Drug Repurposing and Nanotechnology for Topical Skin Cancer Treatment: Redirecting toward Targeted and Synergistic Antitumor Effects.

IF 4.9 Q1 CHEMISTRY, MEDICINAL
ACS Pharmacology and Translational Science Pub Date : 2025-01-23 eCollection Date: 2025-02-14 DOI:10.1021/acsptsci.4c00679
Maria Martins, Francisco Veiga, Ana Cláudia Paiva-Santos, Patrícia C Pires
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引用次数: 0

Abstract

Skin cancer represents a major health concern due to its rising incidence and limited treatment options. Current treatments (surgery, chemotherapy, radiotherapy, immunotherapy, and targeted therapy) often entail high costs, patient inconvenience, significant adverse effects, and limited therapeutic efficacy. The search for novel treatment options is also marked by the high capital investment and extensive development involved in the drug discovery process. In response to these challenges, repurposing existing drugs for topical application and optimizing their delivery through nanotechnology could be the answer. This innovative strategy aims to combine the advantages of the known pharmacological background of commonly used drugs to expedite therapeutic development, with nanosystem-based formulations, which among other advantages allow for improved skin permeation and retention and overall higher therapeutic efficacy and safety. The present review provides a critical analysis of repurposed drugs such as doxycycline, itraconazole, niclosamide, simvastatin, leflunomide, metformin, and celecoxib, formulated into different nanosystems, namely, nanoemulsions and nanoemulgels, nanodispersions, solid lipid nanoparticles, nanostructured lipid carriers, polymeric nanoparticles, hybrid lipid-polymer nanoparticles, hybrid electrospun nanofibrous scaffolds, liposomes and liposomal gels, ethosomes and ethosomal gels, and aspasomes, for improved outcomes in the battle against skin cancer. Enhanced antitumor effects on melanoma and nonmelanoma research models are highlighted, with some nanoparticles even showing intrinsic anticancer properties, leading to synergistic effects. The explored research findings highly evidence the potential of these approaches to complement the currently available therapeutic strategies in the hope that these treatments might one day reach the pharmaceutical market.

局部皮肤癌治疗的药物再利用和纳米技术:定向靶向和协同抗肿瘤作用。
皮肤癌由于发病率上升和治疗选择有限而成为一个主要的健康问题。目前的治疗方法(手术、化疗、放疗、免疫治疗和靶向治疗)往往费用高,给患者带来不便,不良反应显著,治疗效果有限。寻找新的治疗方案也标志着在药物发现过程中涉及的高资本投资和广泛发展。为了应对这些挑战,重新利用现有药物用于局部应用并通过纳米技术优化其递送可能是答案。这一创新策略旨在将常用药物的已知药理背景优势与纳米系统配方结合起来,以加快治疗开发,纳米系统配方的其他优势包括改善皮肤渗透和保留,以及总体上更高的治疗效果和安全性。本文综述了多西环素、伊曲康唑、硝氯沙胺、辛伐他汀、来氟米特、二甲双胍和塞来昔布等被配制成不同纳米体系的药物,即纳米乳液和纳米凝胶、纳米分散体、固体脂质纳米颗粒、纳米结构脂质载体、聚合物纳米颗粒、杂化脂质-聚合物纳米颗粒、杂化电纺纳米纤维支架、脂质体和脂质体凝胶、脂质体和脂质体凝胶以及aspassomes。为了改善对抗皮肤癌的效果。增强的抗肿瘤作用在黑色素瘤和非黑色素瘤研究模型中得到强调,一些纳米颗粒甚至显示出内在的抗癌特性,导致协同效应。所探索的研究结果高度证明了这些方法的潜力,可以补充目前可用的治疗策略,希望这些治疗方法有一天能进入制药市场。
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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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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