Overview
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Key numbers
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- and Cd(II) in the range from 1 to 60 µg L−1 and 5 to 70 µg L−1 , respectively. The limit of detection was
- in Table S1 (8–22). The screen-printed electrode (SPE) has received wide attention for its
- cost (23), which makes it suitable for on-site rapid detection compared with the traditional
- (Hangzhou, China). Sodium acetate (≥99.0%) was obtained from Acros Organics. Acetic
- acid (≥99.7%), bismuth nitrate pentahydrate (≥99.999%), lead nitrate (≥99.999%), cadmium
- nitrate tetrahydrate (≥99.997%), iron nitrate (≥98%), zinc nitrate (≥99%), D-(+)-Glucose
- (≥99.5%), D-(-)-fructose, and Sucrose (≥99.0%) were procured from Sigma Aldrich. N,N-
- Dimethylformamide (≥99.7%), glutamate (≥99.0%), and magnesium nitrate were procured
- are listed in Table S2. The pretreatment method of the milk powder samples was pro-
- H2 O2 (30 wt%) was added into 20 mL of milk to remove the reductive substances in-
- cluding vitamins. After a 15 min sonication, 5 mL of hydrochloric acid (36.5 wt%) and
- 5 mL of acetic acid (50 wt%) were added into the mixture and treated with ultrasound
- Figure 1D. Obviously, there are two peaks in the testing range,
- Moreover, the detection limits (S/N = 3) of 0.10 µg L−1 for Pb(II) and 1.67 µg L−1 for
- revealed in Figure 5A, the relative standard deviations (RSD) of the peak current are 6.6%
- 10.1% for Pb(II)
- responses of the HMIs; the RSD is 4.8% for Pb(II) and 6.9% for Cd(II), respectively, indi-
- Foods 2023, 12, 730 10.1% for Pb(II) and Cd(II) (n = 5), respectively. The stability of the 8 of 12
- responses of the HMIs; the RSD is 4.8% for Pb(II) and 6.9% for Cd(II), respectively,
- responses of the HMIs; the RSD is 4.8% for Pb(II) and 6.9% for Cd(II), respectively, indicating
- Cd(II) were 115.32% and 86.78%, respectively (Table 1), and the testing results of Pb(II)
- in real samples are concluded in Table S4. The average recoveries for Pb(II) and Cd(II)
- Table 1. Recovery measurement for HMI detection in the extracted infant milk powder.
- investigated. The average recovery ratio of 115.32% for Pb(II) and 86.78% for Cd(II) was
- Cd(II). Table S1: Comparison of HMIs detection by electrochemical methods and other widely used
- techniques; Table S2: The main ingredients and nutrients of milk powder from five different brands;
- Table S3: Comparison of the detection performance of Pb(II) and Cd(II) between SPE/NPC and the
- reported methods; Table S4: Recovery measurement for the detection of single variable HMIs in extracted
Methods (brief)
- trometry (ICP-MS) (ELAN DRC-e, PekinElmer, Waltham, MA, USA) as the gold standard.
- 2.4. Real Sample Preparations
- are listed in Table S2. The pretreatment method of the milk powder samples was pro-
- and sp 2 graphitic structure of the NPC samples, respectively (37).To further explore the
- 3.6. Real Samples Application
- of our method for real sample analysis. Briefly, 30 µg L−1 of Pb(II) and Cd(II) were added
- into the pre-treated solution of infant milk powder samples; then, the SPE/NPC was
- the addition of the HMIs in the five samples are shown in Figure S7. To evaluate the
- accuracy of the data obtained from our sensor, a standard method of ICP-MS was used
- in real samples are concluded in Table S4. The average recoveries for Pb(II) and Cd(II)
- operation in the real sample application.
- Sample Added ICP-MS Our Method Recovery Added ICP-MS Our Method Recovery
- linear response ranging from 1 to 60 µg L−1 and 5 to 70 µg L−1 , and satisfactory LOD of
- a promising method for the detection of HMIs in milk powder samples.
- of SPE/NPC in five infant milk powder samples before and after the addition of 30 µg L−1 Pb(II) and
- metal-contaminated soil with various sample pretreatment techniques and detection methods. Environ. Monit. Assess. 2020,
- ICPMS for Fast Analysis of Trace Heavy Metals in Biological Samples. Anal. Chem. 2017, 89, 6878–6885. (CrossRef)
- Microextraction as a Front End to Electrothermal Vaporization-ICPMS for the Analysis of Trace Metals in Cells. Anal. Chem. 2018,
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Update history
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