自愈水凝胶
透明质酸
体内
癌症研究
接种疫苗
原位
生物医学工程
材料科学
磁共振成像
阿霉素
医学
病理
化学
化疗
内科学
生物
放射科
高分子化学
生物技术
有机化学
解剖
作者
Wang Chun,Yi‐Ming Jing,Wenting Yu,Jie Gu,Zijian Wei,Anni Chen,Ying‐Tzu Yen,Xiaowen He,Lanqi Cen,Aoxing Chen,Xueru Song,Yirong Wu,Lixia Yu,Gaojian Tao,Baorui Liu,Shoufeng Wang,Bin Xue,Rutian Li
标识
DOI:10.1002/adhm.202300877
摘要
Doxorubicin (DOX) is the classic soft tissue sarcomas (STS) first-line treatment drug, while dose-dependent myelosuppression and cardiotoxicity limit its application in clinic. This research intends to apply DOX, which is also an inducer of immunogenic cell death as a part for "in situ vaccination" and conjointly uses PD-1 inhibitors to enhance antitumor efficacy. In order to achieve the sustained vaccination effect and real-time monitoring of distribution in vivo, the in situ forming and injectable hydrogel platform with the function of visualization is established for local delivery. The hydrogel platform is synthesized by hyaluronic acid-dopamine coordinated with gadolinium ions (Gd2+ ). Gd2+ provides the ability of magnetic resonance imaging, meanwhile further cross-linking the hydrogel network. Experiments show excellent ability of sustained release and imaging tracking for the hydrogel platform. In mouse STS models, the "in situ vaccination" hydrogels show the best effect of inhibiting tumor growth. Further analysis of tumor tissues show that "in situ vaccination" group can increase T cell infiltration, promote M1-type macrophage polarization and block elevated PD-1/PD-L1 pathway caused by DOX. These results are expected to prove the potential for synthesized hydrogels to achieve a universal platform for "in situ vaccination" strategies on STS treatments.
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