Park Jai Il, Tumarkin Ethan, Kumacheva Eugenia
Department of Chemistry, University of Toronto, 80 Saint George Street, Toronto, ON M5S 3H6, Canada.
Macromol Rapid Commun. 2010 Jan 18;31(2):222-7. doi: 10.1002/marc.200900551. Epub 2009 Dec 17.
A microfluidic route to producing small (<10 µm) bubbles with a narrow size distribution and long-time (at least, up to one month) stability is reported. The bubbles are encapsulated with a protein-polysaccharide shell. The strategy includes the following events, occurring in sequence: (i) a microfluidic generation of bubbles from a mixture of CO(2) and a minute amount of gases with low solubility in water, in an aqueous solution of lysozyme and sodium alginate; (ii) the dissolution of CO(2) leading to the shrinkage of bubbles and a local increase in acidity of the medium; (iii) the deposition of lysozyme at the gas-water interface triggered by the local decrease in pH; (iv) the deposition of alginate onto the lysozyme shell, due to the electrostatically driven complexation of alginate with lysozyme.
报道了一种微流控方法,可产生尺寸小(<10 µm)、尺寸分布窄且具有长期(至少长达一个月)稳定性的气泡。这些气泡被包裹在蛋白质 - 多糖壳中。该策略包括以下依次发生的步骤:(i)在溶菌酶和海藻酸钠的水溶液中,通过微流控从二氧化碳和微量低水溶性气体的混合物中产生气泡;(ii)二氧化碳的溶解导致气泡收缩以及介质酸度局部增加;(iii)局部pH降低引发溶菌酶在气 - 水界面沉积;(iv)由于海藻酸钠与溶菌酶的静电驱动络合作用,海藻酸钠沉积到溶菌酶壳上。