Literature DB >> 33748914

Preparation and Evaluation of Co-amorphous Formulations of Telmisartan-Amino Acids as a Potential Method for Solubility and Dissolution Enhancement.

Mai Khanfar1, Mayyas Al-Remawi2, Faisal Al-Akayleh2, Suha Hmouze3.   

Abstract

Telmisartan (TLM) is a potent antihypertensive drug with pH-dependent aqueous solubility. This work aimed to enhance the solubility and dissolution rate of TLM by the co-amorphous drug amino acid (AA) approach by combining TLM, with different types and ratios of AAs. The co-amorphous TLM-AA blends were prepared by freeze-drying and investigated for solid-state characteristics like the dissolution rate enhancement of TLM. Among the prepared co-amorphous formulations, TLM-arginine (ARG) exhibited the greatest enhancement in solubility with increasing the molar ratio of ARG. The TLM-ARG at 1:2 ratio showed about a 57-fold increase in solubility of TLM and the highest dissolution percentage in phosphate buffer (pH7.5) (100% in 20 minutes) compared to both crystalline TLM (20% in 60 min) and physical mixture. Powder XRD, DSC, FTIR analysis and SEM demonstrated the formation of amorphous form within the co-amorphous formulations. Only TLM:ARG (1:0.5) were stable at (40°C, 75% RH) for a minimum of 90 days. In conclusion, ARG was able to stabilize the amorphous form of TLM and enhances its aqueous solubility and dissolution. The 1:2 w/w ratio of TLM-ARG co-amorphous showed the best solubility and dissolution rate while the 1:0.5 w/w ratio showed the best stability.

Entities:  

Keywords:  amino acid; arginine; aspartic acid; co-amorphous; co-former; proline; telmisartan

Mesh:

Substances:

Year:  2021        PMID: 33748914     DOI: 10.1208/s12249-021-01952-9

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  28 in total

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Journal:  Adv Drug Deliv Rev       Date:  2007-05-29       Impact factor: 15.470

2.  Amorphous ternary cyclodextrin nanocomposites of telmisartan for oral drug delivery: improved solubility and reduced pharmacokinetic variability.

Authors:  Mayur Sangwai; Pradeep Vavia
Journal:  Int J Pharm       Date:  2012-08-28       Impact factor: 5.875

3.  Inclusion of telmisartan in mesocellular foam nanoparticles: drug loading and release property.

Authors:  Yanzhuo Zhang; Tongying Jiang; Qiang Zhang; Siling Wang
Journal:  Eur J Pharm Biopharm       Date:  2010-06-02       Impact factor: 5.571

4.  Co-crystals: a novel approach to modify physicochemical properties of active pharmaceutical ingredients.

Authors:  A V Yadav; A S Shete; A P Dabke; P V Kulkarni; S S Sakhare
Journal:  Indian J Pharm Sci       Date:  2009-07       Impact factor: 0.975

5.  Investigation and correlation of physical stability, dissolution behaviour and interaction parameter of amorphous solid dispersions of telmisartan: a drug development perspective.

Authors:  R Dukeck; P Sieger; P Karmwar
Journal:  Eur J Pharm Sci       Date:  2013-05-16       Impact factor: 4.384

6.  Modulation of microenvironmental pH and crystallinity of ionizable telmisartan using alkalizers in solid dispersions for controlled release.

Authors:  Phuong Ha Lien Tran; Huyen Thi Thanh Tran; Beom-Jin Lee
Journal:  J Control Release       Date:  2008-04-13       Impact factor: 9.776

7.  The effect of mechanical grinding on the formation, crystalline changes and dissolution behaviour of the inclusion complex of telmisartan and β-cyclodextrins.

Authors:  Paola Aline Amarante Borba; Marihá Pinotti; George Ricardo Santana Andrade; Nivan Bezerra da Costa; Luiz Renato Olchanheski Junior; Daniel Fernandes; Carlos Eduardo Maduro de Campos; Hellen Karine Stulzer
Journal:  Carbohydr Polym       Date:  2015-07-09       Impact factor: 9.381

8.  Effect of amorphization method on telmisartan solubility and the tableting process.

Authors:  P Lepek; W Sawicki; K Wlodarski; Z Wojnarowska; M Paluch; L Guzik
Journal:  Eur J Pharm Biopharm       Date:  2012-10-17       Impact factor: 5.571

9.  Co-milling of telmisartan with poly(vinyl alcohol)--An alkalinizer free green approach to ensure its bioavailability.

Authors:  Jinu Isaac; Swastika Ganguly; Animesh Ghosh
Journal:  Eur J Pharm Biopharm       Date:  2016-01-29       Impact factor: 5.571

10.  Development of self-microemulsifying drug delivery system and solid-self-microemulsifying drug delivery system of telmisartan.

Authors:  Parul Jaiswal; Geeta Aggarwal; Sasidharan Leelakumari Harikumar; Kashmir Singh
Journal:  Int J Pharm Investig       Date:  2014-10
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