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功能化 LbL 薄膜用于局部递送 STAT3 siRNA 和奥沙利铂联合治疗结肠癌。

Functionalized LbL Film for Localized Delivery of STAT3 siRNA and Oxaliplatin Combination to Treat Colon Cancer.

机构信息

Birla Institute of Technology and Science (BITS) Pilani, Hyderabad Campus, Hyderabad 500078, Telangana State, India.

出版信息

ACS Appl Mater Interfaces. 2022 Mar 2;14(8):10030-10046. doi: 10.1021/acsami.1c22166. Epub 2022 Feb 16.

Abstract

The aim of the study was to develop and evaluate the efficacy of a functionalized layer-by-layer (LbL) assembled film entrapped with oxaliplatin (OX) and signal transducer and activator of transcription 3 (STAT3) siRNA in the localized treatment of colon cancer. The LbL film was prepared by the sequential layering of chitosan (CS) and alginate to attain desired physical and mechanical properties. The film was functionalized by coating folic acid-conjugated CS on one side. On the other side, polycaprolactone was coated as a backing layer to provide directional drug release. OX was entrapped within the layers of the film, while STAT3 siRNA was complexed with CS to form nanoparticles before entrapment in the LbL film. The CS-siRNA nanoparticles were taken up by the colon carcinoma, Caco-2 cells within 3 h and provided concentration-dependent reduction in STAT3 protein expression. The functionalized LbL film (F-LbL film) selectively adhered to the colon cancer tissue in the mice model, whereas the nonfunctionalized film adhered to the normal colon tissue. The combination of OX and STAT3 siRNA provided significantly greater tumor regression, survival rate, and STAT3 protein suppression after localized delivery through oral administration compared with intravenous administration. Taken together, the F-LbL film can selectively bind to colon tumors for localized delivery of drugs to treat colon cancer.

摘要

本研究旨在开发并评估载有奥沙利铂(OX)和信号转导与转录激活因子 3(STAT3)siRNA 的功能化层层(LbL)组装膜的疗效,用于结肠癌的局部治疗。LbL 膜通过壳聚糖(CS)和海藻酸钠的顺序层层组装来制备,以获得所需的物理和机械性能。通过在一侧涂覆叶酸偶联 CS 对膜进行功能化,另一侧涂覆聚己内酯作为背衬层以提供定向药物释放。OX 被包埋在膜的层中,而 STAT3 siRNA 则与 CS 复合形成纳米颗粒,然后再包埋在 LbL 膜中。CS-siRNA 纳米颗粒在 3 小时内被结肠癌细胞 Caco-2 摄取,并提供浓度依赖性的 STAT3 蛋白表达减少。功能化 LbL 膜(F-LbL 膜)在小鼠模型中选择性地黏附在结肠癌组织上,而非功能化膜则黏附在正常结肠组织上。与静脉给药相比,OX 和 STAT3 siRNA 的联合给药通过口服局部递送可显著提高肿瘤消退率、存活率和 STAT3 蛋白抑制率。总之,F-LbL 膜可选择性地结合结肠肿瘤,用于局部递送药物治疗结肠癌。

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