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Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats

BACKGROUND: In this study, neostigmine-loaded electrospun nanofibers were prepared and then their efficacy and duration of analgesic action were studied after epidural administration in rats by repeated tail flick and formalin tests. METHODS: The neostigmine poly vinyl alcohol (PVA) nanofibers were...

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Autores principales: Yosefifard, Masoomeh, Hassanpour-Ezatti, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243326/
https://www.ncbi.nlm.nih.gov/pubmed/25403313
http://dx.doi.org/10.1186/s40199-014-0073-6
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author Yosefifard, Masoomeh
Hassanpour-Ezatti, Majid
author_facet Yosefifard, Masoomeh
Hassanpour-Ezatti, Majid
author_sort Yosefifard, Masoomeh
collection PubMed
description BACKGROUND: In this study, neostigmine-loaded electrospun nanofibers were prepared and then their efficacy and duration of analgesic action were studied after epidural administration in rats by repeated tail flick and formalin tests. METHODS: The neostigmine poly vinyl alcohol (PVA) nanofibers were fabricated by electrospinning methods. The nanofibers (1 mg) were injected into the lumbar epidural space (L5-L6) of rats (n = 6). Cerebrospinal fluid samples of rats were collected 1, 5 and 24 hours after injection and then were sampled once weekly for 4 weeks. Free-neostigmine concentration was measured in the samples spectrophotometrically. Rat nociceptive responses were evaluated by repeated tail-flick and formalin tests for 5 weeks after the nanofibers (1 mg) injection. Locomotor activity of rats was measured in the open-field at the same period. RESULTS: The cerebrospinal fluid concentration of free neostigmine reached 5 μg/ml five hours after injection and remained constant until the end of the experiments. The tail-flick latency of treated rats was significantly (p < 0.01) increased and remained constant up to 4 weeks. Pain scores of the rats in both phases of formalin test were significantly (p < 0.01) reduced during the same periods, Epidural injection of the nanofibers had no effect on locomotor activity of rats in an open-field. CONCLUSIONS: Our results indicate that the neostigmine nanofibers can provide sustained release of neostigmine for induction of prolonged analgesia after epidural administration. High tissue distribution and penetration of the nanofibers in dorsal horn can increase thermal and chemical analgesia duration without altering locomotor activity in rats for 4 weeks.
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spelling pubmed-42433262014-11-26 Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats Yosefifard, Masoomeh Hassanpour-Ezatti, Majid Daru Research Article BACKGROUND: In this study, neostigmine-loaded electrospun nanofibers were prepared and then their efficacy and duration of analgesic action were studied after epidural administration in rats by repeated tail flick and formalin tests. METHODS: The neostigmine poly vinyl alcohol (PVA) nanofibers were fabricated by electrospinning methods. The nanofibers (1 mg) were injected into the lumbar epidural space (L5-L6) of rats (n = 6). Cerebrospinal fluid samples of rats were collected 1, 5 and 24 hours after injection and then were sampled once weekly for 4 weeks. Free-neostigmine concentration was measured in the samples spectrophotometrically. Rat nociceptive responses were evaluated by repeated tail-flick and formalin tests for 5 weeks after the nanofibers (1 mg) injection. Locomotor activity of rats was measured in the open-field at the same period. RESULTS: The cerebrospinal fluid concentration of free neostigmine reached 5 μg/ml five hours after injection and remained constant until the end of the experiments. The tail-flick latency of treated rats was significantly (p < 0.01) increased and remained constant up to 4 weeks. Pain scores of the rats in both phases of formalin test were significantly (p < 0.01) reduced during the same periods, Epidural injection of the nanofibers had no effect on locomotor activity of rats in an open-field. CONCLUSIONS: Our results indicate that the neostigmine nanofibers can provide sustained release of neostigmine for induction of prolonged analgesia after epidural administration. High tissue distribution and penetration of the nanofibers in dorsal horn can increase thermal and chemical analgesia duration without altering locomotor activity in rats for 4 weeks. BioMed Central 2014-11-18 /pmc/articles/PMC4243326/ /pubmed/25403313 http://dx.doi.org/10.1186/s40199-014-0073-6 Text en © Yosefifard and Hassanpour-Ezatti; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yosefifard, Masoomeh
Hassanpour-Ezatti, Majid
Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
title Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
title_full Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
title_fullStr Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
title_full_unstemmed Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
title_short Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
title_sort epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243326/
https://www.ncbi.nlm.nih.gov/pubmed/25403313
http://dx.doi.org/10.1186/s40199-014-0073-6
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