Evidence map›Paper›PMID 37064815›Full record

ArticleComputers & chemical engineering2023

Surrogate-based Optimization of Capture Chromatography Platforms for the Improvement of Computational Efficiency.

Juan J Romero, Eleanor W Jenkins, Scott M Husson

Abstract read
In one paragraph

Article in Computers & chemical engineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

3 authors.

Juan J RomeroDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC 29634 USA.
Eleanor W JenkinsSchool of Mathematical and Statistical Sciences, Clemson University, Clemson, SC 29634 USA.
Scott M HussonDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC 29634 USA.

Funding

Strategies for continuous biologics purification with new affinity membranesR15GM131341 · NIGMS · CLEMSON UNIVERSITY · PI HUSSON, SCOTT M · 2018 to 2018
$422k
NIGMS NIH HHS R15 GM131341
6 · The paper itself

Abstract

In this work, we discuss the use of surrogate functions and a new optimization framework to create an efficient and robust computational framework for process design. Our model process is the capture chromatography unit operation for monoclonal antibody purification, an important step in biopharmaceutical manufacturing. Simulating this unit operation involves solving a system of non-linear partial differential equations, which can have high computational cost. We implemented surrogate functions to reduce the computational time and make the framework more attractive for industrial applications. This strategy yielded accurate results with a 93% decrease in processing time. Additionally, we developed a new optimization framework to reduce the number of simulations needed to generate a solution to the optimization problem. We demonstrate the performance of our new framework, which uses MATLAB built-in tools, by comparing its performance against individual optimization algorithms for problems with integer, continuous, and mixed-integer variables.

Indexed as

mixed-integer optimizationMonoclonal antibodiesmulti-objective optimization

Identifiers

PMID37064815
PMCPMC10100681

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.