Polyphyllin D-loaded solid lipid nanoparticles for breast cancer: Synthesis, characterization, in vitro, and in vivo studies
[Display omitted] Polyphyllin D (PD), a steroidal saponin in Paris polyphylla, induces apoptosis via the intrinsic apoptotic pathway in different cancer types. However, emerging evidence has shown that the primary issue with PD is its structure's hemolysis and cytotoxicity. This study aimed to...
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Veröffentlicht in: | International journal of pharmaceutics 2023-05, Vol.639, p.122976-122976, Article 122976 |
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creator | Emami, Azadeh Ghafouri, Hossein Sariri, Reyhaneh |
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Polyphyllin D (PD), a steroidal saponin in Paris polyphylla, induces apoptosis via the intrinsic apoptotic pathway in different cancer types. However, emerging evidence has shown that the primary issue with PD is its structure's hemolysis and cytotoxicity. This study aimed to develop and optimize PD-loaded SLN formulation and evaluate its efficacy in breast cancer cell lines. Apoptosis, as the mechanism of cell death, was confirmed by flow cytometry following Annexin V/propidium iodide staining and western blot analysis. In in vivo studies, tumor inhibitory efficacy was compared with different doses of PD-loaded SLN on 4T1-implanted BALB/c mice. The half-maximal inhibitory concentration (IC50) of PD- loaded SLN was calculated to be 33.25 and 35.74 μg/mL for MCF7 and MDA-MB-231 cells, respectively. Flow cytometry analysis further confirmed a significant increase in apoptosis after treatment with PD- loaded SLN. When both cell lines were treated with PD-loaded SLN, Bcl2 and HSP70 proteins were down regulated, while Bax, Bad, P53, Apaf-1, p-p53 and Noxa proteins were upregulated. This effect was also confirmed by test performed on BALB/c mice in vivo. Based on results, PD-loaded SLN may be a promising breast cancer treatment, without recognizable side effects. |
doi_str_mv | 10.1016/j.ijpharm.2023.122976 |
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Polyphyllin D (PD), a steroidal saponin in Paris polyphylla, induces apoptosis via the intrinsic apoptotic pathway in different cancer types. However, emerging evidence has shown that the primary issue with PD is its structure's hemolysis and cytotoxicity. This study aimed to develop and optimize PD-loaded SLN formulation and evaluate its efficacy in breast cancer cell lines. Apoptosis, as the mechanism of cell death, was confirmed by flow cytometry following Annexin V/propidium iodide staining and western blot analysis. In in vivo studies, tumor inhibitory efficacy was compared with different doses of PD-loaded SLN on 4T1-implanted BALB/c mice. The half-maximal inhibitory concentration (IC50) of PD- loaded SLN was calculated to be 33.25 and 35.74 μg/mL for MCF7 and MDA-MB-231 cells, respectively. Flow cytometry analysis further confirmed a significant increase in apoptosis after treatment with PD- loaded SLN. When both cell lines were treated with PD-loaded SLN, Bcl2 and HSP70 proteins were down regulated, while Bax, Bad, P53, Apaf-1, p-p53 and Noxa proteins were upregulated. This effect was also confirmed by test performed on BALB/c mice in vivo. Based on results, PD-loaded SLN may be a promising breast cancer treatment, without recognizable side effects.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2023.122976</identifier><identifier>PMID: 37088118</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Apoptosis ; Breast cancer ; Cell Line, Tumor ; Mice ; Nanoparticles ; Neoplasms ; Polyphyllin D ; Saponins - pharmacology ; Solid lipid nanoparticles ; Tumor Suppressor Protein p53</subject><ispartof>International journal of pharmaceutics, 2023-05, Vol.639, p.122976-122976, Article 122976</ispartof><rights>2023 Elsevier B.V.</rights><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-8a3dc989f72918641aa9e3b543ce0446f91c6d48d18cfa6e4a99a4ce10f9a0e23</citedby><cites>FETCH-LOGICAL-c365t-8a3dc989f72918641aa9e3b543ce0446f91c6d48d18cfa6e4a99a4ce10f9a0e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378517323003964$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37088118$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Emami, Azadeh</creatorcontrib><creatorcontrib>Ghafouri, Hossein</creatorcontrib><creatorcontrib>Sariri, Reyhaneh</creatorcontrib><title>Polyphyllin D-loaded solid lipid nanoparticles for breast cancer: Synthesis, characterization, in vitro, and in vivo studies</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
Polyphyllin D (PD), a steroidal saponin in Paris polyphylla, induces apoptosis via the intrinsic apoptotic pathway in different cancer types. However, emerging evidence has shown that the primary issue with PD is its structure's hemolysis and cytotoxicity. This study aimed to develop and optimize PD-loaded SLN formulation and evaluate its efficacy in breast cancer cell lines. Apoptosis, as the mechanism of cell death, was confirmed by flow cytometry following Annexin V/propidium iodide staining and western blot analysis. In in vivo studies, tumor inhibitory efficacy was compared with different doses of PD-loaded SLN on 4T1-implanted BALB/c mice. The half-maximal inhibitory concentration (IC50) of PD- loaded SLN was calculated to be 33.25 and 35.74 μg/mL for MCF7 and MDA-MB-231 cells, respectively. Flow cytometry analysis further confirmed a significant increase in apoptosis after treatment with PD- loaded SLN. When both cell lines were treated with PD-loaded SLN, Bcl2 and HSP70 proteins were down regulated, while Bax, Bad, P53, Apaf-1, p-p53 and Noxa proteins were upregulated. This effect was also confirmed by test performed on BALB/c mice in vivo. Based on results, PD-loaded SLN may be a promising breast cancer treatment, without recognizable side effects.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis</subject><subject>Breast cancer</subject><subject>Cell Line, Tumor</subject><subject>Mice</subject><subject>Nanoparticles</subject><subject>Neoplasms</subject><subject>Polyphyllin D</subject><subject>Saponins - pharmacology</subject><subject>Solid lipid nanoparticles</subject><subject>Tumor Suppressor Protein p53</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEGLFDEQhYMo7uzqT1By9DA9Jp3udOJFZHVVWFBQz6EmqWYyZDptkhkY8cebpUevXqooeO9V1UfIC842nHH5er_x-3kH6bBpWSs2vG31IB-RFVeDaEQ3yMdkxcSgmp4P4opc57xnjMmWi6fkSgxMKc7Vivz-GsN53p1D8BN934QIDh3NMXhHg59rnWCKM6TibcBMx5joNiHkQi1MFtMb-u08lR1mn9fU1oPAFkz-FxQfpzWtqSdfUlxTmNwynSLN5eg85mfkyQgh4_NLvyE_7j58v_3U3H_5-Pn23X1jhexLo0A4q5Ueh1ZzJTsOoFFs-05YZF0nR82tdJ1yXNkRJHagNXQWORs1MGzFDXm15M4p_jxiLubgs8UQYMJ4zKZVrO-5rNFV2i9Sm2LOCUczJ3-AdDacmQfwZm8u4M0DeLOAr76XlxXH7QHdP9df0lXwdhFgffTkMZlsPVaCzie0xbjo_7PiD0IpmQg</recordid><startdate>20230525</startdate><enddate>20230525</enddate><creator>Emami, Azadeh</creator><creator>Ghafouri, Hossein</creator><creator>Sariri, Reyhaneh</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20230525</creationdate><title>Polyphyllin D-loaded solid lipid nanoparticles for breast cancer: Synthesis, characterization, in vitro, and in vivo studies</title><author>Emami, Azadeh ; Ghafouri, Hossein ; Sariri, Reyhaneh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-8a3dc989f72918641aa9e3b543ce0446f91c6d48d18cfa6e4a99a4ce10f9a0e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Apoptosis</topic><topic>Breast cancer</topic><topic>Cell Line, Tumor</topic><topic>Mice</topic><topic>Nanoparticles</topic><topic>Neoplasms</topic><topic>Polyphyllin D</topic><topic>Saponins - pharmacology</topic><topic>Solid lipid nanoparticles</topic><topic>Tumor Suppressor Protein p53</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Emami, Azadeh</creatorcontrib><creatorcontrib>Ghafouri, Hossein</creatorcontrib><creatorcontrib>Sariri, Reyhaneh</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Emami, Azadeh</au><au>Ghafouri, Hossein</au><au>Sariri, Reyhaneh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyphyllin D-loaded solid lipid nanoparticles for breast cancer: Synthesis, characterization, in vitro, and in vivo studies</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2023-05-25</date><risdate>2023</risdate><volume>639</volume><spage>122976</spage><epage>122976</epage><pages>122976-122976</pages><artnum>122976</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
Polyphyllin D (PD), a steroidal saponin in Paris polyphylla, induces apoptosis via the intrinsic apoptotic pathway in different cancer types. However, emerging evidence has shown that the primary issue with PD is its structure's hemolysis and cytotoxicity. This study aimed to develop and optimize PD-loaded SLN formulation and evaluate its efficacy in breast cancer cell lines. Apoptosis, as the mechanism of cell death, was confirmed by flow cytometry following Annexin V/propidium iodide staining and western blot analysis. In in vivo studies, tumor inhibitory efficacy was compared with different doses of PD-loaded SLN on 4T1-implanted BALB/c mice. The half-maximal inhibitory concentration (IC50) of PD- loaded SLN was calculated to be 33.25 and 35.74 μg/mL for MCF7 and MDA-MB-231 cells, respectively. Flow cytometry analysis further confirmed a significant increase in apoptosis after treatment with PD- loaded SLN. When both cell lines were treated with PD-loaded SLN, Bcl2 and HSP70 proteins were down regulated, while Bax, Bad, P53, Apaf-1, p-p53 and Noxa proteins were upregulated. This effect was also confirmed by test performed on BALB/c mice in vivo. Based on results, PD-loaded SLN may be a promising breast cancer treatment, without recognizable side effects.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>37088118</pmid><doi>10.1016/j.ijpharm.2023.122976</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents - pharmacology Apoptosis Breast cancer Cell Line, Tumor Mice Nanoparticles Neoplasms Polyphyllin D Saponins - pharmacology Solid lipid nanoparticles Tumor Suppressor Protein p53 |
title | Polyphyllin D-loaded solid lipid nanoparticles for breast cancer: Synthesis, characterization, in vitro, and in vivo studies |
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