Interface Wettability Transition‐Driven Drug Release and Dual‐Phase Functionalization in Implant Abutment
Dental implant abutments face dual clinical challenges of early-stage biological contamination and late-stage inflammatory microenvironments. To address the issues, this study developed a smart drug-release coating based on a superhydrophobic-wettable transition mechanism. The coating on the abutment surface was constructed by hydrophobic micelles self-assembling on mesoporous silica nanoparticles loaded with berberine. In the early stage, the superhydrophobic surface can effectively resist the adhesion of proteins and bacteria. With protein deposition, this process induced a transition of the superhydrophobic surface to a hydrophilic state, leading to a sigmoidal drug release profile that passively triggered sustained microenvironment regulation in the later stage. In vivo experiments demonstrated that this coating not only had strong immediate antibacterial efficacy (22.5-fold enhancement) but also significantly reduced inflammation and promoted soft tissue closure. This work provides a sequential functionalization strategy of "early-antifouling-enabled late active regulation" for abutments, offering a potential solution to prevent peri‑implant inflammation and soft tissue dehiscence.
Authors
- Bingyang Lu (ORCID: https://orcid.org/0000-0002-7163-5455)
- Zi Wang (ORCID: https://orcid.org/0000-0002-3953-0493)
- Mingxia Li (ORCID: https://orcid.org/0000-0002-6941-7344)
- Liang Shi
- Jinghan Wang
- Guangping Wang
- Dan Zou (ORCID: https://orcid.org/0000-0002-8147-2557)
Institutions
- Xihua University (CN)
- University of Electronic Science and Technology of China (CN)
- Southwest Medical University (CN)
- Affiliated Hospital of Southwest Medical University (CN)
- First Affiliated Hospital of Sichuan Medical University (CN)
Publication Details
- Journal
- Advanced Science
- Published
- 2026-04-16
- DOI
- https://doi.org/10.1002/advs.75351
- Primary Topic
- Advanced Drug Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 0.00