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基于负载阿霉素的碳纳米颗粒的纳米平台通过产生活性氧来增强细胞凋亡,从而实现有效的癌症治疗。

Nanoplatform based on carbon nanoparticles loaded with doxorubicin enhances apoptosis by generating reactive oxygen species for effective cancer therapy.

作者信息

Liu Yusheng, Zhang Junfeng, Wu Chunying, Lai Yigui, Fan Huijie, Wang Qiang, Lin Zhaolin, Chen Jishang, Zhao Xiaoshan, Jiang Xuefeng

机构信息

Department of Traditional Chinese Medicine, Yangjiang People's Hospital, Yangjiang, Guangdong 529500, P.R. China.

College of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.

出版信息

Oncol Lett. 2024 Apr 30;27(6):288. doi: 10.3892/ol.2024.14421. eCollection 2024 Jun.

Abstract

At present, due to its wide application and relatively low cost, chemotherapy remains a clinically important cancer treatment option; however, a number of chemotherapeutic drugs have important limitations, such as lack of specificity, high toxicity and side effects, and multi-drug resistance. The emergence of nanocarriers has removed numerous clinical application limitations of certain antitumor chemotherapy drugs and has been widely used in the treatment of tumors with nanodrugs. The present study used carbon nanoparticles (CNPs) as a nanocarrier for doxorubicin (DOX) to form the novel nanomedicine delivery system (CNPs@DOX)was demonstrated by UV-vis and fluorescence spectrophotometry, ζ potential and TEM characterization experiments. The results confirmed the successful preparation of CNPs@DOX nanoparticles with a particle size of 96±17 nm, a wide range of absorption and a negatively charged surface. Furthermore, CNPs@DOX produced more reactive oxygen species and induced apoptosis, and thus exhibited higher cytotoxicity than DOX, which is a small molecule anticancer drug without a nanocarrier delivery system.. The present study provides a strategy for the treatment of tumors with nanomedicine.

摘要

目前,由于其广泛应用和相对较低的成本,化疗仍然是临床上重要的癌症治疗选择;然而,一些化疗药物存在重要局限性,如缺乏特异性、高毒性和副作用以及多药耐药性。纳米载体的出现消除了某些抗肿瘤化疗药物的众多临床应用限制,并已广泛用于纳米药物治疗肿瘤。本研究使用碳纳米颗粒(CNPs)作为阿霉素(DOX)的纳米载体,通过紫外可见分光光度法、ζ电位和透射电镜表征实验证明形成了新型纳米药物递送系统(CNPs@DOX)。结果证实成功制备了粒径为96±17nm、吸收范围广且表面带负电荷的CNPs@DOX纳米颗粒。此外,CNPs@DOX产生更多活性氧并诱导凋亡,因此比DOX表现出更高的细胞毒性,DOX是一种没有纳米载体递送系统的小分子抗癌药物。本研究为纳米药物治疗肿瘤提供了一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eda4/11083999/0e2d9b13bc38/ol-27-06-14421-g00.jpg

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