Literature DB >> 1772467

Metabolic fate of exogenous chondroitin sulfate in man.

A Conte1, M de Bernardi, L Palmieri, P Lualdi, G Mautone, G Ronca.   

Abstract

Chondroitin sulfate is administered as a drug to man by intravenous, intramuscular or oral route. However, few data are available on the metabolic fate of exogenous chondroitin sulfate in man. After intravenous administration of 0.5 g of chondroitin sulfate to healthy volunteers, the plasma level decreases according to a two-compartmental open model. The half-lives of distribution and elimination are 25.5 +/- 6.6 and 281 +/- 32 min, respectively. The volumes of central and tissue compartments are 6.0 +/- 1.0 and 22.9 +/- 7.7 l, respectively. More than 50% of the administered chondroitin sulfate is excreted with urine during the first 24 h as high and low molecular weight derivatives. After oral administration of 3 g of chondroitin sulfate to 12 healthy volunteers, a main peak (11.4 +/- 3.7 micrograms/ml) preceded by a lower peak is observed after 190 +/- 21 min. The elimination half-life is 363 +/- 109 min. The absolute bioavailability following oral administration calculated from AUC of plasma concentration is 13.2%. A peak of oligo- and polysaccharides with a molecular weight lower than 5000 Daltons derived from partial digestion of exogenous chondroitin sulfate is also present in plasma. These observations indicate that the metabolic fate of exogenous chondroitin sulfate is similar in man and in experimental animals.

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Year:  1991        PMID: 1772467

Source DB:  PubMed          Journal:  Arzneimittelforschung        ISSN: 0004-4172


  10 in total

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Authors:  Philip J Gregory; Chris Fellner
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3.  Bioavailability of oral chondroitin sulfate.

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Review 4.  Drug Screening Implicates Chondroitin Sulfate as a Potential Longevity Pill.

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5.  Analysis of glycosaminoglycans in human serum after oral administration of chondroitin sulfate.

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9.  Intra-articular use of a medical device composed of hyaluronic acid and chondroitin sulfate (Structovial CS): effects on clinical, ultrasonographic and biological parameters.

Authors:  Yves Henrotin; Jean-Philippe Hauzeur; Pierre Bruel; Thierry Appelboom
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10.  Inhibition of binding of malaria-infected erythrocytes by a tetradecasaccharide fraction from chondroitin sulfate A.

Authors:  J G Beeson; W Chai; S J Rogerson; A M Lawson; G V Brown
Journal:  Infect Immun       Date:  1998-07       Impact factor: 3.441

  10 in total

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