Evidence map›Paper›PMID 40502182›Full record

ArticlebioRxiv : the preprint server for biology2025

Development of a PEGylated Parylene Nanopocket Membrane for the Capture and Release of Lipid Vesicles.

Munther Alsudais, Kevin E Petersen, Atiyeh Hosseinifakhr, Leanna H Frasch, Shayan Gholizadeh, Mehdi Dehghani, Thomas R Gaborski

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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
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.

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

7 authors.

Munther AlsudaisDepartment of Biomedical Engineering, Rochester Institute of Technology, Rochester, New York, United States.
Kevin E PetersenDepartment of Biomedical Engineering, Rochester Institute of Technology, Rochester, New York, United States.
Atiyeh HosseinifakhrDepartment of Biomedical Engineering, Rochester Institute of Technology, Rochester, New York, United States.
Leanna H FraschDepartment of Biomedical Engineering, Rochester Institute of Technology, Rochester, New York, United States.
Shayan GholizadehDepartment of Biomedical Engineering, Rochester Institute of Technology, Rochester, New York, United States.ORCID 0000-0001-5534-460X
Mehdi DehghaniSartorius Corporate Research, Sartorius Stedim North America, Marlborough, Massachusetts, United States.
Thomas R GaborskiDepartment of Biomedical Engineering, Rochester Institute of Technology, Rochester, New York, United States.ORCID 0000-0002-3676-3208

Funding

Engineering Cell-Substrate Interactions on Porous Membranes to Create Physiologically Relevant Model SystemsR35GM153461 · NIGMS · ROCHESTER INSTITUTE OF TECHNOLOGY · PI THOMAS R GABORSKI · 2024 to 2026
$1.1M
Development of size-selective capture and release membranes for purification of extracellular vesiclesR21GM146156 · NIGMS · ROCHESTER INSTITUTE OF TECHNOLOGY · PI GABORSKI, THOMAS R · 2022 to 2023
$407k
NIGMS NIH HHS R21 GM146156NIGMS NIH HHS R35 GM153461
6 · The paper itself

Abstract

Membranes are commonly used for the separation and purification of a variety of biological species. In this study, we developed a nanopocket membrane that can capture nanoparticles and extracellular vesicles in tangential flow filtration by pulling the species of interest into a nanopocket, while tangential flow washes away particles too large to be captured. We developed the pores using a four-step lithography process. By optimizing photolithography parameters, particularly exposure dose, we achieved well-defined pore shapes with the desired wall tilt, forming nanopocket geometries. We validated membrane performance using bead mixtures of varying diameters (50 nm-10 μm), demonstrating its ability to pass small particles, capture mid-sized particles, and exclude larger ones. Surface modification with poly(l-lysine)-grafted poly(ethylene glycol) enhanced this performance by reducing pore size and improving particle release. Additionally, we demonstrated selective capture and release of liposomes as well as EVs in the presence of fluorescently labeled BSA (f-BSA) protein. During this process, EVs were retained and later released, while f-BSA passed through, confirming selective capture and reduced protein contamination. These PEGylated nanopocket membranes constitute a low-pressure platform for gentle, size-selective isolation of nanoscale bioparticles, laying the groundwork for improved extracellular-vesicle analytics and point-of-care diagnostic applications.

Indexed as

extracellular vesiclesmembrane fabricationnanopocket membraneseparationtangential flow filtration

Identifiers

PMID40502182
PMCPMC12157671

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.