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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...

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Autores principales: Zhang, Xiumei, Qiu, Mingfeng, Guo, Pengcheng, Lian, Yumei, Xu, Enge, Su, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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