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TLC-MALDI for analysis of industrial materials
Thin layer chromatography (TLC) is a widely used method for separation of mixture samples.
Introduction
In many cases, sample spots separated on TLC plates must be scraped, extracted, and then analyzed using a variety of techniques. Lately, TLC-MALDI has been already developed to enable direct MS measurement from TLC plates.
To date, most of the samples analyzed using TLC-MALDI are bio-related materials like lipids. Therefore, we explored the use of TLC-MALDI for analysis of industrial materials.
MethodsCharge Transport Materials (CTM) used in organic photo conductor (OPC) drums inside laser printers was employed as a model sample. A mixture con-sists of six CTMs (structures are shown in Figure 1) and titanyl phthalocyanine (TiOPC) also used
Keywords: Industrial materials, Thin Layer Chromatography, ultrafleXtreme, solariX, Oil additives, TLC-MALDI, flexImaging
Authors: Toshiji Kudo, Yoshihiko Morishita, Noriyuki Iwasaki, Takashi Nirasawa; Bruker Japan K.K., Yokohama, Japan
in OPC, was diluted with THF. The diluted sample was applied on to a TLC plate and developed via one and two dimensional thin layer chromatography. MS measurements were performed on a MALDI-TOF MS (ultrafleXtreme, Bruker). For automated acquisition, dedicated TLC-MALDI software was used for 1D developed TLC plates and imaging MS software (flexImaging) was used for 2D TLC plates.
Further, engine oils before and after three months use were compared after analysis by 1D-TLC-MALDI. Afterwards, MALDI-MRMS (solariX, Bruker) was used for detailed analysis.
Results
Figure 2 is a MS image of the CTM-mix after 2D TLC, showing the separated CTMs. Figure 3A shows a mass spectrum of the CTM mixture before TLC separation. The signal of CTM-6 is interfering with the other components (broad signal at m/z 408, which is supposed to be a meta-stable fragment) in this spectrum. But with TLC separation, CTM-6 can be clearly detected (Figure 3B). Figure 4 shows the result from one dimensional MS measurement of CTM-mix after 1D TLC, displayed using the TLC-MALDI viewer. The X-axis represents m/z scale and Y-axis represents the number of spectra, which corresponds to the position or Rf value on TLC plate. MS inten-sity is expressed by color density.
Every component including CTM-6 is clearly visible.
Generally, MS image is easy to understand but its acquisition takes time to cover the whole area of a TLC plate, e.g. a few hours depending on the conditions. On the other hand, a
1D experiment requires much shorter time and its unique data viewer simplifies data interpretation e.g. to find impurities or by-products.
Figure 5 shows a comparison between automotive engine oils using TLC-MALDI via 1D development
Figure 2: MS image of CTM-mix developed two dimensionally on TLC plate
Figure 1: Molecular structures of components in CTM-mix
C38H32N2 Mass: 516.26
C20H19N Mass: 273.15
C34H31N3 Mass: 481.25
C36H40N2 Mass: 500.32
C33H29N3 Mass: 467.24
CTM-1 CTM-2
CTM-3 CTM-4
CTM-5
N(C2H5)2
N N
N N N
N
N N N
C28H40N2 Mass: 408.30
CTM-6
O O
B
A
Figure 3: CTM-mix before separation A and CTM-6 spot on TLC plate B
Inte
nsit
y [a
.U.] 40
50
30
20
10
402 404 406 412408 410 414m/z
CTM-6
Inte
nsit
y [a
.U.] 2.0
2.5
x106
1.5
1.0
0.5
0200 250 300 450350 400 500 550 600 650
m/z
CTM-6?
and subsequent MS measurement. In this case 2,5-dihydroxy benzoic acid (DHB) was used as a matrix, unlike with CTM samples which could be ionized without the addition of a matrix. TLC plates were dipped into DHB solution and dried with hair dryer (Dip Coating Protocol) [1]. After TLC separation, differences between the two samples could be observed indicating many of the compounds are absent in the ‘used’ engine oil. Typically, engine oil consists of base oil and additives. Since the base oil is a non polar hydrocarbon and is
considered to be difficult to ionize with MALDI, the components detected here should be considered additives. Various spots showing differences between used and non-used engine oil were subjected to MALDI-MRMS to elucidate their elemental compo- sition or molecular structure using the extremely high mass resolution and accuracy the techniques provides. Among them, for example, Figure 6 shows a MS/ MS spectrum from a TLC spot shown in Figure 5 indicated by the yellow circle. Its elemental composition was determined using mass difference between precursor and fragment ion to be C13H26. This supports the structure as tritridecylamine.
Summary
1D and 2D TLC MALDI are valuable methods to get a fast inside into com-plexer samples. Applying TLC MALDI to industrial materials expands the range of samples which can be analysed. TLC MALDI can be used efficiently to monitor products or incoming goods.
MRMS is a powerful technique due to its inherent mass accuracy and mass resolving power. Here its use in con-text of TLC MALDI allows for the direct elucidation of compound structures.
Conclusions
• TLC-MALDI is effective also for the analysis of industrial materials
• Simple and easy; scraping and extraction of spot is not necessary
• MALDI-TOF MS is preferable for screening and MALDI-FT-ICR MS is preferable for detailed analysis
Figure 6: FT-ICR MS/MS from a TLC spot shown with yellow circle in Figure 5
Inte
nsit
y 0.8
1.0
x108
0.6
0.4
0.2
200 250 450400350300 500 600550m/z
Figure 4: Result from one dimensional MS measurement of CTM-mix developed one dimensionally on TLC plate
No.
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men
t po
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n/R
f va
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Measurement interval: 0.5 mm)m/z
Figure 5: TLC-MALDI of engine oil before A and after B 3 months use
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9024x1000
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Bru
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© B
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Bruker Daltonik GmbH
Bremen · GermanyPhone +49 (0)421-2205-0
Bruker Scientific LLC
Billerica, MA · USA Phone +1 (978) 663-3660
For Research Use Only. Not for Use in Clinical Diagnostic Procedures.
[email protected] – www.bruker.com
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Reference
[1] Please contact MALDI Application support at: [email protected]