Essential oil-loaded chitosan/zinc (II) montmorillonite synergistic sustained-release system as antibacterial material. Issue 2 (1st February 2023)

• Record Type: Journal Article
• Authors: Zhan, Jinghui; Chen, Huayao; Zhou, Hongjun; Hao, Li; Xu, Hua; Zhou, Xinhua
• Is Part Of: Journal of dispersion science and technology. Volume 44:Issue 2(2023)
• Page Start: 288
• Page End: 298
• Publication Date: 2023-02-01
• Subjects: Chitosan -- montmorillonite -- zinc -- tea tree oil -- antibacterial; Emulsions -- Periodicals; Suspensions (Chemistry) -- Periodicals; Emulsions; Suspensions; 541.34
• DOI: 10.1080/01932691.2021.1947848
• Languages: English
• ISSNs: 0193-2691

Abstract

Abstract: Tea tree oil (TTO) is a broad-spectrum natural antimicrobial agent. Its application is limited due to its volatile property. To reduce its volatility and improve its sustained-release performance, a synergistic sustained-release system was prepared. Montmorillonite (Mt) was ion-exchanged with sodium ions (Na + ) and zinc ions (Zn 2+ ), then organically modified with cetyl trimethyl ammonium bromide (CTAB) and chitosan (CS) to improve its sustained release performance. The results indicated that Mt was exfoliated, but still maintained its ordered layer structure. The surface of CS-Zn-OMt was rough, because some pores and surfaces were filled. The addition of Zn 2+ increased the loading of CS (37.8 − 40.8%) and induced more uniform distribution of CS on Mt. Also, CS-Zn-OMt achieved a high loading capacity for TTO and the loading value was 222.0 mg*g −1 . Furthermore, the release studies showed that CS-Zn-OMt exhibited sustained-release behavior due to the release from the outer layer of CS and the Mt channel simultaneously. The results of antibacterial test showed that the addition of CS inhibited the drift of Mt and showed good antibacterial performance because of strong effective drug-carrier interaction. The developed system can be potentially applied for the delivery of volatile essential oils for antibacterial infection. Graphical Abstract: UF0001