Literature DB >> 28993678

Erratum: Characterization of Mechanically Matched Hydrogel Coatings to Improve the Biocompatibility of Neural Implants.

Kevin C Spencer1, Jay C Sy2,3, Khalil B Ramadi4, Ann M Graybiel5, Robert Langer2,6, Michael J Cima7,8.   

Abstract

A correction to this article has been published and is linked from the HTML version of this paper. The error has not been fixed in the paper.

Entities:  

Year:  2017        PMID: 28993678      PMCID: PMC5634477          DOI: 10.1038/s41598-017-12312-8

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


Scientific Reports 7:1952; doi:10.1038/s41598-017-02107-2; Article published online 16 May 2017 This Article contains an error in the order of the Figures 4 and 5. Figures 4 and 5 were published as Figures 5 and 4 respectively. The correct Figures appear below as Figures 1 and 2. The Figure legends are correct.
Figure 1

Implant Diameter Comparison. Increasing implant diameter increases scarring at 8 weeks post implantation when implant modulus is held constant. Glass capillaries with diameters ranging from 150 μm to 400 μm were implanted into the rodent brain and analyzed at 1, 4, and 8 weeks post implantation. (a) The GFAP activity as a function of distance from the implant at 1 week. A slight decrease in the GFAP reactivity was observed directly around the implants for the larger capillaries. (b) GFAP reactivity at four weeks post implantation. GFAP reactivity was increased around the implant for 400 μm implants at 4 weeks post implantation. The GC400 group had increased scarring compared to GC200 and GC150 groups in the 100 μm surrounding the implant. (c) Representative IF images (scale bar (100 μm) of the GFAP reactivity at 8 weeks post implantation. (d) GFAP reactivity at 8 weeks post implantation. Increased diameter (200 μm and 400 μm) implants were found to produce increased scarring at eight weeks post implantation. **p < 0.01, *p < 0.05 indicates a statistically significant difference between cohorts at a given distance from the implant interface. ##p < 0.01, #p < 0.05 indicates a statistically significant difference compared to background. Cohort sizes (1 wk, 4 wk, 8 wk). GC150 = (11, 11, 18), GC200 = (6, 5, 7), GC400 = (6, 5, 10). Each n corresponds to an individual animal (biological replicate). A minimum of four sections were analyzed per animal.

Figure 2

Increasing implant diameter has additional effects on the biological response at 8 weeks post implantation. (a) Representative IF images of the IgG and ED1 reactivity around implants at 8 weeks post implantation (scale bar 100 μm). (b) Representative IF images of the NeuN staining around glass capillary implants at 8 weeks post implantation. (Scale bar 100 μm). (c,d,e) IgG, NeuN, and ED1 staining around the implants at eight weeks post implantation. Animals with increased diameter implants were found to have increased BBB permeability, IgG (d) decreased neural density, and (e) increased activated macrophages staining in the region directly surrounding the implant location. **p < 0.01, *p < 0.05 indicates a statistically significant difference between cohorts at a given distance from the implant interface. No significant differences were observed beyond the distances shown in the figures. ##p < 0.01, #p < 0.05 indicates a statistically significant difference compared to background. Cohort sizes: GC150: n = 18, GC200: n = 7, GC400: n = 10. Each n corresponds to an individual animal. A minimum of four sections were analyzed per animal.

Implant Diameter Comparison. Increasing implant diameter increases scarring at 8 weeks post implantation when implant modulus is held constant. Glass capillaries with diameters ranging from 150 μm to 400 μm were implanted into the rodent brain and analyzed at 1, 4, and 8 weeks post implantation. (a) The GFAP activity as a function of distance from the implant at 1 week. A slight decrease in the GFAP reactivity was observed directly around the implants for the larger capillaries. (b) GFAP reactivity at four weeks post implantation. GFAP reactivity was increased around the implant for 400 μm implants at 4 weeks post implantation. The GC400 group had increased scarring compared to GC200 and GC150 groups in the 100 μm surrounding the implant. (c) Representative IF images (scale bar (100 μm) of the GFAP reactivity at 8 weeks post implantation. (d) GFAP reactivity at 8 weeks post implantation. Increased diameter (200 μm and 400 μm) implants were found to produce increased scarring at eight weeks post implantation. **p < 0.01, *p < 0.05 indicates a statistically significant difference between cohorts at a given distance from the implant interface. ##p < 0.01, #p < 0.05 indicates a statistically significant difference compared to background. Cohort sizes (1 wk, 4 wk, 8 wk). GC150 = (11, 11, 18), GC200 = (6, 5, 7), GC400 = (6, 5, 10). Each n corresponds to an individual animal (biological replicate). A minimum of four sections were analyzed per animal. Increasing implant diameter has additional effects on the biological response at 8 weeks post implantation. (a) Representative IF images of the IgG and ED1 reactivity around implants at 8 weeks post implantation (scale bar 100 μm). (b) Representative IF images of the NeuN staining around glass capillary implants at 8 weeks post implantation. (Scale bar 100 μm). (c,d,e) IgG, NeuN, and ED1 staining around the implants at eight weeks post implantation. Animals with increased diameter implants were found to have increased BBB permeability, IgG (d) decreased neural density, and (e) increased activated macrophages staining in the region directly surrounding the implant location. **p < 0.01, *p < 0.05 indicates a statistically significant difference between cohorts at a given distance from the implant interface. No significant differences were observed beyond the distances shown in the figures. ##p < 0.01, #p < 0.05 indicates a statistically significant difference compared to background. Cohort sizes: GC150: n = 18, GC200: n = 7, GC400: n = 10. Each n corresponds to an individual animal. A minimum of four sections were analyzed per animal.
  3 in total

Review 1.  Engineering Tissues of the Central Nervous System: Interfacing Conductive Biomaterials with Neural Stem/Progenitor Cells.

Authors:  Rebecca D Bierman-Duquette; Gevick Safarians; Joyce Huang; Bushra Rajput; Jessica Y Chen; Ze Zhong Wang; Stephanie K Seidlits
Journal:  Adv Healthc Mater       Date:  2021-12-16       Impact factor: 9.933

2.  Soft, Conductive, Brain-Like, Coatings at Tips of Microelectrodes Improve Electrical Stability under Chronic, In Vivo Conditions.

Authors:  Arati Sridharan; Jit Muthuswamy
Journal:  Micromachines (Basel)       Date:  2021-06-28       Impact factor: 2.891

3.  Finite Element Modeling of Magnitude and Location of Brain Micromotion Induced Strain for Intracortical Implants.

Authors:  Ali Al Abed; Jason Amatoury; Massoud Khraiche
Journal:  Front Neurosci       Date:  2022-01-06       Impact factor: 4.677

  3 in total

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