Mingyao Li, Ruiyi Li, Zaijun Li
School of Life Sciences and Health Engineering, School of Chemical and Material Engineering, Jiangnan University, Wuxi, 214122, China.
Mikrochim Acta. 2024 Dec 16;192(1):15. doi: 10.1007/s00604-024-06817-z.
A biosensor is reported for electrochemical detection of ampicillin based on AuPt and DNA cycle dual-signal amplification strategy. Firstly, AuPt is prepared by reduction of chloroauric acid and chloroplatinic acid with serine-functionalized graphene quantum dot (SGQD). The resulting AuPt shows an excellent catalytic activity because of the synergy of Au and Pt. Then, AuPt is covalently combined with hairpin DNA and thionine molecule to form a redox probe. The probe was used for construction of the ampicillin biosensor coupling with DNA cycling. In the presence of ampicillin, the DNA cycle was triggered and leads to many redox probes being carried to the biosensor. This produces a significant signal amplification by oxidation and reduction of thionine molecules in these probes. The combination of AuPt catalysis with DNA cycle achieve ultrahigh sensitivity, selectivity, and stability for the electrochemical detection of ampicillin. Differential pulse voltammetry current linearly increases with the increase of ampicillin concentration in the range 1 × 10-1 × 10 M with a detection limit of 3.2 × 10 M (S/N = 3). The proposed analytical method has been satisfactorily used for electrochemical detection of ampicillin in milk.
报道了一种基于金铂和DNA循环双信号放大策略的用于氨苄青霉素电化学检测的生物传感器。首先,通过用丝氨酸功能化的石墨烯量子点(SGQD)还原氯金酸和氯铂酸来制备金铂。由于金和铂的协同作用,所得的金铂表现出优异的催化活性。然后,将金铂与发夹DNA和硫堇分子共价结合以形成氧化还原探针。该探针用于构建与DNA循环耦合的氨苄青霉素生物传感器。在氨苄青霉素存在下,触发DNA循环并导致许多氧化还原探针被携带到生物传感器上。这通过这些探针中硫堇分子的氧化和还原产生显著的信号放大。金铂催化与DNA循环的结合实现了对氨苄青霉素电化学检测的超高灵敏度、选择性和稳定性。在1×10⁻¹×10⁻⁶ M范围内,差分脉冲伏安法电流随氨苄青霉素浓度的增加呈线性增加,检测限为3.2×10⁻⁸ M(S/N = 3)。所提出的分析方法已成功用于牛奶中氨苄青霉素的电化学检测。