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A possible pathogenetic factor of sickle-cell disease based on fluorescent analysis via an optofluidic resonator

Waveguide based optofluidic resonator features high precision and high sensitivity in real-time fluorescent analysis. We present a novel optofluidic resonator following the hollow-core metal-cladding waveguide structure, which is then used to record the real-time binding process of Fe(2+) and Fe(3+)...

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Detalles Bibliográficos
Autores principales: Dai, Hailang, Yin, Cheng, Ye, Xiaona, Jiang, Bei, Ran, Maowu, Cao, Zhuangqi, Chen, Xianfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466609/
https://www.ncbi.nlm.nih.gov/pubmed/28600527
http://dx.doi.org/10.1038/s41598-017-03634-8
Descripción
Sumario:Waveguide based optofluidic resonator features high precision and high sensitivity in real-time fluorescent analysis. We present a novel optofluidic resonator following the hollow-core metal-cladding waveguide structure, which is then used to record the real-time binding process of Fe(2+) and Fe(3+) with protoporphyrin IX (PpIX) in PBS solution, respectively. The central fluorescent wavelength of compound with Fe(2+) is in good accordance with that of the normal hemoglobin, whilst the peaks of the Fe(3+) compound match the hemoglobin specimen from sickle-cell disease (SCD) patients. Similar statement holds when we monitor the real-time oxidation processes of these products by injecting oxygen into the optofluidic chip. These observations lead to the speculation that the SCD is caused by replacing the Fe(2+) in hemoglobin with Fe(3+), which may be insightful in the discovery of new clinical routes to cure this disease.