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Protein, peptide and non-peptide drug PEGylation for therapeutic application

机译:蛋白,肽和非肽药物PEG化用于治疗应用

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摘要

For many years proteins have been investigated as therapeutic agents, but unfortunately their potential advantages could not be completely exploited. The main drawbacks are their intrinsic short life in the body, immunological adverse reaction and proteolytic digestion. Among all the approaches studied for overcoming these problems, PEGylation (the modification of molecules with polyethylene glycol [PEG]) achieved the most interesting results, leading to a novel series of products that have already reached the market, and hopefully other promising agents will soon be available. Since the first studies in this field, the conjugation of PEG to a protein has shown the possibility of improving the pharmacokinetic profile of a linked drug. In the last few years this technology, firstly developed for proteins, has been transferred to non-peptide drugs, opening a new area of investigation that is now receiving increasing interest. This leads to new opportunities for many therapeutic treatments as it is possible to use molecules that could not before be exploited due to limitations such as inadequate water solubility, high nonspecific toxicity and poor pharmacokinetic profiles. In this review the most recent achievements in PEGylation of protein, peptide and non-peptide drugs are described concerning the binding chemistry, and many examples from the literature are reported, in the fields of both protein therapeutics and non-peptide drugs.
机译:多年来,人们一直在研究蛋白质作为治疗剂的作用,但不幸的是,它们的潜在优势无法被完全利用。主要缺点是它们固有的体内寿命短,免疫学不良反应和蛋白水解消化。在解决这些问题的所有方法中,聚乙二醇化(用聚乙二醇[PEG]修饰分子)取得了最有趣的结果,导致了一系列新产品已经投放市场,并希望其他有前途的药物将很快上市。能得到的。自从该领域的第一项研究以来,PEG与蛋白质的结合已显示出改善连接药物的药代动力学特性的可能性。在过去的几年中,首先为蛋白质开发的这项技术已被转移到非肽类药物上,从而开辟了一个新的研究领域,如今该领域受到越来越多的关注。这为许多治疗方法带来了新的机会,因为有可能使用由于诸如水溶性不足,非特异性毒性高和药代动力学特性不佳等限制而无法被开发的分子。在这篇综述中,描述了蛋白质,肽和非肽药物在聚乙二醇化方面的最新成就,涉及结合化学,并且在蛋白质治疗和非肽药物领域都报道了许多来自文献的实例。

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