Economical synthesis of composites of FeNi alloy nanoparticles evenly dispersed in two-dimensional reduced graphene oxide as thin and effective electromagnetic wave absorbers.

Developing electromagnetic wave absorbing materials prepared by a facile and economical way is a great challenge. Herein, we report a feasible route to synthesize a series of two-dimensional FeNi/rGO composites by a hydrothermal method followed by a carbonization process. The characterization confirms that nano-sized FeNi alloy nanoparticles are evenly supported onto graphene sheets without aggregation. The homogeneous dispersion of the nanoparticles may result from the introduction of glucose and the oxygen-containing groups on the surface of the graphene oxide. Measurements show that the microwave attenuation capability of the composites can be improved dramatically by adjusting the proportion of dielectric and magnetic components. Consequently, the two-dimensional magnetic material (FeNi/rGO-100) exhibits an excellent microwave absorption performance. In detail, the minimum reflection loss of -42.6 dB and effective bandwidth of 4.0 GHz can be reached with a thinner thickness of 1.5 mm. This study demonstrates that synergistic effects among the magnetic particles, reduced graphene oxide and amorphous carbon layers give rise to the highlighted microwave attenuation ability. Overall, the FeNi/rGO composite is a promising candidate to be used as a microwave absorber, and the feasible and economical method has shown potential application to construct multitudinous two-dimensional materials.

Systematic polymorphism analysis of the CYP2D6 gene in four different geographical Han populations in mainland China.

In this study, we systematically screened the polymorphisms of the whole CYP2D6 gene in the populations of four different geographical locations in China, namely, Shanghai, Shantou, Shenyang, and Xi'an, using a sample of 100 subjects from each population. Forty-eight different polymorphisms were detected as well as 12 novel ones. One novel nonsynonymous SNP was detected, and one novel intronic SNP was revealed that might inactivate a cryptic donor site 392 nucleotides downstream of the exon 6 natural donor site. In addition, the frequencies of some polymorphisms and alleles demonstrated significant differences among the four populations. Linkage disequilibrium analysis and tag SNP selection were performed separately for each population. Haplotypes were analyzed within the selected tag SNPs. Tag SNP selection and haplotype distributions showed differences across the four populations. This is the first large-scale study to analyze polymorphisms systematically across the whole CYP2D6 gene in the Chinese Han population.

Genetic polymorphism analysis of CYP2C19 in Chinese Han populations from different geographic areas of mainland China.

AIMS: Although many studies have been performed on CYP2C19, most of them have mainly examined the effects of the defective alleles CYP2C19(*)2 and CYP2C19(*)3. A comprehensive search for genetic polymorphisms of the CYP2C19 gene in the Chinese Han population has rarely been conducted. The present study was designed to determine the genetic basis of CYP2C19 polymorphisms. MATERIALS & METHODS: We investigated the 5 -regulatory region, all the exons and their surrounding introns of the CYP2C19 gene in 400 unrelated healthy Chinese Han volunteers from four different geographical locations, namely Shanghai, Shantou, Shenyang and Xi'an, with a sample of 100 subjects in each population, using direct sequencing. RESULTS: A total of 14 different CYP2C19 polymorphisms, including one novel variant (-2306G>A) in the enhancer region and a novel nonsynonymous one (905C>G, T302R) were identified. In addition, CYP2C19(*)1, (*)2, (*)3, (*)15 and (*)17 alleles showed frequencies of 69.7%, 24.7%, 3.3%, 1.2% and 1.2%, respectively, and CYP2C19(*)15 was the first detected in an Asian population. The frequencies of the prevalent defective alleles CYP2C19(*)2 and CYP2C19(*)3 in Chinese Han populations are similar to those in other Asians, and much higher than those reported in American European and other Caucasian populations. Haplotype analysis demonstrated CATCGG was the dominating haplotype with a frequency of 38.6% in the Chinese Han population. Furthermore, homology modeling analysis for CYP2C19 indicates that Thr302Arg could cause the displacement of heme. CONCLUSION: This is the first study that systematically screened the polymorphisms of the whole CYP2C19 gene in a large Chinese Han population. The results suggest that a few low frequent variants show significant differences among the four populations, while the prevalent polymorphisms show no differences. Therefore, our database provides important information on CYP2C19 polymorphisms in the Chinese population, and could be helpful for future personalized medicine studies in Asian populations generally.