The objective of this study was to develop an efficient "real time" measure
ment system able to directly measure, with microgram resolution, the dissol
ution rate of absorbable glass fibers, and utilize the system to evaluate t
he effectiveness of silane-based sizing as a means to delay the fiber disso
lution process. The absorbable glass fiber used was calcium phosphate (CaP)
, with tetramethoxysilane selected as the sizing agent, E-glass fiber was u
sed as a relatively nondegrading control. Both the unsized-CaP and sized-Ca
P degraded linearly at both the 37 degrees C and 60 degrees C test temperat
ure levels used. No significant decrease in weight-loss rate was recorded w
hen the CaP fiber tows were pretreated, using conventional application meth
ods, with the tetramethoxysilane sizing for either temperature condition. T
he unsized-CaP and sized-CaP weight loss rates were each significantly high
er at 60 than at 37 degrees C (both p < 0.02), as expected from dissolution
kinetics, Zn terms of actual weight loss rate measured using our system fo
r phosphate glass fiber, the unsized-CaP fiber we studied dissolved at a ra
te of 10.90 x 10(-09) and 41.20 x 10(-09) g/min-cm(2) at 37 degrees C and 6
0 degrees C, respectively, Considering performance validation of the develo
ped system, the slope of the weight loss vs. time plot for the tested E-gla
ss fiber was not significantly different compared to a slope equal to zero
for both test temperatures. (C) 1999 John Wiley & Sons, Inc.