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A comparative study of the effects of gutta‐percha solvents on human osteoblasts and murine fibroblasts
We aimed to investigate the in vitro physiologic effects of xylene, chloroform, orange oil and eucalyptus oil solvents for dissolving gutta‐percha on L929 and HOB cell lines; 2.5 and 10 μL mL−1 of these solvents were tested for 24, 48 and 72 h. Gutta‐percha solvents inhibited the proliferation rate...
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Published in: | Australian endodontic journal 2021-12, Vol.47 (3), p.569-579 |
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container_title | Australian endodontic journal |
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creator | Gundogan, Gul Ipek Durmus, Sare Ozturk, Gulgun Cansu Kucukyesil, Nazmi Acar, Yasin Talat Balaban, Rumeysa Kig, Cenk |
description | We aimed to investigate the in vitro physiologic effects of xylene, chloroform, orange oil and eucalyptus oil solvents for dissolving gutta‐percha on L929 and HOB cell lines; 2.5 and 10 μL mL−1 of these solvents were tested for 24, 48 and 72 h. Gutta‐percha solvents inhibited the proliferation rate of fibroblasts in a dose‐ and time‐dependent manner; however, no inhibition was detected in HOB (evaluated using MTT assay). None of the solvents induced apoptosis/necrosis in HOB cells at ≤2.5 μL mL−1 concentration in contrast to L929 (determined using acridine orange/ethidium bromide dual staining). Each solvent tested reduced the migration rate of both L929 and HOB cell lines in a dose‐dependent manner (evaluated using a scratch assay). Gutta‐percha solvents can damage fibroblast‐rich tissues. Osteoblasts seemed to be more resistant to the tested solvents, and excessive extrusion of solvents from the root canal may also damage the periradicular tissues and reduce the ability to repair. |
doi_str_mv | 10.1111/aej.12541 |
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Gutta‐percha solvents inhibited the proliferation rate of fibroblasts in a dose‐ and time‐dependent manner; however, no inhibition was detected in HOB (evaluated using MTT assay). None of the solvents induced apoptosis/necrosis in HOB cells at ≤2.5 μL mL−1 concentration in contrast to L929 (determined using acridine orange/ethidium bromide dual staining). Each solvent tested reduced the migration rate of both L929 and HOB cell lines in a dose‐dependent manner (evaluated using a scratch assay). Gutta‐percha solvents can damage fibroblast‐rich tissues. Osteoblasts seemed to be more resistant to the tested solvents, and excessive extrusion of solvents from the root canal may also damage the periradicular tissues and reduce the ability to repair.</description><identifier>ISSN: 1329-1947</identifier><identifier>EISSN: 1747-4477</identifier><identifier>DOI: 10.1111/aej.12541</identifier><identifier>PMID: 34278656</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Acridine orange ; Animals ; Apoptosis ; cell culture ; Cell lines ; Chloroform ; Endodontics ; Essential oils ; Ethidium bromide ; fibroblast ; Fibroblasts ; Gutta-Percha ; gutta‐percha solvents ; Humans ; Mice ; osteoblast ; Osteoblasts ; Root canals ; Solvents ; Xylene</subject><ispartof>Australian endodontic journal, 2021-12, Vol.47 (3), p.569-579</ispartof><rights>2021 Australian Society of Endodontology Inc</rights><rights>2021 Australian Society of Endodontology Inc.</rights><rights>Copyright © 2021 Australian Society of Endodontology Inc</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3531-f9d4086c4d88ee1bdd8c69805bf697b0483a1296e8bb25ad77b4413c923d1e33</citedby><cites>FETCH-LOGICAL-c3531-f9d4086c4d88ee1bdd8c69805bf697b0483a1296e8bb25ad77b4413c923d1e33</cites><orcidid>0000-0002-9438-6113 ; 0000-0001-7710-7613 ; 0000-0002-1135-7967 ; 0000-0002-6318-5001 ; 0000-0001-7129-9394 ; 0000-0002-0997-7577 ; 0000-0001-9964-003X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34278656$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gundogan, Gul Ipek</creatorcontrib><creatorcontrib>Durmus, Sare</creatorcontrib><creatorcontrib>Ozturk, Gulgun Cansu</creatorcontrib><creatorcontrib>Kucukyesil, Nazmi</creatorcontrib><creatorcontrib>Acar, Yasin Talat</creatorcontrib><creatorcontrib>Balaban, Rumeysa</creatorcontrib><creatorcontrib>Kig, Cenk</creatorcontrib><title>A comparative study of the effects of gutta‐percha solvents on human osteoblasts and murine fibroblasts</title><title>Australian endodontic journal</title><addtitle>Aust Endod J</addtitle><description>We aimed to investigate the in vitro physiologic effects of xylene, chloroform, orange oil and eucalyptus oil solvents for dissolving gutta‐percha on L929 and HOB cell lines; 2.5 and 10 μL mL−1 of these solvents were tested for 24, 48 and 72 h. Gutta‐percha solvents inhibited the proliferation rate of fibroblasts in a dose‐ and time‐dependent manner; however, no inhibition was detected in HOB (evaluated using MTT assay). None of the solvents induced apoptosis/necrosis in HOB cells at ≤2.5 μL mL−1 concentration in contrast to L929 (determined using acridine orange/ethidium bromide dual staining). Each solvent tested reduced the migration rate of both L929 and HOB cell lines in a dose‐dependent manner (evaluated using a scratch assay). Gutta‐percha solvents can damage fibroblast‐rich tissues. Osteoblasts seemed to be more resistant to the tested solvents, and excessive extrusion of solvents from the root canal may also damage the periradicular tissues and reduce the ability to repair.</description><subject>Acridine orange</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>cell culture</subject><subject>Cell lines</subject><subject>Chloroform</subject><subject>Endodontics</subject><subject>Essential oils</subject><subject>Ethidium bromide</subject><subject>fibroblast</subject><subject>Fibroblasts</subject><subject>Gutta-Percha</subject><subject>gutta‐percha solvents</subject><subject>Humans</subject><subject>Mice</subject><subject>osteoblast</subject><subject>Osteoblasts</subject><subject>Root canals</subject><subject>Solvents</subject><subject>Xylene</subject><issn>1329-1947</issn><issn>1747-4477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kEtu2zAQhomgQZ24XeQCAYFu0oVs8SVKSyNwmxQBuvGe4GMUy5BEh5RceNcj5Iw9SejYySJAuRly5sM_xIfQFclnJJ25hs2MUMHJGbogksuMcyk_pTujVUYqLifoMsZNnlPOJPmMJoxTWRaiuEDNAlvfbXXQQ7MDHIfR7bGv8bAGDHUNdoiH5-M4DPrf3-ctBLvWOPp2B_1h1OP12Oke-ziAN62Oqal7h7sxND3gujHh1P6CzmvdRvh6qlO0-rFc3d5lD79_3t8uHjLLBCNZXTmel4XlriwBiHGutEVV5sLURSVNzkumCa0KKI2hQjspDeeE2YoyR4CxKbo5xm6DfxohDqprooW21T34MSoqBKNM8LRsir59QDd-DH36nKJF8soElUWivh8pG3yMAWq1DU2nw16RXB30q6RfvepP7PUpcTQduHfyzXcC5kfgT9PC_v9JarH8dYx8AeEBj8E</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>Gundogan, Gul Ipek</creator><creator>Durmus, Sare</creator><creator>Ozturk, Gulgun Cansu</creator><creator>Kucukyesil, Nazmi</creator><creator>Acar, Yasin Talat</creator><creator>Balaban, Rumeysa</creator><creator>Kig, Cenk</creator><general>Wiley Subscription Services, Inc</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>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9438-6113</orcidid><orcidid>https://orcid.org/0000-0001-7710-7613</orcidid><orcidid>https://orcid.org/0000-0002-1135-7967</orcidid><orcidid>https://orcid.org/0000-0002-6318-5001</orcidid><orcidid>https://orcid.org/0000-0001-7129-9394</orcidid><orcidid>https://orcid.org/0000-0002-0997-7577</orcidid><orcidid>https://orcid.org/0000-0001-9964-003X</orcidid></search><sort><creationdate>202112</creationdate><title>A comparative study of the effects of gutta‐percha solvents on human osteoblasts and murine fibroblasts</title><author>Gundogan, Gul Ipek ; 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Gutta‐percha solvents inhibited the proliferation rate of fibroblasts in a dose‐ and time‐dependent manner; however, no inhibition was detected in HOB (evaluated using MTT assay). None of the solvents induced apoptosis/necrosis in HOB cells at ≤2.5 μL mL−1 concentration in contrast to L929 (determined using acridine orange/ethidium bromide dual staining). Each solvent tested reduced the migration rate of both L929 and HOB cell lines in a dose‐dependent manner (evaluated using a scratch assay). Gutta‐percha solvents can damage fibroblast‐rich tissues. 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subjects | Acridine orange Animals Apoptosis cell culture Cell lines Chloroform Endodontics Essential oils Ethidium bromide fibroblast Fibroblasts Gutta-Percha gutta‐percha solvents Humans Mice osteoblast Osteoblasts Root canals Solvents Xylene |
title | A comparative study of the effects of gutta‐percha solvents on human osteoblasts and murine fibroblasts |
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