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Targeted therapy of kidney disease with nanoparticle drug delivery materials.
Shang, Shunlai; Li, Xiangmeng; Wang, Haoran; Zhou, Yena; Pang, Keying; Li, Ping; Liu, Xiaomin; Zhang, Min; Li, Wenge; Li, Qinggang; Chen, Xiangmei.
Afiliação
  • Shang S; Department of Nephrology, China-Japan Friendship Hospital, Beijing, China.
  • Li X; Department of Nephrology, China-Japan Friendship Hospital, Beijing, China.
  • Wang H; Key Laboratory of Bone Metabolism and Physiology in Chronic Kidney Disease of Hebei Province, China.
  • Zhou Y; Peking Union Medical College, Beijing, China.
  • Pang K; Department of Nephrology, First Medical Center of Chinese PLA General Hospital, Nephrology Institute of the Chinese People's Liberation Army, National Key Laboratory of Kidney Diseases, National Clinical Research Center for Kidney Diseases, Beijing Key Laboratory of Kidney Disease Research, Beijing,
  • Li P; School of Medicine, Nankai University, Tianjin, China.
  • Liu X; College of Pharmacy, Hebei University of Chinese Medicine, Shijiazhuang, Hebei Province, China.
  • Zhang M; Department of Nephrology, First Medical Center of Chinese PLA General Hospital, Nephrology Institute of the Chinese People's Liberation Army, National Key Laboratory of Kidney Diseases, National Clinical Research Center for Kidney Diseases, Beijing Key Laboratory of Kidney Disease Research, Beijing,
  • Li W; Department of Nephrology, First Medical Center of Chinese PLA General Hospital, Nephrology Institute of the Chinese People's Liberation Army, National Key Laboratory of Kidney Diseases, National Clinical Research Center for Kidney Diseases, Beijing Key Laboratory of Kidney Disease Research, Beijing,
  • Li Q; Department of Nephrology, Affiliated Beijing Chaoyang Hospital of Capital Medical University, Beijing, China.
  • Chen X; Department of Nephrology, China-Japan Friendship Hospital, Beijing, China.
Bioact Mater ; 37: 206-221, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38560369
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article