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Article: Rhodamine Conjugated Gelatin Methacryloyl Nanoparticles for Stable Cell Imaging

TitleRhodamine Conjugated Gelatin Methacryloyl Nanoparticles for Stable Cell Imaging
Authors
KeywordsGelMA
fluorescent label
rhodamine B
bioimaging
biocompatible nanoparticles
Issue Date2020
Citation
ACS Applied Bio Materials, 2020, v. 3, n. 10, p. 6908-6918 How to Cite?
Abstract© 2020 American Chemical Society. Fluorescent nanomaterials have been widely used in biological imaging due to their selectivity, sensitivity, and noninvasive nature. These characteristics make the materials suitable for real-time and in situ imaging. However, further development of highly biocompatible nanosystems with long-lasting fluorescent intensity and photostability is needed for advanced bioimaging. We have used electrospraying to generate gelatin methacryloyl (GelMA)-based fluorescent nanoparticles (NPs) with chemically conjugated rhodamine B (RB). The extent of conjugation can be controlled by varying the mass ratio of RB and GelMA precursors to obtain RB-conjugated GelMA (RB-GelMA) NPs with optimal fluorescent properties and particle size. These NPs exhibited superior biocompatibility when compared with pure RB in in vitro cell viability and proliferation assays using multiple cell types. Moreover, RB-GelMA NPs showed enhanced cell internalization and improved brightness compared with unconjugated RB. Our experiments demonstrate that engineered RB-GelMA NPs can be used as a biocompatible fluorescent label for bioimaging.
Persistent Identifierhttp://hdl.handle.net/10722/295438
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorXue, Yumeng-
dc.contributor.authorLee, Junmin-
dc.contributor.authorKim, Han Jun-
dc.contributor.authorCho, Hyun Jong-
dc.contributor.authorZhou, Xingwu-
dc.contributor.authorLiu, Yaowen-
dc.contributor.authorTebon, Peyton-
dc.contributor.authorHoffman, Tyler-
dc.contributor.authorQu, Moyuan-
dc.contributor.authorLing, Haonan-
dc.contributor.authorJiang, Xing-
dc.contributor.authorLi, Zhikang-
dc.contributor.authorZhang, Shiming-
dc.contributor.authorSun, Wujin-
dc.contributor.authorAhadian, Samad-
dc.contributor.authorDokmeci, Mehmet R.-
dc.contributor.authorLee, Kang Ju-
dc.contributor.authorKhademhosseini, Ali-
dc.date.accessioned2021-01-18T15:46:52Z-
dc.date.available2021-01-18T15:46:52Z-
dc.date.issued2020-
dc.identifier.citationACS Applied Bio Materials, 2020, v. 3, n. 10, p. 6908-6918-
dc.identifier.urihttp://hdl.handle.net/10722/295438-
dc.description.abstract© 2020 American Chemical Society. Fluorescent nanomaterials have been widely used in biological imaging due to their selectivity, sensitivity, and noninvasive nature. These characteristics make the materials suitable for real-time and in situ imaging. However, further development of highly biocompatible nanosystems with long-lasting fluorescent intensity and photostability is needed for advanced bioimaging. We have used electrospraying to generate gelatin methacryloyl (GelMA)-based fluorescent nanoparticles (NPs) with chemically conjugated rhodamine B (RB). The extent of conjugation can be controlled by varying the mass ratio of RB and GelMA precursors to obtain RB-conjugated GelMA (RB-GelMA) NPs with optimal fluorescent properties and particle size. These NPs exhibited superior biocompatibility when compared with pure RB in in vitro cell viability and proliferation assays using multiple cell types. Moreover, RB-GelMA NPs showed enhanced cell internalization and improved brightness compared with unconjugated RB. Our experiments demonstrate that engineered RB-GelMA NPs can be used as a biocompatible fluorescent label for bioimaging.-
dc.languageeng-
dc.relation.ispartofACS Applied Bio Materials-
dc.subjectGelMA-
dc.subjectfluorescent label-
dc.subjectrhodamine B-
dc.subjectbioimaging-
dc.subjectbiocompatible nanoparticles-
dc.titleRhodamine Conjugated Gelatin Methacryloyl Nanoparticles for Stable Cell Imaging-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acsabm.0c00802-
dc.identifier.scopuseid_2-s2.0-85096478098-
dc.identifier.volume3-
dc.identifier.issue10-
dc.identifier.spage6908-
dc.identifier.epage6918-
dc.identifier.eissn2576-6422-
dc.identifier.isiWOS:000619799800033-
dc.identifier.issnl2576-6422-

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