Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals
Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophi...
Ausführliche Beschreibung
Autor*in: |
Shalabai, V. V. [verfasserIn] Taranchenko, V. F. [verfasserIn] Rybal’chenko, I. V. [verfasserIn] Aksenov, A. V. [verfasserIn] Antokhin, A. M. [verfasserIn] Semchenko, F. M. [verfasserIn] Krymchak, M. S. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2017 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Journal of analytical chemistry - Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000, 72(2017), 6 vom: Juni, Seite 632-638 |
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Übergeordnetes Werk: |
volume:72 ; year:2017 ; number:6 ; month:06 ; pages:632-638 |
Links: |
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DOI / URN: |
10.1134/S1061934817060144 |
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Katalog-ID: |
SPR013454153 |
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245 | 1 | 0 | |a Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
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520 | |a Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. | ||
650 | 4 | |a HPLC |7 (dpeaa)DE-He213 | |
650 | 4 | |a high resolution mass spectrometry |7 (dpeaa)DE-He213 | |
650 | 4 | |a tetrodotoxin |7 (dpeaa)DE-He213 | |
650 | 4 | |a pharmaceutical |7 (dpeaa)DE-He213 | |
700 | 1 | |a Taranchenko, V. F. |e verfasserin |4 aut | |
700 | 1 | |a Rybal’chenko, I. V. |e verfasserin |4 aut | |
700 | 1 | |a Aksenov, A. V. |e verfasserin |4 aut | |
700 | 1 | |a Antokhin, A. M. |e verfasserin |4 aut | |
700 | 1 | |a Semchenko, F. M. |e verfasserin |4 aut | |
700 | 1 | |a Krymchak, M. S. |e verfasserin |4 aut | |
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10.1134/S1061934817060144 doi (DE-627)SPR013454153 (SPR)S1061934817060144-e DE-627 ger DE-627 rakwb eng 540 ASE 35.23 bkl 35.71 bkl 42.03 bkl Shalabai, V. V. verfasserin aut Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. HPLC (dpeaa)DE-He213 high resolution mass spectrometry (dpeaa)DE-He213 tetrodotoxin (dpeaa)DE-He213 pharmaceutical (dpeaa)DE-He213 Taranchenko, V. F. verfasserin aut Rybal’chenko, I. V. verfasserin aut Aksenov, A. V. verfasserin aut Antokhin, A. M. verfasserin aut Semchenko, F. M. verfasserin aut Krymchak, M. S. verfasserin aut Enthalten in Journal of analytical chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 72(2017), 6 vom: Juni, Seite 632-638 (DE-627)334292689 (DE-600)2057336-4 1608-3199 nnns volume:72 year:2017 number:6 month:06 pages:632-638 https://dx.doi.org/10.1134/S1061934817060144 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.23 ASE 35.71 ASE 42.03 ASE AR 72 2017 6 06 632-638 |
spelling |
10.1134/S1061934817060144 doi (DE-627)SPR013454153 (SPR)S1061934817060144-e DE-627 ger DE-627 rakwb eng 540 ASE 35.23 bkl 35.71 bkl 42.03 bkl Shalabai, V. V. verfasserin aut Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. HPLC (dpeaa)DE-He213 high resolution mass spectrometry (dpeaa)DE-He213 tetrodotoxin (dpeaa)DE-He213 pharmaceutical (dpeaa)DE-He213 Taranchenko, V. F. verfasserin aut Rybal’chenko, I. V. verfasserin aut Aksenov, A. V. verfasserin aut Antokhin, A. M. verfasserin aut Semchenko, F. M. verfasserin aut Krymchak, M. S. verfasserin aut Enthalten in Journal of analytical chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 72(2017), 6 vom: Juni, Seite 632-638 (DE-627)334292689 (DE-600)2057336-4 1608-3199 nnns volume:72 year:2017 number:6 month:06 pages:632-638 https://dx.doi.org/10.1134/S1061934817060144 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.23 ASE 35.71 ASE 42.03 ASE AR 72 2017 6 06 632-638 |
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10.1134/S1061934817060144 doi (DE-627)SPR013454153 (SPR)S1061934817060144-e DE-627 ger DE-627 rakwb eng 540 ASE 35.23 bkl 35.71 bkl 42.03 bkl Shalabai, V. V. verfasserin aut Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. HPLC (dpeaa)DE-He213 high resolution mass spectrometry (dpeaa)DE-He213 tetrodotoxin (dpeaa)DE-He213 pharmaceutical (dpeaa)DE-He213 Taranchenko, V. F. verfasserin aut Rybal’chenko, I. V. verfasserin aut Aksenov, A. V. verfasserin aut Antokhin, A. M. verfasserin aut Semchenko, F. M. verfasserin aut Krymchak, M. S. verfasserin aut Enthalten in Journal of analytical chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 72(2017), 6 vom: Juni, Seite 632-638 (DE-627)334292689 (DE-600)2057336-4 1608-3199 nnns volume:72 year:2017 number:6 month:06 pages:632-638 https://dx.doi.org/10.1134/S1061934817060144 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.23 ASE 35.71 ASE 42.03 ASE AR 72 2017 6 06 632-638 |
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10.1134/S1061934817060144 doi (DE-627)SPR013454153 (SPR)S1061934817060144-e DE-627 ger DE-627 rakwb eng 540 ASE 35.23 bkl 35.71 bkl 42.03 bkl Shalabai, V. V. verfasserin aut Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. HPLC (dpeaa)DE-He213 high resolution mass spectrometry (dpeaa)DE-He213 tetrodotoxin (dpeaa)DE-He213 pharmaceutical (dpeaa)DE-He213 Taranchenko, V. F. verfasserin aut Rybal’chenko, I. V. verfasserin aut Aksenov, A. V. verfasserin aut Antokhin, A. M. verfasserin aut Semchenko, F. M. verfasserin aut Krymchak, M. S. verfasserin aut Enthalten in Journal of analytical chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 72(2017), 6 vom: Juni, Seite 632-638 (DE-627)334292689 (DE-600)2057336-4 1608-3199 nnns volume:72 year:2017 number:6 month:06 pages:632-638 https://dx.doi.org/10.1134/S1061934817060144 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.23 ASE 35.71 ASE 42.03 ASE AR 72 2017 6 06 632-638 |
allfieldsSound |
10.1134/S1061934817060144 doi (DE-627)SPR013454153 (SPR)S1061934817060144-e DE-627 ger DE-627 rakwb eng 540 ASE 35.23 bkl 35.71 bkl 42.03 bkl Shalabai, V. V. verfasserin aut Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. HPLC (dpeaa)DE-He213 high resolution mass spectrometry (dpeaa)DE-He213 tetrodotoxin (dpeaa)DE-He213 pharmaceutical (dpeaa)DE-He213 Taranchenko, V. F. verfasserin aut Rybal’chenko, I. V. verfasserin aut Aksenov, A. V. verfasserin aut Antokhin, A. M. verfasserin aut Semchenko, F. M. verfasserin aut Krymchak, M. S. verfasserin aut Enthalten in Journal of analytical chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 72(2017), 6 vom: Juni, Seite 632-638 (DE-627)334292689 (DE-600)2057336-4 1608-3199 nnns volume:72 year:2017 number:6 month:06 pages:632-638 https://dx.doi.org/10.1134/S1061934817060144 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.23 ASE 35.71 ASE 42.03 ASE AR 72 2017 6 06 632-638 |
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Enthalten in Journal of analytical chemistry 72(2017), 6 vom: Juni, Seite 632-638 volume:72 year:2017 number:6 month:06 pages:632-638 |
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Shalabai, V. V. @@aut@@ Taranchenko, V. F. @@aut@@ Rybal’chenko, I. V. @@aut@@ Aksenov, A. V. @@aut@@ Antokhin, A. M. @@aut@@ Semchenko, F. M. @@aut@@ Krymchak, M. S. @@aut@@ |
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|
author |
Shalabai, V. V. |
spellingShingle |
Shalabai, V. V. ddc 540 bkl 35.23 bkl 35.71 bkl 42.03 misc HPLC misc high resolution mass spectrometry misc tetrodotoxin misc pharmaceutical Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
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topic_title |
540 ASE 35.23 bkl 35.71 bkl 42.03 bkl Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals HPLC (dpeaa)DE-He213 high resolution mass spectrometry (dpeaa)DE-He213 tetrodotoxin (dpeaa)DE-He213 pharmaceutical (dpeaa)DE-He213 |
topic |
ddc 540 bkl 35.23 bkl 35.71 bkl 42.03 misc HPLC misc high resolution mass spectrometry misc tetrodotoxin misc pharmaceutical |
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ddc 540 bkl 35.23 bkl 35.71 bkl 42.03 misc HPLC misc high resolution mass spectrometry misc tetrodotoxin misc pharmaceutical |
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ddc 540 bkl 35.23 bkl 35.71 bkl 42.03 misc HPLC misc high resolution mass spectrometry misc tetrodotoxin misc pharmaceutical |
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Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
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Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
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Shalabai, V. V. |
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Journal of analytical chemistry |
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Shalabai, V. V. Taranchenko, V. F. Rybal’chenko, I. V. Aksenov, A. V. Antokhin, A. M. Semchenko, F. M. Krymchak, M. S. |
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10.1134/S1061934817060144 |
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verfasserin |
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use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
title_auth |
Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
abstract |
Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. |
abstractGer |
Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. |
abstract_unstemmed |
Abstract A procedure is developed for the identification and determination of tetrodotoxin in pharmaceuticals by liquid chromatography coupled with high resolution mass spectrometry (HPLC−HRMS). The components of a pharmaceutical sample were separated in the gradient elution mode on a HILIC hydrophilic sorbent and detected by HRMS with electrospray ionization in the mode of registration of selected ion transitions. The calibration curve is linear in the range 0.75−1.25 μg/mL with the correlation coefficient > 0.9995. |
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title_short |
Use of high-performance liquid chromatography coupled with high-resolution mass spectrometry for the identification and quantitative determination of tetrodotoxin in pharmaceuticals |
url |
https://dx.doi.org/10.1134/S1061934817060144 |
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Taranchenko, V. F. Rybal’chenko, I. V. Aksenov, A. V. Antokhin, A. M. Semchenko, F. M. Krymchak, M. S. |
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Taranchenko, V. F. Rybal’chenko, I. V. Aksenov, A. V. Antokhin, A. M. Semchenko, F. M. Krymchak, M. S. |
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2024-07-03T19:48:52.432Z |
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|
score |
7.402895 |