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Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage.
Cheng, Fong-Yu; Chiou, Yuan-Yow; Hung, Shih-Yuan; Lin, Tsun-Mei; Wang, Hao-Kuang; Lin, Chi-Wei; Liou, Hung-Hsiang; Chang, Min-Yu; Wang, Hsi-Hao; Lee, Yi-Che.
Afiliação
  • Cheng FY; Department of Chemistry, Chinese Culture University, Taipei, Taiwan.
  • Chiou YY; Department of Pediatrics, National Cheng Kung University Hospital, Tainan, Taiwan.
  • Hung SY; Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Lin TM; School of Medicine, College of Medicine, I-Shou University, Kaohsiung, Taiwan.
  • Wang HK; Division of Nephrology, Department of Internal Medicine, E-DA Hospital, Kaohsiung, Taiwan.
  • Lin CW; Department of Laboratory Medicine, E-DA Hospital, Kaohsiung, Taiwan.
  • Liou HH; Department of Neurosurgery, E-DA Hospital, Kaohsiung, Taiwan.
  • Chang MY; Department of Medical Education, E-DA Hospital, Kaohsiung, Taiwan.
  • Wang HH; Division of Nephrology, Department of Internal Medicine, Hsin-Jen Hospital, New Taipei City, Taiwan.
  • Lee YC; Division of Nephrology, Department of Internal Medicine, E-DA Hospital, Kaohsiung, Taiwan.
Int J Nanomedicine ; 16: 2137-2146, 2021.
Article em En | MEDLINE | ID: mdl-33731995
ABSTRACT

PURPOSE:

Vitamin D3 is useful for the treatment of peritoneal dialysis (PD)-related peritoneal damage, but its side effects, such as hypercalcemia and vascular calcification, limit its applicability. Thus, we developed vitamin D-loaded magnetic nanoparticles (MNPs) and determined their therapeutic efficacy and side effects in vivo. MATERIALS AND

METHODS:

Alginate-modified MNPs were combined with 1α, 25 (OH)2D3 to generate vitamin D-loaded nanoparticles. The particles were conjugated with an antibody against peritoneum-glycoprotein M6A (GPM6A). The particles' ability to target the peritoneum was examined following intraperitoneal administration to mice and by monitoring their bio-distribution. We also established a PD animal model to determine the therapeutic and side effects of vitamin D-loaded MNPs in vivo.

RESULTS:

Vitamin D-loaded MNPs targeted the peritoneum better than vitamin D3, and had the same therapeutic effect as vitamin D3 in ameliorating peritoneal fibrosis and functional deterioration in a PD animal model. Most importantly, the particles reduced the side effects of vitamin D3, such as hypercalcemia and body weight loss, in mice.

CONCLUSION:

Vitamin D-loaded MNPs could be an ideal future therapeutic option to treat PD-related peritoneal damage.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peritônio / Diálise Peritoneal / Sistemas de Liberação de Medicamentos / Colecalciferol / Nanopartículas de Magnetita Tipo de estudo: Etiology_studies Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peritônio / Diálise Peritoneal / Sistemas de Liberação de Medicamentos / Colecalciferol / Nanopartículas de Magnetita Tipo de estudo: Etiology_studies Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article