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Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation
Although glucocorticoids are highly effective in treating various types of inflammation such as skin disease, rheumatic disease, and allergic disease, their application have been seriously limited for their high incidence of side effects, particularly in long term treatment. To improve efficacy and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320894/ https://www.ncbi.nlm.nih.gov/pubmed/30567356 http://dx.doi.org/10.3390/pharmaceutics10040286 |
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author | Zhang, Xiumei Qiu, Mingfeng Guo, Pengcheng Lian, Yumei Xu, Enge Su, Jing |
author_facet | Zhang, Xiumei Qiu, Mingfeng Guo, Pengcheng Lian, Yumei Xu, Enge Su, Jing |
author_sort | Zhang, Xiumei |
collection | PubMed |
description | Although glucocorticoids are highly effective in treating various types of inflammation such as skin disease, rheumatic disease, and allergic disease, their application have been seriously limited for their high incidence of side effects, particularly in long term treatment. To improve efficacy and reduce side effects, we encapsulated betamethasone phosphate (BSP) into biocompatible red blood cells (RBCs) and explored its long acting-effect. BSP was loaded into rat autologous erythrocytes by hypotonic preswelling method, and the loading amount was about 2.5 mg/mL cells. In vitro, BSP loaded RBCs (BSP-RBCs) presented similar morphology, osmotic fragility to native RBCs (NRBCs). After the loading process, the loaded cells can maintain around 70% of Na(+)/K(+)-ATPase activity of natural cells. In vivo, a series of tests including survival, pharmacokinetics, and anti-inflammatory effect were carried out to examine the long-acting effect of BSP-RBCs. The results shown that the loaded cells could circulate in plasma for over nine days, the release of BSP can last for over seven days and the anti-inflammatory effect can still be observed on day 5 after injection. Totally, BSP-loaded autologous erythrocytes seem to be a promising sustained releasing delivery system with long anti-inflammatory effect. |
format | Online Article Text |
id | pubmed-6320894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63208942019-01-11 Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation Zhang, Xiumei Qiu, Mingfeng Guo, Pengcheng Lian, Yumei Xu, Enge Su, Jing Pharmaceutics Article Although glucocorticoids are highly effective in treating various types of inflammation such as skin disease, rheumatic disease, and allergic disease, their application have been seriously limited for their high incidence of side effects, particularly in long term treatment. To improve efficacy and reduce side effects, we encapsulated betamethasone phosphate (BSP) into biocompatible red blood cells (RBCs) and explored its long acting-effect. BSP was loaded into rat autologous erythrocytes by hypotonic preswelling method, and the loading amount was about 2.5 mg/mL cells. In vitro, BSP loaded RBCs (BSP-RBCs) presented similar morphology, osmotic fragility to native RBCs (NRBCs). After the loading process, the loaded cells can maintain around 70% of Na(+)/K(+)-ATPase activity of natural cells. In vivo, a series of tests including survival, pharmacokinetics, and anti-inflammatory effect were carried out to examine the long-acting effect of BSP-RBCs. The results shown that the loaded cells could circulate in plasma for over nine days, the release of BSP can last for over seven days and the anti-inflammatory effect can still be observed on day 5 after injection. Totally, BSP-loaded autologous erythrocytes seem to be a promising sustained releasing delivery system with long anti-inflammatory effect. MDPI 2018-12-18 /pmc/articles/PMC6320894/ /pubmed/30567356 http://dx.doi.org/10.3390/pharmaceutics10040286 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Xiumei Qiu, Mingfeng Guo, Pengcheng Lian, Yumei Xu, Enge Su, Jing Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation |
title | Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation |
title_full | Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation |
title_fullStr | Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation |
title_full_unstemmed | Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation |
title_short | Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation |
title_sort | autologous red blood cell delivery of betamethasone phosphate sodium for long anti-inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320894/ https://www.ncbi.nlm.nih.gov/pubmed/30567356 http://dx.doi.org/10.3390/pharmaceutics10040286 |
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