RT Journal Article
SR Electronic
T1 Long-term Antibody Release Polycaprolactone (PCL) Capsule and the Release Kinetics In Natural and Accelerated Degradation
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2022.06.06.493286
DO 10.1101/2022.06.06.493286
A1 Waterkotte Thomas
A1 Xingyu He
A1 Apipa Wanasathop
A1 Kevin Li
A1 Yoonjee Park
YR 2022
UL http://biorxiv.org/content/early/2022/06/06/2022.06.06.493286.abstract
AB Although therapy using monoclonal antibodies (mAbs) has been steadily successful over the last 20 years, the means of delivery of mAbs has not been optimized, especially for long-term delivery. Frequent injections or infusions have been current standard of care. In this study, we have developed a long-term antibody biodegradable implant using a porous polycaprolactone (PCL) capsule. It released Bevacizumab (Bev) slowly for 8 months to date. The Bev release kinetics fit a drug release model with experimental data of the diffusion coefficient and partition coefficient through the polymer capsule. Since screening drug release profiles for the long-term (> 6 months) is time consuming, an accelerated degradation method was used after validating characteristics of the PCL capsule in natural and accelerated degradation conditions. The correlation of time period between the natural and the accelerated degradation was determined. Overall, the study suggests mAbs can be released from a porous PCL capsule without an effect of the polymer degradation over the long period (~ 6 months) and the long-term release kinetics can be determined by the accelerated degradation within 14 days.Competing Interest StatementThe authors have declared no competing interest.