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dc.contributor.authorDaraee, H
dc.contributor.authorPourhassanmoghadam, M
dc.contributor.authorAkbarzadeh, A
dc.contributor.authorZarghami, N
dc.contributor.authorRahmati-Yamchi, M
dc.date.accessioned2018-08-26T08:56:25Z
dc.date.available2018-08-26T08:56:25Z
dc.date.issued2016
dc.identifier10.3109/21691401.2015.1031905
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54441
dc.description.abstractAimml: The aim of this project was to synthesize and characterize gold nanoparticles (GNPs) to trace the sequence of the hnRNPB1as a lung cancer biomarker. Methods: In the synthesis of GNPs with characteristics appropriate for conjugation, the size, morphology, and shape of the synthesized GNPs were determined by using spectrophotometry and transmission electron microscopy (TEM), followed by designing a probe for hnRNPB1biomarker with characteristics suitable for conjugation. Next, the GNPs were functionalized with a single-stranded DNA probe that was specific for the biomarker, for the characterization and confirmation of the conjugation process. Finally, for determination of minimum level of detection in solution including DNA target and probe aggregation, the changes in the absorption spectra of the samples in the range of 250-750 nm were determined using the NanoDrop ND 1000 spectrophotometer. Results: The surface of GNPs can be modified by utilizing ligands to selectively attach biomarkers. Thiol-bonding of DNA and chemical functionalization of GNPs are the most common approaches. Colloidal gold was synthesized with the citrate reduction method, as described by Turkevich et al. in 1951. In this study, the probe for hnRNPB1 was designed with a thiol crosslinker. Every set of conjugated GNPs was complementary to one end of the hnRNPB1 biomarker, and the probes were aligned in a tail to tail fashion onto the target. Conclusion: Uniform GNPs were synthesized by the citrate reduction technique, and the outcomes of trials with variation in factors (shape and size of the nanoparticles, gold concentration, and conjugation between GNP and probes) were investigated. The gold nanoprobe-based technique is better than the PCR-based techniques, because there are no requirements of enzymatic amplification and gel electrophoresis, and the evaluation can be done using small amounts of sample. é 2015 Informa Healthcare USA, Inc.
dc.language.isoEnglish
dc.relation.ispartofArtificial Cells, Nanomedicine and Biotechnology
dc.subjectBiological organs
dc.subjectChemical bonds
dc.subjectDiseases
dc.subjectDNA
dc.subjectElectrophoresis
dc.subjectFiber optic sensors
dc.subjectGold
dc.subjectHigh resolution transmission electron microscopy
dc.subjectMetal nanoparticles
dc.subjectNanoparticles
dc.subjectOligonucleotides
dc.subjectOrganic polymers
dc.subjectPolymerase chain reaction
dc.subjectProbes
dc.subjectSynthesis (chemical)
dc.subjectTransmission electron microscopy
dc.subjectChemical functionalization
dc.subjectCitrate reduction methods
dc.subjectEnzymatic amplifications
dc.subjectGold Nanoparticles
dc.subjectGold nanoparticles (GNPs)
dc.subjectHnRNPB1
dc.subjectLung Cancer
dc.subjectOligonucleotide conjugates
dc.subjectBiomarkers
dc.subjectbeta actin
dc.subjectcitric acid
dc.subjectcolloidal gold
dc.subjectDNA
dc.subjectgold nanoparticle
dc.subjectheterogeneous nuclear ribonucleoprotein
dc.subjectheterogeneous nuclear ribonucleoprotein B1
dc.subjectligand
dc.subjectoligonucleotide
dc.subjectthiol
dc.subjectunclassified drug
dc.subjectgold
dc.subjectheterogeneous nuclear ribonucleoprotein group A B
dc.subjecthnRNP A2
dc.subjectmetal nanoparticle
dc.subjectoligodeoxyribonucleotide
dc.subjecttumor marker
dc.subjecttumor protein
dc.subjectabsorption
dc.subjectArticle
dc.subjectchemical analysis
dc.subjectcross linking
dc.subjectDNA probe
dc.subjectdrug synthesis
dc.subjecthuman
dc.subjectlung cancer
dc.subjectoligonucleotide probe
dc.subjectparticle size
dc.subjectprotein aggregation
dc.subjectsequence analysis
dc.subjectspectrophotometer
dc.subjectspectrophotometry
dc.subjectsurface property
dc.subjecttransmission electron microscopy
dc.subjectchemistry
dc.subjectgenetics
dc.subjectLung Neoplasms
dc.subjectBiomarkers, Tumor
dc.subjectGold
dc.subjectHeterogeneous-Nuclear Ribonucleoprotein Group A-B
dc.subjectHumans
dc.subjectLung Neoplasms
dc.subjectMetal Nanoparticles
dc.subjectNeoplasm Proteins
dc.subjectOligodeoxyribonucleotides
dc.titleGold nanoparticle-oligonucleotide conjugate to detect the sequence of lung cancer biomarker
dc.typeArticle
dc.citation.volume44
dc.citation.issue6
dc.citation.spage1417
dc.citation.epage1423
dc.citation.indexScopus
dc.identifier.DOI10.3109/21691401.2015.1031905


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