Structure-based design of charge-conversional drug self-delivery systems for better targeted cancer therapy
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
31901505
DOI
10.1016/j.biomaterials.2019.119701
PII: S0142-9612(19)30819-1
Knihovny.cz E-resources
- Keywords
- Charge conversion, Curcumin, Diarrhea, Irinotecan, Self-delivery, Targeting therapy,
- MeSH
- Camptothecin MeSH
- Pharmaceutical Preparations * MeSH
- Drug Delivery Systems * MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Neoplasms * drug therapy MeSH
- Nanoparticles * MeSH
- Antineoplastic Agents * therapeutic use MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Camptothecin MeSH
- Pharmaceutical Preparations * MeSH
- Antineoplastic Agents * MeSH
Various design and fabrication strategies of carrier-based drug delivery systems have been quickly established and applied for cancer therapy in recent years. These systems contribute greatly to current cancer treatments but further development needs to be made to eliminate obstacles such as low drug loading capacity and severe side effects. To achieve better drug delivery, we propose an innovative strategy for the construction of easy manufactured drug self-delivery systems based on molecular structures, which can be used for the co-delivery of curcuminoids and all the nitrogen-containing derivatives of camptothecin for better targeted cancer therapy with minimized side effects. The formation mechanism investigation demonstrates that the rigid planar structures of camptothecin derivatives and curcuminoids with relevant leaving hydrogens make it possible for them to be assembled into nanoparticles under suitable conditions. These nanoparticles show stabilized particle sizes (100 nm) under various conditions and tunable surface charges which increase from around -10 mV in a normal physiological condition (pH 7.4) to +40 mV under acidic tumor environments. In addition, in vivo mice experiments have demonstrated that, compared to irinotecan (a derivative of camptothecin) itself, the co-delivered irinotecan curcumin nanoparticles exhibited significantly enhanced lung and gallbladder targeting, improved macrophage-clearance escape and ameliorated colorectal cancer treatment with an eradication of life-threatening diarrhea, bringing hope for better targeted chemotherapy and clinical translation. Lastly, the strategy of structure based design of drug self-delivery systems may inspire more research and discoveries of similar self-delivered nano systems for wider pharmaceutical applications.
Centre of Polymer Systems Tomas Bata University in Zlin Zlin 76001 Czech Republic
Quantitative and Systems Biology Program University of California Merced CA 95343 USA
School of Pharmacy Chengdu University of Traditional Chinese Medicine Chengdu 611137 China
References provided by Crossref.org
Self-Monitoring and Self-Delivery of Self-Assembled Fluorescent Nanoparticles in Cancer Therapy