Hyaluronic acid oligosaccharide-modified zeolitic imidazolate framework-8 nanoparticles loaded with oxaliplatin as a targeted drug-delivery system for colorectal cancer therapy

被引:3
|
作者
Li, Bingtai [1 ]
Zhang, Zhicong [2 ]
He, Shenfu [3 ]
Du, Wenlong [4 ]
Yang, Xiaoping [1 ]
Kou, Bangguo [1 ]
Jiang, Yongjie [1 ]
Bian, Pan [1 ]
Yin, Lanning [1 ,3 ]
机构
[1] Lanzhou Univ, Hosp 2, Dept Gen Surg, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[3] Xigu Peoples Hosp, Dept Gen Surg, Lanzhou 730000, Gansu, Peoples R China
[4] Linxia Peoples Hosp, Dept Anorectal Surg, Linxia 731100, Gansu, Peoples R China
关键词
colorectal cancer therapy; drug-delivery system; hyaluronic acid oligosaccharide; metal-organic framework; oxaliplatin; METAL-ORGANIC FRAMEWORKS; MESOPOROUS SILICA; CD44; RESISTANCE;
D O I
10.2217/nnm-2023-0096
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: Exploring a nanoscale targeted drug-delivery system (DDS) for oxaliplatin (Oxa) to improve its therapeutic effect in colorectal cancer. Materials & methods: Nanoparticles were prepared using zeolitic imidazole framework-8 (ZIF-8) modified by hyaluronic acid oligosaccharide (oHA) as an Oxa carrier (oHA@ZIF-8@Oxa). After multiple characterizations, the therapeutic efficacy of the DDS was evaluated by cytotoxicity testing and a nude mouse tumor transplantation experiment in vivo. Results: The results of characterization showed the DDS was homogeneous in morphology and uniform in dispersion. The drug loading of Oxa was 11.82% and the encapsulation efficiency was 90.8%. The cytotoxicity test and in vivo experiments showed that oHA@ZIF-8@Oxa had a more significant anticolorectal cancer effect than free Oxa. Conclusion: This work offers a promising potential DDS for enhancing the anticolorectal cancer effect of Oxa.
引用
收藏
页码:891 / 905
页数:15
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