Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption
15 pages. -- Figure S1: Characterisation data of liposomal formulations used in the study. Figure S2: Assessment of the behaviour function, histological brain changes and weight loss at different time points following induction of ICH model by collagenase injection. -- Figure S3: Histological analys...
| Autores: | , , , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | conjunto de datos |
| Fecha de publicación: | 2022 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/330298 |
| Acceso en línea: | http://hdl.handle.net/10261/330298 |
| Access Level: | acceso abierto |
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Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruptionAl-Ahmady, ZahraaDickie, Ben R.Aldred, IsabelleJasim, DhifafBarrington, JackHaley, Michael J.Lemarchand, EloiseCoutts, GrahamKaur, SatinderdeepBates, JessicaCurran, SarahGoddard, RupertWalker, MeganParry-Jones, AdrianKostarelos, Kostas15 pages. -- Figure S1: Characterisation data of liposomal formulations used in the study. Figure S2: Assessment of the behaviour function, histological brain changes and weight loss at different time points following induction of ICH model by collagenase injection. -- Figure S3: Histological analysis of brain tissues of ICH mice at different time points after ICH without injection of DiI-Lp confirmed that minimum autofluorescence signal (yellow signal) was detected in the injury site due to the presence of RBCs in the brain and tissue damage.-- Figure S4: Representative confocal images of (A) ipsilateral and (B) contralateral side of brain tissues after ICH, suggested enhanced Cav1 positive area 3-5 h after ICH (indicated by white arrows) and showed a clear co-localisation with DiI-Lp positive areas. (C) quantification of Cav1 and (D) DiI-Lp positive areas showed a significant increase 3-5 h after ICH which suggest a role of transcytotic transport in the accumulation of liposomes into the lesion site after ICH. -- Figure S5: Representative widefield overview images were obtained at x40 magnification without oil utilising Leica Thunder imager microscope. -- Figure S6 Histological analysis of iron deposition in the n after ICH using H&E and Prussian Blue stain on two different coordinates from the bregma; -0.58 (A&C) and -0.122 (B&D) both in the lesion core (A-B) and lesion rim (C-D). -- Figure S7: Evaluation of DiI-Lp co-localisation with microglia and astrocytes.. -- Figure S8: representative image analysis using Imaris software. -- Supplementary Table 1. Details of MRI scan time points for each mouse.. -- Graphical abstract and schematic graphes were performed using Biorender.Peer reviewedIvyspring International PublisherConsejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]202320232022info:eu-repo/semantics/datasethttp://purl.org/coar/resource_type/c_ddb1application/pdfhttp://hdl.handle.net/10261/330298reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)InglésAl-Ahmady, Zahraa; Dickie, Ben R.; Aldred, Isabelle; Jasim, Dhifaf; Barrington, Jack; Haley, Michael J.; Lemarchand, Eloise; Coutts, Graham; Kaur, Satinderdeep; Bates, Jessica; Curran, Sarah; Goddard, Rupert; Walker, Megan; Parry-Jones, Adrian; Kostarelos, Kostas. Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption. http://doi.org/10.7150/thno.72167. http://hdl.handle.net/10261/280759http://doi.org/10.7150/thno.72167Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/3302982026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| title |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| spellingShingle |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption Al-Ahmady, Zahraa |
| title_short |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| title_full |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| title_fullStr |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| title_full_unstemmed |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| title_sort |
Supplementary material of the article Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption |
| dc.creator.none.fl_str_mv |
Al-Ahmady, Zahraa Dickie, Ben R. Aldred, Isabelle Jasim, Dhifaf Barrington, Jack Haley, Michael J. Lemarchand, Eloise Coutts, Graham Kaur, Satinderdeep Bates, Jessica Curran, Sarah Goddard, Rupert Walker, Megan Parry-Jones, Adrian Kostarelos, Kostas |
| author |
Al-Ahmady, Zahraa |
| author_facet |
Al-Ahmady, Zahraa Dickie, Ben R. Aldred, Isabelle Jasim, Dhifaf Barrington, Jack Haley, Michael J. Lemarchand, Eloise Coutts, Graham Kaur, Satinderdeep Bates, Jessica Curran, Sarah Goddard, Rupert Walker, Megan Parry-Jones, Adrian Kostarelos, Kostas |
| author_role |
author |
| author2 |
Dickie, Ben R. Aldred, Isabelle Jasim, Dhifaf Barrington, Jack Haley, Michael J. Lemarchand, Eloise Coutts, Graham Kaur, Satinderdeep Bates, Jessica Curran, Sarah Goddard, Rupert Walker, Megan Parry-Jones, Adrian Kostarelos, Kostas |
| author2_role |
author author author author author author author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] |
| description |
15 pages. -- Figure S1: Characterisation data of liposomal formulations used in the study. Figure S2: Assessment of the behaviour function, histological brain changes and weight loss at different time points following induction of ICH model by collagenase injection. -- Figure S3: Histological analysis of brain tissues of ICH mice at different time points after ICH without injection of DiI-Lp confirmed that minimum autofluorescence signal (yellow signal) was detected in the injury site due to the presence of RBCs in the brain and tissue damage.-- Figure S4: Representative confocal images of (A) ipsilateral and (B) contralateral side of brain tissues after ICH, suggested enhanced Cav1 positive area 3-5 h after ICH (indicated by white arrows) and showed a clear co-localisation with DiI-Lp positive areas. (C) quantification of Cav1 and (D) DiI-Lp positive areas showed a significant increase 3-5 h after ICH which suggest a role of transcytotic transport in the accumulation of liposomes into the lesion site after ICH. -- Figure S5: Representative widefield overview images were obtained at x40 magnification without oil utilising Leica Thunder imager microscope. -- Figure S6 Histological analysis of iron deposition in the n after ICH using H&E and Prussian Blue stain on two different coordinates from the bregma; -0.58 (A&C) and -0.122 (B&D) both in the lesion core (A-B) and lesion rim (C-D). -- Figure S7: Evaluation of DiI-Lp co-localisation with microglia and astrocytes.. -- Figure S8: representative image analysis using Imaris software. -- Supplementary Table 1. Details of MRI scan time points for each mouse.. -- Graphical abstract and schematic graphes were performed using Biorender. |
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2022 |
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2022 2023 2023 |
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info:eu-repo/semantics/dataset http://purl.org/coar/resource_type/c_ddb1 |
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http://hdl.handle.net/10261/330298 |
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http://hdl.handle.net/10261/330298 |
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Inglés |
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Inglés |
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Al-Ahmady, Zahraa; Dickie, Ben R.; Aldred, Isabelle; Jasim, Dhifaf; Barrington, Jack; Haley, Michael J.; Lemarchand, Eloise; Coutts, Graham; Kaur, Satinderdeep; Bates, Jessica; Curran, Sarah; Goddard, Rupert; Walker, Megan; Parry-Jones, Adrian; Kostarelos, Kostas. Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption. http://doi.org/10.7150/thno.72167. http://hdl.handle.net/10261/280759 http://doi.org/10.7150/thno.72167 Sí |
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Ivyspring International Publisher |
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