Guichard Marie-Julie, Patil Harshad P, Koussoroplis Salome Juliette, Wattiez Ruddy, Leal Teresinha, Vanbever Rita
Advanced Drug Delivery & Biomaterials, Louvain Drug Research Institute (LDRI), Université catholique de Louvain, Brussels 1200, Belgium.
Department of Proteomic and Microbiology, Research Institute for Biosciences, University of Mons, Mons 7000, Belgium.
Int J Pharm. 2017 May 30;524(1-2):159-167. doi: 10.1016/j.ijpharm.2017.03.057. Epub 2017 Mar 27.
Recombinant human deoxyribonuclease I (rhDNase) is the mucolytic agent most widely used for the treatment of respiratory disease in cystic fibrosis. However, rhDNase is rapidly cleared from the lungs which implies a high dosing frequency and limited patient adherence. The aim of this study was to produce a long-acting PEGylated derivative of rhDNase presenting a preserved enzymatic activity. Site-specific PEGylation on the N-terminal (N-ter) leucine residue of rhDNase was achieved by reductive alkylation at acidic pH using linear 20kDa, linear 30kDa or two-arm 40kDa polyethylene glycol (PEG) propionaldehydes. Yields of mono-PEGylated products ranged between 45% and 61%. Conjugation to PEG fully preserved the secondary structure and the in vitro enzymatic activity of the native protein. These properties offer interesting perspectives for in vivo inhalation studies of the PEGylated enzyme.
重组人脱氧核糖核酸酶I(rhDNase)是治疗囊性纤维化呼吸系统疾病应用最广泛的黏液溶解剂。然而,rhDNase会迅速从肺部清除,这意味着给药频率高且患者依从性有限。本研究的目的是制备一种长效聚乙二醇化rhDNase衍生物,并保留其酶活性。通过在酸性pH条件下使用线性20kDa、线性30kDa或双臂40kDa聚乙二醇(PEG)丙醛进行还原烷基化反应,实现了rhDNase N端(N-ter)亮氨酸残基的位点特异性聚乙二醇化。单聚乙二醇化产物的产率在45%至61%之间。与PEG的缀合完全保留了天然蛋白质的二级结构和体外酶活性。这些特性为聚乙二醇化酶的体内吸入研究提供了有趣的前景。