Gayathri K, Vidya R
Centre for Materials Informatics(C-mAIn), Sir. C.V. Raman Science Block, Anna University Sardar Patel Road, Guindy Chennai 600 025 India
Department of Physics, Anna University Sardar Patel Road, Guindy Chennai 600 025 India.
Nanoscale Adv. 2024 Apr 26;6(16):3992-4014. doi: 10.1039/d4na00278d. eCollection 2024 Aug 6.
The incidence of cancer is increasing worldwide in a life-threatening manner. In such a scenario, the development of anti-cancer drugs with minimal side effects and effective drug delivery systems is of paramount importance. Doxorubicin (DOX) is one of the powerful anti-cancer drugs from the chemical family anthracycline, which is used to treat a wide variety of cancers, including breast, prostate, ovarian, and hematological malignancies. However, DOX has been associated with many side effects, including lethal cardiotoxicity, baldness, gastrointestinal disturbances and cognitive function impairment. Even though DOX is administered in liposomal formulations to reduce its toxicity and enhance its therapeutic profile, the liposomal formulations themselves have certain therapeutic profile limitations such as "palmar-plantar erythrodysesthesia (PPE)", which shows severe swelling and redness in the skin, thus restricting the dosage and reducing patient compliance. In contemporary chemotherapy research, there is a great interest in the utilization of nanomaterials for precise and targeted drug delivery applications, especially using carbon-based nanomaterials. This review provides a comprehensive overview of both experimental and theoretical scientific works, exploring diverse forms of carbon-based materials such as graphene, graphene oxide, and carbon nanotubes that function as carriers for DOX. In addition, the review consolidates information on the fate of the carriers after the delivery of the payload at the site of action through different imaging techniques and the various pathways through which the body eliminates these nanomaterials. In conclusion, the review presents a detailed overview of the toxicities associated with these carriers within the human body, contributing to the development of enhanced drug delivery systems.
全球癌症发病率正以危及生命的方式上升。在这种情况下,开发副作用最小的抗癌药物以及有效的药物递送系统至关重要。阿霉素(DOX)是蒽环类化学家族中一种强大的抗癌药物,用于治疗多种癌症,包括乳腺癌、前列腺癌、卵巢癌和血液系统恶性肿瘤。然而,DOX与许多副作用相关,包括致命的心脏毒性、脱发、胃肠道紊乱和认知功能损害。尽管DOX以脂质体制剂给药以降低其毒性并增强其治疗效果,但脂质体制剂本身存在某些治疗局限性,如“手足红斑感觉异常(PPE)”,表现为皮肤严重肿胀和发红,从而限制了剂量并降低了患者的依从性。在当代化疗研究中,人们对利用纳米材料进行精确和靶向药物递送应用,特别是使用碳基纳米材料,有着浓厚的兴趣。本综述全面概述了实验和理论科学研究,探讨了多种形式的碳基材料,如石墨烯、氧化石墨烯和碳纳米管,它们可作为DOX的载体。此外,该综述整合了有关载体在作用部位递送有效载荷后通过不同成像技术的命运以及人体消除这些纳米材料的各种途径的信息。总之,该综述详细概述了这些载体在人体内的毒性,有助于开发更先进的药物递送系统。