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Preparation and printability of ultrashort self-assembling peptide nanoparticles
Author(s) -
Sarah Ghalayini,
Hepi Hari Susapto,
Sophie Hall,
Kowther Kahin,
Charlotte A. E. Hauser
Publication year - 2019
Publication title -
international journal of bioprinting
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.014
H-Index - 24
eISSN - 2424-7723
pISSN - 2424-8002
DOI - 10.18063/ijb.v5i2.239
Subject(s) - nanotechnology , nanoparticle , materials science , biocompatible material , peptide , self healing hydrogels , microfluidics , drug delivery , chemistry , biomedical engineering , polymer chemistry , biochemistry , medicine
Nanoparticles (NPs) have left their mark on the field of bioengineering. Fabricated from metallic, magnetic, and metal oxide materials, their applications include drug delivery, bioimaging, and cell labeling. However, as they enter the body, the question remains - where do they go after fulfilling their designated function? As most materials used to produce NPs are not naturally found in the body, they are not biodegradable and may accumulate overtime. There is a lack of comprehensive, long-term studies assessing the biodistribution of non-biodegradable NPs for even the most widely studied NPs. There is a clear need for NPs produced from natural materials capable of degradation . As peptides exist naturally within the human body, their non-toxic and biocompatible nature comes as no surprise. Ultrashort peptides are aliphatic peptides designed with three to seven amino acids capable of self-assembling into helical fibers within macromolecular structures. Using a microfluidics flow-focusing approach, we produced different peptide-based NPs that were then three-dimensional (3D) printed with our novel printer setup. Herein, we describe the preparation method of NPs from ultrashort self-assembling peptides and their morphology in both manual and 3D-printed hydrogels, thus suggesting that peptide NPs are capable of withstanding the stresses involved in the printing process.

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