Encapsulation of vinblastine into new liposome formulations prepared from triticum (wheat germ) lipids and its activity against human leukemic cell lines
H. Maswadeh et al., Encapsulation of vinblastine into new liposome formulations prepared from triticum (wheat germ) lipids and its activity against human leukemic cell lines, ANTICANC R, 20(6B), 2000, pp. 4385-4390
Liposomes prepared from lipids isolated from Triticum sp. (wheat germ) were
used to investigate the percentage of Vinblastine encapsulation and its re
tention into liposomes. The wheat germ total lipids (TL) were extracted by
the Bligh-Dyer method and the lipid classes have been isolated using chroma
tographic techniques. The type of lipids and their percentage content have
been examined by TLC coupled with an FID (latroscan). Two liposomal formula
tions, i.e., I and II with encapsulated vinblastine, and formulation III (e
mpty liposomes) have been prepared by thin film hydration method. The cytot
oxic/cytostatic activity of these liposomal formulations have been examined
against nine human leukemic cell lines. The results showed that the percen
tage content of vinblastine into liposomes I and II depended an the lipid c
omposition and it was greater into formulation II (>90%). The retention of
the drug into liposomes was studied and found to be time-dependent at 37 de
grees C. For the cytotoxic/cytostatic activity the parameters GI(50), TGI,
LC50 were estimated according to the instructions given by the NCI. The res
ults shaw that formulation III (empty liposomes), exhibited a growth inhibi
ting activity, against the most tested cell lines. Formulation II showed me
an of LC50 at 124.6 nM, mean of TGI at 71.6 nM and mean of GI(50) at 30.8 n
M.