Journal
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 517, Issue 1-2, Pages 58-66Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijpharm.2016.12.006
Keywords
Nanoparticles; Platform; CD44; pH-sensitive; Targeted cancer therapy
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Funding
- UConn research grant from the University of Connecticut Health Center/Storrs and Regional Campus Incentive Grants (UCIG) Competitive Program
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Nanoparticles as drug delivery carriers have been investigated over the last few decades, particularly for cancer treatment. The rationale in developing such nanoparticles is to maximize drug efficacy while minimizing toxic side effects. This can be most effectively achieved through target specific drug delivery. A novel biocompatible nanoparticle platform prepared using the core-shell self-assembly technique is reported. The core consists of calcium phosphate which is biocompatible and pH-sensitive, and the shell is composed of biocompatible polymers (hyaluronic acid, CD44 targeting moiety; and chitosan, physical cross-linker). Cisplatin was selected as a model drug and incorporated between the core and the shell. The nanoparticle composition was optimized for high serum stability and low protein binding. These nanoparticles demonstrated target specific delivery in human lung cancer cells (which overexpress CD44 receptors). The targeting ability of the nanoparticles was confirmed with an 8-fold increase of drug efficacy (IC50) compared to cisplatin. Furthermore, the pH-sensitive core of the nanoparticle platform led to controlled drug release through destabilization in acidic conditions. This platform technology provides a simple approach for the design of targeted biocompatible nanoparticles for cancer therapy. (C) 2016 Elsevier B.V. All rights reserved.
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