METHOD FOR PREPARING A RADIONUCLIDE-COATED MICROSPHERE

Abstract

A process for delivering a radionuclide material is provided in which the radionuclide, such as holmium oxide, is coated on a glass microsphere. A coating, preferably a dipodal polysiloxane, is applied to the microsphere, which coating has an affinity for the radionuclide. The radionuclide material is milled to decrease agglomerations and then deposited onto the coating to form a radionuclide-coated microsphere. The radionuclide-coated microsphere provides metered delivery of the radionuclide material.

Claims

1. A method for delivering a radionuclide material comprising: a. providing a microsphere; b. providing a coating on the microsphere, the coating having an affinity for the radionuclide; c. milling the radionuclide material to decrease agglomerations; and d. providing the radionuclide material on the coating to form a powder-coated microsphere, in which the radionuclide coated microsphere provides metered delivery of the radionuclide material.

2. The method of claim 1 in which the radionuclide material is coated in a dispersion with a dipodal polysiloxane.

3. The method of claim 2 in which the microspheres are coated by incorporating them with the radionuclide material and dipodal siloxane in the dispersion mixture.

4. The method of claim 1 in which the radionuclide material is milled to decrease agglomerations prior to being provided on the coating,

5. The method claim 1 in which the radionuclide material is powdered holmium oxide.

6. The method of claim 5 in which the microsphere is a glass microsphere.

7. The method of claim 6 in which the glass is A-glass.

8. The method of claim 6 in which the glass is E-glass.

9. The method of claim 5 in which the coating is a dipodal polysiloxane.

10. The method of claim 5 in which the diameter of the microsphere is in the range of 37 μm to 45 μm.

11. The method of claim 5 in which the average diameter of the powdered holmium oxide is in the range of 0.1 μm to 5 μm.

12. The method claim 5 in which the ratio of the average diameter of the powdered holmium oxide to the diameter of the microsphere is in the range of 1:20 to 1:450.

13. The method claim 12 in which the ratio of the average diameter of the powdered holmium oxide to the diameter of the microsphere is in the range of 1:20 to 1:100.

14. The method of claim 5 in which the ratio of the weight of the coating to the weight of the microsphere is in the range of 0.1 to 4% (w/w).

15. The method of claim 5 in which the ratio of the weight of the powdered holmium oxide to the weight of the microsphere is in the range of 0.5 to 10% (w/w).

16. The method of claim 1 in which the coating is a dipodal polysiloxane.

17. A device for delivering a radionuclide material comprising: a. a microsphere; b. a coating provided on the microsphere, the coating having an affinity for the radionuclide material; c. a radionuclide powder formed from the radionuclide material, the radionuclide powder provided on the coating to form a powder-coated microsphere, in which the radionuclide coated microsphere provides metered delivery of the radionuclide material.

18. The device of claim 17 in which the radionuclide powder is a milled radionuclide powder

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0019] FIG. 1 is a chart showing the radioactivity of the coated microspheres prepared in accordance with Example 1.

[0020] FIG. 2 is a chart showing the radioactivity of the coated microspheres prepared in accordance with Example 2.

[0021] FIG. 3a is a photomicrograph of a holmium oxide-coated microsphere in which the holmium oxide has not been milled.

[0022] FIG. 3b is a photomicrograph of a holmium oxide-coated microsphere in which the holmium oxide has been milled.

[0023] FIG. 4a is a photomicrograph showing beads formed using an epoxy-amine coating and milled without dispersant.

[0024] FIG. 4b is a photomicrograph showing beads formed using an epoxy-amine coating and milled with the dispersant.

[0025] FIG. 5a is a photomicrograph showing beads formed using a dipodal polysiloxane coating and milled without dispersant.

[0026] FIG. 5b is a photomicrograph showing beads formed using a dipodal polysiloxane coating and milled with dispersant.

[0027] FIG. 6a is a photomicrograph showing beads in which the holmium oxide was deposited on the glass beads in four separate applications.

[0028] FIG. 6b is a photomicrograph showing beads in which the holmium oxide was deposited on the glass beads in a single application.

PREFERRED FORM OF EMBODIMENT OF THE INVENTION

[0029] Although the present invention is described with reference to preferred embodiments, it will be understood by those skilled in the art that several changes can be made and the equivalents can be replaced by elements thereof. Moreover, although the examples presented below reference the use of holmium and holmium oxide, it will be understood by those skilled in the art that the present invention is applicable to other radionuclides as well.

[0030] Although the examples presented below reference the use of Class A and Class E glass microspheres, it will be understood by those skilled in the art that other classes of glass can be used. It will also be understood by those skilled in the art that both hollow and solid microspheres can be used in the present invention. It will be further understood by those skilled in the art that other silica compounds including quartz can be used as the substrate material.

[0031] Unless otherwise stated in the examples, the weight percentages listed are with respect to the weight of the microsphere.

[0032] It has been found that glass microspheres are an excellent carrier for solid particles such as radionuclide powdered metals. A specific coating applied over the glass microspheres selected based on the nature of the solid particles allows the solid particles to be affixed to the glass microspheres, creating a shield of solid particles around a glass microsphere core. The solid particles can be precisely metered on the glass microspheres. The amount of the solid powder to be delivered can be precisely controlled by selecting the size and surface area of the glass microspheres to which the solid powders are affixed.

[0033] The particle size of the glass microspheres for radionuclides have a broad range depending on the intended application. For holmium oxide radionuclides intended for liver treatment and applied internally in the body, the glass microspheres should preferably have a particle size distribution between 37 μm and 45 μm for most applications. Preferably, glass microspheres smaller than 37 μm are not used nor are glass microspheres larger than 45 μm.

[0034] A presently preferred coating for inorganic radionuclides including holmium oxide is a dipodal polysiloxane coating such as CoatOSil FLX, which is applied over the glass microsphere's surface, in an amount consistent with the specific surface coverage calculation for the size of the glass microsphere. The holmium oxide particles will adhere to the dipodal polysiloxane coating, thereby securing the inorganic particle to the glass microsphere surface.

[0035] A possible coating for organic radionuclides is a vinyl polysiloxane such as Silquest G-170.

[0036] One example of precise delivery of a powdered material is the use of glass microspheres as a carrier for holmium oxide which is used in radiotherapy applications. A dipodal polysiloxane coating secures the solid oxide particles to the microspheres, creating a layer of solid particles around the glass microsphere core.

[0037] The present invention is particularly suitable where the powder material to be delivered is relatively expensive and there is a concern about wasting excess powder in the delivery process. By affixing the desired quantity of powder to the microspheres, there is less waste as the powder will not readily be released from the coating in transport. Moreover, because the powder is isolated on the surface and not the interior of the microsphere, more efficient utilization of the powder material occurs in industrial applications.

[0038] The powder material can be affixed to the microspheres by first coating the holmium oxide particles in dispersion with the dipodal polysiloxane. The microspheres are then coated by incorporating them into the dispersion mixture.

EXAMPLES

[0039] A series of samples of holmium-coated glass beads were prepared using one of seven different processes. The glass beads had a particle size distribution of 37 μm-45 μm.

[0040] In a first method, holmium oxide was bonded to the E-glass beads by coating the glass beads with epoxy silane and coating the holmium oxide with amino silane and mixing them together in the presence of a catalyst to produce fast reactivity between the epoxy and the amino terminal groups.

[0041] In a second method, E-glass microspheres were coated with an epoxysilane onto which powdered holmium oxide was deposited.

[0042] In a third method, powdered holmium oxide was electrostatically assembled onto the surface of the E-glass microsphere.

[0043] In a fourth method, unmilled holmium oxide was mixed with the dipodal polysiloxane and E-glass microspheres were then coated with the mixture.

[0044] In a fifth method, unmilled holmium oxide was mixed with the dipodal polysiloxane and A-glass microspheres were then coated with the mixture.

[0045] In a sixth method, milled holmium oxide was mixed with the dipodal polysiloxane and E-glass microspheres were then coated with the mixture.

[0046] In a seventh method, milled holmium oxide was mixed with the dipodal polysiloxane and A-glass microspheres were then coated with the mixture.

[0047] If the holmium oxide was milled, one of three processes was used. The process used to mill the holmium oxide was performed in an isopropanol solvent using either (a) 1400 μm-1600 μm glass beads at a speed of 1500 rpm, or (b) 1400 μm-1600 μm glass beads at a speed of 9000 rpm, or (c) 0.8 mm Zircosil® milling beads at a speed of 9000 rpm.

[0048] Each of the samples was irradiated in a nuclear reactor. The neutron irradiations were performed in a Rotary Specimen Rack (RSR), and these samples were irradiated for three hours with a thermal neutron flux of 1.Math.10.sup.12 n cm.sup.−2 s.sup.−1, with a Cadmium Ratio of 2.2. The radioactivity was measured and recorded. The samples are presented in Tables 1A and 1B, below and the radioactivity of each is presented in FIG. 1.

TABLE-US-00001 TABLE 1A Sample 1 2 3 4 5 6 7 Method 1 2 3 3 3 3 3 Epoxy Epoxy Electrostatic Electrostatic Electrostatic Electrostatic Electrostatic amino Assembly Assembly Assembly Assembly Assembly Milling (b) (a) (a) (a) (a) (a) (a) process and 15 30 90 30 30 30 30 time (min) Holmium 1.5 wt % 1.5 wt % 1.5 wt % 1.5 wt % 1.5 wt % 4.5 wt % 1.5 wt % oxide Coatosil ® FLX Silane Rhodorsil ®   1 wt % H68 silicone oil Disperbyk ® 0.5 wt % in 180 milling dispersion Epoxysilane 1.5 wt % 0.5 wt % A-187 Amino silane 1:1 stoichi- A-1100 ometry with epoxy Tetraethyl- 1:1 stoichi- ammonium ometry bromide with silanes Radioactivity 4.03 .Math. 10.sup.8 4.0 .Math. 10.sup.7 6.73 .Math. 10.sup.7 3.62 .Math. 10.sup.7 3.59 .Math. 10.sup.7 1.11 .Math. 10.sup.8 4.14 .Math. 10.sup.7 (Bq/g)

TABLE-US-00002 TABLE 1B Sample 8 9 10 11 12 13 14 Method 4 4 4 4 5 6 7 Dipodal Dipodal Dipodal Dipodal Dipodal Dipodal Dipodal polysiloxane polysiloxane polysiloxane polysiloxane polysiloxane polysiloxane polysiloxane Milling Unmilled Unmilled Unmilled Unmilled Unmilled (c) (c) process and 15 15 time (min) Holmium 1.5 wt % 4.5 wt % 4.5 wt % 6 wt % 6 wt % 6 wt % 6 wt % oxide Coatosil ®   1 wt %   3 wt %   3 wt % 4 wt % 4 wt % 4 wt % 4 wt % FLX Silane Rhodorsil ® H68 silicone oil Disperbyk ® 180 Epoxysilane A-187 Amino silane A- 1100 Tetraethyl- ammonium bromide Radioactivity 2.63 .Math. 10.sup.8 8.2 .Math. 10.sup.8 7.74 .Math. 10.sup.8 9.3 .Math. 10.sup.8 1.1 .Math. 10.sup.9 1.1 .Math. 10.sup.9 1.17 .Math. 10.sup.9 (Bq/g)

Example 1

[0049] A first test determined whether the process used to coat the glass beads with holmium oxide affected the measured radioactivity. Samples 1-5 and 7-8 from Tables 1A and 1B were compared. Each of these samples used E-glass beads coated with the same concentration of holmium oxide, but were produced using one of methods 1-4 described above. A comparison of the measured radioactivity for these Samples is presented in Table 2 below and in FIG. 2.

TABLE-US-00003 TABLE 2 Sample 1 2 3 4 5 7 8 Method 1 2 3 3 3 3 4 Epoxy Epoxy Electrostatic Electrostatic Electrostatic Electrostatic Dipodal amino Assembly Assembly Assembly Assembly polysiloxane Radioactivity 4.03 .Math. 10.sup.8 4.0 .Math. 10.sup.7 6.73 .Math. 10.sup.7 3.62 .Math. 10.sup.7 3.59 .Math. 10.sup.7 4.14 .Math. 10.sup.7 2.63 .Math. 10.sup.8 (Bq/g)

[0050] As shown in Table 2, the radioactivity of holmium oxide is dependent on the method used to coat the glass microspheres. Using the same amount of holmium oxide, the final radioactivity can be improved by more than 10 times by using the first method of applying an epoxy silane coating on the glass bead and an amino silane coating on the holmium oxide powder.

Example 2

[0051] It is necessary to maximize the exposed area of holmium oxide in order to achieve a better yield of radioactivity. It has been found that increasing holmium oxide concentration does not linearly increase the radioactivity. An excess of holmium oxide in the mixture probably supports the formation of aggregates, reducing the ratio of active surface compared to the total amount of holmium oxide.

[0052] Breaking holmium oxide aggregates by milling improves the final radioactivity by providing much more exposed surface. FIGS. 3a and 3b show the difference in structure between a non-milled and milled holmium oxide, respectively.

[0053] Table 3 below compares unmilled sample 11 with milled sample 13. Both samples used the same 6% holmium oxide content. By milling the holmium oxide, it is possible to increase the radioactivity approximately 18% (from 9.3×10.sup.8 Bq/g to 11×10.sup.8 Bq/g).

TABLE-US-00004 TABLE 3 Sample 11 13 Method 4 6 Dipodal Dipodal polysiloxane polysiloxane Milling process and Unmilled (c) time (min) 15 Radioactivity (Bq/g) 9.3 .Math. 10.sup.8 1.1 .Math. 10.sup.9

[0054] Sample 1 corroborates the advantage of milling the holmium oxide. The holmium oxide used in Sample 1 was milled and the resultant radioactivity measurements showed a substantial increase over those of unmilled samples using otherwise similar preparation methods.

[0055] Sample 12 shows a higher radioactivity than expected for this unmilled sample. However, the holmium oxide is not perfectly attached to the microsphere in this sample. It is believed that this imperfect attachment of the holmium oxide affected the radioactivity measurement for Sample 12. Although this imperfect attachment provides enhanced activation, it would not be a good carrier for internal application in the body as the holmium oxide is prone to falling off of the microsphere.

[0056] Preferably, the holmium oxide is spread over a carrier with a high surface area to avoid the formation of aggregates. To achieve a good coating over glass beads, the optimum size ratio is 1:50 or higher. So, for glass beads with 50 μm diameter the optimum size for holmium oxide is 1 μm diameter or smaller.

Example 3

[0057] A study was performed to determine whether the sodium content of the microsphere affects the radioactivity of the deposited holmium. Holmium oxide powder was mixed with the dipodal polysiloxane and glass microspheres were then coated with the mixture according to methods 6 and 7. The results of these tests are shown in Table 4 below.

TABLE-US-00005 TABLE 4 Sample 13 14 Method 6 7 Dipodal Dipodal polysiloxane polysiloxane Glass type E-Glass A-Glass Radioactivity (Bq/g) 1.1 .Math. 10.sup.9 1.17 .Math. 10.sup.9

[0058] As shown in Table 4, the radioactivity of the holmium oxide was generally the same regardless of the class of the glass microsphere being used.

Example 4

[0059] Further tests were conducted to determine whether the amount of the dipodal polysiloxane coupling agent could decrease the formation of holmium oxide aggregates. The process above was repeated with the amount of polysiloxane being reduced from 4% to 0.5%. A dispersion of 0.75 wt % holmium oxide particles in isopropanol was milled and the full dispersion was transferred to a glass beaker. The polysiloxane was then added to the dispersion to be mixed with the holmium oxide without the addition of water. Glass beads are then poured onto the mixture. Evaporation of the isopropanol solvent as well as the blend of both of the powders is produced under heating at low temperatures with smooth stirring.

[0060] These tests show that by using less coupling agent, fewer aggregates and clumps of holmium oxide are formed. Moreover, the coated microspheres have a better flowability and improved holmium adhesion. The holmium oxide is better distributed in the matrix and surface of the microspheres.

[0061] Preferably, the amount of coupling agent used is in the range of 0.1 wt %-4 wt %. Flowability of the coated beads is best with a 0.5 wt % coupling agent.

Example 5

[0062] A test was conducted to determine the relevance of the milling process in the final coating. A dispersing agent was introduced to improve the milling, achieving smaller particles sizes. As shown in Table 5, two different coatings were compared with and without dispersant. In both cases, a reduced particle size was observed. FIG. 4a is a photomicrograph showing beads formed using the epoxy-amine coating and milled without dispersant. FIG. 4b is a photomicrograph showing beads formed using the epoxy-amine coating and milled with the dispersant. FIG. 5a is a photomicrograph showing beads formed using the dipodal polysiloxane coating and milled without dispersant. FIG. 5b is a photomicrograph showing beads formed using the dipodal polysiloxane coating and milled with dispersant. FIGS. 4b and 5b show a smaller particle size than FIGS. 4a and 5a, respectively. It is expected that an improvement of radioactivity would occur when the holmium oxide is milled with a dispersant.

TABLE-US-00006 TABLE 5 Sample 15 16 17 18 Method Epoxy- Epoxy- Dipodal Dipodal amino amino polysiloxane polysiloxane Milling 15 15 15 15 time (min) Holmium 6 wt % 6 wt %   6 wt %   6 wt % oxide Coatosil ® 0.5 wt % 0.5 wt % FLX Silane Epoxy 0.5 wt % 0.5 wt % silane 5 μL/g sph 5 μL/g sph A-187 Amino 1:1 1:1 silane Stoichi- Stoichi- A-1100 ometry ometry with epoxy with epoxy Dispersant Disperbyk Disperbyk 2060 2060 Acetic 10 mL 10 mL acid glacial glacial Tetraethyl- 1:1 1:1 ammonium Stoichi- Stoichi- bromide ometry ometry with silane with silane

Example 6

[0063] A test was conducted to determine the effect of applying several coating layers of the holmium oxide over glass beads. A first sample shown in FIG. 6a was prepared in which the holmium oxide was deposited in four separate applications of 1.5 wt % each. A second sample shown in FIG. 6b was prepared in which the holmium oxide was applied in a single application of 6 wt %. No significant differences were revealed in the photomicrographs.

[0064] Although the description above contains certain specificities, they should not be interpreted as limitations to the scope of the invention, but as an example of a preferred embodiment of the same. Therefore, the scope of the present invention must not be determined by the embodiments illustrated, but by the attached set of claims and its legal equivalents.