Codetermination of antimicrobial agents in rabbit tear fluid using LC–MS/MS assay: Insights into ocular pharmacokinetic study
Managing ocular microbial infections typically requires pharmacotherapy using antibiotic eye drops, such as moxifloxacin hydrochloride (MFX), combined with an antifungal agent like amphotericin B (AB). We carried out and validated an LC–MS/MS assay to quantify these compounds in rabbit tear fluid in...
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description | Managing ocular microbial infections typically requires pharmacotherapy using antibiotic eye drops, such as moxifloxacin hydrochloride (MFX), combined with an antifungal agent like amphotericin B (AB). We carried out and validated an LC–MS/MS assay to quantify these compounds in rabbit tear fluid in order to look into the pharmacokinetics of these two drugs. We employed a protein precipitation technique for the extraction of drugs under examination. A Waters Symmetry C18 column was used to separate the analytes and internal standard. The composition of the mobile phase was like (A) 0.1% v/v formic acid in water and (B) methanol. The detection of MFX and AB was accomplished through the utilization of positive ion electrospray ionization under multiple reaction monitoring mode. The linearity curves for both analytes exhibited an acceptable trendline across a concentration range of 2.34–300 ng/mL for MFX and 7.81–1000 ng/mL for AB in surrogate rabbit tear fluid. The lower limit of quantitation for MFX was 2.34 ng/mL, while for AB, it was 7.81 ng/mL. The approach was strictly validated, encompassing tests of selectivity, linearity (with r2 > 0.99), precision, accuracy, matrix effects, and stability. Consequently, we employed this method to evaluate the pharmacokinetics profiles of MFX and AB in rabbit tear fluid following single topical doses. |
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We carried out and validated an LC–MS/MS assay to quantify these compounds in rabbit tear fluid in order to look into the pharmacokinetics of these two drugs. We employed a protein precipitation technique for the extraction of drugs under examination. A Waters Symmetry C18 column was used to separate the analytes and internal standard. The composition of the mobile phase was like (A) 0.1% v/v formic acid in water and (B) methanol. The detection of MFX and AB was accomplished through the utilization of positive ion electrospray ionization under multiple reaction monitoring mode. The linearity curves for both analytes exhibited an acceptable trendline across a concentration range of 2.34–300 ng/mL for MFX and 7.81–1000 ng/mL for AB in surrogate rabbit tear fluid. The lower limit of quantitation for MFX was 2.34 ng/mL, while for AB, it was 7.81 ng/mL. The approach was strictly validated, encompassing tests of selectivity, linearity (with r2 > 0.99), precision, accuracy, matrix effects, and stability. Consequently, we employed this method to evaluate the pharmacokinetics profiles of MFX and AB in rabbit tear fluid following single topical doses.</description><identifier>ISSN: 1076-5174</identifier><identifier>ISSN: 1096-9888</identifier><identifier>EISSN: 1096-9888</identifier><identifier>DOI: 10.1002/jms.5031</identifier><identifier>PMID: 38726684</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Amphotericin B ; Amphotericin B - analysis ; Amphotericin B - pharmacokinetics ; Animals ; Anti-Infective Agents - analysis ; Anti-Infective Agents - pharmacokinetics ; Antimicrobial agents ; bioanalysis ; Chemical kinetics ; chemical species ; Drug therapy ; Drugs ; electrospray ionization mass spectrometry ; eyes ; Formic acid ; Fungicides ; Ionization ; Limit of Detection ; Linear Models ; Linearity ; Liquid Chromatography-Mass Spectrometry ; microbial keratitis ; Microorganisms ; Moxifloxacin ; Moxifloxacin - analysis ; Moxifloxacin - pharmacokinetics ; ocular delivery ; Ophthalmic Solutions - pharmacokinetics ; Pharmacokinetics ; Positive ions ; Rabbits ; Reproducibility of Results ; synergy ; Tandem Mass Spectrometry - methods ; tear fluid ; Tears - chemistry</subject><ispartof>Journal of mass spectrometry., 2024-06, Vol.59 (6), p.e5031-n/a</ispartof><rights>2024 John Wiley & Sons Ltd.</rights><rights>2024 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3821-54aa3b1839bb9d9a683cab0f912cfa74d7fd4731f226df4c3e4646767f4b0423</citedby><cites>FETCH-LOGICAL-c3821-54aa3b1839bb9d9a683cab0f912cfa74d7fd4731f226df4c3e4646767f4b0423</cites><orcidid>0000-0002-3755-407X ; 0000-0003-4841-0140 ; 0000-0002-1427-9247 ; 0009-0008-4656-131X ; 0000-0003-4844-2388 ; 0000-0002-5507-3739</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjms.5031$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjms.5031$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38726684$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bisen, Amol Chhatrapati</creatorcontrib><creatorcontrib>Mishra, Anjali</creatorcontrib><creatorcontrib>Agrawal, Sristi</creatorcontrib><creatorcontrib>Sanap, Sachin Nashik</creatorcontrib><creatorcontrib>Biswas, Arpon</creatorcontrib><creatorcontrib>Verma, Sarvesh Kumar</creatorcontrib><creatorcontrib>Bhatta, Rabi Sankar</creatorcontrib><title>Codetermination of antimicrobial agents in rabbit tear fluid using LC–MS/MS assay: Insights into ocular pharmacokinetic study</title><title>Journal of mass spectrometry.</title><addtitle>J Mass Spectrom</addtitle><description>Managing ocular microbial infections typically requires pharmacotherapy using antibiotic eye drops, such as moxifloxacin hydrochloride (MFX), combined with an antifungal agent like amphotericin B (AB). We carried out and validated an LC–MS/MS assay to quantify these compounds in rabbit tear fluid in order to look into the pharmacokinetics of these two drugs. We employed a protein precipitation technique for the extraction of drugs under examination. A Waters Symmetry C18 column was used to separate the analytes and internal standard. The composition of the mobile phase was like (A) 0.1% v/v formic acid in water and (B) methanol. The detection of MFX and AB was accomplished through the utilization of positive ion electrospray ionization under multiple reaction monitoring mode. The linearity curves for both analytes exhibited an acceptable trendline across a concentration range of 2.34–300 ng/mL for MFX and 7.81–1000 ng/mL for AB in surrogate rabbit tear fluid. The lower limit of quantitation for MFX was 2.34 ng/mL, while for AB, it was 7.81 ng/mL. The approach was strictly validated, encompassing tests of selectivity, linearity (with r2 > 0.99), precision, accuracy, matrix effects, and stability. 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We carried out and validated an LC–MS/MS assay to quantify these compounds in rabbit tear fluid in order to look into the pharmacokinetics of these two drugs. We employed a protein precipitation technique for the extraction of drugs under examination. A Waters Symmetry C18 column was used to separate the analytes and internal standard. The composition of the mobile phase was like (A) 0.1% v/v formic acid in water and (B) methanol. The detection of MFX and AB was accomplished through the utilization of positive ion electrospray ionization under multiple reaction monitoring mode. The linearity curves for both analytes exhibited an acceptable trendline across a concentration range of 2.34–300 ng/mL for MFX and 7.81–1000 ng/mL for AB in surrogate rabbit tear fluid. The lower limit of quantitation for MFX was 2.34 ng/mL, while for AB, it was 7.81 ng/mL. The approach was strictly validated, encompassing tests of selectivity, linearity (with r2 > 0.99), precision, accuracy, matrix effects, and stability. Consequently, we employed this method to evaluate the pharmacokinetics profiles of MFX and AB in rabbit tear fluid following single topical doses.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38726684</pmid><doi>10.1002/jms.5031</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-3755-407X</orcidid><orcidid>https://orcid.org/0000-0003-4841-0140</orcidid><orcidid>https://orcid.org/0000-0002-1427-9247</orcidid><orcidid>https://orcid.org/0009-0008-4656-131X</orcidid><orcidid>https://orcid.org/0000-0003-4844-2388</orcidid><orcidid>https://orcid.org/0000-0002-5507-3739</orcidid></addata></record> |
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subjects | Amphotericin B Amphotericin B - analysis Amphotericin B - pharmacokinetics Animals Anti-Infective Agents - analysis Anti-Infective Agents - pharmacokinetics Antimicrobial agents bioanalysis Chemical kinetics chemical species Drug therapy Drugs electrospray ionization mass spectrometry eyes Formic acid Fungicides Ionization Limit of Detection Linear Models Linearity Liquid Chromatography-Mass Spectrometry microbial keratitis Microorganisms Moxifloxacin Moxifloxacin - analysis Moxifloxacin - pharmacokinetics ocular delivery Ophthalmic Solutions - pharmacokinetics Pharmacokinetics Positive ions Rabbits Reproducibility of Results synergy Tandem Mass Spectrometry - methods tear fluid Tears - chemistry |
title | Codetermination of antimicrobial agents in rabbit tear fluid using LC–MS/MS assay: Insights into ocular pharmacokinetic study |
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