光热治疗
阿霉素
化学
纳米颗粒
药物输送
辣根过氧化物酶
癌症治疗
癌细胞
纳米技术
涂层
光热效应
胶体金
生物物理学
靶向给药
癌症治疗
化疗
毒品携带者
药品
纳米医学
酶
细胞毒性
抗癌药
癌症
材料科学
癌症研究
合理设计
壳聚糖
输送系统
联合疗法
癌症化疗
作者
Manas Kumar Pradhan,Priyanka Payal,Rashi Sharma,Kalyanshi Ubnare,Sharad Gupta,Aasheesh Srivastava
标识
DOI:10.1021/acsanm.5c05215
摘要
Enhanced permeability and retention (EPR) in cancerous cells and tissues provides an opportunity for designing nanomaterials-based drug delivery systems (NanoDDS) for anticancer applications. Chemotherapy (CT) and photothermal therapy (PTT)─two modes of treating cancers─can be employed synergistically by designing suitable NanoDDS to enhance their efficacy. Herein, we engineered an effective multilayered NanoDDS for combination cancer therapy by employing a suitably designed amino acid amphiphile, amenable to reaction by the enzyme horseradish peroxidase (HRP). Coating the precursor particles with polydopamine (PDA) imparted PTT capabilities to these nanoparticles (NPs), and entrapping doxorubicin (Dox) provided CT capabilities. An additional layering of spontaneously formed gold nanoparticles (AuNPs) on these NPs further augmented their PTT capabilities. The resulting PDA_Dox_Au@NPs achieved a solution temperature increase of > + 19 °C upon NIR illumination at 1 W/cm2 for 4 minutes, with a photothermal conversion efficiency of 14%. Moreover, the NIR illumination unraveled these NPs and released the Dox entrapped within, resulting 44% cumulative Dox release. These NPs were efficiently internalized into cancer cells and induced strong anticancer effects. This work highlights the utility of enzyme reactions in engineering multilayered NanoDDS for potential synergistic anticancer therapy.
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