Nanoparticle carrier containing TLR3 ligand in PRRs (pattern recognition receptors) as well as preparation method and application of nanoparticle carrier
A technology of pattern recognition receptors and nanoparticles, applied in the field of medicine, can solve the problems of lack of preventive or therapeutic vaccines, and achieve the effect of enhancing the production of interferon and pro-inflammatory factors
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Embodiment 1
[0046] The present embodiment provides a nanoparticle carrier comprising a TLR3 ligand in a pattern recognition receptor, the nanoparticle carrier uses calcium phosphate nanoparticles as a core, the surface of the core is grafted with PEI, and the surface of the core is adsorbed and loaded with Poly(I: C), the outer core is a silica shell, and the silica of the shell is covalently bonded with thiol groups or amino groups.
[0047] The preparation method of the nanoparticle carrier comprising the TLR3 ligand in the pattern recognition receptor includes the following steps:
[0048] The nanoparticles were prepared using the following chemicals: branched polyethylene (PEI), calcium lactate, diammonium phosphate, tetraethoxysilane (TEOS), trimethoxysilane (MPS), triethoxysilane (APTES), cyclohexane-1-carboxylic acid-3-sulfosuccinimide ester (sulfo-SMCC); , ammonia, cross-linked dextran.
[0049] Step 1: Synthesis of stable PEI-calcium phosphate nanoparticles (CaP / PEI)
[0050] I...
Embodiment 2
[0061] The present embodiment provides a nanoparticle carrier comprising a TLR3 ligand in a pattern recognition receptor, the nanoparticle carrier uses calcium phosphate nanoparticles as a core, the surface of the core is grafted with PEI, and the surface of the core is adsorbed and loaded with Poly(I: C), the outer core is a silica shell, and the silica of the shell is covalently bonded with thiol groups.
[0062] The preparation method of the above-mentioned nanoparticle carrier containing the TLR3 ligand in the pattern recognition receptor is basically the same as that of Example 1, the difference is that:
[0063] Step 2: Synthesis of poly(I:C)-loaded CaP / PEI (CaP / PEI / poly(I:C))
[0064] 1 mL of CaP / PEI was mixed with 100 μL of water-soluble poly(I:C)-Cy5 containing fluorescein, and stirred at room temperature for 30 minutes.
[0065] The poly(I:C)-Cy5 used in this example can also be replaced by poly(I:C)-TRITC. Embodiment three
Embodiment 3
[0066] The present embodiment is to CaP / PEI-Cy5 / Poly(I:C) / SiO 2 The cytotoxicity of -SH was tested, and the specific steps included:
[0067] 1.1 Experimental materials:
[0068] 6-well plates were purchased from Thermo NUNC, Denmark
[0069] RPMI1640 (high glucose), fetal bovine serum, penicillin and streptomycin were purchased from Gibco, USA.
[0070] MTT cell proliferation and cytotoxicity kits were purchased from China Biyuntian Company.
[0071] 1.2 Experimental method:
[0072] 1.2.1 Cell culture
[0073] THP-1 cells were mixed with different concentrations of CaP / PEI-FITC / Poly(I:C) / SiO 2 -SH nanoparticles were cultured for 1h / 24h.
[0074] 1.2.2 MTT cytotoxicity test
[0075] Add 10ul of MTT solution (5mg / ml prepared in PBS, pH=7.4) to each well. Continue to incubate for 4h, terminate the culture, and carefully aspirate and discard the culture supernatant in the well. Add 100ul DMSO to each well and shake for 10min to fully dissolve the crystals. Select a wave...
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