Formulation and stability evaluation of an extemporaneously prepared baclofen suspension (1 mg/mL)
Background Baclofen is prescribed for both adults and children as a muscle relaxant, but no data exists to support an appropriate lower‐dose extemporaneously compounded oral liquid suitable for young children in New Zealand. Aim This study aimed to determine the stability of 1 mg/mL baclofen oral su...
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Published in: | Journal of pharmacy practice and research Vol. 51; no. 4; pp. 314 - 320 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-08-2021
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Subjects: | |
Online Access: | Get full text |
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Summary: | Background
Baclofen is prescribed for both adults and children as a muscle relaxant, but no data exists to support an appropriate lower‐dose extemporaneously compounded oral liquid suitable for young children in New Zealand.
Aim
This study aimed to determine the stability of 1 mg/mL baclofen oral suspension over 30 days.
Method
Baclofen suspensions were compounded (n = 6 per formulation) using suspending vehicles Ora‐Blend® (OB) or Ora‐Blend sugar‐free® (OB SF) and stored at either 25°C/60% relative humidity or 2–8°C for 30 days. Organoleptic properties, sedimentation volume ratio, ease of redispersion, pH and baclofen content were determined.
Results
Formulations required 2–3 inversions to redisperse at each time point. A colour change was observed from day 14 in the OB suspensions stored at both temperatures, likely due to the Maillard reaction, whereas no colour change was observed in any OB SF suspensions. The pH of all formulations remained between 4.5 and 4.6. Both OB and OB SF suspensions retained >90% of the initial baclofen concentration over 30 days.
Conclusion
Although baclofen 1 mg/mL suspensions prepared in both OB and OB SF retained sufficient baclofen to be considered chemically stable in both storage conditions over the study period, OB SF is recommended as a preferred vehicle over OB formulations due to the colour change observed. |
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ISSN: | 1445-937X 2055-2335 |
DOI: | 10.1002/jppr.1750 |