthermore, we explore the mechanism of the formation of this albumin 'corona' and find that monolayer protein adsorption is most likely ruled by hydrophobic interactions. As for many nanotechnology-based biomedical and environmental applications, particle aggregation and sedimentation are undesirable and could substantially increase the risk of toxicological side-effects, the formation of the BSA corona presented here provides a low-cost bio-compatible strategy for nanoparticle stabilization and transport in highly ionic environments.
我们发现,柠檬酸盐稳定的金纳米颗粒在许多体液和血浆的NaCl浓度以下的盐溶液中会聚集并沉淀。我们的实验表明,这是由于溶液中柠檬酸盐阴离子与Na阳离子的络合作用。当牛血清白蛋白吸附到金纳米颗粒表面时,胶体稳定性会显著提高,在NaCl浓度远超过等渗点的恶劣环境条件下,能完全防止纳米颗粒聚集。此外,我们探究了这种白蛋白“冠层”的形成机制,发现单层蛋白质吸附最有可能受疏水相互作用支配。对于许多基于纳米技术的生物医学和环境应用而言,颗粒聚集和沉降是不可取的,并且可能会大幅增加毒理学副作用的风险,此处呈现的BSA冠层的形成提供了一种低成本的生物相容性策略,用于在高离子环境中稳定纳米颗粒并使其运输。