Combining Photothermal Therapy with A NanohybridBased Drug Delivery Strategy for Slow-Released Doxorubicin: A Treatment for Hepatocellular Carcinoma

Muhammad Habiburrahman, A. B. Putra, Muhammad Ilham Dhiya Rakasiwi
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Abstract

Background: Hepatocellular carcinoma (HCC) is the fifth most common malignancy in the world. Surgical intervention remains the primary treatment option for resectable liver cancer. However, the low curative resection ratio, high metastatic ratio, and risk of recurrence make this treatment less than ideal. Additionally, the choice of liver transplantation is limited by the availability of donors. This literature review aimed to discuss the combination strategy of photothermal therapy and nanohybrid-based chemotherapy delivery, which are expected to address the challenges in HCC treatment. Methods: We conducted literature searches in Pubmed, Scopus, ProQuest, and Google Scholar using combined keywords such as “hepatocellular carcinoma”, “polyethylene glycol”, “doxorubicin”, “mesoporous silica”, “CuS”, “nanoparticle”, and “photothermal therapy”. Based on the assessment of validity and applicability aspects using modified Oxford CEBM (Center for Evidence-Based Management) and OHAT (Office of Health Assessment and Translation) checklist tools for preclinical studies, all the selected studies fulfilled the eligibility criteria. Results: Photothermal therapy promotes necrosis and apoptosis of HCC cells by ‘heating’ the cancer cells. Meanwhile, the chemotherapy agent doxorubicin, modified with mesoporous silica nanohybrids and encapsulated copper sulfate polyethylene glycol (PEG-DOX-MSN-CuS), enhances the efficiency and duration of drug circulation in the blood, reduces drug clearance, and minimizes retention by the reticuloendothelial system. By utilizing near-infrared light induction from photothermal therapy, doxorubicin can be slowly released, leading to significantly improved effectiveness. In vitro studies have demonstrated that this this combination strategy achieves over 90% HCC cell death at a chemotherapy concentration of 80 µg/mL, in conjunction with near-infrared light induction. The optimal release time for doxorubicin was recored at a concise 20 minutes. Conclusions: Given the numerous benefits associated with this combination of strategies, photothermal therapy using PEG-DOX-MSN-CuS holds significant expected to be a promising treatment for HCC.
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结合光热疗法和纳米复合缓释阿霉素的药物递送策略:一种治疗肝细胞癌的方法
背景:肝细胞癌(HCC)是世界上第五大常见恶性肿瘤。手术干预仍然是可切除肝癌的主要治疗选择。然而,低治愈率,高转移率和复发风险使这种治疗不太理想。此外,肝移植的选择也受到供体数量的限制。本文献综述旨在讨论光热疗法和纳米混合化疗的联合策略,这有望解决HCC治疗中的挑战。方法:结合关键词“肝细胞癌”、“聚乙二醇”、“阿霉素”、“介孔二氧化硅”、“CuS”、“纳米粒子”、“光热疗法”等,在Pubmed、Scopus、ProQuest和Google Scholar中进行文献检索。采用改良的牛津循证管理中心(CEBM)和健康评估与翻译办公室(OHAT)临床前研究清单工具对有效性和适用性进行评估,所有入选研究均符合入选标准。结果:光热疗法通过“加热”癌细胞促进肝癌细胞坏死和凋亡。同时,化疗药物阿霉素经介孔二氧化硅纳米杂化物和封装硫酸铜聚乙二醇(peg - dox - mnn - cu)修饰后,提高了药物在血液中的循环效率和时间,减少了药物的清除率,并最大限度地减少了网状内皮系统的滞留。利用光热疗法的近红外光诱导,阿霉素可以缓慢释放,从而显著提高疗效。体外研究表明,在80µg/mL的化疗浓度下,结合近红外光诱导,这种联合策略可实现90%以上的HCC细胞死亡。阿霉素的最佳释放时间为20分钟。结论:考虑到与这种策略组合相关的众多益处,使用peg - dox - msn - cu的光热疗法有望成为HCC的一种有前景的治疗方法。
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