Evidence map›Paper›PMID 32596218›Full record

ArticleFrontiers in bioengineering and biotechnology2020

Polylactic Acid-Based Patterned Matrixes for Site-Specific Delivery of Neuropeptides On-Demand: Functional NGF Effects on Human Neuronal Cells.

Olga A Sindeeva, Olga Kopach, Maxim A Kurochkin, Andrei Sapelkin, David J Gould, Dmitri A Rusakov, Gleb B Sukhorukov

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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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

7 authors.

Olga A SindeevaCenter for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, Russia.
Olga KopachUCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Maxim A KurochkinCenter for Photonics and Quantum Materials, Skolkovo Institute of Science and Technology, Moscow, Russia.
Andrei SapelkinSchool of Physics and Astronomy, Queen Mary University of London, London, United Kingdom.
David J GouldBiochemical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Dmitri A RusakovUCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Gleb B SukhorukovCenter for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, Russia.

Funding

Wellcome Trust 212251/Z/18/Z
6 · The paper itself

Abstract

The patterned microchamber arrays based on biocompatible polymers are a versatile cargo delivery system for drug storage and site-/time-specific drug release on demand. However, functional evidence of their action on nerve cells, in particular their potential for enabling patterned neuronal morphogenesis, remains unclear. Recently, we have established that the polylactic acid (PLA)-based microchamber arrays are biocompatible with human cells of neuronal phenotype and provide safe loading for hydrophilic substances of low molecular weight, with successive site-specific cargo release on-demand to trigger local cell responses. Here, we load the nerve growth factor (NGF) inside microchambers and grow N2A cells on the surface of patterned microchamber arrays. We find that the neurite outgrowth in local N2A cells can be preferentially directed towards opened microchambers (upon-specific NGF release). These observations suggest the PLA-microchambers can be an efficient drug delivery system for the site-specific delivery of neuropeptides on-demand, potentially suitable for the migratory or axonal guidance of human nerve cells.

Indexed as

drug delivery systemhuman N2A cellsNGFpatterned microchamber arraypolylactic acid (PLA)

Identifiers

PMID32596218
PMCPMC7304324

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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.