Evidence map›Paper›PMID 36112103›Full record

ArticleTranslational vision science & technology2022

Effect of Recombinant Human Lubricin on Model Tear Film Stability.

Kiara W Cui, Vincent X Xia, Daniel Cirera-Salinas, David Myung, Gerald G Fuller

Open access · goldAbstract read
In one paragraph

Article in Translational vision science & technology, 2022. 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 44% 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

5 authors at 2 institutions in 2 countries.

Kiara W CuiStanford Department of Chemical Engineering, Stanford, CA, USA.
Vincent X XiaStanford Department of Chemical Engineering, Stanford, CA, USA.
Daniel Cirera-SalinasGlobal Drug Development, Novartis Pharma, Basel, Switzerland.
David MyungStanford Department of Chemical Engineering, Stanford, CA, USA.
Gerald G FullerStanford Department of Chemical Engineering, Stanford, CA, USA.
Stanford Medicine · USNovartis (Switzerland) · CH

Funding

Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI TIRIN MOORE · 2017 to 2026
$8.0M
Stanford Chem-H Chemistry/Biology Interface Predoctoral Training ProgramT32GM120007 · NIGMS · STANFORD UNIVERSITY · PI BERTOZZI, CAROLYN · 2016 to 2020
$1.2M
In Situ Bioconjugation as a Therapeutic Delivery Modality to Enhance Ocular Wound HealingK08EY028176 · NEI · STANFORD UNIVERSITY · PI MYUNG, DAVID · 2017 to 2021
$1.1M
NEI NIH HHS K08 EY028176NEI NIH HHS P30 EY026877NIGMS NIH HHS T32 GM120007
6 · The paper itself

Abstract

Purpose: To investigate and quantify the effect of recombinant human lubricin (rh-lubricin) on model tear film stability. Methods: A custom-built, interferometry-based instrument called the Interfacial Dewetting and Drainage Optical Platform was used to create and record the spatiotemporal evolution of model acellular tear films. Image segmentation and analysis was performed in MATLAB to extract the most essential features from the wet area fraction versus time curve, namely the evaporative break-up time and the final wet area fraction (A10). These two parameters indicate the tear film stability in the presence of rh-lubricin in its unstressed and stressed forms. Results: Our parameters successfully captured the trend of increasing tear film stability with increasing rh-lubricin concentration, and captured differences in rh-lubricin efficacy after various industrially relevant stresses. Specifically, aggregation and fragmentation caused by a 4-week, high temperature stress condition negatively impacted rh-lubricin's ability to maintain model tear film stability. Adsorbed rh-lubricin alone was not sufficient to resist break-up and maintain full area coverage of the model tear film surface. Conclusions: Our results demonstrate that fragmentation and aggregation can negatively impact rh-lubricin's ability to maintain a stable tear film. In addition, the ability of rh-lubricin to maintain wetted area coverage is due to both freely dispersed and adsorbed rh-lubricin. Translational Relevance: Our platform and analysis method provide a facile, intuitive, and clinically relevant means to quantify the effect of ophthalmic drugs and formulations intended for improving tear film stability, as well as capture differences between variants related to drug stability and efficacy.

Indexed as

GlycoproteinsTearsHumansInterferometryProteoglycan 4Recombinant ProteinsVision, OcularGlycoproteinsProteoglycan 4Recombinant Proteins

Identifiers

PMID36112103
PMCPMC9487168
OpenAlexW4296029445

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.