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Nostoc commune (Nostoc commune Vaucher ex Born & Flahault) is widely distributed in grasslands within the subtropical region. Because of its morphological changes are more sensitive to moisture, it may affect the soil’s response to infiltration-runoff processes, thus significantly influencing soil moisture dynamics, runoff, and soil loss. However, the exact effects of this phenomenon are not yet fully understood. This study established a one-year monitoring experiment of soil moisture, runoff and soil erosion in the karst area of Southwest China from September 2021 to November 2022. Using bare soil (CK) as the control, two treatments of Nostoc commune cover at 100 % coverage (C1) and 50 % coverage (C2) were set up in 3 repetitions to investigate the shallow soil’s response to Nostoc commune cover and rainfall and to quantify the effects of land cover and rainfall type on runoff and soil loss. The results showed that Nostoc commune cover significantly increased the shallow-soil water content, and the effect of increasing soil water content was more significant with increasing coverage. The cumulative soil water increment (CSWI) varied greatly under different types of rainfall due to the high water-absorbing capacity of Nostoc commune. The CSWI showed C1 C2 > CK under heavy rain and rainstorm events. The temporal pattern of soil moisture changed greatly under different cover treatments and rainfall events. In particular, the response time under different rainfall types varied from 10 min to 250 min. The runoff depth and soil loss in CK were 1.19–2.15 times and 1.92–14.43 times that of C1 and C2, respectively. This indicates that Nostoc commune cover has a significant effect on controlling runoff and soil erosion. In addition, the sensitivity of runoff and soil loss to the maximum 10-min rainfall intensity was higher than that of the maximum 30-min rainfall intensity, which was attributed to the rapid swelling of Nostoc commune in the hydration process, which greatly reduced runoff and soil erosion. This study can contribute to further understanding the hydrological process and soil erosion characteristics under different surface covers in humid karst areas.

An excellent magnetic multi-walled carbon nanotubes (MMWCNT) containing carboxyl material modified with ferroferric oxide (Fe3O4) nanoparticles was synthesized as the adsorbent for magnetic solid-phase extraction (MSPE) of five heavy metal ions (Pb2+, Cu2+, Co2+, Cd2+, Cr4+) in water samples followed by on-line inductively coupled plasma mass spectrometry (ICP-MS) detection. The characteristics of the adsorbent were analyzed using Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), and vibrating sample magnetometer (VSM). Some factors affecting extraction efficiency including pH of sample solution, the amount of adsorbent, extraction method and time, concentration and volume of desorption solvent, desorption time and evaluation of coexisting ions were optimized. Under the optimum conditions, good linearity (r ≥ 0.9951) was obtained within the range of 0.1–50.0 ng·mL−1. The limits of detection (LODs) and limits of quantification (LOQs) were 4.0–25.0 ng·L−1 and 15.0–80.0 ng·L−1, respectively. And satisfactory recoveries of five heavy metal ions ranged from 81.11% to 105.53% were acquired, and the relative standard deviations (RSDs) were no more than 6.05%. The MMWCNT synthesized had strong adsorption force for the five investigated heavy metal ions, respectively. Hence, the proposed method was so suitable and sensitive that it can be applied to the determination of trace analysis of heavy metals in water samples. HIGHLIGHTS A novel material of Fe3O4 nanoparticles modified multi-walled carbon nanotubes was synthesized.; An efficient, rapid and simple method for the determination of five heavy metal ions in different water samples by magnetic solid phase extraction was developed.; This results in the method validation showed good linearity, low limit of detection and satisfactory recovery.;

The complex topography, severe surface fragmentation and landscape heterogeneity of the karst region of southwest China make it extremely difficult to extract information on rocky desertification in the region. In order to overcome the disadvantages of the surface parameter-based feature space approach, which is difficult to construct and apply, this study uses the reflectance of Landsat 8 Operational Land Imager (OLI) in the red (Red), near-infrared (NIR) and shortwave infrared (SWIR) bands as the feature variables, and establishes a two-dimensional SWIR-NIR, Red-NIR and SWIR-Red reflectance spectral feature space. The three models of perpendicular rocky desertification index 1 (PRDI1), perpendicular rocky desertification index 2 (PRDI2) and perpendicular rocky desertification index 3 (PRDI3) were also constructed based on the variation of the degree of rocky desertification in each spectral feature space. The accuracy of the rocky desertification extracted by these three index models was verified and compared with the karst rocky desertification index (KRDI) and rocky desertification difference index (RSDDI), which are constructed based on the surface parameter feature space. The results show that: (1) The waveband reflectance-based feature space model provides a new method for large-scale rocky desertification information extraction, characterized by easy data acquisition, simple index calculation and good stability, and is conducive to the monitoring and quantitative analysis of rocky desertification in karst areas. (2) The overall accuracy and Kappa coefficient of PRDI1 are 0.829 and 0.784, respectively, both higher than other index models, showing the best applicability, accuracy and effectiveness in rocky desertification information extraction. (3) According to the results extracted from PRDI1, the total area of rocky desertification in Huaxi District of Guizhou province is 320.44 km2, with the more serious grades of rocky desertification, such as severe and moderate, mainly distributed in the southwestern, western and southeastern areas of Huaxi District. This study provides important information on the total area and spatial distribution of different degrees of rocky desertification in the study area, and these results can be used to support the local government’s ecological and environmental management decisions. The method proposed in this study is a scientific and necessary complement to the characteristic spatial methods based on different surface parameters, and can provide important methodological support for the rapid and efficient monitoring of karstic rocky desertification over large areas.

Herein, we report a novel sensor to detect trypsin using a purpose-designed fluorescein-labelled peptide with negatively charged carbon nanoparticles (CNPs) modified by acid oxidation. The fluorescence of the fluorescein-labelled peptide was quenched by CNPs. The sensor reacted with trypsin to cleave the peptide, resulting in the release of the dye moiety and a substantial increase in fluorescence intensity, which was dose- and time-dependent, and trypsin could be quantified accordingly. Correspondingly, the biosensor has led to the development of a convenient and efficient fluorescent method to measure trypsin activity, with a detection limit of 0.7 μg/mL. The method allows rapid determination of trypsin activity in the normal and acute pancreatitis range, suitable for point-of-care testing. Furthermore, the applicability of the method has been demonstrated by detecting trypsin in spiked urine samples.

A novel fluorescence chemical sensor-based probe 1-{[(E)-(2-aminophenyl)azanylidene]methyl}naphthalen-2-ol (AMN) was designed and synthesized, which performed a “naked eye” detection ability toward Cu2+ and Co2+ based on aggregation-induced emission (AIE) fluorescence strategy. It has sensitive detection ability for Cu2+ and Co2+. In addition, the color changed from yellow-green to orange under the sunlight, realizing the rapid identification of Cu2+/Co2+, which has the potential of on-site visual detection under the “naked eye”. Moreover, different “on” and “off” fluorescence expressions were exhibited under excessive glutathione (GSH) in AMN-Cu2+ and AMN-Co2+ systems, which could be employed to distinguish Cu2+ from Co2+. The detection limits for Cu2+ and Co2+ were measured to be 8.29 × 10−8 M and 9.13 × 10−8 M, respectively. The binding mode of AMN was calculated to be 2:1 by Jobs’ plot method analysis. Ultimately, the new fluorescence sensor was applied to detect Cu2+ and Co2+ in real samples (tap water, river water, and yellow croaker), and the results were satisfying. Therefore, this high-efficiency bifunctional chemical sensor platform based on “on–off” fluorescence detection will provide significant guidance for the advance development of single-molecule sensors for multi-ion detection.

Drug stability is closely related to drug safety and needs to be considered in the process of drug production, package and storage. To investigate the stability of epalrestat, a carboxylic acid derivative, a reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed in this study and applied to analyzing the degradation kinetics of epalrestat in aqueous solutions in various conditions, such as different pH, temperatures, ionic strengths, oxidation and irradiation. The calibration curve was A = 1.6 × 105C–1.3 × 103 (r = 0.999) with the liner range of 0.5–24 μg/mL, the intra-day and inter-day precision was less than 2.0%, as was the repeatibility. The average accuracy for different concentrations was more than 98.5%, indicating that perfect recoveries were achieved. Degradation kinetic parameters such as degradation rate constants (k), activation energy (Ea) and shelf life (t0.9) under different conditions were calculated and discussed. The results indicated that the degradation behavior of epalrestat was pH-dependent and the stability of epalrestat decreased with the rised irradiation and ionic strength; however, it was more stable in neutral and alkaline conditions as well as lower temperatures. The results showed that the degradation kinetics of epalrestat followed first-order reaction kinetics. Furthermore, the degradation products of epalrestat under stress conditions were identified by UHPLC-PDA-MS/MS, with seven degradation products being detected and four of them being tentatively identified. Keywords: Epalrestat, RP-HPLC, Degradation kinetics, UHPLC-PDA-MS/MS, Degradation products

Antiepileptic drugs are the first choice for epilepsy treatment. Monitoring antiepileptic drugs is important to minimize their adverse side effects by choosing the optimum drug dosage. An accurate and high throughput supercritical fluid chromatography-tandem mass spectrometry method has been developed for the simultaneous quantification of several antiepileptic drugs in human plasma. Plasma samples were extracted with ethyl acetate and the upper organic layer was directly injected into the supercritical fluid chromatography/mass spectrometry (SFC-MS/MS) system without further nitrogen evaporation and subsequent reconstitution. The analytes were eluted on a UPC2TM BEH, 2-EP column (100 × 3 mm, 1.7 μm) at a flow rate of 1.0 mL/min and multi-reaction monitoring (MRM) was performed for determination of the analytes and internal standard (IS) in polarity switching mode. Calibration curves were linear over the concentration ranges of 0.08–40, 0.01–15, 0.01–8 and 0.5–50 μg/mL with lower limit of quantifications of 0.08, 0.01, 0.01 and 0.50 μg/mL for topiramate, carbamazepine, oxcarbazepine and monohydroxycarbamazepine, respectively. This sensitive, accurate, novel method will be very useful for monitoring the above antiepileptic drugs and for pharmacokinetic studies. Keywords: Antiepileptic drugs, SFC-ESI-MS/MS, Human plasma, Therapeutic drug monitoring

Curcumin and its two derivatives of PB-3 and DY-1 were subjected to the forced degradation studies under the conditions of hydrolysis (acidic and alkaline), oxidation, photolysis, and thermal stress recommended by ICH Q1A (R2) by means of UPLC–DAD–MS/MS. Three analytes and their degradation products were separated on a column of ACQUITY UPLC® BEH C18 (100 mm × 2.1 mm, 1.7 μm) with an in-line filter prior to the column using acetonitrile and 10 mM ammonium acetate buffer (pH adjusted to 3.5) as a mobile phase. Both curcumin and DY-1 showed extensive degradation under alkaline condition and gave rise to two degradation products for curcumin and three for DY-1, respectively, while no degradation product was observed under other tested conditions. PB-3 was found to be unstable in acid and alkaline conditions, two degradation products in acidic hydrolytic condition and one in alkaline condition were obtained, while it was stable in photolytic, oxidative and thermal stress conditions. The degradation products of three analytes were characterized as follows by analyzing the mass fragmentation patterns of curcumin and mass analysis of the degradation products: ferulic acid and vanillin for curcumin, 3-methoxyl-4-[3-(1-tetrahydropyrrolyl)propoxyl] benzoic aldehyde, 2,2-di-(1-phenylmethyl)-3-oxo-5-[3-methoxyl-4-(3-tetrahydropyrolylpropoxyl)] pent-4-enoic acid, and tetrapyrolyl propoxyl methoxyl phenyl prop-2-enoic acid for PB-3, 3-oxo-5-[4-hydroxyl-5-methoxyl-3-(1-morpholinylmethyl)] pent-4-enoic aldehyde, 3-oxo-5-(4-hydroxyl-5-methoxyl-3-(1-morpholinylmethyl)) pent-4-enoic acid and 2-hydroxyl-3-methoxyl-5-(7-(3-methoxyl-4-hydroxylphenyl)-3,5-dioxo-4,4-dimethyl hept-1,6-dienyl) benzoic acid for DY-1, respectively. The degradation pathways of curcumin and its derivatives were presented in addition. Keywords: Curcumin, PB-3, DY-1, UPLC–DAD–MS/MS, Degradation products

Surfactants are one of the major pollutants in laundry powder, which have an impact on the environment and human health. Carbon quantum dots (CQDs) are spherical zero-dimensional fluorescent nanoparticles with great potential for fluorescent probing, electrochemical biosensing and ion sensing. Herein, a bottom-up approach was developed for the synthesis of CQDs from biomass to detect laundry detergent and laundry powder. Waste chicken bones were used as carbon precursors after being dried, crushed and reacted with pure water at 180 °C for 4 h to generate CQDs, which exhibited a monodisperse quasi-spherical structure with an average particle size of 3.2 ± 0.2 nm. Functional groups, including -OH, C=O, C=C and C-O, were identified on the surface of the prepared CQDs. The optimal fluorescence excitation wavelength of the yellow-brown CQDs was 380 nm, with a corresponding emission peak at 465 nm. CQDs did not significantly increase cell death in multiple cell lines at concentrations of 200 µg·mL−1. Fluorescence enhancement of CQDs was observed after addition of sodium dodecyl benzene sulphonate, a major anionic surfactant in laundry powder. A linear relationship between fluorescence enhancement CQDs and the concentration of laundry powder was established. Thus, a hydrothermal method was developed to generate CQDs from waste biomass that may be used as a fluorescent probe to detect laundry powder.

A simple, rapid, and sensitive gas chromatography-mass spectrometry (GC-MS) method was developed and validated for the simultaneous determination of two fatty acids, methyl hexadecanoate (MH) and methyl stearate (MS), to allow the evaluation of packaging-drug compatibility. The two migrants were quantified in selective ion-monitoring (SIM) mode, with limits of detection (LOD) of 0.0030 μg/mL and 0.0121 μg/mL. Linear calibration curves for MH and MS were obtained in the concentration ranges of 0.1011–5.0570 μg/mL and 0.2015–10.0740 μg/mL, respectively. The developed method was successfully applied to estimate the safety of the injection of recombinant antitumor-antivirus protein (RAAP). The results showed that the possible maximum daily intake was 3.0 ng and 12.1 ng for MH and MS, respectively. As these values were both below the permitted daily exposure, the migrants can be considered as having low safety risk and do not affect the quality of the injection. Keywords: Compatibility, Rubber stoppers, Injection, Fatty acids, GC-MS

A simple method was established for the determination of β-propiolactone (BPL) in human inactivated rabies vaccine by gas chromatography-mass spectrometry (GC-MS). The determination was performed on an Agilent HP-INNOWAX (30 m × 0.32 mm i.d., 0.25 µm) capillary column at the temperature of 80 °C. Electrospray ionization (ESI) was used by selective ion detection at m/z 42. The temperature for ESI source and inlet was set at 230 °C and 200 °C, respectively. Helium was used as the carrier gas at a flow rate of 25.1 mL/min. The total run time was 8 min. Acetonitrile and other components in the sample did not interfere with the determination of BPL. The results showed good linearity of BPL in the range of 0.50–10.01 μg/mL, with the limit of detection and the limit of quantification of 0.015 μg/mL and 0.050 μg/mL, respectively. Satisfactory precision was achieved for the current developed method. The method was applied to detect 6 batches of vaccine samples, and the results indicated that the target analyte BPL was present in three batches of unpurified samples, but was not detected in the purified samples, indicating the test samples were qualified. The established method was proved to be simple, versatile and sensitive, which can meet the requirements of quality control of BPL in human inactivated rabies vaccine. Keywords: β-propiolactone, Inactivated human rabies vaccine, GC-MS, Hydrolysis

Objective. To establish a method for extraction and determination of antioxidant 264 (2,6-di-tert-butyl-4-methylphenol) in the brominated butyl rubber stopper for injection and migration study in recombinant potent antitumor and antivirus protein injection (Novaferon). Methods. Dichloromethane-ethanol was adopted as the extraction solvent during the process of reflux extraction of antioxidant 264 in the brominated butyl rubber stopper. High-performance liquid chromatography (HPLC) was used for the determination of the migration of antioxidant 264 to Novaferon. The mobile phase consisted of acetonitrile-water (80 : 20, v/v). The flow rate was 1.5 mL/min. The detection wavelength was 280 nm. Results. The linearity range was from 4.003 to 200.150 μg/mL (r2 = 0.99996), and the average recovery of antioxidant 264 was 97.8%. The applicability of the methodology was good, which can be used for the determination of antioxidant 264. The results indicated that antioxidant 264 was not detected in Novaferon after the accelerated test and three months of long-term test. Conclusion. The established validated method in this study can be used for the determination of antioxidant 264 in the rubber stopper, and the brominated butyl rubber stopper has good compatibility with Novaferon.

A simple, rapid and sensitive method based on an ultra-performance liquid chromatographyâtandem mass spectrometry (UPLCâMS/MS) has been developed and validated for the determination of pimavanserin in rat plasma. The analyte was extracted by protein precipitation with methanol and separated on an ACQUITY BEH C18 column (100 à 2.1 mm, 1.7 µm; Waters, USA), with an isocratic elution of acetonitrile-water containing 10 mM ammonium acetate (70:30, v/v), at a flow rate of 0.2 mL/min for 2.5 min. The analyte and clarithromycin (the internal standard) were detected and quantified in positive ion mode using multiple reaction monitoring transitions at m/z 428.2 â 223.0 for pimavanserin and m/z 748.5 â 589.5 for clarithromycin. Relative coefficient (r) for the calibration curve was more than 0.9980. The intra-day and inter-day precisions (relative standard deviation, RSD%) were less than 13.3% and 10.5%, respectively, and the accuracy (relative error, RE%) was within ± 11.5%. The analytical method was successfully applied to a routine pharmacokinetic study of pimavanserin in rats after oral administration at the dose of 10 mg/kg. Keywords: UPLCâMS/MS, Pimavanserin, Pharmacokinetics, Rat plasma

With increasing age, plants will cause changes in soil physicochemical properties. The objective of this study was to investigate differences in the soil physicochemical properties in different-aged Masson pine forest plantations (i.e., 10, 20, 40, and 60 years old). Soil samples were collected in a pure Masson pine forest plantation in Southwest China. The soil determination indexes included organic carbon, nitrogen, phosphorus and potassium contents, water content, bulk density, and pH. The soil pH of a 20-year-old forest was significantly (p < 0.05) higher than that of a 10, 40, and 60-year-old forest. In addition, soil-available phosphorus in a 60-year-old forest was significantly (p < 0.05) higher than that in the other three age forest groups. With increasing forest age, available phosphorus increased, while available nitrogen decreased at 20 years old and then increased at 40 years old. There was a significant positive correlation (p < 0.05) between total nitrogen and available potassium; no significant correlation (p> 0.05) between total phosphorus and total potassium, organic carbon, bulk density, and pH; and a significant negative correlation (p < 0.05) between available phosphorus and the water content. The availability and utilization efficiency of soil nutrients in young forests were higher than those in old forests and the intermediate forest age was an important time point that affected the soil properties. To improve the availability of soil nutrients and ensure the sustainable utilization of soil resources, it is necessary to increase the input of nitrogen and especially phosphorus. More attention should be given to the phytochemometric response with respect to the age of plantations.

The present study was designed to investigate the influence of the pretreatment of piperazine ferulate on pharmacokinetic parameters of methotrexate in methotrexate-induced renal injury rats. A simple and efficient high performance liquid chromatography coupled with mass spectrometry (HPLC-MS) method was developed to determine methotrexate in rat plasma. Methotrexate and syringic acid (internal standard) were extracted from rat plasma samples by protein precipitation with acetonitrile. The analysis was performed on a CAPCELL PAK C18 column (150 mm × 4.6 mm, 5 µm) with acetonitrile and 5 mmol/l ammonium acetate aqueous (10:90, v/v). The linear range was 5.0 × 10−2 to 100.0 µg/ml for methotrexate. Other parameters were all within the acceptance criteria. The validated method was successfully applied the pharmacokinetic study of methotrexate between two methotrexate treated groups (with and without the pretreatment of piperazine ferulate). Compared with the methotrexate treated alone group, the pharmacokinetic parameters in the methotrexate with the pretreatment of piperazine ferulate group showed significantly lower MRT(0-t), MRT(0-∞) and T1/2. Results suggested that methotrexate can be rapidly eliminated, cleared or metabolized in rat blood, which might be related to the pretreatment of piperazine ferulate. The method provided deeper insights into rational clinical use of methotrexate with the pretreatment of piperazine ferulate on cancer patients with renal dysfunction.

Cancer is the leading cause of death all over the world. Among the chemotherapy drugs, taxanes play an important role in cancer treatment. 6258-70 is a new semi-synthetic taxane which has a broad spectrum of antitumor activity. A fast and reliable high performance liquid chromatography-tandem mass spectrometry (HPLC–MS/MS) method was developed for quantification of 6258-70 in rat plasma and tissues in this paper. After extraction by liquid-liquid extraction method with methyl tert-butyl ether, the samples were separated on a Kinetex C18 column (50 mm×2.1 mm, 2.6 µm, Phenomenex, USA) within 3 min. The method was fully validated with the matrix effect between 87.7% and 99.5% and the recovery ranging from 80.3% to 90.1%. The intra- and inter-day precisions were less than 9.5% and the accuracy ranged from −3.8% to 6.5%. The reliable method was successfully applied to the pharmacokinetics and tissue distribution studies of 6258-70 after intravenous administration in rats. The pharmacokinetic results indicated that the pharmacokinetic behavior of 6258-70 in rats was in accordance with linear features within tested dosage of 1 to 4 mg/kg, and there was no significant difference between the two genders. The tissue distribution study showed that 6258-70 had an effective penetration, spread widely and rapidly and could cross blood-brain barrier. The results of pharmacokinetics and tissue distribution may provide a guide for future study.

The detachment and transport of soil particles from soil mass are important effects of falling raindrops on soil erosion during rainfall. The objective of this study was to determine whether soil microrelief affects the detachability and transportability of soil particles by raindrop splash. Experimental microreliefs were manually simulated by two tillage practices: shallow hoeing, contour chisel plowing, and a smooth slope served as control treatment. The experiment included three simulated rainfall intensities (1.0, 1.5, and 2.0 mm/min). A splash board was used to collect sediment splashed upslope as well as that splashed downslope. Results show that microrelief has a positive effect on detachment rate (DRt) and has a negative effect on net downslope movement rate (SPnet). With the exception of DRt of which hoe treatment was less than smooth at the rainfall of 1.0 mm/min intensity, DRt of hoe and chisel treatments were twice as high as that of smooth to other treatments. For all treatments, SPnet of hoe and chisel treatments were less than half of smooth. Regression analysis showed that DRt change with increasing rainfall intensity could be described by a power function for all treatments. The change of SPnet could be described by a logarithmic function for hoe and chisel treatments, while the change of SPnet of the smooth treatment could not be described by a logarithmic function. Statistical results suggest that DRt was significantly influenced by rainfall intensity, while SPnet was not. Conversely, SPnet was significantly influenced by soil microrelief, while DRt was not.

In order to evaluate the pharmacokinetic profile of paliperidone extended-release tablets in vivo, a simple and rapid ultra-high performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS) method was developed and validated for the determination of paliperidone in beagle dog plasma. Paliperidone and diazepam (internal standard) were extracted from plasma samples with diethyl ether, and then separated on a C18 column (2.1 × 50 mm, 2.6 μm) under gradient elution with methanol–0.1% formic acid at a flow rate of 0.3 ml/min. The compounds were detected using a triple-quadrupole mass spectrometer equipped with an electrospray ionization (ESI) source. The validated method was linear over the concentration range of 1.00–1000.00 ng/ml and the lower limit of quantitation was 1.00 ng/ml. The intra-day and inter-day precision values were not more than 15% (relative standard deviation

The objective of this study was to evaluate the difference in the pharmacokinetics of zolpidem tatrate in subjects from five Chinese ethnicities (Han, Mongolian, Uigur, Korean and Hui). Healthy subjects (10 Hans, 10 Mongolians, 10 Uigurs, 10 Koreans and 9 Huis) were recruited and each received a 10 mg tablet-dose of zolpidem tatrate. A total of 12 plasma samples were collected over a 12 h period after administration. The concentrations of zolpidem in plasma were determined by an HPLC-FLU method, after which the pharmacokinetic parameters were determined using DAS 2.0 software and analyzed by SPSS 16.0 software. After normalization by weight, no differences were noted in the pharmacokinetic parameters of zolpidem tatrate among the five ethnic groups (P>0.05). However, there were statistically significant differences between males and females for the pharmacokinetic parameters (P

Hydrophilic interaction-ultra high performance liquid chromatography (HILIC-UHPLC) allows the analysis of highly polar metabolites, providing complementary information to reversed-phase (RP) chromatography. By optimization of the preparation and analytical conditions in HILIC mode, HILIC-UHPLC/MS was applied for the global metabolic profiling of rat plasma samples generated in an experimental model of chronic unpredictable mild stress (CUMS), and the concomitant investigation of the protective effect of fluoxetine was also evaluated. Identification of plasma metabolic profiles indicated that significant changes in specific metabolites occurred after fluoxetine exposure, including increased phenylalanine, serine, acetyl-L-carnitine, carnitine and decreased creatine, betaine, proline, tryptophan, tyrosine, C16:0 LPC. Some novel biomarkers from this HILIC-UHPLC/MS approach were betaine, proline, tyrosine creatine and serine compared with the results of RP-UHPLC/MS. The complementary nature of this technique is confirmed and is on agreement with previously published studies.

In this study, a simple travel time-based runoff model was proposed to simulate a runoff hydrograph on soil surfaces with different microtopographies. Three main parameters, i.e., rainfall intensity (I), mean flow velocity (vm) and ponding time of depression (tp), were inputted into this model. The soil surface was divided into numerous grid cells, and the flow length of each grid cell (li) was then calculated from a digital elevation model (DEM). The flow velocity in each grid cell (vi) was derived from the upstream flow accumulation area using vm. The total flow travel time through each grid cell to the surface outlet was the sum of the sum of flow travel times along the flow path (i.e., the sum of li/vi) and tp. The runoff rate at the slope outlet for each respective travel time was estimated by finding the sum of the rain rate from all contributing cells for all time intervals. The results show positive agreement between the measured and predicted runoff hydrographs.

Purpose. The pharmacokinetics of modafinil were investigated in relation to gender and ethnicity in healthy young volunteers from Han, Mongolian, Korean, Uygur and Hui ( n = 10/group) following administration of a single 200 mg oral dose. Methods. Blood samples were collected over 48 h for the determination of plasma levels of modafinil and its acid metabolite by High performance liquid chromatography with an ultraviolet detector. Pharmacokinetic parameters were evaluated using noncompartmental methods. Results. Modafinil was well tolerated and safe at a single oral dose of 200 mg. All participants reported adverse events, none of which was serious or unexpected. The maximum plasma concentration (Cmax) and area under the curve for modafinil concentration versus time, which was extrapolated to infinity (AUC0-∞), were higher in women compared to men (p < 0.01). No gender-based difference was noted in the total body weight-normalized modafinil oral clearance. The total body weight-normalized modafinil apparent volume of distribution and the t1/2 was found to exhibit an ethnicity-based significant difference. Conclusion. The results of the current study suggest that there might be pharmacokinetic differences related to gender and ethnicity in the pharmacokinetics of modafinil.