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Ternary SLE Measurements for the Systems H2O+ZnCl2+Zn(H2PO2)2 at T= (298, 313 and 333) K T=(298, 313和333)K时H2O+ZnCl2+Zn(H2PO2)2体系的三元SLE测量
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/000984/jcsp/44.01.2022
S. Sevilay DEM RC, Vedat Adig Zel Vedat ADIG ZEL, M. S. N. A. H. E. mer SAH N and Hasan ERGE
The solid-liquid equilibrium (SLE) of H2O+ZnCl2+Zn(H2PO2)2 ternary system at 298, 313 and 333 K have been studied with the use of isothermal method. Solid phase compositions have been determined with Schreinemaker’s method. H2O+ZnCl2+Zn(H2PO2)2 ternary systems have simple eutectic type in 298, 333K. One invariant point, two invariant curves and two crystallization region have been observed in the phase diagrams at 298, 333K. Otherwise, One invariant point, three invariant curves and two crystallization region have been observed in the phase diagrams in 313K. In the crystallization regions; (i) Zn(H2PO2).H2O and ZnCl2, (ii) Zn(H2PO2)2, Zn(H2PO2).H2O and ZnCl2, (iii) Zn(H2PO2)2 and ZnCl2 salts have been observed at 298 K, 313K, and 333 K, respectively. In H2O+ZnCl2+Zn(H2PO2)2 ternary system, the increasing salting-out effect of Zn(H2PO2)2 on ZnCl2 with temperature.
用等温法研究了H2O+ZnCl2+Zn(H2PO2)2三元体系在298、313和333 K时的固液平衡。用施莱因梅克法测定了固相组成。H2O+ZnCl2+Zn(H2PO2)2三元体系在298,333k范围内具有简单共晶型。在298,333k的相图中观察到一个不变量点、两条不变量曲线和两个结晶区。另外,在313K的相图中观察到1个不变点、3条不变曲线和2个结晶区。在结晶区;(我)锌(H2PO2)。H2O和ZnCl2, (ii) Zn(H2PO2)2, Zn(H2PO2)在298 K、313K和333 K下分别观察到H2O和ZnCl2、(iii) Zn(H2PO2)2和ZnCl2盐。在H2O+ZnCl2+Zn(H2PO2)2三元体系中,随着温度的升高,Zn(H2PO2)2对ZnCl2的盐析作用逐渐增强。
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引用次数: 0
In-silico, Antioxidant and Antiepileptic Effect of N(2,3-methylenedioxy-4benzoyloxy-phenthylamine)-3,4-dimethyl-1, propanoamide Derivatives N(2,3-亚甲基二氧基-4苯甲酰氧基-苯胺)-3,4-二甲基-1,丙酰胺衍生物的硅抗氧化和抗癫痫作用
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001073/jcsp/44.04.2022
G. A. M. G A Miana, M. K. M Kanwal, S. M. S Maqsood, Z. T. Z Tariq, F. A. S. F Ali Shah, H. S. H Saddam, M. U. F. A. A. U. K. M Umar Farooq and Arif U Khan
Epilepsy is a severe neurological illness that affects millions of people the globally and is characterized by unpredicted and intermittent seizures.This research aimed to investigate the antiepileptic and antioxidant properties of papaverine derivatives using in-silico, in-vitro, and in-vivo methods.Epileptic seizure was induced in Swiss albino mice of either gender by administering PTZ (pentylenetetrazol). The antioxidant potential of test compounds was computed using previously published DPPH assay methods with minor modifications, while In-silico experiments were conducted using Auto-dock Vina (1.5.6) software and post dock analysis was completed using Discovery Studio Visualizer. The results showed that both compounds have strong antioxidant potential, with a noticeable change in color when compared to ascorbic acid as a control, and very low mortality when anti-epileptic potential was observed. The development of seizures was greatly delayed at first, but after 30 minutes of PTZ, they were completely gone. Both synthesized derivatives also comply the andquot;Lipinskiand#39;s rule of 5andquot;, which states that after structural alterations, extensive investigations, and trials, the chemical products would be evaluated for epilepsy management in the future In-silico investigations demonstrated that ligands with sufficient hydrogen bonds, pi-pi bonds, and Vander-Waals forces have a suitable propensity to engage with the binding pocket of selected protein targets. The current investigation of papaverine derivatives and their binding affinities against gamma aminobutyric acid (GABA) protein may have a vital function in epilepsy aetiology, according to the results of the studies. H1 and H2 were further verified in vivo for their anticonvulsant and antioxidant therapeutic potential. This could lead to more research into neurological problems.
癫痫是一种严重的神经系统疾病,影响着全球数百万人,其特征是不可预测的间歇性癫痫发作。本研究旨在通过硅内、体外和体内方法研究罂粟碱衍生物的抗癫痫和抗氧化性能。给药PTZ(戊四氮)诱导瑞士白化小鼠癫痫发作。测试化合物的抗氧化潜力使用先前发表的DPPH测定方法进行了轻微修改,而In-silico实验使用Auto-dock Vina(1.5.6)软件进行,并使用Discovery Studio Visualizer完成对接后分析。结果表明,这两种化合物都具有很强的抗氧化潜力,与抗坏血酸作为对照相比,其颜色变化明显,并且在观察抗癫痫潜力时死亡率非常低。癫痫发作的发展在一开始被大大推迟,但在30分钟的PTZ后,它们完全消失了。这两种合成的衍生物也符合“利平斯基和5”规则,即经过结构改变、广泛的研究和试验后,化学产品将在未来用于癫痫治疗的评估。硅研究表明,具有足够氢键、pi-pi键和范德-瓦尔斯力的配体具有与选定蛋白质靶点结合的合适倾向。根据研究结果,目前对罂粟碱衍生物及其与γ氨基丁酸(GABA)蛋白结合亲和力的研究可能在癫痫病因学中具有重要作用。在体内进一步验证了H1和H2的抗惊厥和抗氧化治疗潜力。这可能会导致对神经系统问题的更多研究。
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引用次数: 0
Development and Validation of an Analytical Method for Pesticide Residues Analysis in Crude Cottonseed Oil 棉籽油中农药残留分析方法的建立与验证
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/000996/jcsp/44.02.2022
Rashid Muhammad Rashid Muhammad, Karam Ahad Karam Ahad, Muhammad Ishtiaq Muhammad Ishtiaq, Farrakh Mehboob Farrakh Mehboob
This study reports the development and validation of a fast, efficient, and cost effective multiresidue method for determination of 14 lipophilic and analytically problematic pesticides in crude cottonseed oil. Crude cottonseed oil contains high amount of saturated fatty acid and pigments that are problematic in pesticide residues analysis. Modified liquid-liquid partitioning with acetonitrile and n-hexane in 10:1 (v/v) ratio was used to extract pesticides. For clean-up, different combinations of sorbents were used and optimum recovery and minimal matrix effect were obtained with the combination of activated charcoal and primary secondary amine for the selected pesticides. For majority of the analyzed pesticides, the method validation parameters i.e. percent recovery (71.6-140.0%), precision (%RSD 9.7 to 33.0), LOD (0.041 to 0.096 and#181;g/g), LOQ (0.125-0.264 and#181;g/g), linearity (0.998-0.999) and matrix effect (and#177;27%) were in acceptable range as prescribed by EU SANTE guidelines. Two-way Analysis of variance of inter-labs comparison study revealed non-significant interaction effects for most of studied pesticides indicating that the current method can be confidently used in labs for monitoring of these pesticides in crude cottonseed oil.
本研究报道了一种快速、高效、经济的多残留方法,用于测定棉籽油中14种亲脂性农药和分析上存在问题的农药。棉籽油中含有大量的饱和脂肪酸和色素,在农药残留分析中存在问题。采用乙腈与正己烷以10:1 (v/v)比的改进液液分配法提取农药。采用不同的吸附剂组合进行清理,活性炭与伯仲胺组合对所选农药的回收率最佳,基质效应最小。多数农药的回收率(71.6 ~ 140.0%)、精密度(%RSD 9.7 ~ 33.0)、检出限(0.041 ~ 0.096、181 g/g)、定量限(0.125 ~ 0.264、181 g/g)、线性度(0.998 ~ 0.999)、基质效应(177 ~ 27%)均符合欧盟SANTE标准。实验室间比较研究的双向方差分析显示,所研究的大多数农药的交互效应不显著,表明本方法可以在实验室中可靠地用于原棉籽油中农药的监测。
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引用次数: 0
Photocatalytic Properties of Zinc Selenide and Cobalt Selenide Nanocomposite 硒化锌和硒化钴纳米复合材料的光催化性能
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001003/jcsp/44.02.2022
Han Yin Han Yin, Kai Bao Kai Bao, Yi Wang Yi Wang, Maojuan Bai Maojuan Bai, Jun Wan Jun Wan
In recent years, the environmental pollution caused by organic dyes has become more and more serious, so the removal of organic dyes has been paid more and more attention. In this work, ZnSe/CoSe was synthesized by hydrothermal method, and the activity of the composite photocatalytic materials was detected by visible light catalytic degradation of methylene blue. The nanocomposites were characterized by Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), Energy Dispersive Spectrometer (EDS), X-ray Powder Diffraction (XRD), Ultraviolet Diffuse Reflection Spectrum (UV-Vis), Brunner−Emmet−Teller Measurements (BET), and X-ray Photoelectron Spectroscopy (XPS). The catalytic effect was the most obvious when the composite ratio was 1:7.5, with the removal rate reaching to 99.4 % of 20 mg/L MB within 120 min of visible light irradiation. Therefore, ZnSe/CoSe has a broader application prospect due to its high efficiency and low price.
近年来,有机染料对环境的污染越来越严重,因此有机染料的去除越来越受到人们的重视。本文采用水热法合成ZnSe/CoSe,并通过可见光催化降解亚甲基蓝检测复合光催化材料的活性。采用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、能谱仪(EDS)、x射线粉末衍射仪(XRD)、紫外漫反射光谱(UV-Vis)、Brunner - Emmet - Teller测量仪(BET)和x射线光电子能谱(XPS)对纳米复合材料进行了表征。当复合比为1:7.5时,催化效果最明显,在可见光照射120 min内,对20mg /L MB的去除率可达99.4%。因此,ZnSe/CoSe效率高、价格低,具有更广阔的应用前景。
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引用次数: 1
Chemical Diversity and Cytotoxicity of Ganoderma lucidum from Two Different Localities of Pakistan 巴基斯坦两个不同产地灵芝的化学多样性和细胞毒性
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001002/jcsp/44.02.2022
Fatima tuz Zuhra Fatima tuz Zuhra, Shariqa Khawaja Shariqa Khawaja, Bina Shaheen Siddiqui Bina Shaheen Siddiqui, Shabana Usman Simjee Shabana Usman Simjee, Muhammad Ismail Bhatti Muhammad Ismail Bhatti, S. T. A. S T Ali, Sobiya Perwaiz and Sabira Begum Sobiya Perwaiz and Sabira Begum
Ganoderma lucidum is a medicinal mushroom of family Ganodermataceae. It is found in Japan, China, Pakistan and some other parts of Asia. It is reported to exhibit numerous pharmacological properties. In Pakistan this mushroom inhabits areas with different soil and climate conditions which may affect its chemical composition and biological activity. In this context, this study was aimed to investigate the chemical constituents and cytotoxicity of wild growing Ganoderma lucidum from two different localities of Pakistan, Bhawalpur, Punjab (GI-X) and Nawabshah, Sindh (MI-X). These yielded an oily residue (R-GI-X; 2.3 g) and (R-MI-X; 20 g) on extraction with petroleum ether at room temperature. Their cytotoxicity was determined for oral adenosquamous carcinoma (CAL-27) and non-small-lung cancer (NCI-460) cell lines. Only R-MI-X showed toxicity for these cell lines and CAL-27 cells were found more sensitive (IC50 35.68 and#181;M) than NCI-H460 cells which were moderately sensitive (IC50 95.50 and#181;M). R-GI- X was not active for these cell lines. Fractions R-GI-X and R-MI-X contained 40 and 22 compounds respectively. Common compounds were mainly saturated and unsaturated fatty acids and their esters. A major difference was the presence of two ergosterols, 5, 6-dihydroergosterol and (20E)-3-(acetyloxy) ergosta-9(11),20(22)-dien-6-yl acetate in MI-X which may be responsible for its antiproliferative activity as many ergosterols are reported to possess anti-cancer activity against various cell lines.
灵芝是灵芝科的一种药用蘑菇。在日本、中国、巴基斯坦和亚洲其他一些地区都有发现。据报道,它具有许多药理特性。在巴基斯坦,这种蘑菇生长在土壤和气候条件不同的地区,这可能影响其化学成分和生物活性。在此背景下,本研究旨在研究来自巴基斯坦旁遮普省Bhawalpur (GI-X)和信德省Nawabshah (MI-X)两个不同地区的野生灵芝的化学成分和细胞毒性。这些产生了一种油性残留物(R-GI-X;2.3 g)和(R-MI-X;20g)在室温下用石油醚提取。测定了它们对口腔腺鳞癌(CAL-27)和非小肺癌(NCI-460)细胞系的细胞毒性。只有R-MI-X对这些细胞系有毒性作用,CAL-27细胞比中等敏感的NCI-H460细胞更敏感(IC50为35.68和#181;M)。R-GI- X对这些细胞系没有活性。馏分R-GI-X和R-MI-X分别含有40种和22种化合物。常见的化合物主要是饱和脂肪酸和不饱和脂肪酸及其酯类。一个主要的区别是在MI-X中存在两种麦角甾醇,5,6 -二氢麦角甾醇和(20E)-3-(乙酰氧基)麦角甾醇-9(11),20(22)-二烯-6-乙酸酯,这可能是其抗增殖活性的原因,因为许多麦角甾醇据报道对各种细胞系具有抗癌活性。
{"title":"Chemical Diversity and Cytotoxicity of Ganoderma lucidum from Two Different Localities of Pakistan","authors":"Fatima tuz Zuhra Fatima tuz Zuhra, Shariqa Khawaja Shariqa Khawaja, Bina Shaheen Siddiqui Bina Shaheen Siddiqui, Shabana Usman Simjee Shabana Usman Simjee, Muhammad Ismail Bhatti Muhammad Ismail Bhatti, S. T. A. S T Ali, Sobiya Perwaiz and Sabira Begum Sobiya Perwaiz and Sabira Begum","doi":"10.52568/001002/jcsp/44.02.2022","DOIUrl":"https://doi.org/10.52568/001002/jcsp/44.02.2022","url":null,"abstract":"Ganoderma lucidum is a medicinal mushroom of family Ganodermataceae. It is found in Japan, China, Pakistan and some other parts of Asia. It is reported to exhibit numerous pharmacological properties. In Pakistan this mushroom inhabits areas with different soil and climate conditions which may affect its chemical composition and biological activity. In this context, this study was aimed to investigate the chemical constituents and cytotoxicity of wild growing Ganoderma lucidum from two different localities of Pakistan, Bhawalpur, Punjab (GI-X) and Nawabshah, Sindh (MI-X). These yielded an oily residue (R-GI-X; 2.3 g) and (R-MI-X; 20 g) on extraction with petroleum ether at room temperature. Their cytotoxicity was determined for oral adenosquamous carcinoma (CAL-27) and non-small-lung cancer (NCI-460) cell lines. Only R-MI-X showed toxicity for these cell lines and CAL-27 cells were found more sensitive (IC50 35.68 and#181;M) than NCI-H460 cells which were moderately sensitive (IC50 95.50 and#181;M). R-GI- X was not active for these cell lines. Fractions R-GI-X and R-MI-X contained 40 and 22 compounds respectively. Common compounds were mainly saturated and unsaturated fatty acids and their esters. A major difference was the presence of two ergosterols, 5, 6-dihydroergosterol and (20E)-3-(acetyloxy) ergosta-9(11),20(22)-dien-6-yl acetate in MI-X which may be responsible for its antiproliferative activity as many ergosterols are reported to possess anti-cancer activity against various cell lines.","PeriodicalId":17253,"journal":{"name":"Journal of the chemical society of pakistan","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707058","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biosynthesis of Silver Nanoparticles using Echinacea pallida (Nutt.) Nutt. and Antioxidant Activity Thereof 紫锥菊生物合成纳米银的研究纳特。及其抗氧化活性
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001187/jcsp/44.06.2022
Esma Nur Gecer and Ramazan Erenler Esma Nur Gecer and Ramazan Erenler
In this work, silver nanoparticles (Ep-AgNPs) were synthesised using Echinacea pallida (Nutt.) Nutt. The dried leaves of E. pallida were collected and heated at 55 and#176;C in deionized water, and filtered, and the leaf extract was treated with AgNO3 to produce the Ep-AgNPs. The Ep-AgNPs were analyzed by Ultraviolet-visible (UV-Vis), Fourier transform infrared (FTIR), X-ray diffraction (XRD), and scanning electron microscope (SEM). The characteristic hydroxyl gave the peak at 3147 cm-1. In UV-Vis analysis, observation of absorption band at 468 nm proved the achievement of Ep-AgNPs synthesis. SEM analysis presented the spherical shape of nanostructures with an average size of 77.82 nm. The face-centered crystal structure of Ep-AgNPs was revealed by the XRD analysis. The 1,1-diphenyl-2-picryl-hydrazyl radical (DPPH•) scavenging, ferric reducing antioxidant power (FRAP), 2,2and#39;-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) radical cation (ABTS•+) assays were employed for antioxidant study in which Ep-AgNPs exhibited excellent antioxidant effect. Ep-AgNPs displayed outstanding DPPH• activity (6.34, IC50, and#181;g/ml) compared to the standard BHT (10.78, IC50, and#181;g/ml). The high activity was observed for ABTS•+ and reducing power assays as well. Hence, Ep-AgNPs could be a valuable material for the food and pharmaceutical industry.
本研究以紫锥菊为原料合成银纳米粒子(Ep-AgNPs)。纳特。收集苍白树干叶,在55℃和176℃的去离子水中加热,过滤后用AgNO3处理,得到Ep-AgNPs。采用紫外可见(UV-Vis)、傅里叶变换红外(FTIR)、x射线衍射(XRD)和扫描电子显微镜(SEM)对Ep-AgNPs进行了分析。特征羟基在3147 cm-1处出现峰。紫外-可见光谱分析中,在468 nm处观察到的吸收带证明了Ep-AgNPs的合成成功。SEM分析表明,纳米结构呈球形,平均尺寸为77.82 nm。XRD分析揭示了Ep-AgNPs的面心晶体结构。采用1,1-二苯基-2-吡啶-肼基自由基(DPPH•)清除率、铁还原抗氧化能力(FRAP)、2,2和#39;-氮基-双(3-乙基苯并噻唑-6-磺酸)自由基阳离子(ABTS•+)测定法进行抗氧化研究,结果表明Ep-AgNPs具有良好的抗氧化作用。与标准BHT (10.78, IC50, #181;g/ml)相比,Ep-AgNPs显示出出色的DPPH•活性(6.34,IC50, #181;g/ml)。在ABTS•+和降低功率试验中也观察到高活性。因此,Ep-AgNPs可能是食品和制药工业的一种有价值的材料。
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引用次数: 2
Induction of Selenium Nanoparticles Disturbs Behavior, Blood and Serum Biomarkers and Oxidative Stress Markers from Vital Organs of Male and Female Albino Mice 硒纳米颗粒诱导对白化病小鼠行为、血液和血清生物标志物以及重要器官氧化应激标志物的影响
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/000979/jcsp/44.01.2022
Mubashra Salim Mubashra Salim, Maria Shahzeen Maria Shahzeen, Maryam Nasir Khan Maryam Nasir Khan, Rimsha Tariq Rimsha Tariq, Gul Muhammad Gul Muhammad, Ghulam Shabbir Ghulam Shabbir, Laraib Nisar Laraib Nisar, Muhammad Naeem Ashiq and Furhan Iqbal Muhammad Naeem Ashiq and Furhan Iqbal
Current investigation was focused to determine the biological effects of Selenium nanoparticles (Se NPs) in mice. Se NPs (50mg/ml saline/Kg body weight) were intraperitoneally injected to 5 week old albino mice (N = 22) for 14 days. Control group was intraperitoneally injected with saline water (N = 22). In all subjects, a series of neurological tests, hematological parameters and markers of oxidative stress in vital organs were determined. We are reporting that rota rod and open field test performance remained unaffected in Se NPs injected mice when compared with saline treated controls. Male mice injected with Se NPs had significantly less line crossing (P = 0.02) while performing light dark box. They approached object A less frequently (P = 0.02) and spent lesser time with it (P = 0.001) during novel object recognition test (trial 1). % lymphocytes were significantly reduced (P = 0.03) in these mice while % monocytes were higher than control (P = 0.03). Concentration of cholesterol (P = 0.02) and LDL (P = 0.003) was significantly decreased in male mice. Female Se NPs treated mice spent less time (P = 0.05) with B object in trial 1 and 2 (P = 0.04) of novel object recognition test. They had significantly reduced cholesterol level (P = 0.02) and significantly increased catalase activity in the liver (P = 0.01) than control. Remaining parameters of behavior, blood chemistry and markers of oxidative stress from vital organs were non-significantly different upon their comparison between Se NPs and saline injected mice.
目前的研究重点是确定硒纳米颗粒(Se NPs)在小鼠体内的生物学效应。将Se NPs (50mg/ml生理盐水/Kg体重)腹腔注射5周龄白化病小鼠(N = 22) 14 d。对照组腹腔注射生理盐水22例。对所有受试者进行一系列神经学测试、血液学参数和重要器官氧化应激标志物的测定。我们报告说,与生理盐水处理的对照组相比,注射Se NPs的小鼠的旋转棒和开阔场地测试性能未受影响。注射Se NPs的雄性小鼠在进行明暗箱实验时,交叉系明显减少(P = 0.02)。在新目标识别试验(试验1)中,小鼠接近目标A的次数减少(P = 0.02),接触目标A的时间减少(P = 0.001),淋巴细胞百分比显著减少(P = 0.03),单核细胞百分比显著高于对照组(P = 0.03)。雄鼠胆固醇(P = 0.02)和低密度脂蛋白(P = 0.003)浓度显著降低。在新物体识别试验1和试验2中,雌性Se NPs处理小鼠对B物体的识别时间较短(P = 0.05) (P = 0.04)。与对照组相比,它们显著降低了胆固醇水平(P = 0.02),显著提高了肝脏过氧化氢酶活性(P = 0.01)。Se NPs与生理盐水注射小鼠的行为、血液化学和重要器官氧化应激标志物的其余参数比较无显著差异。
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引用次数: 2
Gas Chromatography-Mass Spectrometry-based Phytochemical Analysis and In-Vitro Anti-Lipid Peroxidation, Cyclooxygenase Inhibition Activities of Saudi Eruca sativa Leaves 基于气相色谱-质谱的沙特阿拉伯芥菜叶片植物化学分析及体外抗脂质过氧化、环加氧酶抑制活性
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001001/jcsp/44.02.2022
Mohammed Al bratty Mohammed Al bratty, Neelaveni Thangavel Neelaveni Thangavel, Hassan Ahmad Alhazmi Hassan Ahmad Alhazmi, Asim Najmi Asim Najmi, Amani Ali Jebril Shar Amani Ali Jebril Shar, Bshoor Ali Farhan Alhabsi Bshoor Ali Farhan Alhabsi, Sumaiya Mosa Suliman Ghazwani Sumaiya Mosa Suliman Ghazwani, Safeena Eranhiyil Ashraf Safeena Eranhiyil Ashraf, Ziaur Rehman Ziaur Rehman
Eruca sativa is a wholesome yearly shrubbery herb in Saudi Arabia. Eruca sativa leaves are a conventional food and are consumed raw in salads. The present research reports the phytochemical analysis, in-vitro anti-lipid peroxidation, total anti-oxidant capability, cyclooxygenase-1, and -2 (COX1 and COX2) inhibition activities of Saudi Eruca sativa leaves water decoction (EWD). Gas chromatography-mass spectrometry (GC-MS) of EWD revealed seventeen constituents of six different chemical groups: phenolics (23.60%), aromatic and aliphatic esters (16.97%), terpenoids (31.91%), heterocyclics (14.83%), sulfur containing organics (11.25%), and silyl compounds (1.44%). The presence of Astaxanthin (1.96%), Clionasterol (12.81%), Ingol-12-acetate (4.77%), and Phytol (12.37%) in EWD indicated that the decoction technique was effective in extracting thermostable terpenoids. This research is the first report on Eruca sativa unraveling the thermostable phytochemicals. The EWD exhibited a straight-line relationship between liver lipid peroxidation inhibition and 150 to 400 μg/ml concentrations. The % anti-lipid peroxidation effect produced by EWD and Quercetin was statistically significant. At the highest 400 μg/ml dose, EWD exhibits 68.46 and#177; 0.01% anti-lipid peroxidation activity. The demonstrated IC50 of EWD and Ascorbic acid concerning the total anti-oxidant capability is 217.90 μg/ml and 74.91 μg/ml. The in-vitro assay protocols delineated the modes of inhibition of the biological oxidation processes by Eruca sativa, indicating transfer of hydrogen ion and metal ions reduction. The COX inhibitory potential was screened using Ellmannand#39;s reagent. The IC50 values for COX1 and COX2 inhibitions were 152.31μg/ml and 146.4 μg/ml, respectively, indicating that EWD has a potent COX inhibitory potential compared to Indomethacin. The COX2/COX1 ratio of inhibition, less than one, suggested that EWD phytochemicals would be preferential inhibitors of COX2. The current investigation justifies Eruca sativa leaves as a beneficial health food by establishing the chemical composition of water decoction that contributed to the anti-oxidant and COX inhibition activity.
芥蓝是沙特阿拉伯一种有益健康的一年生灌木草本植物。芥菜的叶子是一种传统的食物,可以在沙拉中生吃。本研究报道了沙乌地阿拉伯芥叶水煎液的植物化学分析、体外抗脂质过氧化、总抗氧化能力、环氧化酶-1和-2 (COX1和COX2)抑制活性。经气相色谱-质谱联用(GC-MS)分析,发现了6个不同化学基团的17种成分:酚类(23.60%)、芳香族和脂肪族酯(16.97%)、萜类(31.91%)、杂环类(14.83%)、含硫有机物(11.25%)和硅基化合物(1.44%)。其中虾青素(1.96%)、甾烷甾醇(12.81%)、Ingol-12-acetate(4.77%)和叶绿醇(12.37%)的含量表明,该方法可有效提取耐热萜类化合物。本研究首次报道了芥蓝的耐热性植物化学物质。EWD与150 ~ 400 μg/ml浓度呈直线关系。EWD与槲皮素的抗脂质过氧化作用有统计学意义。最高剂量400 μg/ml时,EWD值为68.46,#177;0.01%抗脂质过氧化活性。edd和抗坏血酸对总抗氧化能力的IC50分别为217.90和74.91 μg/ml。体外实验方案描述了芥蓝对生物氧化过程的抑制模式,表明氢离子和金属离子的转移还原。采用Ellmannand试剂筛选COX抑制电位。对COX1和COX2的IC50值分别为152.31μg/ml和146.4 μg/ml,表明与吲哚美辛相比,EWD具有较强的COX抑制潜力。COX2/COX1的抑制比小于1,表明EWD植物化学物质可能是COX2的优先抑制剂。本研究通过确定红花叶水煎液中具有抗氧化和抑制COX活性的化学成分,证明了红花叶是一种有益的保健食品。
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引用次数: 0
Preparation, Characterization and Extraction Performance of Rubidium Ions in Water System 水体系中铷离子的制备、表征及萃取性能
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001074/jcsp/44.04.2022
Guo jun Zhang Guo jun Zhang, Hua Fu Hua Fu, Hui yuan Chen Hui yuan Chen, Huo Liu Huo Liu, Wei jun Song Wei jun Song, Chun yan Sun Chun yan Sun, Xin Hu and Yun Zhao Xin Hu and Yun Zhao
In this paper, a valinomycin-functionalized nano-sized magnetic solid-phase extractant (VFE) with the core-shell structure and the Fe3O4 nanospheres as the core is prepared. Related performances are characterized and tested by SEM, PPMS, XRD, FT-IR, TGA, EDS, ICP-MS, and AAS. The optimal extraction conditions are obtained, namely, temperature 50 and#176;C or higher, pH not less than 9.3, and equilibrium extraction time about 35 min. Recycling performance experiments show that the extraction ratio of rubidium ions after 5 extraction-elution cycles is still up to 85.3%. Extraction experiments with the simulated brine, industrial wastewater, and domestic wastewater show that the VFE exhibits good selective extraction ability for rubidium ions in these water systems. This research is expected to provide a new method or a new material for the separation, extraction, enrichment, and detection of rubidium ions in water systems.
本文制备了以Fe3O4纳米微球为核心,具有核壳结构的缬霉素功能化纳米磁性固相萃取剂(VFE)。通过SEM、PPMS、XRD、FT-IR、TGA、EDS、ICP-MS、AAS等手段对相关性能进行了表征和测试。得到了最佳萃取条件:温度50℃,#176℃以上,pH不小于9.3,萃取平衡时间约35 min。循环性能实验表明,经过5次萃取-洗脱循环后,铷离子的提取率仍可达85.3%。模拟卤水、工业废水和生活废水的萃取实验表明,VFE对这些水体系中的铷离子具有良好的选择性萃取能力。本研究有望为水体系中铷离子的分离、提取、富集和检测提供一种新方法或新材料。
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引用次数: 0
Determination of Puerarin, Daidzein, Baicalin and Wogonin in Composite Preparations by Capillary Electrophoresis 毛细管电泳法测定复方制剂中葛根素、大豆苷元、黄芩苷元和枸杞苷元的含量
IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.52568/001075/jcsp/44.04.2022
Cunhong Li and Yan Xu Cunhong Li and Yan Xu
A simple method for the simultaneous determination of four bioactive components (puerarin, daidzein, baicalin, and wogonin) in composite preparations by microemulsion capillary electrophoresis with UV detection has been developed for the first time. A running buffer composed of 8% acetonitrile + 4% microemulsion(3.24% n-heptane + 13.24% sodium dodecyl sulfate (SDS) + 26.44% n-butanol + 57.08% distilled water in weight ratio) + 20 mM borax solution was found to be the most suitable for this separation. The limits of detection for four analytes were over the range of 0.50 - 1.2 μg ml-1. In the tested concentration range, linear relationships (correlation coefficients: 0.997 for baicalin, 0.997 for wogonin, 0.998 for daidzein and 0.999 for puerarin) between the peak areas and the concentrations of the analytes were obtained. This method has been successfully applied to simultaneous determination of the four bioactive components with recoveries from 94.6 to 106.3%.
本文首次建立了同时测定复方制剂中葛根素、大豆苷元、黄芩苷和枸杞苷四种生物活性成分的微乳液毛细管电泳-紫外检测方法。采用8%乙腈+ 4%微乳液(3.24%正庚烷+ 13.24%十二烷基硫酸钠(SDS) + 26.44%正丁醇+ 57.08%蒸馏水重量比)+ 20 mM硼砂溶液组成的流动缓冲液进行分离效果最佳。4种分析物的检出限均在0.50 ~ 1.2 μg ml-1范围内。在检测浓度范围内,黄芩苷、枸杞苷、大豆苷、葛根素的峰面积与浓度呈线性关系(相关系数分别为0.997、0.997、0.998、0.999)。该方法可用于四种活性成分的同时测定,加样回收率为94.6 ~ 106.3%。
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引用次数: 1
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Journal of the chemical society of pakistan
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