Cargando…

Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease

Targeted therapy of Parkinson’s disease is an important challenge because of the blood–brain barrier limitation. Here, we propose a natural killer cell membrane biomimetic nanocomplex (named BLIPO-CUR) delivered via the meningeal lymphatic vessel (MLV) route to further the therapeutic efficacy of Pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Jing, Gao, Duyang, Hu, Dehong, Lan, Siyi, Liu, Yu, Zheng, Hairong, Yuan, Zhen, Sheng, Zonghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAAS 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076012/
https://www.ncbi.nlm.nih.gov/pubmed/37040500
http://dx.doi.org/10.34133/research.0030
_version_ 1785020043439898624
author Liu, Jing
Gao, Duyang
Hu, Dehong
Lan, Siyi
Liu, Yu
Zheng, Hairong
Yuan, Zhen
Sheng, Zonghai
author_facet Liu, Jing
Gao, Duyang
Hu, Dehong
Lan, Siyi
Liu, Yu
Zheng, Hairong
Yuan, Zhen
Sheng, Zonghai
author_sort Liu, Jing
collection PubMed
description Targeted therapy of Parkinson’s disease is an important challenge because of the blood–brain barrier limitation. Here, we propose a natural killer cell membrane biomimetic nanocomplex (named BLIPO-CUR) delivered via the meningeal lymphatic vessel (MLV) route to further the therapeutic efficacy of Parkinson’s disease. The membrane incorporation enables BLIPO-CUR to target the damaged neurons, thus improving their therapeutic efficacy through clearing reactive oxygen species, suppressing the aggregation of α-synuclein, and inhibiting the spread of excess α-synuclein species. Compared with the conventional intravenous injection, this MLV administration can enhance the delivered efficiency of curcumin into the brain by ~20 folds. The MLV route administration of BLIPO-CUR enhances the treatment efficacy of Parkinson’s disease in mouse models by improving their movement disorders and reversing neuron death. Our findings highlight the great potential of MLV route administration used as targeted delivery of drugs to the brain, holding a great promise for neurodegenerative disease therapy.
format Online
Article
Text
id pubmed-10076012
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher AAAS
record_format MEDLINE/PubMed
spelling pubmed-100760122023-04-06 Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease Liu, Jing Gao, Duyang Hu, Dehong Lan, Siyi Liu, Yu Zheng, Hairong Yuan, Zhen Sheng, Zonghai Research (Wash D C) Research Article Targeted therapy of Parkinson’s disease is an important challenge because of the blood–brain barrier limitation. Here, we propose a natural killer cell membrane biomimetic nanocomplex (named BLIPO-CUR) delivered via the meningeal lymphatic vessel (MLV) route to further the therapeutic efficacy of Parkinson’s disease. The membrane incorporation enables BLIPO-CUR to target the damaged neurons, thus improving their therapeutic efficacy through clearing reactive oxygen species, suppressing the aggregation of α-synuclein, and inhibiting the spread of excess α-synuclein species. Compared with the conventional intravenous injection, this MLV administration can enhance the delivered efficiency of curcumin into the brain by ~20 folds. The MLV route administration of BLIPO-CUR enhances the treatment efficacy of Parkinson’s disease in mouse models by improving their movement disorders and reversing neuron death. Our findings highlight the great potential of MLV route administration used as targeted delivery of drugs to the brain, holding a great promise for neurodegenerative disease therapy. AAAS 2023-01-30 2023 /pmc/articles/PMC10076012/ /pubmed/37040500 http://dx.doi.org/10.34133/research.0030 Text en Copyright © 2023 Jing Liu et al. https://creativecommons.org/licenses/by/4.0/Exclusive licensee Science and Technology Review Publishing House. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY 4.0) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Liu, Jing
Gao, Duyang
Hu, Dehong
Lan, Siyi
Liu, Yu
Zheng, Hairong
Yuan, Zhen
Sheng, Zonghai
Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease
title Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease
title_full Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease
title_fullStr Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease
title_full_unstemmed Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease
title_short Delivery of Biomimetic Liposomes via Meningeal Lymphatic Vessels Route for Targeted Therapy of Parkinson’s Disease
title_sort delivery of biomimetic liposomes via meningeal lymphatic vessels route for targeted therapy of parkinson’s disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076012/
https://www.ncbi.nlm.nih.gov/pubmed/37040500
http://dx.doi.org/10.34133/research.0030
work_keys_str_mv AT liujing deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT gaoduyang deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT hudehong deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT lansiyi deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT liuyu deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT zhenghairong deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT yuanzhen deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease
AT shengzonghai deliveryofbiomimeticliposomesviameningeallymphaticvesselsroutefortargetedtherapyofparkinsonsdisease