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Under optimized conditions, the proposed method exhibited acceptable analytical performances in terms of linearity (over a concentration range from 2.00 × 10−6 to 2.25 × 10−5 mol L−1), the detection limit (LOD = 5.81 × 10−7 mol L−1) and the quantification limit (LOQ = 1.94 × 10−6 mol L−1) for a solution containing Flu.
These results meet the target criterion of a pooled RSD of 10% or less and it was determined that the analytical method exhibited acceptable intermediate precision.
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All methods tested exhibited acceptable accuracies, ranging between 80% and 91%.
Besides, 5q exhibited acceptable metabolic stability.
The proposed immunosensor array exhibited acceptable stability and reproducibility.
It is seen that for the case of a clean signal, both approaches exhibited acceptable results.
It was also found that BFRP reinforced beams exhibited acceptable deformability according to CSA S6-14.
Results and discussion: Pellet formulations exhibited acceptable morphological, flow and mechanical properties.
The formulated microparticles exhibited acceptable drug content values that lie in the range 66.20 96.36%.
Furthermore, the hydrogel system exhibited acceptable tissue compatibility by using a mouse subcutaneous implantation model.
Under optimal conditions, the fabricated immunosensor exhibited acceptable reproducibility, selectivity and excellent stability.
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CEO of Professional Science Editing for Scientists @ prosciediting.com