Dual approach for the colorimetric determination of unamplified microRNAs by using citrate capped gold nanoparticles

被引:12
|
作者
Nossier, Ahmed Ibrahim [1 ]
Abdelzaher, Hana [2 ]
Matboli, Marwa [3 ]
Eissa, Sanaa [3 ,4 ]
机构
[1] MUST, Fac Pharm, Biochem Dept, 6th October City, Giza, Egypt
[2] October Univ Modern Sci & Arts, Fac Biotechnol, 6th October City, Cairo, Egypt
[3] Ain Shams Univ, Fac Med, Med Biochem & Mol Biol Dept, Oncol Diagnost Unit, Cairo, Egypt
[4] Ain Shams Res Inst MASRI, Fac Med, Cairo, Egypt
关键词
MicroRNA-210-3p; MicroRNA detection; Bladder cancer; AuNPs; Magnetic nanoparticles; Salt-induced aggregation; Oligonucleotide adsorption; Oligotargeter; Streptavidin; FLUOROMETRIC-DETERMINATION; SIGNAL AMPLIFICATION; STRAND DISPLACEMENT; CANCER-DIAGNOSIS; DNA; SINGLE; ADSORPTION; BIOMARKERS; SEPARATION; PROGNOSIS;
D O I
10.1007/s00604-018-2767-9
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The authors describe a method for the colorimetric determination of unamplified microRNA. It is based on the use of citrate-capped gold nanoparticles (AuNPs) and, alternatively, a microRNA-probe hybrid or a magnetically extracted microRNA that serve as stabilizers against the salt-induced aggregation of AuNPs. The absorbance ratios A(525)/A(625) of the reacted AuNP solutions were used to quantify the amount of microRNA. The assay works in the range of 5-25 pmol microRNA. The lower limit of detection (LOD) is 10 pmol. The performance of the method was tested by detection of microRNA-210-3p in totally extracted urinary microRNA from normal, benign, and bladder cancer subjects. The sensitivity and specificity for qualitative detection of urinary microRNA-210-3p using the assay are 74% and 88% respectively, which is consistent with real time PCR based assays. The assay was applied to the determination of specific microRNA by using its specific oligo targeter or following magnetic isolation of the desired microRNA. The method is simple, cost-efficient, has a short turn-around time and requires minimal equipment and personnel.
引用
收藏
页数:9
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