Peptide-directed self-assembly of functionalized polymeric nanoparticles. Part II: Effects of nanoparticle composition on assembly behavior and multiple drug loading ability
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Peptide-functionalized polymeric nanoparticles were designed and self-assembled into continuous nanoparticle fibers and three-dimensional scaffolds via ionic complementary peptide interaction. Different nanoparticle compositions can be designed to be appropriate for each desired drug, so that the release of each drug is individually controlled and the simultaneous sustainable release of multiple drugs is achieved in a single scaffold. A self-assembled scaffold membrane was incubated with NIH3T3 fibroblast cells in a culture dish that demonstrated non-toxicity and non-inhibition on cell proliferation. This type of nanoparticle scaffold combines the advantages of peptide self-assembly and the versatility of polymeric nanoparticle controlled release systems for tissue engineering. A novel nanoparticle scaffolding system is demonstrated using controlled-release, drug-loaded nanoparticles that yield ordered fibers and scaffolds using ionic complementary peptide-directed self-assembly. The scaffolding system possesses the advantages of individually controlling the release of each loaded drug and the ability to control their assembly sequence.
Peptide-directed self-assembly of functionalized polymeric nanoparticles. Part II: Effects of nanoparticle composition on assembly behavior and multiple drug loading ability.
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