Insulin Detection Enabled by Sensors Employing Fluorescence Signal Amplification Strategy.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Insulin Detection Enabled by Sensors Employing Fluorescence Signal Amplification Strategy.
Συγγραφείς: Wang J; College of Traditional Chinese Medicine and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong, China., Feng T; College of Traditional Chinese Medicine and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong, China.
Πηγή: Luminescence : the journal of biological and chemical luminescence [Luminescence] 2026 Jul; Vol. 41 (7), pp. e70557.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Wiley & Sons Country of Publication: England NLM ID: 100889025 Publication Model: Print Cited Medium: Internet ISSN: 1522-7243 (Electronic) Linking ISSN: 15227235 NLM ISO Abbreviation: Luminescence Subsets: MEDLINE
Imprint Name(s): Original Publication: Chichester, Sussex, UK : Wiley & Sons, c1999-
Ιατρικοί όροι (MeSH): Insulin*/analysis , Aptamers, Nucleotide*/chemistry , Biosensing Techniques*/methods , Fluorescence Resonance Energy Transfer*, Nanotubes, Carbon/chemistry ; Fluorescent Dyes/chemistry ; Fluorescence ; Fluorescent Chemosensor Compounds ; Humans
Περίληψη: We present the development of a fluorescent aptamer sensor for insulin detection, which is based on single-walled carbon nanohorns (SWCNHs). This sensor capitalizes on the high affinity and strong specificity of a FAM-labeled aptamer for insulin. In the absence of insulin, the aptamer is adsorbed onto SWCNHs. This adsorption triggers fluorescence resonance energy transfer (FRET), leading to fluorescence quenching and a low fluorescence intensity. When insulin is present, the FAM-aptamer binds to insulin to form a complex. As a result, the aptamer detaches from the SWCNHs, preventing the SWCNHs from fully quenching the aptamer's fluorescence. The addition of the Cryonase enzyme initiates the hydrolysis of the complex. This process releases both the fluorescent molecules and insulin, allowing them to enter the next cycle. Through multiple hydrolysis cycles, a substantial number of FAM-labeled small oligonucleotide fragments are set free, thereby amplifying the fluorescence signal. The sensor shows a linear detection range from 5 to 250 ng/mL and a detection limit as low as 3.98 ng/mL. This method is simple, sensitive, and exhibits high specificity for insulin detection.
(© 2026 John Wiley & Sons Ltd.)
References: S. Desai and A. Deshmukh, “Mapping of Type 1 Diabetes Mellitus,” Current Diabetes Reviews 16, no. 5 (2020): 438–441.
L. Cloete, “Diabetes Mellitus: An Overview of the Types, Symptoms, Complications and Management,” Nursing Standard 37, no. 1 (2022): 61–66.
S. Dahan, Y. Plakht, A. Shiyovich, et al., “Mean Platelet Volume and Long‐Term Cardiovascular Outcomes in Patients With Type 2 Diabetes Mellitus,” International Journal of Cardiology. Cardiovascular Risk and Prevention 27 (2025): 200535.
X. G. Peng, Y. Cui, J. Sun, et al., “Stratified CT Analysis of Renal, Perirenal and Renal Sinus Fat in Type 2 Diabetes Mellitus and Diabetic Kidney Disease,” Nutrition, Metabolism, and Cardiovascular Diseases 36, no. 2 (2026): 104367.
C. Li, W. Wang, Q. Ji, et al., “Prevalence of Painful Diabetic Peripheral Neuropathy in Type 2 Diabetes Mellitus and Diabetic Peripheral Neuropathy: A Nationwide Cross‐Sectional Study in Mainland China,” Diabetes Research and Clinical Practice 198 (2023): 110602.
M. Poudineh, C. L. Maikawa, E. Y. Ma, et al., “A Fluorescence Sandwich Immunoassay for the Realtime Continuous Detection of Glucose and Insulin in Live Animals,” Nature Biomedical Engineering 5, no. 1 (2021): 53–63.
J. Q. Chong, M. F. Md Shakhih, B. Vijayam, C. Marimuthu, C. T. Ching, and A. Abdul Wahab, “Insulin Quantification Through Electrochemical and Optical Aptasensors: A Review,” Annals of Biomedical Engineering 53, no. 12 (2025): 3345–3375.
N. Foulon, E. Goonatilleke, M. J. MacCoss, M. A. Emrick, and A. N. Hoofnagle, “Multiplexed Quantification of Insulin and C‐Peptide by LC‐MS/MS Without the Use of Antibodies,” Journal of Mass Spectrometry and Advances in the Clinical Lab 25 (2022): 19–26.
G. Yu, Z. Sun, Y. Wu, and N. Sai, “Dual‐QDs Ratios Fluorescent Probe for Sensitive and Stable Detection of Insulin,” Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy 268 (2022): 120641.
M. S. Even, C. B. Sandusky, N. D. Barnard, J. Mistry, and M. K. Sinha, “Development of a Novel ELISA for Human Insulin Using Monoclonal Antibodies Produced in Serum‐Free Cell Culture Medium,” Clinical Biochemistry 40, no. 1–2 (2007): 98–103.
T. E. Park and S. H. Lee, “A Micellized Fluorescence Sensor Based on Amplified Quenching for Highly Sensitive Detection of Non‐Transferrin‐Bound Iron in Serum,” Dalton Transactions 49, no. 15 (2020): 4660–4664.
S. Zhang, W. Qu, S. Chen, et al., “A Specific Visual‐Volumetric Sensor for Mercury Ions Based on Smart Hydrogel,” Analyst 148, no. 23 (2023): 5942–5948.
D. Milićević and J. Hlaváč, “Triple‐FRET Multi‐Purpose Fluorescent Probe for Three‐Protease Detection,” RSC Advances 12, no. 44 (2022): 28780–28787.
K. Charan Behera, D. Mallick, B. Narayan Patra, and B. Bag, “A Pyrene‐Rhodamine FRET Couple as a Chemosensor for Selective Detection of Picric Acid,” Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy 271 (2022): 120934.
H. Y. Tsai and W. R. Algar, “A Dendrimer‐Based Time‐Gated Concentric FRET Configuration for Multiplexed Sensing,” ACS Nano 16, no. 5 (2022): 8150–8160.
P. Sabui, S. Mallick, K. R. Singh, et al., “Potentialities of Fluorescent Carbon Nanomaterials as Sensor for Food Analysis,” Luminescence 38 (2023): 1047–1063.
C. Ji, J. Wei, L. Zhang, et al., “Aptamer‐Protein Interactions: From Regulation to Biomolecular Detection,” Chemical Reviews 123 (2023): 12471–12506.
O. Alkhamis and Y. Xiao, “Systematic Study of In Vitro Selection Stringency Reveals How to Enrich High‐Affinity Aptamers,” Journal of the American Chemical Society 145 (2023): 194–206.
X. Liu, Y. Ying, and J. Ping, “Structure, Synthesis, and Sensing Applications of Single‐Walled Carbon Nanohorns,” Biosensors & Bioelectronics 167 (2020): 112495.
B. He, Y. Shi, Y. Liang, et al., “Single‐Walled Carbon‐Nanohorns Improve Biocompatibility Over Nanotubes by Triggering Less Protein‐Initiated Pyroptosis and Apoptosis in Macrophages,” Nature Communications 9, no. 1 (2018): 2393.
Grant Information: 202303021221158 Natural Science Foundation Project of Shanxi Province; X2025SJ033 Shanxi Graduate Education Innovation Project
Contributed Indexing: Keywords: Cryonase enzyme; fluorescent sensor; insulin; single‐walled carbon nanohorns
Substance Nomenclature: 0 (Insulin)
0 (Aptamers, Nucleotide)
0 (Nanotubes, Carbon)
0 (Fluorescent Dyes)
0 (Fluorescent Chemosensor Compounds)
Entry Date(s): Date Created: 20260630 Date Completed: 20260630 Latest Revision: 20260726
Update Code: 20260726
PubMed Central ID: PMC13349519
DOI: 10.1002/bio.70557
PMID: 42376944
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1522-7243
DOI:10.1002/bio.70557