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1. Identity statement
Reference TypeJournal Article
Siteplutao.sid.inpe.br
Holder Codeisadg {BR SPINPE} ibi 8JMKD3MGPCW/3DT298S
Identifier8JMKD3MGP3W/474P4LL
Repositorysid.inpe.br/plutao/2022/06.15.13.15   (restricted access)
Last Update2022:06.20.17.35.03 (UTC) lattes
Metadata Repositorysid.inpe.br/plutao/2022/06.15.13.15.20
Metadata Last Update2023:01.03.16.52.56 (UTC) administrator
ISSN2574-1241
Labellattes: 3455204481678421 7 WacheskHuCoTaVaCoTr:2022:SyCVDi
Citation KeyWacheskHuCoTaVaCoTr:2022:SyCVDi
TitleSynthesis of CVD Diamond Nanoparticles and Cytotoxicity Evaluation in Murine Metastatic Melanoma Cells
Year2022
Access Date2024, May 19
Type of Workjournal article
Secondary TypePRE PI
Number of Files1
Size2772 KiB
2. Context
Author1 Wachesk, Cristiane da Costa
2 Hurtado, Carolina R.
3 Correia, Rebeca Falcão Borja de Oliveira
4 Tada, Dayane Batista
5 Vasconcelos, Getúlio de
6 Corat, Evaldo José
7 Trava-Airoldi, Vladimir Jesus
Resume Identifier1
2
3
4
5
6 8JMKD3MGP5W/3C9JH33
Group1
2
3
4
5
6 COPDT-CGIP-INPE-MCTI-GOV-BR
7 COPDT-CGIP-INPE-MCTI-GOV-BR
Affiliation1 Universidade Federal de São Paulo (UNIFESP)
2 Universidade Federal de São Paulo (UNIFESP)
3 Universidade Federal de São Paulo (UNIFESP)
4 Universidade Federal de São Paulo (UNIFESP)
5 Instituto de Estudos Avançados (IEAv)
6 Instituto Nacional de Pesquisas Espaciais (INPE)
7 Instituto Nacional de Pesquisas Espaciais (INPE)
Author e-Mail Address1
2
3
4
5
6 evaldo.corat@inpe.br
7 vladimirjta@gmail.com
JournalBiomedical: Journal of Scientific and Technical Research
Volume41
Number3
Pages32695
History (UTC)2022-06-20 17:35:05 :: lattes -> administrator :: 2022
2023-01-03 16:52:56 :: administrator -> simone :: 2022
3. Content and structure
Is the master or a copy?is the master
Content Stagecompleted
Transferable1
Content TypeExternal Contribution
Version Typepublisher
KeywordsNano partículas
Diamante-CVD
Melanoma Cells
citotoxicidade
Murine
AbstractDiamond nanoparticles (DNPs) have demonstrated in vitro and in vivo biomedical applicability due to their low toxicity and biocompatibility. Recent studies have focused on the potential use of DNPs as suitable vehicles to improve drug delivery in cancer treatment. The advantages of DNPs lie in their high stability and small size compared to other carbon-based nanomaterials. In this work, CVD-diamond nanoparticles (CVDDNPs) were synthesized and evaluated for their application as a new drug delivery platform for metastatic melanoma therapy. A new synthesis technique developed DNPs from CVD diamond thin film. This type of diamond has the same physical and chemical properties as a natural diamond: extreme hardness, excellent thermal conductivity, low coefficient of friction, biocompatibility, and is chemically inert at temperatures below 800 °C. The main objective of this study was to produce CVD-DNPs by laser ablation and evaluate their cytotoxicity. A pulsed, ytterbium-doped fiber (Yb) was used to form DNPs in pure aqueous medium (Milli-Q). The final suspension was obtained at high concentration of the CVD-DNPs and was used to evaluate the cytotoxicity in murine metastatic melanoma B16-F10 cells by using colorimetric assays. The characterization by FT-IR, X-Ray, DLS, RAMAN, SEM, and TEM demonstrated the successful synthesis of CVD-DNPs with a hydrodynamic diameter of 57 and 54 nm. In vitro studies performed for 24 h and 48 h resulted in 7080% viability of cells incubated with CVD-DNPs at 250 μg/mL, which demonstrated an insignificant cytotoxic effect. Thus, these results suggest the potential use of CVD-DNPs as a drug delivery platform for antitumoral therapy.
AreaFISMAT
Arrangementurlib.net > BDMCI > Fonds > Produção a partir de 2021 > CGIP > Synthesis of CVD...
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4. Conditions of access and use
Languageen
Target FileBJSTR.MS.ID.006604.pdf
User Grouplattes
Reader Groupadministrator
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Visibilityshown
Read Permissiondeny from all and allow from 150.163
Update Permissionnot transferred
5. Allied materials
Next Higher Units8JMKD3MGPCW/46KUES5
Citing Item Listsid.inpe.br/bibdigital/2022/04.03.23.11 1
Host Collectiondpi.inpe.br/plutao@80/2008/08.19.15.01
6. Notes
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