» Articles » PMID: 20204471

Critical Evaluation of Nanoparticle Tracking Analysis (NTA) by NanoSight for the Measurement of Nanoparticles and Protein Aggregates

Overview
Journal Pharm Res
Specialties Pharmacology
Pharmacy
Date 2010 Mar 6
PMID 20204471
Citations 463
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To evaluate the nanoparticle tracking analysis (NTA) technique, compare it with dynamic light scattering (DLS) and test its performance in characterizing drug delivery nanoparticles and protein aggregates.

Methods: Standard polystyrene beads of sizes ranging from 60 to 1,000 nm and physical mixtures thereof were analyzed with NTA and DLS. The influence of different ratios of particle populations was tested. Drug delivery nanoparticles and protein aggregates were analyzed by NTA and DLS. Live monitoring of heat-induced protein aggregation was performed with NTA.

Results: NTA was shown to accurately analyze the size distribution of monodisperse and polydisperse samples. Sample visualization and individual particle tracking are features that enable a thorough size distribution analysis. The presence of small amounts of large (1,000 nm) particles generally does not compromise the accuracy of NTA measurements, and a broad range of population ratios can easily be detected and accurately sized. NTA proved to be suitable to characterize drug delivery nanoparticles and protein aggregates, complementing DLS. Live monitoring of heat-induced protein aggregation provides information about aggregation kinetics and size of submicron aggregates.

Conclusion: NTA is a powerful characterization technique that complements DLS and is particularly valuable for analyzing polydisperse nanosized particles and protein aggregates.

Citing Articles

Optical label-free microscopy characterization of dielectric nanoparticles.

Garcia Rodriguez B, Olsen E, Skarberg F, Volpe G, Hook F, Midtvedt D Nanoscale. 2025; .

PMID: 40079204 PMC: 11904879. DOI: 10.1039/d4nr03860f.


Anti-Inflammatory and Immunomodulatory Properties of Inorganic Fullerene-Like Tungsten Disulfide Nanoparticles in the Culture of Human Peripheral Blood Mononuclear Cells.

Zecevic S, Popovic D, Tomic S, Bekic M, Rakocevic S, Kosanovic M Nanomaterials (Basel). 2025; 15(5).

PMID: 40072125 PMC: 11901739. DOI: 10.3390/nano15050322.


A synthetic model of bioinspired liposomes to study cancer-cell derived extracellular vesicles and their uptake by recipient cells.

Lopez R, Ben El Khyat C, Chen Y, Tsering T, Dickinson K, Bustamante P Sci Rep. 2025; 15(1):8430.

PMID: 40069225 PMC: 11897354. DOI: 10.1038/s41598-025-91873-5.


Development of a cell-penetrating peptide-based nanocomplex for long-term delivery of intact mitochondrial DNA into epithelial cells.

Wilson K, Holjencin C, Lee H, Annamalai B, Ishii M, Gilbert J Mol Ther Nucleic Acids. 2025; 36(1):102449.

PMID: 39991470 PMC: 11847061. DOI: 10.1016/j.omtn.2025.102449.


Scalable production of anti-inflammatory exosomes from three-dimensional cultures of canine adipose-derived mesenchymal stem cells: production, stability, bioactivity, and safety assessment.

Thongsit A, Oontawee S, Siriarchavatana P, Rodprasert W, Somparn P, Na Nan D BMC Vet Res. 2025; 21(1):81.

PMID: 39979916 PMC: 11841348. DOI: 10.1186/s12917-025-04517-1.


References
1.
Hvidt S . Insulin association in neutral solutions studied by light scattering. Biophys Chem. 1991; 39(2):205-13. DOI: 10.1016/0301-4622(91)85023-j. View

2.
Schellekens H . Bioequivalence and the immunogenicity of biopharmaceuticals. Nat Rev Drug Discov. 2002; 1(6):457-62. DOI: 10.1038/nrd818. View

3.
Mahler H, Muller R, Friess W, Delille A, Matheus S . Induction and analysis of aggregates in a liquid IgG1-antibody formulation. Eur J Pharm Biopharm. 2005; 59(3):407-17. DOI: 10.1016/j.ejpb.2004.12.004. View

4.
Jiskoot W, van Schie R, Carstens M, Schellekens H . Immunological risk of injectable drug delivery systems. Pharm Res. 2009; 26(6):1303-14. DOI: 10.1007/s11095-009-9855-9. View

5.
Cromwell M, Hilario E, Jacobson F . Protein aggregation and bioprocessing. AAPS J. 2006; 8(3):E572-9. PMC: 2761064. DOI: 10.1208/aapsj080366. View