Fluorescent supramolecular hydrogels self-assembled from tetraphenylethene (TPE)/single amino acid conjugatesElectronic supplementary information (ESI) available: Synthesis and characterization. See DOI: 10.1039/c8ra02296h

Herein, we report the synthesis of simple TPE/single amino acid conjugates, TPE-Ser and TPE-Asp with side-chains featuring functional groups that may provide an additional hydrogen bonding network for hydrogelation in aqueous medium. TPE-Ser , which has the lowest molecular weight, containing hydrox...

Full description

Saved in:
Bibliographic Details
Main Authors Chu, Nien-Tzu, Chakravarthy, Rajan Deepan, Shih, Nai-Chia, Lin, Yen-Hsu, Liu, Yen-Chu, Lin, Jhong-Hua, Lin, Hsin-Chieh
Format Journal Article
LanguageEnglish
Published 08.06.2018
Online AccessGet full text

Cover

Loading…
Abstract Herein, we report the synthesis of simple TPE/single amino acid conjugates, TPE-Ser and TPE-Asp with side-chains featuring functional groups that may provide an additional hydrogen bonding network for hydrogelation in aqueous medium. TPE-Ser , which has the lowest molecular weight, containing hydroxyl groups undergoes self-assembly into supramolecular hydrogels under physiological pH conditions. TPE-Asp with a carboxylic group side chain undergoes the self-assembly and hydrogelation processes under slightly acidic conditions (pH = 6.0). UV-vis, IR, PL and rheological studies clearly indicate the formation, stability and fluorescence properties of TPE-amino acid hydrogels. TEM micrographs of the hydrogels indicate that the compounds are self-assembled into a nanosheet morphology with random size and shape. Further, in vitro analysis of TPE-Ser and TPE-Asp with 3A6 cells shows that the compounds exhibit unique fluorescence signals in microcellular environments thus making them suitable candidates for bioimaging applications. Overall, these findings highlight the importance of the structure-hydrogelation relationship and provide new insights into the design of single amino-acid-based supramolecular hydrogels. TPE-Ser molecules exhibit non-covalent interactions necessary for hydrogelation under physiological pH conditions.
AbstractList Herein, we report the synthesis of simple TPE/single amino acid conjugates, TPE-Ser and TPE-Asp with side-chains featuring functional groups that may provide an additional hydrogen bonding network for hydrogelation in aqueous medium. TPE-Ser , which has the lowest molecular weight, containing hydroxyl groups undergoes self-assembly into supramolecular hydrogels under physiological pH conditions. TPE-Asp with a carboxylic group side chain undergoes the self-assembly and hydrogelation processes under slightly acidic conditions (pH = 6.0). UV-vis, IR, PL and rheological studies clearly indicate the formation, stability and fluorescence properties of TPE-amino acid hydrogels. TEM micrographs of the hydrogels indicate that the compounds are self-assembled into a nanosheet morphology with random size and shape. Further, in vitro analysis of TPE-Ser and TPE-Asp with 3A6 cells shows that the compounds exhibit unique fluorescence signals in microcellular environments thus making them suitable candidates for bioimaging applications. Overall, these findings highlight the importance of the structure-hydrogelation relationship and provide new insights into the design of single amino-acid-based supramolecular hydrogels. TPE-Ser molecules exhibit non-covalent interactions necessary for hydrogelation under physiological pH conditions.
Author Liu, Yen-Chu
Lin, Yen-Hsu
Chakravarthy, Rajan Deepan
Shih, Nai-Chia
Chu, Nien-Tzu
Lin, Jhong-Hua
Lin, Hsin-Chieh
AuthorAffiliation Department of Materials Science and Engineering
National Chiao Tung University
AuthorAffiliation_xml – name: National Chiao Tung University
– name: Department of Materials Science and Engineering
Author_xml – sequence: 1
  givenname: Nien-Tzu
  surname: Chu
  fullname: Chu, Nien-Tzu
– sequence: 2
  givenname: Rajan Deepan
  surname: Chakravarthy
  fullname: Chakravarthy, Rajan Deepan
– sequence: 3
  givenname: Nai-Chia
  surname: Shih
  fullname: Shih, Nai-Chia
– sequence: 4
  givenname: Yen-Hsu
  surname: Lin
  fullname: Lin, Yen-Hsu
– sequence: 5
  givenname: Yen-Chu
  surname: Liu
  fullname: Liu, Yen-Chu
– sequence: 6
  givenname: Jhong-Hua
  surname: Lin
  fullname: Lin, Jhong-Hua
– sequence: 7
  givenname: Hsin-Chieh
  surname: Lin
  fullname: Lin, Hsin-Chieh
BookMark eNqFj0FLw0AQhRdRsNZevAvjzR7aJqkG26um2JNCey_jZtJs2eyGmY0Qf6y_xVUED4LO5R3e4_uYM3XsvCOlLtJkmibzxUzfMSZZtsjrIzXIkpt8kiX54lSNRA5JvPw2zfJ0oN5XtvNMoskFkK5lbLwl3VlkqPuS_Z6sgJCtJihCzYulEir2DQQKjG1NrrcUYhBcb5-L8UyM21sCbIzzgNqUoL07dHsMJEVEB_bO6E9Xa6mJWuQejKs8NxiMd3BdbNZjwFc0FqNuCZveRYEYAXSRViOjDsTm7Ws_hQ0RPDytl_D7-XN1UqEVGn3nUF2uiu3944RF71o2TZTvfubzobr6q9-1ZTX_j_EBs26AMg
ContentType Journal Article
DOI 10.1039/c8ra02296h
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
EISSN 2046-2069
EndPage 2927
ExternalDocumentID c8ra02296h
GroupedDBID -JG
0-7
AAEMU
ABGFH
AEFDR
AFVBQ
AGSTE
AUDPV
BSQNT
C6K
EE0
EF-
H~N
J3I
R7C
R7E
R7G
RCNCU
RPMJG
RRC
RSCEA
SLH
SMJ
ID FETCH-rsc_primary_c8ra02296h3
IngestDate Wed Jun 05 04:39:39 EDT 2019
Mon Jan 28 17:14:07 EST 2019
IsPeerReviewed true
IsScholarly true
Issue 37
Language English
LinkModel OpenURL
MergedId FETCHMERGED-rsc_primary_c8ra02296h3
Notes Electronic supplementary information (ESI) available: Synthesis and characterization. See DOI
10.1039/c8ra02296h
PageCount 6
ParticipantIDs rsc_primary_c8ra02296h
ProviderPackageCode J3I
R7E
RRC
R7G
AEFDR
RPMJG
-JG
AGSTE
RCNCU
AUDPV
EF-
SLH
BSQNT
EE0
SMJ
RSCEA
AFVBQ
C6K
H~N
0-7
ABGFH
AAEMU
R7C
PublicationCentury 2000
PublicationDate 2018-June-08
PublicationDateYYYYMMDD 2018-06-08
PublicationDate_xml – month: 06
  year: 2018
  text: 2018-June-08
  day: 08
PublicationDecade 2010
PublicationYear 2018
References_xml – issn: 2005
  issue: vol. 294
  volume-title: Cell Migration: Developmental Methods and Protocols
  publication-title: Methods in Molecular Biology
  doi: Guan
SSID ssj0000651261
Score 4.162016
Snippet Herein, we report the synthesis of simple TPE/single amino acid conjugates, TPE-Ser and TPE-Asp with side-chains featuring functional groups that may provide...
SourceID rsc
SourceType Enrichment Source
Publisher
StartPage 2922
Title Fluorescent supramolecular hydrogels self-assembled from tetraphenylethene (TPE)/single amino acid conjugatesElectronic supplementary information (ESI) available: Synthesis and characterization. See DOI: 10.1039/c8ra02296h
Volume 8
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnZ3NbtpAEIBXNLn0UrVqoyZtojm0UiLLSbBNsHOLCBGp-qdCKnJC6_USOzIGGRyJPGGeos_SGS9eY-FKbS8WeOUFdj5mZkc7M4x9CHBXYZ2OfdP2xanpNF1puqLpmG3bc1p2ELTHnOKQX76e9W6cT8PWsNF4Wju1lC38Y_FYm1fyP1LFeyhXypL9B8nqSfEGvkb54hUljNe_kvFVnE1TVY_JmGezlE-KZrdGuAzS6R0aPmMu47GJLrKc-DF6lyqfRC6oULVMljEl_CpHc_C9-9GiuqAUPoilwSdRMjW4iCjxLbnPKOA275Ztc-bUEFQdPk8pe1DnQdJk3f41BRz4A49iys6iyEN_meCHUQWUPJlOl4pWmaDHqLekcfntOg9S5Hn69GWEm3L0ALwzHbfuhJliWCbm4DGrHlB4wGVagcPvUXddSrS3-g_QD6NQ2ZTI7ISRNkmfVSWFW5yxpzrBFJGQppuf2FLKW-Ya08LNPgKier8U6t1do1jVlyl0tacyold2H9-2a21K7a-t1uguB5-xbQtVHura7R8_b4a3Ot6Hrl4Td6tFhVzbOykfQr8mLfrN5H7N4CV7sdqQwIWi6xVryOQ1-7VGFlTJAk0WVMkCIgs2yIJD5OroRDEFOVNATEEdU1BhCtaYgkMk6gg0T-egaQKkCTZoAqQJkKZz2FyJN2z_qjvo9Excj9FM1VsZlcP2DttKpol8y0AEoiWEZ0m_5TkB97jIi2sKKjHpSovvsp36OXbZXv3AaBaM9_701Dv2vETuPdtapJncR3d04R_kYZyDlbx_A8Tqm_c
link.rule.ids 315,783,787,867,27936,27937
linkProvider Royal Society of Chemistry
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Fluorescent+supramolecular+hydrogels+self-assembled+from+tetraphenylethene+%28TPE%29%2Fsingle+amino+acid+conjugatesElectronic+supplementary+information+%28ESI%29+available%3A+Synthesis+and+characterization.+See+DOI%3A+10.1039%2Fc8ra02296h&rft.au=Chu%2C+Nien-Tzu&rft.au=Chakravarthy%2C+Rajan+Deepan&rft.au=Shih%2C+Nai-Chia&rft.au=Lin%2C+Yen-Hsu&rft.date=2018-06-08&rft.eissn=2046-2069&rft.volume=8&rft.issue=37&rft.spage=2922&rft.epage=2927&rft_id=info:doi/10.1039%2Fc8ra02296h&rft.externalDocID=c8ra02296h