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. 2024 Aug 16;39(1):2372734. doi: 10.1080/14756366.2024.2372734

Table 5.

Quantification of the cellular uptake of PLP and PI-h by H. pylori 26695 strain cells.

Compound Starting inhibitor concentration [µM] Method Observation wavelength [nm] Intracellular accumulation [µM] t-test
PLP 390 UV absorption 388 84.7 ± 17.6 after 4 h
100.4 ± 16.3 after 8 h
****
PI-h 325 UV absorption 318 −8.9 ± 4.9 after 4 h
−10.1 ± 8.2 after 8 h
ns
35.4 UV absorption 318 −1.88 ± 0.77 after 4 h
0.80 ± 0.53 after 8 h
ns
ns
35.4 LC-MS 0.10 ± 0.84 after 4 h
3.58 ± 0.55 after 8 h
ns
***

Notes: The extracellular inhibitor concentration was determined by UV absorption spectra of the tested compounds and LC-MS detection methods 17. The t-test was used to check for a significant difference in the extracellular inhibitor concentration between supernatants incubated with and without H. pylori cells. The intracellular accumulation of each compound was determined using Equation (3) as described in the text. Results of the t-test are marked as follows: **** p < 0.0001; *** p < 0.001; ns p > 0.05, no significant difference.