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Related Concept Videos

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Site-Targeted Drug Delivery Systems: Polymeric Carriers

Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...

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Related Experiment Video

Updated: Jun 19, 2026

A Facile and Eco-friendly Route to Fabricate Poly(Lactic Acid) Scaffolds with Graded Pore Size
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Published on: October 17, 2016

Biodegradable polymeric microcarriers with controllable porous structure for tissue engineering.

Xudong Shi1, Lei Sun, Jian Jiang

  • 1The CAS Key Laboratory of Engineering Plastics, Joint Laboratory of Polymer Science and Materials, Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, PR China.

Macromolecular Bioscience
|October 13, 2009
PubMed
Summary
This summary is machine-generated.

Biodegradable poly(DL-lactide) microspheres were fabricated for tissue engineering. These porous microspheres show potential as cell delivery carriers, supporting MG-63 cell attachment and spreading.

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Fabrication of Extracellular Matrix-derived Foams and Microcarriers as Tissue-specific Cell Culture and Delivery Platforms

Published on: April 11, 2017

Area of Science:

  • Biomaterials Science
  • Tissue Engineering
  • Polymer Chemistry

Background:

  • Biodegradable polymers are crucial for developing effective cell delivery systems in tissue engineering.
  • Porous microspheres offer a promising scaffold for cell cultivation and tissue regeneration.
  • Poly(DL-lactide) (PLA) is a well-established biodegradable polymer with potential for biomedical applications.

Purpose of the Study:

  • To fabricate porous poly(DL-lactide) (PLA) microspheres using a modified double emulsion solvent evaporation method.
  • To investigate the influence of fabrication parameters on the porous structure of PLA microspheres.
  • To evaluate the potential of these microspheres as cell delivery carriers for tissue engineering.

Main Methods:

  • Fabrication of porous PLA microspheres via a modified double emulsion solvent evaporation technique.
  • Systematic variation of fabrication parameters including stirring speed, polymer concentration, solvent type, and post-hydrolysis treatment.
  • Assessment of microsphere morphology and porous structure.
  • Evaluation of MG-63 cell attachment, spreading, and viability on the fabricated microspheres.

Main Results:

  • Successful fabrication of porous poly(DL-lactide) microspheres with controllable structures.
  • Demonstrated influence of key fabrication parameters on microsphere porosity and morphology.
  • Observed good attachment and active spreading of MG-63 cells on the surface of the PLA microspheres.
  • Indicated successful cell integration with the porous microsphere scaffold.

Conclusions:

  • Porous PLA microspheres can be effectively fabricated using a modified double emulsion solvent evaporation method.
  • Fabrication parameters significantly influence the resulting porous structure of the microspheres.
  • The developed PLA microspheres serve as a promising scaffold for cell cultivation and demonstrate potential as cell delivery carriers in tissue engineering applications.