Delivery agent
a technology of delivery agent and delivery tube, which is applied in the field of delivery tube, can solve the problems of certain limitations in the application or efficacy of all the drugs, whether it is the type of target protein, its pi or molecular weight or the type of cells, and achieve the effects of improving the delivery effect, improving the efficiency of transfection according to the invention, and improving the efficiency of delivery
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example 1
Analysis of the Protein Transfection Using pHP
[0094]Transfection of HeLa (Human cervical carcinoma-derived cell line) cells was carried out as follows: one day before the transfection experiment, the cells were seeded in a 24-well tissue culture plate at the density of 5×104 cells per well in the total volume of 1 ml DMEM culture medium supplemented with 10% FBS. The cells were incubated at 37° C. in a CO2 incubator until they reached 70-80% confluency (usually within 24 h). On the day of transfection, the growth medium was removed and replaced with 0.5 ml of warm serum-free medium. Alexa Fluor 488-labeled goat IgG antibody (1 μg) was diluted in 100 μl of 0.15M NaCl solution and mixed with different amounts of polyanions: DNA (1 μg pUC18), sodium polyphosphate (10 mM pP—1 μl) or sodium polytungstate (10 Mm pW—3 μl). Cationic polymer pHP (1 μl) was added into the protein-polyanion mixture and vortexed immediately for few seconds to ensure even distribution of the material. The comple...
example 2
Analysis of the Protein Localization after Polyanion-Polycation Mediated Transfection
[0095]HeLa cell transfection with β-galactosidase (1 μg) was carried out using the same protocol and conditions as described above. The cells were further fractionated using ProteoJET™ Membrane Protein Extraction Kit (Fermentas) in order to separate membrane and cytoplasmic proteins. The enzymatic activity of β-galactosidase in both fractions was estimated using colorimetric assay.
example 3
Analysis of Different Polyanions in pHP-Mediated Protein Transfections
[0096]Several different polyanions were tested for their ability to improve labelled-IgG transfection. Polyanions were grouped as follows: (i) phosphates—heterophosphates (DNA) and homophosphates (sodium polyphosphate—pP), (ii) POMs—without hetero atom (sodium polytungstate, pW, or ammonium molybdate tetrahydrate, pMo) and with hetero atom (sodium phosphotungstate tribasic hydrate, pWP, and sodium phosphomolybdate hydrate, pMoP). HeLa cells were prepared for transfection essentially as described in Example 1. The amount of each polyanion used was: 3 μl of pW, pWP or pMoP, and 2 μl of pMo (each 10 mM stock concentration), 0.5 μl of pP (30 mM stock concentration), 1 μg of DNA. Polyanion-Antibody-pHP mixtures were incubated for 15 min and added to the cells in a drop-wise manner. Transfection results were processed 2 h later using Guava Easy Cyte Plus flow cytometry system (Millipore).
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