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dc.contributor.authorHinkle, David M.
dc.contributor.authorKruh-Garcia, Nicole A.
dc.contributor.authorKruh, Jonathan N.
dc.contributor.authorBroccardo, Carolyn
dc.contributor.authorDoctor, Priyanka
dc.contributor.authorFoster, C. Stephen
dc.date2022-08-11T08:09:48.000
dc.date.accessioned2022-08-23T16:43:49Z
dc.date.available2022-08-23T16:43:49Z
dc.date.issued2017-06-12
dc.date.submitted2017-11-14
dc.identifier.citationOpen Ophthalmol J. 2017 Jun 12;11:107-116. doi: 10.2174/1874364101711010107. eCollection 2017. <a href="https://doi.org/10.2174/1874364101711010107">Link to article on publisher's site</a>
dc.identifier.issn1874-3641 (Linking)
dc.identifier.doi10.2174/1874364101711010107
dc.identifier.pmid28694894
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40377
dc.description.abstractPURPOSE: The aim was to report the aqueous humor moxifloxacin concentration and proteome profile of an individual with bilateral uveitis-like syndrome with pigment dispersion. METHODS: Multiple reactions monitoring mass spectrometry quantified the aqueous concentration of moxifloxacin in the affected individual. Shotgun proteomic analysis performed via liquid chromatography tandem mass spectrometry (LC-MS/MS) defined the protein profile in the affected individual and unaffected control samples. RESULTS: Moxifloxacin was present at higher than expected levels in aqueous humor 18 days following oral administration. One-third of the proteins were identified by significantly lower spectral counts in the aqueous of the individual with moxifloxacin associated uveitis compared to the unaffected control. CONCLUSION: Moxifloxacin was detected in aqueous humor 18 days following the completion of oral administration. These results suggest that moxifloxacin toxicity may be responsible for the uveitis-like syndrome with pigment dispersion syndrome induced by moxifloxacin therapy.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28694894&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2017 Hinkle et al.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectEye Diseases
dc.subjectOphthalmology
dc.titleMoxifloxacin Concentration and Proteomic Analysis of Aqueous Humor in Human Uveitis Associated with Oral Moxifloxacin Therapy
dc.typeJournal Article
dc.source.journaltitleThe open ophthalmology journal
dc.source.volume11
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4190&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3182
dc.identifier.contextkey11050538
refterms.dateFOA2022-08-23T16:43:49Z
html.description.abstract<p>PURPOSE: The aim was to report the aqueous humor moxifloxacin concentration and proteome profile of an individual with bilateral uveitis-like syndrome with pigment dispersion.</p> <p>METHODS: Multiple reactions monitoring mass spectrometry quantified the aqueous concentration of moxifloxacin in the affected individual. Shotgun proteomic analysis performed via liquid chromatography tandem mass spectrometry (LC-MS/MS) defined the protein profile in the affected individual and unaffected control samples.</p> <p>RESULTS: Moxifloxacin was present at higher than expected levels in aqueous humor 18 days following oral administration. One-third of the proteins were identified by significantly lower spectral counts in the aqueous of the individual with moxifloxacin associated uveitis compared to the unaffected control.</p> <p>CONCLUSION: Moxifloxacin was detected in aqueous humor 18 days following the completion of oral administration. These results suggest that moxifloxacin toxicity may be responsible for the uveitis-like syndrome with pigment dispersion syndrome induced by moxifloxacin therapy.</p>
dc.identifier.submissionpathoapubs/3182
dc.contributor.departmentDepartment of Ophthalmology
dc.source.pages107-116


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