| Literature DB >> 28232268 |
Bryn D Monnery1, Michael Wright2, Rachel Cavill3, Richard Hoogenboom4, Sunil Shaunak5, Joachim H G Steinke1, Maya Thanou6.
Abstract
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. CrownEntities:
Keywords: Cytotoxicity; Gene therapy; Hydrolysis; MTT assay; Molecular weight; Phospholipids
Mesh:
Substances:
Year: 2017 PMID: 28232268 DOI: 10.1016/j.ijpharm.2017.02.048
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875