Literature DB >> 16765543

Kinetic study of the transformation of mefenamic acid polymorphs in various solvents and under high humidity conditions.

Fumie Kato1, Makoto Otsuka, Yoshihisa Matsuda.   

Abstract

The transformation kinetics of mefenamic acid form II to form I in three kinds of solvents and under high humidity conditions were extensively investigated. Form II crystals were suspended in water, 50% ethanol and ethanol at 28, 33 and 37 degrees C, or stored at 50, 60 and 70 degrees C at 97% RH. Form II transformed to form I under all storage conditions and the rate of transformation depended on the kind of solvent. The transformation followed the three-dimensional nuclei growth mechanism, depending on temperature. The nuclei formation and growth processes were significantly accelerated in ethanol compared with water. The addition of seed crystals of the stable form I shortened the both nuclei formation and growth processes and therefore the transformation was accelerated.

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Year:  2006        PMID: 16765543     DOI: 10.1016/j.ijpharm.2006.04.020

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  3 in total

1.  Quantum Chemical Study on Mefenamic Acid Polymorphic Forms.

Authors:  Svitlana V Shishkina; Yevhenii A Vaksler; Irina S Konovalova; Victoriya V Dyakonenko; Victoriya V Varchenko
Journal:  ACS Omega       Date:  2022-05-16

2.  In vitro Dissolution Studies on Solid Dispersions of Mefenamic Acid.

Authors:  K R S Sambasiva Rao; M V Nagabhushanam; K P R Chowdary
Journal:  Indian J Pharm Sci       Date:  2011-03       Impact factor: 0.975

3.  Solution growth and thermal treatment of crystals lead to two new forms of 2-((2,6-dimethylphenyl)amino)benzoic acid.

Authors:  Rong Hu; Yunping Zhoujin; Meng Liu; Mingtao Zhang; Sean Parkin; Panpan Zhou; Jianzhi Wang; Faquan Yu; Sihui Long
Journal:  RSC Adv       Date:  2018-04-24       Impact factor: 4.036

  3 in total

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