Development of a custom biological scaffold for investigating ultrasound-mediated intracellular delivery

被引:4
|
作者
Bui, Loan [1 ]
Aleid, Adham [2 ]
Alassaf, Ahmad [3 ,4 ]
Wilson, Otto C. [5 ]
Raub, Christopher B. [5 ]
Frenkel, Victor [6 ,7 ]
机构
[1] Univ Texas Arlington, Dept Bioengn, Arlington, TX 76010 USA
[2] King Saud Univ, Dept Biomed Technol, Riyadh 12372, Saudi Arabia
[3] Univ Miami, Dept Biomed Engn, Coral Gables, FL 33146 USA
[4] Majmaah Univ, Dept Med Equipment Technol, Majmaah City 11952, Saudi Arabia
[5] Catholic Univ Amer, Dept Biomed Engn, Washington, DC 20064 USA
[6] Univ Maryland, Sch Med, Dept Diagnost Radiol & Nucl Med, Baltimore, MD 21201 USA
[7] Univ Maryland, Sch Med, Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA
关键词
Intracellular drug delivery; Biological Scaffolds; Ultrasound; Reflections; Inertial cavitation; Sonoporation; CHITOSAN-GELATIN SCAFFOLDS; GENE-THERAPY; CELLULAR UPTAKE; CELLS; SONOPORATION; DNA; SYSTEMS; PLASMID; ELECTROPORATION; NANOPARTICLES;
D O I
10.1016/j.msec.2016.09.029
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
In vitro investigations of ultrasound mediated, intracellular drug and gene delivery (i.e. sonoporation) are typically carried out in cells cultured in standard plastic well plates. This creates conditions that poorly resemble in vivo conditions, as well as generating unwanted ultrasound phenomena that may confound the interpretation of results. Here, we present our results in the development of a biological scaffold for sonoporation studies. The scaffolds were comprised of cellulose fibers coated with chitosan and gelatin. Scaffold formulation was optimized for adherence and proliferation of mouse fibroblasts in terms of the ratio and relative concentration of the two constituents. The scaffolds were also shown to significantly reduce ultrasound reflections compared to the plastic well plates. A custom treatment chamber was designed and built and the occurrence of acoustic cavitation in the chamber during the ultrasound treatments was detected; a requirement for the process of sonoporation. Finally, experiments were carried out to optimize the ultrasound, exposures to minimize cellular damage. Ultrasound exposure was then shown to enable the uptake of 100 nm fluorescently labeled polystyrene nanoparticles in suspension into the cells seeded on scaffolds, compared to incubation of cell-seeded scaffolds with nanoparticles alone. These preliminary results set the basis for further development of this platform. They also provide motivation for the development of similar platforms for the controlled investigation of other ultrasound mediated cell and tissue therapies. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:461 / 470
页数:10
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