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不同含阿仑膦酸盐商业制剂食管黏附性的体外比较研究

Comparative in vitro study of oesophageal adhesiveness of different commercial formulations containing alendronate.

作者信息

Shakweh Monjed, Bravo-Osuna Irene, Ponchel Gilles

机构信息

Laboratoire de Physicochimie, Pharmacotechnie et Biopharmacie, UMR CNRS 8612, Université Paris-Sud, Chatenay Malabry, France.

出版信息

Eur J Pharm Sci. 2007 Aug;31(5):262-70. doi: 10.1016/j.ejps.2007.03.012. Epub 2007 Apr 8.

Abstract

Cases of oesophageal irritation have been reported in patients ingesting alendronate with little liquid or reclining shortly after taking the medication. Pill-induced oesophagitis principally occurs because of adherence of ingested tablets to the epithelial surface. The objective of this in vitro study was to evaluate the oesophageal bioadhesive characteristics of alendronate generics marketed in Europe, the proprietary Fosamax((R)), one negative and two positive polymer controls. A texture analyser was used for qualitative analysis and to determine the maximal detachment force and the adhesion work developed by each formulation on porcine oesophageal mucosa. Fosamax showed few or no bioadhesive characteristics, but the detachment of few tablets powder particles in some of the experiments does not preclude the potential risk of oesophageal lesions. The 10-mg generic Teva tablets had bioadhesive characteristics similar to a positive control. Other generic formulations (Alenat, Stada, Aliud, Ratiopharm showed "cleavage" rupture, leaving a large piece of the tablet mass attached to the mucosa. The bioadhesive characteristics seem to be related to the inactive ingredients: the presence of adhesive polymers such as HPC or very active disintegration agents, such as sodium croscarmellose. The demonstrated differences in adhesiveness suggest that differences in oesophageal tolerance between Fosamax tablets and generics of sodium alendronate may exist.

摘要

有报告称,患者在摄入阿仑膦酸盐时,如果饮水量很少或服药后不久就躺下,会出现食管刺激症状。药丸引起的食管炎主要是由于摄入的药片附着在上皮表面所致。这项体外研究的目的是评估在欧洲销售的阿仑膦酸盐仿制药、专利药福善美(Fosamax)、一种阴性和两种阳性聚合物对照品的食管生物粘附特性。使用质地分析仪进行定性分析,并确定每种制剂在猪食管黏膜上产生的最大分离力和粘附功。福善美显示出很少或没有生物粘附特性,但在一些实验中少数药片粉末颗粒的分离并不能排除食管病变的潜在风险。10毫克的梯瓦(Teva)仿制药片具有与阳性对照品相似的生物粘附特性。其他仿制药制剂(阿仑膦酸钠片(Alenat)、施达德(Stada)、阿利乌德(Aliud)、德国美纳里尼(Ratiopharm))显示出“裂开”破裂,有一大块药片附着在黏膜上。生物粘附特性似乎与非活性成分有关:存在粘附性聚合物如羟丙基纤维素(HPC)或非常活跃的崩解剂如交联羧甲基纤维素钠。所显示的粘附性差异表明福善美片和阿仑膦酸钠仿制药之间在食管耐受性方面可能存在差异。

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