Tj. Young et al., Encapsulation of lysozyme in a biodegradable polymer by precipitation witha vapor-over-liquid antisolvent, J PHARM SCI, 88(6), 1999, pp. 640-650
Lysozyme was encapsulated in biodegradable polymer microspheres which were
precipitated from an organic solution by spraying the solution into carbon
dioxide. The polymer, either poly(l-lactide) (I-PLA) or poly(DL-lactide-co-
glycolide) (PGLA), in dichloromethane solution with suspended lysozyme was
sprayed into a CO2 vapor phase through a capillary nozzle to form droplets
which solidified after falling into a CO2 liquid phase. By delaying precipi
tation in the vapor phase, the primary particles became sufficiently large,
from 5 to 70 mu m, such that they could encapsulate the lysozyme. At an op
timal temperature of -20 degrees C, the polymer solution mixed rapidly with
CO2, and the precipitated primary particles were sufficiently hard such th
at agglomeration was markedly reduced compared with higher temperatures. Mo
re uniform particles were formed by flowing CO2 at high velocity in a coaxi
al nozzle to mix the droplets at the CO2 vapor-liquid interface. This proce
ss offers a means to produce encapsulated proteins in poly(DL-lactide-co-gl
ycolide) microspheres without earlier limitations of massive polymer agglom
eration and limited protein solubility in organic solvents.