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Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine

PURPOSE: Nose-to-brain drug delivery is an effective approach for poorly soluble drugs to bypass the blood–brain barrier. A new drug intranasal delivery system, a nanosuspension-based in situ gel, was developed and evaluated to improve the solubility and bioavailability of the drug and to prolong it...

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Autores principales: Chen, Yingchong, Liu, Yuling, Xie, Jin, Zheng, Qin, Yue, Pengfei, Chen, Liru, Hu, Pengyi, Yang, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767747/
https://www.ncbi.nlm.nih.gov/pubmed/33380794
http://dx.doi.org/10.2147/IJN.S265659
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author Chen, Yingchong
Liu, Yuling
Xie, Jin
Zheng, Qin
Yue, Pengfei
Chen, Liru
Hu, Pengyi
Yang, Ming
author_facet Chen, Yingchong
Liu, Yuling
Xie, Jin
Zheng, Qin
Yue, Pengfei
Chen, Liru
Hu, Pengyi
Yang, Ming
author_sort Chen, Yingchong
collection PubMed
description PURPOSE: Nose-to-brain drug delivery is an effective approach for poorly soluble drugs to bypass the blood–brain barrier. A new drug intranasal delivery system, a nanosuspension-based in situ gel, was developed and evaluated to improve the solubility and bioavailability of the drug and to prolong its retention time in the nasal cavity. MATERIALS AND METHODS: Breviscapine (BRE) was chosen as the model drug. BRE nanosuspensions (BRE-NS) were converted into BRE nanosuspension powders (BRE-NP). A BRE nanosuspension in situ gelling system (BRE-NG) was prepared by mixing BRE-NP and 0.5% gellan gum (m/v). First, the BRE-NP were evaluated in terms of particle size and by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Subsequently, the critical ionic concentration of the gellan gum phase transition, influence of the deacetylated gellan gum (DGG) concentration on the expansion coefficient (S%), water-holding capacity, rheological properties and in vitro release behaviour of the BRE-NG were investigated. The pharmacokinetics and brain distribution of the BRE-NG after intranasal administration were compared with those of the intravenously injected BRE-NP nanosuspensions in rats. RESULTS: The rheology results demonstrated that BRE-NG was a non-Newtonian fluid with good spreadability and bioadhesion performance. Moreover, the absolute bioavailability estimated for BRE-NG after intranasal administration was 57.12%. The drug targeting efficiency (DTE%) of BRE in the cerebrum, cerebellum and olfactory bulb was 4006, 999 and 3290, respectively. The nose-to-brain direct transport percentage (DTP%) of the cerebrum, cerebellum and olfactory bulb was 0.975, 0.950 and 0.970, respectively. CONCLUSION: It was concluded that the in situ gel significantly increased the drug retention time at the administration site. Therefore, the nanosuspension-based in situ gel could be a convenient and effective intranasal formulation for the administration of BRE.
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spelling pubmed-77677472020-12-29 Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine Chen, Yingchong Liu, Yuling Xie, Jin Zheng, Qin Yue, Pengfei Chen, Liru Hu, Pengyi Yang, Ming Int J Nanomedicine Original Research PURPOSE: Nose-to-brain drug delivery is an effective approach for poorly soluble drugs to bypass the blood–brain barrier. A new drug intranasal delivery system, a nanosuspension-based in situ gel, was developed and evaluated to improve the solubility and bioavailability of the drug and to prolong its retention time in the nasal cavity. MATERIALS AND METHODS: Breviscapine (BRE) was chosen as the model drug. BRE nanosuspensions (BRE-NS) were converted into BRE nanosuspension powders (BRE-NP). A BRE nanosuspension in situ gelling system (BRE-NG) was prepared by mixing BRE-NP and 0.5% gellan gum (m/v). First, the BRE-NP were evaluated in terms of particle size and by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Subsequently, the critical ionic concentration of the gellan gum phase transition, influence of the deacetylated gellan gum (DGG) concentration on the expansion coefficient (S%), water-holding capacity, rheological properties and in vitro release behaviour of the BRE-NG were investigated. The pharmacokinetics and brain distribution of the BRE-NG after intranasal administration were compared with those of the intravenously injected BRE-NP nanosuspensions in rats. RESULTS: The rheology results demonstrated that BRE-NG was a non-Newtonian fluid with good spreadability and bioadhesion performance. Moreover, the absolute bioavailability estimated for BRE-NG after intranasal administration was 57.12%. The drug targeting efficiency (DTE%) of BRE in the cerebrum, cerebellum and olfactory bulb was 4006, 999 and 3290, respectively. The nose-to-brain direct transport percentage (DTP%) of the cerebrum, cerebellum and olfactory bulb was 0.975, 0.950 and 0.970, respectively. CONCLUSION: It was concluded that the in situ gel significantly increased the drug retention time at the administration site. Therefore, the nanosuspension-based in situ gel could be a convenient and effective intranasal formulation for the administration of BRE. Dove 2020-12-23 /pmc/articles/PMC7767747/ /pubmed/33380794 http://dx.doi.org/10.2147/IJN.S265659 Text en © 2020 Chen et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Chen, Yingchong
Liu, Yuling
Xie, Jin
Zheng, Qin
Yue, Pengfei
Chen, Liru
Hu, Pengyi
Yang, Ming
Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine
title Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine
title_full Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine
title_fullStr Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine
title_full_unstemmed Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine
title_short Nose-to-Brain Delivery by Nanosuspensions-Based in situ Gel for Breviscapine
title_sort nose-to-brain delivery by nanosuspensions-based in situ gel for breviscapine
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767747/
https://www.ncbi.nlm.nih.gov/pubmed/33380794
http://dx.doi.org/10.2147/IJN.S265659
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