A colorimetric gold nanoparticle aggregation assay for malathion based on target-induced hairpin structure assembly of complementary strands of aptamer

被引:43
作者
Abnous, Khalil [1 ,2 ]
Danesh, Noor Mohammad [3 ]
Ramezani, Mohammad [1 ]
Alibolandi, Mona [1 ]
Emrani, Ahmad Sarreshtehdar [4 ]
Lavaee, Parirokh [5 ]
Taghdisi, Seyed Mohammad [6 ,7 ]
机构
[1] Mashhad Univ Med Sci, Pharmaceut Res Ctr, Pharmaceut Technol Inst, Mashhad 9177899191, Iran
[2] Mashhad Univ Med Sci, Sch Pharm, Dept Med Chem, Mashhad, Iran
[3] Res Inst Sci & New Technol, Mashhad 9177899191, Iran
[4] Mashhad Univ Med Sci, Sch Med, Cardiovasc Res Ctr, Mashhad 9177899191, Iran
[5] ACECR, Mashhad Branch, Mashhad 9177899191, Iran
[6] Mashhad Univ Med Sci, Targeted Drug Delivery Res Ctr, Pharmaceut Technol Inst, Mashhad 9177899191, Iran
[7] Mashhad Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Mashhad, Iran
关键词
Pesticide; Color change; Serum sample; Salt induced aggregation; Ratiometric detection; Modified AuNPs; LABEL-FREE; VOLTAMMETRIC DETERMINATION; ULTRASENSITIVE DETECTION; APTASENSOR; PESTICIDE; BIOSENSOR; PLATFORM;
D O I
10.1007/s00604-018-2752-3
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 the pesticide malathion. It is based on the use of a hairpin structure consisting of a complementary strand of aptamer and a double-stranded DNA (dsDNA) structure to protect gold nanoparticles (AuNPs) against salt-induced aggregation. In the absence of malathion, the dsDNA structure is preserved on the surface of AuNPs and the color of the AuNPs in solutions containing NaCl remains red. However, in the presence of malathion, a hairpin structure of complementary strand is formed. The Aptamer/Malathion complex and the complementary strand are released from the surface of the AuNPs. As a result, the AuNPs undergo salt-induced aggregation which is accompanied by a color change to blue. The assay allows malathion to be quantified within 35 min (A(650)/A(520) was measured). The detection limit is 1 pM, and response is linear in the 5 pM to 10 nM malathion concentration range. The method is specific and was successfully applied to the determination of malathion in spiked human serum samples.
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页数:7
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