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Penetration enhancers strengthen tough hydrogel bioadhesion and modulate locoregional drug delivery.
Shi, Wenna; Xue, Hui; Du, Tianwei; Liu, Jun-Li; Ling, Victor; Wang, Yuzhuo; Ma, Zhenwei; Gao, Zu-Hua.
Afiliación
  • Shi W; Department of Integrative Oncology, BC Cancer Research Institute, Vancouver, Canada. zuhua.gao@ubc.ca.
  • Xue H; Department of Pharmacy, Shandong Cancer Hospital and Institute, Jinan, China.
  • Du T; Department of Experimental Medicine, BC Cancer Research Institute, Vancouver, Canada.
  • Liu JL; Department of Integrative Oncology, BC Cancer Research Institute, Vancouver, Canada. zuhua.gao@ubc.ca.
  • Ling V; School of Biomedical Engineering, University of British Columbia, Vancouver, Canada.
  • Wang Y; Department of Medicine, McGill University Health Centre Research Institute, Montreal, Canada.
  • Ma Z; Department of Integrative Oncology, BC Cancer Research Institute, Vancouver, Canada. zuhua.gao@ubc.ca.
  • Gao ZH; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Biomater Sci ; 2024 Oct 07.
Article en En | MEDLINE | ID: mdl-39370988
ABSTRACT
The human body possesses natural barriers, such as skin and mucosa, which limit the effective delivery of therapeutics and integration of medical devices to target tissues. Various strategies have been deployed to breach these barriers mechanically, chemically, or electronically. The development of various penetration enhancers (PEs) offers a promising solution due to their ability to increase tissue permeability using readily available reagents. However, existing PE-mediated delivery methods often rely on weak gel or liquid drug formulations, which are not ideal for sustained local delivery. Hydrogel adhesives that can seamlessly interface biological tissues with controlled drug delivery could potentially resolve these issues. Here, we demonstrate that tough adhesion between drug-laden hydrogels and biological tissue (e.g. skin and tumours) can lead to effective local delivery of drugs deep into targeted tissues by leveraging the enhanced tissue penetration mediated by PEs. The drug release profile of the hydrogel adhesives can be fine-tuned by further engineering the nanocomposite hydrogel matrix to elute chemotherapeutics from 2 weeks to 2 months. Using a 3D tumour spheroid model, we demonstrated that PEs increased the cancer-killing effectiveness of doxorubicin by facilitating its delivery into tumour microtissues. Therefore, the proposed tough bioadhesion and drug delivery strategy modulated by PEs holds promise as a platform technique to develop next-generation wearable and implantable devices for cancer management and regenerative medicine.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomater Sci Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomater Sci Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido