<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hong L</submitter><funding>NIEHS NIH HHS</funding><pagination>1101-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3046028</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(5)</volume><pubmed_abstract>Para-aminosalicylic acid (PAS), an approved drug for treatment of tuberculosis, is a promising therapeutic agent for treatment of manganese (Mn)-induced parkinsonian syndromes. Lack of a quantifying method, however, has hindered the clinical evaluation of its efficacy and there upon new drug development. This study was aimed at developing a simple and effective method to quantify PAS and its major metabolite, N-acetyl-para-aminosalicylic acid (AcPAS), in plasma, cerebrospinal fluid (CSF) and tissues. Biological samples underwent one-step protein precipitation. The supernatant was fractionated on a reversed-phase C18 column with a gradient mobile system, followed by on-line fluorescence detection. The lower limits of quantification for both PAS and AcPAS were 50 ng/ml of plasma and 17 ng/g </pubmed_abstract><journal>Journal of pharmaceutical and biomedical analysis</journal><pubmed_title>HPLC analysis of para-aminosalicylic acid and its metabolite in plasma, cerebrospinal fluid and brain tissues.</pubmed_title><pmcid>PMC3046028</pmcid><funding_grant_id>R01ES008146</funding_grant_id><funding_grant_id>R01 ES008146-14</funding_grant_id><funding_grant_id>R01 ES008146</funding_grant_id><pubmed_authors>Hong L</pubmed_authors><pubmed_authors>Zeng S</pubmed_authors><pubmed_authors>Jiang W</pubmed_authors><pubmed_authors>Zheng W</pubmed_authors></additional><is_claimable>false</is_claimable><name>HPLC analysis of para-aminosalicylic acid and its metabolite in plasma, cerebrospinal fluid and brain tissues.</name><description>Para-aminosalicylic acid (PAS), an approved drug for treatment of tuberculosis, is a promising therapeutic agent for treatment of manganese (Mn)-induced parkinsonian syndromes. Lack of a quantifying method, however, has hindered the clinical evaluation of its efficacy and there upon new drug development. This study was aimed at developing a simple and effective method to quantify PAS and its major metabolite, N-acetyl-para-aminosalicylic acid (AcPAS), in plasma, cerebrospinal fluid (CSF) and tissues. Biological samples underwent one-step protein precipitation. The supernatant was fractionated on a reversed-phase C18 column with a gradient mobile system, followed by on-line fluorescence detection. The lower limits of quantification for both PAS and AcPAS were 50 ng/ml of plasma and 17 ng/g </description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Apr</publication><modification>2025-04-04T21:04:02.276Z</modification><creation>2019-03-27T00:39:15Z</creation></dates><accession>S-EPMC3046028</accession><cross_references><pubmed>21159459</pubmed><doi>10.1016/j.jpba.2010.11.031</doi></cross_references></HashMap>