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Anti-Biofilm Impact of Anabasis articulata (Forssk) Moq. Total Methanol Extract Against Pseudomonas aeruginosa Clinical Isolates 关节重根(Forssk) Moq对生物膜的影响。总甲醇提取物抗铜绿假单胞菌临床分离
Pub Date : 2022-05-07 DOI: 10.21608/jampr.2022.131451.1027
Ghada Gamal, Kamelia Abouelsaoud, E. Elekhnawy, Ghada Attia
Anabasis articulata (Forssk) Moq. is a rich bioactive member of Family Amaranthaceae. GC/MS analysis of Anabasis articulata methyl esters fraction notified twenty known fatty acids, including n -hexadecanoic acid, octadecanoic acid and tetradecanoic acid as major constituents. Chromatography analysis of successive fractions revealed the isolation of β -sitosterol 1 from its unsaponifiable fraction , caffeine 2 form its methylene chloride fraction , and 4-acetoxy phenol 3 from the ethyl acetate one. Structural elucidation of these isolates was performed by IR, EI-MS, 1 H NMR and 13 C NMR techniques. Compounds 2 and 3 were isolated for the first time from Anabasis articulata (Forssk) Moq. Meanwhile, methanol extract of the tested plant showed weak total phenolic content. Environmental adaptation of pathogenic microbes through formation of resistible biofilm is constructing a dramatic health hazard, which demanded the exploration of more microbial resisting treatments. One successful strategy is the use of Phytoextracts as noncytotoxic, microbial biofilm inhibitors. Adopting the broth microdilution method, Anabasis articulata (Forssk) Moq. methanol extract (AAME) showed antimicrobial activity against Pseudomonas aeruginosa clinical isolates at range of 32 to 256 µg/mL minimum inhibitory concentrations (MIC). The inhibiting efficiency of AAME against Pseudomonas aeruginosa biofilm formation was concluded at a concentration of half its MIC value using the crystal violet assay (CVA). Our results illustrate the ability of this extract to cutback the percentage of strong, and moderate biofilm forming P. aeruginosa clinical isolates from 41.18 % to 17.65 % and candidate it as futural antibiofilm agent.
关节复位(Forssk) Moq是苋科植物中具有丰富生物活性的一种。通过GC/MS分析,发现了已知的20种脂肪酸,主要成分为正十六酸、十八酸和十四酸。层层析分析表明,β -谷甾醇1从其不可皂化部分分离,咖啡因2从其二氯甲烷部分分离,4-乙酰氧基苯酚3从乙酸乙酯部分分离。通过IR, EI-MS, 1h NMR和13c NMR技术对这些分离物进行了结构鉴定。化合物2和3为首次从该植物中分离得到。同时,被试植物甲醇提取物的总酚含量较低。病原微生物通过形成耐药生物膜对环境的适应正在形成巨大的健康危害,这需要探索更多的微生物耐药治疗方法。一个成功的策略是使用植物提取物作为无细胞毒性的微生物生物膜抑制剂。采用肉汤微量稀释法,测定了关节重木(Forssk) Moq。甲醇提取物(AAME)对铜绿假单胞菌临床分离株的最低抑菌浓度(MIC)为32 ~ 256µg/mL。用结晶紫法(CVA)测定了AAME在MIC值的一半浓度下对铜绿假单胞菌生物膜形成的抑制效果。我们的研究结果表明,该提取物能够将形成强和中等生物膜的铜绿假单胞菌临床分离株的百分比从41.18%降低到17.65%,并有望成为未来的抗生物膜剂。
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引用次数: 0
Marine-Derived Metabolites as Antimalarial Candidates Targeting Various Life Stages 海洋衍生代谢物作为针对不同生命阶段的抗疟疾候选物
Pub Date : 2022-04-10 DOI: 10.21608/jampr.2022.125225.1023
A. Zayed, W. Negm, Amal M. Kabbash, S. Ezzat
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引用次数: 1
Thermodynamic and Kinetic Study of Chiral Separation of Some Non-Steroidal Anti-Inflammatory Drugs on Dinitrobenzamido Tetrahydrophenanthrene Stationary Phase 非甾体类抗炎药在二硝基苄胺四氢菲固定相上手性分离的热力学和动力学研究
Pub Date : 2022-03-29 DOI: 10.21608/jampr.2022.125370.1024
M. Mabrouk, Sherin F Hammad, M. Elshahawy
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引用次数: 1
Different Spectrophotometric Methods of Operating Ratio Spectra for Analyzing Pharmaceutical Combinations of Loratadine and Dexamethasone 不同分光光度法分析氯雷他定与地塞米松联合用药的操作比光谱
Pub Date : 2022-03-25 DOI: 10.21608/jampr.2022.132917.1028
M. Mabrouk, Sherin F Hammad, Noha Elzawawy
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引用次数: 0
Potentiation of paclitaxel antitumor activity by galloflavin or oxamate as lactate dehydrogenase inhibitors 紫杉醇抗肿瘤活性的增强与乳酸脱氢酶抑制剂的作用
Pub Date : 2021-09-30 DOI: 10.21608/jampr.2021.98224.1020
A. Elsisi, S. Sokar, Sara R El-Mahrouk, Sally E Abu-Risha
Increased aerobic glycolysis in cancer, a phenomenon known as the Warburg effect, has been observed in various tumors and represents a major biochemical alteration associated with malignant transformation. Several cancers display an elevated expression of lactate dehydrogenase-A (LDHA), which is involved in tumor initiation, maintenance, and progression. Significantly, inhibition of LDH-A has been reported to have an antiproliferative effect on breast cancer and inhibited tumor progression. Accordingly, several LDH-A inhibitors are being tested for their anticancer activity, such as oxamate and galloflavin. In the current study, the anti-tumor activity of oxamate and galloflavin was tested in vitro using MCF7 and OVCAR-3 human carcinoma cell lines. Furthermore, both drugs were examined in combination with paclitaxel (Taxol). Additionally, the potential anti-tumor effect of oxamate in the solid Ehrlich carcinoma (SEC) mouse model was examined alone and in combination with paclitaxel. Oxamate and galloflavin significantly reduced cell survival of MCF7 and OVCAR3 cell lines. They also caused significant reductions in LDH enzyme activity and ATP cellular content in addition to a significant increase in MDA content. Both oxamate and galloflavin potentiated the anticancer effect of paclitaxel both in vivo and in vitro. Moreover, potentiation of apoptosis and the anti-angiogenic effect of paclitaxel by oxamate were found in vivo. In conclusion, LDH inhibitor may represent a promising agent that enhances the anti-tumor activity of paclitaxel chemotherapy.
癌症中有氧糖酵解的增加,一种被称为Warburg效应的现象,已经在各种肿瘤中观察到,并且代表了与恶性转化相关的主要生化改变。一些癌症显示乳酸脱氢酶a (LDHA)的表达升高,这与肿瘤的发生、维持和进展有关。值得注意的是,据报道,抑制ldl - a对乳腺癌具有抗增殖作用并抑制肿瘤进展。因此,人们正在测试几种ldl - a抑制剂的抗癌活性,如草酸盐和黄素。本研究采用MCF7和OVCAR-3人癌细胞系,在体外测试了草酸酯和没食子黄素的抗肿瘤活性。此外,两种药物联合紫杉醇(紫杉醇)进行了试验。此外,研究了草酸酯在实体埃利希癌(SEC)小鼠模型中的潜在抗肿瘤作用,并与紫杉醇联合使用。草酸酯和没食黄素显著降低MCF7和OVCAR3细胞系的细胞存活率。它们还引起LDH酶活性和ATP细胞含量的显著降低,以及MDA含量的显著增加。在体内和体外实验中,草酸酯和黄素均增强了紫杉醇的抗癌作用。此外,在体内还发现了紫杉醇被草酸酯增强细胞凋亡和抗血管生成的作用。综上所述,LDH抑制剂可能是一种有前景的增强紫杉醇化疗抗肿瘤活性的药物。
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引用次数: 0
Quantitative Determination of Amlodipine and Valsartan in Pharmaceutical Dosage Form 药物剂型中氨氯地平和缬沙坦的定量测定
Pub Date : 2021-09-15 DOI: 10.21608/jampr.2021.85883.1017
Samah F. El-Malla, Sherin F Hammad, S. Khashaba
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引用次数: 0
Analysis of Counterfeit Sildenafil by Validated UV Spectrophotometric Methods 验证紫外分光光度法分析假药西地那非
Pub Date : 2021-09-12 DOI: 10.21608/jampr.2021.89542.1016
M. Mabrouk, Sherin F Hammad, Badiea Soliman, Amira H. Kamal
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引用次数: 0
HPLC/ELSD DETERMINATION AND VALIDATION OF ALPHA LIPOIC ACID AND SUCRALOSE IN BULK AND IN THEIR PHARMACEUTICAL DOSAGE FORMS α硫辛酸和三氯蔗糖原料药和制剂的Hplc / elsd测定和验证
Pub Date : 2021-05-17 DOI: 10.21608/JAMPR.2021.63273.1015
Nourhan M. Abdelbarey, M. Mabrouk, Miranda F. Kamal
Accurate, sensitive, robust and direct isocratic Reversed Phase-HPLC methods, using Evaporative Light Scattering Detector, (ELSD), had been developed and fully validated for the detection and quantification of two non-chromophoric nutraceuticals; Alpha Lipoic Acid (ALA) and Sucralose (SUC). Chromatographic separation was achieved using C18 Zoprax, 5 μm, 15 cm column for both compounds. For ALA, mobile phase was composed of acetonitrile: 0.1 M acetic acid (60:40, v/v), adjusted at pH 2.5, with 0.6 mL/min flow rate. For SUC, acetonitrile: deionized water (70:30, v/v) with 1 mL/min flow rate was used. Temperatures of drift tube, column, and spray chamber have been set to be 40°C and 30°C respectively during both assays. All varying chromatographic parameters were studied carefully. ALA and SUC had eluted at 4.81±0.02 min and 1.70±0.01 min, respectively. The obtained exponential ELSD responses, for the two developed methods, were linearly modeled using logarithmic transformation. Good Linearities had been achieved over the concentration ranges of 100-750 ppm and 16-500 ppm for ALA and SUC estimation respectively. The suggested methods disclosed excellent precision and accuracy levels. All validation parameters were fulfilled according to the USP elements and ICH guidelines. Satisfactory percentages of recovery (>97%) resulted upon methods application for the assay of each dietary supplement in its pharmaceutical formulation. Comparative statistical study was conducted between the proposed HPLC/ELSD methods and the reported HPLC/UV method for ALA and reported HPTLC method for SUC. Student’s t-tests and F-variance ratios for both methods had resulted in satisfactory values.
利用蒸发光散射检测器(ELSD)建立了准确、灵敏、稳健、直接的等容反相高效液相色谱(hplc)方法,并对两种非显色性营养保健品的检测和定量进行了充分验证;α硫辛酸(ALA)和三氯蔗糖(SUC)。用C18 Zoprax, 5 μm, 15 cm色谱柱对两种化合物进行分离。对于ALA,流动相为乙腈:0.1 M乙酸(60:40,v/v),调节pH为2.5,流速为0.6 mL/min。SUC采用乙腈:去离子水(70:30,v/v),流速为1 mL/min。漂移管、色谱柱和喷雾室的温度分别设置为40°C和30°C。仔细研究了各种色谱参数。ALA和SUC的洗脱时间分别为4.81±0.02 min和1.70±0.01 min。对于这两种方法得到的指数型ELSD响应,采用对数变换进行线性建模。ALA和SUC分别在100-750 ppm和16-500 ppm的浓度范围内获得了良好的线性估计。所建议的方法具有优良的精密度和准确度。所有验证参数均符合USP要素和ICH指南。对每种膳食补充剂在其制剂中的测定方法应用后,回收率达到满意的百分比(>97%)。采用HPLC/ELSD方法与文献报道的ALA HPLC/UV法和SUC HPLC/ tlc法进行对比统计研究。两种方法的学生t检验和f方差比结果都令人满意。
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引用次数: 0
Biological Activity Investigation of Some Gymnosperm Plants Belong to Cycadales Order 苏铁目裸子植物的生物活性研究
Pub Date : 2020-06-01 DOI: 10.21608/jampr.2020.23512.1002
W. Negm, K. A. El-Seoud, A. Kabbash, Mona El-Aasr
People are known to utilize plants for treatment of many diseases. Cycadales are one of these ancient plants that contained different active constituents. Due to the lack of adequate research on Cycadales, we conducted this study. The current study investigated and compared different biological activities for four different plants. Cycas thouarsii, Cycas pectinata, Dioon spinulosum and Encephalartos laurentianus were tested for the first time for cytotoxic, antioxidant and antimicrobial activities. Dioon spinulosum displayed significant cytotoxic activity on VERO cell line that was higher than 5-Fluorouracil. D. spinulosum possessed the highest radical scavenging activity followed by Cycas thouarsii. D. spinulosum showed the highest protective activity against DNA damage which was higher than the positive control. D. spinulosum showed the highest antihemolytic antioxidant activity followed by Encephalartos laurentianus. D. spinulosum presented the highest antimicrobial activity among the tested plants. Most Cycadales tested plants especially D. spinulosum displayed significant biological activities that are promising for future drug discovery.
众所周知,人们利用植物来治疗许多疾病。苏铁属植物是一种含有多种活性成分的古老植物。由于对Cycadales缺乏足够的研究,我们进行了这项研究。本研究调查并比较了四种不同植物的不同生物活性。本文首次测定了苏铁、苏铁、刺桐和laurentius的细胞毒、抗氧化和抗菌活性。Dioon spinlosum对VERO细胞株的细胞毒活性显著高于5-氟尿嘧啶。棘木清除自由基的能力最强,其次是苏铁。棘豆对DNA损伤的保护活性最高,高于阳性对照。棘棘的抗溶血抗氧化活性最高,其次是laurentianus。其中棘球菊的抑菌活性最高。大多数苏铁属植物,尤其是刺草,显示出显著的生物活性,对未来的药物开发有很大的前景。
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引用次数: 7
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Journal of Advanced Medical and Pharmaceutical Research
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