Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128, Mainz, Germany.
Graduate School Material Science in Mainz, Staudinger Weg 9, 55128, Mainz, Germany.
Macromol Biosci. 2017 Oct;17(10). doi: 10.1002/mabi.201600377. Epub 2016 Dec 12.
Protein-polymer conjugates are widely used to improve the pharmacokinetic properties of therapeutic proteins. Commercially available conjugates employ poly(ethylene glycol) (PEG) as the protective polymer; however, PEG has a number of shortcomings, including non-biodegradability and immunogenicity, that call for the development of alternatives. Here, the synthesis of biodegradable poly(phosphate), that is, poly(ethyl ethylene phosphate) (PEEP), by organo-catalyzed anionic ring-opening polymerization exhibiting dispersity values Ð < 1.3 is reported. Polymers with molecular weights between 2000 and 33 200 g mol are then ω-functionalized with a succinimidyl carbonate group and subsequently conjugated to model proteins. These are the first conjugates based on polyphosphates which degraded upon exposure to phosphodiesterase. As is the case for PEGylated therapeutics, residual in vitro activity of the PPEylated conjugates depends on the extent of protein modification. These results suggest that PEEP exhibits the desired properties of a biopolymer for use in next generation, fully degradable drug delivery systems.
蛋白质-聚合物缀合物被广泛用于改善治疗性蛋白质的药代动力学性质。市售的缀合物采用聚(乙二醇)(PEG)作为保护聚合物; 然而,PEG 存在许多缺点,包括不可生物降解性和免疫原性,这需要开发替代品。在这里,通过有机催化的阴离子开环聚合合成了可生物降解的聚(磷酸盐),即聚(乙基乙撑磷酸酯)(PEEP),其分散度值 Ð < 1.3。分子量在 2000 至 33200 克/摩尔之间的聚合物随后用琥珀酰亚胺碳酸酯基团进行 ω-官能化,然后与模型蛋白质缀合。这些是基于聚磷酸盐的第一个缀合物,在暴露于磷酸二酯酶时会降解。与 PEG 化治疗剂一样,PEE 化缀合物的体外残留活性取决于蛋白质修饰的程度。这些结果表明,PEEP 表现出作为下一代完全可降解药物递送系统的生物聚合物的所需特性。