脂质体
医学
纳米医学
药物输送
癌症
靶向给药
内吞作用
药品
药理学
毒品携带者
单克隆抗体
癌症研究
癌症治疗
毒性
抗癌药
输送系统
细胞内
化疗
癌症治疗
靶向治疗
癌细胞
作者
Aadi Zaragoza-Jiménez,Luis Fernando López-Lara,Evelyn Dennis Álvarez-Velázquez,Raúl Santiago Aceves-Enríquez,José Francisco Muñoz-Valle,Jorge Hernández‐Bello,Mauricio Salinas‐Santander,Alba Adriana Vallejo‐Cardona,Clara Patricia Ríos-Ibarra
标识
DOI:10.1080/14737140.2025.2604621
摘要
INTRODUCTION: Nanomedicine offers innovative and less invasive therapies by targeting key biological pathways through specific ligands, enhancing precision and minimizing adverse effects. Among nanocarriers, liposomes stand out for their dual aqueous-organic structure, which enables encapsulation of both hydrophilic and hydrophobic compounds, improving drug stability and bioavailability. AREAS COVERED: Cancer remains one of the leading causes of death worldwide, with about 9.6 million deaths annually, according to the World Health Organization (WHO). Despite advances in chemotherapy and radiotherapy, major challenges persist, including toxicity and multidrug resistance. Nanoparticles (NPs) have emerged as promising tools for cancer therapy, acting through direct tumor targeting, modulation of the tumor microenvironment, and activation of immune responses. This review summarizes recent preclinical and clinical findings on liposomal formulations used against breast, liver, pancreatic, and prostate cancers, focusing on their therapeutic potential and translational progress. EXPERT OPINION: Liposome performance depends on molecular surface modifications using carbohydrates, proteins, peptides, aptamers, or monoclonal antibodies. These functionalized liposomes enable ligand-receptor recognition, facilitating endocytosis and controlled intracellular drug release. Consequently, targeted liposomal systems achieve higher specificity and reduced systemic toxicity compared with passively delivered formulations.
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