Enhancing Anticancer Effects: Targeted Doxorubicin Delivery Using UiO-66-NH2-FA Metal-Organic Framework Combined with Autophagy Inhibition by Hydroxychloroquine in Colorectal Cancer Cells

IF 4.5 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Adeleh Saffar, Tahereh Rohani Bastami, Amir Ebrahimi, Sonia Iranpour, Mohammad Hasan Mollaei, Ahmad Reza Bahrami, Maryam M. Matin
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引用次数: 0

Abstract

The use of targeted drug delivery systems to accumulate medications in cancer cells, along with the simultaneous application of multiple drugs, can facilitate the administration of optimal doses, leading to more efficient treatment as well as reduced side effects. We fabricated zirconium-based UiO-66-NH2 metal-organic framework (MOF) nanoparticles (NPs) with folic acid (FA) conjugated onto their surface for targeted delivery of doxorubicin (DOX), and smart drug release within tumor cells. Following the physicochemical characterization of the prepared NPs, the drug release profile was investigated in simulated media with pH 5.4 and 7.4. Subsequently, the internalization and anticancer effects of the NPs were evaluated in HT-29 and HEK-293 cells to assess their selectivity. Simultaneous treatment of HT-29 cells with FA-decorated NPs and hydroxychloroquine (HCQ), an autophagy inhibitor, was performed to sensitize cancer cells. The synergistic effects of combined treatment were assessed through MTT assay and autophagy flux detection. UiO-66-NH2-FA@DOX NPs with a surface area of 323 m²/g and a high loading capacity of 36.25% showed a pH-dependent release with a substantial increase in acidic condition. Higher uptake of targeted NPs in HT-29 cells led to higher cytotoxicity and apoptosis. The combination of HCQ and targeted NPs increased cytotoxic effects against HT-29 cells compared to treatment with targeted NPs alone. Acridine orange staining revealed different patterns of autophagy flux in the co-administered drug groups. This study suggests that our DOX-loaded targeted nanocarrier enhances the therapeutic efficacy through localized drug delivery and reduced potential side effects compared to conventional DOX treatment. Its combination with HCQ may offer a promising strategy for safer and more effective colorectal cancer therapy by enabling dose reduction of both agents. However, further in vivo studies are necessary to validate these findings.

Graphical Abstract

增强抗癌作用:UiO-66-NH2-FA金属有机框架联合羟基氯喹抑制结直肠癌细胞自噬靶向给药阿霉素
使用靶向药物输送系统在癌细胞中积累药物,同时使用多种药物,可以促进最佳剂量的施用,从而更有效地治疗并减少副作用。我们制备了基于锆的UiO-66-NH2金属有机框架(MOF)纳米颗粒(NPs),其表面偶联叶酸(FA),用于靶向递送阿霉素(DOX),并在肿瘤细胞内智能释放药物。对制备的NPs进行理化表征后,在pH为5.4和7.4的模拟介质中研究其药物释放谱。随后,在HT-29和HEK-293细胞中评估NPs的内化和抗癌作用,以评估其选择性。用fa修饰的NPs和自噬抑制剂羟氯喹(HCQ)同时处理HT-29细胞,以使癌细胞增敏。通过MTT试验和自噬通量检测评估联合治疗的协同效应。UiO-66-NH2-FA@DOX NPs的表面积为323 m²/g,负载能力为36.25%,呈现出ph依赖性释放,酸性条件下释放量显著增加。靶向NPs在HT-29细胞中的高摄取导致更高的细胞毒性和凋亡。与单独靶向NPs治疗相比,HCQ和靶向NPs联合治疗增加了对HT-29细胞的细胞毒性作用。吖啶橙染色显示共给药组的自噬通量模式不同。本研究表明,与传统的DOX治疗相比,我们的DOX负载靶向纳米载体通过局部给药提高了治疗效果,减少了潜在的副作用。它与HCQ的联合可能通过减少两种药物的剂量,为更安全、更有效的结直肠癌治疗提供了一种有希望的策略。然而,需要进一步的体内研究来验证这些发现。
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来源期刊
Journal of Materials Science: Materials in Medicine
Journal of Materials Science: Materials in Medicine 工程技术-材料科学:生物材料
CiteScore
8.00
自引率
0.00%
发文量
73
审稿时长
3.5 months
期刊介绍: The Journal of Materials Science: Materials in Medicine publishes refereed papers providing significant progress in the application of biomaterials and tissue engineering constructs as medical or dental implants, prostheses and devices. Coverage spans a wide range of topics from basic science to clinical applications, around the theme of materials in medicine and dentistry. The central element is the development of synthetic and natural materials used in orthopaedic, maxillofacial, cardiovascular, neurological, ophthalmic and dental applications. Special biomedical topics include biomaterial synthesis and characterisation, biocompatibility studies, nanomedicine, tissue engineering constructs and cell substrates, regenerative medicine, computer modelling and other advanced experimental methodologies.
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