I. Lacik et al., NEW CAPSULE WITH TAILORED PROPERTIES FOR THE ENCAPSULATION OF LIVING CELLS, Journal of biomedical materials research, 39(1), 1998, pp. 52-60
A new capsule for the encapsulation and transplantation of pancreatic
islets has been developed. Five active ingredients are involved in the
capsule formation process: high viscosity sodium alginate (SA-HV), ce
llulose sulfate (CS), poly(methylene-co-guanidine) hydrochloride (PMCG
), calcium chloride, and sodium chloride. Complexation reaction exhibi
ts several unique features: (1) solution of SA-HV with CS represents a
physical mixture of two entangled polyanions that provide both pH-sen
sitive (carboxylic) and permanently charged (sulfate) groups; (2) pres
ence of CaCl2 in the cation solution ensures formation of the gelled b
ead after the drop of polyanion solution is immersed in the cation sol
ution; (3) character of the polycation (PMCG), i.e., low molecular wei
ght and unusually high charge density, combines both high mobility and
reactivity; (4) presence of PMCG in cation solution, together with Ca
Cl2, gives rise to the competitive binding of these two cations based
on their diffusion and affinity towards the anion groups; and (5) NaCl
provides the anti-gelling sodium ions that significantly affect the r
eaction of CaCl2 with the polyanion matrix, thus altering the final pr
operties of the capsule surface, shape, and permeability. The capsule
size, mechanical strength, membrane thickness, and permeability can be
precisely adjusted and quantified. Detailed information on the permea
bility aspects is given in another paper by Brissova et al. [J. Biomed
. Mater. Sci., 39, 61 (1998)]. The new features concerning capsule pro
cessing and testing are presented. We believe that the capsule charact
eristics can be optimized in the next step to meet the biological crit
eria. The initial transplantation results suggest that this capsule is
biocompatible and noncytotoxic and is a promising candidate for the i
mmunoisolation of cells such as pancreatic islets. (C) 1998 John Wiley
& Sons, Inc.