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Bioactive Potential of Natural Biomaterials: Identification, Retention and Assessment of Biological Properties

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Date 2021 Mar 19
PMID 33737507
Citations 63
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Abstract

Biomaterials have had an increasingly important role in recent decades, in biomedical device design and the development of tissue engineering solutions for cell delivery, drug delivery, device integration, tissue replacement, and more. There is an increasing trend in tissue engineering to use natural substrates, such as macromolecules native to plants and animals to improve the biocompatibility and biodegradability of delivered materials. At the same time, these materials have favourable mechanical properties and often considered to be biologically inert. More importantly, these macromolecules possess innate functions and properties due to their unique chemical composition and structure, which increase their bioactivity and therapeutic potential in a wide range of applications. While much focus has been on integrating these materials into these devices via a spectrum of cross-linking mechanisms, little attention is drawn to residual bioactivity that is often hampered during isolation, purification, and production processes. Herein, we discuss methods of initial material characterisation to determine innate bioactivity, means of material processing including cross-linking, decellularisation, and purification techniques and finally, a biological assessment of retained bioactivity of a final product. This review aims to address considerations for biomaterials design from natural polymers, through the optimisation and preservation of bioactive components that maximise the inherent bioactive potency of the substrate to promote tissue regeneration.

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References
1.
White L, Taylor A, Faulk D, Keane T, Saldin L, Reing J . The impact of detergents on the tissue decellularization process: A ToF-SIMS study. Acta Biomater. 2016; 50:207-219. PMC: 5592694. DOI: 10.1016/j.actbio.2016.12.033. View

2.
Han W, Singh N, Kim J, Kim H, Kim B, Park J . Directed differential behaviors of multipotent adult stem cells from decellularized tissue/organ extracellular matrix bioinks. Biomaterials. 2019; 224:119496. DOI: 10.1016/j.biomaterials.2019.119496. View

3.
Yang B, Yang B, Savani R, Turley E . Identification of a common hyaluronan binding motif in the hyaluronan binding proteins RHAMM, CD44 and link protein. EMBO J. 1994; 13(2):286-96. PMC: 394807. DOI: 10.1002/j.1460-2075.1994.tb06261.x. View

4.
Tan H, Chu C, Payne K, Marra K . Injectable in situ forming biodegradable chitosan-hyaluronic acid based hydrogels for cartilage tissue engineering. Biomaterials. 2009; 30(13):2499-506. PMC: 2676686. DOI: 10.1016/j.biomaterials.2008.12.080. View

5.
Coxon C, Sadler A, Huo J, Duncan Campbell R . An investigation of hierachical protein recruitment to the inhibitory platelet receptor, G6B-b. PLoS One. 2012; 7(11):e49543. PMC: 3501490. DOI: 10.1371/journal.pone.0049543. View