Cited by 21Advanced Drug Delivery SystemsNanoparticle-Based Drug DeliveryNerve injury and regeneration

Biodegradable microparticles for strictly regulating the release of neurotrophic factors

Gujral, C., Minagawa, Y., Fujimoto, K., Kitano, H., Nakaji-Hirabayashi, T.·2013·Journal of Controlled Release

Abstract

A lot of research has been carried out in the last decade to find a cure for neurodegenerative diseases especially Parkinson's disease but to little avail. In this study we have demonstrated the use of poly(lactic-co-glycolic acid) (PLGA)/collagen biodegradable microparticles formed using water-in-oil-in-water (W/O/W) double emulsion method, as a neurotrophic factor delivery vehicle. The microparticles were encapsulated with glial cell-derived neurotrophic factor (GDNF) fused with collagen binding peptide (CBP) immobilized to the inner collagen phase. The novelty lies in the strict regulation of release of GDNF-CBP from the microparticles as compared to a burst release from standard microparticles. The microparticles were demonstrated to be non-cytotoxic till 300 μg/2 × 10⁵ cells and revealed a maximum release of 250 ng GDNF-CBP/mg microparticles in 0.3% collagenase. Differentiation of neural progenitor cells (NPCs) into mature neurons was demonstrated by co-culturing microparticles with cells in a medium containing collagenase which enabled the release of encapsulated GDNF-CBP, signaling the differentiation of NPCs into microtubule-associated protein 2 (MAP2)-expressing neurons. The successful ability of these microparticles to deliver neurotrophic factors and allow differentiation of NPCs into mature neurons provides some scope in its use for the treatment of Parkinson's disease and other neurodegenerative diseases.

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Crossref · 10.1016/j.jconrel.2013.03.031

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  • PLGA/collagen MS may be used to deliver GDNF, and in vitro application stimulates differentiation of neuronal progenitor cells into mature neurons.

    “Gujral et al. also showed that PLGA/collagen MS may be used to deliver GDNF, and in vitro application suggests that it stimulates the differentiation of neuronal progenitor cells into mature neurons.131”

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References 48 · Cited by 21

Authors
Gujral, C., Minagawa, Y., Fujimoto, K., Kitano, H., & Nakaji-Hirabayashi, T.
Affiliations
University of Toyama (JP)
Corresponding author
Kitano, H.
Venue
Journal of Controlled Release
Publisher
Elsevier BV
Published
2013-06
Volume
168
Issue
3
Pages
307-316
ISSN
0168-3659 (ISSN-L)
OpenAlex
W2065524355
Cited by
21
References
48
Citations by year
2025: 1 · 2024: 2 · 2022: 1 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 3 · 2016: 2 · 2015: 6 · 2014: 1 · 2013: 1
FWCI
2.01
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Controlled Release (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • University of Toyama
  • Japan Society for the Promotion of Science (22350101, 22700468)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
Keywords
biodegradable microparticles, neurotrophic factor delivery, glial cell line-derived neurotrophic factor, collagen-binding peptide, water-in-oil-in-water emulsion, controlled release, burst release, neural progenitor cells, neuronal differentiation, Parkinson's disease, neurodegenerative diseases, collagenase
MeSH terms
Polylactic Acid-Polyglycolic Acid Copolymer, Cell Differentiation, Cell Survival, Cells, Cultured, Collagen, Humans, Neurons, Peptide Fragments, Polyglycolic Acid, Recombinant Proteins, Sialoglycoproteins, Lactic Acid, Glial Cell Line-Derived Neurotrophic Factor, Neural Stem Cells

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