An Inhalable Hybrid Biomimetic Nanoplatform for Sequential Drug Release and Remodeling Lung Immune Homeostasis in Acute Lung Injury Treatment

纳米载体 急性呼吸窘迫综合征 炎症 免疫系统 免疫学 巨噬细胞极化 化学 脂多糖 巨噬细胞 中性粒细胞胞外陷阱 医学 药理学 癌症研究 药品 内科学 体外 生物化学
作者
Chang Liu,Long Fu Xi,Yihan Liu,Jcw Mak,Shirui Mao,Zhenping Wang,Ying Zheng
出处
期刊:ACS Nano [American Chemical Society]
卷期号:17 (12): 11626-11644 被引量:100
标识
DOI:10.1021/acsnano.3c02075
摘要

Interactions of lung macrophages and recruited neutrophils with the lung microenvironment continuously aggravate the dysregulation of lung inflammation in the pathogenesis of acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). Either modulating macrophages or destroying neutrophil counts cannot guarantee a satisfactory outcome in ARDS treatment. Aimed at inhibiting the coordinated action of neutrophils and macrophages and modulating the hyper-inflammatory condition, an inhalable biomimetic sequential drug-releasing nanoplatform was developed for the combinatorial treatment of ALI. The nanoplatform (termed D-SEL) was made by conjugating DNase I, as outer cleavable arms, to a serum exosomal and liposomal hybrid nanocarrier (termed SEL) via a matrix metalloproteinase 9 (MMP-9)-cleavable peptide and then encapsulating methylprednisolone sodium succinate (MPS). In lipopolysaccharide (LPS) induced ALI in mice, the MPS/D-SEL moved through muco-obstructive airways and was retained in the alveoli for over 24 h postinhalation. DNase I was then released from the nanocarrier first after responding to MMP-9, resulting in inner SEL core exposure, which precisely delivered MPS into macrophages for promoting M2 macrophage polarization. Local and sustained DNase I release degraded dysregulated neutrophil extracellular traps (NETs) and suppressed neutrophil activation and the mucus plugging microenvironment, which in turn amplified M2 macrophage polarization efficiency. Such dual-stage drug release behavior facilitated down-regulation of pro-inflammatory cytokines in the lung but anti-inflammatory cytokine production through remodeling lung immune homeostasis, ultimately promoting lung tissue repair. This work presents a versatile hybrid biomimetic nanoplatform for the local pulmonary delivery of dual-drug therapeutics and displays potential in the treatment of acute inflammation.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
FLL完成签到,获得积分10
4秒前
7秒前
科研小白完成签到,获得积分10
7秒前
cdercder应助向往的鱼采纳,获得10
8秒前
11秒前
鸢尾完成签到,获得积分10
11秒前
Angie完成签到,获得积分10
12秒前
12秒前
giao完成签到 ,获得积分10
13秒前
橙子发布了新的文献求助10
17秒前
wali完成签到 ,获得积分0
17秒前
zzzz完成签到,获得积分10
18秒前
烟花应助FLL采纳,获得10
19秒前
19秒前
zyf完成签到,获得积分10
20秒前
cdercder应助zhaozhuangming采纳,获得10
20秒前
Owen应助简单代芙采纳,获得10
21秒前
YuhangZ完成签到 ,获得积分10
22秒前
善良身影完成签到,获得积分10
23秒前
gg完成签到,获得积分10
29秒前
我想毕业完成签到,获得积分10
30秒前
追寻丹妗完成签到 ,获得积分10
31秒前
所所应助羽宇采纳,获得10
31秒前
miemie66完成签到,获得积分10
31秒前
呼呼完成签到 ,获得积分10
32秒前
whisper应助靓丽夜蕾采纳,获得30
35秒前
Licifer完成签到,获得积分10
36秒前
cym完成签到,获得积分10
36秒前
37秒前
wangcw完成签到 ,获得积分10
39秒前
efficient完成签到,获得积分10
39秒前
39秒前
简单乐荷完成签到,获得积分10
40秒前
big发布了新的文献求助10
43秒前
邓洁宜完成签到,获得积分10
44秒前
keyanlv发布了新的文献求助10
44秒前
Silence完成签到 ,获得积分10
46秒前
靓丽夜蕾完成签到,获得积分10
46秒前
Copyright应助若朴祭司采纳,获得10
47秒前
闪闪的绣连完成签到,获得积分10
54秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Nondestructive Testing Handbook: Vol. 4, Thermal and Infrared Testing (IR), 4th ed 800
Understanding Acculturation: The Process of Cultural Adjustment as Applied to International Migration 700
作者名:Kristopher P. Plain,悉尼大学的,目前只能查到其四篇论文,想找到其博士论文 590
Évora na Idade Média 555
Soil mites of the family Rhagidiidae (Actinedida: Eupodoidea). Morphology, Systematics, Ecology 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7370934
求助须知:如何正确求助?哪些是违规求助? 8978519
关于积分的说明 19087621
捐赠科研通 7012975
什么是DOI,文献DOI怎么找? 3224993
关于科研通互助平台的介绍 2388627
邀请新用户注册赠送积分活动 2205666