4.7 Article

Micelle System Based on Molecular Economy Principle for Overcoming Multidrug Resistance and Inhibiting Metastasis

Journal

MOLECULAR PHARMACEUTICS
Volume 15, Issue 3, Pages 1005-1016

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.7b00922

Keywords

D-alpha-tocopheryl polyethylene glycol 1000 succinate; multidrug resistance; metastasis; drug delivery; breast cancer

Funding

  1. National Natural Science Foundation of China [81373360, 81673374]
  2. Fundamental Research Funds for the Central Universities [2015ZDTD048]
  3. Applied Fundamental Research Program of Wuhan [2017060201010146]
  4. Opening Project of Key Laboratory of Drug Targeting and Drug Delivery System, Ministry of Education (Sichuan University)

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The high mortality of cancer is mainly attributed to multidrug resistance (MDR) and metastasis. A simple micelle system was constructed here to codeliver doxorubicin (DOX), adjudin (ADD), and nitric oxide (NO) for overcoming MDR and inhibiting metastasis. It was devised based on the molecular economy principle as the micelle system was easy to fabricate and exhibited high drug loading efficiency, and importantly, each component of the micelles would exert one or more active functions. DOX acted as the main cell killing agent supplemented with ADD, NO, and D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS). MDR was overcome by synergistic effects of mitochondria inhibition agents, TPGS and ADD. A TPGS-based NO donor can be used as a drug carrier, and it can release NO to enhance drug accumulation and penetration in tumor, resulting in a positive cycle of drug delivery. This DOX-ADD conjugate self-assembly system demonstrated controlled drug release, increased cellular uptake and cytotoxicity, enhanced accumulation at tumor site, and improved in vivo metastasis inhibition of breast cancer. The micelles can fully take advantage of the functions of each component, and they provide a potential strategy for nanomedicine design and clinical cancer treatment.

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