SOLID SUPERSATURABLE SMEDDS: A POLYMERIC PRECIPITATION INHIBITOR TO ENHANCE SOLUBILITY AND BIOAVAILABILITY Authors: Dave P , PATEL D, RAVAL B AND JANI RK
ABSTRACT
More than 60% of drugs are poorly water-soluble, and it has less bioavailability. There are many
techniques to overcome these problems, like Cyclodextrins, salt formation, lipid-based
formulation, and solid dispersion. Amongst all approaches, supersaturable self micro emulsifying
drug delivery system has been demonstrated to enhance oral solubility and bioavailability
effectively. Supersaturable formulations are exposed to gastrointestinal fluids, the medication
concentration exceeds equilibrium solubility. High medication concentrations improve oral
absorption of poorly water-soluble medicines in this way. Nevertheless, since many drugs are
thermodynamically unstable at high concentrations, they precipitate rapidly in vivo before
getting absorbed, resulting in poor bioavailability. Precipitation inhibitors are widely valuable for
enhancing solubility, absorption rate, and bioavailability in various formulations. This review
article provides information about various polymers used in supersaturation effects on self-micro
emulsifying drug delivery systems (SMEDDS).
Keywords: Supersaturable, SMEDDS, solubility, bioavailability, solid SMEDDS Publication date: 01/01/2023 https://ijbpas.com/pdf/2023/January/MS_IJBPAS_2023_6726.pdfDownload PDFhttps://doi.org/10.31032/IJBPAS/2023/12.1.6726