Chondroitin product selection for the glucosamine/chondroitin arthritis intervention trial

被引:31
作者
Barnhill, Jamie G.
Fye, Carol L.
Williams, David W.
Reda, Domenic J.
Harris, Crystal L.
Clegg, Daniel O.
机构
[1] US Dept Vet Affairs, Biopharmaceut Pharmacokinet Lab Sect, Cooperat Studies Program, Clin Res Pharm Coordinating Ctr, Albuquerque, NM USA
[2] Univ New Mexico, Coll Pharm, Albuquerque, NM 87131 USA
[3] SMART, Good Clin Practice Review Grp, VA Cooperat Studies Program, Albuquerque, NM USA
[4] Glucosamine Chondroitin Arthritis Intervent Trail, Hines, IL USA
[5] Coordinating Ctr, VA Cooperat Studies Program, Hines, IL USA
[6] Clin Res Pharm Coordinating Ctr, Biopharmaceut Pharmacokinet Lab, VA Cooperat Studies Program, Albuquerque, NM 87106 USA
[7] Univ Utah, Sch Med, Div Rheumatol, Salt Lake City, UT USA
关键词
dietary supplements; chondroitin; glucosamine/chondroitin arthritis intervention trial; osteoarthritis; product selection;
D O I
10.1331/154434506775268616
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To select a high-quality chondroitin dosage form and/ or an appropriate source of sodium chondroitin for the National Institutes of Health's Glucosamine/ Chondroitin Arthritis Intervention Trial ( GAIT). Design: Controlled experimental trials. Setting: Laboratory. Patients or Participants: Not applicable. Interventions: Commercially available chondroitin products were reviewed, and purified sodium chondroitin from two suppliers was evaluated through tests ( infrared and near-infrared identification, moisture content, pH, optical rotation, color and clarity of aqueous solutions prepared from the powders, protein contamination, total residue following ignition and nitrogen content, determination of sodium chondroitin molecular weight, disaccharide analysis, and measurement of chondroitin, sodium, and total glycosaminoglycan content) and an onsite supplier audit. Main Outcome Measures: Purity, potency, and quality of sodium chondroitin powders. Results: No commercially available chondroitin product was deemed appropriate for use in GAIT. Samples of sodium chondroitin powder from two suppliers exhibited similar disaccharide and glycosaminoglycan content. Each contained approximately 2% hyaluronic acid and 8%-9% unsulfated disaccharide. Potency was inconsistent across groups, which might have resulted from different analytical methods and choice of reference standard. Mean potency obtained by five separate methods ranged from 82.2% to 95.5% for one supplier, 92.5% to 110.1% for another, and 95.1% to 112.5% for a commercially obtained reference standard. Critical issues raised by the results include choice of reference standard, selection of assay method, and the consistent appearance of an unidentifiable contaminant present in all three lots from one supplier. Conclusion: This blinded study determined methods to identify acceptable agents and provided results, which, in addition to regulatory compliance supplier audits, formed the basis for chondroitin product selection in GAIT.
引用
收藏
页码:14 / 24
页数:11
相关论文
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