| Literature DB >> 27236097 |
Paola Ringhieri1, Concetta Avitabile2, Michele Saviano3, Giancarlo Morelli1, Alessandra Romanelli4, Antonella Accardo5.
Abstract
Liposomal formulations composed of phospholipids with different unsaturation degrees, head groups and at different cholesterol content have been tested for the encapsulation of Peptide Nucleic Acid (PNA) oligomers. The best loading capability (177μg, ER%=87.2) was obtained for pure liposomes of phosphatidylglycerol (DOPG) with negatively charged head group. The insertion of a 10-20% of cholesterol in DOPG based liposomes provides a slight decrease (∼160μg) of the PNA loading. On the other hand, the cholesterol addition (20-30%) slows down the PNA's release (∼27%) in fetal bovine serum from the liposomal formulation. Based on the encapsulation and the release properties, PEGylated DOPG liposomes with a percentage of cholesterol of 10-20% are the optimal formulation for the loading of PNA-a210.Entities:
Keywords: Cholesterol; DOPG; Formulation; Liposome; Peptide nucleic acid
Mesh:
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Year: 2016 PMID: 27236097 DOI: 10.1016/j.colsurfb.2016.05.034
Source DB: PubMed Journal: Colloids Surf B Biointerfaces ISSN: 0927-7765 Impact factor: 5.268