Am J Health-Syst Pharm
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


American Journal of Health-System Pharmacy, Vol. 64, Issue 6, 644-646
Copyright © 2007 by American Society of Health-System Pharmacists
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cober, M. P.
Right arrow Articles by Johnson, C. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cober, M. P.
Right arrow Articles by Johnson, C. E.

Notes

Stability of an extemporaneously prepared alcohol-free phenobarbital suspension

Mary Petrea Cober and Cary E. Johnson

MARY PETREA COBER, PHARM.D., is Clinical Pharmacist—Pediatric Surgery, Department of Pharmacy, University of Michigan Hospitals and Health Centers (UMHHC), Ann Arbor, and Adjunct Clinical Instructor, College of Pharmacy, University of Michigan (UM), Ann Arbor. CARY E. JOHNSON, PHARM.D., FASHP, is Professor of Pharmacy, College of Pharmacy, UM, and Clinical Pharmacist—Pediatrics, Department of Pharmacy, UMHHC.

Address correspondence to Dr. Cober at the University of Michigan Hospitals and Health Centers, 1500 East Medical Center Drive, UHB2D301, Box 0008, Ann Arbor, MI 48109-0008 (mcober{at}umich.edu).


Purpose. The physical and chemical short-term stability of alcohol-free, oral suspensions of phenobarbital 10 mg/mL prepared from commercially available tablets in both a sugar and a sugar-free vehicle was assessed at room temperature.

Methods. Phenobarbital oral suspension 10 mg/mL was prepared by crushing 10 60-mg tablets of phenobarbital with a mortar and pestle. A small amount of Ora-Plus was added to the phenobarbital powder to sufficiently wet the particles. A 1:1 mixture of Ora-Plus and either Ora-Sweet or Ora-Sweet SF was combined with the phenobarbital powder to produce a final volume of 60 mL. Three identical samples of each of the two different formulations were prepared and stored at room temperature in 2-oz amber plastic bottles. Immediately after preparation and at 15, 30, 60, and 115 days, the samples were assayed in duplicate by stability-indicating high-performance liquid chromatography. The samples were tasted and inspected for color and odor changes. The percent of the initial concentration remaining at each study time for each phenobarbital suspension was determined. Stability was defined as the retention of at least 90% of the initial concentration.

Results. There were no detectable changes in color, odor, and taste and no visible microbial growth in any sample. At least 98% of the initial phenobarbital concentration remained throughout the 115-day study period in both preparations.

Conclusion. An extemporaneously prepared alcohol-free suspension of phenobarbital 10 mg/mL in a 1:1 mixture of Ora-Plus and Ora-Sweet or Ora-Sweet SF was stable for at least 115 days when stored in 2-oz amber plastic bottles at room temperature.

Index terms: Anticonvulsants; Color; Compounding; Concentration; Contamination; Odors; Ora-Plus; Ora-Sweet; Ora-Sweet SF; Phenobarbital; Stability; Storage; Suspensions; Taste; Vehicles

 






HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the American Society of Health-System Pharmacists.