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可再生半合成疫苗级角鲨烯的千克级药品生产质量管理规范(GMP)合成

Kilo-Scale GMP Synthesis of Renewable Semisynthetic Vaccine-Grade Squalene.

作者信息

Fisher Karl J, Shirtcliff Laura, Buchanan Greg, Thompson Andrew W, Woolard Frank X, LaMunyon Donald H, Marshall Jonathan L, Baranouskas Maya B, Voelker Rodger B, Lusk Jason S, Wells Charles E, Mohamath Raodoh, Kinsey Robert, Lykins William R, Ramer-Denisoff Gabi, Fox Christopher B, Paddon Christopher J, McPhee Derek

机构信息

Amyris Inc, 5885 Hollis St, Suite 100, Emeryville, CA 94608, USA.

Actylis Eugene, 90 North Polk St., Suite 200, Eugene OR 97402, USA.

出版信息

Org Process Res Dev. 2023 Dec 15;27(12):2317-2328. doi: 10.1021/acs.oprd.3c00300. Epub 2023 Nov 16.

Abstract

Emulsions of the triterpene squalene ((6,10,14,18)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene, CAS 111-02-4) have been used as adjuvants in influenza vaccines since the 1990s. Traditionally sourced from shark liver oil, the overfishing of sharks and concomitant reduction in the oceanic shark population raises sustainability issues for vaccine adjuvant grade squalene. We report a semisynthetic route to squalene meeting current pharmacopeial specifications for use in vaccines that leverages the ready availability of -β-farnesene ((6)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene, CAS 18794-84-8), manufactured from sustainable sugarcane via a yeast fermentation process. The scalability of the proposed route was verified by a kilo-scale GMP synthesis. We also report data demonstrating the synthesized semi-synthetic squalene's physical stability and biological activity when used in a vaccine adjuvant formulation.

摘要

自20世纪90年代以来,三萜类角鲨烯((6,10,14,18)-2,6,10,15,19,23-六甲基二十四碳-2,6,10,14,18,22-六烯,CAS 111-02-4)乳液已被用作流感疫苗的佐剂。传统上,角鲨烯来源于鲨鱼肝油,鲨鱼的过度捕捞以及随之而来的海洋鲨鱼数量减少,给疫苗佐剂级角鲨烯带来了可持续性问题。我们报道了一条角鲨烯的半合成路线,该路线所制得的角鲨烯符合目前用于疫苗的药典规范,其利用了通过酵母发酵过程从可持续甘蔗中制造的β-法呢烯((6)-7,11-二甲基-3-亚甲基-1,6,10-十二碳三烯,CAS 18794-84-8)的现成可得性。通过千克规模的GMP合成验证了所提出路线的可扩展性。我们还报告了数据,证明合成的半合成角鲨烯在用于疫苗佐剂配方时的物理稳定性和生物活性。

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