Biocompatible Solutions: Evaluating the Safety of Repeated Intra-Articular Injections of pMPCylated Liposomes for Knee Osteoarthritis Therapy in Rat Models
Knee osteoarthritis (OA) poses a significant health care burden globally, necessitating innovative therapeutic approaches. CCoat, a novel poly(2-[methacryloyloxy]ethyl phosphorylcholine) (pMPC)ylated liposome device, protects the cartilage surface of the joint from mechanical wear through an entropy...
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description | Knee osteoarthritis (OA) poses a significant health care burden globally, necessitating innovative therapeutic approaches. CCoat, a novel poly(2-[methacryloyloxy]ethyl phosphorylcholine) (pMPC)ylated liposome device, protects the cartilage surface of the joint from mechanical wear through an entropy-favored process. Two preclinical studies were performed to explore the safety of CCoat following repeated intra-articular (IA) injections into the knee joint (i.e., femorotibial joint) in Sprague-Dawley rats. The studies involved 2 or 3 IA injections, at an interval of 2 or 3 weeks, and an observation period of 1 or 13 weeks after the last injection. Assessments included clinical, histopathological, and immunofluorescent evaluations. In study 1, no mortality or abnormal clinical signs occurred. At 1 week post last injection, histopathology revealed minimal vacuolated macrophages beneath the synovial membrane, predominantly M2-like, indicating a nonadverse response. Immunofluorescent staining supported M2-like macrophage predominance. Study 2 confirmed these findings with no systemic effects over 13 weeks. Statistical analyses indicated no significant differences in body weight, clinical pathology, or organ weights compared with controls. Results affirming the safety of pMPCylated liposomes following repeated IA injections in rat. This novel lubricant coating approach shows promise in OA therapy, with this safety assessment supporting its potential clinical application. |
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CCoat, a novel poly(2-[methacryloyloxy]ethyl phosphorylcholine) (pMPC)ylated liposome device, protects the cartilage surface of the joint from mechanical wear through an entropy-favored process. Two preclinical studies were performed to explore the safety of CCoat following repeated intra-articular (IA) injections into the knee joint (i.e., femorotibial joint) in Sprague-Dawley rats. The studies involved 2 or 3 IA injections, at an interval of 2 or 3 weeks, and an observation period of 1 or 13 weeks after the last injection. Assessments included clinical, histopathological, and immunofluorescent evaluations. In study 1, no mortality or abnormal clinical signs occurred. At 1 week post last injection, histopathology revealed minimal vacuolated macrophages beneath the synovial membrane, predominantly M2-like, indicating a nonadverse response. Immunofluorescent staining supported M2-like macrophage predominance. Study 2 confirmed these findings with no systemic effects over 13 weeks. Statistical analyses indicated no significant differences in body weight, clinical pathology, or organ weights compared with controls. Results affirming the safety of pMPCylated liposomes following repeated IA injections in rat. 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CCoat, a novel poly(2-[methacryloyloxy]ethyl phosphorylcholine) (pMPC)ylated liposome device, protects the cartilage surface of the joint from mechanical wear through an entropy-favored process. Two preclinical studies were performed to explore the safety of CCoat following repeated intra-articular (IA) injections into the knee joint (i.e., femorotibial joint) in Sprague-Dawley rats. The studies involved 2 or 3 IA injections, at an interval of 2 or 3 weeks, and an observation period of 1 or 13 weeks after the last injection. Assessments included clinical, histopathological, and immunofluorescent evaluations. In study 1, no mortality or abnormal clinical signs occurred. At 1 week post last injection, histopathology revealed minimal vacuolated macrophages beneath the synovial membrane, predominantly M2-like, indicating a nonadverse response. Immunofluorescent staining supported M2-like macrophage predominance. Study 2 confirmed these findings with no systemic effects over 13 weeks. Statistical analyses indicated no significant differences in body weight, clinical pathology, or organ weights compared with controls. Results affirming the safety of pMPCylated liposomes following repeated IA injections in rat. This novel lubricant coating approach shows promise in OA therapy, with this safety assessment supporting its potential clinical application.</description><subject>Animals</subject><subject>Biocompatible Materials - chemistry</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Injections, Intra-Articular</subject><subject>Knee Joint - drug effects</subject><subject>Knee Joint - pathology</subject><subject>Liposomes</subject><subject>Male</subject><subject>Original</subject><subject>Osteoarthritis, Knee - drug therapy</subject><subject>Phosphorylcholine - administration & dosage</subject><subject>Phosphorylcholine - analogs & derivatives</subject><subject>Phosphorylcholine - toxicity</subject><subject>Polymethacrylic Acids - administration & dosage</subject><subject>Polymethacrylic Acids - chemistry</subject><subject>Polymethacrylic Acids - toxicity</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0192-6233</issn><issn>1533-1601</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>EIF</sourceid><recordid>eNp9kctu1DAYhS0EokPhAdggL9mk-BLHMRtURqVUTFVUytpynD8zHnni1HYqzbPwsk06pQIhIS8s-3zn-HIQekvJCaVSfiBUsYpxzkrKJC0JeYYWVHBe0IrQ52gx68UMHKFXKW0JofVEvURHXFHFpawX6NdnF2zYDSa7xgP-EfyYXejTR3x2Z_w4bfdrnDeTYjrIexw6fA0DmAwtvuhzNMVpzM6O3sRpvQX74J6x4fL7cu8fwJUbQgo7SLgLEX_rAfBVyhBMzJvoskv4ZgPRDHvsenxtMr4MLfj0Gr3ojE_w5nE-Rj-_nN0svxarq_OL5emqsJzRXDQMeN2ITvBaWEbBqooxxk1FZMOVMkRSWfFG1AqEkiVtjbLGsFrUoi0rI_gx-nTIHcZmB62F-V1eD9HtTNzrYJz-W-ndRq_Dnaa0nAafE94_JsRwO0LKeueSBe9ND2FMmhMla8FkVU0oPaA2hpQidE_nUKLnVvU_rU6ed39e8Mnxu8YJODkAyaxBb8MY--nD_pN4D2SNrMI</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Ramot, Yuval</creator><creator>Kronfeld, Noam</creator><creator>Steiner, Michal</creator><creator>Lee, Eric D.</creator><creator>Goldberg, Ronit</creator><creator>Jahn, Sabrina</creator><creator>Nyska, Abraham</creator><general>SAGE Publications</general><scope>AFRWT</scope><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><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8606-8385</orcidid><orcidid>https://orcid.org/0000-0002-7847-2513</orcidid></search><sort><creationdate>202407</creationdate><title>Biocompatible Solutions: Evaluating the Safety of Repeated Intra-Articular Injections of pMPCylated Liposomes for Knee Osteoarthritis Therapy in Rat Models</title><author>Ramot, Yuval ; Kronfeld, Noam ; Steiner, Michal ; Lee, Eric D. ; Goldberg, Ronit ; Jahn, Sabrina ; Nyska, Abraham</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-b2e38b5f5385c21ec962223a607b399a071763b589e59741da9caa28585d46a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Biocompatible Materials - chemistry</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Injections, Intra-Articular</topic><topic>Knee Joint - drug effects</topic><topic>Knee Joint - pathology</topic><topic>Liposomes</topic><topic>Male</topic><topic>Original</topic><topic>Osteoarthritis, Knee - drug therapy</topic><topic>Phosphorylcholine - administration & dosage</topic><topic>Phosphorylcholine - analogs & derivatives</topic><topic>Phosphorylcholine - toxicity</topic><topic>Polymethacrylic Acids - administration & dosage</topic><topic>Polymethacrylic Acids - chemistry</topic><topic>Polymethacrylic Acids - toxicity</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramot, Yuval</creatorcontrib><creatorcontrib>Kronfeld, Noam</creatorcontrib><creatorcontrib>Steiner, Michal</creatorcontrib><creatorcontrib>Lee, Eric D.</creatorcontrib><creatorcontrib>Goldberg, Ronit</creatorcontrib><creatorcontrib>Jahn, Sabrina</creatorcontrib><creatorcontrib>Nyska, Abraham</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramot, Yuval</au><au>Kronfeld, Noam</au><au>Steiner, Michal</au><au>Lee, Eric D.</au><au>Goldberg, Ronit</au><au>Jahn, Sabrina</au><au>Nyska, Abraham</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biocompatible Solutions: Evaluating the Safety of Repeated Intra-Articular Injections of pMPCylated Liposomes for Knee Osteoarthritis Therapy in Rat Models</atitle><jtitle>Toxicologic pathology</jtitle><addtitle>Toxicol Pathol</addtitle><date>2024-07</date><risdate>2024</risdate><volume>52</volume><issue>5</issue><spage>266</spage><epage>283</epage><pages>266-283</pages><issn>0192-6233</issn><issn>1533-1601</issn><eissn>1533-1601</eissn><abstract>Knee osteoarthritis (OA) poses a significant health care burden globally, necessitating innovative therapeutic approaches. CCoat, a novel poly(2-[methacryloyloxy]ethyl phosphorylcholine) (pMPC)ylated liposome device, protects the cartilage surface of the joint from mechanical wear through an entropy-favored process. Two preclinical studies were performed to explore the safety of CCoat following repeated intra-articular (IA) injections into the knee joint (i.e., femorotibial joint) in Sprague-Dawley rats. The studies involved 2 or 3 IA injections, at an interval of 2 or 3 weeks, and an observation period of 1 or 13 weeks after the last injection. Assessments included clinical, histopathological, and immunofluorescent evaluations. In study 1, no mortality or abnormal clinical signs occurred. At 1 week post last injection, histopathology revealed minimal vacuolated macrophages beneath the synovial membrane, predominantly M2-like, indicating a nonadverse response. Immunofluorescent staining supported M2-like macrophage predominance. Study 2 confirmed these findings with no systemic effects over 13 weeks. 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subjects | Animals Biocompatible Materials - chemistry Disease Models, Animal Female Injections, Intra-Articular Knee Joint - drug effects Knee Joint - pathology Liposomes Male Original Osteoarthritis, Knee - drug therapy Phosphorylcholine - administration & dosage Phosphorylcholine - analogs & derivatives Phosphorylcholine - toxicity Polymethacrylic Acids - administration & dosage Polymethacrylic Acids - chemistry Polymethacrylic Acids - toxicity Rats Rats, Sprague-Dawley |
title | Biocompatible Solutions: Evaluating the Safety of Repeated Intra-Articular Injections of pMPCylated Liposomes for Knee Osteoarthritis Therapy in Rat Models |
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