Evidence map›Paper›PMID 32050432›Full record

ArticlePolymers2020

Clinically Relevant Insulin Degludec and its Interaction with Polysaccharides: A Biophysical Examination.

Shahwar Imran Jiwani, Sha Huang, Oritsegidenene Beji, Philemon Gyasi-Antwi, Richard B Gillis, Gary G Adams

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2020. 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
–field-weighted citation impact, top 99% 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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Shahwar Imran JiwaniUniversity of Nottingham, Faculty of Medicine and Health Sciences, Queen's Medical Centre, Clifton Boulevard, Nottingham NG7 2HA, UK.
Sha HuangUniversity of Nottingham, School of Biosciences, Sutton Bonington Campus, Sutton Bonington, Leicestershire LE12 5RD, UK.
Oritsegidenene BejiUniversity of Nottingham, School of Biosciences, Sutton Bonington Campus, Sutton Bonington, Leicestershire LE12 5RD, UK.
Philemon Gyasi-AntwiUniversity of Nottingham, Faculty of Medicine and Health Sciences, Queen's Medical Centre, Clifton Boulevard, Nottingham NG7 2HA, UK.
Richard B GillisUniversity of Nottingham, Faculty of Medicine and Health Sciences, Queen's Medical Centre, Clifton Boulevard, Nottingham NG7 2HA, UK.
Gary G AdamsUniversity of Nottingham, Faculty of Medicine and Health Sciences, Queen's Medical Centre, Clifton Boulevard, Nottingham NG7 2HA, UK.
University of Nottingham · GB

Funding

InDependent Diabetes Trust ID/T058019/1
6 · The paper itself

Abstract

Protein polysaccharide complexes have been widely studied for multiple industrial applications and are popular due to their biocompatibility. Insulin degludec, an analogue of human insulin, exists as di-hexamer in pharmaceutical formulations and has the potential to form long multi-hexamers in physiological environment, which dissociate into monomers to bind with receptors on the cell membrane. This study involved complexation of two negatively charged bio-polymers xanthan and alginate with clinically-relevant insulin degludec (PIC). The polymeric complexations and interactions were investigated using biophysical methods. Intrinsic viscosity [η] and particle size distribution (PSD) of PIC increased significantly with an increase in temperature, contrary to the individual components indicating possible interactions. [η] trend was X > XA > PIC > A > IDeg. PSD trend was X>A>IDeg>XA>PIC. Zeta (ζ)- potential (with general trend of IDeg < A < XA < X ≈ PIC) revealed stable interaction at lower temperature which gradually changed with an increase in temperature. Likewise, sedimentation velocity indicated stable complexation at lower temperature. With an increase in time and temperature, changes in the number of peaks and area under curve were observed for PIC. Conclusively, stable complexation occurred among the three polymers at 4 °C and 18 °C and the complex dissociated at 37 °C. Therefore, the complex has the potential to be used as a drug delivery vehicle.

Indexed as

alginatecomplexationsinsulin degludecinteractionsxanthan

Identifiers

PMID32050432
PMCPMC7077624
OpenAlexW3004650332

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.