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...

Full description

Bibliographic Details
Main Authors: Xiumei Zhang, Mingfeng Qiu, Pengcheng Guo, Yumei Lian, Enge Xu, Jing Su
Format: Article
Language:English
Published: MDPI AG 2018-12-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/10/4/286
_version_ 1811297660540289024
author Xiumei Zhang
Mingfeng Qiu
Pengcheng Guo
Yumei Lian
Enge Xu
Jing Su
author_facet Xiumei Zhang
Mingfeng Qiu
Pengcheng Guo
Yumei Lian
Enge Xu
Jing Su
author_sort Xiumei Zhang
collection DOAJ
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<sup>+</sup>/K<sup>+</sup>-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.
first_indexed 2024-04-13T06:07:41Z
format Article
id doaj.art-1f3b806dff6d4141b7e081e33a494906
institution Directory Open Access Journal
issn 1999-4923
language English
last_indexed 2024-04-13T06:07:41Z
publishDate 2018-12-01
publisher MDPI AG
record_format Article
series Pharmaceutics
spelling doaj.art-1f3b806dff6d4141b7e081e33a4949062022-12-22T02:59:11ZengMDPI AGPharmaceutics1999-49232018-12-0110428610.3390/pharmaceutics10040286pharmaceutics10040286Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-InflammationXiumei Zhang0Mingfeng Qiu1Pengcheng Guo2Yumei Lian3Enge Xu4Jing Su5School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, ChinaSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, ChinaSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, ChinaSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, ChinaSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, ChinaSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, ChinaAlthough 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<sup>+</sup>/K<sup>+</sup>-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.https://www.mdpi.com/1999-4923/10/4/286red blood cellsdrug delivery systembetamethasone phosphatelong anti-inflammation
spellingShingle Xiumei Zhang
Mingfeng Qiu
Pengcheng Guo
Yumei Lian
Enge Xu
Jing Su
Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation
Pharmaceutics
red blood cells
drug delivery system
betamethasone phosphate
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 red blood cells
drug delivery system
betamethasone phosphate
long anti-inflammation
url https://www.mdpi.com/1999-4923/10/4/286
work_keys_str_mv AT xiumeizhang autologousredbloodcelldeliveryofbetamethasonephosphatesodiumforlongantiinflammation
AT mingfengqiu autologousredbloodcelldeliveryofbetamethasonephosphatesodiumforlongantiinflammation
AT pengchengguo autologousredbloodcelldeliveryofbetamethasonephosphatesodiumforlongantiinflammation
AT yumeilian autologousredbloodcelldeliveryofbetamethasonephosphatesodiumforlongantiinflammation
AT engexu autologousredbloodcelldeliveryofbetamethasonephosphatesodiumforlongantiinflammation
AT jingsu autologousredbloodcelldeliveryofbetamethasonephosphatesodiumforlongantiinflammation