Self-assembled lyotropic liquid crystal gel for osteoarthritis treatment via anti-inflammation and cartilage protection
Osteoarthritis (OA) is a chronic joint disease with occurrence of articular inflammation and cartilage degeneration. An ideal drug delivery system for effective treatment of OA should integrate inflammation alleviation with cartilage protection. Herein, a lyotropic liquid crystal (LLC) precursor co-...
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Veröffentlicht in: | Biomaterials science 2021-10, Vol.9 (21), p.7205-7218 |
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creator | Mei, Liling Wang, Hui Chen, Jintian Zhang, Ziqian Li, Feng Xie, Yecheng Huang, Ying Peng, Tingting Cheng, Guohua Pan, Xin Wu, Chuanbin |
description | Osteoarthritis (OA) is a chronic joint disease with occurrence of articular inflammation and cartilage degeneration. An ideal drug delivery system for effective treatment of OA should integrate inflammation alleviation with cartilage protection. Herein, a lyotropic liquid crystal (LLC) precursor co-loading hyaluronic acid (HA) and celecoxib, formulated as the HLC precursor, was developed for the combined therapeutic efficacy. The
in situ
gelling property of the HLC precursor effectively prolongs drug retention in the articular cavity to achieve a long-term anti-inflammation effect. Based on the rheological tests, HLC gel with a cubic lattice structure endows it with a spring-like effect to buffer joint shock and shows great potential in providing cartilage protection by resisting mechanical destruction, lubricating joint, and decomposing intensive stress (about 50%). Meanwhile, the pharmacodynamics study on the OA-induced SD rats demonstrated that HLC gel was the most effective to reduce inflammation levels and to protect the cartilage against abrasion and degeneration. Furthermore, the
in vivo
degradation behavior and the intra-articular irritation results of LLC/HLC gel demonstrated that it was biodegradable and biocompatible. These results collectively demonstrated that HLC gel with anti-inflammation and cartilage protection performance provides a useful approach to treat OA. |
doi_str_mv | 10.1039/d1bm00727k |
format | Article |
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in situ
gelling property of the HLC precursor effectively prolongs drug retention in the articular cavity to achieve a long-term anti-inflammation effect. Based on the rheological tests, HLC gel with a cubic lattice structure endows it with a spring-like effect to buffer joint shock and shows great potential in providing cartilage protection by resisting mechanical destruction, lubricating joint, and decomposing intensive stress (about 50%). Meanwhile, the pharmacodynamics study on the OA-induced SD rats demonstrated that HLC gel was the most effective to reduce inflammation levels and to protect the cartilage against abrasion and degeneration. Furthermore, the
in vivo
degradation behavior and the intra-articular irritation results of LLC/HLC gel demonstrated that it was biodegradable and biocompatible. These results collectively demonstrated that HLC gel with anti-inflammation and cartilage protection performance provides a useful approach to treat OA.</description><identifier>ISSN: 2047-4830</identifier><identifier>EISSN: 2047-4849</identifier><identifier>DOI: 10.1039/d1bm00727k</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Abrasion ; Arthritis ; Biocompatibility ; Biodegradability ; Biomedical materials ; Cartilage ; Cubic lattice ; Degeneration ; Drug delivery systems ; Hyaluronic acid ; In vivo methods and tests ; Inflammation ; Irritation ; Liquid crystals ; Osteoarthritis ; Precursors ; Rheological properties ; Self-assembly</subject><ispartof>Biomaterials science, 2021-10, Vol.9 (21), p.7205-7218</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-5e4aa135649683dbab762e68157e63ef56f7be1b046d409c154657678c120ec73</citedby><cites>FETCH-LOGICAL-c333t-5e4aa135649683dbab762e68157e63ef56f7be1b046d409c154657678c120ec73</cites><orcidid>0000-0003-1437-2780 ; 0000-0002-9685-9762 ; 0000-0003-1661-0201</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Mei, Liling</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Chen, Jintian</creatorcontrib><creatorcontrib>Zhang, Ziqian</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Xie, Yecheng</creatorcontrib><creatorcontrib>Huang, Ying</creatorcontrib><creatorcontrib>Peng, Tingting</creatorcontrib><creatorcontrib>Cheng, Guohua</creatorcontrib><creatorcontrib>Pan, Xin</creatorcontrib><creatorcontrib>Wu, Chuanbin</creatorcontrib><title>Self-assembled lyotropic liquid crystal gel for osteoarthritis treatment via anti-inflammation and cartilage protection</title><title>Biomaterials science</title><description>Osteoarthritis (OA) is a chronic joint disease with occurrence of articular inflammation and cartilage degeneration. An ideal drug delivery system for effective treatment of OA should integrate inflammation alleviation with cartilage protection. Herein, a lyotropic liquid crystal (LLC) precursor co-loading hyaluronic acid (HA) and celecoxib, formulated as the HLC precursor, was developed for the combined therapeutic efficacy. The
in situ
gelling property of the HLC precursor effectively prolongs drug retention in the articular cavity to achieve a long-term anti-inflammation effect. Based on the rheological tests, HLC gel with a cubic lattice structure endows it with a spring-like effect to buffer joint shock and shows great potential in providing cartilage protection by resisting mechanical destruction, lubricating joint, and decomposing intensive stress (about 50%). Meanwhile, the pharmacodynamics study on the OA-induced SD rats demonstrated that HLC gel was the most effective to reduce inflammation levels and to protect the cartilage against abrasion and degeneration. Furthermore, the
in vivo
degradation behavior and the intra-articular irritation results of LLC/HLC gel demonstrated that it was biodegradable and biocompatible. These results collectively demonstrated that HLC gel with anti-inflammation and cartilage protection performance provides a useful approach to treat OA.</description><subject>Abrasion</subject><subject>Arthritis</subject><subject>Biocompatibility</subject><subject>Biodegradability</subject><subject>Biomedical materials</subject><subject>Cartilage</subject><subject>Cubic lattice</subject><subject>Degeneration</subject><subject>Drug delivery systems</subject><subject>Hyaluronic acid</subject><subject>In vivo methods and tests</subject><subject>Inflammation</subject><subject>Irritation</subject><subject>Liquid crystals</subject><subject>Osteoarthritis</subject><subject>Precursors</subject><subject>Rheological properties</subject><subject>Self-assembly</subject><issn>2047-4830</issn><issn>2047-4849</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkctOwzAQRSMEElXphi-wxAYhBez4lSyhPEURC2AdOc6kuDhxa7ug_j0uRSyYzYxmju4d6WbZMcHnBNPqoiVNj7Es5MdeNiowkzkrWbX_N1N8mE1CWOBUUlZYkFH29QK2y1UI0DcWWmQ3Lnq3NBpZs1qbFmm_CVFZNAeLOueRCxGc8vHdm2gCih5U7GGI6NMopIZocjN0VvW9isYNaZMkEm6smgNaehdBbw9H2UGnbIDJbx9nb7c3r9P7fPZ89zC9nOWaUhpzDkwpQrlglShp26hGigJESbgEQaHjopMNkAYz0TJcacKZ4FLIUpMCg5Z0nJ3udJP1ag0h1r0JGqxVA7h1qAsueUklLouEnvxDF27th_RdokpeESwFTtTZjtLeheChq5fe9MpvaoLrbQz1Nbl6-onhkX4DgYd7wQ</recordid><startdate>20211026</startdate><enddate>20211026</enddate><creator>Mei, Liling</creator><creator>Wang, Hui</creator><creator>Chen, Jintian</creator><creator>Zhang, Ziqian</creator><creator>Li, Feng</creator><creator>Xie, Yecheng</creator><creator>Huang, Ying</creator><creator>Peng, Tingting</creator><creator>Cheng, Guohua</creator><creator>Pan, Xin</creator><creator>Wu, Chuanbin</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1437-2780</orcidid><orcidid>https://orcid.org/0000-0002-9685-9762</orcidid><orcidid>https://orcid.org/0000-0003-1661-0201</orcidid></search><sort><creationdate>20211026</creationdate><title>Self-assembled lyotropic liquid crystal gel for osteoarthritis treatment via anti-inflammation and cartilage protection</title><author>Mei, Liling ; 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An ideal drug delivery system for effective treatment of OA should integrate inflammation alleviation with cartilage protection. Herein, a lyotropic liquid crystal (LLC) precursor co-loading hyaluronic acid (HA) and celecoxib, formulated as the HLC precursor, was developed for the combined therapeutic efficacy. The
in situ
gelling property of the HLC precursor effectively prolongs drug retention in the articular cavity to achieve a long-term anti-inflammation effect. Based on the rheological tests, HLC gel with a cubic lattice structure endows it with a spring-like effect to buffer joint shock and shows great potential in providing cartilage protection by resisting mechanical destruction, lubricating joint, and decomposing intensive stress (about 50%). Meanwhile, the pharmacodynamics study on the OA-induced SD rats demonstrated that HLC gel was the most effective to reduce inflammation levels and to protect the cartilage against abrasion and degeneration. Furthermore, the
in vivo
degradation behavior and the intra-articular irritation results of LLC/HLC gel demonstrated that it was biodegradable and biocompatible. These results collectively demonstrated that HLC gel with anti-inflammation and cartilage protection performance provides a useful approach to treat OA.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d1bm00727k</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-1437-2780</orcidid><orcidid>https://orcid.org/0000-0002-9685-9762</orcidid><orcidid>https://orcid.org/0000-0003-1661-0201</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Abrasion Arthritis Biocompatibility Biodegradability Biomedical materials Cartilage Cubic lattice Degeneration Drug delivery systems Hyaluronic acid In vivo methods and tests Inflammation Irritation Liquid crystals Osteoarthritis Precursors Rheological properties Self-assembly |
title | Self-assembled lyotropic liquid crystal gel for osteoarthritis treatment via anti-inflammation and cartilage protection |
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