2023
DOI: 10.1016/j.jconrel.2023.01.047
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Delivery of macromolecules in unstimulated T cells by photoporation with polydopamine nanoparticles

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Cited by 7 publications
(5 citation statements)
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“…In a follow-up study, we investigated the delivery of 500 kDa FITC-dextran in nonactivated human T cells, finding that smaller BSA@PD NPs of 150 or 250 nm have less impact on T-cell functionality than 400 nm particles. 49 These findings show that photoporation with BSA@PD NPs can be used to deliver compounds in quiescent T cells as well but that the nanoparticles should be small enough to avoid damaging cells too much. Recently, we also reported on the use of a response surface methodology to facilitate finding the optimal parameters for the photoporation of cells with BSA@PD NPs (size, concentration, and laser fluence).…”
Section: Biodegradable Nanoparticlesmentioning
confidence: 88%
See 1 more Smart Citation
“…In a follow-up study, we investigated the delivery of 500 kDa FITC-dextran in nonactivated human T cells, finding that smaller BSA@PD NPs of 150 or 250 nm have less impact on T-cell functionality than 400 nm particles. 49 These findings show that photoporation with BSA@PD NPs can be used to deliver compounds in quiescent T cells as well but that the nanoparticles should be small enough to avoid damaging cells too much. Recently, we also reported on the use of a response surface methodology to facilitate finding the optimal parameters for the photoporation of cells with BSA@PD NPs (size, concentration, and laser fluence).…”
Section: Biodegradable Nanoparticlesmentioning
confidence: 88%
“…This means that the overall yield of living transfected T cells was ∼20%, being 2.5-fold larger than what could be achieved with electroporation as a benchmark technology. In a follow-up study, we investigated the delivery of 500 kDa FITC-dextran in nonactivated human T cells, finding that smaller BSA@PD NPs of 150 or 250 nm have less impact on T-cell functionality than 400 nm particles . These findings show that photoporation with BSA@PD NPs can be used to deliver compounds in quiescent T cells as well but that the nanoparticles should be small enough to avoid damaging cells too much.…”
Section: Single Photothermal Nanostructuresmentioning
confidence: 99%
“…[167][168][169] To overcome this problem, PDA NPs were developed and successfully used for photoporation because they are biocompatible and biodegradable. 170,171 However, further studies are required to validate their in vivo degradation process, which is yet not fully understood. 172 For more elaborate information regarding these PSs and their applications for photoporation, we refer readers to a recent review article published by Xiong et al 23 In this context, single small molecules can be promising due to their small molecular structure making their degradation easier for the body.…”
Section: Photoablation Of Biological Aggregates and Barriers Using Dyesmentioning
confidence: 99%
“…It has been displayed that fragmented gold NPs can potentially intercalate with DNA and induce genotoxicity 167–169 . To overcome this problem, PDA NPs were developed and successfully used for photoporation because they are biocompatible and biodegradable 170,171 . However, further studies are required to validate their in vivo degradation process, which is yet not fully understood 172 .…”
Section: Biomedical Applications Of Dyesmentioning
confidence: 99%
“…[32][33][34] In recent years, researchers have discovered that PDA has an excellent photothermal property, i.e., the ability to generate heat in the presence of light. 35,36 This special property makes PDA an ideal material for photothermal conversion. These properties give PDA a wide range of application prospects in the elds of photothermal therapy, photothermal conversion and photothermal catalysis.…”
Section: Introductionmentioning
confidence: 99%