期刊
AAPS JOURNAL
卷 17, 期 4, 页码 813-827出版社
SPRINGER
DOI: 10.1208/s12248-015-9772-2
关键词
aerobic glycolysis; hypoxia; inflammatory disease; macrophage repolarization; multidrug resistance; targeted biological therapies
资金
- National Cancer Institute's (NCI) Cancer Nanotechnology Platform Partnership (CNPP)
- Dana Farber Cancer Institute-Northeastern University
With the advent of novel and personalized therapeutic approaches for cancer and inflammatory diseases, there is a growing demand for designing delivery systems that circumvent some of the limitation with the current therapeutic strategies. Nanoparticle-based delivery of drugs has provided means of overcoming some of these limitations by ensuring the drug payload is directed to the disease site and insuring reduced off-target activity. This review highlights the challenges posed by the solid tumor microenvironment and the systemic limitations for effective chemotherapy. It then assesses the basis of nanoparticle-based targeting to the tumor tissues, which helps to overcome some of the microenvironmental and systemic limitations to therapy. We have extensively focused on some of the tumor multidrug resistance mechanisms (e.g., hypoxia and aerobic glycolysis) that contribute to the development of multidrug resistance and how targeted nano-approaches can be adopted to overcome drug resistance. Finally, we assess the combinatorial approach and how this platform has been used to develop multifunctional delivery systems for cancer therapy. The review article also focuses on inflammatory diseases, the biological therapies available for its treatment, and the concept of macrophage repolarization for the treatment of inflammatory diseases.
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