Title of Invention	"PORPHYRIN DERIVATES AND METHOD OF PREPARATION OF SAID DERIVATIVE"
Abstract	The invention relates to derivatives of porphyrin, particularly chlorins and/or bacteriochlorins, having formula (I) and (II), which can be used in photodynamic therapy. According to the invention, X1'X2,X3,X4,X5",X6,X7,X8, which may be identical or different, each represent halogen atoms or hydrogen atoms, and R1 , R2 , R3 , R4 , which may be identical or different, are each selected from the following groups: -OH, amino acids, -OR and -NHR and/or a chlorine atom, wherein R is an alkyl group having between 1 and 12 carbon atoms. The invention also relates to an anticancer and/or antiviral and/or antimicrobial medicament for human or animal use, which contains one or more compounds as the main active ingredient.

Title of Invention

"PORPHYRIN DERIVATES AND METHOD OF PREPARATION OF SAID DERIVATIVE"

Abstract

The invention relates to derivatives of porphyrin, particularly chlorins and/or bacteriochlorins, having formula (I) and (II), which can be used in photodynamic therapy. According to the invention, X1'X2,X3,X4,X5",X6,X7,X8, which may be identical or different, each represent halogen atoms or hydrogen atoms, and R1 , R2 , R3 , R4 , which may be identical or different, are each selected from the following groups: -OH, amino acids, -OR and -NHR and/or a chlorine atom, wherein R is an alkyl group having between 1 and 12 carbon atoms. The invention also relates to an anticancer and/or antiviral and/or antimicrobial medicament for human or animal use, which contains one or more compounds as the main active ingredient.

Full Text	NEW PORPHYRIN DERIVATES, IN PARTICULAR CHLORINS AND/OR BACTERIOCHLORINS AND THEIR APPLICATIONS IN PHOTODYNAMIC THERAPY Photodynamic therapy (PDT) is a technique used for treating several types of diseases, in particular certain types of cancer. Such technique consists in marking the pathological tissues with a photosensitizer, then in causing selective destruction of said tissues while exposing them to a light source of a specific wavelength. Such monochromatic light is generally produced by a laser or a laser diode. By photosensitizer is meant any molecule liable to store light energy, to be activated by said energy and to lend itself therefore to numerous biochemical combinations. The photosensitizer, generally between 0.1 and 0.5 micromole/kg of body mass, is delivered to the patient, then picked up by the cells of the whole organism. The photosensitizing molecule accumulates preferably in cancerous cells, but remains inactive until exposed to a light of appropriate wavelength. The illumination or irradiation of the tumour by light activates the molecule, which then interacts with oxygen and forms a transient substance, in particular singlet oxygen. Singlet oxygen is a very reactive and toxic molecule which destroys the cancerous cells wherein the photosensitizer has concentrated. A certain time elapses between the delivery of the photosensitizer and its activation by means of the laser light. The laser light used in photodynamic therapy is focused by means of an optic fibre and is applied only for a few minutes. The practitioner holds the optic fibre in close vicinity of the cancer so as to delivery the correct amount of light. Consequently, photodynamic therapy only damages the healthy cells minimally. At the initial stage of a cancer, the objective of such technique may consist in eliminating completely and curing the cancer but, at an advanced stage, it may consist in reducing the volume of the tumour in order to alleviate symptoms. New normal cells replace those destroyed by photodynamic therapy, which enables rapid healing after treatment and avoids particularly ungracious scars which may form with other others of ablation of tissues. Even patients already treated by surgery, radiotherapy or chemotherapy may be subjected to this technique reliably. By way of examples of diseases which may be treated by photodynamic therapy, one may quote in particular stomach, intestine, lung, breast, uterus, oesophagus, ovary, pancreas, liver, bladder, bile, tongue, brain, skin, thyroid, prostate, parotid gland cancer, as well as certain viral and/or microbial diseases. Photodynamic therapy may also be used as a means for diagnosing certain forms of cancer. In this view, it suffices that the photosensitizing molecules are fluorescent and, hence, capable of emitting light when they receive a radiation. At the moment, the use of certain porphyrin derivatives, in particular hematoporphyrin, as photosensitizers is known in photodynamic therapy. This agent, known under the trademark Photofrin, registered by AXCAN PHARMA INC., is a purified mixture of hematoporphyrin. Hematoporphyrin is in turn a derivative of porcine hemoglobin. Besides, Photofrin® has been the sole photosensitizing molecule until now, which has been authorised for marketing in several countries and, in particular in France, for treating oesophagus cancer. In spite of the advantages shown by Photofrin®, such as its solubility in an aqueous medium, a good throughput of singlet oxygen formation and an easy synthesis, it still exhibits a few shortcomings. First of all, Photofrin® is activated by a 630 nm light. Still, at such wavelength, the penetration of light into the tissues only ranges from 5 to 10 mm, which exhibits a severe handicap when tumours are wider and deeper. Moreover, such photosensitizer causes cutaneous photosensitivity up to six weeks after treatment. Finally, that fact that Photofrin® is a mixture of several molecules, makes the choice of the appropriate dosimetry more difficult, of the photosensitizer as well as of the light delivered. Among other compounds under study, so-called second generation compounds, the document WO-98/50386 describes certain benzoporphyrine derivatives. Such derivatives exhibit certain advantages relative to Photofrin® in that they absorb light at a 690 nm wavelength and, consequently, may be used in the treatment of wider and deeper cancers. Such derivates exhibit moreover better selectivity against cancerous cells. However, certain problem associated with selectivity, light absorption and toxicity persist. The purpose of the present invention is to offer new porphyrin derivatives, such as in particular chlorins and/or bacteriochlorins which remedy the shortcomings aforementioned, in particular as regards preferential accumulation in cancerous cells, better stability and lower phototoxicity. Another aim of the present invention is to offer an anti-cancerous and/or anti-viral and/or anti-microbial medication in order to be used in photodynamic therapy. Other aims and advantages of the invention will appear in the following description which is given only by way of example and without being limited thereto. The present invention relates to a porphyrin derivative, in particular chlorin, of formula: (Figure Removed) - X1 X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms and/or hydrogen atoms ; - R1, R2, R3, R4 are each, identical or different, selected among the moieties : -OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms. The present invention also relates to a porphyrin derivative, in particular bacteriochlorin, of formula : (Figure Removed) wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms and/or hydrogen atoms ; - R1, R2, R3, R4 are each, identical or different, selected among the moieties ; -OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms. One of the advantages of these derivatives lies in the presence of the chlorosulfonyl moiety in the molecule, as described in the present invention, which enables to introduce simply and efficiently a large variety of chemical moieties. The present invention relates, moreover, to an anticancerous and/or antiviral and/or antimicrobial medication for human or animal usage exhibiting as a main active agent one or several compounds described in the present invention. The invention will be understood better when reading the following description, accompanied by the appended drawings among which: - Figure 1 represents the absorption spectrum of chlorin according to the formula (I) in an aqueous solution before (full line) and after (dotted line) irradiation of the sample by the second harmonic of a laser Nd : YAG; - Figure 2 represents the absorption spectrum of bacteriochlorin according to the formula (II) in an aqueous solution before (full line) and after (dotted line) irradiation of the sample by the second harmonic of a laser Nd : YAG. The present invention relates first of all to a porphyrin derivative, in particular chlorin, of formula(Figure Removed) - X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms and/or hydrogen atoms ; - R1, R2, R3, R4 are each, identical or different, selected among the moieties ; - OH, amino acids, -OR and -NHR and/or chlorine atoms, wherein R is an alkyl moiety having 1 to 12 carbon atoms. One of the advantages of such type of derivatives lies in that they are amphiphile. The amphiphilic character is essential so that the molecules may cross the cellular membrane and accumulate inside the cells. By amphiphilic, is meant any molecule which exhibits both a hydrophilic and hydrophobic character. This type of derivatives exhibits an absorption band at 650 nm, as shown on Figure 1. The present invention also relates to the derivatives complying with formula (I), wherein: - X1, X2, X3, X4, X5, X5, X7, X8 are each, identical or different, selected among halogen atoms, and/or hydrogen atoms, such that at least one of the radicals X of each pair X1/ X2, X3/ X4, X5/X6, X7/X8 is a halogen atom, An advantage of this particular type of derivatives lies in the presence of the halogen atoms in the ortho positions of the phenyl moiety which increases the quantum yield of the formation of the triplet state, without reducing significantly the lifetime thereof. With higher quantum yield, the triplet state may transfer its energy more efficiently towards oxygen with consequently higher yield in the formation of singlet oxygen. Moreover, the halogen atoms in the ortho positions of the phenyl moiety make the tetrapyrolic macrocycle more stable and, hence, more efficient in its use in photodynamic therapy. Still according to the present invention, and in compliance with formula (I) : - X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms; - X1, X3, X5 and X7 are hydrogen atoms, - R1, R2, R3, R4 are chlorine atoms. According to another variation of the present invention, and in compliance with formula (I): - X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms; - X1, X3, X5 and X7 are hydrogen atoms, - R1, R2, R3, R4 are-OH moieties. The present invention also relates to derivatives complying with formula (I), wherein: - X1, X2, X3, X4, X5, X5, X7, X8 are chlorine atoms, - R1, R2, R3, R4 are either chlorine atoms, or-OH moieties. The present invention also relates to a porphyrin derivative, in particular bacteriochlorin, of formula : (Figure Removed) : - X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms, and/or hydrogen atoms; - R1, R2, R3, R4 are each, identical or different, selected among the moieties : -OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms. An advantage of such type of derivatives, and such that for the case of chlorins described above, lies in that they are also amphiphilic. Another advantage of these derivatives, in particular bacteriochlorin complying with the formula (II), consists in absorbing light in the red region at 750 nm, as illustrated on Figure 2. At such wavelength, the shielding effects caused by human tissues, in particular by hemoglobin, are not so high, which enables to increase the 'amount' of light reaching the photosensitizers inside the cells. The present invention also relates to the derivatives complying with formula (II), wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms, and/ or hydrogen atoms, such that at least one of the radicals X of each pair X1/ X2, X3/x4 X5/X6, X7/X8 is a halogen atom. As for the case of chlorin described above, the presence of the halogen atoms in the ortho positions of the phenyl moiety, increases the quantum yield of the formation of the triplet state, without reducing significantly the lifetime thereof, and consequently, also increases the increase in the formation of the singlet oxygen. The present invention also relates to certain derivatives, complying with formula (II), wherein: -X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms, - X1, X3, X5 and X7 are hydrogen atoms, - R1, R2, R3, R4 are chlorine atoms. According to another variation of the present invention, and in compliance with formula (II): - X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms, - X1, X3, X5 and X7 are hydrogen atoms, - R1, R2, R3, R4 are-OH moieties. The present invention relates moreover to derivatives complying with formula (II), wherein: X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms, - R1, R2, R3, R4 are either chlorine atoms, or-OH moieties. The presence of the halogen atoms in the ortho positions of the phenyl moiety also makes the tetrapyrrolic macrocycle and its derivatives more stable. According to the present invention, the halogen atoms are fluorine and/or chlorine and/or bromine. Another aim of the present invention consists in the method of preparation of derivatives as described above including the following steps : - a chlorosulfonation step of the corresponding halogenated porphyrin, - a reducing step of the halogenated and chlorosulfonated porphyrin to chlorin and/or to bacteriochlorin with hydrazide and in the presence of organic hindered bases, - a coupling step between the chlorosulfonated moiety and amines and/or amino acids and/or alcohols, or hydrolysing the chlorine of the chlorosulfonated moiety with water. By way of non limiting example, the chemical synthesis of the derivative complying with formula (I) wherein: - X2, X4, X6 and X8 are chlorine atoms ; - X1, X3, X5 and X7 are hydrogen atoms, - R1, R2, R3, R4 are-OH moieties, was conducted as follows: 5,10,15,20-tetrakis(2-chloro-3-chlorosulfonylphenyl)porphyrin (0.0658 g, 6.55 x 10~5 mol) was dissolved in N.N-dimethylformamide and/or toluene, and/or pyridine and/ or picoline (50 ml) dried and distilled beforehand, and the temperature of the reactive mixture was raised from 50°C to 150°C. Then, a solution of p-toluene sulfonyl hydrazide (5.5 x 10-5 mol) and a bulky organic base, such as DABCO and/or DBU in DMF (5ml_) was added to the reactive mixture. The mixture was stirred at 150°C under nitrogen atmosphere and in the absence of light. The evolution of the reaction was followed by spectroscopy of the visible region until the band Q at 650 nm reached its maximum. Then, the solvent was evaporated and the reactive mixture was treated and the product obtained was hydrolysed with water and purified by solvent-solvent extraction. After re-crystallization with a methanol/dichlomethane mixture, the product was obtained with an 80% yield. Mass spectroscopy (FAB), m/z: 1075 (central peak). Vis-UV (buffer solution NaOH, KH2P04), maximal wavelength (in nm) :414, 516, 542, 598, 649. Fluorescence quantum yield: 0.04 Lifetime of the triplet state in a nitrogen-saturated aqueous solution : 235 us Lifetime of the triplet state in an air-saturated aqueous solution : 3.88 us quantum yield of the formation of singlet oxygen in a deuterated aqueous solution: 0.56. Lifetime of singlet oxygen: 65 us in deuterated water Schematically the reaction may be described as follows: (Figure Removed) Also, by way of non limiting example, the chemical synthesis of the derivative complying with formula (II) wherein: - X2, X4, X6 and X8 are chlorine atoms ; -X1, X3, X5 and X7 are hydrogen atoms, - R1, R2, R3, R4 are-OH moieties, was conducted as follows: 5,10,15,20-tetrakis(2-chloro-3-chlorosulfonylphenyl)porphyrin (0.0658 g, 6.55 x 10-5 mol) was dissolved in N,N-dimethylformamide, and/ or pyridine and/ or picoline (50 ml_)dried and distilled beforehand, and the temperature was raised from 50°C°C to 150°C. Then, a solution of p-toluene sulfonyl hydrazide (130.0 x 10~5 mol) and DABCO in DMF (5mL) was added to the reactive mixture. The mixture was stirred at 150°C under nitrogen atmosphere and sheltered from light. The evolution of the reaction was followed by spectroscopy of the visible region until the band Q at 750 nm reached its maximum. Then, the solvent was evaporated and the reactive mixture was treated and the product obtained was hydrolysed with water to provide the requested product with a 77% throughput. Mass spectroscopy (FAB), m/z: 1077 (central peak). Vis-UV (buffer solution NaOH, Kh^PC^), maximal wavelength (in nm): 353,376,486,518,604,748. Fluorescence quantum yield: 0.013 Lifetime of the triplet state in a nitrogen-saturated aqueous solution : 235 us Lifetime of the triplet state in an air-saturated aqueous solution : 3,88 us Quantum yield of the formation of singlet oxygen in a deuterated aqueous solution: greater than 30 %. Lifetime of singlet oxygen: 65 us in deuterated water. Also, schematically the reaction may be described as follows(Figure Removed) porphyrin in the synthesis of chlorin and of bacteriochlorin described above, is known to the man of the art and has been described in the literature, in particular in the Journal of Heterocyclic Chemistry, 28 : 635 (1991). According to the present invention, the quanta yields of the formation of singlet oxygen were obtained by comparison between the phosphorescence intensity of singlet oxygen at 1270 nm wavelength in a solution containing the photosensitizer under study and the phosphorescence intensity obtained from another solution exhibiting the same absorptivity at the same wavelength, and including a reference photosensitizer. According to the present invention, the reference photosensitizer used in meso-tetrakis(3-sulfophenyl)porphyrin (TPPS) whereof the value for the quantum yield of the formation of singlet oxygen in deuterated water is 0.64 at 7.4 pH (photochem. Photobiol, 70 : 391, 1999). The present invention also relates to an anticancerous and/or antiviral and/or antimicrobial medication for human or animal usage exhibiting as a main active agent one or several compounds described in the present invention. This type of medication, used in particular in photodynamic therapy, may also contain one or several pharmaceutically acceptable excipients. Naturally, other embodiments of the present invention, understandable to the man of the art, could have been contemplated without departing from the framework of the invention. CLAIMS 1. Porphyrin derivatives, in particular chlorin, of (Figure Removed) X1, X2, X3, X4, X5; X6, X7, X8 are each, identical or different, selected among halogen atoms, and/or hydrogen atoms, such that at least one of the radicals X of each pair X1/X2, X3/X4, X5/X6, X7/X8 is a halogen atom, - R1, R2, R3, R4 are each, identical or different, selected among the moieties : -OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms. 2. Porphyrin derivatives according to claim 1, complying with formula (I), wherein: - X2, X4, X6 and X8 are chlorine atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are chlorine atoms. 3. Porphyrin derivatives according to claim 1, complying with formula (I), wherein: - X2, X4, X6 and X8 are fluor atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are chlorine atoms. 4. Porphyrin derivatives according to claim 1, complying with formula (I), wherein: - X2, X4, X6 and X8 are fluor atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are -OH moieties. 5. Porphyrin derivatives according to claim 1, complying with formula (I), wherein: - X2, X4, X6 and X8 are fluor atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are -OH moieties. 6. Porphyrin derivatives according to claim 1, complying with formula (I), wherein: - X1, X2, X3. X4, X5, X6, X7, X8 are chlorine atoms ; - R1, R2, R3, R4 are chlorine atoms. 7. Porphyrin derivatives according to claim 1, complying with formula (I), wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms ; - R1, R2, R3, R4 are -OH moieties. 8. Porphyrin derivatives, in particular bacteriochlorin, of formula: R30,S (Figure Removed) wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms, and/or hydrogen atoms ; - R1, R2, R3, R4 are each, identical or different, selected among the moieties : - OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms. 9. Porphyrin derivatives according to claim 8, complying with formula (II), wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms and/or hydrogen atoms, such that at least one of the radicals X of each pair X1/ X2, X3/X4, X5/X6, X7/X8 is a halogen atom, 10. Porphyrin derivatives according to claim 8, complying with formula (II), wherein: - X2, X4, X6 and X8 are chlorine atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are chlorine atoms. 11. Porphyrin derivatives according to claim 8, complying with formula (II), wherein: - X2, X4, X6 and X8 are fluor atoms ; - X1, X3, X5 and X7are hydrogen atoms ; - R1, R2, R3, R4 are chlorine atoms. 12. Porphyrin derivatives according to claim 8, complying with formula (I), wherein: - X2, X4, X6 and X8 are chlorine atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are-OH moieties. 13. Porphyrin derivatives according to claim 8, complying with formula (II), wherein: - X2, X4, X6 and X8 are fluor atoms ; - X1, X3, X5 and X7 are hydrogen atoms ; - R1, R2, R3, R4 are -OH moieties. 14. Porphyrin derivatives according to claim 8, complying with formula (II), wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms ; - R1, R2, R3, R4 are chlorine atoms. 15. Porphyrin derivatives according to claim 8, complying with formula (II), wherein: - X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms ; - R1, R2, R3, R4 are -OH moieties. 16. Porphyrin derivatives according to any of the claims 1 or 8, characterised in that the halogen atoms are fluorine and/or chlorine and/or bromine. 17. A method for the preparation of the porphyrin derivatives according to any of the previous claims, characterised in that it includes: - a reducing step of the corresponding halogenated and chlorosulfonated porphyrin to chlorin and/or to bacteriochlorin with hydrazide and organic bulky bases; - a coupling step between the chlorosulfonated moiety and amines and/or amino acids and/or alcohols. 18. A method of preparation of the derivatives according to any of the previous claims, characterised in that it includes: - a reducing step of the corresponding halogenated and chlorosulfonated porphyrin to chlorin and/or to bacteriochlorin with hydrazide and organic bulky bases; a hydrolysing step of the chlorine of the chlorosulfonated moiety. 19. An anticancerous and/or antiviral and/or antimicrobial medication for human or animal usage exhibiting as a main active agent one or several compounds according to claims 1 to 16.

Full Text

NEW PORPHYRIN DERIVATES, IN PARTICULAR CHLORINS AND/OR BACTERIOCHLORINS AND THEIR APPLICATIONS IN PHOTODYNAMIC THERAPY
Photodynamic therapy (PDT) is a technique used for treating several types of diseases, in particular certain types of cancer. Such technique consists in marking the pathological tissues with a photosensitizer, then in causing selective destruction of said tissues while exposing them to a light source of a specific wavelength. Such monochromatic light is generally produced by a laser or a laser diode.
By photosensitizer is meant any molecule liable to store light energy, to be activated by said energy and to lend itself therefore to numerous biochemical combinations.
The photosensitizer, generally between 0.1 and 0.5 micromole/kg of body mass, is delivered to the patient, then picked up by the cells of the whole organism. The photosensitizing molecule accumulates preferably in cancerous cells, but remains inactive until exposed to a light of appropriate wavelength. The illumination or irradiation of the tumour by light activates the molecule, which then interacts with oxygen and forms a transient substance, in particular singlet oxygen. Singlet oxygen is a very reactive and toxic molecule which destroys the cancerous cells wherein the photosensitizer has concentrated.
A certain time elapses between the delivery of the photosensitizer and its activation by means of the laser light. The laser light used in photodynamic therapy is focused by means of an optic fibre and is applied only for a few minutes. The practitioner holds the optic fibre in close vicinity of the cancer so as to delivery the correct amount of light. Consequently, photodynamic therapy only damages the healthy cells minimally.
At the initial stage of a cancer, the objective of such technique may consist in eliminating completely and curing the cancer but, at an advanced stage, it may consist in reducing the volume of the tumour in order to alleviate symptoms. New normal cells replace those destroyed by photodynamic therapy, which enables rapid healing after treatment and avoids particularly ungracious scars which may form with other others of ablation of tissues.

Even patients already treated by surgery, radiotherapy or chemotherapy may be subjected to this technique reliably.
By way of examples of diseases which may be treated by photodynamic therapy, one may quote in particular stomach, intestine, lung, breast, uterus, oesophagus, ovary, pancreas, liver, bladder, bile, tongue, brain, skin, thyroid, prostate, parotid gland cancer, as well as certain viral and/or microbial diseases.
Photodynamic therapy may also be used as a means for diagnosing certain forms of cancer. In this view, it suffices that the photosensitizing molecules are fluorescent and, hence, capable of emitting light when they receive a radiation.
At the moment, the use of certain porphyrin derivatives, in particular hematoporphyrin, as photosensitizers is known in photodynamic therapy. This agent, known under the trademark Photofrin, registered by AXCAN PHARMA INC., is a purified mixture of hematoporphyrin. Hematoporphyrin is in turn a derivative of porcine hemoglobin.
Besides, Photofrin® has been the sole photosensitizing molecule until now, which has been authorised for marketing in several countries and, in particular in France, for treating oesophagus cancer.
In spite of the advantages shown by Photofrin®, such as its solubility in an aqueous medium, a good throughput of singlet oxygen formation and an easy synthesis, it still exhibits a few shortcomings.
First of all, Photofrin® is activated by a 630 nm light. Still, at such wavelength, the penetration of light into the tissues only ranges from 5 to 10 mm, which exhibits a severe handicap when tumours are wider and deeper. Moreover, such photosensitizer causes cutaneous photosensitivity up to six weeks after treatment. Finally, that fact that Photofrin® is a mixture of several molecules, makes the choice of the appropriate dosimetry more difficult, of the photosensitizer as well as of the light delivered.
Among other compounds under study, so-called second generation compounds, the document WO-98/50386 describes certain benzoporphyrine derivatives. Such derivatives exhibit certain advantages relative to Photofrin® in that they absorb light at a 690 nm wavelength and, consequently, may be used in the

treatment of wider and deeper cancers. Such derivates exhibit moreover better selectivity against cancerous cells.
However, certain problem associated with selectivity, light absorption and toxicity persist.
The purpose of the present invention is to offer new porphyrin derivatives, such as in particular chlorins and/or bacteriochlorins which remedy the shortcomings aforementioned, in particular as regards preferential accumulation in cancerous cells, better stability and lower phototoxicity.
Another aim of the present invention is to offer an anti-cancerous and/or anti-viral and/or anti-microbial medication in order to be used in photodynamic therapy.
Other aims and advantages of the invention will appear in the following description which is given only by way of example and without being limited thereto.
The present invention relates to a porphyrin derivative, in particular chlorin, of formula:
(Figure Removed)
- X1 X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among
halogen atoms and/or hydrogen atoms ;
- R1, R2, R3, R4 are each, identical or different, selected among the moieties : -OH,
amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety
having 1 to 12 carbon atoms.
The present invention also relates to a porphyrin derivative, in particular bacteriochlorin, of formula :
(Figure Removed)
wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen atoms and/or hydrogen atoms ;
- R1, R2, R3, R4 are each, identical or different, selected among the moieties ; -OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms.
One of the advantages of these derivatives lies in the presence of the chlorosulfonyl moiety in the molecule, as described in the present invention, which enables to introduce simply and efficiently a large variety of chemical moieties.
The present invention relates, moreover, to an anticancerous and/or antiviral and/or antimicrobial medication for human or animal usage exhibiting as a main active agent one or several compounds described in the present invention.
The invention will be understood better when reading the following description, accompanied by the appended drawings among which:
- Figure 1 represents the absorption spectrum of chlorin according
to the formula (I) in an aqueous solution before (full line) and after (dotted line)
irradiation of the sample by the second harmonic of a laser Nd : YAG;
- Figure 2 represents the absorption spectrum of bacteriochlorin
according to the formula (II) in an aqueous solution before (full line) and after
(dotted line) irradiation of the sample by the second harmonic of a laser Nd : YAG.
The present invention relates first of all to a porphyrin derivative, in particular chlorin, of formula(Figure Removed)
- X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among
halogen atoms and/or hydrogen atoms ;
- R1, R2, R3, R4 are each, identical or different, selected among the moieties ; -
OH, amino acids, -OR and -NHR and/or chlorine atoms, wherein R is an alkyl
moiety having 1 to 12 carbon atoms.
One of the advantages of such type of derivatives lies in that they are amphiphile. The amphiphilic character is essential so that the molecules may cross the cellular membrane and accumulate inside the cells.
By amphiphilic, is meant any molecule which exhibits both a hydrophilic and hydrophobic character.
This type of derivatives exhibits an absorption band at 650 nm, as shown on Figure 1.
The present invention also relates to the derivatives complying with formula (I), wherein:
- X1, X2, X3, X4, X5, X5, X7, X8 are each, identical or different, selected among
halogen atoms, and/or hydrogen atoms, such that at least one of the radicals X of
each pair X1/ X2, X3/ X4, X5/X6, X7/X8 is a halogen atom,
An advantage of this particular type of derivatives lies in the presence of the halogen atoms in the ortho positions of the phenyl moiety which
increases the quantum yield of the formation of the triplet state, without reducing significantly the lifetime thereof. With higher quantum yield, the triplet state may transfer its energy more efficiently towards oxygen with consequently higher yield in the formation of singlet oxygen.
Moreover, the halogen atoms in the ortho positions of the phenyl moiety make the tetrapyrolic macrocycle more stable and, hence, more efficient in its use in photodynamic therapy.
Still according to the present invention, and in compliance with formula (I) :
- X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms;
- X1, X3, X5 and X7 are hydrogen atoms,
- R1, R2, R3, R4 are chlorine atoms.
According to another variation of the present invention, and in compliance with formula (I):
- X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms;
- X1, X3, X5 and X7 are hydrogen atoms,
- R1, R2, R3, R4 are-OH moieties.
The present invention also relates to derivatives complying with formula (I), wherein:
- X1, X2, X3, X4, X5, X5, X7, X8 are chlorine atoms,
- R1, R2, R3, R4 are either chlorine atoms, or-OH moieties.
The present invention also relates to a porphyrin derivative, in particular bacteriochlorin, of formula :
(Figure Removed)
:
- X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among
halogen atoms, and/or hydrogen atoms;
- R1, R2, R3, R4 are each, identical or different, selected among the moieties : -OH,
amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety
having 1 to 12 carbon atoms.
An advantage of such type of derivatives, and such that for the case of chlorins described above, lies in that they are also amphiphilic.
Another advantage of these derivatives, in particular bacteriochlorin complying with the formula (II), consists in absorbing light in the red region at 750 nm, as illustrated on Figure 2. At such wavelength, the shielding effects caused by human tissues, in particular by hemoglobin, are not so high, which enables to increase the 'amount' of light reaching the photosensitizers inside the cells.
The present invention also relates to the derivatives complying with formula (II), wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among
halogen atoms, and/ or hydrogen atoms, such that at least one of the radicals X of
each pair X1/ X2, X3/x4 X5/X6, X7/X8 is a halogen atom.
As for the case of chlorin described above, the presence of the halogen atoms in the ortho positions of the phenyl moiety, increases the quantum yield of the formation of the triplet state, without reducing significantly the lifetime thereof, and consequently, also increases the increase in the formation of the singlet oxygen.
The present invention also relates to certain derivatives, complying with formula (II), wherein: -X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms,
- X1, X3, X5 and X7 are hydrogen atoms,
- R1, R2, R3, R4 are chlorine atoms.
According to another variation of the present invention, and in compliance with formula (II):
- X2, X4, X6 and X8 are either chlorine atoms, or fluorine atoms,
- X1, X3, X5 and X7 are hydrogen atoms,
- R1, R2, R3, R4 are-OH moieties.
The present invention relates moreover to derivatives complying with formula (II), wherein: X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms,
- R1, R2, R3, R4 are either chlorine atoms, or-OH moieties.
The presence of the halogen atoms in the ortho positions of the phenyl moiety also makes the tetrapyrrolic macrocycle and its derivatives more stable.
According to the present invention, the halogen atoms are fluorine and/or chlorine and/or bromine.
Another aim of the present invention consists in the method of preparation of derivatives as described above including the following steps :
- a chlorosulfonation step of the corresponding halogenated
porphyrin,
- a reducing step of the halogenated and chlorosulfonated porphyrin
to chlorin and/or to bacteriochlorin with hydrazide and in the presence of organic
hindered bases,
- a coupling step between the chlorosulfonated moiety and amines
and/or amino acids and/or alcohols, or hydrolysing the chlorine of the
chlorosulfonated moiety with water.
By way of non limiting example, the chemical synthesis of the derivative complying with formula (I) wherein:
- X2, X4, X6 and X8 are chlorine atoms ;
- X1, X3, X5 and X7 are hydrogen atoms,
- R1, R2, R3, R4 are-OH moieties,
was conducted as follows:
5,10,15,20-tetrakis(2-chloro-3-chlorosulfonylphenyl)porphyrin (0.0658 g, 6.55 x 10~5 mol) was dissolved in N.N-dimethylformamide and/or toluene, and/or pyridine and/ or picoline (50 ml) dried and distilled beforehand, and the temperature of the reactive mixture was raised from 50°C to 150°C. Then, a solution of p-toluene sulfonyl hydrazide (5.5 x 10-5 mol) and a bulky organic base, such as DABCO and/or DBU in DMF (5ml_) was added to the reactive mixture. The mixture was stirred at 150°C under nitrogen atmosphere and in the absence of light.
The evolution of the reaction was followed by spectroscopy of the visible region until the band Q at 650 nm reached its maximum.
Then, the solvent was evaporated and the reactive mixture was treated and the product obtained was hydrolysed with water and purified by solvent-solvent extraction. After re-crystallization with a methanol/dichlomethane mixture, the product was obtained with an 80% yield. Mass spectroscopy (FAB), m/z: 1075 (central peak).
Vis-UV (buffer solution NaOH, KH2P04), maximal wavelength (in nm) :414, 516, 542, 598, 649. Fluorescence quantum yield: 0.04
Lifetime of the triplet state in a nitrogen-saturated aqueous solution : 235 us
Lifetime of the triplet state in an air-saturated aqueous solution : 3.88 us
quantum yield of the formation of singlet oxygen in a deuterated aqueous solution: 0.56.
Lifetime of singlet oxygen: 65 us in deuterated water
Schematically the reaction may be described as follows:
(Figure Removed)
Also, by way of non limiting example, the chemical synthesis of the derivative complying with formula (II) wherein:
- X2, X4, X6 and X8 are chlorine atoms ;
-X1, X3, X5 and X7 are hydrogen atoms,
- R1, R2, R3, R4 are-OH moieties,
was conducted as follows:
5,10,15,20-tetrakis(2-chloro-3-chlorosulfonylphenyl)porphyrin (0.0658 g, 6.55 x 10-5 mol) was dissolved in N,N-dimethylformamide, and/ or pyridine and/ or picoline (50 ml_)dried and distilled beforehand, and the temperature was raised from 50°C°C to 150°C. Then, a solution of p-toluene sulfonyl hydrazide (130.0 x 10~5 mol) and DABCO in DMF (5mL) was added to the reactive mixture. The mixture was stirred at 150°C under nitrogen atmosphere and sheltered from light. The evolution of the reaction was followed by spectroscopy of the visible region until the band Q at 750 nm reached its maximum.
Then, the solvent was evaporated and the reactive mixture was treated and the product obtained was hydrolysed with water to provide the requested product with a 77% throughput. Mass spectroscopy (FAB), m/z: 1077 (central peak).
Vis-UV (buffer solution NaOH, Kh^PC^), maximal wavelength (in nm): 353,376,486,518,604,748.
Fluorescence quantum yield: 0.013
Lifetime of the triplet state in a nitrogen-saturated aqueous solution : 235 us
Lifetime of the triplet state in an air-saturated aqueous solution : 3,88 us
Quantum yield of the formation of singlet oxygen in a deuterated aqueous solution: greater than 30 %.
Lifetime of singlet oxygen: 65 us in deuterated water.
Also, schematically the reaction may be described as follows(Figure Removed)
porphyrin in the synthesis of chlorin and of bacteriochlorin described above, is known to the man of the art and has been described in the literature, in particular in the Journal of Heterocyclic Chemistry, 28 : 635 (1991).
According to the present invention, the quanta yields of the formation of singlet oxygen were obtained by comparison between the phosphorescence intensity of singlet oxygen at 1270 nm wavelength in a solution containing the photosensitizer under study and the phosphorescence intensity obtained from another solution exhibiting the same absorptivity at the same wavelength, and including a reference photosensitizer.
According to the present invention, the reference photosensitizer used in meso-tetrakis(3-sulfophenyl)porphyrin (TPPS) whereof the value for the quantum yield of the formation of singlet oxygen in deuterated water is 0.64 at 7.4 pH (photochem. Photobiol, 70 : 391, 1999).
The present invention also relates to an anticancerous and/or antiviral and/or antimicrobial medication for human or animal usage exhibiting as a main active agent one or several compounds described in the present invention.
This type of medication, used in particular in photodynamic therapy, may also contain one or several pharmaceutically acceptable excipients.
Naturally, other embodiments of the present invention, understandable to the man of the art, could have been contemplated without departing from the framework of the invention.

CLAIMS
1. Porphyrin derivatives, in particular chlorin, of (Figure Removed) X1, X2, X3, X4, X5; X6, X7, X8 are each, identical or different, selected among
halogen atoms, and/or hydrogen atoms, such that at least one of the radicals X of
each pair X1/X2, X3/X4, X5/X6, X7/X8 is a halogen atom,
- R1, R2, R3, R4 are each, identical or different, selected among the moieties : -OH,
amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety
having 1 to 12 carbon atoms.
2. Porphyrin derivatives according to claim 1, complying with formula
(I), wherein:
- X2, X4, X6 and X8 are chlorine atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are chlorine atoms.
3. Porphyrin derivatives according to claim 1, complying with formula
(I), wherein:
- X2, X4, X6 and X8 are fluor atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are chlorine atoms.
4. Porphyrin derivatives according to claim 1, complying with formula (I), wherein:
- X2, X4, X6 and X8 are fluor atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are -OH moieties.
5. Porphyrin derivatives according to claim 1, complying with formula
(I), wherein:
- X2, X4, X6 and X8 are fluor atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are -OH moieties.
6. Porphyrin derivatives according to claim 1, complying with formula
(I), wherein:
- X1, X2, X3. X4, X5, X6, X7, X8 are chlorine atoms ;
- R1, R2, R3, R4 are chlorine atoms.
7. Porphyrin derivatives according to claim 1, complying with
formula (I),
wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms ;
- R1, R2, R3, R4 are -OH moieties.
8. Porphyrin derivatives, in particular bacteriochlorin, of formula:
R30,S
(Figure Removed) wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among halogen
atoms, and/or hydrogen atoms ;
- R1, R2, R3, R4 are each, identical or different, selected among the moieties : -
OH, amino acids, -OR and -NHR and/or chlorine atom, wherein R is an alkyl moiety having 1 to 12 carbon atoms.
9. Porphyrin derivatives according to claim 8, complying with formula
(II), wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are each, identical or different, selected among
halogen atoms and/or hydrogen atoms, such that at least one of the radicals X
of each pair X1/ X2, X3/X4, X5/X6, X7/X8 is a halogen atom,
10. Porphyrin derivatives according to claim 8, complying with formula
(II), wherein:
- X2, X4, X6 and X8 are chlorine atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are chlorine atoms.
11. Porphyrin derivatives according to claim 8, complying with formula
(II), wherein:
- X2, X4, X6 and X8 are fluor atoms ;
- X1, X3, X5 and X7are hydrogen atoms ;
- R1, R2, R3, R4 are chlorine atoms.
12. Porphyrin derivatives according to claim 8, complying with formula
(I), wherein:
- X2, X4, X6 and X8 are chlorine atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are-OH moieties.
13. Porphyrin derivatives according to claim 8, complying with formula
(II), wherein:
- X2, X4, X6 and X8 are fluor atoms ;
- X1, X3, X5 and X7 are hydrogen atoms ;
- R1, R2, R3, R4 are -OH moieties.
14. Porphyrin derivatives according to claim 8, complying with formula
(II),
wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms ;
- R1, R2, R3, R4 are chlorine atoms.
15. Porphyrin derivatives according to claim 8, complying with
formula (II),
wherein:
- X1, X2, X3, X4, X5, X6, X7, X8 are chlorine atoms ;
- R1, R2, R3, R4 are -OH moieties.
16. Porphyrin derivatives according to any of the claims 1 or 8,
characterised in that the halogen atoms are fluorine and/or chlorine and/or bromine.
17. A method for the preparation of the porphyrin derivatives according
to any of the previous claims, characterised in that it includes:
- a reducing step of the corresponding halogenated and chlorosulfonated
porphyrin to chlorin and/or to bacteriochlorin with hydrazide and organic bulky
bases;
- a coupling step between the chlorosulfonated moiety and amines and/or
amino acids and/or alcohols.
18. A method of preparation of the derivatives according to any of the
previous claims, characterised in that it includes:
- a reducing step of the corresponding halogenated and chlorosulfonated
porphyrin to chlorin and/or to bacteriochlorin with hydrazide and organic bulky
bases;
a hydrolysing step of the chlorine of the chlorosulfonated moiety.
19. An anticancerous and/or antiviral and/or antimicrobial medication
for human or animal usage exhibiting as a main active agent one or several
compounds according to claims 1 to 16.

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Patent Number

257295

Indian Patent Application Number

3211/DELNP/2007

PG Journal Number

39/2013

Publication Date

27-Sep-2013

Grant Date

21-Sep-2013

Date of Filing

30-Apr-2007

Name of Patentee

UNIVERSIDADE DE COIMBRA

Applicant Address

PACO DAS ESCOLAS, P-3004-531 COIMBRA, PORTUGAL

Inventors:

#	Inventor's Name	Inventor's Address
1	MARIA MIGUENS PEREIRA,LUIS GUILHERME ARNAUT MOREIRA, SEBASTIAO JOSE FORMOSINHO SIMOES AND CARLOS MONTEIRO	UNIVERSIDADE DE COIMBRA, PACO DAS ESCOLAS, P-3004-531 COIMBRA, PORTUGAL

PCT International Classification Number

A61K 31/409

PCT International Application Number

PCT/EP2005/012212

PCT International Filing date

2005-11-10

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	04/12149	2004-11-16	France