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Updated: Feb 1, 2026

Biofunctionalization of Magnetic Nanomaterials
Published on: July 16, 2020
Membrane reorganization after photochemical internalization to release transferrin-biofunctionalized polystyrene
Inmaculada Mora-Espí1, Lleonard Barrios1, Elena Ibáñez1
1Unitat de Biologia Cel·lular, Departament de Biologia Cel·lular, Fisiologia i Immunologia, Facultat de Biociències, Universitat Autònoma de Barcelona, Bellaterra, 08193, Barcelona, Spain.
Photochemical internalization (PCI) disrupts endolysosomal membranes, allowing soluble drug release. However, PCI does not fully release microparticles from the endolysosome to the cytosol.
Area of Science:
- Cell Biology
- Nanotechnology
- Drug Delivery
Background:
- Therapeutic drug carriers face challenges releasing cargo from endolysosomes.
- Photochemical internalization (PCI) is a proposed method to overcome endolysosomal entrapment.
- The extent of PCI-induced membrane disruption and microparticle release remains unclear.
Purpose of the Study:
- To investigate if PCI facilitates microparticle release from endolysosomes to the cytosol.
- To analyze the ultrastructural effects of PCI on endolysosomal membranes surrounding microparticles.
Main Methods:
- Confocal microscopy to assess membrane disruption and cargo release.
- Transmission electron microscopy (TEM) for ultrastructural analysis.
- Scanning TEM with energy-dispersive X-ray for membrane characterization.
Main Results:
- PCI caused endolysosomal membrane disruption, evidenced by soluble transferrin release.
- Co-localization of LAMP1 and microparticles decreased post-PCI.
- TEM revealed fewer defined membranes around microparticles after PCI.
- Increased endolysosomal membrane width was observed after PCI treatment.
Conclusions:
- PCI alters endolysosomal membrane ultrastructure.
- This alteration is sufficient for soluble cargo release but not complete microparticle liberation.
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