化学传感器
化學傳感器
화학전감기
CHEMICAL SENSORS
2013年
3期
35-41
,共7页
石墨烯%酪氨酸酶%纳米金%有机相酶电极%呋喃丹
石墨烯%酪氨痠酶%納米金%有機相酶電極%呋喃丹
석묵희%락안산매%납미금%유궤상매전겁%부남단
graphene%tyrosinase%gold nanoparticles%carbofuran%organic phase enzyme electrode
采用改进的Hummers法制备了氧化石墨烯(GO),用微波辅助丝素还原法制备了丝素还原石墨烯(SF-GR),并用红外(FT-IR)、紫外(UV-vis)和透射电镜(TEM)对SF-GR进行了表征。然后以丝素同时原位还原的石墨烯-纳米金复合水凝胶包埋酪氨酸酶(Tyr)制备了新型的有机相酶电极(SF-GR-NanoAu-Tyr/GCE),在纯氯仿中对呋喃丹进行了检测。结果表明,在有机相中,丝素水凝胶能较好的保持酪氨酸酶的生物活性,GR和NanoAu促进了电子在电极界面上以及水凝胶内部的电子传递,提高了酶电极的灵敏性。在没有另外添加水或者缓冲液的情况下,酪氨酸酶的抑制率与浓度范围为1.0×10-8~1.0×10-12 mol/L的呋喃丹呈线性关系,检测限为8.0×10-13 mol/L。该有机相酶电极制备简单,检测快速,灵敏度高,适合于有机溶剂中微量农药的定量检测。
採用改進的Hummers法製備瞭氧化石墨烯(GO),用微波輔助絲素還原法製備瞭絲素還原石墨烯(SF-GR),併用紅外(FT-IR)、紫外(UV-vis)和透射電鏡(TEM)對SF-GR進行瞭錶徵。然後以絲素同時原位還原的石墨烯-納米金複閤水凝膠包埋酪氨痠酶(Tyr)製備瞭新型的有機相酶電極(SF-GR-NanoAu-Tyr/GCE),在純氯倣中對呋喃丹進行瞭檢測。結果錶明,在有機相中,絲素水凝膠能較好的保持酪氨痠酶的生物活性,GR和NanoAu促進瞭電子在電極界麵上以及水凝膠內部的電子傳遞,提高瞭酶電極的靈敏性。在沒有另外添加水或者緩遲液的情況下,酪氨痠酶的抑製率與濃度範圍為1.0×10-8~1.0×10-12 mol/L的呋喃丹呈線性關繫,檢測限為8.0×10-13 mol/L。該有機相酶電極製備簡單,檢測快速,靈敏度高,適閤于有機溶劑中微量農藥的定量檢測。
채용개진적Hummers법제비료양화석묵희(GO),용미파보조사소환원법제비료사소환원석묵희(SF-GR),병용홍외(FT-IR)、자외(UV-vis)화투사전경(TEM)대SF-GR진행료표정。연후이사소동시원위환원적석묵희-납미금복합수응효포매락안산매(Tyr)제비료신형적유궤상매전겁(SF-GR-NanoAu-Tyr/GCE),재순록방중대부남단진행료검측。결과표명,재유궤상중,사소수응효능교호적보지락안산매적생물활성,GR화NanoAu촉진료전자재전겁계면상이급수응효내부적전자전체,제고료매전겁적령민성。재몰유령외첨가수혹자완충액적정황하,락안산매적억제솔여농도범위위1.0×10-8~1.0×10-12 mol/L적부남단정선성관계,검측한위8.0×10-13 mol/L。해유궤상매전겁제비간단,검측쾌속,령민도고,괄합우유궤용제중미량농약적정량검측。
Graphene oxide was prepared by the method of modified Hummers. Silk-reduced-graphene (SF-GR) was prepared using microwave-assisted silk fibroin reduction synthesis method. TEM, FT-IR and UV-vis were uti-lized to characterize SF-GR. Then, a novel highly sensitive enzymatic inhibition organic phase enzyme electrode (OPEE) was fabricated by enwrapping tyrosinase in graphene-gold nanoparticles-silk fibroin hydrogel. The SF hy-drogel provided a necessary amount of water and a biocompatible microenvironment around the enzyme molecule to stabilize its biological activity and effectively prevented its inactivation by inhibitors such as pesticides. Under op-timized conditions, the inhibition percentage of carbofuran was proportional to its concentration in the range of 1.0 × 10-8 to 1.0 × 10-12 mol/L with a detection limit of 8.0 × 10-13 mol/L. Thus, the highly sensitive OPEE is a promis-ing new tool for pesticide analysis in organic solvents.