Bioinspired Adaptive Microdrugs Enhance the Chemotherapy of Malignant Glioma: Beyond Their Nanodrugs.
Xuejiao WangXiangrong HaoYangning ZhangQun WuJiajia ZhouZhongman ChengJianping ChenSijia LiuJiahao PanYing WangJun-Bing FanPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Solid nanoparticle-mediated drug delivery systems are usually confined to nanoscale due to the enhanced permeability and retention effect. However, they remain a great challenge for malignant glioma chemotherapy because of poor drug delivery efficiency and insufficient tumor penetration resulting from the blood-brain barrier/blood-brain tumor barrier (BBB/BBTB). Inspired by biological microparticles (e.g., cells) with excellent adaptive deformation, it is demonstrated that the adaptive microdrugs (even up to 3.0 µm in size) are more efficient than their nanodrugs (less than 200 nm in size) to cross BBB/BBTB and penetrate into tumor tissues, achieving highly efficient chemotherapy of malignant glioma. The distinct delivery of the adaptive microdrugs is mainly attributed to the enhanced interfacial binding and endocytosis via adaptive deformation. As expected, the obtained adaptive microdrugs exhibit enhanced accumulation, deep penetration, and cellular internalization into tumor tissues in comparison with nanodrugs, significantly improving the survival rate of glioblastoma mice. It is believed that the bioinspired adaptive microdrugs enable them to efficiently cross physiological barriers and deeply penetrate tumor tissues for drug delivery, providing an avenue for the treatment of solid tumors.
Keyphrases
- drug delivery
- highly efficient
- gene expression
- locally advanced
- type diabetes
- radiation therapy
- metabolic syndrome
- photodynamic therapy
- induced apoptosis
- cancer therapy
- endothelial cells
- oxidative stress
- skeletal muscle
- mass spectrometry
- signaling pathway
- cell proliferation
- binding protein
- endoplasmic reticulum stress