Evidence map›Paper›PMID 31127417›Full record

ArticlePharmaceutical research2019

Understanding the Role of Preferential Exclusion of Sugars and Polyols from Native State IgG1 Monoclonal Antibodies and its Effect on Aggregation and Reversible Self-Association.

Chaitanya M Sudrik, Theresa Cloutier, Neil Mody, Hasige A Sathish, Bernhardt L Trout

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Article in Pharmaceutical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 49 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

5 authors at 2 institutions in 1 country.

Chaitanya M SudrikDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave, Room 66-350, Cambridge, MA, 02139, USA.
Theresa CloutierDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave, Room 66-350, Cambridge, MA, 02139, USA.
Neil ModyFormulation Sciences, MedImmune LLC, Gaithersburg, MD, 20878, USA.
Hasige A SathishFormulation Sciences, MedImmune LLC, Gaithersburg, MD, 20878, USA.
Bernhardt L TroutDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave, Room 66-350, Cambridge, MA, 02139, USA. trout@mit.edu.ORCID http://orcid.org/0000-0003-1417-9470
Massachusetts Institute of Technology · USIIT@MIT · US

Funding

MedImmune LLC NA
6 · The paper itself

Abstract

purposeTo investigate differences in the preferential exclusion of trehalose, sucrose, sorbitol and mannitol from the surface of three IgG1 monoclonal antibodies (mAbs) and understand its effect on the aggregation and reversible self-association of mAbs at high-concentrations.

methodsPreferential exclusion was measured using vapor pressure osmometry. Effect of excipient addition on accelerated aggregation kinetics was quantified using size exclusion chromatography and on reversible self-association was quantified using dynamic light scattering.

resultsThe doubling of excipient concentration in the 0 to 0.5 m range resulted in a doubling of the mAb transfer free energy for all excipients and antibodies tested in this study. Solution pH and choice of buffering agent did not significantly affect the magnitude of preferential exclusion. We find that aggregation suppression for trehalose, sucrose and sorbitol (but not mannitol) correlates with the magnitude of their preferential exclusion from the native state of the three IgG1 mAbs. We also find that addition of sugars and polyols reduced the tendency for reversible self-association in two mAbs that had weakly repulsive or neutral self-interactions in the presence of buffer alone.

conclusionsThe magnitude of preferential exclusion for trehalose, sucrose and sorbitol correlates well with their partial molar volumes in solution. Mannitol is excluded to a greater extent than that expected from its partial molar volume, suggesting specific interactions of mannitol that might be different than the other sugars and polyols tested in this study. Local interactions play a role in the effect of excipient addition on the reversible self-association of mAbs. These results provide further insights into the stabilization of high-concentration mAb formulations by sugars and polyols.

Indexed as

Protein AggregatesAntibodies, MonoclonalExcipientsImmunoglobulin GKineticsMolecular Dynamics SimulationPolymersProtein ConformationSucroseSugar AlcoholsSurface PropertiesTrehaloseAntibodies, MonoclonalExcipientsImmunoglobulin GPolymerspolyolProtein AggregatesSucroseSugar AlcoholsTrehaloseDLSmAb stabilityMannitolSorbitolSucroseTrehalose

Identifiers

PMID31127417
OpenAlexW2944956496

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.