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Development of pH-Responsive Polypills via Semi-Solid Extrusion 3D Printing.

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This study introduces 3D-printed pH-responsive hydrogel drug carriers for improved oral drug bioavailability. Material ratios control drug release in the stomach or intestines, enhancing targeted delivery.

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Area of Science:

  • Pharmaceutical Sciences
  • Biomaterials Engineering
  • Drug Delivery Systems

Background:

  • Low oral drug bioavailability is a major challenge due to gastrointestinal instability.
  • Site-targeted drug delivery systems require carriers stable in diverse pH environments.
  • Developing customizable drug release profiles is crucial for therapeutic efficacy.

Purpose of the Study:

  • To develop a novel 3D-printed hydrogel drug carrier using pH-responsive materials.
  • To enable site-targeted drug release and customize temporal release profiles for oral administration.
  • To investigate the impact of material parameters on hydrogel swelling and drug release.

Main Methods:

  • Utilized semi-solid extrusion 3D printing technology with pH-responsive hydrogels.
  • Analyzed swelling properties of printed tablets in artificial gastric and intestinal fluids.
  • Investigated the effects of sodium alginate and carboxymethyl chitosan mass ratios.
  • Performed drug release experiments to assess site-specific and controlled release.

Main Results:

  • Adjusting the sodium alginate to carboxymethyl chitosan mass ratio significantly altered pH-responsive swelling.
  • A 1:3 ratio facilitated gastric drug release, while a 3:1 ratio enabled intestinal release.
  • Infill density tuning allowed for controlled drug release kinetics.
  • Achieved site-targeted drug release based on material composition and printing parameters.

Conclusions:

  • The 3D-printed pH-responsive hydrogel carrier system effectively addresses oral drug instability and low bioavailability.
  • This technology allows for precise control over drug release location (gastric or intestinal) and timing.
  • Offers potential for customized drug delivery and controlled release of individual components in multi-drug formulations.