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. 2020 Jul 17;25(14):3258. doi: 10.3390/molecules25143258

Table 3.

Recoveries (%) of the silyl derivatives of indolic acids from model solution (derivatization with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) or N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA)), pooled cerebrospinal fluid (CSF) samples and serum samples at three concentration levels using microextraction by packed sorbent (MEPS) as a sample preparation technique and BSTFA as a derivatizing reagent (n = 3, p = 0.95).

Indolic Acid Derivative Model Solution Pooled CSF Blood Serum
BSTFA MTBSTFA 100 a 500 b 1500 c 100 a 500 b 2000 d
Indole-3-acetic acid (3IAA), mono- 80 ± 20 80 ± 10 80 ± 20 80 ± 20 80 ± 10 60 ± 20 60 ± 10 60 ± 20
Indole-3-carboxylic acid (3ICA), mono- 70 ± 10 70 ± 20 60 ± 20 70 ± 20 60 ± 10 60 ± 10 70 ± 20 60 ± 10
Indole-3-propionic acid (3IPA), mono- 62 ± 6 40 ± 10 70 ± 20 70 ± 10 70 ± 10 48 ± 9 50 ± 10 50 ± 10
Indole-3-lactic acid (3ILA), di- 80 ± 20 70 ± 20 80 ± 20 70 ± 20 80 ± 20 50 ± 10 50 ± 10 60 ± 10
5-Hydroxyindole-3-acetic acid (5HIAA), di- 52 ± 8 40 ± 10 40 ± 10 50 ± 10 50 ± 10 40 ± 10 38 ± 6 40 ± 10

a 100 µg/L corresponds to 0.4–0.5 µM; b 500 µg/L corresponds to 2.0–2.5 µM; c 1500 µg/L corresponds to 6–7 µM; d2000 µg/L corresponds to 8–10 µM.