Chrono modulated multiple unit particulate systems (MUPS) via a continuous hot melt double extrusion technique: Investigation of the formulation and process suitability.

Eur J Pharm Biopharm

Department of Pharmaceutics and Drug Delivery, University of Mississippi, University, MS 38677, USA; Pii Center for Pharmaceutical Technology, University of Mississippi, University, MS 38677, USA. Electronic address:

Published: November 2021

AI Article Synopsis

  • The study focuses on creating a new drug delivery system called chrono modulated multiple unit particulate systems (MUPS) for nifedipine, which is a poorly soluble medication, using a continuous double extrusion process.
  • The formulation includes an amorphous solid dispersion (ASD) to enhance drug solubility, incorporating specific polymers and lipids to control drug release rates in both pulsatile and sustained manners.
  • Results from various studies show that the ASD significantly improves the solubility of nifedipine, and MUPS exhibit stable performance and controlled release characteristics over a 12-hour period, suggesting the efficacy of this manufacturing method compared to traditional techniques.

Article Abstract

The current study is aimed at the development of chrono modulated multiple unit particulate systems (MUPS) of nifedipine (ND) by a continuous double extrusion process. ND, a poorly soluble drug was formulated into an amorphous solid dispersion (ASD) to improve its solubility. Further, the ASD was converted into MUPS to control the drug release through a combination of pulsatile and sustained release portions. In the preparation of the ASD, the polymer HPMCAS LG was employed at different concentrations. MUPS were formulated by using Eudragit® FS100, Eudragit® RSPO, Klucel™ HF and lipids Precirol® ATO 5, Geleol™, Compritol® ATO5. The differential scanning calorimetry and powder X-ray diffraction studies of MUPS revealed the amorphous nature of ND. Scanning electron microscopy (SEM) studies depicted the surface morphology of the ASD and the gradual change in the surface of the coated MUPS during in-vitro release studies. The in-vitro drug release profiles of ASD indicated significant improvement (p < 0.05) of solubility of ND and MUPS demonstrated a combination of pulsatile and zero-order controlled release up to 12 h. Accelerated stability studies for MUPS at 40 °C/75% RH revealed the formulations were stable. These findings suggest hot melt double extrusion as a potential alternative for conventional techniques to produce MUPS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666089PMC
http://dx.doi.org/10.1016/j.ejpb.2021.08.014DOI Listing

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