Patent Application
20100056826
The present invention relates to a composition of a radioactive fluorine-labeled amino acid compound. More specifically, it relates to a composition of a radioactive fluorine-labeled amino acid compound useful for detecting tumors by positron emission tomography.
Nuclear medicine examination enables diagnosis by administering an agent containing a compound labeled with a specific radioisotope as an effective ingredient (hereinafter referred to as “radiopharmaceutical”) intravenously to a human body and detecting a radiation emitted from the compound, followed by imaging based on information obtained from the radiation. Nuclear medicine examination is effective in diagnosing a variety of diseases including heart disease and cancer, and characteristic in that it has not only high specificity and sensitivity to diseases, but also an advantage of providing information on the functionality of lesions, compared to other examination techniques.
In such nuclear medicine examination, different diagnostic apparatuses require different nuclides for radiopharmaceuticals to be administered. Single photon emission computed tomography (hereinafter referred to as SPECT) is used for detection of γ rays such as 99mTc, 123I, and 201Tl, and positron emission tomography (hereinafter referred to as PET) is used for detection of positron annihilation radiation such as 11C, 13N and 18F. Most of the agents used for the SPECT examination (hereinafter referred to as SPECT agents) are supplied from pharmaceutical manufacturers. In contrast, since most of the agents used for PET examination (hereinafter referred to as PET agents) contain nuclides shorter in half-life than SPECT agents, PET agents have not conventionally been supplied from pharmaceutical manufacturers, but have been prepared for use in diagnosis by an apparatus called cyclotron in hospitals. However, delivery of PET agents from pharmaceutical manufacturers has recently been started, and PET examination has become possible even in medical institutions having no cyclotron, thanks to changes in surrounding environments such as developments of manufacturing techniques and traffic networks.
Research and development taking the delivery into account is accelerated not only for SPECT agents but also PET agents due to the above-mentioned changes in the surrounding environments. For example, amino acid compounds including [18F]1-amino-3-fluorocyclobuthanecarboxylic acid (hereinafter referred to as anti-[18F]-FACBC) and radioactive fluorine-labeled bodies of nucleic acid compounds such as [18F]-fluorothymidine are synthesized to conduct research and development for PET agents. In radiopharmaceuticals such as PET agents, a problem often arises such that compounds decompose by self-radiation during delivery of the agents so as to cause decrease in radiochemical purity due to so-called radiolysis. Particularly in PET agents, radiolysis often becomes more problematic since the half-life of nuclides used therein is shorter than that of nuclides used in SPECT agents, and thus radioactivity upon shipment must be set larger than SPECT agents, thereby making the resulting radiation energy thereof higher.
For general pharmaceuticals, it is recommended in the guideline of ICH that if decomposed matters in an agent exceed 1.0%, the decomposed matters be subjected to structure determination when the maximum daily dosage of an effective component thereof is as small as not more than 1 mg (Non-Patent Document 1). In most cases, the physical amount of impurities resulting from the radiolysis which may be considered to be one of the decomposition in an agent is as small as about 10−12 mol. Thus, structure determination of the decomposed compounds by NMR analysis is difficult even though their fragments can be just presumed by mass spectrometry which is excellent in detection sensitivity. Consequently, it is very difficult to conduct verification as to whether or not the decomposed matters affect effectiveness such as tumor accumulation of the agent. Therefore, radiolysis in the radioactive diagnostic imaging agent should be maintained as low as possible.
As for a series of radioactive fluorine-labeled amino acid compounds such as the above-mentioned anti-[18F]-FACBC, it is also requisite to reduce radiolysis thereof. In fact, various methods for preventing radiolysis have been disclosed for [18F]-fluorodeoxyglucose (hereinafter referred to as [18F]-FDG) which is a PET agent covered by health insurance and widely used in clinical application.
International Publication No. WO03/090789 pamphlet discloses a method of reducing the radiolysis of [18F]-FDG by adding a weak acid-based buffer to a [18F]-FDG solution and an injection prepared by the method (Patent Document 1) Also, International Publication No. WO04/043497 pamphlet discloses adding ethanol to a [18F]-FDG solution to obtain a composition of injection which may be reduced in radiolysis of [18F]-FDG and improves in stability (Patent Document 2).
Japanese Patent Laid-open (Kokai) No. H10-147542 discloses a technique utilizing an organic compound high in physiological acceptability such as monosaccharides, disaccharides, organic acids and salts or esters thereof as a radiation protecting agent (Patent Document 3). Further, in this publication, the organic compound high in physiological acceptability is defined to have a reaction rate constant with OH radicals, H radicals or hydrated electrons in the range of 1×108 to 5×1010 mol−1s−1.
As described above, International Publication No. WO03/090789 pamphlet and International Publication No. WO04/043497 pamphlet disclose conditions for preventing radiolysis of [18F]-FDG in the solution. However, these documents disclose techniques for reducing radiolysis of [18F]-FDG only, but do not disclose any technique for reducing radiolysis of a series of radioactive fluorine-labeled amino acid compounds.
Japanese Patent Laid-open (Kokai) No. H10-147542 discloses a technique utilizing an organic compound high in physiological acceptability as a radiation protecting agent for pharmaceuticals. However, it is not apparent which compound is selected as the organic compound high in physiological acceptability or how much the compound is added in order to prevent radiolysis of the series of radioactive fluorine-labeled amino acid compounds such as anti-[18F]-FACBC.
The present invention has been made in view of the above circumstances, and aimed at providing a composition comprising a radioactive fluorine-labeled amino acid compound, which is reduced in radiolysis.
As a result of diligent researches, the present inventors have found that the radiolysis can be inhibited by adding a sugar lactone to radioactive fluorine-labeled amino acid compounds, and further have found conditions suitable for inhibiting the radiolysis of radioactive fluorine-labeled amino acid compounds.
The radioactive diagnostic imaging agent according to the present invention is characterized in that it comprises a sugar lactone and a radioactive fluorine-labeled amino acid compound represented by the following formula (1):
The sugar lactone used in the present invention is preferably selected from compounds acceptable as pharmaceutical additives.
As the sugar lactone, one which is selected from the group consisting of ascorbic acid and glucono-σ-lactone can be used preferably. Addition amount thereof needs to be enough to obtain radiolysis inhibition effect, and is preferably not less than 0.5 μmol/mL, further preferably not less than 1.0 μmol/mL, furthermore preferably not less than 5.0 μmol/mL, and particularly preferably not less than 10 μmol/mL. The upper limit of the addition amount needs to be an amount that is acceptable for pharmaceutical additives; for examples, 2.8 g is the upper limit as a total daily dose for ascorbic acid.
In the radioactive diagnostic imaging agent according to the present invention, radioactive concentration is not particularly limited as long as a sufficient amount of radioactivity can be ensured when used. More specifically, the radioactive concentration in use is preferably 25-125 MBq/mL, and more preferably 25-100 MBq/mL.
In the present specification, compounds acceptable as pharmaceutical additives mean compounds that are approved as pharmaceutical additives in the Japanese Pharmacopoeia, the United States Pharmacopoeia, the European Pharmacopoeia, and so on. In addition, sugar lactone means a cyclic ester compound that is derived by oxidation of a sugar.
According to the present invention, a composition of a radioactive fluorine-labeled amino acid compound which can be inhibited in radiolysis is provided.
Hereinafter, the most preferable embodiments for the composition of the radioactive fluorine-labeled amino acid compound according to the present invention will be described.
For production of the radioactive diagnostic imaging agent according to the present invention, a radioactive fluorine-labeled amino acid compound serving as an effective component is first synthesized. The radioactive fluorine-labeled amino acid compound according to the present invention, that is, [18F]-FACBC can be synthesized by the method disclosed in Goodman et al (Goodman et al., The Journal of Nuclear Medicine, (United States), 1999, 40, p. 331-338).
For synthesis of anti-[18F]-FACBC, a mixture comprising [18F] fluoride ion, potassium carbonate and a phase transfer catalyst is first obtained. This mixture can be obtained by the conventional method (for example, a method described in the reference (Radioisotopes, 50, (2001), p. 205-227, Radioisotopes, 50, (2001), p. 228-256, “Production and quality control of radioactive agents for PET—Handbook of synthesis and clinical use—(2nd edition)” edited by PET Chemistry Workshop). [18F]-labeling is conducted by adding, to this mixture, a solution of a labeling precursor 1-(N-(t-butoxycarbonyl)amino)-3-[((trifluoromethyl)sulfonyl)oxy]-cyclobutane-1-carboxylic acid ethylester in acetonitrile, and heating it to allow nucleophilic substitution reaction. This reaction solution is purified to remove the unreacted precursor, and then is given an acidic condition to conduct deprotection of amino groups. The resulting solution is neutralized and purified to obtain an anti-[18F]-FACBC aqueous solution. Conditions in each step may be in accordance with conventional methods (for example, the method described in International Publication No. WO2004/056725 pamphlet).
The radioactive diagnostic imaging agent according to the present invention can be obtained by mixing a required amount of sugar lactone with the radioactive halogen-labeled organic compound obtained as above. The timing of mixing is not limited as long as the required amount of sugar lactone is contained in the final agent, but it is blended preferably before final adjustment operations such as radioactive concentration adjustment and pH adjustment are made for the radioactive diagnostic imaging agent.
The radioactive diagnostic imaging agent according to the present invention needs to have a radioactivity sufficient for PET imaging when it is used, and thus the radioactive concentration at the time of production is adjusted to meet that radioactivity. For example, the agent should have a radioactivity of 1.4 GBq in about 2 mL and contain the above sugar lactone in a proportion of 10 μmol/mL immediately after production. Such a formulation of the agent provides a radioactivity of 50 to 225 MBq when the agent is used, and enables a sufficient PET imaging for adults. In addition, pH may be adjusted to a value acceptable for pharmaceuticals, for example, to 3-8.
Hereinafter, the present invention is described below in more detail by way of Examples. However, these Examples never limit the scope of the present invention.
An anti-[18F]-FACBC solution was prepared in accordance with the literature (Goodman et al., The Journal of Nuclear Medicine, (United States), 1999, 40, p. 331-338). The obtained anti-[18F]-FACBC solution was diluted with a physiological saline solution to prepare a sample solution (with diluting magnification of 4.7-7.0) so that it is supposed to have a radioactive concentration of 92.5 MBq/mL 6.5 hours after the initiation of production. In the present examples, examination was performed, supposing that 0 hour is the time when not only the preparation of the anti-[18F]-FACBC solution but also the preparation of the solution into the sample solution were completed (hereinafter, referred to as sample solution preparation time). Since production time and sample solution preparation time were varied with different production yields, the radioactive concentration at the sample solution preparation time was, in fact, about 400-750 MBq/mL (details are shown in the table) Radioactivity of the sample solution was measured by using RADIOISOTOPE DOSE CALIBRATOR CAPINTEC MODEL CRC-15R (trade name; CAPINTEC, Inc.).
The obtained sample solution was sealed in a vial of 5 mL in volume, analysis was performed by TLC analysis on the following conditions 0 hour and 9 hours after the sample solution preparation time, and radiochemical purity value was calculated in accordance with the following equation (1). Preparation of the sample solution and measurement of radiochemical purity were repeated 5 times, and the resulting value of radiochemical purity was used to evaluate stability.
TLC analysis conditions:
The results are shown in Table 1. For all the sample solutions, the radiochemical purity of anti-[18F]-FACBC solution was decreased, and the decrease (difference) of the radiochemical purity thereof was 1.57% in average. When data 0 hour and 9 hours after the sample solution preparation time were subjected to Student's t test, the results was such that p-value was 0.001, t-value was 4.58, and even in case of 1.0% of significant level, decrease in radiochemical purity was significant. From the above, it was confirmed that the radiochemical purity of the anti-[18F]-FACBC solution was decreased significantly until 9 hours after the preparation of the sample solution in the absence of additives.
The anti-[18F]-FACBC solution was prepared in the same manner as in Comparative Example 1, and diluted with the physiological saline solution under the same conditions as in Comparative Example 1.
Separately, 10, 100 and 200 μmol/mL ascorbic acid-containing physiological saline solutions were prepared.
50 μL of each of the ascorbic acid-containing physiological saline solutions was added to each 1 mL of the above diluted anti-[18F]-FACBC solution, to prepare, as sample solutions, anti-[18F]-FACBC solutions containing ascorbic acid at concentrations of 0.5 (Example 1), 5.0 (Example 2) and 10.0 (Example 3) μmol/mL.
For each sample solution, radiochemical purity 0 hour and 9 hours after the sample solution preparation time was measured under the same condition as in Comparative Example 1, and the obtained values of radiochemical purity were used to evaluate stability. Meanwhile, preparation and measurement of the sample solutions were repeated 3 times for Example 1, and 5 times for Examples 2 and 3.
The results are shown in Table 2. The decrease of radiochemical purity 9 hours after the sample solution preparation time was not more than 1% at all the concentrations of ascorbic acid. When data 0 hour and 9 hours after the sample solution preparation time were subjected to Student's t test, the result was such that the changes of radiochemical purity were not significantly different at the significant level of 1% at all the concentrations of ascorbic acid. The above results indicated that ascorbic acid at concentrations of 0.5-10.0 μmol/mL can inhibit decomposition of the anti-[18F]-FACBC solution.
As indicated in the above Examples, the radiolysis can be inhibited by adding a sugar lactone such as ascorbic acid to the radioactive fluorine-labeled amino acid compound such as anti-[18F]-FACBC. Further, the radiolysis can be inhibited significantly at a concentration of not less than 0.5 μmol/mL. In addition, since the radiolysis was inhibited at a concentration of 700 MBq/mL at maximum, it is considered that the radiolysis is naturally inhibited below that radioactive concentration, and thus a similar effect can be expected at 18.5 MBq/mL which is the minimum radioactive concentration in use.
The present invention can inhibit radiolysis of radioactive fluorine-labeled amino acid compounds which are useful as PET agents, and is useful in the field of radioactive pharmaceuticals.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-304338 | Nov 2006 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2007/067042 | 8/31/2007 | WO | 00 | 5/11/2009 |
