Macrophage membrane (MMs) camouflaged near-infrared (NIR) responsive bone defect area targeting nanocarrier delivery system (BTNDS) for rapid repair: promoting osteogenesis via phototherapy and modulating immunity

Bibliographic Details
Title: Macrophage membrane (MMs) camouflaged near-infrared (NIR) responsive bone defect area targeting nanocarrier delivery system (BTNDS) for rapid repair: promoting osteogenesis via phototherapy and modulating immunity
Authors: Peng Xue, Zhiyong Chang, Hao Chen, Hongzhong Xi, Xiaoxue Tan, Shuai He, Haishi Qiao, Xiaohong Jiang, Xin Liu, Bin Du
Source: Journal of Nanobiotechnology, Vol 22, Iss 1, Pp 1-23 (2024)
Publisher Information: BMC, 2024.
Publication Year: 2024
Collection: LCC:Biotechnology
LCC:Medical technology
Subject Terms: Bone defect targeting, Black phosphorus nanosheets, Anti-inflammation, Osteogenesis, Phototherapy, Biotechnology, TP248.13-248.65, Medical technology, R855-855.5
More Details: Abstract Bone defects remain a significant challenge in clinical orthopedics, but no targeted medication can solve these problems. Inspired by inflammatory targeting properties of macrophages, inflammatory microenvironment of bone defects was exploited to develop a multifunctional nanocarrier capable of targeting bone defects and promoting bone regeneration. The avidin-modified black phosphorus nanosheets (BP-Avidin, BPAvi) were combined with biotin-modified Icaritin (ICT-Biotin, ICTBio) to synthesize Icaritin (ICT)-loaded black phosphorus nanosheets (BPICT). BPICT was then coated with macrophage membranes (MMs) to obtain MMs-camouflaged BPICT (M@BPICT). Herein, MMs allowed BPICT to target bone defects area, and BPICT accelerated the release of phosphate ions (PO4 3−) and ICT when exposed to NIR irradiation. PO4 3− recruited calcium ions (Ca2+) from the microenvironment to produce Ca3(PO4)2, and ICT increased the expression of osteogenesis-related proteins. Additionally, M@BPICT can decrease M1 polarization of macrophage and expression of pro-inflammatory factors to promote osteogenesis. According to the results, M@BPICT provided bone growth factor and bone repair material, modulated inflammatory microenvironment, and activated osteogenesis-related signaling pathways to promote bone regeneration. PTT could significantly enhance these effects. This strategy not only offers a solution to the challenging problem of drug-targeted delivery in bone defects but also expands the biomedical applications of MMs-camouflaged nanocarriers. Graphical Abstract
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1477-3155
Relation: https://doaj.org/toc/1477-3155
DOI: 10.1186/s12951-024-02351-5
Access URL: https://doaj.org/article/b52d934e7912452eb4db52e84518aab5
Accession Number: edsdoj.b52d934e7912452eb4db52e84518aab5
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:14773155
DOI:10.1186/s12951-024-02351-5
Published in:Journal of Nanobiotechnology
Language:English