COMPLEX, CONTRAST AGENT AND METHOD FOR TREATING A DISEASE RELATED TO CXCR4 RECEPTOR

Abstract

Disclosed herein is a complex, a contrast agent and the method for treating a disease related to CXCR4 receptor. The complex is configured to bind the CXCR4 receptor, and is used as a medicament for diagnosis and treatment of cancers and other indications related to the CXCR4 receptor.

Claims

1. A complex configured to bind CXCR4, comprising the following structures: ##STR00009## wherein X is a chelating group, selected from a group consisting of: 1,4,7-triazacyclononane-N,N′,N″-triacetic acid (NOTA), 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), diethylenetriaminepentaacetic acid (DTPA), 1,4,8,11-tetraazacyclotetradecane-N,N′,N″,N′″-tetraacetic acid (TETA), 1,4,7-triazacyclononane phosphinic acid (TRAP) and ethylenediaminetetraacetic acid (EDTA); Y is ##STR00010## and Z is ##STR00011##

2. The complex according to claim 1, wherein the complex is ##STR00012##

3. The complex according to claim 1, further comprising a radioactive metal nuclide or a non-radioactive metal labeled on the complex of formula (I).

4. The complex according to claim 3, wherein the radioactive metal nuclide is indium-111, lutetium-177, gallium-68, gallium-67, yttrium-90 or copper-64.

5. The complex according to claim 4, wherein the radioactive metal is indium-111.

6. A contrast agent, comprising: the complex according to claim 1; and a contrast excipient.

7. A method of using the complex according to claim 1 to treat or diagnose a disease related to CXCR4.

8. The method according to claim 7, wherein the disease is a cancer, and is selected from a group consisting of: lymphoma, multiple myeloma, testicular cancer, thyroid cancer, prostate cancer, throat cancer, cervical cancer, nasopharynx cancer, breast cancer, colorectal cancer, pancreatic cancer, gastric cancer, head-and-neck cancer, esophageal cancer, rectal cancer, bladder cancer, kidney cancer, lung cancer, liver cancer, brain cancer, melanoma and skin cancer.

9. The method according to claim 7, wherein the disease is an immune disease, an infectious disease, a cardiovascular disease or an inflammatory disease.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] To make the foregoing and other objects, features, advantages, and examples of the present invention more comprehensibly, the drawings are described as follows:

[0018] FIG. 1 is a flowchart of synthesizing a complex of the present disclosure according to an implementation of the present invention;

[0019] FIG. 2 is an HPLC chromatogram of a complex of the present disclosure according to an implementation of the present invention;

[0020] FIG. 3 is a mass spectrum of a complex of the present disclosure according to an implementation of the present invention; and

[0021] FIG. 4 is a NanoSPECT/CT image of a complex of the present disclosure in a breast cancer animal model according to an implementation of the present invention.

DETAILED DESCRIPTION OF DISCLOSED EMBODIMENTS

[0022] To make the description of the present disclosure more detailed and complete, the following provides an illustrative text description of the implementations and specific examples of the present invention; but the implementations and specific examples of the present invention are not limited thereto.

[0023] Unless otherwise stated, the scientific and technical terms used in this specification have the same meanings as those understood and commonly used by a person of ordinary skill in the art. In addition, nouns used in this specification include the singular and plural forms of the nouns, unless otherwise specified.

[0024] The word “individual” or “patient” refers to an animal capable of receiving a complex of the present invention. In a preferable implementation, the animal is a mammal, and in particular, is a human.

[0025] The word “disease” herein is a disease related to CXCR4. Specifically, cells expressing CXCR4 participate in the pathogenesis of the disease, causing the development of the disease or symptoms related to the disease. For example, the “disease” may include tumors expressing CXCR4, or is caused by lymphocytes, monocytes and macrophages expressing CXCR4.

[0026] The “cancer” may be a non-solid tumor or a solid tumor. For example, the cancer includes, but is not limited to tumors expressing CXCR4, such as lymphoma, multiple myeloma, testicular cancer, thyroid cancer, prostate cancer, throat cancer, cervical cancer, nasopharynx cancer, breast cancer, colorectal cancer, pancreatic cancer, gastric cancer, head-and-neck cancer, esophageal cancer, rectal cancer, bladder cancer, kidney cancer, lung cancer, liver cancer, brain cancer, melanoma and skin cancer.

[0027] As described in this specification, the term “about” generally means that an actual value falls within plus or minus 10%, 5%, 1%, or 0.5% of a specific value or range. The term “about” herein means that an actual value falls within an acceptable standard error of an average value, depending on the consideration of a person of ordinary skill in the art the present invention pertains. Except for experiment examples, or unless otherwise clearly stated, it should be understood that the ranges, quantities, numerical values, and percentages used herein are all modified by “about”. Therefore, unless otherwise stated, the values or parameters disclosed in this specification and the appended claims are all approximate values, and may be changed as required.

[0028] To resolve the problems existing in the related art, the present inventor provides a novel complex configured to bind CXCR4 for the first time, and the complex mainly has a structure as shown in the complex of formula (I):

##STR00005##

where X is a chelating group, such as a metal ion chelating agent, selected from a group consisting of: 1,4,7-triazacyclononane-N,N′,N″-triacetic acid (NOTA), 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), diethylenetriaminepentaacetic acid (DTPA), 1,4,8,11-tetraazacyclotetradecane-N,N′,N″,N′″-tetraacetic acid (TETA), 1,4,7-triazacyclononane phosphinic acid (TRAP) and ethylenediaminetetraacetic acid (EDTA);

Y is

[0029] ##STR00006##

and

Z is

[0030] ##STR00007##

[0031] The structure of the complex of the present invention may bind to the positions of specific amino acids of CXCR4, as determined by bioinformatics analysis. Compared with conventional small molecular drugs (e.g., AMD3100), the complex provided in the present invention has a stronger ability of binding a CXCR4 receptor. Through calculation and analysis, binding energy of the complex is much lower than that of AMD3100, so that the specificity of a drug can be improved. In addition, the complex of the present invention adds a metal ion chelating agent in the structure, so that it can be labeled with radioactive metal ions or non-radioactive metal ions, and may be used for SPECT/PET medical imaging or used as an Mill contrast agent.

[0032] Furthermore, in an example of the present invention, the experiment results in a tumor animal model show that compared with commercially available CXCR4 antagonists (e.g., AMD3100), the complex of the present invention has a significantly higher aggregation amount in tumors. Therefore, it can be confirmed that the complex of the present invention has potential to be a medicament for diagnosing or treating a disease related to CXCR4.

[0033] According to an implementation of the present invention, the complex provided in the present invention can effectively bind to cells expressing CXCR4. Therefore, regardless of cancers or other diseases related to CXCR4 (for example, cardiovascular disease, inflammatory disease or immune disease), the diseases can be effectively diagnosed or treated by using the complex.

[0034] A plurality of examples is disclosed below to illustrate various different implementations of the present invention, so that those with ordinary knowledge in the technical field of the present invention can implement the technical content disclosed in the present invention according to the disclosure of the specification. Therefore, the examples disclosed below should not be used to limit the scope of the claims of the present invention.

Example 1. Synthesis of a Complex APD of the Present Invention

[0035] ##STR00008##

[0036] A complex of Formula (II) of the invention is submitted to Jinsheng company for synthesis, and synthesizing steps are referred to FIG. 1. Analysis results of synthetic products by HPLC and mass spectrometry (MS) are shown in FIG. 2 to FIG. 3, where the analysis data of NMR is Aromatic H: 7.2˜8.4, N—CH.sub.2CH.sub.2—NH: 2.2˜2.7, C—CH.sub.2—CH: 1.6, N—CH.sub.2—CH: 3.7˜3.8, N—CH.sub.2-ar. H: 4.8. HPLC results show that the peak time of the main component is 11.0 min; the content percentage (chromatographic purity) is 97.52% (>95%). The mass spectrum of the parent molecular ion of the main component is: [M+H] m/z=441, in line with the main component.

Example 2. A Complex APD of the Present Invention Labeled with In-111

[0037] 5 μg to 50 μg of the complex APD of Example 1 is reacted with 1 mCi to 10 mCi of In-111 (with a specific activity greater than 50 mCi/mL) in citrate/acetate buffer solution (pH 3.5˜6.5) at 50° C. to 95° C. for 10 min to 30 min, to obtain a product, the complex APD labeled with In-111.

[0038] Instant thin layer chromatography (iTLC) is used to analyze the efficiency of radioactive labeling, and results show that the labeling efficiency is greater than 95%.

Example 3. Analysis of Binding Efficacy of the Complex APD of the Present Invention

[0039] This experimental example uses BIOVIA software for analysis of binding energy, and results are calculated by docking the complex of the present invention and a control medicament TIQ-15 with amino acids at specific positions of CXCR4 (TRP94, HIS113, TYR116, ASP97, ALA98 and ILE185). See Table 1.

TABLE-US-00001 TABLE 1 Binding energy TIQ-15 (an AMD3100 derivative) −88 kcal/mol APD −300 kcal/mol

[0040] The results show that the binding energy of the complex APD of the present invention is much lower than that of the control medicament, and thus it can be confirmed that the complex of the present invention has better sensitivity and specificity, and is suitable to be used as a medicament for diagnosing or treating cancers and other indications related to CXCR4.

Example 4. Evaluation of the Efficacy of the Radioactive Nuclide-Labeled Complex of the Present Invention by Using a Breast Cancer Animal Model

[0041] 0.1 mCi to 0.5 mCi of the complex of the present invention is injected into mice with breast cancer tumors through tail vein. After biological distribution for 1 h to 6 h, single photon emission computed tomography (SPECT) is used for imaging.

[0042] The result of this experimental example is shown in FIG. 4. The result shows that after two hours of the injection of the complex of the present invention, significant drug aggregation can be seen at the tumor site.

[0043] The specific examples disclosed above are not intended to limit the scope of the claims of the present invention. Those of ordinary skill in the art can make changes according to their common experience within the scope covered by the principles and spirit of the present invention. Therefore, the scope of rights claimed by the present invention should be subject to the scope defined by the claims.