Glycoglycerolipid-coated F/ZnO quantum dots: A biocompatible amphiphilic formulation for fluorescent nanoprobes
Academic Article
Publication Date:
2026
Citation:
Glycoglycerolipid-coated F/ZnO quantum dots: A biocompatible amphiphilic formulation for fluorescent nanoprobes / G.J. Mosca, S. Russo, V. Pelliccioli, M. Quaglia, P. Pettinari, A. Cangiano, D. Colombo, P. Perego, G.L. Beretta, L. Morelli, G. Vitiello. - In: COLLOIDS AND SURFACES. B, BIOINTERFACES. - ISSN 0927-7765. - 264:(2026 Aug), pp. 115674.1-115674.11. [10.1016/j.colsurfb.2026.115674]
abstract:
Colloidal quantum dots (QDs) represent a versatile class of luminescent nanomaterials whose physicochemical
and interfacial properties can be engineered for advanced bio-related applications. Herein, the wet-precipitation
synthesis and surface engineering of ultra-small fluorine-doped ZnO quantum dots (F/ZnO QDs) were proposed
and their formulation into stable amphiphilic nanosystems using synthetic glycoglycerolipids. To control aggregation and interfacial behavior, the QDs were first capped with oleylamine and subsequently functionalized
through an emulsion-based approach with mono-acyl or di-acyl glycoglycerolipids, yielding double-coated
amphiphilic nanoformulations. The resulting materials were extensively characterized by TEM, DLS, zetapotential measurements, XRD, FTIR/ATR, UV–Vis, and fluorescence spectroscopy, allowing to explore correlations between surface chemistry, colloidal stability, and optical properties. Glycoglycerolipid functionalization
led to a marked improvement in aqueous dispersibility and long-term colloidal stability while preserving the
enhanced fluorescence induced by fluorine doping. Biological assays confirmed the cytocompatibility of the
coated QDs and supported their suitability for further biointerface studies. This work highlights
glycoglycerolipid-based amphiphilic coatings as an effective strategy to tailor the surface and colloidal properties
of ZnO-based QDs, enabling the development of stable luminescent nanomaterials as biocompatible nanoprobes
and for bio-interfacial applications.
and interfacial properties can be engineered for advanced bio-related applications. Herein, the wet-precipitation
synthesis and surface engineering of ultra-small fluorine-doped ZnO quantum dots (F/ZnO QDs) were proposed
and their formulation into stable amphiphilic nanosystems using synthetic glycoglycerolipids. To control aggregation and interfacial behavior, the QDs were first capped with oleylamine and subsequently functionalized
through an emulsion-based approach with mono-acyl or di-acyl glycoglycerolipids, yielding double-coated
amphiphilic nanoformulations. The resulting materials were extensively characterized by TEM, DLS, zetapotential measurements, XRD, FTIR/ATR, UV–Vis, and fluorescence spectroscopy, allowing to explore correlations between surface chemistry, colloidal stability, and optical properties. Glycoglycerolipid functionalization
led to a marked improvement in aqueous dispersibility and long-term colloidal stability while preserving the
enhanced fluorescence induced by fluorine doping. Biological assays confirmed the cytocompatibility of the
coated QDs and supported their suitability for further biointerface studies. This work highlights
glycoglycerolipid-based amphiphilic coatings as an effective strategy to tailor the surface and colloidal properties
of ZnO-based QDs, enabling the development of stable luminescent nanomaterials as biocompatible nanoprobes
and for bio-interfacial applications.
IRIS type:
01 - Articolo su periodico
Keywords:
Glycoglycerolipid; Quantum dot; Amphiphilic nanoformulation; Fluorescent nanoprobe; Ovarian cancer cells; Biocompatibility
List of contributors:
G.J. Mosca, S. Russo, V. Pelliccioli, M. Quaglia, P. Pettinari, A. Cangiano, D. Colombo, P. Perego, G.L. Beretta, L. Morelli, G. Vitiello
Link to information sheet: