The extreme toxicity of mercury and its derivatives results from its high affinity for thiol groups in proteins and enzymes, leading to the dysfunction of cells and consequent health problems.
Despite
the significant therapeutic use of cysteamine as drug in
cystinosis, it also has some serious health issues such as idiopathic
intracranial hypertension (IIH), Ehlers–Danlos syndrome, and
eye related problems including blurred or loss of vision and pain
due to eye movement, etc. Thus, it is important to measure accurate
cysteamine levels in the body for clinical studies. However, most
of the conventional methods used to detect cysteamine are time-consuming
and expensive in nature. Therefore, in this regard, we have developed
a chromogenic sensor which sequentially determines the Cu2+ metal ion and, consequently, exhibits potential ratiometric and
selective colorimetric quantification of cysteamine in an aqueous/biological
system. The morphology of the sensor was characterized by TEM, and
it revealed some interesting features in that receptor 1 nanoparticles undergo self-assembly with the addition of Cu2+ metal ions which results in the filament formation (comet
type) in aqueous medium and on subsequent addition of cysteamine to
resultant complex 1·Cu2+; these comet
type nanoparticle filaments undergo further aggregation process and
develop into three-dimensional tree-like structure. Further, on the
basis of obtained colorimetric results, we developed silica-based
solid state sensor strips impregnated with complex 1·Cu2+, which displays colorimetric changes in accordance with
present concentrations of cysteamine in blood serum and urine samples,
wherein the intensity of yellow color decreased gradually after the
addition of cysteamine, as revealed by HSV parameter through lab-on-mobile
based diagnostics. The low detection limit (with naked eye) exhibited
by developed solid state sensors leads to affordable and economic
platforms for easy-to-use, reliable, and rapid colorimetric sensing
of cysteamine in aqueous as well as biological test systems.
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