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Open AccessJournal ArticleDOI

Self‐assembly of peptide amphiphiles: From molecules to nanostructures to biomaterials

Honggang Cui, +2 more
- 01 Jan 2010 - 
- Vol. 94, Iss: 1, pp 1-18
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TLDR
The strategies for using molecular self‐assembly as a toolbox to produce peptide amphiphile nanostructures and materials are highlighted and efforts to translate this technology into applications as therapeutics are reviewed.
Abstract
Peptide amphiphiles are a class of molecules that combine the structural features of amphiphilic surfactants with the functions of bioactive peptides and are known to assemble into a variety of nanostructures. A specific type of peptide amphiphiles are known to self-assemble into one-dimensional nanostructures under physiological conditions, predominantly nanofibers with a cylindrical geometry. The resultant nanostructures could be highly bioactive and are of great interest in many biomedical applications, including tissue engineering, regenerative medicine, and drug delivery. In this context, we highlight our strategies for using molecular self-assembly as a toolbox to produce peptide amphiphile nanostructures and materials and efforts to translate this technology into applications as therapeutics. We also review our recent progress in using these materials for treating spinal cord injury, inducing angiogenesis, and for hard tissue regeneration and replacement.

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Journal ArticleDOI

Peptide Self-Assembly for Crafting Functional Biological Materials

TL;DR: The application of peptide-based materials in the regeneration of bone and enamel, cartilage, and the central nervous system, as well as the transplantation of islets, wound-healing, cardiovascular therapies, and treatment of erectile dysfunction after prostatectomy are discussed.
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Recent advances in amino acid N-carboxyanhydrides and synthetic polypeptides: chemistry, self-assembly and biological applications

TL;DR: Recent advances in amino acid N-carboxyanhydrides (NCAs) and synthetic polypeptides from the aspects of chemistry, self-assembly and biological applications are highlighted.
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Recent advances in self-assembled peptides: Implications for targeted drug delivery and vaccine engineering.

TL;DR: Self‐assembled peptide nanostructures have advantages in biocompatibility, stability against enzymatic degradation, encapsulation of hydrophobic drugs, sustained drug release, shear‐thinning viscoelastic properties, and/or adjuvanting properties.
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Polymeric nanostructured materials for biomedical applications

TL;DR: A comprehensive overview on the various types of polymeric nanostructured materials, their fabrication methods and biomedical applications, as well as the challenges in research and development of future PNMs are presented.
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Self-assembling prodrugs

TL;DR: This review will discuss the various types of self-assembling prodrugs in development, providing an overview of the methods used to control their structure and function and, ultimately, their perspective on their current and future potential.
References
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Journal ArticleDOI

Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule

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PatentDOI

Self-assembly and mineralization of peptide-amphiphile nanofibers

TL;DR: In this paper, pH-induced self-assembly of a peptide-amphiphile was used to make a nanostructured fibrous scaffold reminiscent of extracellular matrix.
Journal ArticleDOI

Regeneration beyond the glial scar

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Journal ArticleDOI

Selective Differentiation of Neural Progenitor Cells by High-Epitope Density Nanofibers

TL;DR: The artificial nanofiber scaffold induced very rapid differentiation of cells into neurons, while discouraging the development of astrocytes, linked to the amplification of bioactive epitope presentation to cells by the nanofibers.
Journal ArticleDOI

Peptide-amphiphile nanofibers: A versatile scaffold for the preparation of self-assembling materials

TL;DR: The scope of amino acid selection and alkyl tail modification in the peptide-amphiphile molecules are investigated, yielding nanofibers varying in morphology, surface chemistry, and potential bioactivity, demonstrating the chemically versatile nature of this supramolecular system.
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