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Automatic methodologies to perform loading and release assays of anticancer drugs from mesoporous silicon nanoparticles
Two automatic methodologies were developed to perform the loading and release assays of drugs from porous silicon (PSi) nanoparticles. 5-Fluorouracil (5-FU) was selected as a model drug, and different functionalized PSi nanoparticles were used. While for drug loading studies the reproducible charact...
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Published in: | Talanta (Oxford) 2019-05, Vol.196 (C), p.277-283 |
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creator | Pereira, Sarah A.P. Passos, Marieta L.C. Correia, Alexandra Mäkilä, Ermei Salonen, Jarno Araujo, André R.S.T. Santos, Hélder A. Saraiva, M. Lúcia M.F.S. |
description | Two automatic methodologies were developed to perform the loading and release assays of drugs from porous silicon (PSi) nanoparticles. 5-Fluorouracil (5-FU) was selected as a model drug, and different functionalized PSi nanoparticles were used. While for drug loading studies the reproducible characteristics of flow systems were explored regarding mixture and volumes taken, in the drug release flow methodology versatility in accommodating different devices around the valve were tested. Fluorescent properties of 5-FU were used with detection limit of 9 × 10−4 mg L−1 and a linear response up to 5 mg L−1 The drug loading and release procedures were optimized in sequential injection analysis (SIA) systems obtaining a huge economy regarding the time spent (4 min towards 2 h). Batch and SIA methods were tested and compared for the different behaviours of the PSi nanoparticles towards both methodologies and no noteworthy differences were obtained with Student's t-test for loading with a calculated t value of 2.04 showing the absence of statistical differences. All the results present a RSD less than 10%. So, the developed automatic methodologies are a viable alternative to load drugs and to study the release profiles from PSi nanoparticles.
[Display omitted]
•Loading and release SIA methods were developed for the first time.•5-FU and different surface functionalised PSi NPs were used in this work.•Advantages of automatic methods are showed in this work.•Less time and involvement and similar results to load and to plot the release profiles. |
doi_str_mv | 10.1016/j.talanta.2018.12.025 |
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[Display omitted]
•Loading and release SIA methods were developed for the first time.•5-FU and different surface functionalised PSi NPs were used in this work.•Advantages of automatic methods are showed in this work.•Less time and involvement and similar results to load and to plot the release profiles.</description><identifier>ISSN: 0039-9140</identifier><identifier>EISSN: 1873-3573</identifier><identifier>DOI: 10.1016/j.talanta.2018.12.025</identifier><identifier>PMID: 30683364</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>5-fluorouracil ; Antineoplastic Agents - chemistry ; Drug Carriers - chemistry ; Drug Liberation ; Fluorouracil - chemistry ; Loading ; Mesoporous silicon nanoparticles ; Nanoparticles - chemistry ; Porosity ; Release ; Sequential injection analysis ; Silicon - chemistry ; Surface Properties ; Technology, Pharmaceutical - methods</subject><ispartof>Talanta (Oxford), 2019-05, Vol.196 (C), p.277-283</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-5f56f5e24a7cc974c697f23ebb7ed4f46a8d614e86f3de52a694b8023c9376253</citedby><cites>FETCH-LOGICAL-c439t-5f56f5e24a7cc974c697f23ebb7ed4f46a8d614e86f3de52a694b8023c9376253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30683364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1636135$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Pereira, Sarah A.P.</creatorcontrib><creatorcontrib>Passos, Marieta L.C.</creatorcontrib><creatorcontrib>Correia, Alexandra</creatorcontrib><creatorcontrib>Mäkilä, Ermei</creatorcontrib><creatorcontrib>Salonen, Jarno</creatorcontrib><creatorcontrib>Araujo, André R.S.T.</creatorcontrib><creatorcontrib>Santos, Hélder A.</creatorcontrib><creatorcontrib>Saraiva, M. Lúcia M.F.S.</creatorcontrib><title>Automatic methodologies to perform loading and release assays of anticancer drugs from mesoporous silicon nanoparticles</title><title>Talanta (Oxford)</title><addtitle>Talanta</addtitle><description>Two automatic methodologies were developed to perform the loading and release assays of drugs from porous silicon (PSi) nanoparticles. 5-Fluorouracil (5-FU) was selected as a model drug, and different functionalized PSi nanoparticles were used. While for drug loading studies the reproducible characteristics of flow systems were explored regarding mixture and volumes taken, in the drug release flow methodology versatility in accommodating different devices around the valve were tested. Fluorescent properties of 5-FU were used with detection limit of 9 × 10−4 mg L−1 and a linear response up to 5 mg L−1 The drug loading and release procedures were optimized in sequential injection analysis (SIA) systems obtaining a huge economy regarding the time spent (4 min towards 2 h). Batch and SIA methods were tested and compared for the different behaviours of the PSi nanoparticles towards both methodologies and no noteworthy differences were obtained with Student's t-test for loading with a calculated t value of 2.04 showing the absence of statistical differences. All the results present a RSD less than 10%. So, the developed automatic methodologies are a viable alternative to load drugs and to study the release profiles from PSi nanoparticles.
[Display omitted]
•Loading and release SIA methods were developed for the first time.•5-FU and different surface functionalised PSi NPs were used in this work.•Advantages of automatic methods are showed in this work.•Less time and involvement and similar results to load and to plot the release profiles.</description><subject>5-fluorouracil</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Liberation</subject><subject>Fluorouracil - chemistry</subject><subject>Loading</subject><subject>Mesoporous silicon nanoparticles</subject><subject>Nanoparticles - chemistry</subject><subject>Porosity</subject><subject>Release</subject><subject>Sequential injection analysis</subject><subject>Silicon - chemistry</subject><subject>Surface Properties</subject><subject>Technology, Pharmaceutical - methods</subject><issn>0039-9140</issn><issn>1873-3573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkE9v1DAQxS0EokvLRwBZ3BP8L05yQlVVClIlLvRszdrjrVdJHNleUL89Dlt65TTS6PfevHmEfOCs5Yzrz8e2wARLgVYwPrRctEx0r8iOD71sZNfL12THmBybkSt2Qd7lfGSMCcnkW3IhmR6k1GpHfl-fSpyhBEtnLI_RxSkeAmZaIl0x-ZhmOkVwYTlQWBxNOCFkpJAzPGUafd1WMSwWE3XpdMjUpzhXsxzXmOIp0xymYONCF1jiCqnSE-Yr8sbDlPH987wkD19vf958a-5_3H2_ub5vrJJjaTrfad-hUNBbO_bK6rH3QuJ-36NTXmkYnOYKB-2lw06AHtV-qG_aUfZadPKSfDr7xlyCyTYUtI81zYK2GK6l5nKDujNkU8w5oTdrCjOkJ8OZ2do2R_PcttnaNlwY9tf841m3nvYzuhfVv3or8OUMYH3xV8C0JcDalQtpC-Bi-M-JP5BaljY</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Pereira, Sarah A.P.</creator><creator>Passos, Marieta L.C.</creator><creator>Correia, Alexandra</creator><creator>Mäkilä, Ermei</creator><creator>Salonen, Jarno</creator><creator>Araujo, André R.S.T.</creator><creator>Santos, Hélder A.</creator><creator>Saraiva, M. Lúcia M.F.S.</creator><general>Elsevier B.V</general><general>Elsevier</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>OTOTI</scope></search><sort><creationdate>20190501</creationdate><title>Automatic methodologies to perform loading and release assays of anticancer drugs from mesoporous silicon nanoparticles</title><author>Pereira, Sarah A.P. ; Passos, Marieta L.C. ; Correia, Alexandra ; Mäkilä, Ermei ; Salonen, Jarno ; Araujo, André R.S.T. ; Santos, Hélder A. ; Saraiva, M. 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Lúcia M.F.S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pereira, Sarah A.P.</au><au>Passos, Marieta L.C.</au><au>Correia, Alexandra</au><au>Mäkilä, Ermei</au><au>Salonen, Jarno</au><au>Araujo, André R.S.T.</au><au>Santos, Hélder A.</au><au>Saraiva, M. Lúcia M.F.S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automatic methodologies to perform loading and release assays of anticancer drugs from mesoporous silicon nanoparticles</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>196</volume><issue>C</issue><spage>277</spage><epage>283</epage><pages>277-283</pages><issn>0039-9140</issn><eissn>1873-3573</eissn><abstract>Two automatic methodologies were developed to perform the loading and release assays of drugs from porous silicon (PSi) nanoparticles. 5-Fluorouracil (5-FU) was selected as a model drug, and different functionalized PSi nanoparticles were used. While for drug loading studies the reproducible characteristics of flow systems were explored regarding mixture and volumes taken, in the drug release flow methodology versatility in accommodating different devices around the valve were tested. Fluorescent properties of 5-FU were used with detection limit of 9 × 10−4 mg L−1 and a linear response up to 5 mg L−1 The drug loading and release procedures were optimized in sequential injection analysis (SIA) systems obtaining a huge economy regarding the time spent (4 min towards 2 h). Batch and SIA methods were tested and compared for the different behaviours of the PSi nanoparticles towards both methodologies and no noteworthy differences were obtained with Student's t-test for loading with a calculated t value of 2.04 showing the absence of statistical differences. All the results present a RSD less than 10%. So, the developed automatic methodologies are a viable alternative to load drugs and to study the release profiles from PSi nanoparticles.
[Display omitted]
•Loading and release SIA methods were developed for the first time.•5-FU and different surface functionalised PSi NPs were used in this work.•Advantages of automatic methods are showed in this work.•Less time and involvement and similar results to load and to plot the release profiles.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30683364</pmid><doi>10.1016/j.talanta.2018.12.025</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 5-fluorouracil Antineoplastic Agents - chemistry Drug Carriers - chemistry Drug Liberation Fluorouracil - chemistry Loading Mesoporous silicon nanoparticles Nanoparticles - chemistry Porosity Release Sequential injection analysis Silicon - chemistry Surface Properties Technology, Pharmaceutical - methods |
title | Automatic methodologies to perform loading and release assays of anticancer drugs from mesoporous silicon nanoparticles |
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