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The proposed method presented a low detection ratio in the QF60 test.
The proposed method presented a LOQ of 0.010 μg mL− 1 and LOD of 0.003 μg mL− 1.
Additionally, the 2D CT measurement method presented a high correlation to the drill sizes used to ream the tunnels and a high intraobserver reliability.
The best fit cylinder method presented a good agreement to the drill size (0.745 of ICC), and the closest mean difference to the drill size 0.04 mm.
NPs prepared by the nanoprecipitation method presented a more prominent burst release (approximately 56% at the first 4 h and 89% at the first 24 h).
Compared to related work, the proposed method presented a better accuracy, required fewer features, and provides a unified approach that expands CRC detection to non-malignant findings.
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The current genotyping method presented an overall detection rate of 295/304 (97.0%), which is similar to previously reported PCR-based methods [3].
Our method presents a false alarm rate of 0.42%%.
In all cases, the method presents a 100% classification success.
Thus, analytical method presents a large error, about 110 %, on switching loss.
Our proposed method presents a slight increase in classification accuracy by 0.01%%.
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