Stability of levofloxacin in an extemporaneously compounded oral liquid

Citation
Hl. Vandenbussche et al., Stability of levofloxacin in an extemporaneously compounded oral liquid, AM J HEAL S, 56(22), 1999, pp. 2316-2318
Citations number
3
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY
ISSN journal
10792082 → ACNP
Volume
56
Issue
22
Year of publication
1999
Pages
2316 - 2318
Database
ISI
SICI code
1079-2082(19991115)56:22<2316:SOLIAE>2.0.ZU;2-8
Abstract
The stability of levofloxacin in an extemporaneously compounded oral liquid was studied. A suspension of levofloxacin 50 mg/mL was prepared from commercially availa ble 500-mg levofloxacin tablets and equal amounts of Ora-Plus and Strawberr y Syrup, NF, to make a final volume of 60 mt. Six identical volumes of the suspension were prepared in amber plastic prescription bottles. Three bottl es were stored at 23-25 degrees C, and three were stored at 3-5 degrees C. Immediately after preparation and at 8, 15, 29, and 57 days, samples were v isually inspected and assayed in duplicate by high-performance liquid chrom atography; pH was also determined. At least 99% of the initial levofloxacin concentration remained in all samp les throughout the study period. The color, odor, and pH of all the samples did not change appreciably. An extemporaneously compounded oral liquid formulation of levofloxacin 50 m g/mL in a 1:1 mixture of Ora-Plus and Strawberry Syrup, NF, was stable at 2 3-25 or 35 degrees C for up to 57 days.