TY - JOUR
T1 - Filter-extruded liposomes revisited
T2 - a study into size distributions and morphologies in relation to lipid-composition and process parameters
AU - Hinna, Askell
AU - Steiniger, Frank
AU - Hupfeld, Stefan
AU - Stein, Paul C.
AU - Kuntsche, Judith
AU - Brandl, Martin
PY - 2016
Y1 - 2016
N2 - Filter-extrusion is a widely used technique for down-sizing of phospholipid vesicles. In order to
gain a detailed insight into size and size distributions of filter-extruded vesicles composed of
egg phosphatidyl-choline (with varying fractions of cholesterol) – in relation to extrusionparameters
(pore-size, number of filter passages, and flow-rate), flow field-flow fractionation in
conjunction with multi-angle laser light scattering (AF4-MALLS, Wyatt Technology Corp., Santa
Barbara, CA) was employed. Liposome size-distributions determined by AF4-MALLS were
compared with those of dynamic light scattering and correlated with cryo-transmission
electron microscopy and 31P-NMR-analysis of lamellarity. Both the mean size of liposome and
the width of size distribution were found to decrease with sequential extrusion through smaller
pore size filters, starting at a size range of &70–415nm upon repeated extrusion through
400nm pore-filters, eventually ending with a size range from &30 to 85nm upon extrusion
through 30nm pore size filters. While for small pores sizes (50 nm), increased flow rates resulted
in smaller vesicles, no significant influence of flow rate on mean vesicle size was seen with
larger pores. Cholesterol at increasing mol fractions up to 0.45 yielded bigger vesicles
(at identical process conditions). For a cholesterol mol fraction of 0.5 in combination with small
filter pore size, a bimodal size distribution was seen indicating cholesterol micro-crystallites.
Finally, a protocol is suggested to prepare large (300 nm) liposomes with rather narrow size
distribution, based on the filter extrusion at defined flow-rates in combination with freeze-/
thaw-cycling and bench-top centrifugation.
AB - Filter-extrusion is a widely used technique for down-sizing of phospholipid vesicles. In order to
gain a detailed insight into size and size distributions of filter-extruded vesicles composed of
egg phosphatidyl-choline (with varying fractions of cholesterol) – in relation to extrusionparameters
(pore-size, number of filter passages, and flow-rate), flow field-flow fractionation in
conjunction with multi-angle laser light scattering (AF4-MALLS, Wyatt Technology Corp., Santa
Barbara, CA) was employed. Liposome size-distributions determined by AF4-MALLS were
compared with those of dynamic light scattering and correlated with cryo-transmission
electron microscopy and 31P-NMR-analysis of lamellarity. Both the mean size of liposome and
the width of size distribution were found to decrease with sequential extrusion through smaller
pore size filters, starting at a size range of &70–415nm upon repeated extrusion through
400nm pore-filters, eventually ending with a size range from &30 to 85nm upon extrusion
through 30nm pore size filters. While for small pores sizes (50 nm), increased flow rates resulted
in smaller vesicles, no significant influence of flow rate on mean vesicle size was seen with
larger pores. Cholesterol at increasing mol fractions up to 0.45 yielded bigger vesicles
(at identical process conditions). For a cholesterol mol fraction of 0.5 in combination with small
filter pore size, a bimodal size distribution was seen indicating cholesterol micro-crystallites.
Finally, a protocol is suggested to prepare large (300 nm) liposomes with rather narrow size
distribution, based on the filter extrusion at defined flow-rates in combination with freeze-/
thaw-cycling and bench-top centrifugation.
U2 - 10.3109/08982104.2015.1022556
DO - 10.3109/08982104.2015.1022556
M3 - Journal article
C2 - 25826203
SN - 0898-2104
VL - 26
SP - 11
EP - 20
JO - Journal of Liposome Research
JF - Journal of Liposome Research
IS - 1
ER -