کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5434544 | 1509144 | 2017 | 11 صفحه PDF | دانلود رایگان |
- A novel biomagnetic separation/preconcentration strategy based on the formation of Pb2+-aptamer complex.
- The current method has a detection limit of 0.05 µg Lâ1.
- The accuracy of method confirmed by the analysis of QCMs of blood and urine is above of 96%.
Lead (Pb) as a topically poisonous metal represents a serious threat to the ecological environment and especially to human beings. Therefore, it is urgent to develop a rapid and reliable monitoring technique for this heavy metal in the environmental samples. In the present study, we have designed a selective and sensitive method for the determination of ultratrace contents of Pb2 + in biological samples, based on the guanine (G)-quadruplex formed by the aptamer with hairpin structure and Pb2 +. For this purpose, Pb2 + specific aptamer serving as affinity probe to capture and separate trace amounts of the analyte, was covalently linked to Fe3O4/graphene oxide (GO) surface by using a suitable cross-linking agent. Then, the G-quadruplex complex was formed by the opening of the “neck- ring” of the hairpin structure of aptamer in the presence of Pb2 +. Inductively coupled plasma mass spectrometry (ICP-MS) was used for determination of Pb2 + in biological matrices. The analysis conditions were optimized and the performance of the proposed method was investigated. Under optimum conditions, the calibration curve was linear over the range of 0.3-867.5 μg Lâ 1 and an enrichment factor (EF) of 50 was obtained. The limit of detection (LOD) was 0.05 μg Lâ 1 and the relative standard deviation (RSD) for single-sorbent repeatability and sorbent-to-sorbent reproducibility were < 4.7% and 8.8% (n = 5), respectively. The accuracy of aptamer-based affinity purification method was confirmed by the analysis of quality control materials (QCMs, Seronorm⢠Blood REF NO 201505 and Urine REF NO 2525).
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Journal: Materials Science and Engineering: C - Volume 77, 1 August 2017, Pages 459-469