Synthesis of Novel Gold Mesoflowers as SERS Tags for Immunoassay with Improved Sensitivity
Source abstract
Abstract
A new class of flowerlike gold mesostructure in high yield is successfully synthesized through a facile one-step route using ascorbic acid as a reducing agent of gold salt with cetyltrimethylammonium chloride (CTAC) as surfactant. The as-prepared Au particles have spherical profiles with an averaged diameter of 770 ± 50 nm, but showing a highly rough surface consisting of many irregular and randomly arranged protrusions. The Au mesoflowers exhibit strong surface-enhanced effects and near-infrared absorption which were utilized in the design of efficient surface-enhanced Raman scattering (SERS) tags as immunosensors for immunoassay with improved sensitivity. The experimental results indicate that a good linear relationship is found between the peak intensity at 1071 cm(-1) and the logarithm of H-IgG concentration in the range between 1 ng/mL and 1 fg/mL, and the limit of detection (LOD) is 1 fg/mL.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Advanced biosensing and bioanalysis techniques · Biosensors and Analytical Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Lab Organic Electronics & Information Displays (KLOEID), and Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, Nanjing 210023, China
References (49)
Show source-provided references
1. Wang Y. R. · Anal. Chem. · 2013 · 85 · 829810.1021/ac4015885 ↗
2. Jin M. J. · Food Agric. Immunol. · 2013 · 24 · 34510.1080/09540105.2012.694096 ↗
3. Wang Y. M. C. · Bioanalysis · 2014 · 6 · 7910.4155/bio.13.302 ↗
4. Wang Y. · Chem. Rev. · 2012 · 113 · 139110.1021/cr300120g ↗
5. Rosi N. L. · Chem. Rev. · 2005 · 105 · 154710.1021/cr030067f ↗
6. Chon H. · Anal. Chem. · 2010 · 82 · 529010.1021/ac100736t ↗
7. Jun B. H. · J. Comb. Chem. · 2007 · 9 · 23710.1021/cc0600831 ↗
8. Vendrell M. · Trends Biotechnol. · 2013 · 31 · 24910.1016/j.tibtech.2013.01.013 ↗
9. Luo Z. H. · Microchim. Acta · 2013 · 180 · 150110.1007/s00604-013-1032-5 ↗
10. Sanda B. · Nanotechnology · 2011 · 22 · 05570210.1088/0957-4484/22/5/055702 ↗
11. Rodriguez-Lorenzo L. · Integr. Biol. · 2011 · 3 · 92210.1039/c1ib00029b ↗
12. Xie J. · ACS Nano · 2008 · 2 · 247310.1021/nn800442q ↗
13. Lu G. · Chem. Sci. · 2011 · 2 · 181710.1039/c1sc00254f ↗
14. Lu G. · Nanoscale · 2012 · 4 · 86010.1039/C1NR10997A ↗
15. Lu G. · Chem. Commun. · 2011 · 47 · 856010.1039/c1cc12027a ↗
16. Lu G. · Small · 2012 · 8 · 133610.1002/smll.201102258 ↗
17. Wu L. · Biosens. Bioelectron. · 2012 · 38 · 9410.1016/j.bios.2012.05.005 ↗
18. Cui Y. · J. Phys. Chem. B · 2006 · 110 · 400210.1021/jp056203x ↗
19. Lee S. · Biosens. Bioelectron. · 2014 · 51 · 23810.1016/j.bios.2013.07.063 ↗
20. Chon H. · Anal. Chem. · 2009 · 81 · 302910.1021/ac802722c ↗
21. Song C. Y. · Colloids Surf., B · 2010 · 81 · 28510.1016/j.colsurfb.2010.07.023 ↗
22. Jia W. · ACS Appl. Mater. Interfaces · 2013 · 5 · 688610.1021/am401006b ↗
23. You H. · J. Mater. Chem. · 2012 · 22 · 199810.1039/C1JM13211C ↗
24. Rodriguez-Lorenzo L. · J. Phys. Chem. C · 2010 · 114 · 733610.1021/jp909253w ↗
25. Hao E. · Nano Lett. · 2004 · 4 · 32710.1021/nl0351542 ↗
26. Bakr O. M. · Chem. Mater. · 2006 · 18 · 329710.1021/cm060681i ↗
27. Kumar P. S. · Nanotechnology · 2008 · 19 · 01560610.1088/0957-4484/19/01/015606 ↗
28. Nhung T. T. · J. Cryst. Growth · 2012 · 373 · 13210.1016/j.jcrysgro.2012.09.042 ↗
29. Sanchez-Gaytan B. L. · J. Phys. Chem. C · 2013 · 117 · 891610.1021/jp401189k ↗
30. Sajanlal P. R. · Nano Res. · 2009 · 2 · 30610.1007/s12274-009-9028-5 ↗
31. Kang K. · J. Phys. Chem. B · 2008 · 113 · 53610.1021/jp807081b ↗
32. Yanxiao L. · Nanotechnology · 2013 · 24 · 27560510.1088/0957-4484/24/27/275605 ↗
33. Xie J. · Chem. Mater. · 2007 · 19 · 282310.1021/cm0700100 ↗
34. Michota A. · J. Raman Spectrosc. · 2003 · 34 · 2110.1002/jrs.928 ↗
35. Yang J. · Nanotechnology · 2010 · 21 · 34510110.1088/0957-4484/21/34/345101 ↗
36. Kelly K. L. · J. Phys. Chem. B · 2002 · 107 · 66810.1021/jp026731y ↗
37. Liang Y. · Talanta · 2007 · 72 · 44310.1016/j.talanta.2006.11.002 ↗
38. Song C. Y. · Biosens. Bioelectron. · 2009 · 25 · 82610.1016/j.bios.2009.08.035 ↗
39. Li L. · Chem. Mater. · 2010 · 22 · 318310.1021/cm100289d ↗
40. Chen L. · J. Colloid Interface Sci. · 2012 · 368 · 28210.1016/j.jcis.2011.10.069 ↗
41. Wang Y. · Anal. Bioanal. Chem. · 2011 · 399 · 127110.1007/s00216-010-4453-6 ↗
42. Qu L. · ACS Appl. Mater. Interfaces · 2014 · 6 · 730910.1021/am5006783 ↗
43. Shen A. · Adv. Funct. Mater. · 2010 · 20 · 96910.1002/adfm.200901847 ↗
44. Zong S. F. · Biosens. Bioelectron. · 2013 · 41 · 74510.1016/j.bios.2012.09.057 ↗
45. Pei Y. W. · J. Mater. Chem. B · 2013 · 1 · 399210.1039/c3tb00519d ↗
46. Ni J. · Anal. Chem. · 1999 · 71 · 490310.1021/ac990616a ↗
47. Chen S. A. · Chem. Commun. · 2011 · 47 · 422510.1039/c0cc05321j ↗
48. Han X. X. · Anal. Chem. · 2009 · 81 · 335010.1021/ac802553a ↗
49. Song C. Y. · J. Raman Spectrosc. · 2011 · 42 · 31310.1002/jrs.2728 ↗