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Novel nanoformulated diethyldithiocarbamate complexes with biosynthesized or green chemosynthesized copper oxide nanoparticles: An in vitro comparative anticancer study
[Display omitted] •Novel nanoformulation of diethyldithiocarbamate by cupper oxide nanoparticles (NPs).•Bacterially (Bio) and green chemically (Chemo) synthesized cupper oxide NPs were used.•Cellular uptake and prooxidant activity of Chemo nanocomplex (CD) was better.•Thus Chemo CD NPs had stronger...
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Published in: | International journal of pharmaceutics 2021-11, Vol.609, p.121149-121149, Article 121149 |
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container_title | International journal of pharmaceutics |
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creator | Abu‑Serie, Marwa M. Eltarahony, Marwa |
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•Novel nanoformulation of diethyldithiocarbamate by cupper oxide nanoparticles (NPs).•Bacterially (Bio) and green chemically (Chemo) synthesized cupper oxide NPs were used.•Cellular uptake and prooxidant activity of Chemo nanocomplex (CD) was better.•Thus Chemo CD NPs had stronger apoptotic anticancer effect than Bio CD NPs (in vitro).•Halting lung, colon, liver and prostate cancer migration was higher in Chemo CD NPs.
Developing more soluble and stable nanoformulation for the potent anticancer complex of copper diethyldithiocarbamate (CD) is extremely desired. Herein, for the first time, CD nanoparticles (NPs) were formulated by chelating diethyldithiocarbamate to bacterially and green chemically prepared copper oxide NPs (Bio CO NPs and Chemo CO NPs, respectively). Chemo CO NPs were produced in simpler and less time-consuming manner with higher NPs homogeneity. These CO NPs were identified, by X-ray diffractometer, as CuO and Cu2O, respectively. The nanoformulated CD complexes (Bio CD NPs and Chemo CD NPs) which have nanosizes (215.7 nm and 148.1 nm, respectively) with negative zeta potentials (∼−20 mv), exhibited not only high serum stability and solubility but also a potent anticancer effect. More importantly, Chemo CD NPs outperformed Bio CD NPs in the terms of synergistic anticancer index, apoptosis induction (>81% and |
doi_str_mv | 10.1016/j.ijpharm.2021.121149 |
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•Novel nanoformulation of diethyldithiocarbamate by cupper oxide nanoparticles (NPs).•Bacterially (Bio) and green chemically (Chemo) synthesized cupper oxide NPs were used.•Cellular uptake and prooxidant activity of Chemo nanocomplex (CD) was better.•Thus Chemo CD NPs had stronger apoptotic anticancer effect than Bio CD NPs (in vitro).•Halting lung, colon, liver and prostate cancer migration was higher in Chemo CD NPs.
Developing more soluble and stable nanoformulation for the potent anticancer complex of copper diethyldithiocarbamate (CD) is extremely desired. Herein, for the first time, CD nanoparticles (NPs) were formulated by chelating diethyldithiocarbamate to bacterially and green chemically prepared copper oxide NPs (Bio CO NPs and Chemo CO NPs, respectively). Chemo CO NPs were produced in simpler and less time-consuming manner with higher NPs homogeneity. These CO NPs were identified, by X-ray diffractometer, as CuO and Cu2O, respectively. The nanoformulated CD complexes (Bio CD NPs and Chemo CD NPs) which have nanosizes (215.7 nm and 148.1 nm, respectively) with negative zeta potentials (∼−20 mv), exhibited not only high serum stability and solubility but also a potent anticancer effect. More importantly, Chemo CD NPs outperformed Bio CD NPs in the terms of synergistic anticancer index, apoptosis induction (>81% and <54%, respectively) and anti-migration efficacy (≥80% and <71%, respectively). This could be attributed to smaller nanosize and Cu2O of Chemo CD NPs causing higher cellular uptake with stronger inhibition of aldehyde dehydrogenase 1A1 and more free radical generation in Chemo CD NPs-treated cancer cells than Bio CD NPs. This distinct anticancer efficacy of novel Chemo CD NPs deserves further investigation using animal models.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2021.121149</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Anti-cancer cell migration ; Apoptosis-dependent anticancer efficacy ; Biosynthesized cupric oxide nanoparticles ; Cellular redox status ; Diethyldithiocarbamate nanocomplexes ; Green chemosynthesized cuprous oxide nanoparticles</subject><ispartof>International journal of pharmaceutics, 2021-11, Vol.609, p.121149-121149, Article 121149</ispartof><rights>2021 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-4b774e460e6c01f0b1f8ae532c6db5d62fddc930c15e5c14e4b0f975a57cad953</citedby><cites>FETCH-LOGICAL-c342t-4b774e460e6c01f0b1f8ae532c6db5d62fddc930c15e5c14e4b0f975a57cad953</cites><orcidid>0000-0002-2739-6231</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Abu‑Serie, Marwa M.</creatorcontrib><creatorcontrib>Eltarahony, Marwa</creatorcontrib><title>Novel nanoformulated diethyldithiocarbamate complexes with biosynthesized or green chemosynthesized copper oxide nanoparticles: An in vitro comparative anticancer study</title><title>International journal of pharmaceutics</title><description>[Display omitted]
•Novel nanoformulation of diethyldithiocarbamate by cupper oxide nanoparticles (NPs).•Bacterially (Bio) and green chemically (Chemo) synthesized cupper oxide NPs were used.•Cellular uptake and prooxidant activity of Chemo nanocomplex (CD) was better.•Thus Chemo CD NPs had stronger apoptotic anticancer effect than Bio CD NPs (in vitro).•Halting lung, colon, liver and prostate cancer migration was higher in Chemo CD NPs.
Developing more soluble and stable nanoformulation for the potent anticancer complex of copper diethyldithiocarbamate (CD) is extremely desired. Herein, for the first time, CD nanoparticles (NPs) were formulated by chelating diethyldithiocarbamate to bacterially and green chemically prepared copper oxide NPs (Bio CO NPs and Chemo CO NPs, respectively). Chemo CO NPs were produced in simpler and less time-consuming manner with higher NPs homogeneity. These CO NPs were identified, by X-ray diffractometer, as CuO and Cu2O, respectively. The nanoformulated CD complexes (Bio CD NPs and Chemo CD NPs) which have nanosizes (215.7 nm and 148.1 nm, respectively) with negative zeta potentials (∼−20 mv), exhibited not only high serum stability and solubility but also a potent anticancer effect. More importantly, Chemo CD NPs outperformed Bio CD NPs in the terms of synergistic anticancer index, apoptosis induction (>81% and <54%, respectively) and anti-migration efficacy (≥80% and <71%, respectively). This could be attributed to smaller nanosize and Cu2O of Chemo CD NPs causing higher cellular uptake with stronger inhibition of aldehyde dehydrogenase 1A1 and more free radical generation in Chemo CD NPs-treated cancer cells than Bio CD NPs. This distinct anticancer efficacy of novel Chemo CD NPs deserves further investigation using animal models.</description><subject>Anti-cancer cell migration</subject><subject>Apoptosis-dependent anticancer efficacy</subject><subject>Biosynthesized cupric oxide nanoparticles</subject><subject>Cellular redox status</subject><subject>Diethyldithiocarbamate nanocomplexes</subject><subject>Green chemosynthesized cuprous oxide nanoparticles</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhS0EEkvpT6jkI5csdhzHCRdUVRQqVXApZ8sZT4hXiR1s79LtL-Jn4nZ74dTTSDPvvdHTR8gFZ1vOePtxt3W7dTJx2das5ltec970r8iGd0pUolHta7JhQnWV5Eq8Je9S2jHG2pqLDfn7PRxwpt74MIa47GeT0VLrME_H2bo8uQAmDmYpewphWWe8x0T_lAsdXEhHnydM7qGYQqS_IqKnMOHy3wXCumKk4d5ZfHq1mpgdzJg-0UtPnacHl2N4yjfRZHdAanxRGA_Fl_LeHt-TN6OZE54_zzPy8_rL3dW36vbH15ury9sKRFPnqhmUarBpGbbA-MgGPnYGpaihtYO0bT1aC71gwCVK4EU6sLFX0kgFxvZSnJEPp9w1ht97TFkvLgHOs_EY9knXUvWsk51silSepBBDShFHvUa3mHjUnOlHMnqnn8noRzL6RKb4Pp98WHocHEadwGGpal1EyNoG90LCP2bioNk</recordid><startdate>20211120</startdate><enddate>20211120</enddate><creator>Abu‑Serie, Marwa M.</creator><creator>Eltarahony, Marwa</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2739-6231</orcidid></search><sort><creationdate>20211120</creationdate><title>Novel nanoformulated diethyldithiocarbamate complexes with biosynthesized or green chemosynthesized copper oxide nanoparticles: An in vitro comparative anticancer study</title><author>Abu‑Serie, Marwa M. ; Eltarahony, Marwa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-4b774e460e6c01f0b1f8ae532c6db5d62fddc930c15e5c14e4b0f975a57cad953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anti-cancer cell migration</topic><topic>Apoptosis-dependent anticancer efficacy</topic><topic>Biosynthesized cupric oxide nanoparticles</topic><topic>Cellular redox status</topic><topic>Diethyldithiocarbamate nanocomplexes</topic><topic>Green chemosynthesized cuprous oxide nanoparticles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abu‑Serie, Marwa M.</creatorcontrib><creatorcontrib>Eltarahony, Marwa</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abu‑Serie, Marwa M.</au><au>Eltarahony, Marwa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel nanoformulated diethyldithiocarbamate complexes with biosynthesized or green chemosynthesized copper oxide nanoparticles: An in vitro comparative anticancer study</atitle><jtitle>International journal of pharmaceutics</jtitle><date>2021-11-20</date><risdate>2021</risdate><volume>609</volume><spage>121149</spage><epage>121149</epage><pages>121149-121149</pages><artnum>121149</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
•Novel nanoformulation of diethyldithiocarbamate by cupper oxide nanoparticles (NPs).•Bacterially (Bio) and green chemically (Chemo) synthesized cupper oxide NPs were used.•Cellular uptake and prooxidant activity of Chemo nanocomplex (CD) was better.•Thus Chemo CD NPs had stronger apoptotic anticancer effect than Bio CD NPs (in vitro).•Halting lung, colon, liver and prostate cancer migration was higher in Chemo CD NPs.
Developing more soluble and stable nanoformulation for the potent anticancer complex of copper diethyldithiocarbamate (CD) is extremely desired. Herein, for the first time, CD nanoparticles (NPs) were formulated by chelating diethyldithiocarbamate to bacterially and green chemically prepared copper oxide NPs (Bio CO NPs and Chemo CO NPs, respectively). Chemo CO NPs were produced in simpler and less time-consuming manner with higher NPs homogeneity. These CO NPs were identified, by X-ray diffractometer, as CuO and Cu2O, respectively. The nanoformulated CD complexes (Bio CD NPs and Chemo CD NPs) which have nanosizes (215.7 nm and 148.1 nm, respectively) with negative zeta potentials (∼−20 mv), exhibited not only high serum stability and solubility but also a potent anticancer effect. More importantly, Chemo CD NPs outperformed Bio CD NPs in the terms of synergistic anticancer index, apoptosis induction (>81% and <54%, respectively) and anti-migration efficacy (≥80% and <71%, respectively). This could be attributed to smaller nanosize and Cu2O of Chemo CD NPs causing higher cellular uptake with stronger inhibition of aldehyde dehydrogenase 1A1 and more free radical generation in Chemo CD NPs-treated cancer cells than Bio CD NPs. This distinct anticancer efficacy of novel Chemo CD NPs deserves further investigation using animal models.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.ijpharm.2021.121149</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-2739-6231</orcidid></addata></record> |
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subjects | Anti-cancer cell migration Apoptosis-dependent anticancer efficacy Biosynthesized cupric oxide nanoparticles Cellular redox status Diethyldithiocarbamate nanocomplexes Green chemosynthesized cuprous oxide nanoparticles |
title | Novel nanoformulated diethyldithiocarbamate complexes with biosynthesized or green chemosynthesized copper oxide nanoparticles: An in vitro comparative anticancer study |
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