Journal of Analytical Methods in Chemistry / 2018 / Article / Tab 1 / Research Article
A Stability Indicating HPLC Assay Method for Analysis of Rivastigmine Hydrogen Tartrate in Dual-Ligand Nanoparticle Formulation Matrices and Cell Transport Medium Table 1 Summary of published HPLC conditions for RHT determinations.
Column Sample matrix Mobile phase Flow rate Detection technique Analysis time Detection limits Reference Waters Spherisorb silica Human plasma Acetonitrile-50 mM aqueous sodium dihydrogen phosphate (17 : 83 v/v, pH 3.1) 1.3 mL/min UV: 200 nm 6 minutes LOD: 0.2 ng/mL [26 ] LOQ: 0.5 ng/mL Inertsil ODS-3V C18 Rat plasma and brain Ammonium acetate buffer (20 mM, pH 4.5) and acetonitrile 74 : 26 (v/v) 1.0 mL/min Fluorescence detector, Ex/Em wavelength: 220/293 nm 16 minutes LOD: not given [16 ] LOQ: 10 ng/mL XTerra RP18 C18 Raw material 10 mM sodium-1-heptane sulphonate (pH 3.0) and acetonitrile 72 : 28 (v/v) 1.0 mL/min UV: 217 nm 13 minutes LOD: 100 ng/mL [27 ] LOQ: 300 ng/mL Monomeric C18 Rat plasma Acetonitrile and 20 mmol/L phosphate buffer, pH 3.0 (25 : 75) 1.0 mL/min Fluorescence detector, Ex/Em wavelength:220/293 nm 20 minutes LOD: not given [28 ] LOQ: 25 ng/mL 5C18 -MS Capsule Methanol and water (90 : 10) 1.0 mL/min UV: 217 nm Not given LOD: not given [29 ] LOQ: 10.9 µ g/mL Kromasil C8 Liposomes 20 mmol·L−1 phosphate buffer (pH 3.0) and acetonitrile (75 : 25%, v/v) 1.0 mL/min UV: 210 nm 20 minutes LOD: not given [17 ] LOQ: 10 ng/mL C18 Solid lipid nanoparticles Acetonitrile and potassium dihydrogen orthophosphate buffer (pH 6.0) (20 : 80 v/v) 1.0 mL/min UV: 215 nm Not given LOD: not given [14 ] LOQ: 1 µ g/mL ODS C18 Liposomes Acetonitrile : water (20 mM NaH2 PO4 ·2H2 O, 10 mM Na2 HPO4 ·12H2 O) (25 : 75, v/v) 1.0 mL/min UV: 218 nm Not given LOD: not given [15 ] LOQ: not given