Preparation and Rheological Properties of Cross-linked Liposomes Using Hydroxypropylmethylcellulose Bearing a Hydrophobic Anchor
Hydrophobically-modified hydroxypropylmethylcellulose (HM-HPMC) is a thickener with a long hydrophobic alkyl side chain. In this study, we investigated the gelation ability and rheological properties of a liposome/HM-HPMC mixed solution. The liposome suspension and the HM-HPMC aqueous solution each...
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Veröffentlicht in: | YAKUGAKU ZASSHI 2020/03/01, Vol.140(3), pp.435-441 |
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description | Hydrophobically-modified hydroxypropylmethylcellulose (HM-HPMC) is a thickener with a long hydrophobic alkyl side chain. In this study, we investigated the gelation ability and rheological properties of a liposome/HM-HPMC mixed solution. The liposome suspension and the HM-HPMC aqueous solution each had low viscosities, but the viscosity increased rapidly when they were mixed. This is thought to be due to the formation of a 3D network structure caused by the hydrophobic group of HM-HPMC penetrating into the liposomal bilayer membrane, crosslinking the liposomes together. This hypothesis was supported by the fact that gelation did not occur when hydroxypropylmethylcellulose without a hydrophobic group was used. The viscosity of the liposome/HM-HPMC mixed solution decreased rapidly when a shear was applied, but immediately returned to the original gel state when the shear was removed, indicating a reversible reaction. When a strong shear is applied, the hydrophobic group of HM-HPMC detaches from the liposome. When the shear is removed, the liposome is again cross-linked by HM-HPMC. From these results, it was revealed that liposome cross-linked gels can be prepared when HM-HPMC is used. |
doi_str_mv | 10.1248/yakushi.19-00235 |
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In this study, we investigated the gelation ability and rheological properties of a liposome/HM-HPMC mixed solution. The liposome suspension and the HM-HPMC aqueous solution each had low viscosities, but the viscosity increased rapidly when they were mixed. This is thought to be due to the formation of a 3D network structure caused by the hydrophobic group of HM-HPMC penetrating into the liposomal bilayer membrane, crosslinking the liposomes together. This hypothesis was supported by the fact that gelation did not occur when hydroxypropylmethylcellulose without a hydrophobic group was used. The viscosity of the liposome/HM-HPMC mixed solution decreased rapidly when a shear was applied, but immediately returned to the original gel state when the shear was removed, indicating a reversible reaction. When a strong shear is applied, the hydrophobic group of HM-HPMC detaches from the liposome. When the shear is removed, the liposome is again cross-linked by HM-HPMC. From these results, it was revealed that liposome cross-linked gels can be prepared when HM-HPMC is used.</description><identifier>ISSN: 0031-6903</identifier><identifier>EISSN: 1347-5231</identifier><identifier>DOI: 10.1248/yakushi.19-00235</identifier><identifier>PMID: 32115566</identifier><language>jpn</language><publisher>TOKYO: The Pharmaceutical Society of Japan</publisher><subject>crosslink ; hydrogel ; hydrophobically-modified hydroxypropylmethylcellulose ; Life Sciences & Biomedicine ; liposome ; Pharmacology & Pharmacy ; rheology ; Science & Technology ; small angle X-ray scattering</subject><ispartof>YAKUGAKU ZASSHI, 2020/03/01, Vol.140(3), pp.435-441</ispartof><rights>2020 The Pharmaceutical Society of Japan</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>5</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000517669700017</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c406t-34b6e17c2fff0d0152d1a0106e069bb4ff3ce1b0355c63816b190b51d3b623b33</citedby><cites>FETCH-LOGICAL-c406t-34b6e17c2fff0d0152d1a0106e069bb4ff3ce1b0355c63816b190b51d3b623b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1884,27928,27929,28252</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32115566$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hashizaki, Kaname</creatorcontrib><creatorcontrib>Umeda, Risa</creatorcontrib><creatorcontrib>Miura, Motofumi</creatorcontrib><creatorcontrib>Taguchi, Hiroyuki</creatorcontrib><creatorcontrib>Fujii, Makiko</creatorcontrib><title>Preparation and Rheological Properties of Cross-linked Liposomes Using Hydroxypropylmethylcellulose Bearing a Hydrophobic Anchor</title><title>YAKUGAKU ZASSHI</title><addtitle>YAKUGAKU ZASSHI</addtitle><addtitle>YAKUGAKU ZASSHI</addtitle><description>Hydrophobically-modified hydroxypropylmethylcellulose (HM-HPMC) is a thickener with a long hydrophobic alkyl side chain. In this study, we investigated the gelation ability and rheological properties of a liposome/HM-HPMC mixed solution. The liposome suspension and the HM-HPMC aqueous solution each had low viscosities, but the viscosity increased rapidly when they were mixed. This is thought to be due to the formation of a 3D network structure caused by the hydrophobic group of HM-HPMC penetrating into the liposomal bilayer membrane, crosslinking the liposomes together. This hypothesis was supported by the fact that gelation did not occur when hydroxypropylmethylcellulose without a hydrophobic group was used. The viscosity of the liposome/HM-HPMC mixed solution decreased rapidly when a shear was applied, but immediately returned to the original gel state when the shear was removed, indicating a reversible reaction. When a strong shear is applied, the hydrophobic group of HM-HPMC detaches from the liposome. When the shear is removed, the liposome is again cross-linked by HM-HPMC. From these results, it was revealed that liposome cross-linked gels can be prepared when HM-HPMC is used.</description><subject>crosslink</subject><subject>hydrogel</subject><subject>hydrophobically-modified hydroxypropylmethylcellulose</subject><subject>Life Sciences & Biomedicine</subject><subject>liposome</subject><subject>Pharmacology & Pharmacy</subject><subject>rheology</subject><subject>Science & Technology</subject><subject>small angle X-ray scattering</subject><issn>0031-6903</issn><issn>1347-5231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><recordid>eNqNkUFv1DAQhS0EoqvSOyeUIxJK8cSJkxxLBF2klagQPUe2M9mYOnGwE5Xc-On1brbbKz7YI_l7ozdvCHkP9BqStPi8iIfZd_oaypjShGWvyAZYmsdZwuA12VDKIOYlZRfkynstAxNOBsVbcsESgCzjfEP-3TkchROTtkMkhib62aE1dq-VMNGdsyO6SaOPbBtVznofGz08YBPt9Gi97cPPvdfDPtoujbN_lzEoFtPj1C1GoTGzsR6jLyjcARIrNnZWahXdDKqz7h150wrj8er0XpL7b19_Vdt49-P2e3Wzi1VK-RSzVHKEXCVt29KGQpY0IChQjpSXUqZtyxSCpCzLFGcFcAkllRk0TPKEScYuyce1b7D4Z0Y_1b32B4tiQDv7OmG8LPIiKXlA6Yqqw8QO23p0uhduqYHWh-jrU_Q1lPUx-iD5cOo-yx6bs-A56AB8WoFHlLb1SuOg8IxRSjPIOS_zUEEe6OL_6UpPx_VVdh6mIN2u0t9-EvsXkQh7VAZfrKe0Zsf7eYgzojrhahzYEz9CvkU</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Hashizaki, Kaname</creator><creator>Umeda, Risa</creator><creator>Miura, Motofumi</creator><creator>Taguchi, Hiroyuki</creator><creator>Fujii, Makiko</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Soc Japan</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200301</creationdate><title>Preparation and Rheological Properties of Cross-linked Liposomes Using Hydroxypropylmethylcellulose Bearing a Hydrophobic Anchor</title><author>Hashizaki, Kaname ; Umeda, Risa ; Miura, Motofumi ; Taguchi, Hiroyuki ; Fujii, Makiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-34b6e17c2fff0d0152d1a0106e069bb4ff3ce1b0355c63816b190b51d3b623b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>2020</creationdate><topic>crosslink</topic><topic>hydrogel</topic><topic>hydrophobically-modified hydroxypropylmethylcellulose</topic><topic>Life Sciences & Biomedicine</topic><topic>liposome</topic><topic>Pharmacology & Pharmacy</topic><topic>rheology</topic><topic>Science & Technology</topic><topic>small angle X-ray scattering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashizaki, Kaname</creatorcontrib><creatorcontrib>Umeda, Risa</creatorcontrib><creatorcontrib>Miura, Motofumi</creatorcontrib><creatorcontrib>Taguchi, Hiroyuki</creatorcontrib><creatorcontrib>Fujii, Makiko</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>YAKUGAKU ZASSHI</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashizaki, Kaname</au><au>Umeda, Risa</au><au>Miura, Motofumi</au><au>Taguchi, Hiroyuki</au><au>Fujii, Makiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and Rheological Properties of Cross-linked Liposomes Using Hydroxypropylmethylcellulose Bearing a Hydrophobic Anchor</atitle><jtitle>YAKUGAKU ZASSHI</jtitle><stitle>YAKUGAKU ZASSHI</stitle><addtitle>YAKUGAKU ZASSHI</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>140</volume><issue>3</issue><spage>435</spage><epage>441</epage><pages>435-441</pages><issn>0031-6903</issn><eissn>1347-5231</eissn><abstract>Hydrophobically-modified hydroxypropylmethylcellulose (HM-HPMC) is a thickener with a long hydrophobic alkyl side chain. In this study, we investigated the gelation ability and rheological properties of a liposome/HM-HPMC mixed solution. The liposome suspension and the HM-HPMC aqueous solution each had low viscosities, but the viscosity increased rapidly when they were mixed. This is thought to be due to the formation of a 3D network structure caused by the hydrophobic group of HM-HPMC penetrating into the liposomal bilayer membrane, crosslinking the liposomes together. This hypothesis was supported by the fact that gelation did not occur when hydroxypropylmethylcellulose without a hydrophobic group was used. The viscosity of the liposome/HM-HPMC mixed solution decreased rapidly when a shear was applied, but immediately returned to the original gel state when the shear was removed, indicating a reversible reaction. When a strong shear is applied, the hydrophobic group of HM-HPMC detaches from the liposome. When the shear is removed, the liposome is again cross-linked by HM-HPMC. From these results, it was revealed that liposome cross-linked gels can be prepared when HM-HPMC is used.</abstract><cop>TOKYO</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>32115566</pmid><doi>10.1248/yakushi.19-00235</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | crosslink hydrogel hydrophobically-modified hydroxypropylmethylcellulose Life Sciences & Biomedicine liposome Pharmacology & Pharmacy rheology Science & Technology small angle X-ray scattering |
title | Preparation and Rheological Properties of Cross-linked Liposomes Using Hydroxypropylmethylcellulose Bearing a Hydrophobic Anchor |
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