» Articles » PMID: 38560369

Targeted Therapy of Kidney Disease with Nanoparticle Drug Delivery Materials

Overview
Journal Bioact Mater
Date 2024 Apr 1
PMID 38560369
Authors
Affiliations
Soon will be listed here.
Abstract

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 short-term 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.

Citing Articles

Advances in medical devices using nanomaterials and nanotechnology: Innovation and regulatory science.

Lin C, Huang X, Xue Y, Jiang S, Chen C, Liu Y Bioact Mater. 2025; 48:353-369.

PMID: 40060145 PMC: 11889687. DOI: 10.1016/j.bioactmat.2025.02.017.


Recent advances in self-targeting natural product-based nanomedicines.

Liu H, Jin X, Liu S, Liu X, Pei X, Sun K J Nanobiotechnology. 2025; 23(1):31.

PMID: 39833846 PMC: 11749302. DOI: 10.1186/s12951-025-03092-9.


Nanoparticle-Based Drug Delivery for Vascular Applications.

Naskar A, Kilari S, Baranwal G, Kane J, Misra S Bioengineering (Basel). 2025; 11(12.

PMID: 39768040 PMC: 11673055. DOI: 10.3390/bioengineering11121222.


Multifunctional extracellular vesicles and edaravone-loaded scaffolds for kidney tissue regeneration by activating GDNF/RET pathway.

Lee S, Park J, Rhim W, Lee E, Lee S, Kim J Nano Converg. 2024; 11(1):43.

PMID: 39460807 PMC: 11512987. DOI: 10.1186/s40580-024-00450-5.


Dual-responsive renal injury cells targeting nanoparticles for vitamin E delivery to treat ischemia reperfusion-induced acute kidney injury.

Zhang J, Ren X, Nie Z, You Y, Zhu Y, Chen H J Nanobiotechnology. 2024; 22(1):626.

PMID: 39407248 PMC: 11481814. DOI: 10.1186/s12951-024-02894-7.


References
1.
Dias A, da Silva Santos S, da Silva J, Parise-Filho R, Ferreira E, El Seoud O . Dendrimers in the context of nanomedicine. Int J Pharm. 2019; 573:118814. DOI: 10.1016/j.ijpharm.2019.118814. View

2.
Ho T, Chang C, Chan H, Chung T, Shu C, Chuang K . Hydrogels: Properties and Applications in Biomedicine. Molecules. 2022; 27(9). PMC: 9104731. DOI: 10.3390/molecules27092902. View

3.
Zuckerman J, Gale A, Wu P, Ma R, Davis M . siRNA delivery to the glomerular mesangium using polycationic cyclodextrin nanoparticles containing siRNA. Nucleic Acid Ther. 2015; 25(2):53-64. PMC: 4376487. DOI: 10.1089/nat.2014.0505. View

4.
Chen Z, Li W, Shi L, Jiang L, Li M, Zhang C . Kidney-targeted astaxanthin natural antioxidant nanosystem for diabetic nephropathy therapy. Eur J Pharm Biopharm. 2020; 156:143-154. DOI: 10.1016/j.ejpb.2020.09.005. View

5.
Gabizon A, Shmeeda H, Barenholz Y . Pharmacokinetics of pegylated liposomal Doxorubicin: review of animal and human studies. Clin Pharmacokinet. 2003; 42(5):419-36. DOI: 10.2165/00003088-200342050-00002. View