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

被引:1
作者
Gawade, Ashwini [1 ]
Boldhane, Sanjay [2 ]
Pawar, Anil [1 ]
Pujari, Rohini [1 ]
Kuchekar, Ashwin [1 ]
机构
[1] World Peace Univ, Dr Vishwanath Karad Maharashtra Inst Pharm MIP, Sch Pharm, Pune 411038, Maharashtra, India
[2] Dev Micro Labs Ltd, Micro Adv Res Ctr Marc, 58-3 Kudlu Village,Post Bangalore, Singasandra 560068, Karnataka, India
关键词
Dabigatran Etexilate Mesylate; Cocrystals; Anticoagulant; Immediate Release; Cutaneous Bleeding; Clotting Time; DIRECT THROMBIN INHIBITOR; PHARMACEUTICAL COCRYSTALS; VENOUS THROMBOEMBOLISM; HEPARIN-ANTITHROMBIN; SOLUBILITY; INACTIVATION; DISSOLUTION; PREVENTION; DESIGN; VITRO;
D O I
10.13189/app.2022.100101
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
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页码:1 / 7
页数:7
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