A convenient method for the relative and absolute quantification of lipid components in liposomes by 1H- and 31P NMR-spectroscopy.

Liposomes are promising delivery systems for pharmaceutical applications and have been used in medicine in the recent past. Preparation of liposomes requires reliable characterization and quantification of the phospholipid components for which the traditional cumbersome molybdate method is used frequently. The objective was to improve relative and absolute quantification of lipid components from liposomes. A reliable method for quantification of lipid composition in liposome formulations in the 1–10 μmol range with 1H- and 31P NMR spectroscopy at 600 MHz has been developed. The method is based on three crystalline small-molecule standards (Ph 3 PO 4 , (Tol) 3 PO 4 , and Ph 3 PO) in CDCl 3. Excellent calibration linearity and chemical stability of the standards was observed. The method was tested in blind fashion on liposomes containing POPC, PEG-ceramide and a pH-sensitive trans -aminocyclohexanol-based amphiphile (TACH). 1 1 Et 3 PO 4 Triethyl phosphate, Ph 3 PO 4 triphenyl phosphate, (Tol) 3 PO 4 tritolyl phosphate, Ph 3 PO triphenylphosphine oxide, POPC 1-palmitoyl-2-oleyl- sn -glycero-3-phosphocholine, DPPC 1,2-dipalmitoyl- sn -glycero-3-phosphocholine, DOPC 1,2-dioleyl- sn -glycero-3-phosphocholine, DOPE 1,2-dioleoyl- sn -glycero-3-phosphoethanolamine, POPE 1-palmitoyl-2-oleoyl- sn -glycero-3-phosphoethanolamine, PEG-ceramide N -palmitoyl-sphingosine-1-(succinyl[methoxy(polyethylene glycol)2000]), COSY correlation spectroscopy, TOCSY total correlation spectroscopy, HMBC heteronuclear multiple-bond correlation, TACH trans -aminocyclohexanol, ANTS 8-aminonaphthalene-1,3,6-trisulfonic acid, disodium salt, DPX p -xylene-bis-pyridinium bromide, HEPES 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid, pfg pulse-field gradient. Relative quantification (percentage of components) as well as determination of absolute lipid amount was possible with excellent reproducibility with an average error of 5 %. Quantification (triplicate) was accomplished in 15 min based on 1H NMR and in 1 h based on 31P NMR. Very little change in mixture composition was observed over multiple preparative steps. Liposome preparations containing POPC, POPE, DOPC, DPPC, TACH, and PEG-ceramide can be reliably characterized and quantified by 1H NMR and 31P NMR spectroscopy at 600 MHz in the μmol range. [Display omitted] • Reliable liposome lipid quantification around 1–10 μmol with 1H/31P NMR spectroscopy was possible. • Quantification in 15 min (1H) and in 1 h (31P). • Very little change in liposome composition was observed over multiple preparative steps. [ABSTRACT FROM AUTHOR]