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dc.contributor.authorKuosmanen, Riikka
dc.contributor.authorPuttreddy, Rakesh
dc.contributor.authorWillman, Roosa-Maria
dc.contributor.authorÄijäläinen, Ilkka
dc.contributor.authorGalandáková, Adéla
dc.contributor.authorUlrichová, Jitka
dc.contributor.authorSalo, Hannu
dc.contributor.authorRissanen, Kari
dc.contributor.authorSievänen, Elina
dc.date.accessioned2016-04-13T08:05:49Z
dc.date.available2017-02-22T22:45:09Z
dc.date.issued2016
dc.identifier.citationKuosmanen, R., Puttreddy, R., Willman, R.-M., Äijäläinen, I., Galandáková, A., Ulrichová, J., Salo, H., Rissanen, K., & Sievänen, E. (2016). Biocompatible Hydrogelators Based on Bile Acid Ethyl Amides. <i>Steroids</i>, <i>108</i>, 7-16. <a href="https://doi.org/10.1016/j.steroids.2016.02.014" target="_blank">https://doi.org/10.1016/j.steroids.2016.02.014</a>
dc.identifier.otherCONVID_25553703
dc.identifier.otherTUTKAID_69214
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/49320
dc.description.abstractFour novel bile acid ethyl amides were synthetized using a well-known method. All the four compounds were characterized by IR, SEM, and X-ray crystal analyses. In addition, the cytotoxicity of the compounds was tested. Two of the prepared compounds formed organogels. Lithocholic acid derivative 1 formed hydrogels as 1% and 2% (w/v) in four different aqueous solutions. This is very intriguing regarding possible uses in biomedicine.
dc.language.isoeng
dc.publisherElsevier Inc.
dc.relation.ispartofseriesSteroids
dc.subject.otherbile acid
dc.subject.otheramide
dc.subject.otherself-assembly
dc.subject.othersupramolecular hydrogel
dc.subject.otherbiocompatibility
dc.titleBiocompatible Hydrogelators Based on Bile Acid Ethyl Amides
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201604112041
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-04-11T12:15:02Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange7-16
dc.relation.issn0039-128X
dc.relation.numberinseries0
dc.relation.volume108
dc.type.versionacceptedVersion
dc.rights.copyright© 2016 Elsevier Inc. This is a final draft version of an article whose final and definitive form has been published by Elsevier. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1016/j.steroids.2016.02.014
dc.type.okmA1


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