Biomaterials Synthesized via Sol–Gel Methods
A special issue of Materials (ISSN 1996-1944).
Deadline for manuscript submissions: closed (30 September 2021) | Viewed by 29098
Special Issue Editor
Interests: Geopolymers; sol–gel technology; biomaterials; bioglass; organic/inorganic hybrid materials; drug delivery; thin films
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Dear Colleagues,
The requirement of improving the life quality of people affected by diseases that need replacements of tissues or body parts has encouraged the development of new materials with high performance in terms of tolerability and integration capability. These promising so-called "Biomaterials" are able to interact with human tissue and body fluids to treat, improve, or replace anatomical elements of the human body, without adverse reactions in the host organism. They can be applied to permanent structures such as implants and artificial organs or devices that stay in contact with the human body for a limited time such as sutures or scaffolds. Despite advances in the biomaterials field, today a good combination between properties (mechanical, chemical, and tribological) and biocompatibility of the materials has not been yet achieved. This is the cause of the early failure of the implants, which entails the need for the subsequent replacement of the prosthetic devices, especially in young patients.
An ideal method to prepare biomaterials is the sol–gel technique. It is a versatile synthesis process used to produce ceramics and/or glasses materials at low temperatures.
The process starts when water is added to a solution of metal alkoxyde precursors in alcohol. The hydrolysis of metal alkoxide precursor and the polycondensation of the formed oligomers cause the transition of the system from a mostly colloidal liquid (sol) into a solid (gel). By drying the obtained wet gel, it is possible to prepare xerogels (by exposure to low temperatures) or aerogels (by solvent extraction under supercritical conditions) or dense ceramic and glass by means of a further heat treatment at higher temperatures. The sol–gel method has many advantages, such as the purity of products and the possibility of controlling the chemical composition, the microstructure and, thus, the properties of the obtained materials through the modulation of the parameters of the sol–gel process, such as the molar ratios of the reagents, pH, inhibitor/catalyst addition, and heat treatment. Moreover, sol–gel chemistry and the low processing temperature used allow for embedding in inorganic glassy materials of various thermolabile molecules (e.g., polymers, drugs, biomolecules, etc.) during the formation of the glassy matrix, via the dissolution of those molecules in a liquid sol–gel system, producing organic/inorganic hybrids.
Assoc. Prof. Michelina Catauro
Guest Editor
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Keywords
- biomaterials
- drug delivery
- sol-gel method
- hybrid materials
- bioactivity
- biocompatibility
- cell viability
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