Chemical Biology Section, Department of Chemistry, Imperial College London, London SW7 2AZ, UK.
Institute of Pharmaceutical Science, King's College London,Franklin-Wilkins Building, London, SE1 9NH, UK.
Int J Pharm. 2017 Apr 15;521(1-2):249-258. doi: 10.1016/j.ijpharm.2017.02.048. Epub 2017 Feb 21.
The mechanism of polycation cytotoxicity and the relationship to polymer molecular weight is poorly understood. To gain an insight into this important phenomenon a range of newly synthesised uniform (near monodisperse) linear polyethylenimines, commercially available poly(l-lysine)s and two commonly used PEI-based transfectants (broad 22kDa linear and 25kDa branched) were tested for their cytotoxicity against the A549 human lung carcinoma cell line. Cell membrane damage assays (LDH release) and cell viability assays (MTT) showed a strong relationship to dose and polymer molecular weight, and increasing incubation times revealed that even supposedly "non-toxic" low molecular weight polymers still damage cell membranes. The newly proposed mechanism of cell membrane damage is acid catalysed hydrolysis of lipidic phosphoester bonds, which was supported by observations of the hydrolysis of DOPC liposomes.
聚阳离子细胞毒性的机制及其与聚合物分子量的关系尚不清楚。为了深入了解这一重要现象,我们测试了一系列新合成的均匀(近单分散)线性聚乙烯亚胺、市售的聚(L-赖氨酸)以及两种常用的基于 PEI 的转染试剂(宽分布 22kDa 线性和 25kDa 支化)对 A549 人肺癌细胞系的细胞毒性。细胞膜损伤测定(LDH 释放)和细胞活力测定(MTT)表明,细胞毒性与剂量和聚合物分子量有很强的相关性,并且随着孵育时间的延长,即使是所谓的“低毒性”低分子量聚合物也会损伤细胞膜。新提出的细胞膜损伤机制是脂酰磷酸酯键的酸催化水解,这一机制得到了 DOPC 脂质体水解观察的支持。