Recent innovative approaches for drug delivery systems targeting cancer and CNS disorders

Abstract

Advancements in drug delivery systems (DDSs) have revolutionized pharmaceutical development by enhancing therapeutic precision, minimizing off-target effects, and improving patient compliance. Modern DDS technologies, such as lipid nanoparticles (LNPs), liquid-liquid phase separated (LLPS) systems, inorganic nanoparticles, GalNac systems, small molecules, dendrimers, polymers, peptides, and silk fibroin (SF) hydrogels, have significantly expanded the range of anticancer therapeutics. These advancements extend beyond conventional chemotherapeutics to include biologics such as nucleic acids (NAs), peptides, proteins, and monoclonal antibodies. These innovations have transformed oncology treatment paradigms and are gradually being adapted for central nervous system (CNS) disorders, where effective drug delivery is hindered by the protective blood-brain barrier (BBB) and the intricate architecture of neural networks. In this context, stimuli-responsive DDSs have emerged as promising tools, capable of crossing the BBB and releasing drugs in response to pathological cues. Theranostic DDS, which integrate diagnostic and therapeutic functionalities into a single platform, hold particular promise in imaging-guided interventions. This review provides a comprehensive overview of DDS applications in both oncology and neurodegenerative diseases (NDDs), emphasizing mechanistic insights, delivery strategies, and material innovations. Furthermore, it explores key translational considerations-including safety, efficacy, and clinical scalabilityessential for advancing next-generation DDS platforms from bench to bedside, thereby maximizing therapeutic outcomes in complex diseases.

Article information

Article type
Review Article
Submitted
19 Feb 2026
Accepted
27 Apr 2026
First published
28 Apr 2026

J. Mater. Chem. B, 2026, Accepted Manuscript

Recent innovative approaches for drug delivery systems targeting cancer and CNS disorders

M. K. Anand, E. Premalatha, H. Moorthy and T. Govindaraju, J. Mater. Chem. B, 2026, Accepted Manuscript , DOI: 10.1039/D6TB00411C

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