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Publication numberUS3749556 A
Publication typeGrant
Publication dateJul 31, 1973
Filing dateAug 19, 1971
Priority dateAug 19, 1971
Publication numberUS 3749556 A, US 3749556A, US-A-3749556, US3749556 A, US3749556A
InventorsM Barak, H Winchell
Original AssigneeMedi Physics Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Radiopharmaceutical generator kit
US 3749556 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

July 31, 1973 M. BARAK ET AL 3,749,556

RADIOPHARMACEUTICAL GENERATOR KIT Filed Aug. 19, 1971 INVENTORS MORTON BARAK HARRY S. INC ELL //I w ai 1 ATTORNEYS 3 749,556 RADIOPHARMACEIEJTICAL GENERATOR KIT Morton llarak, Walnut Creek, and Harry S. Winchell, Lafayette, Califl, assignars to Medi-lhysics, Inc. Filed Aug. 19, 1971, Ser. No. 173,099 int. Cl. A611; 27/04; B913 1/04 US. Cl. 23-252 R 4 Claims ABSTRACT OF THE DISCLOSURE benign cations are substituted for uncombined reducing agent and isotope ions. A new technetium-99m labeled radiopharmaceutical useful in liver imaging is produced by interaction with the column packing in one specific aspect of the procedure.

This invention relates generally to medical radioisotope organ imaging and function studies and more particularly to simple apparatus and method for producing known technetium-99m labeled radiopharmaceuticals and for producing new technetium-99m labeled radiopharmaceuticals useful in nuclear medicine diagnostic procedures.

One object of this invention is to provide a kit for assembly into a simple radiopharmaceutical generator useful in making technetium-99m labeled radiopharmaceuticals quickly and without the need for a skilled chemist or pharmacist.

Another object of this invention is to provide a simple two-step process for making technetium-99m labeled pharmaceuticals quickly and without the need for a skilled chemist or pharmacist.

Still another object of this invention is to provide apparatus and methods which employ a packing of reducing agent for technetium-99m pertechnetate to isolate and concentrate it to any desired level of radioactivity so that radiopharmaceuticals of known specific concentrations of radioactivity can be made.

An object of this invention also is to provide simple methods and apparatus for eliminating chemical and radionuclidic contaminants from the processed radiopharmaceutical.

One other obj-ect of this invention is to provide new and useful pharmaceuticals labeled with technetium-99m.

Other objects and advantages will become apparent from a consideration of the following description and the accompanying drawing wherein FIG. 1 is a cross-sectional view of the components of the kit of this invention prior to assembly;

FIG. 2 is a perspective view of the kit of this invention shown in FIG. 1 before assembly;

FIG. 3 is a vertical sectional view of the kit of this invention assembled for generation of a radiopharmaceutical; and

- atent FIG. 4 illustrates in perspective the assembled kit of FIG. 3.

This invention includes procedures and apparatus for making pharmaceuticals labeled with technetium-99m which are useful in nuclear medicine for organ imaging. As used herein the term biological compounds include single elements, chemical compounds, mixtures of either or both or complexes of other sorts which are chelating agents for reduced technetium'99m that may be administered internally or otherwise without adverse effects to living organisms, particularly to human beings.

The technetium-99m isotope is conveniently available in isotonic solution in the form of the chemically stable pertechnetate ion (TcO Sodium pertechnetate solutions usually are eluted by saline solution in generators or cows from the long-lived parent molybdenum-99. The inherent chemical properties of technetium-99m and a number of undersirable characteristics of pertechnetate solutions originating from such generators normally require time consuming and complicated chemicals processing performed by skilled chemists or pharmacists with substantial radiation exposure to make useful technetium- 99m labeled pharmaceuticals.

The cow eluate frequently contains variable amounts of non-radioactive contaminants such as aluminum and molybdenum ions. It often contains as well, variable amounts of long-lived radionuclidic impurities such as Mo, the parent isotope, and neutron activation and fission products such as cesium, Zr- Nb, 5b, (10 or Sc. The specific concentration of Tc obtained from the cow also varies considerably.

Tc in the chemical form of pertechnetate (TcO ion is commonly used to image some areas of the body. But due to the imperfect nature of its biological distribution as the pertechnetate ion, drugs such as perchlorate or iodide ion or atropine are often administered to the patient to suppress uptake in areas that might interfere with scan interpretation or to reduce radiation dose to uninvolved organs. For example before Tc-pertechnate is given for brain scanning, relatively large amounts of the aforementioned suppressive drugs are administered to the patient to suppress characteristic uptake in the salivary glands and choroid plexus-events that might interfere with scan interpretation. Thyroid uptake is suppressed as well, thus rescuing this organ from an otherwise gratuitous radiation dose.

It is therefore beneficial to combine Tc with substances which result in a radiopharmaceutical that has a more specific afiinity for the organ of interest and a reduced tendency to concentrate elsewhere. For example, T00 treated with an iron salt plus ascorbic acid, results in a radiopharmaceutical that concentrates in the cortex of the kidney to such a degree that usefully informative scintiphotographs may be taken of that organ. Other preparations of Tc labeled compounds are useful for liver and lung imaging and for placenta localization. Almost all of the chemical processes required to convert pertechnetate ion to useful pharmaceuticals are time consuming and complex. They require services of a skilled radiochemist and substantial radiation exposure.

THE GENERATOR KIT The generator kit disclosed in FIGS. 1 and 2 assembles into what is essentially a small chromatographic column illustrated in FIGS. 3 and 4. The kit includes a first tubular section referred to generally as 1. It has an elongated tubular shell 2; an integral liquid inlet 3 at one end, such as the illustrated female luer slip fitting; and at the other end a first joinder means 4, such as the illustrated male taper which assembles to a corresponding taper in the second tubular section referred to generally as 5.

The second tubular section 5 includes an elongated tubular shell 6; a second joinder means 7 at one end, such as the female taper 7 for quick and vacuum-tight assembly to male taper 4 of the first tubular section of the kit as is shown in FIG. 3; and at the other end an integral liquid outlet 8 such as the illustrated male luer slip fitting. A first inert porous disc 9 and a second inert porous disc 10 define with shell 2 a first processing zone within the first tubular section 1 which is packed with a particulate or sintered reducing agent 11 for technetium-99m pertechnetate. The porous discs 9, 10 may be inert coarse filters press-fit into shell 2 or one of them, such as porous disc 9 may be integrally molded with the shell from linear polyethylene or polypropylene or other physiologically and chemically inert materials. The pore size permits liquid flow but confines the reducing agent packing within the first processing zone. Porous disc 10 press-fits into shell 2 after reducing agent 11 is packed. The reducing agent for technetium-99m pertechnetate is a particulate metal powder or sinter which is aseptically packed dry and dry heat sterilized. Plastic caps 12 and 13 over each of its ends, seal the first tubular section 1 and preserve sterility until its use.

The second tubular section 5 carries a third porous disc 14 at its lower end adjacent to liquid outlet 8. This disc has a pore size in the order of 5 microns in diameter. It may be molded integrally with a polyethylene or polypropylene shell 6 or may be press-fit filter material such as nylon, Teflon, sintered stainless steel or a glass frit. Shell 6 between the end of female taper 7 and porous disc 14 defines a second processing zone packed with a cation exchange resin 15. Such resins normally are autoclave sterilized and stored Wet. Plastic caps 16 and 17 close the ends of the second tubular section 5 of the kit and preserve sterility until its use.

For use in processing a radiopharmaceutical, protective plastic caps 12, 13, 16 and 17 are stripped from the kit components and the first and second tubular sections are assembled into a complete column as is illustrated in FIG. 3. The joint between the tapered joinder means 4 is vacuum tight. Liquids to be processed through the column are introduced through inlet 3 by means of hypodermic syringe 20. They are moved or assisted through the column by needle 21 attached to outlet 8 and afiixed to vacuum bottle 22.

For the examples described herein tubular shells 2, 6 were 7-8 millimeters in inside diameter and defined first and second processing zones about 10 centimeters long. While the precise dimensions are not critical, the first processing zone must provide enough reducing agent packing and residence time to adjust the pH of the eluant during the second processing step and to buffer it to physiologically acceptable levels within the range of 5 to 8. On the other hand, the second processing zone must provide enough cation exchange resin and residence time to remove all uncombined reducing agent and radioisotope-carrier ions.

THE PROCESS AND PRODUCT The described kit is used to generate radioisotope labeled pharmaceuticals by a simple two-step procedure.

In a first step hypodermic syringe of an appropriate size introduces the labeling technetium-99m pertechnetronegative than hydrogen, such as iron. Needle 21 and vacuum bottle 22 assist the syringe contents to pass through the column.

The reducing agent 11 adsorbs or isolates substantially all of the technetium-99m in the initial portion of the zone-with the dimensions described, within the first onefourth inch of the packing. Substantially all of the radioactivity collects upon this portion of the packing regardless of the concentration of the technetium-99m pertechnetate in the first carrier liquid or the quantity of the carrier liquid put through the column. Thus, as much radioactivity as is desired may be concentrated on the initial portion of the reducing agent packing. The total amount of trapped radioactivity can be measured directly by its radiation. The first carrier liquid passes through the column and collects in vacuum bottle 22 stripped of substantially all of its radioactive component. With it pass all chemical and radionuclidic impurities in the cow eluate that do not adhere to the column packing materials.

In a second step another hypodermic syringe introduces a known volume of special eluant to the column assisted by a second sterile vacuum bottle 22 afiixed to needle 21 at the bottom of the column. The eluant is a physiologically benign second carrier liquid carrying a dispersion, either in solution or suspension, of a biological compound that combines irreversibly with the reduced technetium-99m residing on the reducing agent packing in the initial portion of the first processing zone. The biological compound may be one of the group of instantly labeled chelating agents including albumin which are known to concentrate in particular human organs of interest in predictable amounts. It should be effective at physiological ion concentrations (about 150 meq. per liter) and should not precipitate or form large particles during passage through the column. The pH of the special eluant is adjusted, as required, to provide the requisite environment for combination of the biological compound and reduced technetium-99m. The pH of the special eluant initially should be less than 6.

The eluant carries the biological compound, now labeled with technetium-99m, through the remainder of the first processing zone wherein its reaction with the reducing agent packing adjusts the pH to and buffers it at physiologically acceptable levels, in the pH range of 5-8 for example. The second carrier liquid and its dispersion then passes through the second processing zone packed with cation exchange resin. A strongly acidic cation exchange resin composed of nuclear sulphonic acid exchange groups attached to a styrene-divinylbenzene polymer lattice is used. The resin is sodium cycled so that physiologically benign sodium ions are substituted for any uncombined reducing agent or radioisotope or other cations present in the passing eluant.

Pharmaceuticals and desired specific concentration are made by eluting the column in the second step with a volume of eluant that corresponds to the measured amount of radioactivity isolated in the first zone packing. Typical process parameters are shown in the following examples.

Example I.Technetium-99m-iron-ascorbic acid complex A technetium-99m iron ascorbic acid complex of the type often used for kidney imaging has been generated by the process and kit described in 5 to 10 minutes by a nonskilled technican. The first zone of the kit was packed with about 6 grams of 325 mesh (U.S. seive size) powdered iron. The second zone was packed with about 8 cc. (wet) of 100-200 mesh sodium cycled cation exchange resin, such as AG50W-X8 manufactured by Bio Rad Company of Richmond, Calif.

About 10 cc.- of a normal saline solution carrying pertechnetate ions eluted directly from the Mo cow at a radioactivity concentration of about 2 millicuries per cc. Was introduced by syringe to the assembled kit in a first step. This material was run through the column at a slow rate on the order of one-tenth cc. per second. Ninety-nine percent of the original radioactivity adhered to the first one to two millimeters of powdered iron in the first zone of the column.

Then a second syringe introduced to the column four millimeters of 0.15 normal aqueous ascorbic acid solution. The net yield of technetium-99m labeled pharmaceutical was 55 percent of the total technetium-99m activity initially present in the cow eluate.

The biological distribution of the resulting pharmaceutical in rats three hours after intravenous injection was 8 percent in the kidneys, 53.7 percent in the urine-bladder and 3.5 percent in the liver.

Example II.-Technetium-99m-iron-albumin complex A new technetium-99m-iron-serum albumin complex has been generated in 5-10 minutes which concentrates in the liver and is useful for liver imaging.

Six grams of 100 mesh (U.S. sieve size) hydrogen reduced iron pack the first zone of the kit and 8 cc. of so dium cycled cation exchange resin as in Example I pack the second zone. Ten cc. of the saline pertechnetate solution as used in Example I was introduced to the kit in a first step as in Example I. The pertechnetate trapping efliciency was about 92 percent. In a second step four milliliters of eluant comprising ten mililgrams per milliliter of bovine serum albumin dissolved in 0.6 normal hydrochloric acid was then introduced to the column.

The net yield of technetium-99m labeled pharmaceutical was 55 percent of the total technetium-99m activity initially present in the cow eluate. Combined iron in the effluent pharmaceutical from the column was 0.35 milligram of elemental iron per milliliter or a total of 1.4 milligrams. Biological distribution in rats /2 hour after intravenous injection was 69.5 percent in the liver and 1.0 percent in the spleen. There was no reaction to the foreign protein.

This pharmaceutical is unique in its composition. It is believed to be an albumin-technetium-99m-iron complex which, if particulate, has a particle size of less than 0.22 micron. In this state the complex is useful for liver imaging.

Application of heat, for example heating the pharmaceutical at 100 F. for 5 minutes, agglomerates the complex into particles barely visible to the naked eye. These particles averaging -100 microns in size concentrate in the lungs like known technetium-99m labeled macroaggregated human serum albumin.

Example III.-Technetium-99m tin colloid complex A technetium-99m labeled tin colloid for use in liver imaging was similarly prepared in 5-10 minutes. The packing in the first zone was tin powder of greater than 325 mesh (U.S. sieve size) with the same cation exchange resin and saline solution of pertechnetate ions as in Examples I and II. The trapping efiiciency for the pertechnetate ion was 98.8 percent.

In a second step four milliliters of two normal hydrochloric acid was eluted through the column to yield 74.5 percent of technetium-99m labeled pharmaceutical based on the original technetium-99m activity in the cow eluate. A high concentration in the liver of experimental rats is observed after intravenous injection.

The radiopharmaceuticals listed below have been prepared using the described procedures and kit with satisfactory yields. They have useful biological distributions and are physiologically benign.

D0..." H01 plus serum albumin Do. D0... 1161 plus serum albumin plus heat.-. Lungs.

Tin HCl Liver.

mg Ascorbic acid Same as TcO-n The above examples and the described apparatus and procedures are for illustrative purposes only. It will be apparent to those skilled in the art that other technetium- 99m labeled pharmaceuticals may be similarly prepared and the process parameters may be modified within the scope of the invention defined in the following claims.

We claim:

1. A kit for assembly into a packed column for making technetium-99m labeled pharmaceuticals comprising a first tubular section having a first tubular shell;

a liquid inlet at one end of said first tubular shell;

first joinder means at the other end of said first tubular shell;

a first and a second porous disc enclosing a first processing zone within said first tubular shell adjacent said inlet;

a reducing agent for technetium-99m pertechnetate packed Within said first processing zone;

a second tubular section having a second tubular shell;

a liquid outlet at one end of said second tubular shell;

second joinder means at the other end of said second tubular shell for airtight assembly to said first joinder means;

a third porous disc adjacent said. liquid outlet;

and a cation exchange resin packed within a second processing zone defined in the second tubular shell between said first processing zone and said third porous disc.

2. The kit of claim 1 further comprising removable asceptic sealing means on said liquid inlet, said first and second joinder means, and said liquid outlet.

3. The kit of claim 1 wherein said reducing agent is a metal more electronegative than hydrogen.

4. The kit of claim 1 wherein said reducing agent is one of iron, tin and magnesium.

References Cited UNITED STATES PATENTS 3,156,532 11/1964 Doering et a1 23-252 R 3,369,121 2/1968 Bruno et al. 250-106 T 3,446,965 5/1969 Ogier et a1 250-106 T 3,462,245 8/1969 Eudes et al 23-252 R 3,466,361 9/1969 Richards et al. 424-1 3,535,085 10/1970 Schumate 23-252 R 3,561,932 2/1971 Gruverman et al.

252-3011 R X 3,564,256 2/1971 Arlman et al. 250-106 T 3,566,124 2/1971 Gemmill 250-106 T 3,655,981 4/1972 Montgomery et al. 250-106 T 3,657,541 4/1972 Deutsch et al. 250-106 T X JOSEPH SCOVRONEK, Primary Examiner US. Cl. X.R.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3911096 *Jun 23, 1972Oct 7, 1975Professional Staff Ass Of TheRadioimmunoassay for measurement of thyroxine (T{HD 4{B ) and triiodothyonine (T{HD 3{B ) in blood serum
US3983227 *Apr 19, 1974Sep 28, 1976The Procter & Gamble CompanyDry mixture containing diphosphonates and a stannous salt useful in the preparation of Tc99M containing bone scanning agents
US4010109 *Jul 2, 1973Mar 1, 1977Kurt SauerweinDevice for marking fluent materials
US4027005 *Jun 7, 1974May 31, 1977New England Nuclear CorporationDiagnostic agents
US4054645 *Aug 24, 1976Oct 18, 1977Minnesota Mining And Manufacturing CompanyRadiodiagnostic complexes employing fluorine-containing tin reducing agents
US4088747 *Feb 3, 1976May 9, 1978Australian Atomic Energy CommissionPhenolic amino-carboxylic acid radiopharmaceuticals
US4091088 *Sep 30, 1976May 23, 1978Australian Atomic Energy CommissionPhenolic amino-carboxylic acid complexes for forming radiopharmaceuticals
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US5662882 *Mar 23, 1995Sep 2, 1997Mallinckrodt Medical, Inc.Radiopharmaceutical formulations having non-stannous reductants
US7700926 *Jul 3, 2007Apr 20, 2010Draximage General PartnershipSystems and methods for radioisotope generation
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U.S. Classification250/303, 250/432.0PD
International ClassificationG01N30/52, A61K51/12, G01N30/60
Cooperative ClassificationA61K2123/00, G01N30/52, G01N30/6034, A61K51/1282
European ClassificationA61K51/12T
Legal Events
Aug 8, 1983AS02Assignment of assignor's interest
Owner name: MEDI-PHYSICS, INC.
Effective date: 19820812
Aug 8, 1983ASAssignment
Effective date: 19820812