Dipartimento di Scienze Chimiche, Università di Cagliari-CSGI and CNBS, Cittadella Universitaria, S.S. 554 bivio Sestu, 09042 Monserrato (CA), Italy.
J Colloid Interface Sci. 2010 May 15;345(2):448-53. doi: 10.1016/j.jcis.2010.01.063. Epub 2010 Jan 28.
In this work, we present the synthesis and characterization of n(+)-type porous silicon (PSi) layers. Our final aim is the fabrication of a biosensor that exploits the semiconductive properties of this material. PSi wafers were used as a matrix for enzyme adsorption. These wafers, as a result of their porous nanostructure, had a high surface area (360 m(2)/g) and pore size in the range 5-20 nm. The freshly prepared PSi was stabilized through controlled anodic oxidation. Two classes of samples differing for the level of oxidation were prepared. The first class was oxidized up to 2V (LO-PSi), whereas the second class was oxidized up to 10 V (HO-PSi). Both samples were used for the adsorption of Candida rugosa lipase. A significantly higher loading was ascertained for LO-PSi (140 mg/g) compared to HO-PSi (47 mg/g). The different hydrophobic-hydrophilic balance of the PSi surfaces induced by the different oxidation voltage affects the physical interactions that address the adsorption process of the lipase. The higher loading achieved with the LO-PSi resulted in a higher activity of the immobilized biocatalyst but in a lower catalytic efficiency. The two biocatalysts showed an acceptable stability toward storage (pH 5 buffer solution at 5 °C) within 2 weeks.
在这项工作中,我们展示了 n(+)-型多孔硅 (PSi) 层的合成和表征。我们的最终目标是制造一种利用这种材料的半导体特性的生物传感器。PSi 晶片被用作酶吸附的基质。这些晶片由于其多孔纳米结构,具有高表面积(360 m(2)/g)和 5-20nm 的孔径范围。新制备的 PSi 通过受控阳极氧化进行稳定。制备了两类不同氧化水平的样品。第一类氧化至 2V(LO-PSi),而第二类氧化至 10V(HO-PSi)。两种样品都用于吸附 Candida rugosa 脂肪酶。与 HO-PSi(47mg/g)相比,LO-PSi(140mg/g)的吸附量明显更高。不同氧化电压引起的 PSi 表面的不同疏水性-亲水性平衡影响了吸附脂肪酶的物理相互作用。与 LO-PSi 相比,较高的负载量导致固定化生物催化剂的活性更高,但催化效率较低。两种生物催化剂在 2 周内对储存(pH5 的缓冲溶液在 5°C)表现出良好的稳定性。
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