Hierarchical mesoporous silicon and albumin composite microparticles delivering DOX and FU for liver cancer treatment

被引:3
|
作者
Xu, Tianyuan [1 ,2 ,3 ,4 ,5 ]
Fan, Lu [4 ]
Wang, Li [4 ]
Ren, Haozhen [3 ]
Zhang, Qingfei [1 ,2 ,4 ,6 ]
Sun, Weijian [1 ,2 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Gastrointestinal Surg, Wenzhou 325027, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Peoples R China
[3] Nanjing Univ, Nanjing Drum Tower Hosp, Med Sch, Dept Hepatobiliary Surg, Nanjing 210008, Peoples R China
[4] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Zhejiang, Peoples R China
[5] Guangxi Med Univ, Natl Ctr Int Res Biotargeting Theranost, Collaborat Innovat Ctr Targeting Tumor Diag & Ther, State Key Lab Targeting Oncol,Guangxi Key Lab Biot, Nanning 530021, Guangxi, Peoples R China
[6] Wenzhou Med Univ, Affiliated Hosp 2, Key Lab Pediat Hematol & Oncol Dis Wenzhou, Wenzhou 325027, Peoples R China
基金
中国国家自然科学基金;
关键词
Bovine serum albumin; Microfluidics; Microparticle; Liver cancer; Mesoporous silicon nanoparticle; DRUG-RELEASE; NANOPARTICLES; MICROFLUIDICS;
D O I
10.1016/j.ijbiomac.2024.131732
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drug delivery systems based on hydrogel microcarriers have shown enormous achievements in tumor treatment. Current research direction mainly concentrated on the improvement of the structure and function of the microcarriers to effectively deliver drugs for enhanced cancer treatment with decreased general toxicity. Herein, we put forward novel hierarchical mesoporous silicon nanoparticles (MSNs) and bovine serum albumin (BSA) composite microparticles (MPMSNs@DOX/FU) delivering doxorubicin (DOX) and 5-fluorouracil (FU) for effective tumor therapy with good safety. The DOX and FU could be efficiently loaded in the MSNs, which were further encapsulated into methacrylate BSA (BSAMA) microparticles by applying a microfluidic technique. When transported to the tumor area, DOX and FU will be persistently released from the MPMSNs@DOX/FU and kept locally to lessen general toxicity. Based on these advantages, MPMSNs@DOX/FU could observably kill liver cancer cells in vitro, and evidently suppress the tumor development of liver cancer nude mice model in vivo. These results suggest that such hierarchical hydrogel microparticles are perfect candidates for liver cancer treatment, holding promising expectations for impactful cancer therapy.
引用
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页数:10
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