Arsenic sorption onto natural hematite, magnetite, and goethite

In this work the sorption of As(III) and As(V) on different natural iron oxides (hematite, magnetite, and goethite) has been studied as a function of different parameters. The sorption kinetics for the three iron oxides shows that equilibrium is reached in less than 2 days and the kinetics of sorption seems to be faster for goethite and magnetite than for hematite. The variation of the arsenic sorbed on the three different sorbents as a function of the equilibrium arsenic concentration in solution has been fitted with a non-competitive Langmuir isotherm. The main trend observed in the variation of the arsenic sorbed with pH is the decrease of the sorption on the three sorbents at alkaline pH values, which agrees with results found in the literature. Highest As(III) sorption was observed on hematite surface in all the pH range compared to goethite and magnetite. Natural minerals studied in this work had similar sorption capacities for arsenic than synthetic sorbents.     

Optimized Li4Ti5O12 nanoparticles by solvothermal route for Li-ion batteries

Li4Ti5O12 (LTO) nanoparticles were successfully synthesized by solvothermal technique using cost-effective precursors in polyol medium and post-annealed at temperatures of 400, 500, and 600 degrees C. The XRD patterns of the samples were clearly indexed to the spinel shaped Li4Ti5O12 (space group, Fd-3 m). The particle size and morphology of samples were identified using field-emission SEM. The electrochemical performance of solvothermal samples revealed fairly high initial discharge/charge specific capacities in the range 230-235 and 170-190 mAh/g, at 1 C-rate, while that registered for the solid-state sample has been 160 and 150 mAh/g, respectively. Furthermore, among these samples, LTO annealed at 500 degrees C exhibited highly improved rate performances at C-rates as high as 30 and 60 C. This was attributed to the achievement of small particle sizes with high crystallinity in nano-scale dimensions and hence shorter diffusion paths combined with larger contact area at the electrode/electrolyte interface.     

Persistence of four s-triazine herbicides in river, sea and groundwater samples exposed to sunlight and darkness under laboratory conditions

The persistence of terbuthylazine, simazine, atrazine and prometryn (s-triazine herbicides) was studied in sea, river and groundwaters during long-term laboratory incubation (127 days) under different laboratory conditions (light-darkness at 20 degrees C). Analysis of herbicides was performed by GC-NPD and their identity was confirmed by GC-MSD. A micro on-line method for the isolation of herbicide residues was used. The results showed that light had little effect on the removal of the four herbicides in riverwater but had a marked effect on their removal from sea and groundwater. Surprisingly, this removal appeared to be inversely proportional to the concentration of dissolved organic materials. In general, the degradation order was similar in sea and riverwaters; simazine was the most readily degraded compound (t(1/2)= 29-49 days), while terbuthylazine was the most persistent with the longest half-lives (76-331 days). In groundwater, terbuthylazine also showed greater persistence but prometryn was the compound with a fastest degradation rate, half-lives ranged from 88 days for prometryn to approximately 100 days for the other three compounds in light conditions and 263-366 days for prometryn and terbuthylazine, respectively, in darkness. Only for terbuthylazine was the remaining percentage at the end of the experiment higher than 50% under light conditions in riverwater, while in the other cases, the remaining percentage varied from 7 to 43% for simazine in seawater and atrazine in groundwater, respectively. Finally, a greater persistence was observed in groundwater for the four compounds.     

A Genomic Information Management System for Maintaining Healthy Genomic States and Application of Genomic Big Data in Clinical Research

Improvements in next-generation sequencing (NGS) technology and computer systems have enabled personalized therapies based on genomic information. Recently, health management strategies using genomics and big data have been developed for application in medicine and public health science. In this review, I first discuss the development of a genomic information management system (GIMS) to maintain a highly detailed health record and detect diseases by collecting the genomic information of one individual over time. Maintaining a health record and detecting abnormal genomic states are important; thus, the development of a GIMS is necessary. Based on the current research status, open public data, and databases, I discuss the possibility of a GIMS for clinical use. I also discuss how the analysis of genomic information as big data can be applied for clinical and research purposes. Tremendous volumes of genomic information are being generated, and the development of methods for the collection, cleansing, storing, indexing, and serving must progress under legal regulation. Genetic information is a type of personal information and is covered under privacy protection; here, I examine the regulations on the use of genetic information in different countries. This review provides useful insights for scientists and clinicians who wish to use genomic information for healthy aging and personalized medicine.     

Effect of Hyaluronic Acid on the Self-Assembly of a Dipeptide-Based Supramolecular Gel

The combination of polymers and low molecular weight (LMW) compounds is a powerful approach to prepare new supramolecular materials. Here we prepare two-component hydrogels made by a well-known and biologically active polymer, hyaluronic acid ( HA ), and a dipeptide-based supramolecular gelator. We undertake a detailed study of materials with different compositions including macroscopic (hydrogel formation, rheology) and micro/nanoscopic characterization (electron microscopy, X-ray powder diffraction). We observe that the two components mutually benefit in the new materials: a minimum amount of HA helps to reduce the polymorphism of the LMW network leading to reproducible hydrogels with improved mechanical properties; the LMW component network holds HA without the need for an irreversible covalent crosslinking. These materials have a great potential for biomedical application as, for instance, extracellular matrix mimetics for cell growth. As a proof of concept, we have observed that this material is effective for cell growth in suspension and avoids cell sedimentation even in the presence of competing cell-adhesive surfaces. This may be of interest to advanced cell delivery techniques.     

Antiparasitic Derivatives of the Furoquinoline Alkaloids Kokusaginine And Flindersiamine

We report the synthesis of 16 new compounds obtained from kokusaginine and flindersiamine, the main alkaloids isolated from the bark of Balfourodendron riedelianum. The activity of the compounds against axenic cultures of Trypanosoma cruzi epimastigtotes and trypomastigotes, as well as intracellular amastigotes, is described, together with their cytotoxic activity against three different human cell lines. The synthetic strategy for the preparation of the new compounds was based on the reactivity at the C4 position of the furoquinoline core towards nucleophiles. The new derivatives were synthesized by a Buchwald-Hartwig reaction, in most cases under green, solvent-free conditions. Compounds 1 c and 1 e displayed better in-vitro activity against trypomastigotes than benznidazole and nifurtimox (positive controls) with IC₅₀<4 μM. In addition, both compounds were not cytotoxic against the three human cell lines K562 (erytroleukimia), LM2 (breast cancer), and HaCat (keratinocyte). Interestingly, when evaluated against intracellular amastigotes, compound 1 c was able to significantly reduce the number of this parasite form, compared to the negative control.