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Renal Proximal Tubular Cells: A New Site for Targeted Delivery Therapy of Diabetic Kidney Disease

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Publisher MDPI
Specialty Chemistry
Date 2022 Dec 23
PMID 36558944
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Abstract

Diabetic kidney disease (DKD) is a major complication of diabetes mellitus (DM) and the leading cause of end-stage kidney disease (ESKD) worldwide. A significant number of drugs have been clinically investigated for the treatment of DKD. However, a large proportion of patients still develop end-stage kidney disease unstoppably. As a result, new effective therapies are urgently needed to slow down the progression of DKD. Recently, there is increasing evidence that targeted drug delivery strategies such as large molecule carriers, small molecule prodrugs, and nanoparticles can improve drug efficacy and reduce adverse side effects. There is no doubt that targeted drug delivery strategies have epoch-making significance and great application prospects for the treatment of DKD. In addition, the proximal tubule plays a very critical role in the progression of DKD. Consequently, the purpose of this paper is to summarize the current understanding of proximal tubule cell-targeted therapy, screen for optimal targeting strategies, and find new therapeutic approaches for the treatment of DKD.

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References
1.
Paluszkiewicz P, Martuszewski A, Zareba N, Wala K, Banasik M, Kepinska M . The Application of Nanoparticles in Diagnosis and Treatment of Kidney Diseases. Int J Mol Sci. 2022; 23(1). PMC: 8745391. DOI: 10.3390/ijms23010131. View

2.
Dolman M, Harmsen S, Pieters E, Sparidans R, Lacombe M, Szokol B . Targeting of a platinum-bound sunitinib analog to renal proximal tubular cells. Int J Nanomedicine. 2012; 7:417-33. PMC: 3273977. DOI: 10.2147/IJN.S26485. View

3.
Haraguchi R, Kohara Y, Matsubayashi K, Kitazawa R, Kitazawa S . New Insights into the Pathogenesis of Diabetic Nephropathy: Proximal Renal Tubules Are Primary Target of Oxidative Stress in Diabetic Kidney. Acta Histochem Cytochem. 2020; 53(2):21-31. PMC: 7212204. DOI: 10.1267/ahc.20008. View

4.
Mukherjee A, Waters A, Kalyan P, Singh Achrol A, Kesari S, Yenugonda V . Lipid-polymer hybrid nanoparticles as a next-generation drug delivery platform: state of the art, emerging technologies, and perspectives. Int J Nanomedicine. 2019; 14:1937-1952. PMC: 6430183. DOI: 10.2147/IJN.S198353. View

5.
Hasanein Asfour M, Salama A, Mohsen A . Fabrication of All-Trans Retinoic Acid loaded Chitosan/Tripolyphosphate Lipid Hybrid Nanoparticles as a Novel Oral Delivery Approach for Management of Diabetic Nephropathy in Rats. J Pharm Sci. 2021; 110(9):3208-3220. DOI: 10.1016/j.xphs.2021.05.007. View