Evidence map›Paper›PMID 35835184›Full record

ArticleJournal of pharmaceutical sciences2022

Machine Learning Analysis Provides Insight into Mechanisms of Protein Particle Formation Inside Containers During Mechanical Agitation.

Nidhi G Thite, Saba Ghazvini, Nicole Wallace, Naomi Feldman, Christopher P Calderon, Theodore W Randolph

Abstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
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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.

Nidhi G ThiteDepartment of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80309, United States.
Saba GhazviniAstraZeneca Gaithersburg, Maryland 20878, United States.
Nicole WallaceAstraZeneca Gaithersburg, Maryland 20878, United States.
Naomi FeldmanAstraZeneca Gaithersburg, Maryland 20878, United States.
Christopher P CalderonDepartment of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80309, United States; Ursa Analytics, Denver, CO 80212, United States.
Theodore W RandolphDepartment of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80309, United States. Electronic address: theodore.randolph@colorado.edu.

Funding

Quantitative Biotherapeutic Particle Characterization via Deep Neural NetworksR41GM130513 · NIGMS · URSA ANALYTICS, INC. · PI CALDERON, CHRISTOPHER PETER, RANDOLPH, THEODORE W · 2018 to 2018
$222k
NIGMS NIH HHS R41 GM130513
6 · The paper itself

Abstract

Container choice can influence particle generation within protein formulations. Incompatibility between proteins and containers can manifest as increased particle concentrations, shifts in particle size distributions and changes in particle morphology distributions. In this study, flow imaging microscopy (FIM) combined with machine learning-based goodness-of-fit hypothesis testing algorithms were used in accelerated stability studies to investigate the impact of containers on particle formation. Containers in four major container categories subdivided into eleven container types were filled with monoclonal antibody formulations and agitated with and without headspace, producing subvisible particles. Digital images of the particles were recorded using flow imaging microscopy and analyzed with machine learning algorithms. Particle morphology distributions depended on container category and type, revealing differences that would not have been obvious by analysis of particle concentrations or container surface characteristics alone. Additionally, the algorithm was used to compare morphologies of particles generated in containers against those generated using isolated stresses at air-liquid and container-air-liquid interfaces. These comparisons showed that the morphology distributions of particles formed during agitation most closely resemble distributions that result from exposure of proteins to moving triple interface lines at points where container-air-liquid interfaces intersect. The approach described here can be used to identify dominant causes of particle generation due to protein-container interactions.

Indexed as

Antibodies, MonoclonalMachine LearningDrug CompoundingParticle SizeAntibodies, MonoclonalImage analysisMachine learningMonoclonal antibodiesProtein aggregationProtein formulation

Identifiers

PMID35835184
PMCPMC9481670

What OpenQuestion holds

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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.