Embolic agent as well as preparation method thereof
A technology of embolic agents and liposomes, applied in the field of pharmaceuticals for the treatment of liver cancer, can solve the problems of being easily taken out of the embolism area, difficult to find/treat, and no synergistic comprehensive application, etc., to achieve good embolism stability and biological safety. Effect
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Embodiment 1
[0025] Embolic agent of the present invention is made by following method:
[0026] (1) Synthetic package has 131 Liposomes of I-iodol and magnetic nanoparticles;
[0027] (1a) the oil-soluble F e3 o 4 Nanoparticles dispersed in 131 In I-iodol, a mixed solution is formed;
[0028] (1b) Add the mixed solution described in step (1a) as an oil phase to the aqueous phase containing aminated polyethylene glycol (PEG) monostearate, and stir for 30 minutes to form a colostrum cloudy solution;
[0029] (1c) Ultrasonic the colostrum turbid liquid described in step (1b) for 5 minutes with an ultrasonic breaker, and the colostrum turbid liquid is converted into a stable oil-in-water nanoemulsion, finally obtaining a suitable size, good uniformity, good stability, Transparent and clear magnetic with high biocompatibility 131 I-iodol nanoemulsion; the magnetic 131 I-iodol nanoemulsion is coated with magnetic nanoparticles and 131 The liposome of 1-iodol, its particle diameter is 10...
Embodiment 2
[0036] Embolic agent of the present invention is made by following method:
[0037] (1) Synthetic package has 131 Liposomes of I-iodol and magnetic nanoparticles;
[0038] (1a) the oil-soluble γ -Fe 2 o 3 The nanoparticles are dispersed in the iodine-131 carburetion injection to form a mixed solution;
[0039] (1b) adding the mixed solution described in step (1a) as an oil phase into an aqueous phase containing carboxylated polyethylene glycol (PEG) monostearate, stirring for 60 min to form a colostrum turbid solution;
[0040] (1c) Ultrasonic the colostrum turbid liquid described in step (1b) for 30 minutes with an ultrasonic breaker, and the colostrum turbid liquid is converted into a stable oil-in-water nanoemulsion, finally obtaining a suitable size, good uniformity, good stability, Transparent and clear magnetic with high biocompatibility 131 I-iodol nanoemulsion; the magnetic 131 I-iodol nanoemulsion is coated with magnetic nanoparticles and 131 The liposome of 1...
Embodiment 3
[0047] The average survival rate of 30 patients with liver cancer (not receiving any treatment) was selected as the control group. 125 The survival rate of patients with liver cancer after interventional therapy with I-iodol embolism was used as the control group 2. 131 I-iodine's metuximab injection carries out the survival rate of patients with liver cancer after radioimmunotherapy as a control group 3, and the survival rate of patients with liver cancer after the embolization agent (embodiment 1) interventional therapy provided by the present invention is used as an experimental group .
[0048] Efficacy comparison: experimental data shows that the survival rate of liver cancer patients (liver cancer patients who survived to 24 months) in the control group is less than 10%. 131 The survival rate of patients with liver cancer after I-iodine metuximab treatment (liver cancer patients who survived to 24 months) was less than 50%, using 125 The survival rate of liver cancer p...
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