Evidence map›Paper›PMID 32024534›Full record

ArticleJournal of nanobiotechnology2020

Local delivery of minocycline-loaded PLGA nanoparticles from gelatin-coated neural implants attenuates acute brain tissue responses in mice.

Alexander Dontsios Holmkvist, Johan Agorelius, Matilde Forni, Ulf J Nilsson, Cecilia Eriksson Linsmeier, Jens Schouenborg

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  9. Commonly Overlooked Factors in Biocompatibility Studies of Neural Implants.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  10. Review
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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

6 authors at 1 institution in 1 country.

Alexander Dontsios HolmkvistNeuronano Research Center, Department of Experimental Medical Science, Faculty of Medicine, Lund University, Medicon Village, Building 404 A2, Scheelevägen 2, 223 81, Lund, Sweden. Alexander.Holmkvist@med.lu.se.ORCID http://orcid.org/0000-0002-3013-7468
Johan AgoreliusNeuronano Research Center, Department of Experimental Medical Science, Faculty of Medicine, Lund University, Medicon Village, Building 404 A2, Scheelevägen 2, 223 81, Lund, Sweden.
Matilde ForniNeuronano Research Center, Department of Experimental Medical Science, Faculty of Medicine, Lund University, Medicon Village, Building 404 A2, Scheelevägen 2, 223 81, Lund, Sweden.
Ulf J NilssonCentre for Analysis and Synthesis, Department of Chemistry, Lund University, Box 124, 221 00, Lund, Sweden.
Cecilia Eriksson LinsmeierNeuronano Research Center, Department of Experimental Medical Science, Faculty of Medicine, Lund University, Medicon Village, Building 404 A2, Scheelevägen 2, 223 81, Lund, Sweden.
Jens SchouenborgNeuronano Research Center, Department of Experimental Medical Science, Faculty of Medicine, Lund University, Medicon Village, Building 404 A2, Scheelevägen 2, 223 81, Lund, Sweden. Jens.Schouenborg@med.lu.se.
Lund University · SE

Funding

Magnus Bergvalls Foundation 2015-01176Swedish Research Council 2016-06195
6 · The paper itself

Abstract

backgroundNeural interfaces often elicit inflammatory responses and neuronal loss in the surrounding tissue which adversely affect the function and longevity of the implanted device. Minocycline, an anti-inflammatory pharmaceutics with neuroprotective properties, may be used for reducing the acute brain tissue responses after implantation. However, conventional administration routes require high doses which can cause adverse systemic side effects. Therefore, the aim of this study was to develop and evaluate a new drug-delivery-system for local and sustained administration of minocycline in the brain.

methodsStainless steel needles insulated with Parylene-C were dip-coated with non-crosslinked gelatin and minocycline-loaded PLGA nanoparticles (MC-NPs) were incorporated into the gelatin-coatings by an absorption method and subsequently trapped by drying the gelatin. Parylene-C insulated needles coated only with gelatin were used as controls. The expression of markers for activated microglia (CD68), all microglia (CX3CR1-GFP), reactive astrocytes (GFAP), neurons (NeuN) and all cell nuclei (DAPI) surrounding the implantation sites were quantified at 3 and 7 days after implantation in mice.

resultsMC-NPs were successfully incorporated into gelatin-coatings of neural implants by an absorption method suitable for thermosensitive drug-loads. Immunohistochemical analysis of the in vivo brain tissue responses, showed that MC-NPs significantly attenuate the activation of microglial cells without effecting the overall population of microglial cells around the implantation sites. A delayed but significant reduction of the astrocytic response was also found in comparison to control implants. No effect on neurons or total cell count was found which may suggest that the MC-NPs are non-toxic to the central nervous system.

conclusionsA novel drug-nanoparticle-delivery-system was developed for neural interfaces and thermosensitive drug-loads. The local delivery of MC-NPs was shown to attenuate the acute brain tissue responses nearby an implant and therefore may be useful for improving biocompatibility of implanted neuro-electronic interfaces. The developed drug-delivery-system may potentially also be used for other pharmaceutics to provide highly localized and therefore more specific effects as compared to systemic administration.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory AgentsAstrocytesBiocompatible MaterialsBiological TransportBrainCD68 MoleculeFemaleFluorescent DyesGelatinHumansMaleMiceMice, TransgenicAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory AgentsBiocompatible MaterialsCD68 antigen, humanCD68 MoleculeFluorescent DyesGelatinMinocyclineNanocapsulesparylenePolylactic Acid-Polyglycolic Acid CopolymerPolymersXylenesBiocompatibilityBrainDrug-delivery-systemsGelatinImmunohistochemistryMinocyclineNanoparticlesNeural interfacePLGATissue responses

Identifiers

PMID32024534
PMCPMC7003334
OpenAlexW3004778360

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.