Structure-based design of charge-conversional drug self-delivery systems for better targeted cancer therapy
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31901505
DOI
10.1016/j.biomaterials.2019.119701
PII: S0142-9612(19)30819-1
Knihovny.cz E-zdroje
- Klíčová slova
- Charge conversion, Curcumin, Diarrhea, Irinotecan, Self-delivery, Targeting therapy,
- MeSH
- kamptothecin MeSH
- léčivé přípravky * MeSH
- lékové transportní systémy * MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- nádory * farmakoterapie MeSH
- nanočástice * MeSH
- protinádorové látky * terapeutické užití MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- kamptothecin MeSH
- léčivé přípravky * MeSH
- protinádorové látky * 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
Citace poskytuje Crossref.org
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