Adsorption material for blood purification and preparation method thereof
An adsorption material and blood purification technology, applied in chemical instruments and methods, blood circulation treatment, other chemical processes, etc., can solve problems such as poor blood compatibility, hidden dangers to patient health and safety, and destruction of formed components, and achieve stereoselectivity Strong, personalized and functional, simple reaction conditions
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Embodiment 1
[0053] Synthesis of adsorbent materials for blood purification by photoinitiated polymerization:
[0054] 1. Synthesis of low-density lipoprotein adsorption material
[0055] (1) Add 18wt% sodium hydroxide solution to the resin, pretreat at 20°C for 24 hours, then filter and rinse until the rinse solution is neutral, and dry in the air;
[0056] (2) Under the condition of 4 ℃ and dark, soak the resin obtained in step (1) with 0.10wt% photoinitiator Quantacure BTC and 0.10wt% acrylic acid monomer solution for 4h, then suction filter to obtain the photoinitiator deposited on the surface and acrylic resins;
[0057] (3) Place the resin with photoinitiator and acrylic acid deposited on the surface of the obtained step (2) in the photoreactor, form a 1.0cm thick resin layer at the bottom of the photoreactor, then add a quartz glass upper cover, and deoxygenate with nitrogen for 8min After that, turn on the UV light for 20 minutes;
[0058] (4) Soak in water to clean the resin ob...
Embodiment 2
[0065] Synthesis of Adsorbent Materials for Blood Purification by Plasma Jet Deposition:
[0066] Resin as a carrier
[0067] 1. Activated resin
[0068] on the resin surface by using NH 3 Plasma polymerization method (Plasma Science, USA, Type PS 0350 Plasma Surface Treatment System) for modification, code number PD-0.
[0069] The amount of primary amines on the surface of the obtained resin was determined by trinitrotoluene sulfonate (TNBS) assay.
[0070] 2. Synthetic protein A immunoadsorbent material
[0071] The resin PD-0 was added to a mixed solution of 0.25 times the mass of glutaraldehyde and 2 times the mass of 0.2M phosphate buffer (pH 7.4), and reacted at 37° C. and 120 rpm for 3 hours. After washing with pH 7.4, 0.1M phosphate buffer, add the resin to borate buffer containing 3M mercapto-ammonium acid ammonium of SPA 3mg / mL, pH 8.2, 37℃, 120rpm for 24h, and then use pH7 .4. Wash with 0.1M phosphate buffer, and finally use NaBH 3 The double bond generated d...
Embodiment 3
[0093] Mercapto-ene click reaction synthesis of adsorbent materials for blood purification:
[0094] Resin as a carrier
[0095] 1. Ligand thiolation
[0096] First activate cysteine, add 1eq cysteine, 2-(7-azobenzotriazole)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HATU, 2eq ) as condensing agent, N,N-diisopropylethylamine (DIPEA) (4eq) as base, N,N-dimethylformamide (DMF) as solvent, react at room temperature, and then add 2eq amino group The ligand (n-butylamine, polymyxin B sulfate, colistin B, lysozyme) was reacted for 6 hours to obtain the thiolated ligand, numbered QX-0.
[0097] 2. Synthesis of Bilirubin Adsorbent Material
[0098] 2g of mercaptolated n-butylamine was dissolved in 20ml of absolute ethanol, 2mg of photoinitiator was added, and then added to the resin after swelling and suction filtration washing with ethylene dichloride (in the system, the carbon-carbon double bond and thiol The molar ratio is 1:1), light reaction under 254nm ultraviolet lig...
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