Loading…
Therapeutic effect of oxidized bletilla striata polysaccharide-natamycin eye drops on fungal keratitis
Fungal keratitis (FK) usually develops to a poor clinical prognosis due to the fungal invasion and excessive inflammatory reaction. In order to enhance the therapeutic effect of natamycin (NAT), we used the anti-inflammatory biological polysaccharide bletilla striata polysaccharide (BSP) combined wi...
Saved in:
Published in: | Journal of biomaterials applications 2024-08, p.8853282241280844 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c183t-61731aaf40bcf7775340167a0084691f170b273a56f3248b0ae023dfc00184ad3 |
container_end_page | |
container_issue | |
container_start_page | 8853282241280844 |
container_title | Journal of biomaterials applications |
container_volume | |
creator | Tian, Xue Ji, Xiaoyue Zhang, Ranran Long, Xiaojing Lin, Jing Zhang, Yingxue Zhan, Lu Luan, Junjie Zhao, Guiqiu Peng, Xudong |
description | Fungal keratitis (FK) usually develops to a poor clinical prognosis due to the fungal invasion and excessive inflammatory reaction. In order to enhance the therapeutic effect of natamycin (NAT), we used the anti-inflammatory biological polysaccharide bletilla striata polysaccharide (BSP) combined with NAT to prepare a new eye drop -- oxidized bletilla striata polysaccharide-natamycin (OBN).
UV-vis, FT-IR, and fluorescence spectroscopy were used to identify the synthesis of OBN. Biocompatibility of OBN was determined by CCK-8, scratch assay, and corneal toxicity test. RAW264.7 cells and C57BL/6 mice were stimulated with
and treated with PBS, OBN, or NAT. The anti-inflammatory activity of OBN was detected by RT-PCR and ELISA. In mice with FK, the clinical scores were used to evaluate the effect of OBN; HE staining was performed to assess the corneal pathological changes; MPO assay and immunofluorescence staining were used to investigate neutrophil infiltration.
OBN was synthesized by combining oxidized bletilla striata polysaccharide (OBSP) with NAT through Schiff base reaction. OBN did not affect cell viability at a concentration of 160 μg/mL in HCECs, RAW264.7 cells, and mouse corneas. OBN versus NAT significantly improved the prognosis of
keratitis by reducing disease severity, neutrophil infiltration, and expression of inflammatory factors
. Additionally, OBN treatment down-regulated the mRNA and protein expression levels of inflammatory factors IL-1β, TNF-α, and IL-6 in RAW264.7 and mouse models.
OBN is a compound prepared by covalently linking OBSP to the imino group of NAT through Schiff base reaction. OBN treatment down-regulated inflammation and improved the prognosis of mice with
keratitis. |
doi_str_mv | 10.1177/08853282241280844 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3099799373</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3099799373</sourcerecordid><originalsourceid>FETCH-LOGICAL-c183t-61731aaf40bcf7775340167a0084691f170b273a56f3248b0ae023dfc00184ad3</originalsourceid><addsrcrecordid>eNplkMtOwzAURC0EoqXwAWyQl2wC14_EzhJVvKRKbMo6chybGtI42I5E-HpStbBhdaW5Z0aaQeiSwA0hQtyClDmjklJOqATJ-RGak5xBJoHSYzTf_bMdMENnMb4DQF7y4hTNWElBMijnyK43JqjeDMlpbKw1OmFvsf9yjfs2Da5bk1zbKhxTcCop3Pt2jErrjQquMVk3adtRuw6b0eAm-D5i32E7dG-qxR9TdnLJxXN0YlUbzcXhLtDrw_16-ZStXh6fl3erTBPJUlYQwYhSlkOtrRAiZxxIIRRM5YqSWCKgpoKpvLCMclmDMkBZYzUAkVw1bIGu97l98J-DianauqjNVKAzfojV1LkUZckEm1CyR3XwMQZjqz64rQpjRaDazVv9m3fyXB3ih3prmj_H757sB9yJdZM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3099799373</pqid></control><display><type>article</type><title>Therapeutic effect of oxidized bletilla striata polysaccharide-natamycin eye drops on fungal keratitis</title><source>Sage Journals Online</source><creator>Tian, Xue ; Ji, Xiaoyue ; Zhang, Ranran ; Long, Xiaojing ; Lin, Jing ; Zhang, Yingxue ; Zhan, Lu ; Luan, Junjie ; Zhao, Guiqiu ; Peng, Xudong</creator><creatorcontrib>Tian, Xue ; Ji, Xiaoyue ; Zhang, Ranran ; Long, Xiaojing ; Lin, Jing ; Zhang, Yingxue ; Zhan, Lu ; Luan, Junjie ; Zhao, Guiqiu ; Peng, Xudong</creatorcontrib><description>Fungal keratitis (FK) usually develops to a poor clinical prognosis due to the fungal invasion and excessive inflammatory reaction. In order to enhance the therapeutic effect of natamycin (NAT), we used the anti-inflammatory biological polysaccharide bletilla striata polysaccharide (BSP) combined with NAT to prepare a new eye drop -- oxidized bletilla striata polysaccharide-natamycin (OBN).
UV-vis, FT-IR, and fluorescence spectroscopy were used to identify the synthesis of OBN. Biocompatibility of OBN was determined by CCK-8, scratch assay, and corneal toxicity test. RAW264.7 cells and C57BL/6 mice were stimulated with
and treated with PBS, OBN, or NAT. The anti-inflammatory activity of OBN was detected by RT-PCR and ELISA. In mice with FK, the clinical scores were used to evaluate the effect of OBN; HE staining was performed to assess the corneal pathological changes; MPO assay and immunofluorescence staining were used to investigate neutrophil infiltration.
OBN was synthesized by combining oxidized bletilla striata polysaccharide (OBSP) with NAT through Schiff base reaction. OBN did not affect cell viability at a concentration of 160 μg/mL in HCECs, RAW264.7 cells, and mouse corneas. OBN versus NAT significantly improved the prognosis of
keratitis by reducing disease severity, neutrophil infiltration, and expression of inflammatory factors
. Additionally, OBN treatment down-regulated the mRNA and protein expression levels of inflammatory factors IL-1β, TNF-α, and IL-6 in RAW264.7 and mouse models.
OBN is a compound prepared by covalently linking OBSP to the imino group of NAT through Schiff base reaction. OBN treatment down-regulated inflammation and improved the prognosis of mice with
keratitis.</description><identifier>ISSN: 0885-3282</identifier><identifier>ISSN: 1530-8022</identifier><identifier>EISSN: 1530-8022</identifier><identifier>DOI: 10.1177/08853282241280844</identifier><identifier>PMID: 39208309</identifier><language>eng</language><publisher>England</publisher><ispartof>Journal of biomaterials applications, 2024-08, p.8853282241280844</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c183t-61731aaf40bcf7775340167a0084691f170b273a56f3248b0ae023dfc00184ad3</cites><orcidid>0000-0001-6140-4162</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/39208309$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tian, Xue</creatorcontrib><creatorcontrib>Ji, Xiaoyue</creatorcontrib><creatorcontrib>Zhang, Ranran</creatorcontrib><creatorcontrib>Long, Xiaojing</creatorcontrib><creatorcontrib>Lin, Jing</creatorcontrib><creatorcontrib>Zhang, Yingxue</creatorcontrib><creatorcontrib>Zhan, Lu</creatorcontrib><creatorcontrib>Luan, Junjie</creatorcontrib><creatorcontrib>Zhao, Guiqiu</creatorcontrib><creatorcontrib>Peng, Xudong</creatorcontrib><title>Therapeutic effect of oxidized bletilla striata polysaccharide-natamycin eye drops on fungal keratitis</title><title>Journal of biomaterials applications</title><addtitle>J Biomater Appl</addtitle><description>Fungal keratitis (FK) usually develops to a poor clinical prognosis due to the fungal invasion and excessive inflammatory reaction. In order to enhance the therapeutic effect of natamycin (NAT), we used the anti-inflammatory biological polysaccharide bletilla striata polysaccharide (BSP) combined with NAT to prepare a new eye drop -- oxidized bletilla striata polysaccharide-natamycin (OBN).
UV-vis, FT-IR, and fluorescence spectroscopy were used to identify the synthesis of OBN. Biocompatibility of OBN was determined by CCK-8, scratch assay, and corneal toxicity test. RAW264.7 cells and C57BL/6 mice were stimulated with
and treated with PBS, OBN, or NAT. The anti-inflammatory activity of OBN was detected by RT-PCR and ELISA. In mice with FK, the clinical scores were used to evaluate the effect of OBN; HE staining was performed to assess the corneal pathological changes; MPO assay and immunofluorescence staining were used to investigate neutrophil infiltration.
OBN was synthesized by combining oxidized bletilla striata polysaccharide (OBSP) with NAT through Schiff base reaction. OBN did not affect cell viability at a concentration of 160 μg/mL in HCECs, RAW264.7 cells, and mouse corneas. OBN versus NAT significantly improved the prognosis of
keratitis by reducing disease severity, neutrophil infiltration, and expression of inflammatory factors
. Additionally, OBN treatment down-regulated the mRNA and protein expression levels of inflammatory factors IL-1β, TNF-α, and IL-6 in RAW264.7 and mouse models.
OBN is a compound prepared by covalently linking OBSP to the imino group of NAT through Schiff base reaction. OBN treatment down-regulated inflammation and improved the prognosis of mice with
keratitis.</description><issn>0885-3282</issn><issn>1530-8022</issn><issn>1530-8022</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNplkMtOwzAURC0EoqXwAWyQl2wC14_EzhJVvKRKbMo6chybGtI42I5E-HpStbBhdaW5Z0aaQeiSwA0hQtyClDmjklJOqATJ-RGak5xBJoHSYzTf_bMdMENnMb4DQF7y4hTNWElBMijnyK43JqjeDMlpbKw1OmFvsf9yjfs2Da5bk1zbKhxTcCop3Pt2jErrjQquMVk3adtRuw6b0eAm-D5i32E7dG-qxR9TdnLJxXN0YlUbzcXhLtDrw_16-ZStXh6fl3erTBPJUlYQwYhSlkOtrRAiZxxIIRRM5YqSWCKgpoKpvLCMclmDMkBZYzUAkVw1bIGu97l98J-DianauqjNVKAzfojV1LkUZckEm1CyR3XwMQZjqz64rQpjRaDazVv9m3fyXB3ih3prmj_H757sB9yJdZM</recordid><startdate>20240829</startdate><enddate>20240829</enddate><creator>Tian, Xue</creator><creator>Ji, Xiaoyue</creator><creator>Zhang, Ranran</creator><creator>Long, Xiaojing</creator><creator>Lin, Jing</creator><creator>Zhang, Yingxue</creator><creator>Zhan, Lu</creator><creator>Luan, Junjie</creator><creator>Zhao, Guiqiu</creator><creator>Peng, Xudong</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6140-4162</orcidid></search><sort><creationdate>20240829</creationdate><title>Therapeutic effect of oxidized bletilla striata polysaccharide-natamycin eye drops on fungal keratitis</title><author>Tian, Xue ; Ji, Xiaoyue ; Zhang, Ranran ; Long, Xiaojing ; Lin, Jing ; Zhang, Yingxue ; Zhan, Lu ; Luan, Junjie ; Zhao, Guiqiu ; Peng, Xudong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c183t-61731aaf40bcf7775340167a0084691f170b273a56f3248b0ae023dfc00184ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tian, Xue</creatorcontrib><creatorcontrib>Ji, Xiaoyue</creatorcontrib><creatorcontrib>Zhang, Ranran</creatorcontrib><creatorcontrib>Long, Xiaojing</creatorcontrib><creatorcontrib>Lin, Jing</creatorcontrib><creatorcontrib>Zhang, Yingxue</creatorcontrib><creatorcontrib>Zhan, Lu</creatorcontrib><creatorcontrib>Luan, Junjie</creatorcontrib><creatorcontrib>Zhao, Guiqiu</creatorcontrib><creatorcontrib>Peng, Xudong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomaterials applications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tian, Xue</au><au>Ji, Xiaoyue</au><au>Zhang, Ranran</au><au>Long, Xiaojing</au><au>Lin, Jing</au><au>Zhang, Yingxue</au><au>Zhan, Lu</au><au>Luan, Junjie</au><au>Zhao, Guiqiu</au><au>Peng, Xudong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Therapeutic effect of oxidized bletilla striata polysaccharide-natamycin eye drops on fungal keratitis</atitle><jtitle>Journal of biomaterials applications</jtitle><addtitle>J Biomater Appl</addtitle><date>2024-08-29</date><risdate>2024</risdate><spage>8853282241280844</spage><pages>8853282241280844-</pages><issn>0885-3282</issn><issn>1530-8022</issn><eissn>1530-8022</eissn><abstract>Fungal keratitis (FK) usually develops to a poor clinical prognosis due to the fungal invasion and excessive inflammatory reaction. In order to enhance the therapeutic effect of natamycin (NAT), we used the anti-inflammatory biological polysaccharide bletilla striata polysaccharide (BSP) combined with NAT to prepare a new eye drop -- oxidized bletilla striata polysaccharide-natamycin (OBN).
UV-vis, FT-IR, and fluorescence spectroscopy were used to identify the synthesis of OBN. Biocompatibility of OBN was determined by CCK-8, scratch assay, and corneal toxicity test. RAW264.7 cells and C57BL/6 mice were stimulated with
and treated with PBS, OBN, or NAT. The anti-inflammatory activity of OBN was detected by RT-PCR and ELISA. In mice with FK, the clinical scores were used to evaluate the effect of OBN; HE staining was performed to assess the corneal pathological changes; MPO assay and immunofluorescence staining were used to investigate neutrophil infiltration.
OBN was synthesized by combining oxidized bletilla striata polysaccharide (OBSP) with NAT through Schiff base reaction. OBN did not affect cell viability at a concentration of 160 μg/mL in HCECs, RAW264.7 cells, and mouse corneas. OBN versus NAT significantly improved the prognosis of
keratitis by reducing disease severity, neutrophil infiltration, and expression of inflammatory factors
. Additionally, OBN treatment down-regulated the mRNA and protein expression levels of inflammatory factors IL-1β, TNF-α, and IL-6 in RAW264.7 and mouse models.
OBN is a compound prepared by covalently linking OBSP to the imino group of NAT through Schiff base reaction. OBN treatment down-regulated inflammation and improved the prognosis of mice with
keratitis.</abstract><cop>England</cop><pmid>39208309</pmid><doi>10.1177/08853282241280844</doi><orcidid>https://orcid.org/0000-0001-6140-4162</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0885-3282 |
ispartof | Journal of biomaterials applications, 2024-08, p.8853282241280844 |
issn | 0885-3282 1530-8022 1530-8022 |
language | eng |
recordid | cdi_proquest_miscellaneous_3099799373 |
source | Sage Journals Online |
title | Therapeutic effect of oxidized bletilla striata polysaccharide-natamycin eye drops on fungal keratitis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T01%3A59%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Therapeutic%20effect%20of%20oxidized%20bletilla%20striata%20polysaccharide-natamycin%20eye%20drops%20on%20fungal%20keratitis&rft.jtitle=Journal%20of%20biomaterials%20applications&rft.au=Tian,%20Xue&rft.date=2024-08-29&rft.spage=8853282241280844&rft.pages=8853282241280844-&rft.issn=0885-3282&rft.eissn=1530-8022&rft_id=info:doi/10.1177/08853282241280844&rft_dat=%3Cproquest_cross%3E3099799373%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c183t-61731aaf40bcf7775340167a0084691f170b273a56f3248b0ae023dfc00184ad3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3099799373&rft_id=info:pmid/39208309&rfr_iscdi=true |