Magnetic graphene oxide nanosheets with amidoamine dendronized crosslinks for dual pH and redox-sensitive doxorubicin delivery

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY BMC Chemistry Pub Date : 2024-09-28 DOI:10.1186/s13065-024-01301-4
Amir Reza Sarikhani, Mehdi Abedi, Samira Sadat Abolmaali, Sedigheh Borandeh, Ali Mohammad Tamaddon
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Abstract

Delivering anticancer drugs to the appropriate site within the body poses a critical challenge in cancer treatment with chemotherapeutic agents like doxorubicin (DOX). Magnetic graphene oxide (GO) nanosheets with generation 1 (G1) amidoamine-dendronized crosslinks were developed by coupling cystamine-functionalized GO nanosheets with Fe3O4 nanoparticles modified with primary amine and methyl acrylate. These magnetic GO nanosheets were loaded with DOX to create a dual pH- and redox-responsive delivery system for cancer chemotherapy. The prepared magnetic nanosheets underwent characterization using FTIR, XRD, DLS, VSM, FE-SEM, and TEM. Physical DOX adsorption was evaluated using various isotherms, including Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich. The in-vitro release profiles of DOX from the magnetic nanosheets were studied under different pH conditions, with and without glutathione (GSH), and the drug release data were fitted with various kinetic models. Additionally, an MTT assay was employed to assess the compatibility and antitumor activity of DOX-loaded magnetic nanosheets in the HepG2 cell line. The results showed that the maximum drug loading was 13.1% (w/w) at a drug/carrier ratio of 1. Without GSH addition, the maximum drug release after 10 days was only 17.9% and 24.1% at pH 7.4 and 5.3, respectively. However, in the presence of GSH, the maximum drug release reached 51.7% and 64.8% at pH 7.4 and 5.3, respectively. Finally, the research findings suggest that the magnetic nanosheets exhibited pH- and redox-stimuli drug release, high biocompatibility, and superior antitumor activity compared to free DOX.

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具有氨基胺树枝化交联的磁性氧化石墨烯纳米片可实现对 pH 值和氧化还原反应双重敏感的多柔比星递送
在使用多柔比星(DOX)等化疗药物治疗癌症的过程中,如何将抗癌药物输送到体内的适当部位是一项严峻的挑战。通过将胱胺化的氧化石墨烯(GO)纳米片与用伯胺和丙烯酸甲酯修饰的 Fe3O4 纳米颗粒耦合,开发出了具有第一代(G1)氨基胺化树胶交联的磁性氧化石墨烯(GO)纳米片。这些磁性 GO 纳米片装载了 DOX,形成了一种用于癌症化疗的 pH 和氧化还原双重响应给药系统。利用傅立叶变换红外光谱(FTIR)、XRD、DLS、VSM、FE-SEM 和 TEM 对制备的磁性纳米片进行了表征。利用各种等温线(包括 Langmuir、Freundlich、Temkin 和 Dubinin-Radushkevich)对 DOX 的物理吸附进行了评估。研究了在不同 pH 值条件下、有谷胱甘肽(GSH)和无谷胱甘肽(GSH)情况下,DOX 从磁性纳米片中的体外释放曲线,并用各种动力学模型拟合了药物释放数据。此外,还采用 MTT 法评估了载药磁性纳米片在 HepG2 细胞系中的相容性和抗肿瘤活性。结果表明,当药物/载体比为 1 时,最大载药量为 13.1%(w/w);在不添加 GSH 的情况下,pH 值为 7.4 和 5.3 时,10 天后的最大药物释放量分别为 17.9% 和 24.1%。然而,在添加 GSH 的情况下,药物在 pH 值为 7.4 和 5.3 时的最大释放量分别达到 51.7% 和 64.8%。最后,研究结果表明,与游离 DOX 相比,磁性纳米片具有 pH 和氧化还原刺激药物释放、高生物相容性和卓越的抗肿瘤活性。
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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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