Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway

Allergic asthma is one of the most common chronic airway diseases, and there is still a lack of effective drugs for the treatment of allergic asthma. The purpose of this work is to formulate rhynchophylline (Rhy)-solid lipid nanoparticles (SLNs) to improve their therapeutic efficacy in a mice allerg...

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Autores principales: Chuanfeng Lv, Hui Li, Hongxia Cui, Qianyu Bi, Meng Wang
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Publicado: Taylor & Francis Group 2021
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spelling oai:doaj.org-article:d216f51b4fa2462083b67359b31e7e652021-11-04T15:51:53ZSolid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway2165-59792165-598710.1080/21655979.2021.1988364https://doaj.org/article/d216f51b4fa2462083b67359b31e7e652021-01-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.1988364https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Allergic asthma is one of the most common chronic airway diseases, and there is still a lack of effective drugs for the treatment of allergic asthma. The purpose of this work is to formulate rhynchophylline (Rhy)-solid lipid nanoparticles (SLNs) to improve their therapeutic efficacy in a mice allergic model of asthma. A solvent injection method was employed to prepare the Rhy-SLNs. Physicochemical characterization of Rhy-SLNs was measured, and the release assessment was investigated, followed by the release kinetics. Next, a model of murine experimental asthma was established. Mice were subcutaneously injected with 20 μg ovalbumin mixed with 1 mg aluminum hydroxide on days 0, 14, 28, and 42 and administrated aerosolized 1% ovalbumin (w/v) by inhalation from day 21 to day 42. Mice were intraperitoneally injected with 20 mg/kg Rhy-SLNs or Rhy at one hour before the airway challenge with ovalbumin. The results showed that Rhy-SLNs revealed a mean particle size of 62.06 ± 1.62 nm with a zeta potential value of −6.53 ± 0.04 mV and 82.6 ± 1.8% drug entrapment efficiency. The release curve of Rhy-SLNs was much higher than the drug released in phosphate buffer saline at 0, 1, 1.5, 2, 4, or 6 h. Moreover, Rhy-SLNs exerted better effects on inhibiting ovalbumin-induced airway inflammation, oxidative stress, airway remodeling (including collagen deposition and mucus gland hyperplasia) than Rhy in murine experimental asthma. Subsequently, we found that Rhy-SLNs relieved allergic asthma via the upregulation of the suppressor of cytokine signaling 1 by repressing the p38 signaling pathway.Chuanfeng LvHui LiHongxia CuiQianyu BiMeng WangTaylor & Francis Grouparticlerhynchophyllinesolid lipid nanoparticleallergic asthmasuppressor of cytokine signaling 1p38 signaling pathwayBiotechnologyTP248.13-248.65ENBioengineered, Vol 12, Iss 1, Pp 8635-8649 (2021)
institution DOAJ
collection DOAJ
language EN
topic rhynchophylline
solid lipid nanoparticle
allergic asthma
suppressor of cytokine signaling 1
p38 signaling pathway
Biotechnology
TP248.13-248.65
spellingShingle rhynchophylline
solid lipid nanoparticle
allergic asthma
suppressor of cytokine signaling 1
p38 signaling pathway
Biotechnology
TP248.13-248.65
Chuanfeng Lv
Hui Li
Hongxia Cui
Qianyu Bi
Meng Wang
Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
description Allergic asthma is one of the most common chronic airway diseases, and there is still a lack of effective drugs for the treatment of allergic asthma. The purpose of this work is to formulate rhynchophylline (Rhy)-solid lipid nanoparticles (SLNs) to improve their therapeutic efficacy in a mice allergic model of asthma. A solvent injection method was employed to prepare the Rhy-SLNs. Physicochemical characterization of Rhy-SLNs was measured, and the release assessment was investigated, followed by the release kinetics. Next, a model of murine experimental asthma was established. Mice were subcutaneously injected with 20 μg ovalbumin mixed with 1 mg aluminum hydroxide on days 0, 14, 28, and 42 and administrated aerosolized 1% ovalbumin (w/v) by inhalation from day 21 to day 42. Mice were intraperitoneally injected with 20 mg/kg Rhy-SLNs or Rhy at one hour before the airway challenge with ovalbumin. The results showed that Rhy-SLNs revealed a mean particle size of 62.06 ± 1.62 nm with a zeta potential value of −6.53 ± 0.04 mV and 82.6 ± 1.8% drug entrapment efficiency. The release curve of Rhy-SLNs was much higher than the drug released in phosphate buffer saline at 0, 1, 1.5, 2, 4, or 6 h. Moreover, Rhy-SLNs exerted better effects on inhibiting ovalbumin-induced airway inflammation, oxidative stress, airway remodeling (including collagen deposition and mucus gland hyperplasia) than Rhy in murine experimental asthma. Subsequently, we found that Rhy-SLNs relieved allergic asthma via the upregulation of the suppressor of cytokine signaling 1 by repressing the p38 signaling pathway.
format article
author Chuanfeng Lv
Hui Li
Hongxia Cui
Qianyu Bi
Meng Wang
author_facet Chuanfeng Lv
Hui Li
Hongxia Cui
Qianyu Bi
Meng Wang
author_sort Chuanfeng Lv
title Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
title_short Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
title_full Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
title_fullStr Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
title_full_unstemmed Solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
title_sort solid lipid nanoparticle delivery of rhynchophylline enhanced the efficiency of allergic asthma treatment via the upregulation of suppressor of cytokine signaling 1 by repressing the p38 signaling pathway
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/d216f51b4fa2462083b67359b31e7e65
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AT huili solidlipidnanoparticledeliveryofrhynchophyllineenhancedtheefficiencyofallergicasthmatreatmentviatheupregulationofsuppressorofcytokinesignaling1byrepressingthep38signalingpathway
AT hongxiacui solidlipidnanoparticledeliveryofrhynchophyllineenhancedtheefficiencyofallergicasthmatreatmentviatheupregulationofsuppressorofcytokinesignaling1byrepressingthep38signalingpathway
AT qianyubi solidlipidnanoparticledeliveryofrhynchophyllineenhancedtheefficiencyofallergicasthmatreatmentviatheupregulationofsuppressorofcytokinesignaling1byrepressingthep38signalingpathway
AT mengwang solidlipidnanoparticledeliveryofrhynchophyllineenhancedtheefficiencyofallergicasthmatreatmentviatheupregulationofsuppressorofcytokinesignaling1byrepressingthep38signalingpathway
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