梁强,王昕,杨宝,支旭勃,李倩楠,刘建利,张忠旗,赵金礼.化学通报,2022,85(6):722-727.
阿基瑞林制备方法的改进研究
Study on the improvement of preparation method of argireline
投稿时间:2021-08-17  修订日期:2021-10-22
DOI:
中文关键词:  阿基瑞林  酰胺化反应  差向异构  氨基保护与脱保护
英文关键词:Argireline, Amidation, Epimerization, Amino  Protection and  Deprotection
基金项目:西安市博士后创新基地项目(市人社:2019-683号)
作者单位E-mail
梁强* 陕西慧康生物科技有限责任公司 liangqiang@huikangbio.com 
王昕 陕西慧康生物科技有限责任公司  
杨宝 陕西慧康生物科技有限责任公司  
支旭勃 陕西慧康生物科技有限责任公司  
李倩楠 陕西慧康生物科技有限责任公司  
刘建利 陕西慧康生物科技有限责任公司  
张忠旗 陕西慧康生物科技有限责任公司  
赵金礼 陕西慧康生物科技有限责任公司  
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中文摘要:
      阿基瑞林,又称乙酰基六肽-8、六胜肽等。它作为肉毒毒素的安全替代品,具有显著的抗皱活性,是美妆市场上需求潜力很大的抗皱多肽原料。 当前阿基瑞林主要是通过固相合成方法得到的,由于所使用的Rink Amide AM Resin单价高、上载量低,造成了阿基瑞林原料价格高昂,不利于其大规模生产及推广应用。本文中使用固-液相结合的方法:首先用高上载量、单价低的2-CTC Resin合成六肽片段,六肽片段再经酰胺化处理得阿基瑞林粗品,粗品经纯化后得95%以上阿基瑞林,收率59.77%;本方法成本低、收率高,使2-CTC Resin方法较Rink Amide AM Resin方法每公斤合成成本降低了19.74%,收率提高了13.25%,Rink Amide AM Resin和2-CTC Resin每公斤规模化生产批次产量由406.4g提高到908.0g,更适用于规模化生产。同时本方法对C端酰胺化多肽的合成提供了一种新思路。
英文摘要:
      Argireline, also known as Acetyl Hexapeptide-8 and Hexapeptide. As a safe alternative of botulinum toxin, it has significant anti-wrinkle activity and is a potential anti-wrinkle peptide material in beauty makeup market. At present, Argireline is mainly obtained by solid phase synthesis. However, due to high unit price, low uploading quantity and low yield of Rink Amide AM Resin used, the raw material price of Argireline is high, which is not conducive to its large-scale production and application. In this paper, the method of solid-liquid phase combination was used: first, hexapeptide fragment was synthesized with 2-CTC Resin with high loading capacity and low unit price. Hexapeptide fragment was aminated to get crude achirylin. After purification, more than 95% achirylin was obtained with 59.77% yield. Compared with Rink Amide AM Resin, the synthesis cost of 2-CTC Resin decreased by 19.74% per kilogram and the yield increased by 13.25%. Rink Amide AM Resin and 2-CTC Resin yield per kilogram of large-scale production batches increased from 406.4g to 908.0g. This method provides a new idea for the synthesis of C-terminal aminated polypeptides.
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