Loading…

In situ formation of steroidal supramolecular gels designed for drug release

In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthe...

Full description

Saved in:
Bibliographic Details
Published in:Molecules (Basel, Switzerland) Switzerland), 2013-03, Vol.18 (4), p.3745-3759
Main Authors: Bunzen, Hana, Kolehmainen, Erkki
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173
cites cdi_FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173
container_end_page 3759
container_issue 4
container_start_page 3745
container_title Molecules (Basel, Switzerland)
container_volume 18
creator Bunzen, Hana
Kolehmainen, Erkki
description In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthesis or directly in situ during the gel forming process. The gels prepared by both methods were studied and it was found that they had very similar macro- and microscopic properties. Furthermore, the possibility to use the gels as carriers for aromatic drugs such as 5-chloro-8-hydroxyquinoline, pyrazinecarboxamide, and antipyrine was investigated and the prepared two-component gels were studied with regard to their potential applications in drug delivery, particularly in a pH-controlled drug release.
doi_str_mv 10.3390/molecules18043745
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_014893def1324c02bd772e6d3ad8f32c</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_014893def1324c02bd772e6d3ad8f32c</doaj_id><sourcerecordid>1320164018</sourcerecordid><originalsourceid>FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173</originalsourceid><addsrcrecordid>eNplkU-PFCEQxYnRuOvqB_BiOvHiZbT409BcTMxG10km8aJnQkPRMqGbEbpN9ttvjzNudjUcINR7v6J4hLym8J5zDR_GnNAtCSvtQHAl2ifkkgoGGw5CP31wviAvat0DMCpo-5xcMN4yDVxckt12amqclybkMto55qnJoakzlhy9TU1dDsWe-9jSDJhq47HGYUJ_9DS-LENTMKGt-JI8CzZVfHXer8iPL5-_X3_d7L7dbK8_7TZOaD5vJIKjnevsukKrXdf3Vsjgew1InaSMMR9QY6-CAw9KYtf2mivf0hYkVfyKbE9cn-3eHEocbbk12Ubz5yKXwdgyR5fQABWd5h4D5Uw4YL1XiqH03PoucOZW1scT67D0I3qH01xsegR9XJniTzPk30YyBdCKFfDuDCj514J1NmOsDlOyE-almrUxUCmAdqv07T_SfV7KtH6VoS2XSmouj0B6UrmSay0Y7h9DwRxzN__lvnrePJzi3vE3aH4HZPisJg</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1536769364</pqid></control><display><type>article</type><title>In situ formation of steroidal supramolecular gels designed for drug release</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Bunzen, Hana ; Kolehmainen, Erkki</creator><creatorcontrib>Bunzen, Hana ; Kolehmainen, Erkki</creatorcontrib><description>In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthesis or directly in situ during the gel forming process. The gels prepared by both methods were studied and it was found that they had very similar macro- and microscopic properties. Furthermore, the possibility to use the gels as carriers for aromatic drugs such as 5-chloro-8-hydroxyquinoline, pyrazinecarboxamide, and antipyrine was investigated and the prepared two-component gels were studied with regard to their potential applications in drug delivery, particularly in a pH-controlled drug release.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules18043745</identifier><identifier>PMID: 23529034</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>acid-responsive ; Chloroquinolinols - chemistry ; Cholesterol ; Delayed-Action Preparations ; Design ; Drug Delivery Systems - methods ; drug release ; Gels - chemistry ; Hydrogen-Ion Concentration ; in situ gelation ; Magnetic Resonance Spectroscopy ; organogel ; Solvents ; Steroids</subject><ispartof>Molecules (Basel, Switzerland), 2013-03, Vol.18 (4), p.3745-3759</ispartof><rights>Copyright MDPI AG 2013</rights><rights>2013 by the authors; licensee MDPI, Basel, Switzerland. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173</citedby><cites>FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1536769364/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1536769364?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23529034$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bunzen, Hana</creatorcontrib><creatorcontrib>Kolehmainen, Erkki</creatorcontrib><title>In situ formation of steroidal supramolecular gels designed for drug release</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthesis or directly in situ during the gel forming process. The gels prepared by both methods were studied and it was found that they had very similar macro- and microscopic properties. Furthermore, the possibility to use the gels as carriers for aromatic drugs such as 5-chloro-8-hydroxyquinoline, pyrazinecarboxamide, and antipyrine was investigated and the prepared two-component gels were studied with regard to their potential applications in drug delivery, particularly in a pH-controlled drug release.</description><subject>acid-responsive</subject><subject>Chloroquinolinols - chemistry</subject><subject>Cholesterol</subject><subject>Delayed-Action Preparations</subject><subject>Design</subject><subject>Drug Delivery Systems - methods</subject><subject>drug release</subject><subject>Gels - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>in situ gelation</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>organogel</subject><subject>Solvents</subject><subject>Steroids</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkU-PFCEQxYnRuOvqB_BiOvHiZbT409BcTMxG10km8aJnQkPRMqGbEbpN9ttvjzNudjUcINR7v6J4hLym8J5zDR_GnNAtCSvtQHAl2ifkkgoGGw5CP31wviAvat0DMCpo-5xcMN4yDVxckt12amqclybkMto55qnJoakzlhy9TU1dDsWe-9jSDJhq47HGYUJ_9DS-LENTMKGt-JI8CzZVfHXer8iPL5-_X3_d7L7dbK8_7TZOaD5vJIKjnevsukKrXdf3Vsjgew1InaSMMR9QY6-CAw9KYtf2mivf0hYkVfyKbE9cn-3eHEocbbk12Ubz5yKXwdgyR5fQABWd5h4D5Uw4YL1XiqH03PoucOZW1scT67D0I3qH01xsegR9XJniTzPk30YyBdCKFfDuDCj514J1NmOsDlOyE-almrUxUCmAdqv07T_SfV7KtH6VoS2XSmouj0B6UrmSay0Y7h9DwRxzN__lvnrePJzi3vE3aH4HZPisJg</recordid><startdate>20130325</startdate><enddate>20130325</enddate><creator>Bunzen, Hana</creator><creator>Kolehmainen, Erkki</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130325</creationdate><title>In situ formation of steroidal supramolecular gels designed for drug release</title><author>Bunzen, Hana ; Kolehmainen, Erkki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>acid-responsive</topic><topic>Chloroquinolinols - chemistry</topic><topic>Cholesterol</topic><topic>Delayed-Action Preparations</topic><topic>Design</topic><topic>Drug Delivery Systems - methods</topic><topic>drug release</topic><topic>Gels - chemistry</topic><topic>Hydrogen-Ion Concentration</topic><topic>in situ gelation</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>organogel</topic><topic>Solvents</topic><topic>Steroids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bunzen, Hana</creatorcontrib><creatorcontrib>Kolehmainen, Erkki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bunzen, Hana</au><au>Kolehmainen, Erkki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ formation of steroidal supramolecular gels designed for drug release</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2013-03-25</date><risdate>2013</risdate><volume>18</volume><issue>4</issue><spage>3745</spage><epage>3759</epage><pages>3745-3759</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthesis or directly in situ during the gel forming process. The gels prepared by both methods were studied and it was found that they had very similar macro- and microscopic properties. Furthermore, the possibility to use the gels as carriers for aromatic drugs such as 5-chloro-8-hydroxyquinoline, pyrazinecarboxamide, and antipyrine was investigated and the prepared two-component gels were studied with regard to their potential applications in drug delivery, particularly in a pH-controlled drug release.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>23529034</pmid><doi>10.3390/molecules18043745</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1420-3049
ispartof Molecules (Basel, Switzerland), 2013-03, Vol.18 (4), p.3745-3759
issn 1420-3049
1420-3049
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_014893def1324c02bd772e6d3ad8f32c
source Publicly Available Content Database; PubMed Central
subjects acid-responsive
Chloroquinolinols - chemistry
Cholesterol
Delayed-Action Preparations
Design
Drug Delivery Systems - methods
drug release
Gels - chemistry
Hydrogen-Ion Concentration
in situ gelation
Magnetic Resonance Spectroscopy
organogel
Solvents
Steroids
title In situ formation of steroidal supramolecular gels designed for drug release
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T06%3A12%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=In%20situ%20formation%20of%20steroidal%20supramolecular%20gels%20designed%20for%20drug%20release&rft.jtitle=Molecules%20(Basel,%20Switzerland)&rft.au=Bunzen,%20Hana&rft.date=2013-03-25&rft.volume=18&rft.issue=4&rft.spage=3745&rft.epage=3759&rft.pages=3745-3759&rft.issn=1420-3049&rft.eissn=1420-3049&rft_id=info:doi/10.3390/molecules18043745&rft_dat=%3Cproquest_doaj_%3E1320164018%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c493t-6e0c18c8a8a8f59c8bba46fdb90e1c61222dfe9eb7fc0d076e85b937d51506173%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1536769364&rft_id=info:pmid/23529034&rfr_iscdi=true