Loading…

ChABC-loaded PLGA nanoparticles: A comprehensive study on biocompatibility, functional recovery, and axonal regeneration in animal model of spinal cord injury

[Display omitted] Spinal Cord Injury (SCI) is one of the leading causes of physical disability. In this study, spherical PLGA nanoparticles (NPs) containing ChABC enzyme were manufactured and fully characterized for SCI therapy. The NPs were used in the rat’s contused spinal cord to assess the funct...

Full description

Saved in:
Bibliographic Details
Published in:International journal of pharmaceutics 2020-03, Vol.577, p.119037, Article 119037
Main Authors: Azizi, Monireh, Farahmandghavi, Farhid, Joghataei, Mohammad Taghi, Zandi, Mojgan, Imani, Mohammad, Bakhtiari, Mehrdad, Omidian, Hamid
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3
cites cdi_FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3
container_end_page
container_issue
container_start_page 119037
container_title International journal of pharmaceutics
container_volume 577
creator Azizi, Monireh
Farahmandghavi, Farhid
Joghataei, Mohammad Taghi
Zandi, Mojgan
Imani, Mohammad
Bakhtiari, Mehrdad
Omidian, Hamid
description [Display omitted] Spinal Cord Injury (SCI) is one of the leading causes of physical disability. In this study, spherical PLGA nanoparticles (NPs) containing ChABC enzyme were manufactured and fully characterized for SCI therapy. The NPs were used in the rat’s contused spinal cord to assess the functional improvement and scar digestion. Twenty-three adult male Wistar rats (275 ± 25 g) were assigned into four groups of control, sham, blank-treated particle, and ChABC-treated particle. Throughout the survey, the BBB scores were obtained for all the groups. Finally, the injured sections of animals were dissected, and histological studies were conducted using Luxol fast blue and Bielschowsky. The biocompatibility and non-toxicity effects of the NPs on olfactory ensheathing cells (OECs) were confirmed by the MTT test. The flow-cytometry revealed the purity of cultured OECs with p75+/GFAP+ at around 87.9 ± 2.4%. Animals in the control and the blank-treated groups exhibited significantly lower BBB scores compared with the ChABC-treated particle group. Histological results confirmed the induced contusion models in the injured site. Myelin was observed in the treated groups, especially when the ChABC-loaded nanoparticles were utilized. The immunohistochemistry results indicated the scar glial degradation in animals treated by the ChABC-loaded particles. According to this study, the loaded particles can potentially serve as a suitable candidate for spinal cord repair, functional recovery and axonal regeneration.
doi_str_mv 10.1016/j.ijpharm.2020.119037
format article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_ijpharm_2020_119037</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0378517320300193</els_id><sourcerecordid>31953081</sourcerecordid><originalsourceid>FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3</originalsourceid><addsrcrecordid>eNqFkMtO4zAUhi0EgnJ5BJAfgHTsODezQaUCBqkSLGBtOfYJdZTYkZ1W05fhWXHUDltWx_ovx0cfQteUzCmhxZ92btphLX0_T0kaNcoJK4_QjFYlS1hWFsdoFpUqyWnJztB5CC0hpEgpO0VnjPKckYrO0NdyvXhYJp2TGjR-Wz0vsJXWDdKPRnUQ7vACK9cPHtZgg9kCDuNG77CzuDZucuRoatOZcXeLm41Vo3FWdtiDclvwUZRWY_nvIH6CBS-nDDY2WqaPcu80dNg1OAxmiinndbTbjd9dopNGdgGuDvMCfTw9vi__JqvX55flYpUoVuRjIivO06rMaKFqyHheAGcNSVmlIIMSSl6wUjYqvphOYyZTPGP55Cle11qyC5Tv9yrvQvDQiMHH2_xOUCIm3qIVB95i4i32vGPvZt8bNnUP-qf1H3AM3O8DEK_fGvAiKANWgTYR0Si0M7988Q2poZeM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>ChABC-loaded PLGA nanoparticles: A comprehensive study on biocompatibility, functional recovery, and axonal regeneration in animal model of spinal cord injury</title><source>Elsevier</source><creator>Azizi, Monireh ; Farahmandghavi, Farhid ; Joghataei, Mohammad Taghi ; Zandi, Mojgan ; Imani, Mohammad ; Bakhtiari, Mehrdad ; Omidian, Hamid</creator><creatorcontrib>Azizi, Monireh ; Farahmandghavi, Farhid ; Joghataei, Mohammad Taghi ; Zandi, Mojgan ; Imani, Mohammad ; Bakhtiari, Mehrdad ; Omidian, Hamid</creatorcontrib><description>[Display omitted] Spinal Cord Injury (SCI) is one of the leading causes of physical disability. In this study, spherical PLGA nanoparticles (NPs) containing ChABC enzyme were manufactured and fully characterized for SCI therapy. The NPs were used in the rat’s contused spinal cord to assess the functional improvement and scar digestion. Twenty-three adult male Wistar rats (275 ± 25 g) were assigned into four groups of control, sham, blank-treated particle, and ChABC-treated particle. Throughout the survey, the BBB scores were obtained for all the groups. Finally, the injured sections of animals were dissected, and histological studies were conducted using Luxol fast blue and Bielschowsky. The biocompatibility and non-toxicity effects of the NPs on olfactory ensheathing cells (OECs) were confirmed by the MTT test. The flow-cytometry revealed the purity of cultured OECs with p75+/GFAP+ at around 87.9 ± 2.4%. Animals in the control and the blank-treated groups exhibited significantly lower BBB scores compared with the ChABC-treated particle group. Histological results confirmed the induced contusion models in the injured site. Myelin was observed in the treated groups, especially when the ChABC-loaded nanoparticles were utilized. The immunohistochemistry results indicated the scar glial degradation in animals treated by the ChABC-loaded particles. According to this study, the loaded particles can potentially serve as a suitable candidate for spinal cord repair, functional recovery and axonal regeneration.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2020.119037</identifier><identifier>PMID: 31953081</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Cells, Cultured ; Chondroitin ABC Lyase - chemistry ; Chondroitin ABC Lyase - pharmacology ; Chondroitinase ABC ; Cicatrix - drug therapy ; Locomotion - drug effects ; Male ; Materials Testing - methods ; Nanoparticles - chemistry ; Nerve Regeneration - drug effects ; OECs ; Olfactory Mucosa - pathology ; PLGA nanoparticle ; Polylactic Acid-Polyglycolic Acid Copolymer - chemistry ; Protein delivery ; Rats ; Recovery of Function - drug effects ; Spinal Cord Injuries - drug therapy ; Spinal Cord Injuries - pathology ; Spinal cord injury</subject><ispartof>International journal of pharmaceutics, 2020-03, Vol.577, p.119037, Article 119037</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3</citedby><cites>FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3</cites><orcidid>0000-0002-2917-2645 ; 0000-0001-5154-0881</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31953081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Azizi, Monireh</creatorcontrib><creatorcontrib>Farahmandghavi, Farhid</creatorcontrib><creatorcontrib>Joghataei, Mohammad Taghi</creatorcontrib><creatorcontrib>Zandi, Mojgan</creatorcontrib><creatorcontrib>Imani, Mohammad</creatorcontrib><creatorcontrib>Bakhtiari, Mehrdad</creatorcontrib><creatorcontrib>Omidian, Hamid</creatorcontrib><title>ChABC-loaded PLGA nanoparticles: A comprehensive study on biocompatibility, functional recovery, and axonal regeneration in animal model of spinal cord injury</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted] Spinal Cord Injury (SCI) is one of the leading causes of physical disability. In this study, spherical PLGA nanoparticles (NPs) containing ChABC enzyme were manufactured and fully characterized for SCI therapy. The NPs were used in the rat’s contused spinal cord to assess the functional improvement and scar digestion. Twenty-three adult male Wistar rats (275 ± 25 g) were assigned into four groups of control, sham, blank-treated particle, and ChABC-treated particle. Throughout the survey, the BBB scores were obtained for all the groups. Finally, the injured sections of animals were dissected, and histological studies were conducted using Luxol fast blue and Bielschowsky. The biocompatibility and non-toxicity effects of the NPs on olfactory ensheathing cells (OECs) were confirmed by the MTT test. The flow-cytometry revealed the purity of cultured OECs with p75+/GFAP+ at around 87.9 ± 2.4%. Animals in the control and the blank-treated groups exhibited significantly lower BBB scores compared with the ChABC-treated particle group. Histological results confirmed the induced contusion models in the injured site. Myelin was observed in the treated groups, especially when the ChABC-loaded nanoparticles were utilized. The immunohistochemistry results indicated the scar glial degradation in animals treated by the ChABC-loaded particles. According to this study, the loaded particles can potentially serve as a suitable candidate for spinal cord repair, functional recovery and axonal regeneration.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Chondroitin ABC Lyase - chemistry</subject><subject>Chondroitin ABC Lyase - pharmacology</subject><subject>Chondroitinase ABC</subject><subject>Cicatrix - drug therapy</subject><subject>Locomotion - drug effects</subject><subject>Male</subject><subject>Materials Testing - methods</subject><subject>Nanoparticles - chemistry</subject><subject>Nerve Regeneration - drug effects</subject><subject>OECs</subject><subject>Olfactory Mucosa - pathology</subject><subject>PLGA nanoparticle</subject><subject>Polylactic Acid-Polyglycolic Acid Copolymer - chemistry</subject><subject>Protein delivery</subject><subject>Rats</subject><subject>Recovery of Function - drug effects</subject><subject>Spinal Cord Injuries - drug therapy</subject><subject>Spinal Cord Injuries - pathology</subject><subject>Spinal cord injury</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMtO4zAUhi0EgnJ5BJAfgHTsODezQaUCBqkSLGBtOfYJdZTYkZ1W05fhWXHUDltWx_ovx0cfQteUzCmhxZ92btphLX0_T0kaNcoJK4_QjFYlS1hWFsdoFpUqyWnJztB5CC0hpEgpO0VnjPKckYrO0NdyvXhYJp2TGjR-Wz0vsJXWDdKPRnUQ7vACK9cPHtZgg9kCDuNG77CzuDZucuRoatOZcXeLm41Vo3FWdtiDclvwUZRWY_nvIH6CBS-nDDY2WqaPcu80dNg1OAxmiinndbTbjd9dopNGdgGuDvMCfTw9vi__JqvX55flYpUoVuRjIivO06rMaKFqyHheAGcNSVmlIIMSSl6wUjYqvphOYyZTPGP55Cle11qyC5Tv9yrvQvDQiMHH2_xOUCIm3qIVB95i4i32vGPvZt8bNnUP-qf1H3AM3O8DEK_fGvAiKANWgTYR0Si0M7988Q2poZeM</recordid><startdate>20200315</startdate><enddate>20200315</enddate><creator>Azizi, Monireh</creator><creator>Farahmandghavi, Farhid</creator><creator>Joghataei, Mohammad Taghi</creator><creator>Zandi, Mojgan</creator><creator>Imani, Mohammad</creator><creator>Bakhtiari, Mehrdad</creator><creator>Omidian, Hamid</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2917-2645</orcidid><orcidid>https://orcid.org/0000-0001-5154-0881</orcidid></search><sort><creationdate>20200315</creationdate><title>ChABC-loaded PLGA nanoparticles: A comprehensive study on biocompatibility, functional recovery, and axonal regeneration in animal model of spinal cord injury</title><author>Azizi, Monireh ; Farahmandghavi, Farhid ; Joghataei, Mohammad Taghi ; Zandi, Mojgan ; Imani, Mohammad ; Bakhtiari, Mehrdad ; Omidian, Hamid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Chondroitin ABC Lyase - chemistry</topic><topic>Chondroitin ABC Lyase - pharmacology</topic><topic>Chondroitinase ABC</topic><topic>Cicatrix - drug therapy</topic><topic>Locomotion - drug effects</topic><topic>Male</topic><topic>Materials Testing - methods</topic><topic>Nanoparticles - chemistry</topic><topic>Nerve Regeneration - drug effects</topic><topic>OECs</topic><topic>Olfactory Mucosa - pathology</topic><topic>PLGA nanoparticle</topic><topic>Polylactic Acid-Polyglycolic Acid Copolymer - chemistry</topic><topic>Protein delivery</topic><topic>Rats</topic><topic>Recovery of Function - drug effects</topic><topic>Spinal Cord Injuries - drug therapy</topic><topic>Spinal Cord Injuries - pathology</topic><topic>Spinal cord injury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Azizi, Monireh</creatorcontrib><creatorcontrib>Farahmandghavi, Farhid</creatorcontrib><creatorcontrib>Joghataei, Mohammad Taghi</creatorcontrib><creatorcontrib>Zandi, Mojgan</creatorcontrib><creatorcontrib>Imani, Mohammad</creatorcontrib><creatorcontrib>Bakhtiari, Mehrdad</creatorcontrib><creatorcontrib>Omidian, Hamid</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Azizi, Monireh</au><au>Farahmandghavi, Farhid</au><au>Joghataei, Mohammad Taghi</au><au>Zandi, Mojgan</au><au>Imani, Mohammad</au><au>Bakhtiari, Mehrdad</au><au>Omidian, Hamid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChABC-loaded PLGA nanoparticles: A comprehensive study on biocompatibility, functional recovery, and axonal regeneration in animal model of spinal cord injury</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2020-03-15</date><risdate>2020</risdate><volume>577</volume><spage>119037</spage><pages>119037-</pages><artnum>119037</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted] Spinal Cord Injury (SCI) is one of the leading causes of physical disability. In this study, spherical PLGA nanoparticles (NPs) containing ChABC enzyme were manufactured and fully characterized for SCI therapy. The NPs were used in the rat’s contused spinal cord to assess the functional improvement and scar digestion. Twenty-three adult male Wistar rats (275 ± 25 g) were assigned into four groups of control, sham, blank-treated particle, and ChABC-treated particle. Throughout the survey, the BBB scores were obtained for all the groups. Finally, the injured sections of animals were dissected, and histological studies were conducted using Luxol fast blue and Bielschowsky. The biocompatibility and non-toxicity effects of the NPs on olfactory ensheathing cells (OECs) were confirmed by the MTT test. The flow-cytometry revealed the purity of cultured OECs with p75+/GFAP+ at around 87.9 ± 2.4%. Animals in the control and the blank-treated groups exhibited significantly lower BBB scores compared with the ChABC-treated particle group. Histological results confirmed the induced contusion models in the injured site. Myelin was observed in the treated groups, especially when the ChABC-loaded nanoparticles were utilized. The immunohistochemistry results indicated the scar glial degradation in animals treated by the ChABC-loaded particles. According to this study, the loaded particles can potentially serve as a suitable candidate for spinal cord repair, functional recovery and axonal regeneration.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31953081</pmid><doi>10.1016/j.ijpharm.2020.119037</doi><orcidid>https://orcid.org/0000-0002-2917-2645</orcidid><orcidid>https://orcid.org/0000-0001-5154-0881</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0378-5173
ispartof International journal of pharmaceutics, 2020-03, Vol.577, p.119037, Article 119037
issn 0378-5173
1873-3476
language eng
recordid cdi_crossref_primary_10_1016_j_ijpharm_2020_119037
source Elsevier
subjects Animals
Cells, Cultured
Chondroitin ABC Lyase - chemistry
Chondroitin ABC Lyase - pharmacology
Chondroitinase ABC
Cicatrix - drug therapy
Locomotion - drug effects
Male
Materials Testing - methods
Nanoparticles - chemistry
Nerve Regeneration - drug effects
OECs
Olfactory Mucosa - pathology
PLGA nanoparticle
Polylactic Acid-Polyglycolic Acid Copolymer - chemistry
Protein delivery
Rats
Recovery of Function - drug effects
Spinal Cord Injuries - drug therapy
Spinal Cord Injuries - pathology
Spinal cord injury
title ChABC-loaded PLGA nanoparticles: A comprehensive study on biocompatibility, functional recovery, and axonal regeneration in animal model of spinal cord injury
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T16%3A43%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ChABC-loaded%20PLGA%20nanoparticles:%20A%20comprehensive%20study%20on%20biocompatibility,%20functional%20recovery,%20and%20axonal%20regeneration%20in%20animal%20model%20of%20spinal%20cord%20injury&rft.jtitle=International%20journal%20of%20pharmaceutics&rft.au=Azizi,%20Monireh&rft.date=2020-03-15&rft.volume=577&rft.spage=119037&rft.pages=119037-&rft.artnum=119037&rft.issn=0378-5173&rft.eissn=1873-3476&rft_id=info:doi/10.1016/j.ijpharm.2020.119037&rft_dat=%3Cpubmed_cross%3E31953081%3C/pubmed_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c365t-a899287416cbe4956e93f0238ce4e7e79637afc7e73d26cb4c9435e4e7c9bbda3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/31953081&rfr_iscdi=true