14 research outputs found

    Sex discrimination based on morphological traits in Mystus mysticetus Roberts, 1992

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    This study supplemented the way of sex determination of fish based on the regression relationship of some morphological indicators of Mystus mysticetus. A total of 425 fish specimens were collected by trawl nets at Cai Rang - Can Tho and Long Phu - Soc Trang from January to July 2022. After collection, the fish were transferred to the laboratory to determine their total length (TL), standard length (SL), eye diameter (ED), eye distance (DE), body height (BD), head length (HL), and mouth width (MD) before anatomy for sex determination based on gonads. The regression analysis results of TL-SL, TL-ED, TL-DE, TL-BD, TL-HL, and TL-MD showed that SL, DE, and MD could be used to determine the sex of this fish species because SL and DE were dominant in growth in males, and MD was prevalent in females. In addition, SL could be used to determine the sampling time and HL to determine the distribution environment

    Morphometrics allometry changes and sexual dimorphism in Caragobius urolepis (Gobiiformes: Gobiidae)

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    The present study reported an alternative way of sex-determining for scaleless worm goby Caragobius urolepis based on the regression relationship of some morphological parameters. A total of 328 samples were collected at the trawl nets in two coastal regions in Bac Lieu and Ca Mau from April to August 2022. After collection, the samples were transported to the laboratory in order to measure the total length (TL), body height (BD), head length (HL), the distance of eye (DE), and mouth width (MD) before surgery for accurate sex determination based on gonads. Regression analysis results of TL-BD (growth pattern A+ in females and I in males), TL-HL (growth pattern A+ in females and A- in males), and TL- MD (growth pattern A- in females and A+ in males) could be used to determine the sex of this fish. Moreover, TL-DE and TL-BD could be used to estimate when the samples were collected, e.g , in the dry or wet season, because DE and BD displayed A+ in the wet season but A- in the dry one. The findings could be used as an alternative way to determine fish sex and catching season for this species and others in the Mekong Delta

    Structure of general-population antibody titer distributions to influenza A virus.

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    Seroepidemiological studies aim to understand population-level exposure and immunity to infectious diseases. Their results are normally presented as binary outcomes describing the presence or absence of pathogen-specific antibody, despite the fact that many assays measure continuous quantities. A population's natural distribution of antibody titers to an endemic infectious disease may include information on multiple serological states - naiveté, recent infection, non-recent infection, childhood infection - depending on the disease in question and the acquisition and waning patterns of immunity. In this study, we investigate 20,152 general-population serum samples from southern Vietnam collected between 2009 and 2013 from which we report antibody titers to the influenza virus HA1 protein using a continuous titer measurement from a protein microarray assay. We describe the distributions of antibody titers to subtypes 2009 H1N1 and H3N2. Using a model selection approach to fit mixture distributions, we show that 2009 H1N1 antibody titers fall into four titer subgroups and that H3N2 titers fall into three subgroups. For H1N1, our interpretation is that the two highest-titer subgroups correspond to recent and historical infection, which is consistent with 2009 pandemic attack rates. Similar interpretations are available for H3N2, but right-censoring of titers makes these interpretations difficult to validate

    Safety and efficacy of fluoxetine on functional outcome after acute stroke (AFFINITY): a randomised, double-blind, placebo-controlled trial

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    Background Trials of fluoxetine for recovery after stroke report conflicting results. The Assessment oF FluoxetINe In sTroke recoverY (AFFINITY) trial aimed to show if daily oral fluoxetine for 6 months after stroke improves functional outcome in an ethnically diverse population. Methods AFFINITY was a randomised, parallel-group, double-blind, placebo-controlled trial done in 43 hospital stroke units in Australia (n=29), New Zealand (four), and Vietnam (ten). Eligible patients were adults (aged ≥18 years) with a clinical diagnosis of acute stroke in the previous 2–15 days, brain imaging consistent with ischaemic or haemorrhagic stroke, and a persisting neurological deficit that produced a modified Rankin Scale (mRS) score of 1 or more. Patients were randomly assigned 1:1 via a web-based system using a minimisation algorithm to once daily, oral fluoxetine 20 mg capsules or matching placebo for 6 months. Patients, carers, investigators, and outcome assessors were masked to the treatment allocation. The primary outcome was functional status, measured by the mRS, at 6 months. The primary analysis was an ordinal logistic regression of the mRS at 6 months, adjusted for minimisation variables. Primary and safety analyses were done according to the patient's treatment allocation. The trial is registered with the Australian New Zealand Clinical Trials Registry, ACTRN12611000774921. Findings Between Jan 11, 2013, and June 30, 2019, 1280 patients were recruited in Australia (n=532), New Zealand (n=42), and Vietnam (n=706), of whom 642 were randomly assigned to fluoxetine and 638 were randomly assigned to placebo. Mean duration of trial treatment was 167 days (SD 48·1). At 6 months, mRS data were available in 624 (97%) patients in the fluoxetine group and 632 (99%) in the placebo group. The distribution of mRS categories was similar in the fluoxetine and placebo groups (adjusted common odds ratio 0·94, 95% CI 0·76–1·15; p=0·53). Compared with patients in the placebo group, patients in the fluoxetine group had more falls (20 [3%] vs seven [1%]; p=0·018), bone fractures (19 [3%] vs six [1%]; p=0·014), and epileptic seizures (ten [2%] vs two [<1%]; p=0·038) at 6 months. Interpretation Oral fluoxetine 20 mg daily for 6 months after acute stroke did not improve functional outcome and increased the risk of falls, bone fractures, and epileptic seizures. These results do not support the use of fluoxetine to improve functional outcome after stroke

    Fabrication of Porous Hydroxyapatite Granules as an Effective Adsorbent for the Removal of Aqueous Pb(II) Ions

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    Porous hydroxyapatite (HAp) granules have been successfully fabricated from a HAp powder precursor and polyvinyl alcohol (PVA) additive by a simple sintering process. The composition and microstructures of the HAp were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM) equipped with an energy dispersive X-ray (EDX) spectrometer. The effects of sintering temperature and PVA/HAp mass ratios on color, water stability, morphology, and chemical composition of HAp are discussed. Optimum conditions for the fabrication of HAp granules were found to be a PVA/HAp mass ratio of 3/20 and a sintering temperature of 600°C for 4 h. Accordingly, the obtained HAp is white in color, is in the granular form with a size of about 2 × 10 mm, and has a specific surface area of 70.6 m2/g. The adsorption of Pb2+ onto the as-prepared HAp granules was carried out in aqueous solution by varying the pH, the adsorbent dose, the initial concentration of Pb2+, and the contact time. The results of adsorption stoichiometry of Pb2+ on the HAp granule adsorbent were fitted to the Langmuir adsorption isotherm model (R2 = 0.99). The adsorption capacity and removal efficiency of the HAp granule adsorbent for Pb2+ under optimal conditions were found to be 7.99 mg/g and 95.92%, respectively. The adsorption process obeyed a pseudo-second-order kinetic model with R2∼1. The porous HAp granules studied in this work showed potential for the removal of Pb2+ from industrial wastewater

    Study of Nasal Fractional Exhaled Nitric Oxide (FENO) in Children with Allergic Rhinitis

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    (1) Background: Exhaled nitric oxide (NO) has been considered as a biomarker of airway inflammation. The measurement of fractional exhaled NO (FENO) is a valuable test for assessing local inflammation in subjects with allergic rhinitis (AR). (2) Objective: To evaluate (a) the correlation between nasal FENO with anthropometric characteristics, symptoms of AR and nasal peak flows in children without and with AR; and (b) the cut-off of nasal FENO for diagnosis of AR in symptomatic children. (3) Methods: The study was a descriptive and cross-sectional study in subjects with and without AR &lt; 18 years old. All clinical and functional characteristics of the study subjects were recorded for analysis. They were divided into healthy subjects for the control group and subjects with AR who met all inclusion criteria. (4) Results: 100 subjects (14 ± 3 years) were included, including 32 control subjects and 68 patients with AR. Nasal FENO in AR patients was significantly higher than in control subjects: 985 ± 232 ppb vs. 229 ± 65 ppb (p &lt; 0.001). In control subjects, nasal FENO was not correlated with anthropometric characteristics and nasal inspiratory or expiratory peak flows (IPF or EPF) (p &gt; 0.05). There was a correlation between nasal FENO and AR symptoms in AR patients and nasal IPF and EPF (p = 0.001 and 0.0001, respectively). The cut-off of nasal FENO for positive AR diagnosis with the highest specificity and sensitivity was ≥794 ppb (96.7% and 92.6%, respectively). (5) Conclusion: The use of nasal FENO as a biomarker of AR provides a useful tool and additional armamentarium in the management of allergic rhinitis

    Characterizations and Antibacterial Efficacy of Chitosan Oligomers Synthesized by Microwave-Assisted Hydrogen Peroxide Oxidative Depolymerization Method for Infectious Wound Applications

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    The use of naturally occurring materials with antibacterial properties has gained a great interest in infected wound management. Despite being an abundant resource in Vietnam, chitosan and its derivatives have not yet been intensively explored for their potential in such application. Here, we utilized a local chitosan source to synthesize chitosan oligomers (OCS) using hydrogen peroxide (H2O2) oxidation under the microwave irradiation method. The effects of H2O2 concentration on the physicochemical properties of OCS were investigated through molecular weight, degree of deacetylation, and heavy metal contamination for optimization of OCS formulation. Then, the antibacterial inhibition was examined; the minimum inhibitory concentration and minimum bactericidal concentration (MIC and MBC) of OCS-based materials were determined against common skin-inhabitant pathogens. The results show that the local Vietnamese chitosan and its derivative OCS possessed high-yield purification while the molecular weight of OCS was inversely proportional and proportional to the concentration of H2O2, respectively. Further, the MIC and MBC of OCS ranged from 3.75 to less than 15 mg/mL and 7.5–15 mg/mL, respectively. Thus, OCS-based materials induce excellent antimicrobial properties and can be attractive for wound dressings and require further investigation

    Fabrication of silver nanoparticle-containing electrospun polycaprolactone membrane coated with chitosan oligosaccharides for skin wound care

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    An ideal wound dressing should have several qualities to protect the wound from infection and other adverse factors. This study aimed to fabricate a wound care membrane combining the two well-known bioactive agents silver nanoparticles (AgNPs) and chitosan oligosaccharides (COS). In specific, this multilayer membrane (PCL-Ag/POX/COS) consisted of (1) the electrospun basement layer of poly(ε-caprolactone) (PCL) and AgNPs; (2) the intermediate amphiphilic layer of PCL and poloxamer 407 (POX); and (3) the coating layer of COS and poly(N-vinyl pyrrolidone) (PVP). Several characterisation tests showed that the membrane was successfully coated with COS and owned suitable characteristics as a wound dressing, including proper tensile strength (more significant than the typical value of the skin), the hydrophilic and fluid-absorbable innermost surface, the waterproof outermost basement, vapour permeability, rapid COS release, and gradual AgNP release. In vitro experiments proved its haemostatic effect and antibacterial activities. Though its 100% extract solution reduced in vitro fibroblast viability, through the skin-defected mouse model experiment, PCL-Ag/POX/COS was compatible with the wound tissue and exhibited several positive effects on wound healing. In conclusion, PCL-Ag/POX/COS was proven for its potential for wound care, but it needs further investigations to allow translation from bench to bedside
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