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Please use this identifier to cite or link to this item: http://scholars.ntou.edu.tw/handle/123456789/21522
DC FieldValueLanguage
dc.contributor.authorLin, Pei-Hsuanen_US
dc.contributor.authorJian, Hong-Jyuanen_US
dc.contributor.authorLi, Yu-Jiaen_US
dc.contributor.authorHuang, Yu-Fenen_US
dc.contributor.authorAnand, Anishaen_US
dc.contributor.authorHuang, Chih-Chingen_US
dc.contributor.authorLin, Han-Jiaen_US
dc.contributor.authorLai, Jui-Yangen_US
dc.date.accessioned2022-05-05T01:11:15Z-
dc.date.available2022-05-05T01:11:15Z-
dc.date.issued2022-03-15-
dc.identifier.issn1742-7061-
dc.identifier.urihttp://scholars.ntou.edu.tw/handle/123456789/21522-
dc.description.abstractMost dry eye syndromes (DES) are caused by oxidative stress and an overactive inflammatory response, leading to tear deficiency and excessive tear evaporation. Conventional eye drops for DES treatment re-quire high doses and frequent administration due to their insufficient precorneal residence time. To over-come these problems, in this study, we have developed carbonized nanogels (CNGs) via the straight-forward pyrolysis of lysine hydrochloride (Lys) to provide a long-lasting eye drop formulation for topical DES therapy. This methodology thermally converts Lys-into nitrogen-doped crosslinked polymers with embedded nanographitic structures, which enable efficient free radical scavenging. The cationic and crosslinked polymeric features of the Lys-CNGs also prolong the precorneal retention time and improve ocular bioavailability. These Lys-CNGs exhibit high biocompatibility with corneal epithelial cells both in vitro and in vivo, indicating their safety as eye drops. In a DES rabbit model, a single dose of Lys-CNGs (50 mu g mL(-1)) can effectively alleviate the signs of DES within 4 days, whereas multiple treatments of 10-fold higher concentration of cyclosporine A are needed to achieve similar therapeutic effects (one dose every 12 h; 500 mu g mL(-1)). The topical administration of Lys-CNGs enable a reduced therapeutic dose and extended dosing interval, thereby demonstrating a superior therapeutic efficacy compared to the commercial cyclosporine A eye drops. These Lys-CNGs, which exhibit significant free radical scavenging, anti-inflammatory activity, high biocompatibility, and a remarkable ocular bioadhesive property, hold great potential as a long-lasting eye drop formulation for the treatment of dry eye disease.& nbsp;Statement of significance & nbsp;Multifunctional nanobiomaterial-based eye drops can render an ideal pharmaceutical formulation for the treatment of a variety of ocular surface diseases. To our knowledge, this is the first report describing the development of carbonized nanogels as topically administered therapeutics for alleviating dry eye syndrome (DES). We present evidence that the thermal transformation of lysine hydrochloride into car-bonized nanogels (Lys-CNGs) endows superior antioxidant, anti-inflammatory, and bioadhesive properties. While a single dose of Lys-CNGs (50 mu g mL(-1)) is sufficient to relieve the symptoms of DES for 4 days, multiple treatments of 10-fold higher concentration of commercially available cyclosporine eye drops are needed to achieve similar therapeutic outcomes (one dose every 12 h; 500 mu g mL(-1)), suggesting an effective and long-lasting ocular carbonized nanomedicine.& nbsp;(c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoEnglishen_US
dc.publisherELSEVIER SCI LTDen_US
dc.relation.ispartofACTA BIOMATERIALIAen_US
dc.subjectDry eye syndromeen_US
dc.subjectCarbonized nanogelsen_US
dc.subjectAnti-inflammatory activityen_US
dc.subjectOphthalmic dropsen_US
dc.subjectMucinen_US
dc.titleAlleviation of dry eye syndrome with one dose of antioxidant, anti-inflammatory, and mucoadhesive lysine-carbonized nanogelsen_US
dc.typejournal articleen_US
dc.identifier.doi10.1016/j.actbio.2022.01.044-
dc.identifier.isiWOS:000772079600002-
dc.relation.journalvolume141en_US
dc.relation.pages140-150en_US
dc.identifier.eissn1878-7568-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.languageiso639-1English-
item.fulltextno fulltext-
item.grantfulltextnone-
item.openairetypejournal article-
crisitem.author.deptCollege of Life Sciences-
crisitem.author.deptDepartment of Bioscience and Biotechnology-
crisitem.author.deptNational Taiwan Ocean University,NTOU-
crisitem.author.deptCenter of Excellence for the Oceans-
crisitem.author.deptCollege of Life Sciences-
crisitem.author.deptDepartment of Bioscience and Biotechnology-
crisitem.author.deptNational Taiwan Ocean University,NTOU-
crisitem.author.deptBachelor Degree Program in Marine Biotechnology-
crisitem.author.deptCenter of Excellence for the Oceans-
crisitem.author.orcid0000-0002-0363-1129-
crisitem.author.orcid0000-0002-4929-6573-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
crisitem.author.parentorgCollege of Life Sciences-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
crisitem.author.parentorgCollege of Life Sciences-
crisitem.author.parentorgCollege of Life Sciences-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
Appears in Collections:生命科學暨生物科技學系
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