Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K9/00—Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
  • C09K9/02—Organic tenebrescent materials
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/10—Spiro-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
  • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
  • C07D491/10—Spiro-condensed systems
  • C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B57/00—Other synthetic dyes of known constitution
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/02—Printing inks
  • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
  • C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/50—Sympathetic, colour changing or similar inks
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
  • C09K2211/10—Non-macromolecular compounds
  • C09K2211/1018—Heterocyclic compounds
  • C09K2211/1025—Heterocyclic compounds characterised by ligands
  • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
  • C09K2211/10—Non-macromolecular compounds
  • C09K2211/1018—Heterocyclic compounds
  • C09K2211/1025—Heterocyclic compounds characterised by ligands
  • C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T436/00—Chemistry: analytical and immunological testing
  • Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
  • Y10T436/141111—Diverse hetero atoms in same or different rings [e.g., alkaloids, opiates, etc.]

Definitions

• the present invention relates to a photochromic ink, the process for its preparation which is based on a photochromic spiropyran powder obtainable by melting, cooling and crushing, and to a new form of a photochromic spiropyran obtainable thereby.
• photochromic ink is meant a formulation formed as fluid ink which changes color when exposed to UV light radiation and provides a sufficiently high color density for use in the printing processes.
• the International Application WO2005075978 (Freshpoint) describes the preparation of solvent-based or water-based printing inks comprising a spiropyran, an acrylate polymer as binder, a solvent or water and additives.
• the spiropyran is added as finely ground powder.
• Spiropyrans used for preparing printing inks for time temperature indicators have to be easily dispersible. Therefore a small particle size of the spiropyran is required, for example obtained by intensively milling using standard bead mills.
• This method has at least two drawbacks. First, the milling operation is a time-intensive process, as long milling times are required to produce small enough particles to enable the formation of a stable dispersion. Second, the milling operation can not be used for all spiropyrans as some spiropyrans irreversibly change their color during milling.
• a good dispersibility is needed to obtain a high color strength.
• the use in aqueous and solvent-based systems is desired.
• the problem underlying the present invention is to reduce the milling time and to prepare an easily activable spiropyran which can be easily converted into a colored spiropyran having a high color strength.
• "excellent activable” or “easily converted” means that only short exposure to UV light is required.
• the invention relates to a process to prepare a photochromic ink comprising the steps of a) heating and melting a spiropyran, i.e. a photochromic spiropyran at a temperature below 250 0 C, i.e. heating a photochromic spiropyran until it has melted, b) cooling the melt to obtain a solidified spiropyran, c) crushing the solidified spiropyran to obtain a powder, d) optionally adding the powder to a binder providing the basis for the photochromic ink.
• the invention further relates to a photochromic ink obtainable according to the process of claim 1.
• the invention further relates to a photochromic spiropyran in the form of a powder which, after dispersion in a printing ink, has at least the double color strength than known forms of the same spiropyran, said powder being obtainable by a) heating and melting a photochromic spiropyran at a temperature below 250 0 C, i.e. carefully heating the spiropyran until it has melted, b) cooling the melt to obtain a solidified spiropyran, and c) crushing the solidified spiropyran to obtain a powder.
• the inventive process allows the preparation of easily activable time temperature indicators in powder form which can be used in various ink formulations.
• the decomposition temperature of spiropyrans is below 250 0 C, i.e. all spiropyrans so far tested by the present inventors at least start decomposing below or even far below 250 0 C.
• a certain degree, e.g. up to 20%, 30%, 40% or even 50%, of decomposition is acceptable since the gain in color strength by the inventive process more than compensates for the loss of intact spiropyrans by decomposition.
• some spiropyrans tend to decompose rather rapidly, some even explosively.
• due care should be taken not to raise the temperature more than is necessary to obtain a complete melt or not to use explosive spiropyrans in the process of the present invention, especially not in larger scale.
• Spiropyrans which are suitable for being used in the process of the present invention can easily be detected and selected, e.g. by heating an undangerously small amount of them until they melt and watching the decomposition behaviour.
• the preferred manner of carrying out process step a) above is to heat the spiropyran until it has melted, i.e. to heat it only slightly, e.g. 2, 5 or 10 0 C above its melting point which is usually in the range of 140-200 0 C, especially 150-190 0 C.
• heating is continued until melting is complete, i.e. all of the spiropyran has melted, but in order to avoid circumvention of the patent protection the respective patent claim comprises also those modifications of the process wherein only a substantial portion, e.g. 10, 20, 30, 40, 50, 60, 70, 80 or 90 per cent (percent), of the spiropyran has melted.
• the solidified spiropyran is in a transparent form.
• Solidified is crystalline or semi amorphous.
• si-amorphous herein means a spiropyran having an intermediate structure of an amorphous structure and a crystalline structure.
• Cooling means for example, cooling to room temperature or a temperature below room temperature and comprisesalso shock cooling.
• Shock cooling is preferably performed by pooring the melt on solid carbon dioxide (also called dry ice or carbon dioxide snow) or into liquid nitrogen whereupon the melt usually splits into tiny pieces.
• the melting is carried out using any method of heat transfer, for example the melting is formed by heating using an oil bath, by melt extrusion, by radiation, e.g. NIR/IR radiation, heating using a hot air technology, heating by using a cold plasma and the like.
• the melting is formed by heating using an oil bath, by melt extrusion, by radiation, e.g. NIR/IR radiation, heating using a hot air technology, heating by using a cold plasma and the like.
• a short heating treatment is preferred to avoid the decomposition of the spiropyrans.
• Polymeric binders for inks include all polymers known to be used in inks, e.g. homopolymers, copolymers (random or block-copolymers) or mixtures thereof including polymers of acrylic acid or methacrylic acid, acrylates or methacrylates (e.g. methyl acrylate or methyl methacrylate), styrene, acrylamide, vinyl acetate, vinyl alcohol, vinyl chloride, polyurethanes, cellulose nitrate, carboxymethyl cellulose.
• Preferred is a water-soluble or water- dispersible acrylic polymer.
• the binder is thus preferably an acrylic binder.
• Inks contain a variety of additives to eliminate foaming, dispersion of pigments, rheological modifiers, and slip agents.
• the inks comprise a total content of spiropyran of from 1 to 20 % by weight, preferably 1.5- 20% by weight, 2-20% by weight, 3-20% by weight based on the total weight of the ink.
• the spiropyran-dispersed ink composition can be produced by employing various methods which have so far conventionally been known. For example, it can readily be obtained by blending the respective components (binder, additive, spiropyran powder) and mixing and stirring them by means of a stirrer such as a dissolver or mixing and crushing them by means of a ball mill.
• a stirrer such as a dissolver or mixing and crushing them by means of a ball mill.
• the spiropyran compound is for example a spiropyran as disclosed (including processes for its manufacture) in WO 2008/083925 A1 or WO 2005075978 A2 (Freshpoint), or a spiropyran as disclosed in the European Application EP08156605 (Ciba), filed May 21 , 2008 (corresponding to PCT/EP2009/05564 filed May 1 1 , 2009 and published as WO2009141237 A1 ), all of which publications are incorporated herein by reference.
• Ri is hydrogen, -Ci-Ci 8 alkoxy, -CrCi 8 alkylthio, halogen, -d-d 8 alkyl, -NO 2 or a phenyl radical, like preferably phenyl,
• R 2 is hydrogen, -d-d 8 alkoxy or NO 2 ;
• R 3 is NO 2 or halogen;
• R 4 is hydrogen, -Ci-Ci 8 alkoxy or halogen
• R 5 is hydrogen, halogen, -Ci-Ci 8 alkoxy, -COOH, -COO-Ci-Ci ⁇ alkyI, -CF 3 or phenyl;
• Re is hydrogen or R 6 and R 7 form together a phenyl ring; R 7 is hydrogen;
• R 3 is hydrogen or -CrC 6 alkyl
• Rb is hydrogen or -CrC ⁇ alkyl, or together with R a form a 5-6 membered ring;
• Y is phenyl or benzyl wherein the phenyl or benzyl group may be substituted by one or more groups selected from NO 2 , fluorine, bromine, chlorine, CF 3 or phenyl and may carry an annealed benzo ring, or
• Y is-CH 2 -COO- d-Ci ⁇ alkyl or -CH 2 -COOH or -CH 2 -CO-N(Ri 0 )-R 9 ; or -CH 2 -CO- N(Rio)-L-N(Rio) CO-CH 2 - ;
• R 9 is hydrogen, d-Ci 8 alkyl , phenyl, mesityl, phenyl once or more than once substituted by halogen, -CF 3 , d-C 6 alkyl, -d-C 6 alkoxy, carboxy, -COO-d-C ⁇ alkyl, -S-phenyl or -CO-phenyl;
• L is 1 ,3 phenylene or 1 ,4 phenylene wherein the phenylene linker is optionally substituted by once or more than once by halogen, -CF 3 , Ci-Ci 8 alkyl, -d-d 8 alkoxy, carboxy , -COO-Ci-Ci ⁇ alkyI, -CONH 2 , -CON(d-d 8 alkyl) 2 , nitro; or L is naphthalene, biphenylene or phenylene-O-phenylene wherein the naphthalene, biphenylene or phenylene-O-phenylene linker is optionally substituted once or more than once by halogen, -CF 3 , d-d 8 alkyl, -Ci-Ci 8 alkoxy, carboxy , -COO-Ci-Ci ⁇ alkyI, -CONH 2 , - CON(Ci-Ci 8 alkyl) 2 , nitro.
• Phenyl or benzyl Y carrying an is napthyl or napthylmethyl.
• Y does not carry an annealed benzo ring.
• Ri is hydrogen, -Ci-Ci 8 alkoxy, -CrCi 8 alkylthio, halogen, -d-d 8 alkyl or -NO 2
• R 2 is hydrogen or -d-d 8 alkoxy
• R 3 is NO 2 or halogen
• R 4 is hydrogen, -d-d 8 alkoxy or halogen
• R 5 is hydrogen, halogen, -d-d 8 alkoxy, -COOH, -C00-d-d 8 alkyl, -CF 3 or phenyl
• R 6 is hydrogen or R 6 and R 7 form together a phenyl ring
• R 7 is hydrogen
• R 3 is hydrogen or -CrC 6 alkyl
• R b is hydrogen or -CrC 6 alkyl, or together with R a form a 5-6 membered ring;
• Y is phenyl or benzyl wherein the phenyl or benzyl group may be substituted by one or more groups selected from fluorine, bromine, chlorine, CF 3 or phenyl or Y is-CH 2 -COO- d-Ci ⁇ alkyl or -CH 2 -COOH or -CH 2 -CO-N(R 1 O)-R 9 ; or -CH 2 -CO- N(R 1 O)-L-N(R 10 ) CO-CH 2 - ;
• R 9 is hydrogen, CrC 18 alkyl , phenyl, mesityl, phenyl once or more than once substituted by halogen, -CF 3 , C r C 6 alkyl, -C 1 -C 6 alkoxy, carboxy, -COO-d-Cealkyl,
• R 10 is hydrogen, CrC 18 alkyl
• L is 1 ,3 phenylene or 1 ,4 phenylene wherein the phenylene linker is optionally substituted by once or more than once by halogen, -CF 3 , CrC 18 alkyl, -C 1 -C 18 alkoxy, carboxy , -COO-C r C 18 alkyl, -CONH 2 , -CON(C r C 18 alkyl) 2 , nitro; or L is naphthalene, biphenylene or phenylene-O-phenylene wherein the naphthalene, biphenylene or phenylene-O-phenylene linker is optionally substituted once or more than once by halogen, -CF 3 , C r C 18 alkyl, -C 1 -C 18 alkoxy, carboxy , -COO-C r C 18 alkyl, -CONH 2 , - CON(C r C 18 alkyl) 2 , nitro.
• Ri is CrC 6 alkoxy, preferably methoxy
• R 2 is hydrogen
• R 3 is NO 2 ,
• R 4 is hydrogen
• R 5 is hydrogen or CrC 6 alkoxy
• R 6 is hydrogen
• R 7 is hydrogen
• Ra is methyl
• Rb is methyl
• R 10 O is NO 2 , bromine, fluorine or CF 3 , preferably bromine, fluorine or CF 3 , R 2 00 is hydrogen or fluorine.
• Y is nitro-benzyl, like especially 4-nitro-benzyl, preferably Y is 4-fluoro-benzyl or 2,4-difluoro-benzyl,
• R 1 is methoxy
• R 2 is hydrogen
• R 3 is NO 2
• R 4 is hydrogen
• R 5 is hydrogen
• R 6 is hydrogen
• R 7 is hydrogen
• R 3 is methyl, Rb is methyl,
• the preferred compound has the following formula
• the spiropyran compounds are molten and re-solidified by cooling to room temperature.
• the re-solidified spiropyran can easily be dispersed in an ink formulation.
• the milling time is reduced by factor 5 compared to unmolten spiropyrans.
• the exposure time of the ink formulation by UV radiation is less (approximately 4-40%, preferably 4-10%) compared to an ink formulation containing an unmolten spiropyran.
• Ri is CrC 6 alkoxy, CrC 6 alkylthio, or a phenyl radical, like especially phenyl, preferably Ri is Ci-C 6 alkoxy or d-C 6 alkylthio, R is -C-i-C ⁇ alkoxy or -NHR 9 wherein R 9 is phenyl, phenyl once or more than once substituted by halogen, -CF 3 , d-C 6 alkyl, -CrC 6 alkoxy, -S-phenyl or -CO-phenyl,
• R 2 is hydrogen
• R 3 is NO 2 ,
• R 4 is hydrogen
• R 5 is hydrogen
• R 6 is hydrogen
• R 7 is hydrogen
• R 3 is methyl
• Rb is methyl
• Pulverisette 7 Pulverisette 7 to obtain a printing ink.
• the basic ink formulation is described below.
• the printing ink is then applied to a paper using a wiper.
• the film thickness is approximately 12 ⁇ m.
• the label obtained is activated using UV light.
• the Table below shows that the molten and re-solidified spiropyran according to the invention needs only 1/10 of the UV Dosis to reach the same color strength as the unmolten spiropyran.
• the radiation time is reduced from 2 seconds to 0.2 seconds.
• L, a and b used in the present text are informal abbreviations of the coordinates of the CIE color space L * , a * and b * and should not be mixed up with the Hunter values L, a and b.
• L (and L * ) define the lightness axis of the CIE color space with 0 meaning black and 100 meaning white; a (and a * ) define the location on the red - green axis (positive values are red, negative values are green, and 0 is neutral); and b (and b * ) define the location on the blue - yellow axis (positive values are yellow, negative values are blue, and 0 is neutral).
• the bleaching kinetic is the same for both products.
• * LF2923 carries a benzo ring which is annealed to the C-atom carrying the substituent R 1O o and the C-atom marked with * in the above formula.
• * * OMe means methoxy, i.e. OCH 3 .
• the following spiropyrans having an ester or amid group Y are treated analogously as described in Example 1.
• the following spiropyran compound is molten in a glass tube at
• a CoIMn Teachline extruder E 20 T is heated to 16O 0 C.
• the extruder is loaded with
• the spiropyran is molten during the extrusion process and exites out as a high viscous liquid which is then cooled. Glassy plates are formed. The plates are crushed and added to an aqueous based basic ink formulation using a planetary mill (available from Fritsch GmbH, Planetary Fritsch Pulverisette 7) to obtain a printing ink. molten 2 seconds activated
• 3 g of the following spiropyran is molten in a microwave (800W) for 2 minutes.
• the molten mass is cooled to room temperature and pulverized.
• the powder is then added to an aqueous based basic ink formulation using a planetary mill (available from Fritsch GmbH, Planetary Fritsch Pulverisette 7) to obtain a printing ink
• Step 1 Basic printing ink
• Step 2 preparation of the TTI-printing ink: 1 g spiropyran (TTI) 9g Basic printing ink 35g zirconium oxide -balls having a diameter of 0.7-0.9mm
• the same compound after melting step is also dispersed according to the usual dispersion process and the coloristical properties (especially L-Value -> color development) are checked after 5, 15 and 30 minutes dispersion time.
• the color development after irradiation with UV light (cf. Example 3) shows that a very high and constant L-value is already obtained after only 5 minutes processing time (dispersion time).
• Example 3 color strength comparison of crystalline, milled and molten LF2807
• Step 1 A solution of 2,3,3-trimethylindolenine (5.0 g, 31.4 mmol) and 4-fluorobenzylbromide (3.0 g, 15.7 mmol) in dry toluene 30 ml is stirred overnight at 80-85 0 C. The mixture is cooled to room temperature, filtered through a glass filter, washed with diethyl ether and dried under reduced pressure. The crude product is dissolved in CH 2 CI 2 and treated with 5% aqueous NaOH under stirring for 30 minutes.
• the organic phase is separated, dried over Na 2 SO 4 , passed through a short alumina column in equal parts per volume of hexane-CH 2 CI 2 and evaporated giving rise to a corresponding free base, which is immediately dissolved in 10 ml ethanol containing a few drops of triethylamine.
• Step 2 A solution of 1-(4'-fluorobenzyl)-3,3-dimethyl-2-methylene-indoline (2.7 g, 10.0 mmol) and 2-hydroxy-3-methoxy-5-nitrobenzaldehyde (3.6 g, 13.0 mmol) is refluxed in 25 ml ethanol for 2 hours, cooled to room temperature, filtered, triturated with 1% triethylamine (in water), washed with water, crystallized from ethanol, and dried under reduced pressure yielding crystalline LF2807. Color strength comparison:
• Crystalline LF2807 is dispersed and milled in 5% loading in the printing ink described above using a perl mill (pulverisette) with zirconium oxide beads (650 rpm) for 10 minutes.
• Crystalline LF2807 is molten, re-solidified, dispersed and milled in 1% loading in the printing ink described above using a perl mill (pulverisette) with zirconium oxide beads (650 rpm) for 10 minutes.
• the molten, re-solidified and milled LF2807 exhibits about the same L- value as the unmolten and milled LF2807 (Experiment B) despite the fact that the concentration of the active material in Experiment C is 5 times lower. Therefore the color strength for the molten, re-solidified and milled LF2807 is 500% as compared to the unmolten and milled LF2807 for which the color strength is set as 100%. The color strength of crystalline LF2807 which is not milled, but only stirred in the printing ink is extremely low.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Life Sciences & Earth Sciences (AREA)
• Wood Science & Technology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)
• Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)

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• 2009
  • 2009-12-23 KR KR1020117018305A patent/KR20110106434A/ko not_active Withdrawn
  • 2009-12-23 JP JP2011544834A patent/JP2012514671A/ja active Pending
  • 2009-12-23 AU AU2009336680A patent/AU2009336680A1/en not_active Abandoned
  • 2009-12-23 US US13/141,718 patent/US8287776B2/en not_active Expired - Fee Related
  • 2009-12-23 MX MX2011007275A patent/MX2011007275A/es active IP Right Grant
  • 2009-12-23 WO PCT/EP2009/067825 patent/WO2010079098A1/en not_active Ceased
  • 2009-12-23 EP EP09799639A patent/EP2385972A1/en not_active Withdrawn
  • 2009-12-23 BR BRPI0923937A patent/BRPI0923937A2/pt not_active IP Right Cessation
  • 2009-12-23 CN CN2009801541524A patent/CN102272250A/zh active Pending
• 2011
  • 2011-06-28 IL IL213815A patent/IL213815A0/en unknown
• 2012
  • 2012-09-18 US US13/621,957 patent/US20130026428A1/en not_active Abandoned

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