In vivo Anticoagulant Activity of Immediate Release Tablets of Dabigatran Etexilate Mesylate Cocrystals

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Advances in Pharmacology and Pharmacy Pub Date : 2022-01-01 DOI:10.13189/app.2022.100101
A. Gawade, S. Boldhane, Anil Pawar, R. Pujari, A. Kuchekar
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引用次数: 1

Abstract

Dabigatran Etexilate Mesylate (DEM), a salt of prodrug dabigatran etexilate, is a potent, oral, reversible and direct thrombin inhibitor with low oral bioavailability. The present research investigation focused on the formulation of immediate release (IR) tablets of DEM cocrystals and evaluation of In vivo anticoagulant activity. The results of the study showed that the formulated IR tablets of DEM showed improved efficacy in comparison with the plain drug by enhancing the pre-compression parameters such as bulk density, tap density, Carr's index, angle of repose and Hausner's ratio and post-compression parameters like thickness and weight variation, hardness and friability, In vitro dissolution parameters. The improved efficacy was confirmed by improvement in the pharmacodynamic parameters such as cutaneous bleeding time and clotting time indicative of enhanced bioavailability of dabigatran. Thus, it can be concluded that the IR tablets of dabigatran cocrystals can be proven to be more effective in producing the anticoagulant effect in clinical practice as compared to the plain drug resulting in more patient compliance.
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甲磺酸达比加群酯速释片体内抗凝血活性的研究
达比加群依替西酯甲酸盐(DEM)是一种前药达比加群依替西酯盐,是一种有效的、口服的、可逆的、直接的凝血酶抑制剂,具有低口服生物利用度。本研究主要对DEM共晶速释片的制备及体内抗凝血活性进行了研究。研究结果表明,通过提高DEM红外片的容重、轻叩密度、卡尔指数、休止角、豪斯纳比等预压参数和压后厚度、重量变化、硬度、脆度、体外溶出度等参数,与普通药物相比,其疗效有所提高。改善的疗效通过改善的药效学参数,如皮肤出血时间和凝血时间,表明提高了达比加群的生物利用度。由此可见,在临床实践中,达比加群共晶IR片的抗凝作用比普通药物更有效,患者依从性更高。
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Advances in Pharmacology and Pharmacy
Advances in Pharmacology and Pharmacy PHARMACOLOGY & PHARMACY-
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