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用于控制阿霉素释放的压电六方氮化硼纳米载体的协同抗癌作用

Synergistic anti-cancer effects of piezoelectric hexagonal boron nitride nanocarriers for controlled doxorubicin release.

作者信息

Cicek Nilay, Cobandede Zehra, Adiguzel Sevin, Yilmaz Hulya, Culha Mustafa

机构信息

Sabanci University Nanotechnology Research and Application Center (SUNUM), Tuzla Istanbul, Turkey.

Chemistry and Biochemistry Department, College of Science and Mathematics, Augusta University, Augusta, GA, USA.

出版信息

Nanomedicine (Lond). 2025 Mar;20(5):455-466. doi: 10.1080/17435889.2025.2459055. Epub 2025 Jan 31.

Abstract

AIMS

This study aims to develop a piezoelectric drug delivery system based on hexagonal boron nitride nanosheets (hBNs).

MATERIALS AND METHODS

hBNs were synthesized using the chemical vapor deposition (CVD) method and characterized through imaging and spectroscopic techniques. Their piezoelectric properties were evaluated to confirm their functionality. Subsequently, the potential of hBNs as nanocarriers was assessed through in vitro experiments with doxorubicin (Dox) as a model drug.

RESULTS

The piezoelectric hBNs were successfully synthesized and exhibited efficient loading and controlled release of Dox. In vitro experiments conducted on PC3 (human prostate cancer) and PNT1A (normal adult prostate epithelial) cell lines demonstrated that ultrasound (US)-induced Dox-loaded hBNs (hBN-Dox) significantly inhibited the proliferation of prostate cancer cells, achieving efficacy at a much lower Dox concentration compared to conventional methods. The system enhanced reactive oxygen species (ROS) generation, impaired cancer cell colony formation, and induced both early and late apoptosis.

CONCLUSIONS

These findings highlight the potential of piezoelectric hBNs as nanocarriers for efficient drug delivery, leveraging the synergistic effect of piezoelectricity-induced drug release and the degradation products of hBNs in biological media. Their ability to enhance drug efficacy while reducing the required dose holds promise for advanced cancer therapies.

摘要

目的

本研究旨在开发一种基于六方氮化硼纳米片(hBNs)的压电药物递送系统。

材料与方法

采用化学气相沉积(CVD)法合成hBNs,并通过成像和光谱技术对其进行表征。评估其压电性能以确认其功能。随后,以阿霉素(Dox)为模型药物,通过体外实验评估hBNs作为纳米载体的潜力。

结果

成功合成了压电hBNs,并表现出对Dox的高效负载和控释。在PC3(人前列腺癌)和PNT1A(正常成人前列腺上皮)细胞系上进行的体外实验表明,超声(US)诱导的载Dox的hBNs(hBN-Dox)显著抑制前列腺癌细胞的增殖,与传统方法相比,在低得多的Dox浓度下即可达到疗效。该系统增强了活性氧(ROS)的产生,损害了癌细胞集落形成,并诱导了早期和晚期凋亡。

结论

这些发现突出了压电hBNs作为高效药物递送纳米载体的潜力,利用了压电诱导药物释放和hBNs在生物介质中的降解产物的协同效应。它们在提高药物疗效的同时降低所需剂量的能力为先进的癌症治疗带来了希望。

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