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Nanoporous capsules of block co-polymers of [(MeO-PEG-NH)-b-(L-GluA)]-PCL for the controlled release of anticancer drugs for therapeutic applications
Herein, new nanoporous capsules of the block co-polymers of MeO-PEG-NH-(L-GluA)10 and polycaprolactone (PCL) have been synthesized through a surfactant-free cost-effective self-assembled soft-templating approach for the controlled release of drugs and for therapeutic applications. The nanoporous pol...
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Published in: | Nanotechnology 2016-03, Vol.27 (12), p.125101-125112 |
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container_title | Nanotechnology |
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creator | Amgoth, Chander Dharmapuri, Gangappa Kalle, Arunasree M Paik, Pradip |
description | Herein, new nanoporous capsules of the block co-polymers of MeO-PEG-NH-(L-GluA)10 and polycaprolactone (PCL) have been synthesized through a surfactant-free cost-effective self-assembled soft-templating approach for the controlled release of drugs and for therapeutic applications. The nanoporous polymer capsules are designed to be biocompatible and are capable of encapsulating anticancer drugs (e.g., doxorubicin hydrochloride (DOX) and imatinib mesylate (ITM)) with a high extent (∼279 and ∼480 ng g−1, respectively). We have developed a nanoformulation of porous MeO-PEG-NH-(L-GluA)10-PCL capsules with DOX and ITM. The porous polymer nanoformulations have been programmed in terms of the release of anticancer drugs with a desired dose to treat the leukemia (K562) and human carcinoma cells (HepG2) in vitro and show promising IC50 values with a very high mortality of cancer cells (up to ∼96.6%). Our nanoformulation arrests the cell divisions due to 'cellular scenescence' and kills the cancer cells specifically. The present findings could enrich the effectiveness of idiosyncratic nanoporous polymer capsules for use in various other nanomedicinal and biomedical applications, such as for killing cancer cells, immune therapy, and gene delivery. |
doi_str_mv | 10.1088/0957-4484/27/12/125101 |
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The nanoporous polymer capsules are designed to be biocompatible and are capable of encapsulating anticancer drugs (e.g., doxorubicin hydrochloride (DOX) and imatinib mesylate (ITM)) with a high extent (∼279 and ∼480 ng g−1, respectively). We have developed a nanoformulation of porous MeO-PEG-NH-(L-GluA)10-PCL capsules with DOX and ITM. The porous polymer nanoformulations have been programmed in terms of the release of anticancer drugs with a desired dose to treat the leukemia (K562) and human carcinoma cells (HepG2) in vitro and show promising IC50 values with a very high mortality of cancer cells (up to ∼96.6%). Our nanoformulation arrests the cell divisions due to 'cellular scenescence' and kills the cancer cells specifically. 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The nanoporous polymer capsules are designed to be biocompatible and are capable of encapsulating anticancer drugs (e.g., doxorubicin hydrochloride (DOX) and imatinib mesylate (ITM)) with a high extent (∼279 and ∼480 ng g−1, respectively). We have developed a nanoformulation of porous MeO-PEG-NH-(L-GluA)10-PCL capsules with DOX and ITM. The porous polymer nanoformulations have been programmed in terms of the release of anticancer drugs with a desired dose to treat the leukemia (K562) and human carcinoma cells (HepG2) in vitro and show promising IC50 values with a very high mortality of cancer cells (up to ∼96.6%). Our nanoformulation arrests the cell divisions due to 'cellular scenescence' and kills the cancer cells specifically. 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Dharmapuri, Gangappa ; Kalle, Arunasree M ; Paik, Pradip</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-d9186be616bf6438a4990cd00207a136fc4edf5cefa09bc951c78fd038cb81ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Blocking</topic><topic>Cancer</topic><topic>cancer therapy</topic><topic>Capsules - chemistry</topic><topic>Cell Survival - drug effects</topic><topic>Cellular</topic><topic>Controlled release</topic><topic>Copolymers</topic><topic>Delayed-Action Preparations</topic><topic>DOX</topic><topic>Doxorubicin - pharmacology</topic><topic>Drugs</topic><topic>Enrichment</topic><topic>Glucose Transporter Type 1</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Imatinib Mesylate - pharmacology</topic><topic>ITM</topic><topic>K562 Cells</topic><topic>nanomedicine</topic><topic>Nanopores</topic><topic>Nanostructure</topic><topic>Neoplasms - drug therapy</topic><topic>Particle Size</topic><topic>Polyesters - chemistry</topic><topic>polymer capsules</topic><topic>Polymers - chemical synthesis</topic><topic>Polymers - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amgoth, Chander</creatorcontrib><creatorcontrib>Dharmapuri, Gangappa</creatorcontrib><creatorcontrib>Kalle, Arunasree M</creatorcontrib><creatorcontrib>Paik, Pradip</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Nanotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amgoth, Chander</au><au>Dharmapuri, Gangappa</au><au>Kalle, Arunasree M</au><au>Paik, Pradip</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanoporous capsules of block co-polymers of [(MeO-PEG-NH)-b-(L-GluA)]-PCL for the controlled release of anticancer drugs for therapeutic applications</atitle><jtitle>Nanotechnology</jtitle><stitle>NANO</stitle><addtitle>Nanotechnology</addtitle><date>2016-03-29</date><risdate>2016</risdate><volume>27</volume><issue>12</issue><spage>125101</spage><epage>125112</epage><pages>125101-125112</pages><issn>0957-4484</issn><eissn>1361-6528</eissn><coden>NNOTER</coden><abstract>Herein, new nanoporous capsules of the block co-polymers of MeO-PEG-NH-(L-GluA)10 and polycaprolactone (PCL) have been synthesized through a surfactant-free cost-effective self-assembled soft-templating approach for the controlled release of drugs and for therapeutic applications. The nanoporous polymer capsules are designed to be biocompatible and are capable of encapsulating anticancer drugs (e.g., doxorubicin hydrochloride (DOX) and imatinib mesylate (ITM)) with a high extent (∼279 and ∼480 ng g−1, respectively). We have developed a nanoformulation of porous MeO-PEG-NH-(L-GluA)10-PCL capsules with DOX and ITM. The porous polymer nanoformulations have been programmed in terms of the release of anticancer drugs with a desired dose to treat the leukemia (K562) and human carcinoma cells (HepG2) in vitro and show promising IC50 values with a very high mortality of cancer cells (up to ∼96.6%). Our nanoformulation arrests the cell divisions due to 'cellular scenescence' and kills the cancer cells specifically. The present findings could enrich the effectiveness of idiosyncratic nanoporous polymer capsules for use in various other nanomedicinal and biomedical applications, such as for killing cancer cells, immune therapy, and gene delivery.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>26891479</pmid><doi>10.1088/0957-4484/27/12/125101</doi><tpages>12</tpages></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Blocking Cancer cancer therapy Capsules - chemistry Cell Survival - drug effects Cellular Controlled release Copolymers Delayed-Action Preparations DOX Doxorubicin - pharmacology Drugs Enrichment Glucose Transporter Type 1 HEK293 Cells Humans Imatinib Mesylate - pharmacology ITM K562 Cells nanomedicine Nanopores Nanostructure Neoplasms - drug therapy Particle Size Polyesters - chemistry polymer capsules Polymers - chemical synthesis Polymers - chemistry |
title | Nanoporous capsules of block co-polymers of [(MeO-PEG-NH)-b-(L-GluA)]-PCL for the controlled release of anticancer drugs for therapeutic applications |
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