Evidence map›Paper›PMID 40378074›Full record

ArticleAnalytical chemistry2025

Derivation of Particle Number Concentration from the Size Distribution: Theory and Applications.

Natalia Farkas, John A Kramar, Antonio R Montoro Bustos, George Caceres, Monique Johnson, Matthias Roesslein, Elijah J Petersen

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Natalia FarkasMicrosystems and Nanotechnology Division, Physical Measurement Laboratory, NIST, Gaithersburg, Maryland 20899, United States.
John A KramarMicrosystems and Nanotechnology Division, Physical Measurement Laboratory, NIST, Gaithersburg, Maryland 20899, United States.ORCID 0000-0001-6038-637X
Antonio R Montoro BustosChemical Sciences Division, Material Measurement Laboratory, NIST, Gaithersburg, Maryland 20899, United States.ORCID 0000-0001-5945-2333
George CaceresChemical Sciences Division, Material Measurement Laboratory, NIST, Gaithersburg, Maryland 20899, United States.
Monique JohnsonChemical Sciences Division, Material Measurement Laboratory, NIST, Gaithersburg, Maryland 20899, United States.ORCID 0000-0001-5096-2003
Matthias RoessleinParticles-Biology Interactions Laboratory, Empa, Swiss Federal Laboratories for Material Testing and Research, St. Gallen 9015, Switzerland.
Elijah J PetersenBiosystems and Biomaterials Division, Material Measurement Laboratory, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland 20899, United States.ORCID 0000-0001-8215-9127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The particle number concentration (PNC) in a suspension is a key measurand in nanotechnology. A common approach for deriving PNC is to divide the total mass concentration by the per-particle mass, calculated as density times volume. The volume is most frequently derived from the arithmetic mean diameter (AMD) of the size distribution. The harmonic mean volume (HMV) has also been used. Given a known size distribution, we show that the correct PNC is obtained by using the arithmetic mean volume (AMV). The AMD-based volume results in an overestimate in PNC that increases superlinearly with increasing coefficient of variation (CV), reaching 12% at CV = 0.2 for a normal distribution. HMV would yield a much greater overestimate, exceeding 50%. The error in the AMD-derived PNC shows only weak skew dependence, suggesting a simple approximate correction as a function of CV in the common situation where AMD and CV are known but the overall size distribution is unknown. Using published data sets of gold nanoparticles, we demonstrate an overall consistency of ±1.1% in comparing the PNC directly determined by single-particle inductively coupled plasma-mass spectrometry (spICP-MS) and the PNCs derived from AMV using size distributions independently measured by high-resolution scanning electron microscopy and spICP-MS. We further compare AMV and AMD-derived PNCs for well-characterized polystyrene nanoparticle standards, illustrating sensitivity to distributional characteristics along with common errors to avoid. Nanoparticles in environmental samples, food additives, and nanomedicines often have CVs greater than 0.3, for which uncorrected AMD-derived PNC errors can exceed 35%.

Identifiers

PMID40378074
PMCPMC12138877

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.