Targeted therapy of kidney disease with nanoparticle drug delivery materials

被引:0
作者
Shang, Shunlai [1 ]
Li, Xiangmeng [1 ,2 ,3 ]
Wang, Haoran [4 ]
Zhou, Yena [5 ]
Pang, Keying [6 ]
Li, Ping [4 ]
Liu, Xiaomin [4 ]
Zhang, Min [7 ]
Li, Wenge [1 ]
Li, Qinggang [4 ]
Chen, Xiangmei [4 ]
机构
[1] China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R China
[2] Key Lab Bone Metab & Physiol Chron Kidney Dis Hebe, Baoding, Peoples R China
[3] Peking Union Med Coll, Beijing, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Natl Key Lab Kidney Dis, Dept Nephrol,Natl Clin Res Ctr Kidney Dis,Nephrol, Beijing, Peoples R China
[5] Nankai Univ, Sch Med, Tianjin, Peoples R China
[6] Hebei Univ Chinese Med, Coll Pharm, Shijiazhuang, Hebei, Peoples R China
[7] Capital Med Univ, Affiliated Beijing Chaoyang Hosp, Dept Nephrol, Beijing, Peoples R China
基金
北京市自然科学基金; 中国博士后科学基金;
关键词
Nanomedicine; Materials; Targeted drugs; Kidney disease; MESOPOROUS SILICA NANOPARTICLES; PEGYLATED LIPOSOMAL DOXORUBICIN; ENHANCED PERMEABILITY; MESANGIAL CELLS; HYDROGEL; NANOTECHNOLOGY; RETENTION; MICELLES; CHITOSAN; RELEASE;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
With the development of nanomedicine, nanomaterials have been widely used, offering specific drug delivery to target sites, minimal side effects, and significant therapeutic effects. The kidneys have filtration and reabsorption functions, with various potential target cell types and a complex structural environment, making the strategies for kidney function protection and recovery after injury complex. This also lays the foundation for the application of nanomedicine in kidney diseases. Currently, evidence in preclinical and clinical settings supports the feasibility of targeted therapy for kidney diseases using drug delivery based on nanomaterials. The prerequisite for nanomedicine in treating kidney diseases is the use of carriers with good biocompatibility, including nanoparticles, hydrogels, liposomes, micelles, dendrimer polymers, adenoviruses, lysozymes, and elastin-like polypeptides. These carriers have precise renal uptake, longer half-life, and targeted organ distribution, protecting and improving the efficacy of the drugs they carry. Additionally, attention should also be paid to the toxicity and solubility of the carriers. While the carriers mentioned above have been used in preclinical studies for targeted therapy of kidney diseases both in vivo and in vitro, extensive clinical trials are still needed to ensure the shortterm and long-term effects of nano drugs in the human body. This review will discuss the advantages and limitations of nanoscale drug carrier materials in treating kidney diseases, provide a more comprehensive catalog of nanocarrier materials, and offer prospects for their drug-loading efficacy and clinical applications.
引用
收藏
页码:206 / 221
页数:16
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