An Improved and Validated HPLC Method for the Determination of Methylprednisolone Sodium Succinate and its Degradation Products in Nanoparticles

Author(s): Yasemin Karabey-Akyurek, Emirhan Nemutlu, Erem Bilensoy, Levent Oner

Journal Name: Current Pharmaceutical Analysis

Volume 13 , Issue 2 , 2017


Become EABM
Become Reviewer
Call for Editor

Graphical Abstract:


Abstract:

Background: A reversed-phase high-performance liquid chromatographic method is developed for quantitative analysis of methylprednisolone sodium succinate (MPSS) in nanoparticles.

Method: An ACE 5AQ column (4.6 × 210 mm, 5 µm, Advanced Chromatography Technologies) was used as stationary phase and phosphate buffered saline (PBS, pH 7.4): acetonitrile (70:30 v/v) at a flowrate of 1.5 mL min-1 was used as mobile phase. The retention time of MPSS was around 5 min. The UV detection was performed at 243 nm. The proposed method was precise, accurate, and linear over the concentration range of analysis (1-100 µg mL-1, R2=0.9999) with a limit of detection and a limit of quantification of 0.03 and 0.12 µg mL-1, respectively.

Result: No interference was observed from the nanoparticle formulation ingredients. The method validated was applied for the analysis of MPSS in-vitro release samples of polycaprolactone (PCL) nanoparticles.

Keywords: Methylprednisolone sodium succinate, HPLC, validation, nanoparticles, pharmaceuticals.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 13
ISSUE: 2
Year: 2017
Published on: 17 January, 2017
Page: [162 - 168]
Pages: 7
DOI: 10.2174/1573412913666161107155008
Price: $65

Article Metrics

PDF: 30
HTML: 1
EPUB: 1