H. Ratz et al., Separation and quantitation of alkylphosphocholines and analogues of different liposome formulations by HPTLC, J AOAC INT, 84(4), 2001, pp. 1277-1282
High-performance thin-layer chromatographic (HPTLC) analysis of non UV-acti
ve phospholipids in biological matrixes is a common method for separation,
detection, and quantitation. Liposomes containing new alkylphosphocholines
and analogues with enhanced cytostatic activity had been prepared. The lipo
somal formulations were designed to enable the intravenous application of t
he alkylphosphocholines and analogues and to reduce dose-limiting toxicitie
s observed after oral administration. For quality control the liposomes wer
e analyzed by HPTLC for content of 1,2-dipalmitoyl-sn-glycero-3-phosphoglyc
erol (DPPG), cholesterol, alkylphosphocholines, and analogues and their rel
ated compounds (main degradation products). Due to the differences in lipop
hily of the compounds, different mobile phases were necessary to achieve se
paration. Automated Multiple Development was used to reduce the number of p
lates and to improve the selectivity and the capacity of the chromatographi
c system to separate the described alkylphosphocholines and analogues from
DPPG and 1,2-dipaimitoyl-sn-glycero-3-phosphocholine in one chromatographic
system.