Cargando…

Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect

Liver fibrosis remains a significant public health problem. However, few drugs have yet been validated. Costunolide (COS), as a monomeric component of the traditional Chinese medicinal herb Saussurea Lappa, has shown excellent anti-fibrotic efficacy. However, COS displays very poor aqueous solubilit...

Descripción completa

Detalles Bibliográficos
Autores principales: Niu, Xia, Wang, Xiaomei, Niu, Bingyu, Meng, Yanan, He, Hongwei, Wang, Yucheng, Li, Guiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539632/
https://www.ncbi.nlm.nih.gov/pubmed/34681175
http://dx.doi.org/10.3390/ph14100951
_version_ 1784588793989300224
author Niu, Xia
Wang, Xiaomei
Niu, Bingyu
Meng, Yanan
He, Hongwei
Wang, Yucheng
Li, Guiling
author_facet Niu, Xia
Wang, Xiaomei
Niu, Bingyu
Meng, Yanan
He, Hongwei
Wang, Yucheng
Li, Guiling
author_sort Niu, Xia
collection PubMed
description Liver fibrosis remains a significant public health problem. However, few drugs have yet been validated. Costunolide (COS), as a monomeric component of the traditional Chinese medicinal herb Saussurea Lappa, has shown excellent anti-fibrotic efficacy. However, COS displays very poor aqueous solubility and poor stability in gastric juice, which greatly limits its application via an oral administration. To increase the stability, improve the dissolution rate and enhance the anti-liver fibrosis of COS, pH-responsive mesoporous silica nanoparticles (MSNs) were selected as a drug carrier. Methacrylic acid copolymer (MAC) as a pH-sensitive material was used to coat the surface of MSNs. The drug release behavior and anti-liver fibrosis effects of MSNs-COS-MAC were evaluated. The results showed that MSNs-COS-MAC prevented a release in the gastric fluid and enhanced the dissolution rate of COS in the intestinal juice. At half the dose of COS, MSNs-COS-MAC still effectively ameliorated parenchymal necrosis, bile duct proliferation and excessive collagen. MSNs-COS-MAC significantly repressed hepatic fibrogenesis by decreasing the expression of hepatic fibrogenic markers in LX-2 cells and liver tissue. These results suggest that MSNs-COS-MAC shows great promise for anti-liver fibrosis treatment.
format Online
Article
Text
id pubmed-8539632
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-85396322021-10-24 Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect Niu, Xia Wang, Xiaomei Niu, Bingyu Meng, Yanan He, Hongwei Wang, Yucheng Li, Guiling Pharmaceuticals (Basel) Article Liver fibrosis remains a significant public health problem. However, few drugs have yet been validated. Costunolide (COS), as a monomeric component of the traditional Chinese medicinal herb Saussurea Lappa, has shown excellent anti-fibrotic efficacy. However, COS displays very poor aqueous solubility and poor stability in gastric juice, which greatly limits its application via an oral administration. To increase the stability, improve the dissolution rate and enhance the anti-liver fibrosis of COS, pH-responsive mesoporous silica nanoparticles (MSNs) were selected as a drug carrier. Methacrylic acid copolymer (MAC) as a pH-sensitive material was used to coat the surface of MSNs. The drug release behavior and anti-liver fibrosis effects of MSNs-COS-MAC were evaluated. The results showed that MSNs-COS-MAC prevented a release in the gastric fluid and enhanced the dissolution rate of COS in the intestinal juice. At half the dose of COS, MSNs-COS-MAC still effectively ameliorated parenchymal necrosis, bile duct proliferation and excessive collagen. MSNs-COS-MAC significantly repressed hepatic fibrogenesis by decreasing the expression of hepatic fibrogenic markers in LX-2 cells and liver tissue. These results suggest that MSNs-COS-MAC shows great promise for anti-liver fibrosis treatment. MDPI 2021-09-23 /pmc/articles/PMC8539632/ /pubmed/34681175 http://dx.doi.org/10.3390/ph14100951 Text en © 2021 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
Niu, Xia
Wang, Xiaomei
Niu, Bingyu
Meng, Yanan
He, Hongwei
Wang, Yucheng
Li, Guiling
Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect
title Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect
title_full Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect
title_fullStr Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect
title_full_unstemmed Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect
title_short Costunolide Loaded in pH-Responsive Mesoporous Silica Nanoparticles for Increased Stability and an Enhanced Anti-Fibrotic Effect
title_sort costunolide loaded in ph-responsive mesoporous silica nanoparticles for increased stability and an enhanced anti-fibrotic effect
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539632/
https://www.ncbi.nlm.nih.gov/pubmed/34681175
http://dx.doi.org/10.3390/ph14100951
work_keys_str_mv AT niuxia costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect
AT wangxiaomei costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect
AT niubingyu costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect
AT mengyanan costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect
AT hehongwei costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect
AT wangyucheng costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect
AT liguiling costunolideloadedinphresponsivemesoporoussilicananoparticlesforincreasedstabilityandanenhancedantifibroticeffect