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首页> 外文期刊>International Journal of Pharmaceutical Sciences Review and Research >Formulation and Evaluation of Sustained Release Matrix Tablets of Ciprofloxacin HCL Using Gum Kondagogu and Chitosan as Matrix Forming Polymers”
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Formulation and Evaluation of Sustained Release Matrix Tablets of Ciprofloxacin HCL Using Gum Kondagogu and Chitosan as Matrix Forming Polymers”

机译:以口香糖和壳聚糖为基质形成聚合物的环丙沙星盐酸盐缓释基质片剂的制备与评价”

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摘要

Hepatitis B virus (HBV) infects around 350 million of the global population. The current antivirals are laden with side effects as well as expense burden. An alternative medication based on Ayurveda is being proposed to counter this scenario. Hep-1 to Hep-6 are herbal formulations used for the treatment of hepatitis B virus. They are also indicated for alleviation of hepatotoxicity. The molecular mechanism involved in the anti-HBV activity of these formulations is being studied using in-vitro models for the first time. Inhibition of Hepatitis B surface antigen (HBsAg) secretion from the transfected human hepatocarcinoma PLC/PRF/5 cells, as well as inhibition of the surface antigen binding was taken up in the present study. These anti-HBV activities were detected by HBsAg specific antibody-mediated enzyme assay (ELISA) at concentrations ranging from 50 to 250μg/mL. The results indicate that the suppression of HBsAg production and inhibition were best observed at 150μg/mL across the extracts. This concentration was used to determine the hepatoprotectivity of these extracts in a Kupffer cell-hepatocyte in-vitro co-culture; determined by the expression of cytokines TNF-α, IL-6 and IL-10, in presence of bacterial lipopolysaccharide. Hep-1 was found to be the most suitable formulation showing both anti-HBV activity and optimum hepatoprotectivity during the study. This extract could thus be beneficial in the treatment of liver inflammation.
机译:乙型肝炎病毒(HBV)感染全球约3.5亿人口。当前的抗病毒药具有副作用以及费用负担。针对这种情况,正在提出一种基于阿育吠陀的替代药物。 Hep-1至Hep-6是用于治疗乙型肝炎病毒的草药配方。它们还被指示用于减轻肝毒性。首次使用体外模型研究了这些制剂抗HBV活性的分子机制。本研究研究了转染人肝癌PLC / PRF / 5细胞对乙肝表面抗原(HBsAg)分泌的抑制作用以及对表面抗原结合的抑制作用。这些抗HBV活性通过HBsAg特异性抗体介导的酶测定(ELISA)在50至250μg/ mL的浓度范围内进行检测。结果表明,在整个提取物中,对HBsAg产生的抑制和抑制作用最好在150μg/ mL处。该浓度用于确定这些提取物在库普弗细胞-肝细胞体外共培养中的肝保护性。通过在细菌脂多糖存在下细胞因子TNF-α,IL-6和IL-10的表达来确定。发现Hep-1是最合适的制剂,在研究期间显示出抗HBV活性和最佳的肝保护性。因此,该提取物在治疗肝脏炎症中可能是有益的。

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