DEVELOPMENT AND CHARACTERIZATION OF LANSOPRAZOLE NANOSPONGES FOR ENHANCED SOLUBILITY AND CONTROLLED DRUG RELEASE Authors: Patel A* And Patel R
ABSTRACT
This study presents the preparation and characterization of Lansoprazole nanosponges using soluble
chitosan, polyvinyl alcohol (PVA), and Pluronic F68 via the emulsion solvent diffusion method. The
nanosponges were formulated to enhance the drug's solubility and controlled release profile.
Differential Scanning Calorimetry (DSC) confirmed the transition of Lansoprazole to an amorphous
state, indicating uniform distribution within the nanosponge matrix. Scanning Electron Microscopy
(SEM) revealed spherical, porous nanosponges. Dynamic Light Scattering (DLS) analysis showed an
average particle size of 332.4 nm with a moderate polydispersity index (PDI) of 0.52, while zeta
potential measurements indicated moderate stability with a value of -15.3 mV. Fourier-transform
infrared (FTIR) spectroscopy confirmed the entrapment of Lansoprazole without significant
interactions with the polymers. The in vitro drug release study demonstrated a controlled and sustained
release profile, achieving nearly complete drug release over 11 hours. These findings suggest that the
prepared Lansoprazole nanosponges possess the desired characteristics for potential therapeutic
applications, offering improved solubility, stability, and a controlled release mechanism.
Keywords: Lansoprazole, Nanosponges, Soluble Chitosan, Polyvinyl Alcohol (PVA), Pluronic
F68, Emulsion Solvent Diffusion, Controlled Release, Differential Scanning Calorimetry (DSC),
Scanning Electron Microscopy (SEM), Dynamic Light Scattering (DLS), Zeta Potential Publication date: 01/05/2026 https://www.ijbpas.com/pdf/2026/May/MS_IJBPAS_2026_9465.pdfDownload PDFhttps://doi.org/10.31032/IJBPAS/2026/15.5.9465