Nano vaccine of LAMP-2 epitope peptide and preparation method of nano vaccine
A technology of LAMP-2, 1.LAMP-2, applied in the field of biomedicine, can solve problems such as failure to find, achieve the effect of enhancing drug efficacy and eliminating spontaneous immune response
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Embodiment 1
[0045] Example 1 loaded with LAMP-2 epitope peptide P 331-341 Preparation of Nanovaccine
[0046] Weigh 5mg of LAMP-2 epitope peptide P with electronic balance 331-341 (purity>95%, Hangzhou Zhongpei Biochemical Co., Ltd.) and 15mg poly(lactic-co-glycolic acid) (LA:GA=50 / 50, sigma), put in a 10ml centrifuge tube, add 0.6ml dichloromethane, and vortex to mix Stir it into a homogeneous mixture, add 6ml of phosphate buffer (pH 6.5) containing 1% polyvinyl alcohol, and place it under the ultrasonic probe for 20s (power 90W, time 20s, pause interval 1s every 3s). Pour the emulsion into 20ml of phosphate buffer solution (pH 6.5) containing 0.3% polyvinyl alcohol, put it into a stirring bar, and stir with a magnetic stirrer for 3 hours at room temperature to evaporate the organic solvent. Pour the emulsion after the organic solvent has evaporated into an EP tube, put it into a centrifuge tube and centrifuge (15000rpm, 10min), pour off the supernatant, add double-distilled water, and...
Embodiment 2
[0047] Example 2 is loaded with LAMP-2 epitope peptide P 41-49 Preparation of Nanovaccine
[0048] Weigh 5mg of LAMP-2 epitope peptide P with electronic balance 41-49 (purity>95%, Hangzhou Zhongpei Biochemical Co., Ltd.) and 15mg poly(lactic-co-glycolic acid) (LA:GA=50 / 50, sigma), put in a 10ml centrifuge tube, add 0.6ml dichloromethane, and vortex to mix Stir it into a homogeneous mixture, add 6ml of phosphate buffer (pH 6.5) containing 1% polyvinyl alcohol, and place it under the ultrasonic probe for 20s (power 90W, time 20s, pause interval 1s every 3s). Pour the emulsion into 20ml of phosphate buffer solution (pH 6.5) containing 0.3% polyvinyl alcohol, put it into a stirring bar, and stir with a magnetic stirrer for 3 hours at room temperature to evaporate the organic solvent. Pour the emulsion after the organic solvent has evaporated into an EP tube, put it into a centrifuge tube and centrifuge (15000rpm, 10min), pour off the supernatant, add double-distilled water, and ...
experiment example 3
[0049] Evaluation of Experimental Example 3 Nano Vaccine
[0050] (1) Morphological observation of the prepared nano-vaccine
[0051] Dilute the nanoparticle suspension washed in Examples 1 and 2 and evenly spread it on the mica sheet. After natural drying, observe the morphology with a scanning electron microscope (S-3400N electron microscope). The test results show that the nanoparticles prepared by the emulsified solvent volatilization method have good spheroidity, good shape and uniform particle size. like figure 1 Shown is the scanning electron micrograph of the nano-vaccine prepared in Example 2.
[0052] (2) Particle size test of the prepared nano-vaccine
[0053] The nanoparticles washed in Examples 1 and 2 were diluted with double distilled water and loaded into the sample cell of a particle size analyzer (Malvern Company) to measure the particle size distribution. The test results show that the particle size of the nanoparticles loaded with epitope peptide is bet...
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