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測(cè)量應(yīng)用案例-20210402

來(lái)源:美國(guó)布魯克海文儀器公司   2021年05月20日 16:08  
 

文獻(xiàn)名:An oligopeptide/aptamer-conjugated dendrimer-based nanocarrier for dual-targeting delivery to bone

 

 

作者 Mingxing Ren,abc   Yuzhou Li,abc   He Zhang,abc   Lingjie Li,abc   Ping He,abc   Ping Jiabc  and  Sheng Yang abc  

a College of Stomatology, Chongqing Medical University, 426 Songshibei Road, Yubei District, Chongqing, China
b Chongqing Key Laboratory of Oral Diseases and Biomedical Sciences, Chongqing, China

c Chongqing Municipal Key Laboratory of Oral Biomedical Engineering of Higher Education, Chongqing, China

 

 

摘要:Bone targeting is one of the most potentially valuable therapeutic methods for medically treating bone diseases, such as osteoarthritis, osteoporosis, nonunion bone defects, bone cancer, and myeloma-related bone disease, but its efficacy remains a challenge due to unfavorable bone biodistribution, off-target effects, and the lack of cell specificity. To address these problems, we synthesized a new dual-targeting nanocarrier for delivery to bone by covalently modifying the G4.0 PAMAM dendrimer with the C11 peptide and the CH6 aptamer (CH6-PAMAM-C11). The molecular structure was confirmed using 1H-NMR and FT-IR spectroscopy. CLSM results showed that the novel nanocarrier could successfully accumulate in the targeted cells, mineralized areas and tissues. DLS and TEM demonstrated that CH6-PAMAM-C11 was approximately 40–50 nm in diameter. In vitro targeting experiments confirmed that the C11 ligand had a high affinity for HAP, while the CH6 aptamer had a high affinity for osteoblasts. The in vivo biodistribution analysis showed that CH6-PAMAM-C11 could rapidly accumulate in bone within 4 h and 12 h and then deliver drugs to sites of osteoblast activity. The components of CH6-PAMAM-C11 were well excreted via the kidneys. The accumulation of many more CH6-PAMAM-C11 dual-targeting nanocarriers than single-targeting nanocarriers was observed in the periosteal layer of the rat skull, along with aggregation at sites of osteoblast activity. All of these results indicate that CH6-PAMAM-C11 may be a promising nanocarrier for the delivery of drugs to bone, particularly for the treatment of osteoporosis, and our research strategy may serve as a reference for research in targeted drug, small molecule drug and nucleic acid delivery.

 

 

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