A dandelion polysaccharide and its selenium nanoparticles: Structure features and evaluation of anti-tumor activity in zebrafish models

In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and T...

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Veröffentlicht in:Carbohydrate Polymers Jg. 270; S. 118365
Hauptverfasser: Zhang, Shaojie, Song, Ziteng, Shi, Lijuan, Zhou, Linan, Zhang, Jie, Cui, Jianlin, Li, Yuhao, Jin, Da-Qing, Ohizumi, Yasushi, Xu, Jing, Guo, Yuanqiang
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Veröffentlicht: England Elsevier Ltd 15.10.2021
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ISSN:0144-8617, 1879-1344, 1879-1344
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Abstract In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and Tween 80 were tightly wrapped on the surface of SeNPs by forming CO⋯Se bonds or through hydrogen bonding interaction (OH⋯Se). In vitro anti-tumor assay showed that Tw-TMP-SeNP treatment could significantly inhibit the proliferation of cancer cells (HepG2, A549, and HeLa) in a dose-dependent manner, while HepG2 cells were more susceptible to Tw-TMP-SeNP with an IC50 value of 46.8 μg/mL. The apoptosis induction of HepG2 cells by Tw-TMP-SeNP was evidenced by increasing the proportion of apoptotic cells ranging from 12.5% to 27.4%. Furthermore, in vivo zebrafish model confirmed the anti-tumor activity of Tw-TMP-SeNP by inhibiting the proliferation and migration of tumor cells as well as the angiogenesis of zebrafish embryos. •An inulin fructan, TMP50-2, was purified and characterized from dandelion.•A fructan-based nanoparticle (Tw-TMP-SeNP) was designed, fabricated, and characterized.•Tw-TMP-SeNP exerted anti-tumor activity by inducing apoptosis.•Tw-TMP-SeNP blocked tumor proliferation and migration in the zebrafish xenograft model.•Tw-TMP-SeNP inhibited angiogenesis in the transgenic zebrafish model.
AbstractList In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and Tween 80 were tightly wrapped on the surface of SeNPs by forming CO⋯Se bonds or through hydrogen bonding interaction (OH⋯Se). In vitro anti-tumor assay showed that Tw-TMP-SeNP treatment could significantly inhibit the proliferation of cancer cells (HepG2, A549, and HeLa) in a dose-dependent manner, while HepG2 cells were more susceptible to Tw-TMP-SeNP with an IC value of 46.8 μg/mL. The apoptosis induction of HepG2 cells by Tw-TMP-SeNP was evidenced by increasing the proportion of apoptotic cells ranging from 12.5% to 27.4%. Furthermore, in vivo zebrafish model confirmed the anti-tumor activity of Tw-TMP-SeNP by inhibiting the proliferation and migration of tumor cells as well as the angiogenesis of zebrafish embryos.
In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and Tween 80 were tightly wrapped on the surface of SeNPs by forming CO⋯Se bonds or through hydrogen bonding interaction (OH⋯Se). In vitro anti-tumor assay showed that Tw-TMP-SeNP treatment could significantly inhibit the proliferation of cancer cells (HepG2, A549, and HeLa) in a dose-dependent manner, while HepG2 cells were more susceptible to Tw-TMP-SeNP with an IC50 value of 46.8 μg/mL. The apoptosis induction of HepG2 cells by Tw-TMP-SeNP was evidenced by increasing the proportion of apoptotic cells ranging from 12.5% to 27.4%. Furthermore, in vivo zebrafish model confirmed the anti-tumor activity of Tw-TMP-SeNP by inhibiting the proliferation and migration of tumor cells as well as the angiogenesis of zebrafish embryos.In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and Tween 80 were tightly wrapped on the surface of SeNPs by forming CO⋯Se bonds or through hydrogen bonding interaction (OH⋯Se). In vitro anti-tumor assay showed that Tw-TMP-SeNP treatment could significantly inhibit the proliferation of cancer cells (HepG2, A549, and HeLa) in a dose-dependent manner, while HepG2 cells were more susceptible to Tw-TMP-SeNP with an IC50 value of 46.8 μg/mL. The apoptosis induction of HepG2 cells by Tw-TMP-SeNP was evidenced by increasing the proportion of apoptotic cells ranging from 12.5% to 27.4%. Furthermore, in vivo zebrafish model confirmed the anti-tumor activity of Tw-TMP-SeNP by inhibiting the proliferation and migration of tumor cells as well as the angiogenesis of zebrafish embryos.
In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and Tween 80 were tightly wrapped on the surface of SeNPs by forming CO⋯Se bonds or through hydrogen bonding interaction (OH⋯Se). In vitro anti-tumor assay showed that Tw-TMP-SeNP treatment could significantly inhibit the proliferation of cancer cells (HepG2, A549, and HeLa) in a dose-dependent manner, while HepG2 cells were more susceptible to Tw-TMP-SeNP with an IC₅₀ value of 46.8 μg/mL. The apoptosis induction of HepG2 cells by Tw-TMP-SeNP was evidenced by increasing the proportion of apoptotic cells ranging from 12.5% to 27.4%. Furthermore, in vivo zebrafish model confirmed the anti-tumor activity of Tw-TMP-SeNP by inhibiting the proliferation and migration of tumor cells as well as the angiogenesis of zebrafish embryos.
In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of TMP50-2, a monodisperse and stable spherical nanoparticle (Tw-TMP-SeNP, 50 nm) was fabricated. Physico-chemical analysis revealed that TMP50-2 and Tween 80 were tightly wrapped on the surface of SeNPs by forming CO⋯Se bonds or through hydrogen bonding interaction (OH⋯Se). In vitro anti-tumor assay showed that Tw-TMP-SeNP treatment could significantly inhibit the proliferation of cancer cells (HepG2, A549, and HeLa) in a dose-dependent manner, while HepG2 cells were more susceptible to Tw-TMP-SeNP with an IC50 value of 46.8 μg/mL. The apoptosis induction of HepG2 cells by Tw-TMP-SeNP was evidenced by increasing the proportion of apoptotic cells ranging from 12.5% to 27.4%. Furthermore, in vivo zebrafish model confirmed the anti-tumor activity of Tw-TMP-SeNP by inhibiting the proliferation and migration of tumor cells as well as the angiogenesis of zebrafish embryos. •An inulin fructan, TMP50-2, was purified and characterized from dandelion.•A fructan-based nanoparticle (Tw-TMP-SeNP) was designed, fabricated, and characterized.•Tw-TMP-SeNP exerted anti-tumor activity by inducing apoptosis.•Tw-TMP-SeNP blocked tumor proliferation and migration in the zebrafish xenograft model.•Tw-TMP-SeNP inhibited angiogenesis in the transgenic zebrafish model.
ArticleNumber 118365
Author Jin, Da-Qing
Xu, Jing
Guo, Yuanqiang
Song, Ziteng
Zhang, Shaojie
Zhou, Linan
Cui, Jianlin
Zhang, Jie
Ohizumi, Yasushi
Shi, Lijuan
Li, Yuhao
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  surname: Song
  fullname: Song, Ziteng
  organization: State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, People's Republic of China
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  givenname: Lijuan
  surname: Shi
  fullname: Shi, Lijuan
  organization: State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, People's Republic of China
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  surname: Zhou
  fullname: Zhou, Linan
  organization: State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, People's Republic of China
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  surname: Zhang
  fullname: Zhang, Jie
  organization: Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003, People's Republic of China
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  fullname: Cui, Jianlin
  organization: School of Medicine, Nankai University, Tianjin 300071, People's Republic of China
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  surname: Li
  fullname: Li, Yuhao
  organization: School of Medicine, Nankai University, Tianjin 300071, People's Republic of China
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  givenname: Da-Qing
  surname: Jin
  fullname: Jin, Da-Qing
  organization: School of Medicine, Nankai University, Tianjin 300071, People's Republic of China
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  givenname: Yasushi
  surname: Ohizumi
  fullname: Ohizumi, Yasushi
  organization: Kansei Fukushi Research Institute, Tohoku Fukushi University, Sendai 989-3201, Japan
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  fullname: Xu, Jing
  email: xujing611@nankai.edu.cn
  organization: State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, People's Republic of China
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  givenname: Yuanqiang
  surname: Guo
  fullname: Guo, Yuanqiang
  email: victgyq@nankai.edu.cn
  organization: State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, People's Republic of China
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ISSN 0144-8617
1879-1344
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Keywords Zebrafish
Fructan
Selenium nanoparticles
Taraxacum mongolicum Hand.-Mazz
Anti-tumor activity
Language English
License Copyright © 2021 Elsevier Ltd. All rights reserved.
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PMID 34364610
PQID 2559669159
PQPubID 23479
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crossref_primary_10_1016_j_carbpol_2021_118365
crossref_citationtrail_10_1016_j_carbpol_2021_118365
nii_cinii_1870583642719290880
elsevier_sciencedirect_doi_10_1016_j_carbpol_2021_118365
PublicationCentury 2000
PublicationDate 2021-10-15
PublicationDateYYYYMMDD 2021-10-15
PublicationDate_xml – month: 10
  year: 2021
  text: 2021-10-15
  day: 15
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Carbohydrate Polymers
PublicationTitleAlternate Carbohydr Polym
PublicationYear 2021
Publisher Elsevier Ltd
Elsevier BV
Publisher_xml – name: Elsevier Ltd
– name: Elsevier BV
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Snippet In this study, an inulin fructan (TMP50-2) with moderate anti-tumor activity was obtained from dandelion. To further improve the anti-tumor activity of...
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SubjectTerms A549 Cells
angiogenesis
Animals
Anti-tumor activity
antineoplastic activity
Antineoplastic Agents
Antineoplastic Agents - pharmacology
Apoptosis
Apoptosis - drug effects
Cell Proliferation
Cell Proliferation - drug effects
Danio rerio
dose response
Fructan
Fructans
Fructans - chemistry
Fructans - pharmacology
HeLa Cells
Hep G2 Cells
Humans
hydrogen
Hydrogen Bonding
inulin
Nanoparticles
Nanoparticles - chemistry
Neoplasms
Neoplasms - drug therapy
Neoplasms - metabolism
Neoplasms - pathology
Polysaccharides
Polysaccharides - chemistry
Polysaccharides - pharmacology
polysorbates
Selenium
Selenium - chemistry
Selenium - pharmacology
Selenium nanoparticles
Taraxacum
Taraxacum - chemistry
Taraxacum mongolicum Hand.-Mazz
Zebrafish
Title A dandelion polysaccharide and its selenium nanoparticles: Structure features and evaluation of anti-tumor activity in zebrafish models
URI https://dx.doi.org/10.1016/j.carbpol.2021.118365
https://cir.nii.ac.jp/crid/1870583642719290880
https://www.ncbi.nlm.nih.gov/pubmed/34364610
https://www.proquest.com/docview/2559669159
https://www.proquest.com/docview/2636472214
Volume 270
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