Biodegradable
polymer clips as multidimensional soft tissue biopsy
markers were developed with better biocompatibility and imaging features.
Unlike the commercially available metallic biopsy markers, the developed
polymer clips are temporary implants with similar efficacies as metal
markers in imaging and detection and get absorbed within the body
with time. Herein, we evaluate the degradation rate of three resorbable
polymer-based marker compounds in an in vivo murine model. Three polymers,
abbreviated as Polymer A (PLGA poly(lactic-
co
-glycolic
acid)50:50), Polymer B (PLGA (poly(lactic-
co
-glycolic
acid)) 75:25), and Polymer C (polycaprolactone (PCL)), mixed with
20% lipiodol and 0.2% iron oxide and a control polymer were implanted
into nine mice, followed by CT and MRI imaging. Images were evaluated
for conspicuity. Specimens were examined for tissue analysis of iodine
and iron contents. Significant differences in polymer resorption and
visualization on CT were noted, particularly at 8 weeks (
p
< 0.027). Polymers A, B, and C were visible by CT at 4, 6, and
8 weeks, respectively. All marker locations were detected on MRI (T1
and SWI) after 24 weeks, with tattooing of the surrounding soft tissue
by iron deposits. CT and MR visible polymer markers can be constructed
to possess variable resorption, with stability ranging between 4 and
14 weeks post placement, making this approach suitable for distinct
clinical scenarios with varying time points.