COMPARISON OF ACOUSTOFLUIDIC AND STATIC SYSTEMS FOR ULTRASOUND-MEDIATED MOLECULAR DELIVERY TO T LYMPHOCYTES

被引:2
作者
Centner, Connor S. [1 ]
Moore, John T. [1 ]
Baxter, Mary E. [1 ]
Yaddanapudi, Kavitha [2 ]
Bates, Paula J. [3 ]
Kopechek, Jonathan A. [1 ,4 ]
机构
[1] Univ Louisville, Dept Bioengn, Louisville, KY USA
[2] Univ Louisville, Dept Surg, Louisville, KY USA
[3] Univ Louisville, Sch Med, Louisville, KY USA
[4] Univ Louisville, Dept Bioengn, 2301 South Third St,Lutz Hall,Room 419, Louisville, KY 40292 USA
基金
美国国家科学基金会;
关键词
Acoustofluidics; Sonoporation; Drug delivery; fluorescein isothiocyanate; dextran; T lymphocytes; B-CELL; ELECTRIC-FIELD; SONOPORATION; MEMBRANE; DESTRUCTION; ATTENUATION; RECEPTORS; CHILDREN; THERAPY; BLOOD;
D O I
10.1016/j.ultrasmedbio.2022.08.005
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Continuous-flow acoustofluidic technologies can potentially improve processing of T lymphocytes for cell therapies by addressing the limitations with viral and non-viral delivery methods. The objective of this study was to assess the intracellular delivery efficiency with acoustofluidic treatment compared with that of static ultrasound treatment. Optimization of parameters in acoustofluidic and static configurations was performed by assessing intracellular delivery of a fluorescent compound (calcein) in viable human Jurkat T lymphocytes. Ultrasound pressure and the concentration of cationic phospholipid-coated microbubbles influenced calcein delivery in both systems. In the static system, a treatment time of 45 s increased molecular delivery compared with 0-30 s (p < 0.01). Refined parameters were used to assess molecular delivery of small and large compounds (0.6-kDa calcein and 150-kDa fluorescein isothiocyanate- dextran, respectively) after ultrasound treatment with the acoustofluidic or static systems. Molecular delivery was similar with refined parameters for acoustofluidic treatment and static treatment (p > 0.05), even though acoustofluidic treatment had lower microbubble concentration (24 mu g/mL vs. 94 mu g/mL) and shorter treatment time (similar to 2-3 s vs. 45 s). This study indicates that the acoustofluidic system can significantly enhance intracellular molecular delivery, which could potentially enable acoustofluidic cell transfection during continuous flow processing for manufacture of cell therapies or other applications. (c) 2022 World Federation for Ultrasound in Medicine & Biology. All rights reserved.
引用
收藏
页码:90 / 105
页数:16
相关论文
共 61 条
[1]   The Evolution and Future of CAR T Cells for B-Cell Acute Lymphoblastic Leukemia [J].
Annesley, Colleen E. ;
Summers, Corinne ;
Ceppi, Francesco ;
Gardner, Rebecca A. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2018, 103 (04) :591-598
[2]  
Barnkob R., 2009, Proceedings of Meetings on Acoustics, V6, P020001
[3]   Applications of CRISPR technologies in research and beyond [J].
Barrangou, Rodolphe ;
Doudna, Jennifer A. .
NATURE BIOTECHNOLOGY, 2016, 34 (09) :933-941
[4]   Acoustofluidic sonoporation for gene delivery to human hematopoietic stem and progenitor cells [J].
Belling, Jason N. ;
Heidenreich, Liv K. ;
Tian, Zhenhua ;
Mendoza, Alexandra M. ;
Chiou, Tzu-Ting ;
Gong, Yao ;
Chen, Natalie Y. ;
Young, Thomas D. ;
Wattanatorn, Natcha ;
Park, Jae Hyeon ;
Scarabelli, Leonardo ;
Chiang, Naihao ;
Takahashi, Jack ;
Young, Stephen G. ;
Stieg, Adam Z. ;
De Oliveira, Satiro ;
Huang, Tony Jun ;
Weiss, Paul S. ;
Jonas, Steven J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (20) :10976-10982
[5]   EFFECT OF MOLECULAR WEIGHT ON SONOPORATION-MEDIATED UPTAKE IN HUMAN CELLS [J].
Bhutto, Danyal F. ;
Murphy, Emily M. ;
Priddy, Mariah C. ;
Centner, Connor C. ;
Moore, Joseph B. ;
Bolli, Roberto ;
Kopechek, Jonathan A. .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2018, 44 (12) :2662-2672
[6]   Genetically targeted T cells eradicate systemic acute lymphoblastic leukemia xenografts [J].
Brentjens, Renier J. ;
Santos, Elmer ;
Nikhamin, Yan ;
Yeh, Raymond ;
Matsushita, Maiko ;
La Perle, Krista ;
Quintas-Cardama, Alfonso ;
Larson, Steven M. ;
Sadelain, Michel .
CLINICAL CANCER RESEARCH, 2007, 13 (18) :5426-5435
[7]   Forthcoming Lab on a Chip tutorial series on acoustofluidics: Acoustofluidics-exploiting ultrasonic standing wave forces and acoustic streaming in microfluidic systems for cell and particle manipulation [J].
Bruus, Henrik ;
Dual, Jurg ;
Hawkes, Jeremy ;
Hill, Martyn ;
Laurell, Thomas ;
Nilsson, Johan ;
Radel, Stefan ;
Sadhal, Satwindar ;
Wiklund, Martin .
LAB ON A CHIP, 2011, 11 (21) :3579-3580
[8]  
Buzhor E, 2014, REGEN MED, V9, P649, DOI [10.2217/RME.14.35, 10.2217/rme.14.35]
[9]   Contrast agent-free sonoporation: The use of an ultrasonic standing wave microfluidic system for the delivery of pharmaceutical agents [J].
Carugo, Dario ;
Ankrett, Dyan N. ;
Glynne-Jones, Peter ;
Capretto, Lorenzo ;
Boltryk, Rosemary J. ;
Zhang, Xunli ;
Townsend, Paul A. ;
Hill, Martyn .
BIOMICROFLUIDICS, 2011, 5 (04)
[10]  
Centner C.S., 2021, J VISUAL EXP, V167, P62035