4.7 Article

Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers

期刊

PHARMACEUTICS
卷 14, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics14071444

关键词

polyamidoamine dendrimers; diabetic retinopathy; protein kinase C-beta inhibitor; nanoparticles; ruboxistaurin

资金

  1. King Saud University, Riyadh, Saudi Arabia [RSP-2021/340]

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This study developed RBX nanoparticles using PAMAM dendrimers for the treatment of diabetic retinopathy, providing a safe and effective method for RBX administration. The drug loading efficiency and in vitro release of the RBX:PAMAM dendrimer complexes were evaluated, and the 5:1 complex showed the highest loading efficiency and drug release. The nanoformulation improved the therapeutic outcomes of anti-VEGF therapy and the bioavailability of RBX for preventing vision loss in patients with diabetic retinopathy.
Ruboxistaurin (RBX) is an anti-vascular endothelial growth factor (anti-VEGF) agent that is used in the treatment of diabetic retinopathy and is mainly given intravitreally. To provide a safe and effective method for RBX administration, this study was designed to develop RBX nanoparticles using polyamidoamine (PAMAM) dendrimer generation 5 for the treatment of diabetic retinopathy. Drug loading efficiency, and in vitro release of proposed complexes of RBX: PAMAM dendrimers were determined and the complexation ratio that showed the highest possible loading efficiency was selected. The drug loading efficiency (%) of 1:1, 2.5:1, and 5:1 complexes was 89.2%, 96.4%, and 97.6%, respectively. Loading capacities of 1:1, 2.5:1, and 5:1 complexes were 1.6%, 4.0%, and 7.2% respectively. In comparison, the 5:1 complex showed the best results in the aforementioned measurements. The in vitro release studies showed that in 8 h, the RBX release from 1:1, 2.5:1, and 5:1 complexes was 37.5%, 35.9%, and 77.0%, respectively. In particular, 5:1 complex showed the highest drug release. In addition, particle size measurements showed that the diameter of empty PAMAM dendrimers was 214.9 +/- 8.5 nm, whereas the diameters of loaded PAMAM dendrimers in 1:1, 2.5:1, 5:1 complexes were found to be 461.0 +/- 6.4, 482.4 +/- 12.5, and 420.0 +/- 7.1 nm, respectively. Polydispersity index (PDI) showed that there were no significant changes in the PDI between the free and loaded PAMAM dendrimers. The zeta potential measurements showed that the free and loaded nanoparticles possessed neutral charges due to the presence of anionic and cationic terminal structures. Furthermore, the safety of this formulation was apparent on the viability of the MIO-M1 cell lines. This nanoformulation will improve the therapeutic outcomes of anti-VEGF therapy and the bioavailability of RBX to prevent vision loss in patients with diabetic retinopathy.

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