Transport and calorimetry study of 20% La-doped CeIn3.

CeIn3, a prototypical antiferromagnet, is an ideal candidate for investigating the relationship between magnetism and superconductivity, as superconductivity is induced as the magnetic transition temperature (T N) is lowered to 0 K by applying pressure. When La is substituted for Ce, T N of CeIn3 decreases to 0 K owing to the Ce dilution effects, thereby providing an alternative route to the zero-temperature quantum phase transition. In this study, we report a combinatorial approach to gain access to the critical point by applying external pressure to 20% La-doped CeIn3. Electrical resistivity measurements of La0.2Ce0.8In3 show that the T N of 8.4 K at 1 bar is gradually suppressed under pressure and can be extrapolated to 0 K at approximately 2.47 GPa, thereby showing a similar pressure dependence of T N as shown by undoped CeIn3. The kink-like feature in resistivity at T N of CeIn3 changed to an obvious jump in the doped compound for pressures higher than 1.64 GPa, indicating depletion in the carrier density due to a gap opening. AC calorimetry measurements under applied pressure show that the size of the specific heat jump at T N decreases with increasing pressure, but any signatures associated with the gap opening are not obvious, suggesting that the pressure-induced kink-to-jump change at T N in the resistivity is not a phase transition, but rather a gradual crossover. The low-temperature specific heat divided by temperature, C/T, does not strongly diverge with decreasing temperature, but is almost saturated near the projected quantum critical point, which can be attributed to a weak enhancement in the effective mass up to 2.6 GPa.

Seasonal variations of several pharmaceutical residues in surface water and sewage treatment plants of Han River, Korea.

We collected influent and effluent samples from four sewage treatment plants (STPs) as well as surface water samples in Han River of Seoul, Korea, in three sampling events representing different flow conditions, i.e., April, June, and August, 2005, and analyzed for eleven pharmaceuticals including acetaminophen, caffeine, carbamazepine, cimetidine, diltiazem, trimethoprim, and five sulfonamide antibiotics, using LC-MS-ESI. Pharmaceuticals of high annual production amount were detected in higher level in STP influents. Levels of pharmaceutical residues in the influents were the highest for acetaminophen (average 27,089 ng/L), followed by caffeine (23,664 ng/L), cimetidine (8045 ng/L), and sulfamethoxazole (523 ng/L). Levels of acetaminophen and caffeine in STP effluents were very low compared to the influent concentrations. However cimetidine was detected in relatively high levels even in STP effluent samples. In effluent samples, cimetidine showed the highest level (5380 ng/L), followed by caffeine (278 ng/L), sulfamethoxazole (193 ng/L), and carbamazepine (111 ng/L). The concentration of cimetidine was also the highest in surface water samples (average 281 ng/L), which is the highest level reported from surface water worldwide to our knowledge. Caffeine (268.7 ng/L), acetaminophen (34.8 ng/L), and sulfamethoxazole (26.9 ng/L) were also detected in relatively high levels. Levels of pharmaceuticals detected in surface water samples upstream STPs were generally very low compared to the downstream samples, suggesting that the STPs potentially be a major source of the test pharmaceuticals into Han River. The hazard quotients (HQs) were calculated for the test pharmaceuticals based on their occurrences in surface water, and no pharmaceutical resulted in HQ greater than one, suggesting that their potential environmental impact may be low.

Anti-ulcer actions of phytosphingosine hydrochloride in different experimental rat ulcer models.

The gastroprotective activity of phytosphingosine hydrochloride (PS-HCl, CAS 554-62-1) was assessed in four different rat models of experimentally induced gastric ulcer. Various doses (2.5-10 mg/kg) of PS-HCI were orally administered to rats 30 min before the treatment with HCl/ethanol, indometacin, cysteamine, or to rats with ligated pylorus. Oral administration of PS-HCl (2.5-10 mg/kg) to rats prevented the acute ulcer formation in 4 different types of ulcer in a dose-dependent manner as follows: (1) HCl/ethanol-induced gastric mucosal membrane lesions (20.1-47.8% inhibition), (2) indometacin-induced gastric mucosal membrane lesions (4.6-31.9% inhibition), (3) duodenal ulcer induced by cysteamine (10-20% inhibition), (4) gastric secretion and ulceration following pylorus ligation (33.3-61.9% inhibition). These results indicate that PS-HCI may be useful for the prevention of gastric ulcer.