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A Sensitive LC-MS/MS Method for the Simultaneous Determination of Two Thia-Analogous Indirubin N -Glycosides and Indirubin-3'-Monoxime in Plasma and Cell Culture Medium
Indirubin was identified as an active component of Danggui Longhui Wan, an herbal mixture used in traditional Chinese medicine, and showed anticancer activity in clinical trials in patients with chronic leukemia. Investigations on the mechanisms of antitumor action of indirubins have mainly focused...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2022-05, Vol.27 (9), p.3031 |
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description | Indirubin was identified as an active component of Danggui Longhui Wan, an herbal mixture used in traditional Chinese medicine, and showed anticancer activity in clinical trials in patients with chronic leukemia. Investigations on the mechanisms of antitumor action of indirubins have mainly focused on the indirubin derivative indirubin-3'-monoxime (I3M). Meanwhile, antiproliferative and cytotoxic properties on cancer cells have also been demonstrated for several synthetic indirubin
-glycosides. In the present study, we demonstrate cytotoxic activity of the thia-analogous indirubin
-glycosides KD87 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-glucopyranosyl)-oxindole) and KD85 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-mannopyranosyl)-oxindole) against melanoma and squamous cell carcinoma cells as well as lung cancer and glioblastoma cells. The advanced state of preclinical studies on the effects of indirubins conducted to date underscores the need for pharmacokinetic data from cellular, animal, and human studies for which reliable quantification is required. Therefore, a sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the simultaneous measurement of KD87, KD85, and I3M in plasma and cell culture medium. Experimental conditions for sample preparation were optimized for human plasma protein precipitation and liquid-liquid extraction from plasma and cell culture medium. The methods were successfully validated in accordance with the U.S. Food and Drug Administration Bioanalytical Method Validation and evaluated for selectivity, sensitivity, matrix effect, recovery, carryover, calibration curve linearity, accuracy, precision, and stability. The applicability of the methods was demonstrated by the determination of KD87 in mouse plasma after prior intraperitoneal administration to mice. |
doi_str_mv | 10.3390/molecules27093031 |
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-glycosides. In the present study, we demonstrate cytotoxic activity of the thia-analogous indirubin
-glycosides KD87 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-glucopyranosyl)-oxindole) and KD85 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-mannopyranosyl)-oxindole) against melanoma and squamous cell carcinoma cells as well as lung cancer and glioblastoma cells. The advanced state of preclinical studies on the effects of indirubins conducted to date underscores the need for pharmacokinetic data from cellular, animal, and human studies for which reliable quantification is required. Therefore, a sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the simultaneous measurement of KD87, KD85, and I3M in plasma and cell culture medium. Experimental conditions for sample preparation were optimized for human plasma protein precipitation and liquid-liquid extraction from plasma and cell culture medium. The methods were successfully validated in accordance with the U.S. Food and Drug Administration Bioanalytical Method Validation and evaluated for selectivity, sensitivity, matrix effect, recovery, carryover, calibration curve linearity, accuracy, precision, and stability. The applicability of the methods was demonstrated by the determination of KD87 in mouse plasma after prior intraperitoneal administration to mice.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules27093031</identifier><identifier>PMID: 35566381</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animals ; Antineoplastic Agents - pharmacokinetics ; Antitumor activity ; Biological activity ; Blood plasma ; Breast cancer ; Calibration ; Cell culture ; Cell Culture Techniques ; Chromatography, Liquid - methods ; Clinical trials ; Culture media ; Cyclin-dependent kinases ; Cytotoxicity ; Glioblastoma ; Glioblastoma cells ; Glycosides ; Herbal medicine ; Humans ; Indoles ; Kinases ; LC-MS/MS ; Leukemia ; Liquid chromatography ; Liquid-liquid extraction ; Lung cancer ; Melanoma ; Methods ; Mice ; Noise ; Oximes ; Oxindoles ; Pharmacokinetics ; Plasma ; protein precipitation ; Proteins ; Reproducibility of Results ; Sample preparation ; Selectivity ; Sensitivity analysis ; Skin cancer ; Spectrometry ; Squamous cell carcinoma ; Tandem Mass Spectrometry - methods ; thia-analogous indirubin N-glycosides ; validation</subject><ispartof>Molecules (Basel, Switzerland), 2022-05, Vol.27 (9), p.3031</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4081-707e101994e57b11a489dffccedcd6a508a5e1fd27c7d94c128ba4af47bb2c443</citedby><cites>FETCH-LOGICAL-c4081-707e101994e57b11a489dffccedcd6a508a5e1fd27c7d94c128ba4af47bb2c443</cites><orcidid>0000-0002-5826-1217 ; 0000-0003-0098-6546 ; 0000-0002-2529-0732</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2663050103/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2663050103?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35566381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fischle, Alica</creatorcontrib><creatorcontrib>Schwarz, Rico</creatorcontrib><creatorcontrib>Wendt, Franziska</creatorcontrib><creatorcontrib>Kordt, Marcel</creatorcontrib><creatorcontrib>Ramer, Robert</creatorcontrib><creatorcontrib>Boeckmann, Lars</creatorcontrib><creatorcontrib>Hein, Martin</creatorcontrib><creatorcontrib>Langer, Peter</creatorcontrib><creatorcontrib>Emmert, Steffen</creatorcontrib><creatorcontrib>Vollmar, Brigitte</creatorcontrib><creatorcontrib>Hinz, Burkhard</creatorcontrib><title>A Sensitive LC-MS/MS Method for the Simultaneous Determination of Two Thia-Analogous Indirubin N -Glycosides and Indirubin-3'-Monoxime in Plasma and Cell Culture Medium</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>Indirubin was identified as an active component of Danggui Longhui Wan, an herbal mixture used in traditional Chinese medicine, and showed anticancer activity in clinical trials in patients with chronic leukemia. Investigations on the mechanisms of antitumor action of indirubins have mainly focused on the indirubin derivative indirubin-3'-monoxime (I3M). Meanwhile, antiproliferative and cytotoxic properties on cancer cells have also been demonstrated for several synthetic indirubin
-glycosides. In the present study, we demonstrate cytotoxic activity of the thia-analogous indirubin
-glycosides KD87 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-glucopyranosyl)-oxindole) and KD85 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-mannopyranosyl)-oxindole) against melanoma and squamous cell carcinoma cells as well as lung cancer and glioblastoma cells. The advanced state of preclinical studies on the effects of indirubins conducted to date underscores the need for pharmacokinetic data from cellular, animal, and human studies for which reliable quantification is required. Therefore, a sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the simultaneous measurement of KD87, KD85, and I3M in plasma and cell culture medium. Experimental conditions for sample preparation were optimized for human plasma protein precipitation and liquid-liquid extraction from plasma and cell culture medium. The methods were successfully validated in accordance with the U.S. Food and Drug Administration Bioanalytical Method Validation and evaluated for selectivity, sensitivity, matrix effect, recovery, carryover, calibration curve linearity, accuracy, precision, and stability. The applicability of the methods was demonstrated by the determination of KD87 in mouse plasma after prior intraperitoneal administration to mice.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacokinetics</subject><subject>Antitumor activity</subject><subject>Biological activity</subject><subject>Blood plasma</subject><subject>Breast cancer</subject><subject>Calibration</subject><subject>Cell culture</subject><subject>Cell Culture Techniques</subject><subject>Chromatography, Liquid - methods</subject><subject>Clinical trials</subject><subject>Culture media</subject><subject>Cyclin-dependent kinases</subject><subject>Cytotoxicity</subject><subject>Glioblastoma</subject><subject>Glioblastoma cells</subject><subject>Glycosides</subject><subject>Herbal medicine</subject><subject>Humans</subject><subject>Indoles</subject><subject>Kinases</subject><subject>LC-MS/MS</subject><subject>Leukemia</subject><subject>Liquid chromatography</subject><subject>Liquid-liquid extraction</subject><subject>Lung cancer</subject><subject>Melanoma</subject><subject>Methods</subject><subject>Mice</subject><subject>Noise</subject><subject>Oximes</subject><subject>Oxindoles</subject><subject>Pharmacokinetics</subject><subject>Plasma</subject><subject>protein precipitation</subject><subject>Proteins</subject><subject>Reproducibility of Results</subject><subject>Sample preparation</subject><subject>Selectivity</subject><subject>Sensitivity analysis</subject><subject>Skin cancer</subject><subject>Spectrometry</subject><subject>Squamous cell carcinoma</subject><subject>Tandem Mass Spectrometry - 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pharmacokinetics</topic><topic>Antitumor activity</topic><topic>Biological activity</topic><topic>Blood plasma</topic><topic>Breast cancer</topic><topic>Calibration</topic><topic>Cell culture</topic><topic>Cell Culture Techniques</topic><topic>Chromatography, Liquid - methods</topic><topic>Clinical trials</topic><topic>Culture media</topic><topic>Cyclin-dependent kinases</topic><topic>Cytotoxicity</topic><topic>Glioblastoma</topic><topic>Glioblastoma cells</topic><topic>Glycosides</topic><topic>Herbal medicine</topic><topic>Humans</topic><topic>Indoles</topic><topic>Kinases</topic><topic>LC-MS/MS</topic><topic>Leukemia</topic><topic>Liquid chromatography</topic><topic>Liquid-liquid extraction</topic><topic>Lung cancer</topic><topic>Melanoma</topic><topic>Methods</topic><topic>Mice</topic><topic>Noise</topic><topic>Oximes</topic><topic>Oxindoles</topic><topic>Pharmacokinetics</topic><topic>Plasma</topic><topic>protein precipitation</topic><topic>Proteins</topic><topic>Reproducibility of Results</topic><topic>Sample preparation</topic><topic>Selectivity</topic><topic>Sensitivity analysis</topic><topic>Skin cancer</topic><topic>Spectrometry</topic><topic>Squamous cell carcinoma</topic><topic>Tandem Mass Spectrometry - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fischle, Alica</au><au>Schwarz, Rico</au><au>Wendt, Franziska</au><au>Kordt, Marcel</au><au>Ramer, Robert</au><au>Boeckmann, Lars</au><au>Hein, Martin</au><au>Langer, Peter</au><au>Emmert, Steffen</au><au>Vollmar, Brigitte</au><au>Hinz, Burkhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Sensitive LC-MS/MS Method for the Simultaneous Determination of Two Thia-Analogous Indirubin N -Glycosides and Indirubin-3'-Monoxime in Plasma and Cell Culture Medium</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2022-05-09</date><risdate>2022</risdate><volume>27</volume><issue>9</issue><spage>3031</spage><pages>3031-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>Indirubin was identified as an active component of Danggui Longhui Wan, an herbal mixture used in traditional Chinese medicine, and showed anticancer activity in clinical trials in patients with chronic leukemia. Investigations on the mechanisms of antitumor action of indirubins have mainly focused on the indirubin derivative indirubin-3'-monoxime (I3M). Meanwhile, antiproliferative and cytotoxic properties on cancer cells have also been demonstrated for several synthetic indirubin
-glycosides. In the present study, we demonstrate cytotoxic activity of the thia-analogous indirubin
-glycosides KD87 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-glucopyranosyl)-oxindole) and KD85 (3-[3'-oxo-benzo[
]thiophen-2'-(
)-ylidene]-1-(β-d-mannopyranosyl)-oxindole) against melanoma and squamous cell carcinoma cells as well as lung cancer and glioblastoma cells. The advanced state of preclinical studies on the effects of indirubins conducted to date underscores the need for pharmacokinetic data from cellular, animal, and human studies for which reliable quantification is required. Therefore, a sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the simultaneous measurement of KD87, KD85, and I3M in plasma and cell culture medium. Experimental conditions for sample preparation were optimized for human plasma protein precipitation and liquid-liquid extraction from plasma and cell culture medium. The methods were successfully validated in accordance with the U.S. Food and Drug Administration Bioanalytical Method Validation and evaluated for selectivity, sensitivity, matrix effect, recovery, carryover, calibration curve linearity, accuracy, precision, and stability. The applicability of the methods was demonstrated by the determination of KD87 in mouse plasma after prior intraperitoneal administration to mice.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35566381</pmid><doi>10.3390/molecules27093031</doi><orcidid>https://orcid.org/0000-0002-5826-1217</orcidid><orcidid>https://orcid.org/0000-0003-0098-6546</orcidid><orcidid>https://orcid.org/0000-0002-2529-0732</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic Agents - pharmacokinetics Antitumor activity Biological activity Blood plasma Breast cancer Calibration Cell culture Cell Culture Techniques Chromatography, Liquid - methods Clinical trials Culture media Cyclin-dependent kinases Cytotoxicity Glioblastoma Glioblastoma cells Glycosides Herbal medicine Humans Indoles Kinases LC-MS/MS Leukemia Liquid chromatography Liquid-liquid extraction Lung cancer Melanoma Methods Mice Noise Oximes Oxindoles Pharmacokinetics Plasma protein precipitation Proteins Reproducibility of Results Sample preparation Selectivity Sensitivity analysis Skin cancer Spectrometry Squamous cell carcinoma Tandem Mass Spectrometry - methods thia-analogous indirubin N-glycosides validation |
title | A Sensitive LC-MS/MS Method for the Simultaneous Determination of Two Thia-Analogous Indirubin N -Glycosides and Indirubin-3'-Monoxime in Plasma and Cell Culture Medium |
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