体内
膀胱癌
抗癌药
药物输送
药品
材料科学
单宁酸
泌尿科
生物相容性
医学
原位癌
排尿
生物医学工程
纳米技术
癌症
药理学
内科学
化学
泌尿系统
冶金
有机化学
生物技术
生物
作者
Guangyu Wu,Hanyu Liang,Hexin Nan,Zhentao Shao,Shi Wang,Yan Zhou,Juan Li
标识
DOI:10.1021/acsabm.1c01186
摘要
Intravesical instillation therapy is increasingly recognized as one of the most common clinical treatment strategies for bladder cancer. However, the antitumor efficacy of chemotherapy drugs is still limited due to their rapid clearance by periodic urination. To circumvent this issue, a drug-loaded thin film comprising the self-assembly of tannic acid (TA) and ferric ions (Fe3+) was in situ fabricated on the bladder wall in vivo. As expected, the TA@Fe film with adjustable thickness could effectively prolong the residence time of anticancer drugs in the bladder and realize sustained release of anticancer drugs. Together with the antibacterial properties, the TA@Fe film enabled improved chemotherapeutic efficacy. Moreover, the TA@Fe film caused no adverse effects on bladder function, demonstrating the in vivo biocompatibility. In addition, the T2 contrast effect of Fe3+ was employed to real-time monitor the disassembly of the TA@Fe film and the ensuing drug release process by magnetic resonance imaging. We believe that the TA@Fe-based drug delivery platform with enhanced retention in the bladder would be of great potential for treating various bladder diseases.
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