| Literature DB >> 33915726 |
Daria Tretiakova1, Irina Le-Deigen2, Natalia Onishchenko1, Judith Kuntsche3, Elena Kudryashova2, Elena Vodovozova1.
Abstract
Previously, a liposomal formulation of a chemotherapeutic agent melphalan (Mlph) incorporated in a fluid lipid bilayer of natural phospholipids in the form of dioleoylglyceride ester (MlphDG) was developed and the antitumor effect was confirmed in mouse models. The formulation composed of egg phosphatidylcholine (ePC), soybean phosphatidylinositol (PI), and MlphDG (8:1:1, by mol) showed stability in human serum for at least 4-5 h. On the contrary, replacing PI with pegylation of the liposomes, promoted fast dissociation of the components from the bilayer. In this work, interactions of MlphDG-liposomes with the most abundant plasma protein-albumin-in function of the presence of PI in the formulation were explored using Fourier transform infrared spectroscopy. The release of MlphDG from the liposomes was studied by asymmetrical flow field-flow fractionation (AF4) using micelles formed by a polyethylene glycol conjugate with phosphatidylethanolamine to mimic the physiological lipid sink like lipoproteins. Our results show that PI actually protects the membrane of MlphDG-liposomes from the protein penetration, presumably due to pairing between the positively charged MlphDG and negatively charged PI, which compensates for the heterogeneity of the lipid bilayer. The AF4 technique also evidences high stability of the formulation as a drug carrier.Entities:
Keywords: ATR-FTIR spectroscopy; albumin; asymmetrical flow field-flow fractionation; formulation stability; lipophilic prodrug; melphalan; nanosized liposomes; phosphatidylinositol
Year: 2021 PMID: 33915726 DOI: 10.3390/pharmaceutics13040473
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321