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An injectable soft implant for long-acting, reversible, ultra-stable release of therapeutics

Stevens, M. M.; Kütahya, C.; Panariello, L.; Najer, A.; Rizou, T.; Shamsabadi, A.; Brachi, G.; Peeler, D. J.; Zharova, L.; Fernandez Debets, T. F. F.; Peschke, P.; Constantinou, A. P.; Xie, R.; Cheng, Y.; Burdis, R.; Suarez-Bonnet, A.; Cihova, M.; Yeow, J.; Schaufelberger, F.; Malanchi, I.

2026-02-26 bioengineering
10.64898/2026.02.25.707913 bioRxiv
Show abstract

Providing long-term (>6 months) zero-order drug release from easily administered formulations is a key challenge in improving patient adherence and facilitating access. Herein, we report the design and development of an injectable, biodegradable, long-acting polymeric microparticle-embedded hydrogel platform for prolonged, zero-order release of therapeutics. This "soft implant" is injectable for ease of administration and can be retrieved via a small incision, allowing for discontinuation of therapy if desired. Central to the platform are surface-eroding poly(orthoester) (POE) microparticles, which were molecularly tailored to tune zero-order drug release across a wide range of timeframes. We demonstrate the clinical potential of the "soft implant" using levonorgestrel, a contraceptive agent requiring sustained dosing. In vitro, we observed zero-order release for 300 days, projected for >12 months, with behavior consistent with surface erosion further supported through Raman chemical mapping. In vivo studies confirmed zero-order release for six months, projected to 12 months, from a subcutaneous injection in rats. We envision that our platform could transform therapies that require long-term, regular drug dosing, significantly improving compliance and therapy outcomes.

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