Stimuli responsive nanocarrier for an effective delivery of multi-frontline tuberculosis drugs
Pulmonary delivery, of both individual nanoparticles and encapsulated within carrier particles, is attractive method in antitubercular therapy; however, literature reports of these system have not shown consistently successful results due to poor loading of the frontline drug and inefficient sustain...
Gespeichert in:
Veröffentlicht in: | Polymer chemistry 2014-04, Vol.5 (8), p.2725-2735 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2735 |
---|---|
container_issue | 8 |
container_start_page | 2725 |
container_title | Polymer chemistry |
container_volume | 5 |
creator | Mane, Shivshankar R. Chatterjee, Koushik Dinda, Himadri Sarma, Jayasri Das Shunmugam, Raja |
description | Pulmonary delivery, of both individual nanoparticles and encapsulated within carrier particles, is attractive method in antitubercular therapy; however, literature reports of these system have not shown consistently successful results due to poor loading of the frontline drug and inefficient sustained release profile. Here, a multifaceted synthetic strategy is employed to prepare stimuli responsive polymeric nanocarrier,
RCP-2
, with high purity, reproducibility, and precisely controlled stoichiometry of the drug motifs to demonstrate the high drug content as well as controlled release in a systematic manner. The drug release profile of
RCP-2
in mild acidic conditions implies the smart drug delivery nature of the nanocarrier. Cancerous cell lines, 4 T and A549, are employed due to their acidic nature to demonstrate the proposed pH responsive design. Surprisingly, the preliminary MTT assay against A549 cells (Lung cancer cell lines) shows a high anticancer efficacy. Taken together, these results demonstrate the significance of our unique design in which multi-frontline TB drugs are efficiently attached to produce the multi-task nanocarrier for potential therapeutic treatment. |
doi_str_mv | 10.1039/C3PY01589K |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1520372868</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1520372868</sourcerecordid><originalsourceid>FETCH-LOGICAL-c305t-94c6706f9d8bd2482a3c51b41c5f518a83605f6c252ad6af9728395c2943645a3</originalsourceid><addsrcrecordid>eNpFUEtLAzEYDKJgqb34C3IUYTXvJkcpvrCgoB68uKTZRCLppn7JCv33bqnoXGZgHodB6JSSC0q4uVzwpzdCpTYPB2hC59I0xih2-KelOEazUj7JCE4F42qC3p9rXA8pYvBlk_sSvz3ubZ-dBYgecMiAbY99CN7Vndn5NBJscQ54LNbYBMh9TbH3uA4rD25IucSCOxg-ygk6CjYVP_vlKXq9uX5Z3DXLx9v7xdWycZzI2hjh1JyoYDq96pjQzHIn6UpQJ4Ok2mquiAzKMclsp2wwc6a5kY4ZwZWQlk_R2X53A_lr8KW261icT8n2Pg-lpZIRPpaUHqPn-6iDXAr40G4gri1sW0ra3Y_t_4_8BxWTZik</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1520372868</pqid></control><display><type>article</type><title>Stimuli responsive nanocarrier for an effective delivery of multi-frontline tuberculosis drugs</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Mane, Shivshankar R. ; Chatterjee, Koushik ; Dinda, Himadri ; Sarma, Jayasri Das ; Shunmugam, Raja</creator><creatorcontrib>Mane, Shivshankar R. ; Chatterjee, Koushik ; Dinda, Himadri ; Sarma, Jayasri Das ; Shunmugam, Raja</creatorcontrib><description>Pulmonary delivery, of both individual nanoparticles and encapsulated within carrier particles, is attractive method in antitubercular therapy; however, literature reports of these system have not shown consistently successful results due to poor loading of the frontline drug and inefficient sustained release profile. Here, a multifaceted synthetic strategy is employed to prepare stimuli responsive polymeric nanocarrier,
RCP-2
, with high purity, reproducibility, and precisely controlled stoichiometry of the drug motifs to demonstrate the high drug content as well as controlled release in a systematic manner. The drug release profile of
RCP-2
in mild acidic conditions implies the smart drug delivery nature of the nanocarrier. Cancerous cell lines, 4 T and A549, are employed due to their acidic nature to demonstrate the proposed pH responsive design. Surprisingly, the preliminary MTT assay against A549 cells (Lung cancer cell lines) shows a high anticancer efficacy. Taken together, these results demonstrate the significance of our unique design in which multi-frontline TB drugs are efficiently attached to produce the multi-task nanocarrier for potential therapeutic treatment.</description><identifier>ISSN: 1759-9954</identifier><identifier>EISSN: 1759-9962</identifier><identifier>DOI: 10.1039/C3PY01589K</identifier><language>eng</language><subject>Mycobacterium</subject><ispartof>Polymer chemistry, 2014-04, Vol.5 (8), p.2725-2735</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c305t-94c6706f9d8bd2482a3c51b41c5f518a83605f6c252ad6af9728395c2943645a3</citedby><cites>FETCH-LOGICAL-c305t-94c6706f9d8bd2482a3c51b41c5f518a83605f6c252ad6af9728395c2943645a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Mane, Shivshankar R.</creatorcontrib><creatorcontrib>Chatterjee, Koushik</creatorcontrib><creatorcontrib>Dinda, Himadri</creatorcontrib><creatorcontrib>Sarma, Jayasri Das</creatorcontrib><creatorcontrib>Shunmugam, Raja</creatorcontrib><title>Stimuli responsive nanocarrier for an effective delivery of multi-frontline tuberculosis drugs</title><title>Polymer chemistry</title><description>Pulmonary delivery, of both individual nanoparticles and encapsulated within carrier particles, is attractive method in antitubercular therapy; however, literature reports of these system have not shown consistently successful results due to poor loading of the frontline drug and inefficient sustained release profile. Here, a multifaceted synthetic strategy is employed to prepare stimuli responsive polymeric nanocarrier,
RCP-2
, with high purity, reproducibility, and precisely controlled stoichiometry of the drug motifs to demonstrate the high drug content as well as controlled release in a systematic manner. The drug release profile of
RCP-2
in mild acidic conditions implies the smart drug delivery nature of the nanocarrier. Cancerous cell lines, 4 T and A549, are employed due to their acidic nature to demonstrate the proposed pH responsive design. Surprisingly, the preliminary MTT assay against A549 cells (Lung cancer cell lines) shows a high anticancer efficacy. Taken together, these results demonstrate the significance of our unique design in which multi-frontline TB drugs are efficiently attached to produce the multi-task nanocarrier for potential therapeutic treatment.</description><subject>Mycobacterium</subject><issn>1759-9954</issn><issn>1759-9962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpFUEtLAzEYDKJgqb34C3IUYTXvJkcpvrCgoB68uKTZRCLppn7JCv33bqnoXGZgHodB6JSSC0q4uVzwpzdCpTYPB2hC59I0xih2-KelOEazUj7JCE4F42qC3p9rXA8pYvBlk_sSvz3ubZ-dBYgecMiAbY99CN7Vndn5NBJscQ54LNbYBMh9TbH3uA4rD25IucSCOxg-ygk6CjYVP_vlKXq9uX5Z3DXLx9v7xdWycZzI2hjh1JyoYDq96pjQzHIn6UpQJ4Ok2mquiAzKMclsp2wwc6a5kY4ZwZWQlk_R2X53A_lr8KW261icT8n2Pg-lpZIRPpaUHqPn-6iDXAr40G4gri1sW0ra3Y_t_4_8BxWTZik</recordid><startdate>20140421</startdate><enddate>20140421</enddate><creator>Mane, Shivshankar R.</creator><creator>Chatterjee, Koushik</creator><creator>Dinda, Himadri</creator><creator>Sarma, Jayasri Das</creator><creator>Shunmugam, Raja</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20140421</creationdate><title>Stimuli responsive nanocarrier for an effective delivery of multi-frontline tuberculosis drugs</title><author>Mane, Shivshankar R. ; Chatterjee, Koushik ; Dinda, Himadri ; Sarma, Jayasri Das ; Shunmugam, Raja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c305t-94c6706f9d8bd2482a3c51b41c5f518a83605f6c252ad6af9728395c2943645a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Mycobacterium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mane, Shivshankar R.</creatorcontrib><creatorcontrib>Chatterjee, Koushik</creatorcontrib><creatorcontrib>Dinda, Himadri</creatorcontrib><creatorcontrib>Sarma, Jayasri Das</creatorcontrib><creatorcontrib>Shunmugam, Raja</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mane, Shivshankar R.</au><au>Chatterjee, Koushik</au><au>Dinda, Himadri</au><au>Sarma, Jayasri Das</au><au>Shunmugam, Raja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stimuli responsive nanocarrier for an effective delivery of multi-frontline tuberculosis drugs</atitle><jtitle>Polymer chemistry</jtitle><date>2014-04-21</date><risdate>2014</risdate><volume>5</volume><issue>8</issue><spage>2725</spage><epage>2735</epage><pages>2725-2735</pages><issn>1759-9954</issn><eissn>1759-9962</eissn><abstract>Pulmonary delivery, of both individual nanoparticles and encapsulated within carrier particles, is attractive method in antitubercular therapy; however, literature reports of these system have not shown consistently successful results due to poor loading of the frontline drug and inefficient sustained release profile. Here, a multifaceted synthetic strategy is employed to prepare stimuli responsive polymeric nanocarrier,
RCP-2
, with high purity, reproducibility, and precisely controlled stoichiometry of the drug motifs to demonstrate the high drug content as well as controlled release in a systematic manner. The drug release profile of
RCP-2
in mild acidic conditions implies the smart drug delivery nature of the nanocarrier. Cancerous cell lines, 4 T and A549, are employed due to their acidic nature to demonstrate the proposed pH responsive design. Surprisingly, the preliminary MTT assay against A549 cells (Lung cancer cell lines) shows a high anticancer efficacy. Taken together, these results demonstrate the significance of our unique design in which multi-frontline TB drugs are efficiently attached to produce the multi-task nanocarrier for potential therapeutic treatment.</abstract><doi>10.1039/C3PY01589K</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1759-9954 |
ispartof | Polymer chemistry, 2014-04, Vol.5 (8), p.2725-2735 |
issn | 1759-9954 1759-9962 |
language | eng |
recordid | cdi_proquest_miscellaneous_1520372868 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Mycobacterium |
title | Stimuli responsive nanocarrier for an effective delivery of multi-frontline tuberculosis drugs |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T09%3A39%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Stimuli%20responsive%20nanocarrier%20for%20an%20effective%20delivery%20of%20multi-frontline%20tuberculosis%20drugs&rft.jtitle=Polymer%20chemistry&rft.au=Mane,%20Shivshankar%20R.&rft.date=2014-04-21&rft.volume=5&rft.issue=8&rft.spage=2725&rft.epage=2735&rft.pages=2725-2735&rft.issn=1759-9954&rft.eissn=1759-9962&rft_id=info:doi/10.1039/C3PY01589K&rft_dat=%3Cproquest_cross%3E1520372868%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1520372868&rft_id=info:pmid/&rfr_iscdi=true |