Literature DB >> 27323428

Long-term Stability of Zonisamide, Amitriptyline, and Glycopyrrolate in Extemporaneously Prepared Liquid-dosage Forms at Two Temperatures.

Milap C Nahata.   

Abstract

The lack of commercially available liquid dosage forms for pediatric patients prompted this study. The objectives of our study were to determine the stability of zonisamide, amitriptyline, and glycopyrrolate in extemporaneously prepared oral suspensions in plastic prescription bottles. One group of suspensions was prepared in OraPlus:OraSweet (1:1) for each drug and stored either under refrigeration (4°C) or at room temperature (25°C). A second group of suspensions were compounded in 1% methylcellulose:simple syrup at a 1:10 proportion for zonisamide, amitriptyline, and glycopyrrolate; these suspensions were stored at either under refrigeration (4°C) or at room temperature (25°C). The drug concentrations were measured by the stability-indicating high-performance liquid chromatographic methods. The mean concentration of zonisamide (10 mg/mL) remained above 95% of the original concentration for 91 days in each group of suspensions at both 4°C and 25°C. The mean concentration of amitriptyline (20 mg/mL) was above 95% for 91 days in the suspensions containing OraPlus/ OraSweet at both 4°C and 25°C. However, in the suspensions containing methylcellulose:simple syrup, the mean concentration of amitriptyline was about 95% for 42 days at 4°C and 28 days at 25°C. The mean concentration of glycopyrrolate (0.2 mg/mL) was above 95% in each group of suspensions during the 14-day study period. These data indicate that zonisamide, amitriptyline, and glycopyrrolate can be prepared extemporaneously as suspensions and stored in plastic prescription bottles for varying periods at 4°C and 25°C for use in pediatric patients.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27323428

Source DB:  PubMed          Journal:  Int J Pharm Compd        ISSN: 1092-4221


  3 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
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.