Molecularly Imprinted Plasmonic Substrates for Specific and Ultrasensitive Immunoassay of Trace Glycoproteins in Biological Samples

被引:84
|
作者
Muhammad, Pir [1 ]
Tu, Xueying [1 ]
Liu, Jia [1 ]
Wang, Yijia [1 ]
Liu, Zhen [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
molecularly imprinted polymer; immunoassay; glycoprotein; plasmon-enhanced Raman scattering; self-assembled monolayer; BORONATE-AFFINITY; ANTIBODY MIMICS; DRUG-DELIVERY; CANCER-CELLS; NANOPARTICLES; ASSAY; RECOGNITION; AMPLIFICATION; POLYMERS; DISEASE;
D O I
10.1021/acsami.7b00628
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Assays of glycoproteins hold significant biological importance and clinical values, for which immunoassay has been the workhorse tool. As immunoassays are associated with disadvantages such as poor availability of high-specificity antibodies, limited stability of biological reagents, and tedious procedure, innovative alternatives that can overcome these drawbacks are highly desirable. Plasmonic immunosandwich, assay (PISA) has emerged as an appealing alternative to immunoassay for fast and sensitive determination of trace glycoproteins in biosamples. Plasmonic substrates play key roles in PISA, not only in determining the specificity but also in greatly influencing the detection sensitivity. Herein, we-report a new type of molecularly imprinted plasmonic substrates for rapid and ultrasensitive PISA assay Of trace glycoproteins in complex real samples. The substrates were fabricated from glass slides, first coated with self-assembled monolayer (SAM) of gold nanoparticles (AuNPs) and then molecularly imprinted with organo-siloxane polymer in the presence of template glycoproteins. The prepared molecularly imprinted substrates exhibited not only a significant plasmonic effect but also excellent binding properties, ensuring the sensitivity as well as the specificity of the assay. Alkaline phosphatase (ALP) and alpha-fetoprotein (AFP), glycoproteins that are routinely used as disease markers in clinical diagnosis, were used as representative targets. The limit of detection (LOD) was 3.1 X 10(-12) M for ALP and 1.5 x 10(-14) M for AFP, which is the best among the PISA approaches reported. The sample volume required was only 5 mu L, and the total time required was within 30 min for each assay. Specific and ultrasensitive determination of ALP and AFP in human serum was demonstrated. Because many disease biomarkers are glycoproteins, the developed PISA approach holds great promise in disease diagnostics.
引用
收藏
页码:12082 / 12091
页数:10
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