Evidence map›Paper›PMID 29425047›Full record

ArticleMolecular pharmaceutics2018

Protein Adsorption and Layer Formation at the Stainless Steel-Solution Interface Mediates Shear-Induced Particle Formation for an IgG1 Monoclonal Antibody.

Cavan K Kalonia, Frank Heinrich, Joseph E Curtis, Sid Raman, Maria A Miller, Steven D Hudson

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
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

11 citing papers in PubMed, 65 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Cavan K KaloniaMaterial Measurement Laboratory , National Institute of Standards and Technology (NIST) , Gaithersburg , Maryland 20899 , United States.
Frank HeinrichNIST Center for Neutron Research , National Institute of Standards and Technology , Gaithersburg , Maryland 20899 , United States.
Joseph E CurtisNIST Center for Neutron Research , National Institute of Standards and Technology , Gaithersburg , Maryland 20899 , United States.
Sid RamanFormulation Sciences Department , MedImmune Inc. , Gaithersburg , Maryland 20878 , United States.
Maria A MillerFormulation Sciences Department , MedImmune Inc. , Gaithersburg , Maryland 20878 , United States.
Steven D HudsonMaterial Measurement Laboratory , National Institute of Standards and Technology (NIST) , Gaithersburg , Maryland 20899 , United States.ORCID 0000-0002-3203-4833
National Institute of Standards and Technology · US

Funding

Intramural NIST DOC 9999-NIST
6 · The paper itself

Abstract

Passage of specific protein solutions through certain pumps, tubing, and/or filling nozzles can result in the production of unwanted subvisible protein particles (SVPs). In this work, surface-mediated SVP formation was investigated. Specifically, the effects of different solid interface materials, interfacial shear rates, and protein concentrations on SVP formation were measured for the National Institute of Standards and Technology monoclonal antibody (NISTmAb), a reference IgG1 monoclonal antibody (mAb). A stainless steel rotary piston pump was used to identify formulation and process parameters that affect aggregation, and a flow cell (alumina or stainless steel interface) was used to further investigate the effect of different interface materials and/or interfacial shear rates. SVP particles produced were monitored using flow microscopy or flow cytometry. Neutron reflectometry and a quartz crystal microbalance with dissipation monitoring were used to characterize adsorption and properties of NISTmAb at the stainless steel interface. Pump/shear cell experiments showed that the NISTmAb concentration and interface material had a significant effect on SVP formation, while the effects of interfacial shear rate and passage number were less important. At the higher NISTmAb concentrations, the adsorbed protein became structurally altered at the stainless steel interface. The primary adsorbed layer remained largely undisturbed during flow, suggesting that SVP formation at high NISTmAb concentration was caused by the disruption of patches and/or secondary interactions.

Indexed as

AdsorptionAntibodies, MonoclonalImmunoglobulin GParticle SizeQuartz Crystal Microbalance TechniquesStainless SteelSurface PropertiesAntibodies, MonoclonalImmunoglobulin GStainless Steelbioprocess developmentmonoclonal antibodyprotein adsorptionprotein aggregationsolid−liquid interfacesubvisible particles

Identifiers

PMID29425047
PMCPMC5997281
OpenAlexW2792177350

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.