Method for detecting a radical compound derived from a lipid and a compound derived from the radical compound

Abstract

[Problem] To provide a method of scavenging an unstable radical derived from a lipid and analyzing structures of those radicals. [Means for solution] A fluorescent nitroxide (NBD-Pen) is made to act to scavenge a lipid radical or a fragment radical thereof, and fluorescent detection liquid chromatography (LC/FL) and mass spectrometry (MS) are combined to identify lipid-derived radicals contained in a lipid extract.

Claims

1. A compound, which is the following compound (C′): ##STR00009## wherein R is selected from a group consisting of CH.sub.3, C.sub.2H.sub.5, C.sub.3H.sub.7, C.sub.4H.sub.9, C.sub.6H.sub.13, C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.8H.sub.15O, C.sub.9H.sub.15, C.sub.9H.sub.15O.sub.2, C.sub.9H.sub.13O.sub.3, C.sub.10H.sub.17O, C.sub.11H.sub.19O.sub.2, and C.sub.12H.sub.21O.sub.2; or R is selected from a group consisting of AA-O.sub.2, CH.sub.3, C.sub.2H.sub.5, C.sub.3H.sub.7, C.sub.4H.sub.9, C.sub.6H.sub.13, C.sub.6H.sub.9O.sub.3, C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.8H.sub.13O.sub.2, C.sub.8H.sub.15O, C.sub.9H.sub.17, C.sub.9H.sub.15O.sub.2, C.sub.9H.sub.13O.sub.3, C.sub.10H.sub.17O, C.sub.11H.sub.19, C.sub.11H.sub.17O, C.sub.11H.sub.19O, C.sub.11H.sub.19O.sub.2, C.sub.12H.sub.19O, C.sub.12H.sub.19O.sub.2, C.sub.13H.sub.19O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.23O, and C.sub.15H.sub.23O, and wherein AA represents arachidonic acid; or R is selected from a group consisting of ALA-O.sub.2, CH.sub.3, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.15H.sub.21O.sub.2, and C.sub.15H.sub.21O.sub.3 and, wherein ALA represents α-linolenic acid; or R is selected from a group consisting of EPA-O.sub.2, CH.sub.3, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.12H.sub.17O, C.sub.12H.sub.17O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.19O, C.sub.15H.sub.21O, C.sub.15H.sub.21O.sub.2, C.sub.15H.sub.21O.sub.3, C.sub.17H.sub.23O, and C.sub.18H.sub.25O and, wherein EPA represents eicosapentaenoic acid; or R is selected from a group consisting of DHA-O.sub.2, CH.sub.3, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.12H.sub.17O, C.sub.12H.sub.17O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.19O, C.sub.15H.sub.21O, C.sub.15H.sub.21O.sub.2, C.sub.15H.sub.21O.sub.3, C.sub.17H.sub.23O, C.sub.18H.sub.25O, and C.sub.21H.sub.31O.sub.4 and, wherein DHA represents docosahexaenoic acid.

2. The compound of claim 1, wherein R is selected from a group consisting of C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.8H.sub.15O, C.sub.9H.sub.15, C.sub.9H.sub.15O.sub.2, C.sub.9H.sub.13O.sub.3, C.sub.10H.sub.17O, C.sub.11H.sub.19O.sub.2, and C.sub.12H.sub.21O.sub.2; or R is selected from a group consisting of AA-O.sub.2, C.sub.6H.sub.9O.sub.3, C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.8H.sub.13O.sub.2, C.sub.8H.sub.15O, C.sub.9H.sub.17, C.sub.9H.sub.15O.sub.2, C.sub.9H.sub.13O.sub.3, C.sub.10H.sub.17O, C.sub.11H.sub.19, C.sub.11H.sub.17O, C.sub.11H.sub.19O, C.sub.11H.sub.19O.sub.2, C.sub.12H.sub.19O, C.sub.12H.sub.19O.sub.2, C.sub.13H.sub.19O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.23O, and C.sub.15H.sub.23O, and wherein AA represents arachidonic acid; or R is selected from a group consisting of ALA-O.sub.2, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.15H.sub.21O.sub.2, and C.sub.15H.sub.21O.sub.3 and, wherein ALA represents α-linolenic acid; or R is selected from a group consisting of EPA-O.sub.2, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.5H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.12H.sub.17O, C.sub.12H.sub.17O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.19O, C.sub.15H.sub.21O, C.sub.15H.sub.21O.sub.2, C.sub.15H.sub.21O.sub.3, C.sub.17H.sub.23O, and C.sub.18H.sub.25O and, wherein EPA represents eicosapentaenoic acid; or R is selected from a group consisting of DHA-O.sub.2, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.5H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.12H.sub.17O, C.sub.12H.sub.17O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.19O, C.sub.15H.sub.21O, C.sub.15H.sub.21O.sub.2, C.sub.15H.sub.21O.sub.3, C.sub.17H.sub.23O, C.sub.18H.sub.25O, and C.sub.21H.sub.31O.sub.4 and, wherein DHA represents docosahexaenoic acid.

Description

BRIEF EXPLANATION OF THE DRAWINGS

(1) FIG. 1 A schematic chart of lipid peroxidation reactions.

(2) FIG. 2 Age-related macular degeneration (AMD) onset and progression routes summarized by the present inventors.

(3) FIG. 3 A graph showing reactivities of NBD-nitroxides with reactive oxygen species and lipid radicals.

(4) FIG. 4 A graph showing reactivities of NBD-Pen with reactive oxygen species and lipid radicals.

(5) FIG. 5 Graphs showing suppression of stimulus with lipid radicals by nitroxides.

(6) FIG. 6 Schematic views showing suppression of hepatocellular carcinoma-induction with lipid radicals by nitroxides (a); and a graph showing the numbers of tumors (b).

(7) FIG. 7 A schematic view of fluorescent detection of lipid radicals according to the present invention.

(8) FIG. 8 A schematic diagram showing one embodiment of a LC/FL/MS system according to the present invention.

(9) FIG. 9 Detection results of arachidonic acid (AA)-derived radical compound produced by AAPH stimulation.

(10) FIG. 10 Detection results of docosahexaenoic acid (DHA)-derived radical compound produced by AAPH stimulation.

(11) FIG. 11 Detection results of radical compound induced within a hepatocellular carcinoma model mouse by using NBD-Pen.

MODE FOR CARRYING OUT THE INVENTION

Reference Example 1: Development of Fluorescent Nitroxide

(12) The present inventors developed a novel method of synthesizing a 2,6-substituted TEMPO-based nitroxide 2,2,6,6-tetramethylpiperadine-N-oxyl represented by the chemical structure (2):

(13) ##STR00002##
and found that an alkyl group is introduced in the vicinity of a radical part to enhance lipid affinity and an ability of suppressing lipid peroxidation and, then, lipid radicals can be effectively scavenged.

(14) Additionally, the nitroxide (NO.) is a stable radical having paramagnetism and a property of decaying fluorescence by intersystem crossing due to photoinduced electron transfer and electron-spin exchange associating with charge separated states. A fluorescent nitroxide in which a fluorophore attaches to a nitroxide is in an intermolecular quenching state. However, it was confirmed that when the nitroxide reacted with a free radical to lose paramagnetism, it became a fluorescence emitting state. That is, the fluorescent nitroxide is useful as a probe to detect scavenging of lipid radicals by fluorometry.

(15) The present inventors converted the carbonyl group at the 4th position into an amino group and covalently attached a fluorophore 7-nitrobenzofurazan (NBD) represented by the chemical structure (3):

(16) ##STR00003##
so as to make proximity with a radical moiety on the TEMPO-based nitroxide.

(17) Most of lipid molecules to be detected exist within living body membrane to achieve a hydrophobic environment. Therefore, an environment-responsive fluorophore in which its fluorescence decays under hydrophilic environment and emits selectively high fluorescence under hydrophobic environment is best. For that reason, the present inventors chose NBD which widely used as a fluorophore in a lipid field such as phase transition and membrane fusion within a living body membrane or intercellular lipid metabolism and the like.

(18) NBD derivatives are very useful to apply to imaging with a fluorescent microscopy because their excitation wavelength is around 470 nm which is suitable for argon laser excitation (488 nm). Further, since its emission maximum is around 530 nm, use of NBD derivatives is useful from the viewpoint of reducing autofluorescence from substances in a living body.

(19) The present inventors found that introduction of a chain alkyl group in the vicinity of the radical moiety of TEMPO-based nitroxide changes the lipid affinity and steric hindrance of the compound and, thereby, lipid radicals can be effectively scavenged. For example, extending the alkyl chain at the 2.sup.nd position (or the 6.sup.th position) of nitroxide increased the lipid peroxidation suppressive ability.

(20) The present inventors synthesized, as NBD-nitroxides with high lipid reactivity, Compound A (NBD-Me) and Compound B (NBD-Et) in which the 2.sup.nd and 6.sup.th positions were substituted, respectively, with two methyl groups or ethyl groups, and Compound C (NBD-Pen) in which the 2.sup.nd position was substituted with two methyl groups and the 6.sup.th position was substituted with pentyl group.

(21) ##STR00004##

(22) It was revealed that extension of one of the two alkyl groups attached to the 2.sup.nd (or 6.sup.th) position increased the reactivity with the lipid radicals and that the complex of a nitroxide derivative and a lipid was thermally stable. That is, among Compounds A to C, Compound C: NBD-Pen was predominant.

Reference Example 2: Detection Sensitivity of Lipid Radical of NBD-Nitroxide

(23) (1) Reactivity of NBD-Nitroxide with Reactive Oxygen Species and Lipid Radicals

(24) In order to investigate reaction selectivities of the above three types of NBD-nitroxide (NBD-Me, NBD-Et and NBD-Pen), reactivities with various ROS and lipid radical were evaluated by fluorometry. When each NBD-nitroxide was reacted with hydrogen peroxide, hypochlorous acid, superoxide anion radical, hydroxy radical or nitric oxide, fluorescence did not increase much in any nitroxide. In addition, in the reaction with these compounds, no significant difference in fluorescence intensity was observed between these nitroxides, and there was no difference between the 2.sup.nd and 6.sup.th position substituents. On the other hand, it was revealed that when each NBD-nitroxide was reacted with lipid radical produced using lipoxygenase (LOX) for linoleic acid (LA), α-linolenic acid (ALA), or arachidonic acid (AA), its fluorescence intensity was significantly elevated, and lipid radical could be detected selectively and with high sensitivity. In particular, when NBD-Pen was used, it was found that the fluorescence intensity increased by about 10 to 26 times by reaction with lipid radical (FIG. 3).

(25) (2) Reactivity of NBD-Pen with Reactive Oxygen Species and Lipid Radicals

(26) For fluorescence detection of lipid radicals, the reactivity of the most sensitive NBD-Pen was further investigated.

(27) When NBD-Pen was reacted with hydrogen peroxide, hypochlorous acid, superoxide anion radical or hydroxy radical, the same results as above were reproduced and the fluorescence did not increase much. On the other hand, when NBD-Pen was reacted with lipid radicals induced by activating LA, ALA, and AA, respectively, with any one of radical-inducing agents of lipoxygenase (LOX), 2,2′-azobis(2-methylpropion amidine) dihydrochoride (AAPH), and 2,2′-azobis(4-methoxy-2,4′-dimethylvaleronitorile (MeO-AMVN), the fluorescence intensity remarkably increased (FIG. 4).

Reference Example 3: Cytotoxicity of NBD-Nitroxide

(28) Cytotoxicity of NBD-nitroxide was evaluated using human umbilical vein endothelial cell (HUVEC). When each concentration of the compound was added to HUVEC and the number of viable cells after incubation for 24 hours was counted, cytotoxicity was not observed up to 10 μM in any NBD-nitroxide.

Reference Example 4: Possibility of Hepatocellular Carcinogenesis with Lipid Radicals

(29) In addition, diethylnitrosamine (DEN) is metabolically activated by cytochrome P450 to produce a carbon centered radical. It is known that this radical alkylates a DNA and induces hepatocellular carcinoma [Non-patent literature 3].

(30) ##STR00005##

(31) In a study on preparation of hepatocellular carcinoma model mice using DEN, it is already known that the carcinogenesis rate of obese mice is high [Non-patent literature 4], and that a large amount of ROS accumulates in a body of a hepatocellular carcinoma model mouse [Non-patent literature 5].

(32) From the above two findings, the present inventors speculated that ROS activates a lipid and produces a lipid radical, and such a lipid radical also induces hepatocellular carcinoma.

(33) The present inventors had confirmed that lipid radicals generated only 1 hour after administration of DEN in rats, but it was unknown whether the lipid radicals induced hepatocellular carcinoma.

(34) Therefore, it was investigated whether inhibition of lipid radical generation affects hepatocellular carcinogenesis. The present inventors first synthesized Nitroxide compound D (4-hydroxy-2,2,6-trimethyl-6-pentylpiperidine-1-oxyl; OH-Pen) and Piperidine compound E (4-hydroxy-1-methoxy-2,2,6-trimethyl-6-pentylpiperidine-1-oxyl; OH-Pen-NOMe) lacking a lipid radical scavenging ability due to modification with a methyl group on the part of its nitroxide part of the nitroxide compound D. OH-Pen is a compound in which the fluorescent chromophore of NBD-Pen is unbound.

(35) ##STR00006##

(36) Six week-old male rats (F344) were divided into 4 groups, and as a control, rats in Group 1 were administered with saline (PBS) by intraperitoneal injection. Rats in Groups 2-4 were administered with DEN at 100 mg/kg by intraperitoneal injection.

(37) One hour after DEN administration, physiological saline was administered to rats in Group 2 by intraperitoneal injection, rats in Group 3 were administered with a 500 μM OH-Pen solution at 4 ml/kg, and rats in Group 4 were administered with a 500 μM OH-Pen-NOMe solution at 4 ml/kg.

(38) Twenty-four hours after DEN administration, livers were excised from rats in the respective groups and lipid extraction was carried out. For extracts, amounts of malondialdehyde; MDA as a peroxidized lipid marker, alanine transaminase (glutamate pyruvate transferase; ALT (GPT)) as a hepatic injury marker, and interleukin-6; IL-6 as an inflammatory marker were measured. The results are shown in FIG. 5.

(39) As is apparent from the above results, as compared with the control (Group 1), each marker value increased by administration of DEN (Group 2), but when OH-Pen having lipid radical scavenging ability was administered, each marker value significantly decreased (Group 3). On the other hand, when OH-Pen-NOMe lacking lipid radical scavenging ability was administered, there was almost no drop in each marker value (Group 4).

(40) Three months after DEN administration, rats in the respective groups were subjected to mixed anesthesia of 3 species, and they were sacrificed and livers were taken out promptly. Photographs of the livers taken from the rats of the respective groups are shown in FIG. 6, and the result of counting the number of tumor foci is shown in FIG. 6b.

(41) As is clear from the above results, hepatocellular carcinoma was induced by DEN administration (Group 2), but administration of OH-Pen having a lipid radical scavenging ability suppressed hepatocellular carcinogenesis (Group 3). On the other hand, when OH-Pen-NOMe lacking a lipid radical scavenging ability was administered, hepatocellular carcinogenesis was not suppressed at all (Group 4).

Example 1

(42) (1) Aim of the Experiments

(43) In the reference example above, it was confirmed that NBD-Pen have a lipid radical scavenging ability, fluorescence sensitivity when a lipid radical is scavenged, nor cytotoxic at a concentration of 10 μM or less.

(44) The present inventors predicted that NBD-nitroxide with a lipid radical scavenging ability could scavenge lipid radicals induced in the living body and its structure could be analyzed.

(45) As mentioned above, it was found that lipids in living body become lipid radicals, and peroxidized lipids by chain reactions, and further metabolites and the like, and that they involved in diseases. Thus, if structural analysis would be possible on lipid radicals which have not been observed until now, it becomes possible to comprehensively analyze the relationship between lipids and its derivatives present in living body and diseases.

(46) (2) In Vitro Scavenging of Lipid Radicals by NBD-Pen

(47) The present inventors presumed that when NBD-Pen scavenges lipid radical (L.) and the radical adduct NBD-Pen-L is produced, fluorescence chromatogram and mass spectrometry may be combined to perform structural analysis of the scavenged lipid (LH).

(48) For example, if three kinds of radical species respectively having R.sub.1, R.sub.2 or R.sub.3 groups are contained in a sample, when liquid chromatogram of the sample to which NBD-Pen has been applied is observed by fluorometry, and fractions obtained at the respective column retention time is subject to mass analysis, the structures of R.sub.1, R.sub.2 and R.sub.3 can be determined. A conceptual diagram of fluorescence detection of such a lipid radical according to the present invention is shown in FIG. 7.

(49) In this Example, with 2,2′-azobis(2-methylpropion amidine) dihydrochoride (AAPH), lipid radicals were induced by activating linoleic acid (LA) and arachidonic acid (AA) as omega-6 fatty acid; and α-linolenic acid (ALA), eicosapentaenoic acid (EPA), and docosahexanoic acid (DHA) as omega-3 fatty acid.

(50) An ethanol solution of each fatty acid 100 mM was prepared and diluted to a final concentration (500 μM) by adding a phosphate buffer solution thereto. To these fatty acid solutions, a 50 mM AAPH solution in phosphate buffer was added.

(51) ##STR00007##

(52) By making NBD-Pen react with a solution in which lipid radicals are induced, a lipid was extracted from the reacted solution. The extract was analyzed using a LC/FL/MS system integrating fluorescence (FL) and mass spectrometer (MS) with high performance liquid chromatography (HPLC).

(53) A schematic diagram showing one embodiment of a LC/FL/MS system according to the present invention is depicted in FIG. 8. A LC/FL/MS system 1 comprises a pump 11, a valve 12, a HPLC column 13, a fluorescence detector 14, a valve 15, an ion source for mass spectrometry 16, an ion detector for mass spectrometry 17, and a sampler 18 providing a sample via the valve 12 to the column 13. Additionally, a sample solution flowing out from the fluorescence detector may be disposed via the valve 15, when mass spectrometry is not performed.

(54) It is appropriately selected according to the present invention, but not limited to, HPLC analysis is performed in this Example by injecting 10 μL of a sample solution into an InertSusteain® C18 analytical column (filled with ES silica having a particle size of 3 μm, 2.0×150 mm) manufactured by Mitsubishi Chemical Corporation, which is eluted with a mobile phase (A: 5.0 mM ammonium acetate in H.sub.2O, B:ACN:H.sub.2O (95:5)) at 40° C. at a rate of 0.4 ml/min. The time program of mobile phase elution was set to B %: 0 to 22 min; 60%, 22 to 60 min; 80%, 60 to 70 min; 100%.

(55) For each fraction eluted, fluorescence observation from NBD-Pen was performed at excitation wavelength (470 nm) and emission wavelength (530 nm) with a fluorescence detector (RF-20A xs manufactured by Shimadzu Corporation).

(56) Next, each fraction thus obtained was introduced into an ion detector (Q Exactive™ Hibrid Quadrupole-Orbitrap™ MS manufactured by Thermo Fisher Scientific Co., Ltd.) by electrospray ionization (ESI) and subjected to mass spectrometry.

(57) The structure of the radical adduct was analyzed by comparing the fluorescence peak observed at the LC/FL site with the precise mass analysis result at the column retention time.

(58) Then, surprisingly, from the solution of docosahexaenoic acid (DHA) as omega-3 fatty acid, obtained were not only three adducts: an adduct in which arachidonic acid radical is attached to NBD-Pen (NBD-Pen-AA); an adduct in which one oxygen molecule is attached to that (NBD-Pen-AA-O1); and an adduct in which two oxygen molecules are attached (NBD-Pen-AA-O2), and also 25 types of adducts including adducts in which each of species .C.sub.5H.sub.11, .C.sub.8H.sub.15, .C.sub.7H.sub.13O is attached to NBD-Pen, wherein 23 types out of which were novel adducts (FIG. 9).

(59) In addition, from the solution of arachidonic acid (AA) as omega-6 fatty acid, obtained were not only three adducts: an adduct in which docosahexaenoic acid radical is attached to NBD-Pen (NBD-Pen-DHA); an adduct in which one oxygen molecule is attached to that (NBD-Pen-DHA-O1); and an adduct in which two oxygen molecules are attached (NBD-Pen-DHA-O2) and also 37 types of adducts including adducts in which each of species .C.sub.5H.sub.9, .C.sub.4H.sub.7O, .C.sub.7H.sub.11O is attached to NBD-Pen, wherein 35 types out of which were novel adducts (FIG. 10).

(60) Table 1 summarizes radical compound constituting radical adducts derived from the respective lipids: LA (18:2n-6), AA (20:4n-6), ALA (18:3n-3), EPA (20:5n-3) and DHA (22:6n-3) obtained by the method of the present invention.

(61) As used herein, the term “radical compound” means a radical of a lipid itself (lipid radical) and a radical of a fragmented lipid (fragment lipid radical). Additionally, adducts in which radical compound are respectively attached to NBD-nitroxides (NBD-Me, NBD-Et, NBD-Pen):

(62) ##STR00008##
are collectively mentioned as “NBD-nitroxide R (NBD-Me-R, NBD-Et-R, NBD-Pen-R)”, for example, an adduct in which a lipid radical is attached to NBD-Pen may be mentioned as “NBD-Pen-L”.

(63) TABLE-US-00001 TABLE 1 Lipid Radical compound ω-6 LA •LA, •LA-O.sub.1, •LA-O.sub.2 •CH.sub.3, •C.sub.2H.sub.5, •C.sub.3H.sub.7, •C.sub.4H.sub.9, •C.sub.5H.sub.11, •C.sub.6H.sub.13, •C.sub.7H.sub.13, •C.sub.7H.sub.13O, •C.sub.8H.sub.15, •C.sub.8H.sub.15O, •C.sub.9H.sub.15, •C.sub.9H.sub.15O.sub.2, •C.sub.9H.sub.13O.sub.3, •C.sub.10H.sub.17O, •C.sub.11H.sub.19O.sub.2, •C.sub.12H.sub.21O.sub.2 AA •AA, •AA-O.sub.1, •AA-O.sub.2, •CH.sub.3, •C.sub.2H.sub.5, •C.sub.3H.sub.7, •C.sub.4H.sub.9, •C.sub.5H.sub.11, •C.sub.6H.sub.13, •C.sub.6H.sub.9O.sub.3, •C.sub.7H.sub.13, •C.sub.7H.sub.13O, •C.sub.8H.sub.15, •C.sub.8H.sub.13O.sub.2, •C.sub.8H.sub.15O, •C.sub.9H.sub.17, •C.sub.9H.sub.15O.sub.2, •C.sub.9H.sub.13O.sub.3, •C.sub.10H.sub.17O, •C.sub.11H.sub.10, •C.sub.11H.sub.17O, •C.sub.11H.sub.19O, •C.sub.11H.sub.19O.sub.2, •C.sub.12H.sub.19O, •C.sub.12H.sub.19O.sub.2, •C.sub.13H.sub.19O.sub.2, •C.sub.14H.sub.21O, •C.sub.14H.sub.23O, •C.sub.15H.sub.23O ω-3 ALA •ALA, •ALA-O.sub.1, •ALA-O.sub.2 •CH.sub.3, •C.sub.2H.sub.5, •C.sub.5H.sub.9, •C.sub.5H.sub.9O, •C.sub.6H.sub.9O, •C.sub.6H.sub.11O, •C.sub.7H.sub.11O, •C.sub.8H.sub.13, •C.sub.8H.sub.11O, •C.sub.8H.sub.11O.sub.3, •C.sub.8H.sub.13O, •C.sub.9H.sub.13O, •C.sub.9H.sub.13O.sub.2, •C.sub.10H.sub.15O, •C.sub.11H.sub.17, •C.sub.11H.sub.15O, •C.sub.11H.sub.17O, •C.sub.11H.sub.15O.sub.3, •C.sub.15H.sub.21O.sub.2, •C.sub.15H.sub.21O.sub.3 EPA •EPA, •EPA-O.sub.1, •EPA-O.sub.2 •CH.sub.3, •C.sub.2H.sub.5, •C.sub.5H.sub.9, •C.sub.5H.sub.9O, •C.sub.6H.sub.9O, •C.sub.6H.sub.11O, •C.sub.7H.sub.11O, •C.sub.8H.sub.13, •C.sub.8H.sub.11O, •C.sub.8H.sub.11O.sub.3, •C.sub.9H.sub.13O, •C.sub.9H.sub.13O, •C.sub.9H.sub.13O.sub.2, •C.sub.10H.sub.15O, •C.sub.11H.sub.17, •C.sub.11H.sub.15O, •C.sub.11H.sub.17O, •C.sub.11H.sub.15O.sub.3, •C.sub.12H.sub.17O, •C.sub.12H.sub.17O.sub.2, •C.sub.14H.sub.21O, •C.sub.14H.sub.19O, •C.sub.15H.sub.21O, •C.sub.15H.sub.21O.sub.2, •C.sub.15H.sub.21O.sub.3, •C.sub.17H.sub.23O, •C.sub.18H.sub.25O DHA •DHA, •DHA-O, •DHA-O.sub.2, •CH.sub.3, •C.sub.2H.sub.5, •C.sub.5H.sub.9, •C.sub.5H.sub.9O, •C.sub.6H.sub.9O, •C.sub.6H.sub.11O, •C.sub.7H.sub.11O, •C.sub.8H.sub.13, •C.sub.8H.sub.11O, •C.sub.8H.sub.11O.sub.3, •C.sub.8H.sub.13O, •C.sub.9H.sub.13O, •C.sub.9H.sub.13O.sub.2, •C.sub.10H.sub.15O, •C.sub.11H.sub.17, •C.sub.11H.sub.15O, •C.sub.11H.sub.17O, •C.sub.11H.sub.15O.sub.3, •C.sub.12H.sub.17O, •C.sub.12H.sub.17O.sub.2, •C.sub.14H.sub.21O, •C.sub.14H.sub.19O, •C.sub.15H.sub.21O, •C.sub.15H.sub.21O.sub.2, •C.sub.15H.sub.21O.sub.3, •C.sub.17H.sub.23O, •C.sub.18H.sub.25O, •C.sub.21H.sub.31O.sub.4 *Radical compound newly found according to the present invention are shown in italics.

(64) A LC/FL/MS analysis involving use of NBD-Pen was performed on linoleic acid (LA) radical-induced with AAPH to newly obtained compounds represented by NBD-Pen-R, wherein R is selected from a group consisting of CH.sub.3, C.sub.2H.sub.5, C.sub.3H.sub.7, C.sub.4H.sub.9, C.sub.6H.sub.13, C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.8H.sub.15O, C.sub.9H.sub.15, C.sub.9H.sub.15O.sub.2, C.sub.9H.sub.13O.sub.3, C.sub.10H.sub.17O, C.sub.11H.sub.19O.sub.2, and C.sub.12H.sub.21O.sub.2.

(65) A LC/FL/MS analysis involving use of NBD-Pen was performed on arachidonic acid (AA) radical-induced with AAPH to newly obtained compounds represented by NBD-Pen-R, wherein R is selected from a group consisting of AA-O.sub.2, CH.sub.3, C.sub.2H.sub.5, C.sub.3H.sub.7, C.sub.4H.sub.9, C.sub.6H.sub.13, C.sub.6H.sub.9O.sub.3, C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.9H.sub.3O.sub.2, C.sub.9H.sub.15O, C.sub.91317, C.sub.9H.sub.15O.sub.2, C.sub.9H.sub.13O.sub.3, C.sub.10H.sub.17O, C.sub.11H.sub.19, C.sub.11H.sub.17O, C.sub.11H.sub.19O, C.sub.11H.sub.19O.sub.2, C.sub.12H.sub.19O, C.sub.12H.sub.19O.sub.2, C.sub.13H.sub.19O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.23O, and C.sub.15H.sub.23O.

(66) A LC/FL/MS analysis involving use of NBD-Pen was performed on α-linolenic acid (ALA) radical-induced with AAPH to newly obtained compounds represented by NBD-Pen-R, wherein R is selected from a group consisting of ALA-O.sub.2, CH.sub.3, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.9H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.91H.sub.3O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.15H.sub.21O.sub.2, and H.sub.21O.sub.3.

(67) A LC/FL/MS analysis involving use of NBD-Pen was performed on eicosapentaenoic acid (EPA) radical-induced with AAPH to newly obtained compounds represented by NBD-Pen-R, wherein R is selected from a group consisting of EPA-O.sub.2, CH.sub.3, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.13O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.12H.sub.17O, C.sub.12H.sub.17O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.19O, C.sub.15H.sub.21O, C.sub.15H.sub.21O.sub.2, C.sub.15H.sub.21O.sub.3, C.sub.17H.sub.23O, and C.sub.18H.sub.25O.

(68) A LC/FL/MS analysis involving use of NBD-Pen was performed on docosahexaenoic acid (DHA) radical-induced with AAPH to newly obtained compounds represented by NBD-Pen-R, wherein R is selected from a group consisting of DHA-O.sub.2, CH.sub.3, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.8H.sub.13O, C.sub.9H.sub.3O, C.sub.9H.sub.13O.sub.2, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, C.sub.11H.sub.17O, C.sub.11H.sub.15O.sub.3, C.sub.12H.sub.17O, C.sub.12H.sub.17O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.19O, C.sub.15H.sub.21O, C.sub.15H.sub.21O.sub.2, C.sub.15H.sub.21O.sub.3, C.sub.17H.sub.23O, C.sub.18H.sub.25O, and C.sub.2H.sub.31O.sub.4.

(69) Additional analysis revealed that as R of the compounds whose structure was determined for omega-3 fatty acid, at least C.sub.5H.sub.9, C.sub.5H.sub.9O, C.sub.6H.sub.9O, C.sub.6H.sub.11O, C.sub.7H.sub.11O, C.sub.8H.sub.13, C.sub.8H.sub.11O, C.sub.8H.sub.11O.sub.3, C.sub.10H.sub.15O, C.sub.11H.sub.17, C.sub.11H.sub.15O, and C.sub.11H.sub.17O are common; as R of the compounds whose structure was determined for omega-6 fatty acid, at least C.sub.5H.sub.11, C.sub.6H.sub.13, C.sub.7H.sub.13, C.sub.7H.sub.13O, C.sub.8H.sub.15, C.sub.8H.sub.15O, C.sub.9H.sub.15, and C.sub.10H.sub.17O are common; and the common structure for omega-3 fatty acid and that for omega-6 fatty acid are different from each other.

(70) Further, among omega-6 fatty acid, at least C.sub.8H.sub.5, C.sub.8H.sub.15O, C.sub.11H.sub.19, C.sub.11H.sub.17O, C.sub.11H.sub.19O, C.sub.11H.sub.19O.sub.2, C.sub.12H.sub.9O, C.sub.12H.sub.9O.sub.2, C.sub.12H.sub.19O.sub.2, C.sub.13H.sub.19O.sub.2, C.sub.14H.sub.21O, C.sub.14H.sub.23O, C.sub.15H.sub.23O as R of the compounds whose structure was specified per arachidonic acid (AA) were found to be different from those of the compounds whose structure was specified for linoleic acid (LA).

Example 2

(71) (1) Aim of Experiment

(72) Example 1 suggests that, with a LC/FL/MS analysis using NBD-Pen, based on the combination of obtained radical compounds, fatty acids contained in an unknown sample can be identified.

(73) Therefore, radical compounds produced in a living body of a mouse were detected with a LC/FL/MS analysis using NBD-Pen.

(74) (2) Scavenging of Lipid Radicals Induced in Hepatocellular Carcinoma Model Mouse by NBD-Pen

(75) Male mice (C57BL/6J) at 8 weeks of age were divided into two groups. As a control, physiological saline (PBS) was administered to mice in Group 1 by intraperitoneal injection. DEN at 100 mg/kg was administered to mice in Group 2 by intraperitoneal injection.

(76) Four hours after DEN administration, a 500 μM NBD-Pen solution was administered at 4 ml/kg to mice in Groups 1 and 2 by intraperitoneal injection.

(77) Fifteen minutes after administration of NBD-Pen, livers were excised from the mice in the respective groups and lipid extraction was performed. LC/FL/MS analysis was performed on extracts under the same conditions as in Example 1. The structure of the radical adduct was analyzed by comparing the fluorescence peak observed at the LC/FL site with the precise mass analysis result at that column retention time. The results are described in Table 2 and FIG. 11.

(78) TABLE-US-00002 TABLE 2 Fluorescent intensity of Hepatocellular Lipid NBD-Pen-R (a.u.) carcinoma radical R inducing agent scavenger C.sub.2H.sub.5 C.sub.3H.sub.7 C.sub.5H.sub.11 C.sub.5H.sub.15 Gr. 1 — NBD-Pen 72.95 143.69 393.38 29.72 Gr. 2 DEN NBD-Pen 704.15 1604.07 3511.72 353.94

(79) Since NBD-Pen-C.sub.5H.sub.11, which is an identification marker for omega-6 fatty acid and, further NBD-Pen-C.sub.8H.sub.15 were detected as understood from Table 2, generation of arachidonic acid (AA) was verified.

INDUSTRIAL AVAILABILITY

(80) By using the fluorescent nitroxide according to the present invention, lipid-derived radicals induced with reactive oxygen species (ROS) in a living body can be scavenged to determine the radical structures thereof. By this method, it is possible to elucidate the relevance to diseases caused by lipid radicals such as age-related macular degeneration and hepatocellular carcinoma.

EXPLANATION FOR SIGNS

(81) 1 LC/FL/MS system 11 Pump 12 Valve 13 Liquid chromatography column 14 Fluorescence detector 15 Valve 16 Ion source for mass spectrometry 17 Ion detector for mass spectrometry 18 Sampler