posted on 2021-06-02, 15:49authored byXiongqi Han, Joseph Ho Chi Lai, Jianpan Huang, Se Weon Park, Yang Liu, Kannie Wai Yan Chan
Imaging hydrogel-based local drug
delivery to the brain after tumor
resection has implications for refining treatments, especially for
brain tumors with poor prognosis and high recurrence rate. Here, we
developed a series of self-healing chitosan–dextran (CD)-based
hydrogels for drug delivery to the brain. These hydrogels are injectable,
self-healing, mechanically compatible, and detectable by chemical
exchange saturation transfer magnetic resonance imaging (CEST MRI).
CD hydrogels have an inherent CEST contrast at 1.1 ppm, which decreases
as the stiffness increases. We further examined the rheological properties
and CEST contrast of various chemotherapeutic-loaded CD hydrogels,
including gemcitabine (Gem), doxorubicin, and procarbazine. Among
these formulations, Gem presented the best compatibility with the
rheological (G′: 215.3 ± 4.5 Pa) and
CEST properties of CD hydrogels. More importantly, the Gem-loaded
CD hydrogel generated another CEST readout at 2.2 ppm (11.6 ±
0.1%) for monitoring Gem. This enabled independent and simultaneous
imaging of the drug and hydrogel integrity using a clinically relevant
3 T MRI scanner. In addition, the Gem-loaded CD hydrogel exhibited
a longitudinal antitumor efficacy of Gem over a week in vitro. Furthermore, the CD hydrogel could be visualized by CEST after
brain injection with a contrast of 7.38 ± 2.31%. These natural
labels on both the chemotherapeutics and hydrogels demonstrate unique
image-guided local drug delivery for brain applications.