The present study compares solid lipid nanoparticles (SLN) formulated with
either wax or glyceride bulk material. While most published data deal with
glyceride SLN, little knowledge is reported on wax carriers. The two types
were compared with respect to drug encapsulation efficacy, particle size di
stribution after production and storage, and crystal packing. The inclusion
of retinol as a model drug was investigated. Retinol is chemically unstabl
e in water and rather stable in lipid phases. Thus, rapid degradation of re
tinol indicates rapid drug expulsion from the carrier. Good stability indic
ates an effective drug encapsulation in the lipid phase of the nanoparticle
s. Particle size distribution was measured by laser diffractometry. Subcell
packing and assignment of polymorphic forms was investigated by WAXS measu
rements. Glyceride SLN showed good drug encapsulation, while physical stabi
lity was poor. In contrast, wax SLN possessed good physical stability but l
acked sufficient drug encapsulation in the solidified state. These differen
ces were attributed in part to different crystal packing. Less ordered crys
tal lattices favour successful drug inclusion, as in the case of glyceryl m
onosterate and glyceryl behenate SLN. The highly ordered crystal packing of
wax SLN comprised of beeswax or cetyl palmitate, for instance. leads to dr
ug expulsion, but also to superior physical stability. (C) 2000 Elsevier Sc
ience B.V. All rights reserved.