Nylon 610 is a hydrophilic polymer with considerable potential as a me
mbrane for drug microencapsulation. To better understand drug transpor
t through such membranes, the influence of the solvents and monomers u
sed in the synthesis of nylon films were examined using a full factori
al study. Nylon 610 films were synthesized by an interfacial polyconde
nsation reaction using hexamethylenediamine (HD) in the water phase an
d sebacoyl chloride (SC) in the organic phase, which was a solvent ble
nd of chloroform and trichlorotrifluoroethane at ratios of 1:1, 1:4, a
nd 4:1. Monomer concentrations studied were 0.2, 0.4, and 0.6 M with r
espect to their appropriate phase, while the monomer ratios were 1:1,
3:1, and 1:3. The molecular weight, porosity, thickness, and crystalli
nity of the films were characterized. The transport of potassium chlor
ide, hydrocortisone, and m-cresol was studied at 25 degrees C as a fun
ction of the syntheses variables. Potassium chloride was selected to m
easure the porosity of the membrane. Hydrocortisone and m-cresol, a kn
own solvent for nylon 610, were used to study pore and solution-diffus
ion transport, respectively. The molecular weight of the films was pro
portional to the chloroform concentration. As the molecular weight inc
reased, film thickness, porosity, and hydrocortisone permeability incr
eased. As the molecular weight decreased, film thickness and porosity
decreased, while m-cresol permeability increased. These results can be
explained on the basis of HD ability to readily partition into a good
solvent such as chloroform permitting high molecular weight polymer t
o form before precipitation.