Design and development of spirulina polysaccharide-loaded nanoemulsions with improved the antitumor effects of paclitaxel / Manling Du, Zhenjiang Yang, Wenping Lu, Bingyue Wang, Qi Wang, Zhen Chen, Lianyu Chen, Shuyan Han, Tiange Cai, Yu Cai
Abstract Aims: In this study, we prepared spirulina polysaccharides into spirulina polysaccharide-loaded nanoemulsions (SPS-NEs), and determined the antitumor effect of SPS-NEs, when combined with paclitaxel (PTX). Methods: SPS-NEs were prepared by a phase transformation method. The Characterisation and stability of SPS-NEs was measured. The antitumor effect of SPS-NEs combined with PTX was determined by S180 cells or RAW 264.7 macrophages and S180 tumour-bearing mice. Results: SPS-NEs were spherical and stable, the particle size of SPS-NEs was 84.6 ± 3.31 nm, PDI = 0.235 ± 0.02. PTX + SPS-NEs exhibited a much greater toxicity against RAW 264.7 cells than PTX. PTX + SPS-NEs increased the release of NO, IL-6 and TNF-α, and the expression of p-p65 NF-κB, p-I-κB, TLR4. In addition, PTX + SPS-NEs significantly inhibited tumour growth by 72.82% and increased the secretion of serum IL-2, TNF-α and IFN-γ. Conclusions: SPS-NEs can regulate immunity through TLR4/NF-κB signalling pathways, which enhances the anti-tumour effect of PTX.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2020 |
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Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:37 |
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Enthalten in: |
Journal of microencapsulation - 37(2020), 6, Seite 403-412 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Du, Manling [VerfasserIn] |
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Links: |
FID Access [lizenzpflichtig] |
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Themen: |
Nanoemulsions |
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Umfang: |
1 Online-Ressource (10 p) |
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doi: |
10.1080/02652048.2020.1767224 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
KFL011204168 |
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520 | |a Abstract Aims: In this study, we prepared spirulina polysaccharides into spirulina polysaccharide-loaded nanoemulsions (SPS-NEs), and determined the antitumor effect of SPS-NEs, when combined with paclitaxel (PTX). Methods: SPS-NEs were prepared by a phase transformation method. The Characterisation and stability of SPS-NEs was measured. The antitumor effect of SPS-NEs combined with PTX was determined by S180 cells or RAW 264.7 macrophages and S180 tumour-bearing mice. Results: SPS-NEs were spherical and stable, the particle size of SPS-NEs was 84.6 ± 3.31 nm, PDI = 0.235 ± 0.02. PTX + SPS-NEs exhibited a much greater toxicity against RAW 264.7 cells than PTX. PTX + SPS-NEs increased the release of NO, IL-6 and TNF-α, and the expression of p-p65 NF-κB, p-I-κB, TLR4. In addition, PTX + SPS-NEs significantly inhibited tumour growth by 72.82% and increased the secretion of serum IL-2, TNF-α and IFN-γ. Conclusions: SPS-NEs can regulate immunity through TLR4/NF-κB signalling pathways, which enhances the anti-tumour effect of PTX | ||
653 | |a Spirulina polysaccharide | ||
653 | |a nanoemulsions | ||
653 | |a paclitaxel | ||
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700 | 1 | |a Wang, Qi |e verfasserin |4 aut | |
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700 | 1 | |a Chen, Lianyu |e verfasserin |4 aut | |
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700 | 1 | |a Cai, Yu |e verfasserin |4 aut | |
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