Program Information
Next Generation Radiotherapy Biomaterials Loaded With Gold Nanoparticles
G Cifter1,2*, E Sajo2 , H Korideck1 , R Kumar1,3 , S Sridhar3 , R Cormack1 , G Makrigiorgos1 , W Ngwa1,2 , (1) Dana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, (2) Univ Massachusetts Lowell, Lowell, MA, (3) Northeastern University, Boston, MA,
Presentations
MO-FG-BRA-5 (Monday, July 13, 2015) 4:30 PM - 6:00 PM Room: Ballroom A
Purpose:It has been proposed that routinely used inert radiotherapy (RT) biomaterials (e.g. fiducials, spacers) can be upgraded to smarter ones by coating/loading them with radiosensitizing gold nanoparticles (GNPs), for sustained in-situ release after implantation to enhance RT. In this work, we developed prototypes of such RT biomaterials and investigated the sustained release of GNPs from the biomaterials as a function of design parameters.
Methods:Prototype smart biomaterials were produced by incorporating the GNPs in poly(D,L-lactide-co-glycolide) (PLGA) polymer millirods during the gel phase of production. For comparison, commercially available spacers were also coated with a polymer film loaded with fluorescent GNP. Optical/spectroscopy methods were used to monitor in vitro release of GNPs over time as a function of different design parameters: polymer weighting, type, and initial (loading) GNP concentrations. Inductively coupled plasma mass spectrometry was employed to verify GNP release.
Results:Results showed that gold nanoparticles could be successfully loaded in the new RT biomaterial prototypes. Burst release of GNPs could be achieved within 1 to 25 days depending on the preparation approach. Burst release was followed by sustained release profile over time. The amount of released GNP increased with increasing loading concentration as expected. The release profiles could also be customized as a function of polymer weighting, or preparation approaches.
Conclusion:Considered together, our results highlight potential for the development of next generation RT biomaterials loaded with GNPs customizable to different RT schedules. Such biomaterials could be employed as needed instead of currently used inert spacers/fiducials at no additional inconvenience to patients, to enhance RT.
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