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. Author manuscript; available in PMC: 2021 May 5.
Published in final edited form as: Anal Chem. 2020 Apr 16;92(9):6613–6621. doi: 10.1021/acs.analchem.0c00392

Table 1.

Matrix effects on the results of direct tissue SALDI MSI and iMSI detection of different lipid standards in different brain regions.

Approach Region [CEr+Na]+ (m/z 588.5) [CEr+K]+ (m/z 604.5) [PE+Na]+ (m/z 750.6) [PE+K]+ (m/z 766.6) [CB+Na]+ (m/z 850.6) [CB+K]+ (m/z 866.6)
Direct tissue SALDI MSI CTX 18± 8 1330±670 0.34±0.08 53±25 85±47 1230±750
CC 7±3 320± 140 17±5 455±50 326±50 6490±1300
CA1 11±8 475±367 44 ±14 212±121 264±183 4560±3700
CA3 46±17 890±370 1.3 ±0. 3 0.11± 0.03 0.10±0.03 28±6
iMSI CTX 76±32 67±30 7±3 10±3 33±8 11±3
CC 84±11 43±26 12±6 16±6 124±25 12±6
CA1 89±18 29±52 21±16 27±6 51±6 34±12
CA3 32±33 5±3 10±5 16±3 46±17 20±7

CTX, cortex; CC, corpus callosum; CA1, region I of hippocampus proper; CA3, region III of hippocampus proper; Cer, ceramide; PE, phosphatidylethanolamine; CB, cerebroside. Mean ± standard deviations for all points/pixels were assessed. Matrix effects determined as ratios of lipid standard signal areas determined by measurements of arrays of microspots deposited onto (1) tissue slices and clean ITO glass surfaces (SALDI MSI) (n=2 animals); (2) tissue imprints and clean ITO glass slides coated with TiO2-DA monolith (iMSI) (n=2 animals).