Literature DB >> 21159459

HPLC analysis of para-aminosalicylic acid and its metabolite in plasma, cerebrospinal fluid and brain tissues.

Lan Hong1, Wendy Jiang, Wei Zheng, Su Zeng.   

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 of tissues. The intra-day and inter-day precision values did not exceed 5% and 8%, respectively, in all three matrices. The method was used to quantify PAS and AcPAS in rat plasma and brain following a single iv injection of PAS. Data showed a greater amount of PAS than AcPAS in plasma, while a greater amount of AcPAS than PAS was found in brain tissues. The method has been proven to be sensitive, reproducible, and practically useful for laboratory and clinical investigations of PAS in treatment of Mn Parkinsonism.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21159459      PMCID: PMC3046028          DOI: 10.1016/j.jpba.2010.11.031

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  25 in total

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Authors:  Jonathan E Myers; Mary Lou Thompson; Suzan Ramushu; Taryn Young; Mohamed F Jeebhay; Leslie London; Eric Esswein; Kevin Renton; Adri Spies; Andrew Boulle; Inakshi Naik; Anders Iregren; David J Rees
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2.  Bioavailability of aminosalicylic acid and its various salts in humans IV: comparison of four brands of the sodium salt.

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3.  Pharmacokinetics of para-aminosalicylic acid granules under four dosing conditions.

Authors:  C A Peloquin; M Zhu; R D Adam; M D Singleton; D E Nix
Journal:  Ann Pharmacother       Date:  2001-11       Impact factor: 3.154

4.  Chronic manganese intoxication.

Authors:  D G Cook; S Fahn; K A Brait
Journal:  Arch Neurol       Date:  1974-01

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Authors:  M C Gennaro; R Calvino; C Abrigo
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6.  Quantitative determination of p-aminosalicylic acid and its degradation product m-aminophenol in pellets by ion-pair high-performance liquid chromatography applying the monolithic Chromolith Speedrod RP-18e column.

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Review 9.  Clinical pharmacokinetics of the antituberculosis drugs.

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2.  Brain regional pharmacokinetics of p-aminosalicylic acid and its N-acetylated metabolite: effectiveness in chelating brain manganese.

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3.  Pharmacokinetics of para-aminosalicylic acid in HIV-uninfected and HIV-coinfected tuberculosis patients receiving antiretroviral therapy, managed for multidrug-resistant and extensively drug-resistant tuberculosis.

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Journal:  Antimicrob Agents Chemother       Date:  2014-08-11       Impact factor: 5.191

4.  Roles of P-glycoprotein and multidrug resistance protein in transporting para-aminosalicylic acid and its N-acetylated metabolite in mice brain.

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5.  Sodium Para-aminosalicylic Acid Inhibits Lead-Induced Neuroinflammation in Brain Cortex of Rats by Modulating SIRT1/HMGB1/NF-κB Pathway.

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Review 6.  Manganese Toxicity Upon Overexposure: a Decade in Review.

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9.  The 1H NMR profile of healthy dog cerebrospinal fluid.

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10.  Development of a highly biocompatible antituberculosis nanodelivery formulation based on para-aminosalicylic acid-zinc layered hydroxide nanocomposites.

Authors:  Bullo Saifullah; Palanisamy Arulselvan; Mohamed Ezzat El Zowalaty; Sharida Fakurazi; Thomas J Webster; Benjamin Geilich; Mohd Zobir Hussein
Journal:  ScientificWorldJournal       Date:  2014-06-23
  10 in total

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