Abstract

Despite the lack of safety, efficacy and pharmacokinetic (PK) studies, multicomponent dietary supplements (nutraceuticals) have become increasingly popular as primary or adjunct therapies for clinical osteoarthritis in veterinary medicine. Phycox® is a line of multicomponent joint support supplements marketed for joint health in dogs and horses. Many of the active constituents are recognized anti-inflammatory and antioxidant agents. Due to a lack of PK studies in the literature for the product, a pilot PK study of select constituents in Phycox® was performed in healthy dogs. Two novel methods of analysis were developed and validated for quantification of glucosamine and select polyphenols using liquid chromatography-tandem mass spectrometry. After a single oral (PO) administrated dose of Phycox®, a series of blood samples from dogs were collected for 24 h post-dose and analyzed for concentrations of glucosamine HCl, hesperetin, resveratrol and naringenin. Non-compartmental PK analyses were carried out. Glucosamine was detected up to 8 h post-dose with a Tmax of 2 h and Cmax of 9.69 μg/mL. The polyphenols were not found at detectable concentrations in serum samples. Co-administration of glucosamine in the Phycox® formulation may enhance the absorption of glucosamine as determined by comparison of glucosamine PK data in the literature.

Highlights

  • Osteoarthritis (OA) continues to present significant therapeutic problems in humans, equines, canines and other companion animals despite its clinical prevalence

  • Optimal separation was achieved with the combination of a Primesep 200 mixed function cation exchange column and pH gradient mobile phase consisting of: (A) 0.05% aqueous formic acid; and (B) 1% formic acid, in 50% aqueous acetonitrile with the following gradient: 0% B for

  • ±hesperetin, trans-resveratrol and ±naringenin was employed to determine the amount of each compound in a single dose of Phycox® as it is not disclosed on the label claim

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Summary

Introduction

Osteoarthritis (OA) continues to present significant therapeutic problems in humans, equines, canines and other companion animals despite its clinical prevalence. Non-steroidal anti-inflammatory agents (NSAIDs) remain the most common therapies across species for attenuation of clinical signs of OA [1,2,3]. NSAIDs act by inhibiting cyclooxygenases, which are involved in the production of prostaglandins resulting in analgesic, anti-inflammatory and antipyretic effects [4,5]. Due to the possible adverse effects of NSAIDs, there has been an interest in human and veterinary medicine to identify dietary supplements (nutraceuticals) that may serve as safer, efficacious alternatives or adjuncts to NSAIDs for the management of OA [8].

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