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Related Concept Videos

Bioplastics01:27

Bioplastics

42
Bioplastics derived from microbial processes present a sustainable alternative to conventional petroleum-based plastics. Among these, polyhydroxyalkanoates (PHAs), particularly polyhydroxybutyrates (PHBs), have emerged as prominent candidates due to their biodegradability and biocompatibility. These polymers are synthesized by a variety of bacteria, such as Cupriavidus necator and Pseudomonas putida, which naturally accumulate PHAs as intracellular carbon and energy reserves, especially under...
42

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Development of prilling process for biodegradable microspheres through experimental designs.

Violet Fabien1, Le Minh-Quan1, Sergent Michelle2

  • 1LUNAM Université, Micro et Nanomédecines Biomimétiques (MINT), F-49933 Angers, France; INSERM U1066, F-49933 Angers, France.

International Journal of Pharmaceutics
|December 15, 2015
PubMed
Summary

This study optimized the prilling process for producing poly(lactic-co-glycolic) acid (PLGA) microspheres without toxic solvents. These microspheres are suitable for pharmaceutical production and tissue regeneration therapies.

Keywords:
Experimental designGlycofurolMicrospherePLGAPrilling

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Area of Science:

  • Biomaterials Engineering
  • Regenerative Medicine
  • Pharmaceutical Technology

Background:

  • Poly(lactic-co-glycolic) acid (PLGA) microspheres are promising for drug delivery and tissue engineering.
  • Current production methods often involve toxic solvents, limiting pharmaceutical scalability.
  • Developing solvent-free methods is crucial for advancing regenerative therapies.

Purpose of the Study:

  • To develop and optimize a solvent-free prilling process for producing PLGA microspheres.
  • To create a scalable method for manufacturing monodispersed microspheres for pharmaceutical applications.
  • To establish PLGA microspheres as a viable tool for tissue regeneration.

Main Methods:

  • Utilized the prilling process for microsphere fabrication.
  • Employed experimental designs to study and optimize seventeen process parameters.
  • Focused on achieving high production quality and control over microsphere characteristics.

Main Results:

  • Successfully developed a solvent-free prilling method for PLGA microsphere production.
  • Identified key parameters and mechanisms governing microsphere formation.
  • Achieved an acceptable production quality through process optimization.

Conclusions:

  • The solvent-free prilling process offers a scalable and controllable method for producing PLGA microspheres.
  • These microspheres are suitable for pharmaceutical applications and hold potential for tissue regeneration therapies.
  • Further optimization confirmed the feasibility of this approach for industrial implementation.