Literature DB >> 25882013

Design and stability study of a paediatric oral solution of methotrexate 2 mg/ml.

Sandy Vrignaud1, Thomas Briot2, Aurélie Launay3, Marie Kempf4, Frédéric Lagarce2.   

Abstract

Oral paediatric forms development by pharmaceutical industry is still insufficient. The present study was performed to propose an adapted and pleasant formulation of liquid oral formulation of MTX. The solution is composed of injectable methotrexate, water, Ora Sweet(®) and sodium bicarbonate. After 120 days storage, pH remained stable at about 8 in all formulations, insuring no risk of MTX precipitation. MTX content in solution formulation, determined by high performance liquid chromatography measurements, remained in the specifications of >90% of the initial concentration when stored at 4 and 25°C. Forced degradation of MTX by heat and acidic conditions allowed formation and detection of degradation products by the analytical method. Microbial study of the preparation shows that the solution remains in the specifications during all the storage, or after one sample each week during one month, eventually indicating the microbial properties are not affected by patient use. To conclude, we here propose a new MTX liquid formulation stable for at least 120 days.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  HPLC; Methotrexate; Oral paediatric solution; Stability study

Mesh:

Substances:

Year:  2015        PMID: 25882013     DOI: 10.1016/j.ijpharm.2015.04.016

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


  4 in total

1.  Stability of Diazoxide in Extemporaneously Compounded Oral Suspensions.

Authors:  Mihaela Friciu; Sarra Zaraa; V Gaëlle Roullin; Grégoire Leclair
Journal:  PLoS One       Date:  2016-10-11       Impact factor: 3.240

2.  Stability of gabapentin in extemporaneously compounded oral suspensions.

Authors:  Mihaela Friciu; V Gaëlle Roullin; Grégoire Leclair
Journal:  PLoS One       Date:  2017-04-17       Impact factor: 3.240

3.  Validation of a stability-indicating HPLC-UV method for the quantification of acetazolamide in Oral-Mix and Oral-Mix SF.

Authors:  Charlotte Gillium; Mihaela Friciu; Nicolas Abatzoglou; Grégoire Leclair
Journal:  MethodsX       Date:  2020-02-27

4.  Hydrolytic stability of anticancer drugs and one metabolite in the aquatic environment.

Authors:  Michał Toński; Joanna Dołżonek; Piotr Stepnowski; Anna Białk-Bielińska
Journal:  Environ Sci Pollut Res Int       Date:  2021-06-08       Impact factor: 4.223

  4 in total

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