肺病
药物输送
医学
粘液
光热治疗
慢性阻塞性肺病
材料科学
化学
内科学
纳米技术
生物物理学
药理学
药品
生物
生态学
作者
Zhibin Li,Guanghong Luo,Weiping Hu,Jian-lan Hua,Shengyong Geng,Paul K. Chu,Jing Zhang,Huaiyu Wang,Xue‐Feng Yu
标识
DOI:10.1002/anie.202008379
摘要
Abstract Chronic obstructive pulmonary disease (COPD) is an intractable disease involving a sticky mucus layer and nanoagents with mucus‐penetrating capability offer a new way to deliver drugs. However, drug release from nanovehicles requires optimization to enhance the therapeutic effects of COPD therapy. Herein, black phosphorus quantum dots (BPQDs) are combined with PEGylated chitosan nanospheres containing the antibiotic amikacin (termed PEG@CS/BPQDs‐AM NPs). As a drug‐delivery system, the hydrophilicity of PEG and positive charge of CS facilitate the penetration of nanovehicles through the mucus layer. The nanovehicles then adhere to the mucous membrane. Furthermore, the BPQDs degrade rapidly into nontoxic PO 4 3− and acidic H + , thereby promoting the dissociation of PEGylated CS nanospheres, accelerating the release of AM, decreasing the vitality of biofilms for ease of eradication. Our results reveal that drug delivery mediated by BPQDs is a feasible and desirable strategy for precision medicine and promising for the clinical therapy of COPD.
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