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Analyzing the surface of functional nanomaterials-how to quantify the total and derivatizable number of functional groups and ligands

期刊

MICROCHIMICA ACTA
卷 188, 期 10, 页码 -

出版社

SPRINGER WIEN
DOI: 10.1007/s00604-021-04960-5

关键词

Functional group quantification; Surface ligand; Nanomaterial; Nanoparticle; Bead; Dye-based assay; Optical detection; Electrochemical titration; Instrumental analysis; Nanosafety; Safe-by-design

资金

  1. Projekt DEAL
  2. Federal Institute for Materials Research and Testing (BAM)
  3. German Federal Ministry for Economic Affairs and Energy (BMWi) [03TNK005A]
  4. European Metrology Programme for Innovation and Research (EMPIR) [18HLT01, 18HLT02]
  5. European Union
  6. EMPIR

向作者/读者索取更多资源

The surface chemistry of functional nanomaterials plays a crucial role in their properties and impact on human health and the environment. Analytical methods such as electrochemical titration, optical assays, nuclear magnetic resonance, and vibrational spectroscopy are utilized for chemical identification and quantification of functional groups. These methods are essential for reliable detection and quantification of functional groups on nanomaterial surfaces.
Functional nanomaterials (NM) of different size, shape, chemical composition, and surface chemistry are of increasing relevance for many key technologies of the twenty-first century. This includes polymer and silica or silica-coated nanoparticles (NP) with covalently bound surface groups, semiconductor quantum dots (QD), metal and metal oxide NP, and lanthanide-based NP with coordinatively or electrostatically bound ligands, as well as surface-coated nanostructures like micellar encapsulated NP. The surface chemistry can significantly affect the physicochemical properties of NM, their charge, their processability and performance, as well as their impact on human health and the environment. Thus, analytical methods for the characterization of NM surface chemistry regarding chemical identification, quantification, and accessibility of functional groups (FG) and surface ligands bearing such FG are of increasing importance for quality control of NM synthesis up to nanosafety. Here, we provide an overview of analytical methods for FG analysis and quantification with special emphasis on bioanalytically relevant FG broadly utilized for the covalent attachment of biomolecules like proteins, peptides, and oligonucleotides and address method- and material-related challenges and limitations. Analytical techniques reviewed include electrochemical titration methods, optical assays, nuclear magnetic resonance and vibrational spectroscopy, as well as X-ray based and thermal analysis methods, covering the last 5-10 years. Criteria for method classification and evaluation include the need for a signal-generating label, provision of either the total or derivatizable number of FG, need for expensive instrumentation, and suitability for process and production control during NM synthesis and functionalization.

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