Chitosan coated MOF/GO nanohybrid as a co-anticancer drug delivery vehicle: Synthesis, characterization, and drug delivery application

被引:66
作者
Asl, Elnaz Aghazadeh [1 ]
Pooresmaeil, Malihe [1 ]
Namazi, Hassan [1 ,2 ]
机构
[1] Univ Tabriz, Fac Chem, Res Lab Dendrimers & Nanobiopolymers, POB 51666, Tabriz, Iran
[2] Tabriz Univ Med Sci, Biomed Inst, Res Ctr Pharmaceut Nanotechnol, Tabriz, Iran
关键词
Chitosan; Graphene oxide; Aluminum-succinic acid metal-organic frame-works; Encapsulation; Dual drug delivery; Biocompatibility; METAL-ORGANIC FRAMEWORK; GRAPHENE OXIDE; ADSORPTION CAPACITY; HYALURONIC-ACID; DOXORUBICIN; NANOCOMPOSITE; RELEASE; SYSTEM; MICROSPHERES; NANOCARRIERS;
D O I
10.1016/j.matchemphys.2022.126933
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In the current research work, at first, aluminum-succinic acid-based metal-organic framework (Al-MOF) was synthesized in the presence of graphene oxide (GO) via a green procedure (Al-MOF/GO). The fabricated Al-MOF/ GO loaded about 78.4% and 65.7% of 5-fluorouracil (5-Fu) and doxorubicin (DOX) (DOX@5-Fu@Al-MOF/GO). Then the DOX@5-Fu@Al-MOF/GO was encapsulated with chitosan (CS) as a biocompatible and pH-sensitive coat (CS/DOX@5-Fu@Al-MOF/GO). The observed pH-dependent drug release pattern could be approved the positive role of CS having abundant amine functional groups in its structure. The in vitro experimental drug release results followed the first-order and Higuchi kinetic models respectively for 5-Fu and DOX. The biodeg-radation and swelling tests respectively exhibited a pH-sensitive swelling profile and degradation of 71.2% of CS/ DOX@5-Fu@Al-MOF/GO after 30 days which could be attributed to the CS coat. In sum outcome of this research work showed that the CS shell not only leads to the biodegradability and biocompatibility of the system but also leads to the release of anticancer drugs to a greater extent at pH 5.0, suggesting its potential for local cancer therapy.
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页数:13
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