Newly emerging mesoporous strontium hydroxyapatite nanorods: microwave synthesis and relevance as doxorubicin nanocarrier
A new synthesis method is developed for preparation of mesoporous strontium hydroxyapatite (SrHAp) nanorods using CEM Discover microwave synthesizer. Nanorods preparation with surfactants SrHAp(+) and without surfactants SrHAp(−) were successfully achieved at 160 °C temperature and 15 min of hold ti...
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| Veröffentlicht in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2018-09, Vol.20 (9), p.1-11, Article 230 |
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| creator | Agrawal, Shital Kelkar, Madhura De, Abhijit Kulkarni, Ajit R. Gandhi, Mayuri N. |
| description | A new synthesis method is developed for preparation of mesoporous strontium hydroxyapatite (SrHAp) nanorods using CEM Discover microwave synthesizer. Nanorods preparation with surfactants SrHAp(+) and without surfactants SrHAp(−) were successfully achieved at 160 °C temperature and 15 min of hold time. Particle sizes with standard deviation were found to be 67 ± 18 and 69 ± 24 nm respectively. Mesoporous nanorods were thoroughly characterized using different methods, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field-emission gun transmission electron microscopy (FEG-TEM), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) surface area and porosity measurement. It was observed that use of trisodium citrate and CTAB resulted in quite agglomerated particles, whereas nanorods synthesized without citrate and CTAB were well dispersed. Cell toxicity of both these materials synthesized was tested in MCF-7 and Zr-75 cell lines using MTT assay. SrHAp nanorods concentration up to 0.25 mg/ml was non-toxic at 48 hours (h) time point in both the cell lines. As SrHAp(−) were found to serve better in terms of cytotoxicity, they were chosen for doxorubicin (Dox) loading, pH depended release and cell uptake study. The successful loading of Dox was ascertained by UV-Visible and FTIR spectroscopy. Entrapment efficiency of Dox in SrHAp nanoparticles was found to be 83.71%, and loading capacity was 0.017 μg Dox per μg SrHAp nanoparticles. Rapid release was observed in the initial hours followed by slow release. Even until 31 days, only 27 and 32% drug was released at pH 7.4 and pH 4.5 respectively, which shows controlled release behavior. Further, cellular uptake of Dox-loaded nanoparticles at different time points was studied in the two breast cancer cell lines by fluorescence imaging. These nanoparticles were found to internalize within both these cells after 3 h of incubation and continued further until 24 h. Overall, high Dox loading efficacy, sustained release behavior, and cell uptake potential render SrHAp nanoparticles to give promising results when applied in vivo and emerge as a robust drug carrier towards solving purpose of slow and prolonged drug release.
Graphical abstract
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| doi_str_mv | 10.1007/s11051-018-4335-y |
| format | Article |
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Graphical abstract
ᅟ</description><identifier>ISSN: 1388-0764</identifier><identifier>EISSN: 1572-896X</identifier><identifier>DOI: 10.1007/s11051-018-4335-y</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Biocompatibility ; Biotechnology ; Breast cancer ; Characterization and Evaluation of Materials ; Chemistry and Materials Science ; Citric acid ; Controlled release ; Cytotoxicity ; Doxorubicin ; Drug carriers ; Drug delivery systems ; Entrapment ; Fluorescence ; Fourier transforms ; Hydroxyapatite ; Infrared spectroscopy ; Inorganic Chemistry ; Lasers ; Materials Science ; Microscopy ; Nanoparticles ; Nanorods ; Nanotechnology ; Optical Devices ; Optics ; pH effects ; Photonics ; Physical Chemistry ; Porosity ; Research Paper ; Scanning electron microscopy ; Sodium citrate ; Spectrum analysis ; Strontium ; Surfactants ; Sustained release ; Synthesis ; Toxicity ; Transmission electron microscopy ; Tumor cell lines ; X-ray diffraction ; Zirconium</subject><ispartof>Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology, 2018-09, Vol.20 (9), p.1-11, Article 230</ispartof><rights>Springer Nature B.V. 2018</rights><rights>Journal of Nanoparticle Research is a copyright of Springer, (2018). All Rights Reserved.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-8a7718cd394affce43cbe7c9959fda5dcc1cf215c4f2a683e5f7c927356279c43</citedby><cites>FETCH-LOGICAL-c316t-8a7718cd394affce43cbe7c9959fda5dcc1cf215c4f2a683e5f7c927356279c43</cites><orcidid>0000-0002-6382-9137</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11051-018-4335-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11051-018-4335-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Agrawal, Shital</creatorcontrib><creatorcontrib>Kelkar, Madhura</creatorcontrib><creatorcontrib>De, Abhijit</creatorcontrib><creatorcontrib>Kulkarni, Ajit R.</creatorcontrib><creatorcontrib>Gandhi, Mayuri N.</creatorcontrib><title>Newly emerging mesoporous strontium hydroxyapatite nanorods: microwave synthesis and relevance as doxorubicin nanocarrier</title><title>Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology</title><addtitle>J Nanopart Res</addtitle><description>A new synthesis method is developed for preparation of mesoporous strontium hydroxyapatite (SrHAp) nanorods using CEM Discover microwave synthesizer. Nanorods preparation with surfactants SrHAp(+) and without surfactants SrHAp(−) were successfully achieved at 160 °C temperature and 15 min of hold time. Particle sizes with standard deviation were found to be 67 ± 18 and 69 ± 24 nm respectively. Mesoporous nanorods were thoroughly characterized using different methods, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field-emission gun transmission electron microscopy (FEG-TEM), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) surface area and porosity measurement. It was observed that use of trisodium citrate and CTAB resulted in quite agglomerated particles, whereas nanorods synthesized without citrate and CTAB were well dispersed. Cell toxicity of both these materials synthesized was tested in MCF-7 and Zr-75 cell lines using MTT assay. SrHAp nanorods concentration up to 0.25 mg/ml was non-toxic at 48 hours (h) time point in both the cell lines. As SrHAp(−) were found to serve better in terms of cytotoxicity, they were chosen for doxorubicin (Dox) loading, pH depended release and cell uptake study. The successful loading of Dox was ascertained by UV-Visible and FTIR spectroscopy. Entrapment efficiency of Dox in SrHAp nanoparticles was found to be 83.71%, and loading capacity was 0.017 μg Dox per μg SrHAp nanoparticles. Rapid release was observed in the initial hours followed by slow release. Even until 31 days, only 27 and 32% drug was released at pH 7.4 and pH 4.5 respectively, which shows controlled release behavior. Further, cellular uptake of Dox-loaded nanoparticles at different time points was studied in the two breast cancer cell lines by fluorescence imaging. These nanoparticles were found to internalize within both these cells after 3 h of incubation and continued further until 24 h. Overall, high Dox loading efficacy, sustained release behavior, and cell uptake potential render SrHAp nanoparticles to give promising results when applied in vivo and emerge as a robust drug carrier towards solving purpose of slow and prolonged drug release.
Graphical abstract
ᅟ</description><subject>Biocompatibility</subject><subject>Biotechnology</subject><subject>Breast cancer</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry and Materials Science</subject><subject>Citric acid</subject><subject>Controlled release</subject><subject>Cytotoxicity</subject><subject>Doxorubicin</subject><subject>Drug carriers</subject><subject>Drug delivery systems</subject><subject>Entrapment</subject><subject>Fluorescence</subject><subject>Fourier transforms</subject><subject>Hydroxyapatite</subject><subject>Infrared spectroscopy</subject><subject>Inorganic Chemistry</subject><subject>Lasers</subject><subject>Materials Science</subject><subject>Microscopy</subject><subject>Nanoparticles</subject><subject>Nanorods</subject><subject>Nanotechnology</subject><subject>Optical Devices</subject><subject>Optics</subject><subject>pH effects</subject><subject>Photonics</subject><subject>Physical Chemistry</subject><subject>Porosity</subject><subject>Research Paper</subject><subject>Scanning electron microscopy</subject><subject>Sodium citrate</subject><subject>Spectrum analysis</subject><subject>Strontium</subject><subject>Surfactants</subject><subject>Sustained release</subject><subject>Synthesis</subject><subject>Toxicity</subject><subject>Transmission electron microscopy</subject><subject>Tumor cell lines</subject><subject>X-ray 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Abstracts</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><jtitle>Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agrawal, Shital</au><au>Kelkar, Madhura</au><au>De, Abhijit</au><au>Kulkarni, Ajit R.</au><au>Gandhi, Mayuri N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Newly emerging mesoporous strontium hydroxyapatite nanorods: microwave synthesis and relevance as doxorubicin nanocarrier</atitle><jtitle>Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology</jtitle><stitle>J Nanopart Res</stitle><date>2018-09-01</date><risdate>2018</risdate><volume>20</volume><issue>9</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><artnum>230</artnum><issn>1388-0764</issn><eissn>1572-896X</eissn><abstract>A new synthesis method is developed for preparation of mesoporous strontium hydroxyapatite (SrHAp) nanorods using CEM Discover microwave synthesizer. Nanorods preparation with surfactants SrHAp(+) and without surfactants SrHAp(−) were successfully achieved at 160 °C temperature and 15 min of hold time. Particle sizes with standard deviation were found to be 67 ± 18 and 69 ± 24 nm respectively. Mesoporous nanorods were thoroughly characterized using different methods, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field-emission gun transmission electron microscopy (FEG-TEM), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) surface area and porosity measurement. It was observed that use of trisodium citrate and CTAB resulted in quite agglomerated particles, whereas nanorods synthesized without citrate and CTAB were well dispersed. Cell toxicity of both these materials synthesized was tested in MCF-7 and Zr-75 cell lines using MTT assay. SrHAp nanorods concentration up to 0.25 mg/ml was non-toxic at 48 hours (h) time point in both the cell lines. As SrHAp(−) were found to serve better in terms of cytotoxicity, they were chosen for doxorubicin (Dox) loading, pH depended release and cell uptake study. The successful loading of Dox was ascertained by UV-Visible and FTIR spectroscopy. Entrapment efficiency of Dox in SrHAp nanoparticles was found to be 83.71%, and loading capacity was 0.017 μg Dox per μg SrHAp nanoparticles. Rapid release was observed in the initial hours followed by slow release. Even until 31 days, only 27 and 32% drug was released at pH 7.4 and pH 4.5 respectively, which shows controlled release behavior. Further, cellular uptake of Dox-loaded nanoparticles at different time points was studied in the two breast cancer cell lines by fluorescence imaging. These nanoparticles were found to internalize within both these cells after 3 h of incubation and continued further until 24 h. Overall, high Dox loading efficacy, sustained release behavior, and cell uptake potential render SrHAp nanoparticles to give promising results when applied in vivo and emerge as a robust drug carrier towards solving purpose of slow and prolonged drug release.
Graphical abstract
ᅟ</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11051-018-4335-y</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6382-9137</orcidid></addata></record> |
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| subjects | Biocompatibility Biotechnology Breast cancer Characterization and Evaluation of Materials Chemistry and Materials Science Citric acid Controlled release Cytotoxicity Doxorubicin Drug carriers Drug delivery systems Entrapment Fluorescence Fourier transforms Hydroxyapatite Infrared spectroscopy Inorganic Chemistry Lasers Materials Science Microscopy Nanoparticles Nanorods Nanotechnology Optical Devices Optics pH effects Photonics Physical Chemistry Porosity Research Paper Scanning electron microscopy Sodium citrate Spectrum analysis Strontium Surfactants Sustained release Synthesis Toxicity Transmission electron microscopy Tumor cell lines X-ray diffraction Zirconium |
| title | Newly emerging mesoporous strontium hydroxyapatite nanorods: microwave synthesis and relevance as doxorubicin nanocarrier |
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