Self-assembled calcium pyrophosphate nanostructures for targeted molecular delivery

被引:7
作者
Bassett, David C. [1 ]
Robinson, Thomas E. [1 ]
Hill, Reghan J. [2 ]
Grover, Liam M. [1 ]
Barralet, Jake E. [3 ]
机构
[1] Univ Birmingham, Healthcare Technol Inst, Sch Chem Engn, Birmingham, England
[2] McGill Univ, Dept Chem Engn, Montreal, PQ, Canada
[3] McGill Univ, Dept Dent, Montreal, PQ, Canada
来源
BIOMATERIALS ADVANCES | 2022年 / 140卷
关键词
Calcium pyrophosphate; Nanofibre microsphere; Nanotube; Self; -assembly; Drug delivery; BIODEGRADABLE POLYMERIC MICROSPHERES; DRUG-DELIVERY; MICROPARTICLES; BIOMATERIALS; DISSOLUTION; CHALLENGES; RELEASE;
D O I
10.1016/j.bioadv.2022.213086
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Nanostructured, inorganic microspheres have many industrial applications, including catalysis, electronics, and particularly drug delivery, with several advantages over their organic counterparts. However, many current production methods require high energy input, use of harmful chemicals, and extensive processing. Here, the self-assembly of calcium pyrophosphate into nanofibre microspheres is reported. This process takes place at ambient temperature, with no energy input, and only salt water as a by-product. The formation of these materials is examined, as is the formation of nanotubes when the system is agitated, from initial precipitate to crystallisation. A mechanism of formation is proposed, whereby the nanofibre intermediates are formed as the system moves from kinetically favoured spheres to thermodynamically stable plates, with a corresponding increase in aspect ratio. The functionality of the nanofibre microspheres as targeted enteric drug delivery vehicles is then demonstrated in vitro and in vivo, showing that the microspheres can pass through the stomach while protecting the activity of a model protein, then release their payload in intestinal conditions.
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页数:10
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