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Dual targeting nanoparticles for epilepsy therapy

For epilepsy therapy, one-third of the patients worldwide are resistant to antiepileptic drugs mainly due to the existence of the blood–brain barrier (BBB) that prevents the drugs from reaching the epileptic lesions. Here, we design a double targeting nanoparticle carrying lamotrigine (LTG) to cross...

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Autores principales: Hou, Qinghong, Wang, Lulu, Xiao, Feng, Wang, Le, Liu, Xiaoyan, Zhu, Lina, Lu, Yi, Zheng, Wenfu, Jiang, Xingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645397/
https://www.ncbi.nlm.nih.gov/pubmed/36519053
http://dx.doi.org/10.1039/d2sc03298h
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author Hou, Qinghong
Wang, Lulu
Xiao, Feng
Wang, Le
Liu, Xiaoyan
Zhu, Lina
Lu, Yi
Zheng, Wenfu
Jiang, Xingyu
author_facet Hou, Qinghong
Wang, Lulu
Xiao, Feng
Wang, Le
Liu, Xiaoyan
Zhu, Lina
Lu, Yi
Zheng, Wenfu
Jiang, Xingyu
author_sort Hou, Qinghong
collection PubMed
description For epilepsy therapy, one-third of the patients worldwide are resistant to antiepileptic drugs mainly due to the existence of the blood–brain barrier (BBB) that prevents the drugs from reaching the epileptic lesions. Here, we design a double targeting nanoparticle carrying lamotrigine (LTG) to cross the BBB and further concentrate at the neurons. We prepare the nanoparticles on a microfluidic chip by encapsulating LTG in poly(lactic-co-glycolic acid) (PLGA) to form a core (PL) and capping the core with a shell of lipids conjugated with the D-T7 peptide (targeting the BBB) and Tet1 peptide (targeting the neuron) to form D-T7/Tet1-lipids@PL nanoparticles (NPs). In vitro and in vivo experiments show that D-T7/Tet1-lipids@PL NPs have excellent neuron targeting, antiepileptic, and protecting effects. Our approach provides a new strategy for improving the therapeutic efficacy of existing antiepileptic drugs.
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spelling pubmed-96453972022-12-13 Dual targeting nanoparticles for epilepsy therapy Hou, Qinghong Wang, Lulu Xiao, Feng Wang, Le Liu, Xiaoyan Zhu, Lina Lu, Yi Zheng, Wenfu Jiang, Xingyu Chem Sci Chemistry For epilepsy therapy, one-third of the patients worldwide are resistant to antiepileptic drugs mainly due to the existence of the blood–brain barrier (BBB) that prevents the drugs from reaching the epileptic lesions. Here, we design a double targeting nanoparticle carrying lamotrigine (LTG) to cross the BBB and further concentrate at the neurons. We prepare the nanoparticles on a microfluidic chip by encapsulating LTG in poly(lactic-co-glycolic acid) (PLGA) to form a core (PL) and capping the core with a shell of lipids conjugated with the D-T7 peptide (targeting the BBB) and Tet1 peptide (targeting the neuron) to form D-T7/Tet1-lipids@PL nanoparticles (NPs). In vitro and in vivo experiments show that D-T7/Tet1-lipids@PL NPs have excellent neuron targeting, antiepileptic, and protecting effects. Our approach provides a new strategy for improving the therapeutic efficacy of existing antiepileptic drugs. The Royal Society of Chemistry 2022-10-19 /pmc/articles/PMC9645397/ /pubmed/36519053 http://dx.doi.org/10.1039/d2sc03298h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Hou, Qinghong
Wang, Lulu
Xiao, Feng
Wang, Le
Liu, Xiaoyan
Zhu, Lina
Lu, Yi
Zheng, Wenfu
Jiang, Xingyu
Dual targeting nanoparticles for epilepsy therapy
title Dual targeting nanoparticles for epilepsy therapy
title_full Dual targeting nanoparticles for epilepsy therapy
title_fullStr Dual targeting nanoparticles for epilepsy therapy
title_full_unstemmed Dual targeting nanoparticles for epilepsy therapy
title_short Dual targeting nanoparticles for epilepsy therapy
title_sort dual targeting nanoparticles for epilepsy therapy
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645397/
https://www.ncbi.nlm.nih.gov/pubmed/36519053
http://dx.doi.org/10.1039/d2sc03298h
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