Efficient mRNA Delivery with Lyophilized Human Serum Albumin-Based Nanobubbles

被引:5
|
作者
Kida, Hiroshi [1 ]
Yamasaki, Yutaro [1 ]
Feril Jr., Loreto B. B. [1 ]
Endo, Hitomi [1 ]
Itaka, Keiji [2 ]
Tachibana, Katsuro [1 ]
机构
[1] Fukuoka Univ, Fac Med, Dept Anat, 7-45-1 Nanakuma,Jonan Ku, Fukuoka 8140180, Japan
[2] Tokyo Med & Dent Univ TMDU, Inst Biomat & Bioengn, Dept Biofunct Res, 2-3-10 Kanda Surugadai, Tokyo 1010062, Japan
关键词
nanobubble; lyophilization; sonoporation; mRNA; drug delivery system; ultrasound; ULTRASOUND CONTRAST AGENT; LOADED MICROBUBBLES; CAVITATION NUCLEI; GENE DELIVERY; PROTEINS; SONOPORATION; COMBINATION; DESTRUCTION; ENHANCE; CELLS;
D O I
10.3390/nano13071283
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we developed an efficient mRNA delivery vehicle by optimizing a lyophilization method for preserving human serum albumin-based nanobubbles (HSA-NBs), bypassing the need for artificial stabilizers. The morphology of the lyophilized material was verified using scanning electron microscopy, and the concentration, size, and mass of regenerated HSA-NBs were verified using flow cytometry, nanoparticle tracking analysis, and resonance mass measurements, and compared to those before lyophilization. The study also evaluated the response of HSA-NBs to 1 MHz ultrasound irradiation and their ultrasound (US) contrast effect. The functionality of the regenerated HSA-NBs was confirmed by an increased expression of intracellularly transferred Gluc mRNA, with increasing intensity of US irradiation. The results indicated that HSA-NBs retained their structural and functional integrity markedly, post-lyophilization. These findings support the potential of lyophilized HSA-NBs, as efficient imaging, and drug delivery systems for various medical applications.
引用
收藏
页数:18
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