从实验室到临床:推进阿霉素脂质体靶向癌症治疗

Mohammad Zaki Ahmad , Gulam Mustafa , Basel A. Abdel-Wahab , Kalyani Pathak , Aparoop Das , Jon Jyoti Sahariah , Parimita Kalita , Afroze Alam , Partha Protim Borthakur
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引用次数: 0

摘要

脂质体已成为癌症治疗中靶向药物输送的变革性平台,解决了阿霉素(DOX)等传统化疗药物的主要局限性。虽然传统的蒽环类药物非常有效,但其严重的心脏毒性和全身副作用限制了其临床应用。脂质体包封通过将药物包封在脂质双层内增强了这种方法,实现了控制释放,改善了肿瘤靶向性,降低了脱靶毒性。值得注意的是,聚乙二醇化脂质体DOX制剂,如Doxil®,在保持强大的抗癌功效的同时,显著改善了药代动力学,延长了循环时间,降低了心脏毒性。本文系统地分析了DOX脂质体配方的发展,从早期的进展到下一代功能化配方。我们批判性地研究了最近的创新,包括抗体-,肽-,适体-和细胞穿透肽偶联脂质体,它们已经证明了增强的肿瘤特异性和克服多药耐药的潜力。此外,热敏性脂质体(TSLs),特别是溶热敏性变体,为高温引发的局部药物释放提供了一种很有前途的策略。同时,ph敏感和糖偶联脂质体利用肿瘤微环境的独特特征进行精确靶向。尽管取得了这些进展,但在优化配体密度、可扩展性和长期稳定性方面仍然存在重大挑战,这阻碍了临床转化。这篇综述总结了最近的进展,比较了新出现的策略,并强调了翻译的关键障碍。通过解决目前临床应用中的差距并提出潜在的解决方案,本工作为肿瘤学多功能脂质体制剂的未来提供了前瞻性的视角。最终,这篇综述旨在指导未来研究更安全、更有效和以患者为中心的癌症治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From bench to bedside: Advancing liposomal doxorubicin for targeted cancer therapy
Liposomes have emerged as a transformative platform for targeted drug delivery in cancer therapy, addressing key limitations of traditional chemotherapeutics like doxorubicin (DOX. Although conventional anthracyclines are highly effective, their severe cardiotoxicity and systemic side effects restrict their clinical use. Liposomal encapsulation enhances this approach by encapsulating drugs within lipid bilayers, enabling controlled release, improved tumor targeting, and reduced off-target toxicity. Notably, PEGylated liposomal DOX formulations, such as Doxil®, have significantly improved pharmacokinetics, extended circulation times, and decreased cardiotoxicity while maintaining strong anticancer efficacy. This review systematically analyzes the development of liposome-based formulations for DOX, from early advancements to next-generation functionalized formulations. We critically examine recent innovations, including antibody-, peptide-, aptamer-, and cell-penetrating peptide-conjugated liposomes, which have demonstrated enhanced tumor specificity and the potential to overcome multidrug resistance. Additionally, thermosensitive liposomes (TSLs), particularly lyso-thermosensitive variants, present a promising strategy for localized drug release triggered by hyperthermia. Concurrently, pH-sensitive and sugar-conjugated liposomes exploit the unique characteristics of the tumor microenvironment for precise targeting. Despite these advancements, significant challenges remain in optimizing ligand density, scalability, and long-term stability, which hinder clinical translation. This review consolidates recent progress, compares emerging strategies, and highlights critical barriers to translation. By addressing current gaps in clinical application and proposing potential solutions, this work offers a forward-looking perspective on the future of multifunctional liposomal formulations in oncology. Ultimately, this review aims to guide future research toward safer, more effective, and patient-centered cancer therapies.
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