A comprehensive review on using injectable chitosan microgels for osteochondral tissue repair.

J Biomater Sci Polym Ed

School of Mechanical Engineering, Iran University of Science and Technology, Tehran, Iran.

Published: October 2024

AI Article Synopsis

  • Restoring healthy cartilage is difficult due to low cell density and current treatment methods are not suitable for clinical use.
  • Engineering cell microaggregates in higher concentrations can promote new cartilage growth without the need for additional growth factors.
  • Chitosan is highlighted as an effective injectable hydrogel for cartilage repair, with its use in encapsulating stem cells and potential for 3D printing discussed.

Article Abstract

Restoring cartilage to healthy state is challenging due to low cell density and hence low regenerative capacity. The current platforms are not compatible with clinical translation and require dedicated handling of trained personnel. However, by engineering and implanting cell microaggregates in higher concentrations, efficient formation of new cartilage can be achieved, even in the absence of exogenous growth factors. Therefore, one-step surgeries are preferable for novel treatments and we need cell laden microgels allowing the formation of microaggregaets . Injectability is a key parameter for forming the shape and minimally invasive clinical applications. Hydrogels as bioinks can restore damaged tissues to their primary shape. Chitosan is a polysaccharide derived from chitin with abundant usage in tissue engineering. This review highlights the use of chitosan as an injectable hydrogel for osteochondral defects. Several studies focused on encapsulating mesenchymal stem cells within chitosan hydrogels have been categorized and incorporating microfluidic devices has been identified in the forefront to form microgels. Additionally, the printability is another convenience of chitosan for using in 3D printing for cartilage tissue engineering which is described in this review.

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Source
http://dx.doi.org/10.1080/09205063.2024.2419715DOI Listing

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