Highly penetrative liposome nanomedicine generated by a biomimetic strategy for enhanced cancer chemotherapy
Liposome nanomedicine has been successfully applied for cancer chemotherapy in patients. However, in general, the therapeutic efficacy is confined by its limited accumulation and penetration in solid tumors. Here, we established a biomimetic strategy for the preparation of highly penetrative liposom...
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Veröffentlicht in: | Biomaterials science 2018-05, Vol.6 (6), p.1546-1555 |
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creator | Jia, Yali Sheng, Zonghai Hu, Dehong Yan, Fei Zhu, Mingting Gao, Guanhui Wang, Pan Liu, Xin Wang, Xiaobing Zheng, Hairong |
description | Liposome nanomedicine has been successfully applied for cancer chemotherapy in patients. However, in general, the therapeutic efficacy is confined by its limited accumulation and penetration in solid tumors. Here, we established a biomimetic strategy for the preparation of highly penetrative liposome nanomedicine for enhanced chemotherapeutic efficacy. By applying this unique type of nanomedicine, membrane proteins on the cancer cells are used as highly penetrative targeting ligands. Biomimetic liposomes are highly stable, exhibiting a superior in vitro homologous targeting ability, and a 2.25-fold deeper penetration in 3D tumor spheroids when compared to conventional liposome nanomedicine. The fluorescence/photoacoustic dual-modal imaging approach demonstrated enhanced tumor accumulation and improved tumor penetration of the biomimetic liposome in C6 glioma tumor-bearing nude mice. Following the intravenous administration of biomimetic liposome nanomedicine, the tumor inhibition rate reached up to 93.3%, which was significantly higher when compared to that of conventional liposome nanomedicine (69.3%). Moreover, histopathological analyses demonstrated that biomimetic liposome nanomedicine has limited side effects. Therefore, these results suggested that a cancer cell membrane-based biomimetic strategy may provide a breakthrough approach for enhancing drug penetration and improving treatment efficacy, holding a great promise for further clinical studies. |
doi_str_mv | 10.1039/c8bm00256h |
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However, in general, the therapeutic efficacy is confined by its limited accumulation and penetration in solid tumors. Here, we established a biomimetic strategy for the preparation of highly penetrative liposome nanomedicine for enhanced chemotherapeutic efficacy. By applying this unique type of nanomedicine, membrane proteins on the cancer cells are used as highly penetrative targeting ligands. Biomimetic liposomes are highly stable, exhibiting a superior in vitro homologous targeting ability, and a 2.25-fold deeper penetration in 3D tumor spheroids when compared to conventional liposome nanomedicine. The fluorescence/photoacoustic dual-modal imaging approach demonstrated enhanced tumor accumulation and improved tumor penetration of the biomimetic liposome in C6 glioma tumor-bearing nude mice. Following the intravenous administration of biomimetic liposome nanomedicine, the tumor inhibition rate reached up to 93.3%, which was significantly higher when compared to that of conventional liposome nanomedicine (69.3%). Moreover, histopathological analyses demonstrated that biomimetic liposome nanomedicine has limited side effects. Therefore, these results suggested that a cancer cell membrane-based biomimetic strategy may provide a breakthrough approach for enhancing drug penetration and improving treatment efficacy, holding a great promise for further clinical studies.</description><identifier>ISSN: 2047-4830</identifier><identifier>EISSN: 2047-4849</identifier><identifier>DOI: 10.1039/c8bm00256h</identifier><identifier>PMID: 29694474</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Accumulation ; Animals ; Antibiotics, Antineoplastic - administration & dosage ; Antibiotics, Antineoplastic - pharmacokinetics ; Antibiotics, Antineoplastic - therapeutic use ; Biomimetic Materials - metabolism ; Biomimetics ; Cancer ; Cell Line, Tumor ; Chemotherapy ; Doxorubicin - administration & dosage ; Doxorubicin - pharmacokinetics ; Doxorubicin - therapeutic use ; Effectiveness ; Fluorescence ; Glioma - drug therapy ; Glioma - pathology ; Homology ; Humans ; Liposomes ; Liposomes - metabolism ; Mice, Inbred BALB C ; Mice, Nude ; Nanomedicine ; Penetration ; Proteins ; Side effects ; Spheroids ; Strategy ; Tumors</subject><ispartof>Biomaterials science, 2018-05, Vol.6 (6), p.1546-1555</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-5187b1c776fdb902187e6a2cd4b719b493fb34c3069518423c6b45af7ad2a9083</citedby><cites>FETCH-LOGICAL-c315t-5187b1c776fdb902187e6a2cd4b719b493fb34c3069518423c6b45af7ad2a9083</cites><orcidid>0000-0003-3569-3938 ; 0000-0001-5868-8037</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29694474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jia, Yali</creatorcontrib><creatorcontrib>Sheng, Zonghai</creatorcontrib><creatorcontrib>Hu, Dehong</creatorcontrib><creatorcontrib>Yan, Fei</creatorcontrib><creatorcontrib>Zhu, Mingting</creatorcontrib><creatorcontrib>Gao, Guanhui</creatorcontrib><creatorcontrib>Wang, Pan</creatorcontrib><creatorcontrib>Liu, Xin</creatorcontrib><creatorcontrib>Wang, Xiaobing</creatorcontrib><creatorcontrib>Zheng, Hairong</creatorcontrib><title>Highly penetrative liposome nanomedicine generated by a biomimetic strategy for enhanced cancer chemotherapy</title><title>Biomaterials science</title><addtitle>Biomater Sci</addtitle><description>Liposome nanomedicine has been successfully applied for cancer chemotherapy in patients. However, in general, the therapeutic efficacy is confined by its limited accumulation and penetration in solid tumors. Here, we established a biomimetic strategy for the preparation of highly penetrative liposome nanomedicine for enhanced chemotherapeutic efficacy. By applying this unique type of nanomedicine, membrane proteins on the cancer cells are used as highly penetrative targeting ligands. Biomimetic liposomes are highly stable, exhibiting a superior in vitro homologous targeting ability, and a 2.25-fold deeper penetration in 3D tumor spheroids when compared to conventional liposome nanomedicine. The fluorescence/photoacoustic dual-modal imaging approach demonstrated enhanced tumor accumulation and improved tumor penetration of the biomimetic liposome in C6 glioma tumor-bearing nude mice. Following the intravenous administration of biomimetic liposome nanomedicine, the tumor inhibition rate reached up to 93.3%, which was significantly higher when compared to that of conventional liposome nanomedicine (69.3%). Moreover, histopathological analyses demonstrated that biomimetic liposome nanomedicine has limited side effects. Therefore, these results suggested that a cancer cell membrane-based biomimetic strategy may provide a breakthrough approach for enhancing drug penetration and improving treatment efficacy, holding a great promise for further clinical studies.</description><subject>Accumulation</subject><subject>Animals</subject><subject>Antibiotics, Antineoplastic - administration & dosage</subject><subject>Antibiotics, Antineoplastic - pharmacokinetics</subject><subject>Antibiotics, Antineoplastic - therapeutic use</subject><subject>Biomimetic Materials - metabolism</subject><subject>Biomimetics</subject><subject>Cancer</subject><subject>Cell Line, Tumor</subject><subject>Chemotherapy</subject><subject>Doxorubicin - administration & dosage</subject><subject>Doxorubicin - pharmacokinetics</subject><subject>Doxorubicin - therapeutic use</subject><subject>Effectiveness</subject><subject>Fluorescence</subject><subject>Glioma - drug therapy</subject><subject>Glioma - pathology</subject><subject>Homology</subject><subject>Humans</subject><subject>Liposomes</subject><subject>Liposomes - metabolism</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Nanomedicine</subject><subject>Penetration</subject><subject>Proteins</subject><subject>Side effects</subject><subject>Spheroids</subject><subject>Strategy</subject><subject>Tumors</subject><issn>2047-4830</issn><issn>2047-4849</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kFFLwzAQx4Mobsy9-AEk4JtQTZo0aR51qBMmvuhzSdJ0zWibmrRCv72Zm7uX_x387g5-AFxjdI8REQ86Vy1CacbqMzBPEeUJzak4P_UEzcAyhB2KxblADF-CWSqYoJTTOWjWdls3E-xNZwYvB_tjYGN7F1xrYCe7GKXVtjNwG4kImBKqCUqorGttawarYdgvmu0EK-eh6WrZ6UjpfXioa9O6oY6r_XQFLirZBLM85gJ8vTx_rtbJ5uP1bfW4STTB2ZBkOOcKa85ZVSqB0jgaJlNdUsWxUFSQShGqCWIiojQlmimayYrLMpUC5WQBbg93e---RxOGYudG38WXRbTCCBWY40jdHSjtXQjeVEXvbSv9VGBU7N0Wq_zp_c_tOsI3x5OjikpO6L9J8gvF7HUV</recordid><startdate>20180529</startdate><enddate>20180529</enddate><creator>Jia, Yali</creator><creator>Sheng, Zonghai</creator><creator>Hu, Dehong</creator><creator>Yan, Fei</creator><creator>Zhu, Mingting</creator><creator>Gao, Guanhui</creator><creator>Wang, Pan</creator><creator>Liu, Xin</creator><creator>Wang, Xiaobing</creator><creator>Zheng, Hairong</creator><general>Royal Society of Chemistry</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>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0003-3569-3938</orcidid><orcidid>https://orcid.org/0000-0001-5868-8037</orcidid></search><sort><creationdate>20180529</creationdate><title>Highly penetrative liposome nanomedicine generated by a biomimetic strategy for enhanced cancer chemotherapy</title><author>Jia, Yali ; Sheng, Zonghai ; Hu, Dehong ; Yan, Fei ; Zhu, Mingting ; Gao, Guanhui ; Wang, Pan ; Liu, Xin ; Wang, Xiaobing ; Zheng, Hairong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-5187b1c776fdb902187e6a2cd4b719b493fb34c3069518423c6b45af7ad2a9083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Accumulation</topic><topic>Animals</topic><topic>Antibiotics, Antineoplastic - administration & dosage</topic><topic>Antibiotics, Antineoplastic - pharmacokinetics</topic><topic>Antibiotics, Antineoplastic - therapeutic use</topic><topic>Biomimetic Materials - metabolism</topic><topic>Biomimetics</topic><topic>Cancer</topic><topic>Cell Line, Tumor</topic><topic>Chemotherapy</topic><topic>Doxorubicin - administration & dosage</topic><topic>Doxorubicin - pharmacokinetics</topic><topic>Doxorubicin - therapeutic use</topic><topic>Effectiveness</topic><topic>Fluorescence</topic><topic>Glioma - drug therapy</topic><topic>Glioma - pathology</topic><topic>Homology</topic><topic>Humans</topic><topic>Liposomes</topic><topic>Liposomes - metabolism</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Nanomedicine</topic><topic>Penetration</topic><topic>Proteins</topic><topic>Side effects</topic><topic>Spheroids</topic><topic>Strategy</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jia, Yali</creatorcontrib><creatorcontrib>Sheng, Zonghai</creatorcontrib><creatorcontrib>Hu, Dehong</creatorcontrib><creatorcontrib>Yan, Fei</creatorcontrib><creatorcontrib>Zhu, Mingting</creatorcontrib><creatorcontrib>Gao, Guanhui</creatorcontrib><creatorcontrib>Wang, Pan</creatorcontrib><creatorcontrib>Liu, Xin</creatorcontrib><creatorcontrib>Wang, Xiaobing</creatorcontrib><creatorcontrib>Zheng, Hairong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Biomaterials science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jia, Yali</au><au>Sheng, Zonghai</au><au>Hu, Dehong</au><au>Yan, Fei</au><au>Zhu, Mingting</au><au>Gao, Guanhui</au><au>Wang, Pan</au><au>Liu, Xin</au><au>Wang, Xiaobing</au><au>Zheng, Hairong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly penetrative liposome nanomedicine generated by a biomimetic strategy for enhanced cancer chemotherapy</atitle><jtitle>Biomaterials science</jtitle><addtitle>Biomater Sci</addtitle><date>2018-05-29</date><risdate>2018</risdate><volume>6</volume><issue>6</issue><spage>1546</spage><epage>1555</epage><pages>1546-1555</pages><issn>2047-4830</issn><eissn>2047-4849</eissn><abstract>Liposome nanomedicine has been successfully applied for cancer chemotherapy in patients. However, in general, the therapeutic efficacy is confined by its limited accumulation and penetration in solid tumors. Here, we established a biomimetic strategy for the preparation of highly penetrative liposome nanomedicine for enhanced chemotherapeutic efficacy. By applying this unique type of nanomedicine, membrane proteins on the cancer cells are used as highly penetrative targeting ligands. Biomimetic liposomes are highly stable, exhibiting a superior in vitro homologous targeting ability, and a 2.25-fold deeper penetration in 3D tumor spheroids when compared to conventional liposome nanomedicine. The fluorescence/photoacoustic dual-modal imaging approach demonstrated enhanced tumor accumulation and improved tumor penetration of the biomimetic liposome in C6 glioma tumor-bearing nude mice. Following the intravenous administration of biomimetic liposome nanomedicine, the tumor inhibition rate reached up to 93.3%, which was significantly higher when compared to that of conventional liposome nanomedicine (69.3%). Moreover, histopathological analyses demonstrated that biomimetic liposome nanomedicine has limited side effects. Therefore, these results suggested that a cancer cell membrane-based biomimetic strategy may provide a breakthrough approach for enhancing drug penetration and improving treatment efficacy, holding a great promise for further clinical studies.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>29694474</pmid><doi>10.1039/c8bm00256h</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3569-3938</orcidid><orcidid>https://orcid.org/0000-0001-5868-8037</orcidid></addata></record> |
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subjects | Accumulation Animals Antibiotics, Antineoplastic - administration & dosage Antibiotics, Antineoplastic - pharmacokinetics Antibiotics, Antineoplastic - therapeutic use Biomimetic Materials - metabolism Biomimetics Cancer Cell Line, Tumor Chemotherapy Doxorubicin - administration & dosage Doxorubicin - pharmacokinetics Doxorubicin - therapeutic use Effectiveness Fluorescence Glioma - drug therapy Glioma - pathology Homology Humans Liposomes Liposomes - metabolism Mice, Inbred BALB C Mice, Nude Nanomedicine Penetration Proteins Side effects Spheroids Strategy Tumors |
title | Highly penetrative liposome nanomedicine generated by a biomimetic strategy for enhanced cancer chemotherapy |
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