Catechin-Functionalized Cationic Lipopolymer Based Multicomponent Nanomicelles for Lung-Targeting Delivery

© 2023 Wiley‐VCH GmbH.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 17 vom: 31. Apr., Seite e2302985
Auteur principal: Jin, Min (Auteur)
Autres auteurs: Liu, Bangheng, Zhang, Zhen, Mu, Yulei, Ma, Liang, Yao, Hang, Wang, Dong-An
Format: Article en ligne
Langue:English
Publié: 2024
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article bioavailability catechin cationic lipopolymers lung‐targeting delivery nano‐micelle Catechin 8R1V1STN48 Micelles Cations plus... Liposomes Reactive Oxygen Species Polymers Drug Carriers
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520 |a Catechins from green tea are one of the most effective natural compounds for cancer chemoprevention and have attracted extensive research. Cancer cell-selective apoptosis-inducing properties of catechins depend on efficient intracellular delivery. However, the low bioavailability limits the application of catechins. Herein, a nano-scaled micellar composite composed of catechin-functionalized cationic lipopolymer and serum albumin is constructed. Cationic liposomes tend to accumulate in the pulmonary microvasculature due to electrostatic effects and are able to deliver the micellar system intracellularly, thus improving the bioavailability of catechins. Albumin in the system acts as a biocompatible anti-plasma absorbent, forming complexes with positively charged lipopolymer under electrostatic interactions, contributing to prolonged in vivo retention. The physicochemical properties of the nano-micellar complexes are characterized, and the antitumor properties of catechin-functionalized materials are confirmed by reactive oxygen species (ROS), caspase-3, and cell apoptosis measurements. The role of each functional module, cationic polymeric liposome, and albumin is revealed by cell penetration, in vivo animal assays, etc. This multicomponent micellar nanocomposite has the potential to become an effective vehicle for the treatment of lung diseases such as pneumonia, lung tumors, sepsis-induced lung injury, etc. This study also demonstrates that it is a great strategy to create a delivery system that is both tissue-targeted and biologically active by combining cationic liposomes with the native bioactive compound catechins 
650 4 |a Journal Article 
650 4 |a bioavailability 
650 4 |a catechin 
650 4 |a cationic lipopolymers 
650 4 |a lung‐targeting delivery 
650 4 |a nano‐micelle 
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650 7 |a 8R1V1STN48  |2 NLM 
650 7 |a Micelles  |2 NLM 
650 7 |a Cations  |2 NLM 
650 7 |a Liposomes  |2 NLM 
650 7 |a Reactive Oxygen Species  |2 NLM 
650 7 |a Polymers  |2 NLM 
650 7 |a Drug Carriers  |2 NLM 
700 1 |a Liu, Bangheng  |e verfasserin  |4 aut 
700 1 |a Zhang, Zhen  |e verfasserin  |4 aut 
700 1 |a Mu, Yulei  |e verfasserin  |4 aut 
700 1 |a Ma, Liang  |e verfasserin  |4 aut 
700 1 |a Yao, Hang  |e verfasserin  |4 aut 
700 1 |a Wang, Dong-An  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 36(2024), 17 vom: 31. Apr., Seite e2302985  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnas 
773 1 8 |g volume:36  |g year:2024  |g number:17  |g day:31  |g month:04  |g pages:e2302985 
856 4 0 |u http://dx.doi.org/10.1002/adma.202302985  |3 Volltext 
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