Evidence map›Paper›PMID 29946984›Full record

ArticlePharmaceutical research2018

Use of Cyclodextrin as a Novel Agent in the SEC-HPLC Mobile Phase to Mitigate the Interactions of Proteins or Peptide or their Impurities with the Residual Silanols of Commercial SEC-HPLC Columns with Improved Separation and Resolution.

Indu Javeri, Kaliappanadar Nellaiappan, Charles McNemar, Kirill Yakovlevsky, Amina Soukrati, Phanindra Velisetty, Bijay Misra

Abstract read
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Article in Pharmaceutical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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 at 1 institution in 1 country.

Indu JaveriCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA.
Kaliappanadar NellaiappanCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA. Nellaiappan@curirx.com.ORCID http://orcid.org/0000-0002-0028-1178
Charles McNemarCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA.
Kirill YakovlevskyCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA.
Amina SoukratiCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA.
Phanindra VelisettyCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA.
Bijay MisraCuriRx, Inc, 205 Lowell St, Suite 1C, Wilmington, Massachusetts, 01887, USA.
CuriRx (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAccurate quantification of the intact proteins, antibodies or peptides and their impurities without interaction to silanols of HPLC column.

methodsHydroxypropyl ß Cyclodextrin (HPCD) is added in the mobile phase at different concentrations. Different commercial SEC-HPLC columns and biologics with a molecular weight ranging from 5.8 kDa to 150kDa were assessed with and without cyclodextrin.

resultsAddition of non-ionic sugars such as Hydroxypropyl ß Cyclodextrin in the mobile phase, resulted improved peak performance such as theoretical plates, peak resolution, peak width, peak height, and improved quantification of aggregates in biologics such as antibodies Humira and Actemra, and peptides such as insulin. There is an increase in peak height, reduced retention time, increased plate and reduced peak width with increasing concentration of cyclodextrin studied. DISCUSSION: High ionic strength, basic amino acids such as arginine, organic solvents (with a concentration low enough not to precipitate protein), sodium perchlorate and ion pairing agents in the mobile phase used for separation of peptides, proteins and antibodies to prevent silanol interaction. These commonly used solutions are not always successful, as they not only interact with the biologic, but are sometimes, not compatible. The non-ionic cyclodextrin itself does not cause protein aggregation but prevents the nonspecific binding or interaction of protein itself and thereby allowing for improved resolution, and accurate quantification of aggregates in antibodies, and peptides. The data on the separation in presence of cyclodextrin in the mobile phase showed higher peak resolution, improved peak shape, accurate apparent molecular weight, improved efficiency, and less peak tailing for biological products.

conclusionHydroxypropyl ß Cyclodextrin in the mobile phase, resulted improved SEC-HPLC resolution, and quantitation of aggregates in biologics by preventing the interaction of biologics to silanol of the commercial SEC-HPLC columns.

Indexed as

2-Hydroxypropyl-beta-cyclodextrinAdalimumabAnimalsAntibodies, Monoclonal, HumanizedChromatography, GelChromatography, High Pressure LiquidHumansImmunoglobulin GInsulinPeptidesProtein AggregatesProteinsRatsSilanes2-Hydroxypropyl-beta-cyclodextrinAdalimumabAntibodies, Monoclonal, HumanizedImmunoglobulin GInsulinPeptidesProtein AggregatesProteinsSilanessilanoltocilizumabhydroxypropyl ß Cyclodextrinproteins and peptidesSEC-HPLC column interactionsilanol

Identifiers

PMID29946984
OpenAlexW2809878561

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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.