Research and application of K/S value in stain identification

Purpose The intelligent identification of stains can quickly and accurately identify stains. At present, stains are identified subjectively by appearance, color, taste, feel, location, etc. Color is an important factor in identifying stains. K/S value is used to analyze the color of textile fabric, and it has additivity. The purpose of the study is to explore its application in stain recognition is of great significance to intelligent washing. Design/methodology/approach A certain method used to stain the textile, then the K/S value of the textile before and after the stain was analyzed and tested by the color difference instrument. The K/S curve of the stain was calculated by the addition of K/S, and then the stain was identified and distinguished. Findings The K/S value of the textile stained with stains could be deducted by the K/S value of the color difference meter. After deducting the base cloth, the K/S curve of the same stain is basically the same. Then the stain can be identified and analyzed. Research limitations/implications The K/S value can be used for stain analysis, but it needs to be analyzed and tested in the laboratory. Practical implications This study provides a simple method for stains identification. Originality/value In addition to common methods of stain identification, such as appearance, color, feel, smell, location, stain removal materials, breaking the substrate, IR, etc., K/S value can be used for stain analysis. Identifying stains and washing them in a targeted way to achieve a better washing effect could provide certain technical support for the development of smart washing and smart home appliances.

Yeast Cell as a Bio-Model for Measuring the Toxicity of Fish-Killing Flagellates

Harmful algal blooms are a significant environmental problem. Cells that bloom are often associated with intercellular or dissolved toxins that are a grave concern to humans. However, cells may also excrete compounds that are beneficial to their competition, allowing the cells to establish or maintain cells in bloom conditions. Here, we develop a yeast cell assay to assess whether the bloom-forming species can change the toxicity of the water environment. The current methods of assessing toxicity involve whole organisms. Here, yeast cells are used as a bioassay model to evaluate eukaryotic cell toxicity. Yeast is a commonly used, easy to maintain bioassay species that is free from ethical concerns, yet is sensitive to a wide array of metabolic and membrane-modulating agents. Compared to methods in which the whole organism is used, this method offers rapid and convenient cytotoxicity measurements using a lower volume of samples. The flow cytometer was employed in this toxicology assessment to measure the number of dead cells using alive/dead stain analysis. The results show that yeast cells were metabolically damaged after 1 h of exposure to our model toxin-producing euryhaline flagellates (Heterosigma akashiwo and Prymnesium parvum) cells or extracts. This amount was increased by extending the incubation time.

IR Imaging of Solid Lubricant Coatings on Concealed/Disjointed Surfaces for Transparent Polymer Delivery Device Applications

Transparent polymer delivery devices often contain a solid lubricant coating on a stronger bulk polymer. The distribution of lubricant coating must be monitored for device optimisation appraisals and to ensure consistency during mass production. However, coating evaluation is difficult to perform as surfaces are often concealed and/or disjointed. Dye stain analysis, which is destructive and time-consuming, is the current industry standard. We present a prototype IR transmission microscope to evaluate micron-level coating coverage of polyurethane and/or polyvinylpyrrolidone on a poly(propylene)-based delivery device. The device has a common industrial configuration, containing a duct and bevel. Inferred absorption of the coating was used to identify coating coverage and a multivariate analysis was used to remove the effects of absorption and scattering by the bulk. Coverage on concealed and disjointed surfaces was imaged and evaluated from a single camera viewpoint and ≈50 μm defects were detectable. The industrial applicability of the prototype was demonstrated using comparisons with dye stain analysis by estimating water dilution of coating and identifying artifacts in coating, which may indicate machine malfunction. The sensitivity and speed of the IR technique makes it a favourable alternative to the current industry standard.

Aerobic exercise and octopamine protect against deep-frying oil-induced cardiomyocyte apoptosis through modulation of caspase and pro-caspase 3

Background: Deep-frying is a common cooking method accompanied by production of carcinogenesis substance such as acrolein. Acrolein is a toxic byproduct of lipid peroxidation that is involved in the development of pulmonary, cardiac, and neurodegenerative diseases. This study aimed to explore the effect of aerobic exercise (EXE) and octopamine (OCT) on caspase 3 and pro-caspase 3 expression levels in the heart tissue of rats were fed deep-frying oil (DFO).Methods: 30 male Wistar rats were divided into 5 groups (n=6 in each) including 1) control (CO), 2) DFO, 3) DFO+EXE, 4) DFO+OCT and 5) DFO+EXE+OCT. The apoptotic effects of DFO on heart and cardiomyocytes’ fibers were examined by TUNEL assay and Masson's trichrome staining respectively. Also caspase 3 and pro-caspase 3 genes and proteins expression in all groups were evaluated using quantitative real-time PCR and western blotting method, respectively. Results: Data showed a significant increase in apoptotic cells in the DFO group (P <0.05). Masson's trichrome stain analysis demonstrated that the number of cardiomyocytes' fibers are decreased, and collagen deposition is increased in the DFO group. In comparison, the collagen percentage was significantly reduced in DFO+EXE, DFO +OCT and DFO+EXE+OCT groups. Also, the expression level of caspase 3 and pro-caspase 3 was significantly decreased in DFO+EXE+OCT group (P <0.05). Conclusions: The results of this study show that DFO lead to programmed cell death via the activation of caspases in heart tissue. However, it seems that aerobic exercise with octopamine supplementation improves heart tissue through decreasing in the expression of caspase 3 and pro-caspase 3 that inhibit apoptosis.

Aerobic exercise and octopamine protects against deep-frying oil-induced cardiomyocyte apoptosis through modulation of caspase and pro-caspase 3

Background : Deep-frying is a common cooking method in which cooking is accompanied by carcinogenic byproducts such as acrolein. Acrolein is a toxic byproduct of lipid peroxidation, which has been implicated in pulmonary, cardiac, and neurodegenerative diseases. This study aimed to explore the effect of aerobic exercise and octopamine on caspase 3 and pro-caspase 3 expression levels in the heart tissue of rat exposed deep-frying oil. Methods : 30 male Wistar rats were divided into 5 groups (n=6 in each) including 1) control (CO), 2) deep-frying oil (DFO), 3) deep-frying oil+exercise (DFO+EXE), 4) deep-frying oil+octopamine (DFO+OCT), and 5) deep-frying oil+exercise+octopamine (DFO+EXE+OCT). The apoptotic effects of DFO in heart tissue were examined by TUNEL assay. Masson's trichrome stain used to study cardiomyocytes’ fibers. Moreover, caspase 3 and pro-caspase 3 genes and proteins expression in all groups were evaluated using quantitative real-time PCR and western blotting method, respectively. Results : Data showed a significant increase in apoptotic cells in the DFO-treated group ( P <0.05). Masson's trichrome stain analysis demonstrated that the number of cardiomyocytes' fibers are decreased, and collagen deposition is increased in the DFO group. In comparison, the collagen percentage was significantly reduced in exercise, OCT, and exercise+OCT groups. Also, the expression level of caspase 3 and pro-caspase 3 was significantly decreased in deep-frying oil+exercise+OCT group ( P <0.05). Conclusions : The results of our study show that DFO lead to programmed cell death via the activation of caspase in heart tissue. However, it seems that aerobic exercise with octopamine supplementation improves heart tissue by significantly decrease the expression of caspase 3 and pro-caspase 3 that inhibit apoptosis.

NIMG-17. CLINICOPATHOLOGIC AND ULTRASOUND VARIABLES ASSOCIATED WITH THE UNFAVORABLE PATHOLOGY IN NEUROBLASTOMA

BACKGROUND The International Neuroblastoma Pathology Classification has a prognostic impact that distinguishes two neuroblastoma categories: favorable histology (FH) and unfavorable histology (UFH). The aim of this study was to identify the clinicopathological and ultrasound variables that were associated with the UFH. METHODS With ethic approval, the clinical, pathologic, and ultrasonographic data of the 104 patients with the pathologic diagnosis of neuroblastoma were retrospectively analyzed. Pathologic findings were ascertained by the paraffin pathologic, fluorescent in situ hybridization (FISH), and the immunohistochemical stain analysis. Tumors were assessed for the following ultrasonographic characteristics: size, boundary, shape, internal echo, acoustic pattern, posterior features, calcification, internal blood flow, and pushing peripheral organs. Univariate and multivariate logistic regression analyses were used to assess the clinicopathologic and ultrasound variables that were associated with UFH. RESULTS There were 27 neuroblastoma cases (26.0%) of the UFH group. The independent clinicopathologic variables for the UFH were: older than one year (Odds ratio [OR]=32.84, p=0.003), presence of metastases (OR=4.92, p=0.032), and the MYCN amplification ratio >5 (OR=47.06, p=0.003). The independent ultrasound feature of neuroblastoma which associated with UFH was the ill-defined boundary (OR=4.64, p=0.047) and tumor size ≥50mm (OR=15.77, p=0.05). CONCLUSION Patients older than one year, with the presence of metastases, and the MYCN amplification ratio >5 on the FISH analysis as well as the ill-defined boundary and tumor size ≥50mm on an ultrasound assessment were associated with the UFH in neuroblastoma. These characteristics of the neuroblastoma should be considered in patient stratification and prognostic evaluation. Key words: Neuroblastoma; Unfavorable histology; Ultrasound