Chitosan-based drug delivery systems: From synthesis strategy to osteomyelitis treatment – A review
•Chitosan is a polycation polysaccharide with excellent biological properties.•Chitosan can be a carrier for osteomyelitis-targeting drug delivery.•Chitosan modifying can prevent implant-related infection and promote osseointegration.•Chitosan derivatives can improve the therapeutic effects of osteo...
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Veröffentlicht in: | Carbohydrate polymers 2021-01, Vol.251, p.117063-117063, Article 117063 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •Chitosan is a polycation polysaccharide with excellent biological properties.•Chitosan can be a carrier for osteomyelitis-targeting drug delivery.•Chitosan modifying can prevent implant-related infection and promote osseointegration.•Chitosan derivatives can improve the therapeutic effects of osteomyelitis.
Osteomyelitis is a complex disease in orthopedics mainly caused by bacterial pathogens invading bone or bone marrow. The treatment of osteomyelitis is highly difficult and it is a major challenge in orthopedic surgery. The long-term systemic use of antibiotics may lead to antibiotic resistance and has limited effects on eradicating local biofilms. Localized antibiotic delivery after surgical debridement can overcome the problem of antibiotic resistance and reduce systemic toxicity. Chitosan, a special cationic polysaccharide, is a product extracted from the deacetylation of chitin. It has numerous advantages, such as nontoxicity, biocompatibility, and biodegradability. Recently, chitosan has attracted significant attention in bacterial inhibition and drug delivery. Because chitosan contains many functional bioactive groups conducive to chemical reaction and modification, some chitosan-based biomaterials have been applied as the local antibiotic delivery systems in the treatment of osteomyelitis. This review aims to introduce recent advances in the biomedical applications of chitosan-based drug delivery systems in osteomyelitis treatment and to highlight the perspectives for further studies. |
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ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2020.117063 |