|
|
|
|
LEADER |
01000naa a22002652 4500 |
001 |
NLM156846748 |
003 |
DE-627 |
005 |
20231223075007.0 |
007 |
tu |
008 |
231223s2005 xx ||||| 00| ||eng c |
028 |
5 |
2 |
|a pubmed24n0523.xml
|
035 |
|
|
|a (DE-627)NLM156846748
|
035 |
|
|
|a (NLM)16049946
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a Sandvoss, Martin
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a HPLC-SPE-NMR in pharmaceutical development
|b capabilities and applications
|
264 |
|
1 |
|c 2005
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
|
338 |
|
|
|a Band
|b nc
|2 rdacarrier
|
500 |
|
|
|a Date Completed 23.09.2005
|
500 |
|
|
|a Date Revised 15.11.2012
|
500 |
|
|
|a published: Print
|
500 |
|
|
|a Citation Status MEDLINE
|
520 |
|
|
|a Copyright 2005 John Wiley & Sons, Ltd.
|
520 |
|
|
|a High-performance liquid chromatography-solid phase extraction-NMR spectroscopy (HPLC-SPE-NMR) has recently become commercially available and has been evaluated with regard to its applicability in a pharmaceutical environment. The addition of an automated SPE unit to an HPLC-NMR system for peak trapping results in an improved NMR signal-to-noise ratio (S/N) and also has other practical advantages. The trapping efficiency is shown to depend on compound polarity and is highest for compounds eluting late on reversed-phase HPLC systems. Multiple peak trapping further increases the S/N, again with the best results for less polar compounds. For polar compounds, multiple peak trapping resulted in no S/N gain as the amount of material retained on the SPE cartridge was equivalent to that from a single injection. When compared with conventional HPLC-NMR, a S/N gain of up to five-fold could be achieved for some compounds in a single trapping step. A major advantage of the technique is the independence of the chromatographic step from the NMR step, resulting in greater versatility than conventional HPLC-NMR in the HPLC solvents and NMR solvents that can be used. Practical applications from both drug metabolite and drug impurity identification are presented
|
650 |
|
4 |
|a Journal Article
|
650 |
|
7 |
|a Acetonitriles
|2 NLM
|
650 |
|
7 |
|a Acids, Carbocyclic
|2 NLM
|
650 |
|
7 |
|a Ketones
|2 NLM
|
650 |
|
7 |
|a Pharmaceutical Preparations
|2 NLM
|
650 |
|
7 |
|a Solvents
|2 NLM
|
650 |
|
7 |
|a acetonitrile
|2 NLM
|
650 |
|
7 |
|a Z072SB282N
|2 NLM
|
700 |
1 |
|
|a Bardsley, Ben
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Beck, Tony L
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Lee-Smith, Emma
|e verfasserin
|4 aut
|
700 |
1 |
|
|a North, Stephanie E
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Moore, Peter J
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Edwards, Andrew J
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Smith, Richard J
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 43(2005), 9 vom: 01. Sept., Seite 762-70
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
|
773 |
1 |
8 |
|g volume:43
|g year:2005
|g number:9
|g day:01
|g month:09
|g pages:762-70
|
912 |
|
|
|a GBV_USEFLAG_A
|
912 |
|
|
|a SYSFLAG_A
|
912 |
|
|
|a GBV_NLM
|
912 |
|
|
|a GBV_ILN_350
|
951 |
|
|
|a AR
|
952 |
|
|
|d 43
|j 2005
|e 9
|b 01
|c 09
|h 762-70
|