The disclosure pertains to a strontium-90 scaled source, such as may be used with treatment of the eye or other medical, brachytherapeutic or industrial processes. In particular, a relatively constant absorbed dose rate is sought throughout a target volume of tissue of therapeutic interest that is to be treated with radiation (hereinafter referred to as “a flat radiation profile”).
The prior art of radiological or radioactive sources of various types for medical, industrial and other processes is well-developed. For example, U.S. Pat. No. 8,430,804, entitled “Methods and Devices for Minimally-Invasive Extraocular Delivery of Radiation to the Posterior Portion of the Eye”, issued on Apr. 30, 2013 to Brigatti et al., and assigned on its face to Salutaris Medical Devices, Inc., discloses an applicator for minimally-invasive delivery of beta radiation from a radionuclide brachytherapy source to the posterior portion of the eye. In particular, this is adapted for the treatment of various diseases of the eye, such as, but not limited to, wet age-related macular degeneration. Other prior art includes U.S. Pat. No. 9,873,001 entitled “Methods and Devices for Minimally-Invasive Delivery of Radiation to the Eye”, issued on Jan. 23, 2018 to Lutz et al. and assigned on its face to Salutaris Medical Devices, Inc.; PCT/US2014/056135 entitled “Radiation System with Emanating Source Surrounding an Internal Attenuation Component”, filed on Mar. 18, 2016; U.S. Pat. No. 7,070,554 entitled “Brachytherapy Devices and Methods of Using Them”, issued on Jul. 4, 2006 to White et al., and assigned on its face to Theragenics Corporation and U.S. Pat. No. 6,413,881, entitled “Ophthalmic Brachytherapy Device”, issued on Sep. 3, 2002 to Finger.
While this prior art is well-developed and suited for its intended purposes, further improvements are sought in the radioactive sources used in the disclosed devices. In particular, a collimated distribution of radiation, rather than an isotropic (spherical “4π”) distribution of radiation, would allow a radiological source to direct radiation at the tissues under treatment, while reducing radiation directed at surrounding tissues which are not under treatment and also while preventing excessive radiation to be directed to the tissues under treatment in the center of the emitted radiation beam.
It is therefore an object of the present disclosure to provide improvements in the radiological sources used in brachytherapy and in other medical or industrial applications. In particular, it is an object of the present disclosure to provide improved radiological sources for known applicators for treatment of diseases of the eye, including, but not limited to, wet age-related macular degeneration. These radiological sources are intended to concentrate the radiation more uniformly on the diseased tissue, rather than using isotropic radiation which would expose more of the surrounding healthy tissue to unnecessary radiation and could overexpose tissue under treatment at the center of the radiation beam.
This and other objects are attained by providing a beta radiological source, typically containing strontium-90, wherein the radiological insert has increased radioactivity around its periphery and less radioactivity at its center. This may be achieved by a toroidal or annular shape, (such as a donut-type shape with a hole or aperture in the middle) or with the central portion of a disk having reduced thickness or reduced radioactivity content. This may further be achieved by a minus lens meniscus shape wherein the lower concave surface has a shorter radius of curvature than the upper concave surface, thereby resulting in a raised thinner portion and a lower thicker peripheral portion. This is further achieved by providing an encapsulation with increased shielding in the center of the face from which the therapeutic radiation is emitted, thereby substantially attenuating the radiation emitted from the central portion of a source. It is further possible to use a separate denser attenuating disk in front of the activity, either on the inside or outside of the encapsulation. Material in the attenuating disk may include, but is not limited to, silver, copper, lead, tungsten, gold and/or iridium.
Further objects and advantages of the disclosure will become apparent from the following description and from the accompanying drawings, wherein:
Referring now to the drawings in detail wherein like numerals refer to like elements throughout the several views, one sees that
The toroidal shape of the strontium-90 radiological insert 318, with its thickened periphery, leads to increased radiation emission around the periphery and a reduced radiation output within the center. This, in combination with the increased beta shielding in the central area of central plateau 304, results in a flat beam profile, achieving a more constant absorbed dose rate throughout a target volume of tissue of therapeutic interest that is located in front of the source as illustrated in
It is noted that the strontium-90 beta radiation insert 130 may be made of various materials, such as a strontium ceramic, strontium glass, or a collection of tightly packed ceramic beads (of various possible shapes) or a refractory-metal composite. Refractory ceramics and glasses containing Strontium-90 can be made from a wide variety of materials in combination, such as those containing metal oxides of aluminum, silicon, zirconium, titanium, magnesium, calcium amongst others. It is envisioned that other additional materials may be selected from, but not limited to, such strontium-90 compounds as SrF2, Sr2P2O7, SrTiO3, SrO, Sr2TiO4, SrZrO3, SrCO3, Sr(NbO3)2, SrSiO3, 3SrO.Al2O3, SrSO4, SrB6, SrS, SrBr2, SrC2, SrCl2, SrI2 and SrWO4. Additionally, beta emitters based on materials other than strontium-90 may also be compatible with this disclosure. Such beta emitters may include Copper-66, Lead-209, Praseodymium-145, Tellurium-127, Tin-121, Nickel-66, Yttrium-90, Bismuth-210, Erbium-169, Praseodymium-143, Phosphorus-32, Phosphorus-33, Strontium-89, Yttrium-91, Tungsten-188, Sulfur-35, Tin-123, Calcium-45, Berkelium-249, Ruthenium-106, Thulium-171, Promethium-147, Krypton-85, Hydrogen-3, Cadmium-113m, Plutonium-241, Strontium-90, Argon-42, Samarium-151, Nickel-63, Silicon-32, Argon-39, Carbon-14, Technetium-99, Selenium-79, Beryllium-10, Cesium-135, Palladium-107, Rhenium-187, Indium-115 and Cadmium-113. In particular, after commercial and technical considerations (e.g., energy level and half-life), the following are of particular interest—Strontium-90/Yttrium-90, Strontium-89, Phosphorus-32, Tin-123 and Yttrium-91.
The embodiment of radiological source 100 in
The embodiment of radiological source 100 in
The embodiment of
The embodiment of
The embodiment of
The embodiment of
The embodiment of
The embodiments of
Further alternatives to the present disclosure include fixation of the active insert using glass, such as glass pre-melted into a stainless steel insert, glass powder co-compacted with a ceramic and glass powder mixed with a ceramic and then compacted. Additionally, alternatives include fixation of the active insert using mechanical methods such as soft materials such as copper, silver, aluminum, etc. or the use of springs of various types (wave, conical, folded disk, etc.). Further alternatives include active insert centering features to prevent positional errors such as tapered ceramic disks or a disk with an aperture or protrusion which interfaces with the capsule lid.
Similarly, the various embodiments of the radiological sources which include a cavity could be implemented by filling the cavity with radioactive microspheres. Such shapes would be defined by the shape of the cavity inside the source, while the microspheres could be immobilized using washers, spaces or similar devices during assembly. Further alternative embodiments include radioactive microspheres which are bonded using a fused glass/enamel bonding material to an insert (e.g., a metal or ceramic support) to immobilize the microspheres and define their shape.
In a further aspect of this disclosure, aqueous ammonia solution (NH4OH) is added to a mixed aqueous solution containing dissolved radioactive strontium nitrate 90Sr(NO3)2 and dissolved silver nitrate (AgNO3) (gold or copper may be substituted for silver in some applications, mixtures of silver, gold or copper may also be used) and a mixed precipitate can form of sparingly soluble silver hydroxide AgOH (some of which may convert to silver oxide Ag2O plus water in situ) and strontium hydroxide 90Sr(OH)2. Soluble ammonium nitrate NH4NO3 remains in solution. Excess ammonium hydroxide produces a water-soluble ammoniacal silver complex [Ag(NH3)2OH] while the strontium hydroxide remains insoluble. The solution and/or the mixed precipitates can be evaporated so that all solids co-precipitate or crystalize out of solution to produce an intimate mixture. These solids are baked dry so that the ammonium nitrate decomposes and sublimes (above 250° Centigrade) leaving substantially nothing behind, silver hydroxide decomposes to silver oxide then further decomposes to silver metal and the strontium hydroxide decomposes to strontium oxide. What is left is an intimate mixture of silver metal and strontium oxide (90SrO+Ag). Because silver is a soft semi-precious metal, such an intimate mixture of silver and radioactive strontium oxide can be mechanically and/or thermally formed into thin toroidal insert shapes by processes such as pressing, forging, rolling, extrusion and/or sintering.
Silver hydroxide or silver oxide can be prepared and pressed into a disk shape (toroidal or flat) at a pressure sufficient to bind the particles together to produce a handleable green-state disk (an organic or inorganic binder can be added if needed) but at a pressure that is low enough to leave porosity or microporosity within the disk. Aqueous strontium nitrate 90Sr(NO3)2 can then be soaked into the disk and then dried down to achieve intimate mixing. The dried disk can be sintered to produce a fully dense cermet containing strontium oxide embedded or immobilized within the matrix formed of copper oxide, silver oxide, copper hydroxide, silver hydroxide, gold hydroxide (i.e., auric acid) or mixtures thereof. The proportions of strontium and silver (or gold, copper or mixtures thereof) can be varied, resulting in different mechanical properties. Less strontium produces more ductility but a thicker more-attenuating disk. The typical range of composition can be 2-50 mol percent of strontium oxide in silver, gold or copper, preferably 5-40 mol percent, more preferably 10-30 mol percent. Cermet disks can be re-pressed or otherwise mechanically or thermally treated after sintering to further densify or remold the shape of the disks.
In a further aspect of this disclosure, Strontium-90 compounds are incorporated or mixed with aluminum to make a composite material. This may be performed by a method of incorporating Strontium-90 into aluminum by mixing or blending strontium fluoride (90SrF2) powder with aluminum powder, compressing the mixture into a billet, then heating it to about 10° Centigrade below the melting point of aluminum (660.3° Centigrade) before extruding the billet through an aperture in a metal collar to produce a wire of 90SrF2+Al. The resulting material can be formed into a toroidal disk or similar configuration as described in this disclosure.
Strontium fluoride is a stable material. It melts at 1477° Centigrade and is insoluble in water (Ksp value is approximately 2.0×10−10 at 25° Centigrade). It can be made from commercially available strontium nitrate 90Sr(NO3)2 by adding soluble ammonium fluoride to a strontium nitrate solution, precipitating insoluble strontium fluoride (90SrF2) and mixing/blending the dried salt with aluminum powder before pressing the mixture/blend into a disk. Useful ratios of 90SrF2 to Al could typically be in the range 5-50% of 90SrF2, preferably 10-30% (by weight). The resulting material can be formed into a toroidal disk or similar configuration as described in this disclosure.
Alternatively, an aqueous solution of 90Sr(NO3)2 could be absorbed into a disk made of porous or microporous aluminum and then dried down and baked above the decomposition temperature of 90Sr(NO3)2 of 570° Centigrade but below the melting point of aluminum 660.3° Centigrade in a non-oxidizing atmosphere, to convert the strontium nitrate into strontium oxide. This could be achieved in a vacuum oven or under an inert gas such as argon or a reducing atmosphere such as an argon-hydrogen mixture. Other soluble forms of Strontium-90 could be absorbed and baked in similar ways. The resulting material can be formed into a toroidal disk or similar configuration as described in this disclosure.
Thus the several aforementioned objects and advantages are most effectively attained. Although preferred embodiments of the invention have been disclosed and described in detail herein, it should be understood that this invention is in no sense limited thereby.
This application is a continuation-in-part application of U.S. patent application Ser. No. 15/571,310, filed on Nov. 2, 2017, now U.S. Pat. No. 10,714,226, which claims priority of PCT/US2016/022437, filed Mar. 15, 2016, which claims priority under 35 U.S.C. 119(e) of U.S. provisional application Ser. No. 62/158,091, filed on May 7, 2015, the contents of all of which is hereby incorporated by reference in its entirety and for all purposes.
Number | Name | Date | Kind |
---|---|---|---|
2517568 | Hissong | Aug 1950 | A |
4284887 | Kusumoto et al. | Aug 1981 | A |
6030333 | Sioshansi | Feb 2000 | A |
6443881 | Finger | Sep 2002 | B1 |
6907106 | McIntyre et al. | Jun 2005 | B1 |
7070554 | White et al. | Jul 2006 | B2 |
8430804 | Brigatti et al. | Apr 2013 | B2 |
9873001 | Lutz et al. | Jan 2018 | B2 |
20040242953 | Good | Dec 2004 | A1 |
20090156881 | Stokes | Jun 2009 | A1 |
20100004499 | Brigatti et al. | Jan 2010 | A1 |
20130240761 | Wang | Sep 2013 | A1 |
20150105601 | Finger | Apr 2015 | A1 |
20160184606 | Fluhs | Jun 2016 | A1 |
20160375267 | Lutz et al. | Dec 2016 | A1 |
20180296855 | Lohrenz | Oct 2018 | A1 |
Number | Date | Country |
---|---|---|
101951965 | Jan 2001 | CN |
1413748 | Apr 2003 | CN |
1529554 | May 2005 | EP |
2350718 | Dec 2000 | GB |
2011-508654 | Mar 2011 | JP |
9203179 | Mar 1992 | WO |
2000075692 | Dec 2000 | WO |
0187409 | Nov 2001 | WO |
2015105539 | Jul 2015 | WO |
PCTUS2014056135 | Mar 2016 | WO |
2016178746 | Nov 2016 | WO |
Entry |
---|
International Search Report issued in PCT/US2020/039845 dated Feb. 3, 2021. |
Number | Date | Country | |
---|---|---|---|
20190336791 A1 | Nov 2019 | US |
Number | Date | Country | |
---|---|---|---|
62158091 | May 2015 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 15571310 | US | |
Child | 16513032 | US |