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Recombinant glucagon: a differential biological activity

机译:重组胰高血糖素:不同的生物活性

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摘要

In Brazil, there is a growing demand for specialised pharmaceuticals, and the high cost of their importation results in increasing costs, reaching US$ 1.34 billion in 2012 and US$ 1.61 billion in 2013. Worldwide expenses related to drugs could reach US$ 1.3 trillion in 2018, especially due to new treatments for hepatitis C and cancer. Specialised or high-cost pharmaceutical drugs used for the treatment of viral hepatitis, multiple sclerosis, HIV and diabetes are distributed free of charge by the Brazilian government. The glucagon peptide was included in this group of high-cost biopharmaceuticals in 2008. Although its main application is the treatment of hypoglycaemia in diabetic patients, it can also be used with patients in an alcoholic coma, for those patients with biliary tract pain, and as a bronchodilator. Therefore, in order to reduce biopharmaceutical production costs, the Brazilian government passed laws focusing on the development and increase of a National Pharmaceutical Industrial Centre, including the demand for the national production of glucagon. For that reason and given the importance and high cost of recombinant glucagon, the purpose of this study was to develop methods to improve production, purification and performance of the biological activity of recombinant glucagon. Glucagon was recombined into a plasmid vector containing a Glutathione S-transferase tag, and the peptide was expressed in a heterologous Escherichia coli system. After purification procedures and molecular analyses, the biological activity of this recombinant glucagon was examined using in vivo assays and showed a highly significant (p < 0.00001) and prolonged effect on glucose levels when compared with the standard glucagon. The experimental procedure described here facilitates the high level production of recombinant glucagon with an extended biological activity.Electronic supplementary materialThe online version of this article (doi:10.1186/s13568-015-0099-2) contains supplementary material, which is available to authorized users.
机译:在巴西,对特殊药品的需求不断增长,其进口的高成本导致成本增加,2012年达到13.4亿美元,2013年达到16.1亿美元。全球与毒品有关的支出可能达到1.3万亿美元在2018年,尤其是由于丙型肝炎和癌症的新疗法。巴西政府免费分发用于治疗病毒性肝炎,多发性硬化症,HIV和糖尿病的专业或昂贵药物。胰高血糖素肽于2008年被包括在这组昂贵的生物药物中。尽管其主要应用是治疗糖尿病患者的低血糖症,但它也可用于酒精性昏迷患者,胆道疼痛患者和作为支气管扩张剂。因此,为了降低生物制药生产成本,巴西政府通过了以发展和增加国家制药工业中心为重点的法律,其中包括对国内胰高血糖素生产的需求。因此,鉴于重组胰高血糖素的重要性和高成本,本研究的目的是开发提高重组胰高血糖素生物活性的生产,纯化和性能的方法。胰高血糖素重组到含有谷胱甘肽S-转移酶标签的质粒载体中,并且该肽在异源大肠杆菌系统中表达。经过纯化程序和分子分析后,使用体内测定法检查了该重组胰高血糖素的生物活性,与标准胰高血糖素相比,该重组胰高血糖素具有很高的显着性(p <0.00001),并且对葡萄糖水平的影响延长。本文所述的实验程序有助于高水平生产具有扩展生物活性的重组胰高血糖素。电子补充材料本文的在线版本(doi:10.1186 / s13568-015-0099-2)包含补充材料,授权用户可以使用。

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