加拿大品牌和通用双膦酸盐体外崩解时间的差异。

IF 1.1 Q3 ORTHOPEDICS
Journal of Osteoporosis Pub Date : 2014-01-01 Epub Date: 2014-10-02 DOI:10.1155/2014/420451
Wojciech P Olszynski, Jonathan D Adachi, K Shawn Davison
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引用次数: 2

摘要

本研究的目的是比较加拿大上市品牌(阿仑膦酸盐70毫克,阿仑膦酸盐70毫克加维生素D 5600 IU,利塞膦酸盐35毫克)和通用(新阿仑膦酸盐70毫克和阿普阿仑膦酸盐70毫克)每周服用一次的双膦酸盐的崩解时间。所有崩解试验均使用范德坎普崩解仪进行。当除了不溶性包衣或胶囊壳的碎片外,没有任何残余物可见时,即认为发生了崩解。每个双膦酸盐组分别测试了18至20个样本。apo -阿仑膦酸钠(26±5.6秒)和novo -阿仑膦酸钠(13±1.1秒)的平均崩解时间(±标准差)显著(P < 0.05)快于品牌阿仑膦酸钠(147±50.5秒)、品牌阿仑膦酸钠加维生素D(378±60.5秒)和品牌立塞膦酸钠(101±20.6秒)。与品牌双膦酸盐相比,仿制药的崩解速度明显更快,这可能会对患者进行这些治疗的安全性和有效性产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Differences in In Vitro Disintegration Time among Canadian Brand and Generic Bisphosphonates.

Differences in In Vitro Disintegration Time among Canadian Brand and Generic Bisphosphonates.

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 significantly (P < 0.05) faster for Apo-alendronate (26 ± 5.6 seconds) and Novo-alendronate (13 ± 1.1 seconds) as compared to brand alendronate (147 ± 50.5 seconds), brand alendronate plus vitamin D (378 ± 60.5 seconds), or brand risedronate (101 ± 20.6 seconds). 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.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
6
审稿时长
20 weeks
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