Microsphere and preparation method thereof
Provided is a microsphere including a glass sphere core. The glass sphere core includes a first nuclide, a second nuclide and a diffusion region extending inwardly from an outer surface of the glass sphere core, with the second nuclide distributed in the diffusion region. The first nuclide and the second nuclide become radioactive after being activated by neutrons to produce radiations including β-rays or γ-rays, or simultaneously β-rays and γ-rays. A preparation method of a microsphere is also provided.
1. A microsphere, comprising:
a glass sphere core comprising a first nuclide, a second nuclide, and a diffusion region extending inwardly from an outer surface of the glass sphere core, wherein the size of the diffusion region is less than the size of the glass sphere core,
wherein the first nuclide is distributed throughout the glass sphere core, the second nuclide is only distributed in the diffusion region and not present out of the diffusion region, and the first nuclide and the second nuclide both are capable of being radioactive to produce radiations comprising γ-rays or β-rays, or simultaneously γ-rays and β-rays.
2. The microsphere of claim 1 , further comprising a shell layer coating the glass sphere core.
3. The microsphere of claim 2 , wherein a material of the shell layer comprises one of an organic material, an inorganic material, or a combination thereof.
4. The microsphere of claim 1 , wherein the first nuclide comprises one of yttrium, aluminum, silicon, or a combination thereof.
5. The microsphere of claim 1 , wherein the second nuclide is at least one selected from the group consisting of: phosphorus, calcium, sodium, rhenium, scandium, lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, erbium, thulium, ytterbium, lutetium, actinium, antimony, arsenic, barium, bismuth, californium, carbon, cesium, chromium, cobalt, fluorine, gallium, gold, holmium, hydrogen, indium, iodine, iridium, iron, krypton, molybdenum, nitrogen, oxygen, palladium, radon, radium, rhodium, selenium, strontium, technetium, thallium, xenon and yttrium.
6. The microsphere of claim 3 , wherein the material is an organic material, and the organic material comprises an acid group, a hydroxyl group, an amine group or a biodegradable material.
7. The microsphere of claim 6 , wherein the organic material is at least one selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, carboxymethyl cellulose, methyl cellulose, hydroxypropyl methylcellulose, hydroxypropyl cellulose, polyethylene glycol, gum arabic and a copolymer of polylactic acid and polylactic acid-glycolic acid.
8. The microsphere of claim 3 , wherein the material is an inorganic material, and the inorganic material comprises a phosphate compound, a sulfate compound, a chlorine salt compound, a nitrate compound or a borate compound.
9. The microsphere of claim 3 , wherein the shell layer is further grafted with a radioactive therapeutic agent or a radioactive contrast agent.
10. A method for preparing a microsphere, comprising:
heating glass powder comprising a first nuclide to spheroidize and form a glass sphere core; and
reacting the glass sphere core with a cooling source, wherein the cooling source is a saturated liquid containing a second nuclide liquid phase component with a second nuclide diffused into the glass sphere core by being thermally activated to form a diffusion region extending inwardly from an outer surface of the glass sphere core,
wherein the first nuclide and the second nuclide are capable of being radioactive to produce radiations comprising β-rays or γ-rays, or simultaneously β-rays and γ-rays.
11. The method of claim 10 , further comprising forming a shell layer coating the glass sphere core by a spray process.
12. The method of claim 11 , wherein the shell layer is grafted with a radioactive therapeutic agent or a radioactive contrast agent.