High loading and sustained-release system of doxorubicin-carbon dots as nanocarriers for cancer therapeutics.

Aswathy Prasad, Ram Prasad Sekar, Mariyam Razana C A, Smitha Devi Sudhamani, Anagha Das, Jayakrishnan Athipettah, Lightson Ngashangva
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Abstract

Nanocarriers for drugs have been investigated for decades, yet it is still challenging to achieve sustained release from nanomaterials due to drug loading inefficiency and burst release. In this study, we developed novel functional carbon dots (CDs) and investigated the therapeutic efficacy by studying the loading efficiency and release behavior of the anticancer drug doxorubicin (DOX). CDs were successfully synthesized using a one-step pyrolysis method with varying concentrations of citric acid (CA) and thiourea (TU). Functional groups, morphology, particle size, and zeta potential of synthesized CT-CDs and DOX loaded CT-CDs were investigated by UV-visible, Fluorescence, dynamic light scattering, Zeta Potential measurements, FTIR, and transmission electron microscopy. The zeta potential data revealed DOX loading onto CT-CDs by charge difference, i.e. -24.6 ± 0.44 mV (CT-CDs) and 20.57 ± 0.55 mV (DOX-CT-CDs). DOX was loaded on CDs with a loading efficiency of 88.67 ± 0.36%.In vitrodrug release studies confirmed pH-dependent biphasic drug release, with an initial burst effect and sustained release of DOX was found to be 21.42 ± 0.28% (pH 5), 13.30 ± 0.03% (pH 7.4), and 13.95 ± 0.18% (pH 9) even after 144 h at 37 °C. The CT-CDs were non-toxic and biocompatible with L929 Fibroblasts cells. The cytotoxic effect of DOX-CT-CDs showed a concentration-dependent effect after 48 h with Glioblastoma U251 cells. Flow cytometry was used to examine the cellular uptake of CT-CDs and DOX-CT-CDs in L929 and U251 cells. It was observed that the maximum CT-CDs uptake was around 75% at the end of 24 h. This study showed that the synthesized fluorescent CT-CDs demonstrated a high drug loading capacity, pH-dependent sustained release of DOX, and high cellular uptake by mammalian cells. We believe this work provides practical and biocompatible CDs for chemotherapeutic drug delivery that can be applied to other drugs for certain therapeutic aims.

作为癌症治疗纳米载体的多柔比星-碳点高负载和持续释放系统。
对药物纳米载体的研究已有数十年历史,但由于药物负载效率低和猝灭释放,实现纳米材料的持续释放仍具有挑战性。在这项研究中,我们开发了新型功能碳点(CDs),并通过研究抗癌药物多柔比星(DOX)的负载效率和释放行为考察了其治疗效果。采用不同浓度的柠檬酸(CA)和硫脲(TU)一步热分解法成功合成了CD。通过紫外可见光、荧光、DLS、Zeta 电位测量、傅立叶变换红外光谱和 TEM 对合成的 CT-CDs 和负载 DOX 的 CT-CDs 的官能团、形态、粒度和 Zeta 电位进行了研究。Zeta 电位数据显示,DOX 通过电荷差负载到 CT-CDs 上,即 -24.6 ± 0.44 mV(CT-CDs)和 20.57 ± 0.55 mV(DOX-CT-CDs)。DOX 在 CD 上的负载效率为 88.67±0.36%。体外药物释放研究证实,DOX 的释放与 pH 值呈双相依赖关系,具有初始猝灭效应,即使在 37 °C 下放置 144 小时后,DOX 的持续释放率分别为 21.42 ± 0.28 %(pH 值为 5)、13.30 ± 0.03 %(pH 值为 7.4)和 13.95 ± 0.18 %(pH 值为 9)。CT-CD 对 L929 成纤维细胞无毒且具有生物相容性。在与胶质母细胞瘤 U251 细胞作用 48 小时后,DOX-CT-CDs 的细胞毒性效应表现出浓度依赖性。流式细胞仪用于检测 L929 和 U251 细胞对 CT-CDs 和 DOX-CT-CDs 的细胞摄取。这项研究表明,合成的荧光 CT-CD 具有很高的药物负载能力、DOX 的 pH 依赖性持续释放以及哺乳动物细胞的高细胞摄取率。我们相信,这项工作为化疗药物的递送提供了实用且生物相容性好的 CD,可应用于其他药物以达到特定的治疗目的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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