TY - JOUR
T1 - Development of Gold Nanoparticle (AuNP)-based Colorimetric Aptasensor for Penicillin G Detection
AU - Darmawati, null
AU - Mustopa, Apon Zaenal
AU - Budiarto, Bugi Ratno
AU - Rahmawati, Siti Irma
AU - Izzati, Fauzia Nurul
AU - Harmoko, Rikno
AU - Saepudin, Endang
AU - Mahsunah, Anis H.
N1 - Funding Information:
The authors would like to thank Research Center for Biotechnology, Indonesian Institute of Sciences (LIPI) for the use of their lab equipment and funding of this research.
Publisher Copyright:
© 2022 Published by ITB Institute for Research and Community Services,.
PY - 2022/7/18
Y1 - 2022/7/18
N2 - Antibiotics are chemical or biological substances that have the ability to kill pathogens selectively. Currently, high-performance liquid chromatography (HPLC) is used routinely in the detection of antibiotics. However, the cost of analysis and running time are bottlenecks for HPLC to be used for routine tests to detect antibiotics. Alternative methods need to be developed to overcome this issue. In this study, the development of a penicillin G specific biosensor by using a DNA aptamer and gold nanoparticles (AuNPs) was done. Optimal aptasensor conditions were achieved with the concentrations of NaCl and aptamer at 0.25 M and 2 μM, respectively. An aptasensor of this type showed LOD for penicillin G at 3 mg/L and was able to detect penicillin G in the range of 3 to 27 mg/L. The established aptasensor showed specific sensitivity toward penicillin G after testing with several antibiotics, i.e., ampicillin, kanamycin, chloramphenicol, and erythromycin. The aptasensor could detect the presence of penicillin G from culture medium of wild-type, ultraviolet irradiation mutant, gamma irradiation mutant, and ultraviolet irradiation and gamma irradiation mutant strains of P. chrysogenum, at detection concentrations of 9.75 ± 0.004; 25.25 ± 0.005; 37.5 ± 0.005; and 45 ± 0.004 mg/L, respectively.
AB - Antibiotics are chemical or biological substances that have the ability to kill pathogens selectively. Currently, high-performance liquid chromatography (HPLC) is used routinely in the detection of antibiotics. However, the cost of analysis and running time are bottlenecks for HPLC to be used for routine tests to detect antibiotics. Alternative methods need to be developed to overcome this issue. In this study, the development of a penicillin G specific biosensor by using a DNA aptamer and gold nanoparticles (AuNPs) was done. Optimal aptasensor conditions were achieved with the concentrations of NaCl and aptamer at 0.25 M and 2 μM, respectively. An aptasensor of this type showed LOD for penicillin G at 3 mg/L and was able to detect penicillin G in the range of 3 to 27 mg/L. The established aptasensor showed specific sensitivity toward penicillin G after testing with several antibiotics, i.e., ampicillin, kanamycin, chloramphenicol, and erythromycin. The aptasensor could detect the presence of penicillin G from culture medium of wild-type, ultraviolet irradiation mutant, gamma irradiation mutant, and ultraviolet irradiation and gamma irradiation mutant strains of P. chrysogenum, at detection concentrations of 9.75 ± 0.004; 25.25 ± 0.005; 37.5 ± 0.005; and 45 ± 0.004 mg/L, respectively.
KW - aptamer
KW - aptasensor
KW - colorimetry
KW - gold nanoparticles
KW - penicillin G
UR - http://www.scopus.com/inward/record.url?scp=85134495757&partnerID=8YFLogxK
U2 - 10.5614/j.eng.technol.sci.2022.54.4.13
DO - 10.5614/j.eng.technol.sci.2022.54.4.13
M3 - Article
AN - SCOPUS:85134495757
SN - 2337-5779
VL - 54
JO - Journal of Engineering and Technological Sciences
JF - Journal of Engineering and Technological Sciences
IS - 4
M1 - 220413
ER -