Method for promoting nanoparticles to enter cells efficiently based on nanosecond pulsed electric field
A nanoparticle and pulsed electric field technology, applied in the field of biology, can solve the problems of limiting clinical application and lack of uniform use standards
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Embodiment 1
[0031] Human cervical cancer HeLa cells in the logarithmic growth phase with an adhesion rate of 80% were digested, centrifuged and resuspended into a single cell suspension, and the cell concentration was adjusted to 6×10 by cell counting. 5 cells / mL, proceed as follows:
[0032] 1) Blank control group: without any treatment;
[0033] 2) Individual pulse group: apply nsPEF: parameters are selected as 100ns, 20kV / cm, 10Pulses;
[0034] 3) Magnetic particle treatment group alone: co-incubate with magnetic nanoparticles (final concentration: 4 mg / mL) with an average particle size of about 10 nm in a 6-well plate for 8 hours;
[0035] 4) Combined treatment group: mixed with magnetic nanoparticles (final concentration: 4 mg / mL) with an average particle size of about 10 nm, and after the above nanosecond short pulse treatment, the cells were seeded into a 6-well plate and incubated for 8 hours.
[0036] The cell culture medium inoculated on the 6-well plate was discarded, gentl...
Embodiment 2
[0038] Human normal HaCaT cells in logarithmic growth phase with 80% adherence rate were digested, centrifuged and resuspended into a single cell suspension, and the cell concentration was adjusted to 6×10 by cell counting. 5 cells / mL, proceed as follows:
[0039] 1) Blank control group: without any treatment;
[0040] 2) Individual pulse group: apply nsPEF: parameters are selected as 100ns, 20kV / cm, 10Pulses;
[0041] 3) Magnetic particle treatment group alone: co-incubate with magnetic nanoparticles (final concentration: 4 mg / mL) with an average particle size of about 10 nm in a 6-well plate for 8 hours;
[0042] 4) Combined treatment group: mixed with magnetic nanoparticles (final concentration: 4 mg / mL) with an average particle size of about 10 nm, and after the above nanosecond short pulse treatment, the cells were seeded into a 6-well plate and incubated for 8 hours.
[0043]The cell culture medium inoculated on the 6-well plate was discarded, gently washed with PBS ...
Embodiment 3
[0045] Collect human cervical cancer cell HeLa cells in the logarithmic growth phase with an adhesion rate of 80%, digest, centrifuge and resuspend into a single cell suspension, and adjust the cell concentration to 6×10 for cell counting. 5 Cells / mL were grouped as follows. After the treatment, 3000 cells per well were seeded in 96-well plates, with 3 replicate wells in each group. Place the 96-well plate at 37°C, 5% CO 2 , in an incubator with saturated humidity, after culturing for 24 hours, 10 μL of CCK-8 solution per well was added to a 96-well plate for cell viability detection.
[0046] Experimental group:
[0047] 1) Blank control group: without any treatment;
[0048] 2) Pure alternating magnetic field treatment group: the magnetic field frequency is 287kHz, the current is 35A, and the treatment time is 50min;
[0049] 3) Individual pulse group: apply nsPEF processing with different parameters: 100ns, 10 / 20 / 30kV / cm, 10 / 30Pulses;
[0050] 4) Individual heating grou...
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