pH-Sensitive Stimulus Responsive ZIF-8 Composites Nanoparticles Coated with Folic Acid-Conjugated Chitosan for Targeted Delivery of Curcumin

被引:8
|
作者
Luo, Honghuan [1 ,2 ]
Chen, Menglan [1 ,2 ]
Song, Fangxiang [3 ]
Cai, Xiaoqin [1 ,2 ]
Yan, Yibing [1 ,2 ]
Li, Tingxian [1 ,2 ]
Li, Yan [1 ,2 ]
机构
[1] Guizhou Univ, Sch Pharm, Guiyang 550025, Peoples R China
[2] Guizhou Univ, Guizhou Engn Lab Synthet Drug, Guiyang 550025, Peoples R China
[3] Guizhou Univ, Sch Chem & Chem Engn, Guiyang 550025, Peoples R China
关键词
ZIF-8; Composites; CS-FA; pH-sensitive; Drug delivery; MESOPOROUS SILICA NANOPARTICLES; ZEOLITIC IMIDAZOLATE FRAMEWORK-8; METAL-ORGANIC FRAMEWORKS; DRUG-DELIVERY; CERVICAL-CANCER; IN-VITRO; STABILITY; WATER; DOXORUBICIN; THERAPY;
D O I
10.1007/s10876-024-02602-3
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Zeolitic imidazolate framework-8 (ZIF-8) is a promising material for drug delivery, but its poor stability limits its wide application. In this work, homogeneous dodecahedral ZIF-8 was prepared by the room-temperature solution stirring method, and to improve the stability of ZIF-8, ZIF-8@mSiO2 and DZIF-8 (ZIF-8 after calcination) @PMO composites with the core-shell structure were obtained using mesoporous silica (mSiO2) and periodic mesoporous organic silica (PMO) coatings. Folic acid-coupled chitosan (CS-FA) was modified on nanoparticles, and curcumin (CUR) was used as a model anti-tumor drug to obtain the drug delivery systems with targeting and pH stimulation response: ZIF-8@mSiO2@CUR@CS-FA and DZIF-8@PMO@CUR@CS-FA, which exhibited good dispersion and high drug loading capability. In addition, we used the MTT assay to assess the cytotoxicity of the drug-carrying systems and selected human cervical cancer cells (Hela) as model cells. The results of the in vitro experiments suggested that the final CUR-loaded drug delivery systems had significantly increased anticancer efficiency compared with the free drug CUR, which improved the therapeutic effect of the hydrophobic CUR on tumors. In conclusion, the pH-responsive nanocarriers provided potential for the targeted delivery of anticancer medication, resulting in a platform for drug-controlled release and cancer therapy.
引用
收藏
页码:1533 / 1547
页数:15
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