posted on 2013-04-08, 00:00authored byN. Samadi, C. F. van Nostrum, T. Vermonden, M. Amidi, W. E. Hennink
The
purpose of this study was to gain mechanistic insights into
the effect of different formulation parameters on the degradation
and release behavior of protein-loaded nanoparticulate carrier systems
based on an aliphatic polyester with pendant hydroxyl groups, poly(lactic-co-glycolic-hydroxymethyl glycolic acid) (pLGHMGA). Bovine
serum albumin (BSA) was used as a model protein. BSA-loaded pLGHMGA
nanospheres of 400–700 nm were prepared using a solvent evaporation
method using pLGHMGA of different molecular weights and different
compositions. Also, the concentration of pLGHMGA in the organic phase
was varied. The nanospheres showed a continuous mass loss accompanied
by continuous decrease in number average molecular weight, which indicates
that the degradation of the nanospheres is by bulk degradation with
a rapid release of water-soluble low molecular weight fragments. On
the basis of NMR analysis, it is concluded that intramolecular transesterification
precedes extensive hydrolysis of the polymer and degradation of the
nanospheres. BSA-loaded freeze-dried nanospheres showed a significant
burst release of 40–50% of the BSA loading. In contrast, nonfreeze-dried
samples showed a small burst of around 10–20%, indicating that
freeze-drying induced pore formation. Nonlyophilized nanospheres prepared
from pLGHMGA with 64/18/18 lactic/glycolic/hydroxymethylglycolic acid
(L/G/HMG) ratio showed a relatively fast release of BSA for the next
30 days. Nanospheres prepared from a more hydrophobic pLGHMGA (74/13/13,
L/G/HMG) showed a two-phase release. Circular dichroism analysis showed
that the secondary structure of the released protein was preserved.
This study shows a correlation between release behavior and particle
erosion rate, which can be modulated by the copolymer composition.