Serum albumin nanoparticles combined with fluorescent dyes and coomassie brilliant blue as well as preparation method and application thereof in tumor diagnosis and treatment
A technology of serum albumin and Coomassie brilliant blue, applied in the field of new organic nanomaterials, can solve the problems of undiscovered preparation and application of serum albumin nanoparticles, inability to direct chemotherapy, poor biocompatibility, etc., and achieves important scientific significance. and application value, good biosafety, good effect of histocompatibility
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Embodiment 1
[0035] Embodiment one: if figure 1 , a preparation method of serum albumin nanoparticles combined with fluorescent dye and Coomassie brilliant blue, comprising the following steps:
[0036] S101: Mix the Coomassie Brilliant Blue G250 solution and the human serum albumin (HSA) solution according to the mass ratio of 1:10, and stir and react at 25°C for 7h;
[0037] S102: After ultrafiltration with an ultrafiltration tube with a molecular weight cut-off of 30KD, remove the filtrate, wash twice with dimethyl sulfoxide with a volume of 30%, and disperse with phosphate buffer solution (PBS) to obtain the intermediate product G250-HSA;
[0038] S103: Add 4% by weight fluorescent dye Cy5.5-NHS to the intermediate product G250-HSA, and stir at 25°C for 7h;
[0039] S104: Human serum albumin nanoparticles (Cy5.5-HSA-G250) co-combined with Cy5.5 fluorescent dye and Coomassie Brilliant Blue G250 of the present invention were obtained after 48 hours of dialysis using a dialysis bag with ...
Embodiment 2
[0040] Embodiment 2: A preparation method of serum albumin nanoparticles co-combined with fluorescent dye and Coomassie brilliant blue, comprising the following steps:
[0041] S101: Mix the Coomassie Brilliant Blue G250 solution and the mouse serum albumin (MSA) solution according to the mass ratio of 1:40, and stir and react at 4°C for 15h;
[0042] S102: the ultrafiltration with molecular weight cut-off is 10KD after ultrafiltration, removes filtrate, washes 3 times with its volume 30% dimethylformamide (DMF), uses phosphate buffer solution dispersion (PBS), obtains intermediate product MSA -G250;
[0043] S103: Add 1% by weight fluorescent dye Cy5.5-NHS to the intermediate product MSA-G250, and stir at 4°C for 15h;
[0044] S104: The mouse serum albumin nanoparticles (Cy5.5-MSA-G250) co-bound with Cy5.5 fluorescent dye and Coomassie Brilliant Blue (G250) of the present invention were prepared after dialysis with a dialysis bag with a molecular weight cut-off of 10 kD for ...
Embodiment 3
[0045] Embodiment 3: A preparation method of serum albumin nanoparticles co-combined with fluorescent dye and Coomassie brilliant blue, comprising the following steps:
[0046] S101: Mix the Coomassie Brilliant Blue G250 solution and the bovine serum albumin (BSA) solution according to the mass ratio of 1:5, and stir and react at 50°C for 0.5h;
[0047]S102: the ultrafiltration tube ultrafiltration with a molecular weight cut-off of 50KD afterward, remove the filtrate, wash 3 times with its volume 40% dimethylformamide (DMF), use phosphate buffer solution to disperse (PBS), obtain the intermediate product BSA -G250;
[0048] S103: Add 10% by weight fluorescent dye Cy7-NHS to the intermediate product BSA-G250, and stir at 30°C for 0.5h;
[0049] S104: Bovine serum albumin nanoparticles (Cy7-BSA-G250) co-bound with fluorescent dye Cy7-NHS and Coomassie Brilliant Blue (G250) of the present invention were obtained after 48 h of dialysis using a dialysis bag with a molecular weigh...
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