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Reconstructed membrane vesicles from the microalga Dunaliella as a potential drug delivery system

Bioelectrochemistry 2022 11 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Irem Demir-Yilmaz, Nadica Ivošević DeNardis Maja Levak, Irem Demir-Yilmaz, Irem Demir-Yilmaz, Cécile Formosa‐Dague, Ana Butorac, Cécile Formosa‐Dague, Ivna Vrana, Blaženka Gašparović, Irem Demir-Yilmaz, Lucija Horvat, Cécile Formosa‐Dague, Ana Butorac, Ruža Frkanec, Cécile Formosa‐Dague, Cécile Formosa‐Dague, Maja Levak, Ivna Vrana, Nadica Ivošević DeNardis Nadica Ivošević DeNardis Lucija Horvat, Blaženka Gašparović, Nadica Ivošević DeNardis

Summary

Researchers reconstructed tiny bubble-like vesicles from microalgae cell membranes and tested their potential as drug delivery vehicles. The vesicles proved soft, water-friendly, and semi-permeable to certain molecules, pointing to a sustainable, ocean-inspired approach for transporting medicines or studying how materials move across biological membranes.

The aim of this biophysical study is to characterize reconstructed membrane vesicles obtained from microalgae in terms of their morphology, properties, composition, and ability to transport a model drug. The reconstructed vesicles were either emptied or non-emptied and exhibited a non-uniform distribution of spherical surface structures that could be associated with surface coat proteins, while in between there were pore-like structures of up to 10 nm that could contribute to permeability. The reconstructed vesicles were very soft and hydrophilic, which could be attributed to their composition. The vesicles were rich in proteins and were mostly derived from the cytoplasm and chloroplasts. We demonstrated that all lipid classes of D. tertiolecta are involved in the formation of the reconstructed membrane vesicles, where they play fundamental role to maintain the vesicle structure. The vesicles appeared to be permeable to calcein, impermeable to FITC-ovalbumin, and semipermeable to FITC-concanavalin A, which may be due to a specific surface interaction with glucose/mannose units that could serve as a basis for the development of drug carriers. Finally, the reconstructed membrane vesicles could pave a new way as sustainable and environmentally friendly marine bioinspired carriers and serve for studies on microtransport of materials and membrane-related processes contributing to advances in life sciences and biotechnology.

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