Differences inIn VitroDisintegration Time among Canadian Brand and Generic Bisphosphonates

Author:

Olszynski Wojciech P.1,Adachi Jonathan D.2,Davison K. Shawn3

Affiliation:

1. Saskatoon Osteoporosis Centre and Department of Medicine, University of Saskatchewan, Suite 103, 39-23rd Street East, Saskatoon, SK, Canada S7K 0H6

2. Department of Medicine, St. Joseph’s Hospital, McMaster University, 501-25 Charlton Avenue E., Hamilton, ON, Canada L8N 1Y2

3. University of Victoria, P.O. Box 1700 STN CSC, Victoria, BC, Canada V8W 2Y2

Abstract

The objective of this study was to compare the disintegration times among Canadian-marketed brand (alendronate 70 mg, alendronate 70 mg plus vitamin D 5600 IU, and risedronate 35 mg) and generic (Novo-alendronate 70 mg and Apo-alendronate 70 mg) once-weekly dosed bisphosphonates. All disintegration tests were performed with a Vanderkamp Disintegration Tester. Disintegration was deemed to have occurred when no residue of the tablet, except fragments of insoluble coating or capsule shell, was visible. Eighteen to 20 samples were tested for each bisphosphonate group. The mean (±standard deviation) disintegration times were significantlyP<0.05faster for Apo-alendronate (26±5.6seconds) and Novo-alendronate (13±1.1seconds) as compared to brand alendronate (147±50.5seconds), brand alendronate plus vitamin D (378±60.5seconds), or brand risedronate (101±20.6seconds). The significantly faster disintegration of the generic tablets as compared to the brand bisphosphonates may have concerning safety and effectiveness implications for patients administering these therapies.

Publisher

Hindawi Limited

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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