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Background: Evidence for the effect of dietary sodium intake on the risk of cardiovascular disease has been controversial. One of the main explanations for the conflicting results lies in the great variability associated with measurement methods for sodium intake. Spot urine collection is a convenient method commonly used for sodium estimation, but its validity for predicting 24-h urinary sodium excretion at the individual level has not been well evaluated among the general population.Objective: The aim of this study was to evaluate the validity of the Kawasaki, the International Cooperative Study on Salt, Other Factors, and Blood Pressure (INTERSALT), and the Tanaka formulas in predicting 24-h urinary sodium excretion by using spot urine samples in Chinese adults.Design: We analyzed the relative and absolute differences and misclassification at the individual level from 3 commonly used methods for estimating sodium intake among 141 Chinese community residents.Results: The mean measured 24-h sodium excretion was 220.8 mmol/d. The median (95% CIs) differences between measured sodium and those estimated from the Kawasaki, INTERSALT, and Tanaka methods were 6.4 mmol/d (-17.5, 36.8 mmol/d), -67.3 mmol/d (-96.5, -46.9 mmol/d), and -42.9 mmol/d (-59.1, -24.8 mmol/d), respectively. The proportions of relative differences >40% with the Kawasaki, INTERSALT, and Tanaka methods were 31.2%, 41.1%, and 22.0%, respectively; and the absolute difference for the 3 methods was >51.3 mmol/d (3 g salt) in approximately half of the participants. The misclassification rate was 63.1% for the Kawasaki method, 78.7% for the INTERSALT method, and 66.0% for the Tanaka method at the individual level.Conclusion: The results from our study do not support the use of spot urine to estimate 24-h urinary sodium excretion at the individual level because of its poor performance with respect to misclassification. This trial was registered at www.chictr.org.cn as ChiCTR-IOR-16010278.

Carbon nano onions (CNOs) with diameters of 70–100 nm were fabricated by chemical vapor deposition at 800 °C, using methane as carbon source and high-temperature steam treated 316 stainless steel mesh as catalyst. The CNOs were isolated from the substrate by HNO3 refluxing, calcination in air at 500 °C and magnetic separation. The morphology, microstructures and magnetic properties of the CNOs were characterized by SEM, TEM, XRD, Raman spectroscopy, FT-IR spectroscopy and vibration sample magnetometer tests. Results showed that the surface-attached catalyst particles and amorphous carbon can be effectively removed from raw CNOs through HNO3-refluxing and calcination. Magnetic separation can selectively remove the CNOs encapsulating a [Ni, Fe] magnetic catalyst from the CNOs that are hollow. [New Carbon Materials 2014, 29(5): 398–403]