生物加工
原位
纤维素
多重耐药
化学
微生物学
医学
生物医学工程
生物
生物化学
抗生素
有机化学
组织工程
作者
Filipe V. Ferreira,Nazanin Zanjanizadeh Ezazi,Caio G. Otoni,Ana Carolina de Aguiar,Jhonatan R. O. Bianchi,João Henrique Lopes,Danilo Martins dos Santos,Luiz G. Greca,Hernane da Silva Barud,Hélder A. Santos,Orlando J. Rojas,Luiz H. C. Mattoso
出处
期刊:ACS applied polymer materials
[American Chemical Society]
日期:2024-04-01
标识
DOI:10.1021/acsapm.3c02851
摘要
The colon is a main absorption site (nutrients and drugs) and a target for oral therapeutic delivery. However, the latter is challenged by the fact that most drugs degrade during transit in the gastrointestinal tract (GIT). Herein, we rationally designed a universal controlled-release system based on cubosomes contained in microbial nanocellulose capsules that enabled oral administration and pH-triggered delivery of bioactives. We show that the bicontinuous cubosome structure allows the simultaneous incorporation of drugs with differing polarity or surface energy. Furthermore, the multidrug cubosomes combined with the cellulose carrier by in situ biofabrication was demonstrated as a route toward multicomponent 3D capsules with added protection in the GIT. The obtained capsules were subsequently coated with sodium alginate to enable responsiveness, achieving dual cargo-controlled release and site-specific administration. In sum, we successfully engineered pH-responsive, nontoxic microcapsules as a versatile platform for colon-targeted multidrug delivery.
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