Mannose functionalized protein gold nano-cluster, and preparation method and application thereof
A mannose, protein gold technology, applied in chemical instruments and methods, nanotechnology for materials and surface science, nanotechnology, etc., can solve the problem of gold nanoclusters with toxicity, limited application and poor biocompatibility And other issues
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Embodiment 1
[0059] Example 1 provides a method for preparing protein gold nanoclusters functionalized with mannose, the method comprising: mixing 100 mg of bovine serum albumin, 30 mg of NH 2 - Mannose and 10 mg of EDC were sequentially added to 5 ml of phosphate buffer solution with a pH value of 7, stirred at 25 degrees Celsius for 12 hours, purified with an ultrafiltration tube with a molecular weight cut-off of 10 kDa, and then concentrated to obtain mannose- Bovine Serum Albumin Conjugate. The mannose-bovine serum albumin conjugate was redissolved in 2 ml of phosphate buffer, and 3 ml of chloroauric acid solution with a concentration of 8 mmol was added. After stirring for 2 minutes, 200 microliters of a concentration of 1 mol / L of sodium hydroxide solution, adjust the pH value to 11, stir at 37 degrees Celsius for 12 hours, purify and concentrate with an ultrafiltration tube with a molecular weight cut-off of 10kDa to obtain protein gold nanoclusters, and disperse the protein gold ...
Embodiment 2
[0062] Example 2 provides a method for preparing mannose-functionalized protein gold nanoclusters, the method comprising: 90 mg of bovine serum albumin, 30 mg of NH 2 -Mannose and 10 mg of EDC were sequentially added to 5 ml of 4-hydroxyethylpiperazineethanesulfonic acid buffer with a pH value of 7, stirred at 30 °C for 14 hours, and then filtered with an ultrafiltration tube with a molecular weight cut-off of 10 kDa Concentrate after purification to obtain mannose-bovine serum albumin conjugate. Re-dissolve the mannose-bovine serum albumin conjugate in 3 ml of 4-hydroxyethylpiperazineethanesulfonic acid buffer, add 3 ml of chloroauric acid solution with a concentration of 9 mmol, stir for 2 minutes, and then Add 200 microliters of sodium hydroxide solution with a concentration of 1mol / L, adjust the pH value to 10, stir at 38 degrees Celsius for 15 hours, purify with an ultrafiltration tube with a molecular weight cut-off of 10kDa, and concentrate to obtain protein gold nanocl...
Embodiment 3
[0065] Example 3 provides a method for preparing mannose-functionalized protein gold nanoclusters, the method comprising: mixing 110 mg of bovine serum albumin, 30 mg of NH 2 - Mannose and 10 mg of EDC were sequentially added to 5 ml of phosphate buffer with a pH value of 7, stirred at 35 degrees Celsius for 11 hours, purified with an ultrafiltration tube with a molecular weight cut-off of 10 kDa, and then concentrated to obtain mannose- Bovine Serum Albumin Conjugate. Redissolve the mannose-bovine serum albumin conjugate in 2 ml of phosphate buffer, add 3 ml of a 10 mmol / m chloroauric acid solution, stir for 2 minutes, then add 200 μl of a 1 mol / L of sodium hydroxide solution, adjust the pH value to 10, stir at 30 degrees Celsius for 14 hours, purify and concentrate with an ultrafiltration tube with a molecular weight cut-off of 10kDa to obtain protein gold nanoclusters, and disperse the protein gold nanoclusters in 5 ml of phosphate buffer.
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