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还原氧化石墨烯/苋菜提取物/AuNPs 复合水凝胶对肿瘤细胞的作用:作为局部和多重协同治疗的集成平台。

Reduced Graphene Oxide/Amaranth Extract/AuNPs Composite Hydrogel on Tumor Cells as Integrated Platform for Localized and Multiple Synergistic Therapy.

机构信息

†School of Chemistry and Chemical Engineering, Anhui University, Hefei 230601, People's Republic of China.

§Collaborative Innovation Center of Modern Bio-Manufacture Anhui University, Hefei 230601, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2015 Jun 3;7(21):11246-56. doi: 10.1021/acsami.5b03907. Epub 2015 May 22.

DOI:10.1021/acsami.5b03907
PMID:25978657
Abstract

Integration of multimodal treatment strategies combined with localized therapy to enhance antitumor efficacy and reduce side effects is still a challenge. Herein, a novel composite hydrogel containing rGO, amaranth extract (AE) and gold nanoparticles (AuNPs) was prepared by using AE as both reductant and cross-linking agent. The chlorophyll derivatives in AE were also employed as a photodynamic therapy drug. Meanwhile, AuNPs and rGO both have obvious photothermal effects and can accelerate the generation of cytotoxic singlet oxygen (1O2). The temperature increase of rGO/AE/AuNPs precursor is up to 6.3 °C under 808 nm laser irradiation at a power density of 200 mW·cm(-2). The hydrogel shell on in situ tumor cells was easily formed and regulated by near-infrared irradiation within 10 min, which could both retain a high concentration of drugs on the lesion site and prevent them from migrating to normal tissue, thus reducing the side effects. Compared with rGO/AE and AE, rGO/AE/AuNPs showed a remarkably improved and synergistic antitumor effect. The hydrogel possesses good biocompatibility and high hydrophilicity and could be used for loading chemotherapeutics, which provides a new approach for located and multiple antitumor therapies.

摘要

整合多种治疗策略与局部治疗相结合,以提高抗肿瘤疗效并降低副作用仍然是一个挑战。在此,通过使用 AE 作为还原剂和交联剂,制备了一种新型的包含 rGO、苋菜提取物 (AE) 和金纳米粒子 (AuNPs) 的复合水凝胶。AE 中的叶绿素衍生物也被用作光动力治疗药物。同时,AuNPs 和 rGO 都具有明显的光热效应,可以加速细胞毒性单线态氧 (1O2) 的产生。在 808nm 激光照射下,功率密度为 200mW·cm(-2)时,rGO/AE/AuNPs 前体的温度升高可达 6.3°C。原位肿瘤细胞的水凝胶壳可以通过近红外辐射在 10 分钟内轻松形成和调节,既能保持病变部位的药物高浓度,又能防止药物迁移到正常组织,从而降低副作用。与 rGO/AE 和 AE 相比,rGO/AE/AuNPs 表现出显著改善的协同抗肿瘤作用。该水凝胶具有良好的生物相容性和高亲水性,可用于负载化疗药物,为定位和多种抗肿瘤治疗提供了新途径。

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