Cargando…

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

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 poly...

Descripción completa

Detalles Bibliográficos
Autores principales: Alshammari, Rehab A., Aleanizy, Fadilah S., Aldarwesh, Amal, Alqahtani, Fulwah Y., Mahdi, Wael A., Alquadeib, Bushra, Alqahtani, Qamraa H., Haq, Nazrul, Shakeel, Faiyaz, Abdelhady, Hosam G., Alsarra, Ibrahim A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322846/
https://www.ncbi.nlm.nih.gov/pubmed/35890338
http://dx.doi.org/10.3390/pharmaceutics14071444
_version_ 1784756404879360000
author Alshammari, Rehab A.
Aleanizy, Fadilah S.
Aldarwesh, Amal
Alqahtani, Fulwah Y.
Mahdi, Wael A.
Alquadeib, Bushra
Alqahtani, Qamraa H.
Haq, Nazrul
Shakeel, Faiyaz
Abdelhady, Hosam G.
Alsarra, Ibrahim A.
author_facet Alshammari, Rehab A.
Aleanizy, Fadilah S.
Aldarwesh, Amal
Alqahtani, Fulwah Y.
Mahdi, Wael A.
Alquadeib, Bushra
Alqahtani, Qamraa H.
Haq, Nazrul
Shakeel, Faiyaz
Abdelhady, Hosam G.
Alsarra, Ibrahim A.
author_sort Alshammari, Rehab A.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-9322846
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93228462022-07-27 Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers Alshammari, Rehab A. Aleanizy, Fadilah S. Aldarwesh, Amal Alqahtani, Fulwah Y. Mahdi, Wael A. Alquadeib, Bushra Alqahtani, Qamraa H. Haq, Nazrul Shakeel, Faiyaz Abdelhady, Hosam G. Alsarra, Ibrahim A. Pharmaceutics Article 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. MDPI 2022-07-11 /pmc/articles/PMC9322846/ /pubmed/35890338 http://dx.doi.org/10.3390/pharmaceutics14071444 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alshammari, Rehab A.
Aleanizy, Fadilah S.
Aldarwesh, Amal
Alqahtani, Fulwah Y.
Mahdi, Wael A.
Alquadeib, Bushra
Alqahtani, Qamraa H.
Haq, Nazrul
Shakeel, Faiyaz
Abdelhady, Hosam G.
Alsarra, Ibrahim A.
Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers
title Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers
title_full Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers
title_fullStr Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers
title_full_unstemmed Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers
title_short Retinal Delivery of the Protein Kinase C-β Inhibitor Ruboxistaurin Using Non-Invasive Nanoparticles of Polyamidoamine Dendrimers
title_sort retinal delivery of the protein kinase c-β inhibitor ruboxistaurin using non-invasive nanoparticles of polyamidoamine dendrimers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322846/
https://www.ncbi.nlm.nih.gov/pubmed/35890338
http://dx.doi.org/10.3390/pharmaceutics14071444
work_keys_str_mv AT alshammarirehaba retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT aleanizyfadilahs retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT aldarweshamal retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT alqahtanifulwahy retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT mahdiwaela retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT alquadeibbushra retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT alqahtaniqamraah retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT haqnazrul retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT shakeelfaiyaz retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT abdelhadyhosamg retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers
AT alsarraibrahima retinaldeliveryoftheproteinkinasecbinhibitorruboxistaurinusingnoninvasivenanoparticlesofpolyamidoaminedendrimers