TEPZZ _7 8 6A_T EP A1 (19) (11) EP A1 (12) EUROPEAN PATENT APPLICATION. (43) Date of publication: Bulletin 2017/22

Transcription

1 (19) TEPZZ _7 8 6A_T (11) EP A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: Bulletin 17/22 (1) Int Cl.: G02B 1/04 (06.01) C09B 69/ (06.01) (21) Application number: (22) Date of filing: (84) Designated Contracting States: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR Designated Extension States: BA ME Designated Validation States: MA MD (71) Applicant: Pegavision Corporation Taoyuan City 333 (TW) Yu, Hsiao-Ting Taoyuan City (TW) Chang, Han-Yi Taoyuan City (TW) Lai, Yu-Chin Taoyuan City (TW) (74) Representative: Zimmermann & Partner Patentanwälte mbb Josephspitalstr München (DE) (72) Inventors: Chiang, Te-Ju Taoyuan City (TW) (4) HYDROGEL COMPOSITION AND HYDROGEL CONTACT LENSES MADE OF THE COMPOSITION (7) A hydrogel composition and a hydrogel contact lens made of the hydrogel composition are provided. The hydrogel composition includes a hydrophilic monomer, a blue light-blocking monomer, a crosslinker and an initiator. The hydrophilic monomer is in a range from to parts by weight. The blue light-blocking monomer is in a range from 0.02 to 0. parts by weight and has a yellow dye. The crosslinker is in a range from 0.1 to 1 parts by weight. The initiator is in a range from 0.2 to 2 parts by weight. EP A1 Printed by Jouve, 7001 PARIS (FR)

2 Description BACKGROUND Field of Disclosure [0001] The present disclosure relates to a hydrogel composition. More particularly, the present disclosure relates to a blue light-blocking hydrogel composition. Description of Related Art 1 [0002] Since contact lenses made of hydrogel have good moisturizing capabilities, hydrogel contact lenses can provide sufficient water content to cornea even wearing them for a long time and improve the uncomfortable symptoms of eyes caused by the dryness of cornea. Therefore, hydrogel has become one of the preferred components of contact lenses. [0003] A lot of electronic display devices such as television screens, computer monitors, tablets, mobile phones have used a light emitting diode (LED) as a light source for twenty years. It is well known that blue light, which is characterized by a wavelength of nanometers (nm) and emitted from the LED, easily causes eye diseases. In the case of prolonged use of tablet or mobile phone may damage retina, and further induce the early development of cataract and macular degeneration because eyes are prolonged exposure to blue light. [0004] In the current market, however, there is a lack of contact lenses which can block blue light and have a high water content. Therefore, it is essential for manufacturing a hydrogel contact lens which can block blue light and have a high water content. 2 3 SUMMARY [000] In view of the issue un-met in the art, the present disclosure provides a hydrogel composition which can block blue light, and a hydrogel contact lens made of the hydrogel composition may have a high water content and blue lightblocking efficacy. [0006] The present disclosure provides a hydrogel composition for manufacturing a hygrogel contact lens. The hydrogel composition includes a hydrophilic monomer, a blue light-blocking monomer, a crosslinker and an initiator. The hydrophilic monomer is in a range from to parts by weight. The blue light-blocking monomer is in a range from 0.02 to 0. part by weight and has a yellow dye. The crosslinker is in a range from 0.1 to 1 part by weight. The initiator is in a range from 0.2 to 2 parts by weight. [0007] In various embodiments of the present disclosure, the hydrophilic monomer is in a range from 96. to parts by weight. [0008] In various embodiments of the present disclosure, the hydrogel composition further includes a silicone component selected from a group consisting of a silicone monomer, a silicone macromer and a silicone prepolymer, and in which the silicone component is in a range from to 9 parts by weight, and the hydrophilic monomer is in a range from to 60 parts by weight. [0009] In various embodiments of the present disclosure, the silicone monomer has a structure of formula (1): 4 0 which V 1 is 2

3 L 1 is a C3 C7 alkylene group or 1 and R 1 is a methyl group or 2 which * is a linkage position of V 1, L 1 and R 1 in the structure of formula (1). [00] In various embodiments of the present disclosure, the silicone macromer has a structure of formula (2): which L 2 is a C3 C alkylene group, 3 4 and S 2 is 0 which R 2 is C3 C alkyl group, n is an integer from 2 to 4, and * is a linkage position of V 2 and S 2 in the structure of formula (2). [0011] In various embodiments of the present disclosure, the silicone prepolymer has a structure of formula (3): 3

4 which V 3 is 1 L 3 is a C2 C alkylene group, and m is an integer from to 0, which * is a linkage position of V 3 in the structure of formula (3). [0012] In various embodiments of the present disclosure, the yellow dye has a structure of formula (4): 2 which R 3 is -OH or -CH 3, and R 4 is -O- or -CH 2 CH 2 NH-. [0013] In various embodiments of the present disclosure, when R 3 is -OH and R 4 is -CH 2 CH 2 NH- in the structure of formula (4), the yellow dye has a structure of formula (): 3 [0014] In various embodiments of the present disclosure, when R 3 is -CH 3 and R 4 is -O- in the structure of formula (4), the yellow dye has a structure of formula (6): 4 0 [001] In various embodiments of the present disclosure, the yellow dye has a sulfonyl group or a sulfonate group. 4

5 [0016] In various embodiments of the present disclosure, when the yellow dye has the sulfonyl group, the yellow dye has a structure of formula (7): 1 2 [0017] In various embodiments of the present disclosure, when the yellow dye has the sulfonate group, the yellow dye has a structure of formula (8): 3 [0018] In various embodiments of the present disclosure, the yellow dye has an amide group. [0019] In various embodiments of the present disclosure, when the yellow dye has the amide group, the yellow dye has a structure of formula (9): 4 0 [00] In various embodiments of the present disclosure, the hydrophilic monomer is selected from a group consisting of N-vinyl pyrrolidone (NVP), 2-hydroxyethyl methacrylate (HEMA), glyceryl methacrylate (GM), methacrylic acid, acrylic acid, N,N-dimethyl acrylamide (DMA), N,N-dimethyl methacrylamide and N-vinyl-N-methyl acetamide. [0021] In various embodiments of the present disclosure, the crosslinker is selected from a group consisting of ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimeth-

6 1 2 3 acrylate, ally dimethacrylate, ethylene glycol dially ether, triethylene glycol dially ether, tetraethylene glycol dially ether, triallyl-s-triazine-2,4,6(1h,3h,h)-trione and 1,1,1 -trimethylolpropane trimethacrylate. [0022] In various embodiments of the present disclosure, the initiator is a photoinitiator. [0023] In various embodiments of the present disclosure, the photoinitiator is a phosphine-oxide-based initiator, a titanium metallocene-based initiator or a combination thereof. [0024] In various embodiments of the present disclosure, the phosphine-oxide-based initiator is selected from a group consisting of diphenyl (2,4,6-triphenyl)phosphine oxide, bis(2,4,6-trimethylbenzoyl)phenyl phosphine oxide and bis(2,6- dimethoxylbenzoyl)(2,4,4-trimethylpentyl) phosphine oxide. [002] In various embodiments of the present disclosure, the titanium metallocene-based initiator comprises dicyclopentadienyl bis[2,4-difluoro-3-(1-pyrrolyl) phenyl] titanium. [0026] In various embodiments of the present disclosure, the hydrogel composition further includes an UV-blocking monomer in a range from 0. to 2 parts by weight. [0027] In various embodiments of the present disclosure, the UV-blocking monomer has benzophenone, benzotriazole or a combination thereof. [0028] In various embodiments of the present disclosure, when the UV-blocking monomer has benzophenone, the UV-blocking monomer is selected from a group consisting of 4-methacryloxy-2-hydroxy benzophenone and 4-(2-acryloxyethoxy-2-hydroxy benzophenone. [0029] In various embodiments of the present disclosure, when the UV-blocking monomer has benzotriazole, the UVblocking monomer is selected from a group consisting of 2-(2-hydroxy--methacryloxyethylphenyl)-2H-benzotriazole, 2-(2-hydroxy--methacryloxyethylphenyl)-2H-6-chloro-benzotriazole, 2-(2-hydroxy--methacryloxyethylphenyl)-2H- 6- methoxybenzotriazole, 2-[3 -t-butyl- -(3"-dimethylvinylsilylpropoxy)-2 -hydroxyphenyl]--methoxybenzo triazole, 2-[3 - t-butyl- -(3"-methacryloylozypropyl)phenyl]--chlorobenzotriazole and 2-[2 -hydroxy- -(γ-methacryloyloxypropoxy)-3 - tert-butylphenyl]--methoxy-2h-benzotriazole. [00] In various embodiments of the present disclosure, the hydrogel composition further includes a hydrophobic monomer in a range from 1 to parts by weight. [0031] In various embodiments of the present disclosure, the hydrophobic monomer is selected from a group consisting of methyl methacrylate, butyl methacrylte, n-hexyl methacrylate and isobornyl methacrylate. [0032] In various embodiments of the present disclosure, the hydrogel composition further includes an organic solvent in a range from 1 to parts by weight. [0033] In various embodiments of the present disclosure, the organic solvent is selected from a group consisting of glycerol, n-butanol, t-butanol, t-amyl alcohol and n-hexanol. [0034] The present disclosure also provides a hydrogel contact lens. The hydrogel contact lens includes a contact lens body made of the hydrogel composition stated above. [003] These and other features, aspects, and advantages of the present disclosure will become better understood with reference to the following description and appended claims. [0036] It is to be understood that both the foregoing general description and the following detailed description are by examples, and are intended to provide further explanation of the invention as claimed. 4 0 DETAILED DESCRIPTION [0037] Reference will now be made in detail to the present embodiments of the invention, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers are used in the drawings and the description to refer to the same or like parts. [0038] The following embodiments are disclosed for detailed description. For illustration clarity, many details of practice are explained in the following descriptions. However, it should be understood that these details of practice do not intend to limit the present invention. That is, these details of practice are not necessary in parts of embodiments of the present invention. Furthermore, for simplifying the drawings, some of the conventional structures and elements are shown with schematic illustrations. [0039] The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms "a", "an" and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms "comprises" and/or "comprising", or "includes" and/or "including" or "has" and/or "having" when used in this specification, specify the presence of stated features, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof. [00] As aforementioned problems, it is noted that eyes prolonged exposure to blue light are easy to cause eye diseases. However, while full blockage of blue light can offer the best protection of eyes, it may cause poor vision, especially during the evening. Therefore, how to manufacture a hydrogel contact lens which can simultaneously protect 6

7 1 eyes and maintain a good vision, especially in the evening, is still an issue un-met in the art. [0041] In view of the issue un-met in the art, the present disclosure provides a hydrogel composition for manufacturing a hygrogel contact lens. A hydrogel contact lens made of the hydrogel composition can block blue light partially to protect eyes and has a clear vision even during evening. [0042] The present disclosure provides a hydrogel composition for manufacturing a hygrogel contact lens. The hydrogel composition includes a hydrophilic monomer, a blue light-blocking monomer, a crosslinker and an initiator. The hydrophilic monomer is in a range from to parts by weight. The blue light-blocking monomer is in a range from 0.02 to 0. part by weight and has a yellow dye. The crosslinker is in a range from 0.1 to 1 partby weight. The initiator is in a range from 0.2 to 2 parts by weight. [0043] In various embodiments of the present disclosure, the hydrophilic monomer is in a range from 96. to parts by weight. [0044] For instance, the hydrophilic monomer is selected from a group consisting of N-vinyl pyrrolidone (NVP), 2- hydroxyethyl methacrylate (HEMA), glyceryl methacrylate (GM), methacrylic acid, acrylic acid, N,N-dimethyl acrylamide (DMA), N,N-dimethyl methacrylamide and N-vinyl-N-methyl acetamide. [004] In various embodiments of the present disclosure, the hydrogel composition further includes a silicone component selected from a group consisting of a silicone monomer, a silicone macromer and a silicone prepolymer. When the hydrogel composition includes a silicone component, the hydrogel composition includes the silicone component in a range from to 9 parts by weight, the hydrophilic monomer in a range from to 60 parts by weight, the blue lightblocking monomer in a range from 0.02 to 0. part by weight and has a yellow dye, the crosslinker in a range from 0.1 to 1 part by weight and the initiator in a range from 0.2 to 2 parts by weight. [0046] Specifically, the silicone component may be selected from a group consisting of a silicone monomer, a silicone macromer and a silicone prepolymer. The silicone monomer, the silicone macromer and the silicone prepolymer may be selected from various components listed in Table

8 Silicone monomer 1 Table

9 (continued) Silicone macromer

10 (continued) Silicone prepolymer [0047] In various embodiments of the present disclosure, the yellow dye may be a component which have an ethylenically- based polymerizable group, a sulfonyl group, a sulfonate group and an amide group, as shown in Table 2. The yellow dye having the ethylenically- Structure 1 Table 2 3 based polymerizable group Structure 2 4 0

11 (continued) The yellow dye having the sulfonyl group Structure 3 1 The yellow dye having the sulfonate group Structure The yellow dye having the amide group Structure 4 0 [0048] In various embodiments of the present disclosure, the crosslinker is selected from a group consisting of ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, ally dimethacrylate, ethylene glycol dially ether, triethylene glycol dially ether, tetraethylene glycol dially ether, triallyl-s-triazine-2,4,6(1h,3h,h)-trione and 1,1,1 -trimethylolpropane trimethacrylate. [0049] In various embodiments of the present disclosure, the initiator is a photoinitiator. The photoinitiator is a phosphine-oxide-based initiator, a titanium metallocene-based initiator or a combination thereof. [000] In various embodiments of the present disclosure, the phosphine-oxide-based initiator is selected from a group consisting of diphenyl (2,4,6-triphenyl)phosphine oxide, bis(2,4,6-trimethylbenzoyl)phenyl phosphine oxide and bis(2,6- dimethoxylbenzoyl)(2,4,4-trimethylpentyl) phosphine oxide. [001] In various embodiments of the present disclosure, the titanium metallocene-based initiator comprises dicyclopentadienyl bis[2,4-difluoro-3-(1-pyrrolyl) phenyl] titanium. [002] In various embodiments of the present disclosure, the hydrogel composition further includes an UV-blocking monomer in a range from 0. to 2 parts by weight. The UV-blocking monomer has benzophenone, benzotriazole or a combination thereof. [003] In various embodiments of the present disclosure, when the UV-blocking monomer has benzophenone, the UV-blocking monomer is selected from a group consisting of 4-methacryloxy-2-hydroxy benzophenone and 4-(2-acry- 11

12 1 2 3 loxyethoxy-2-hydroxy benzophenone. [004] In various embodiments of the present disclosure, when the UV-blocking monomer has benzotriazole, the UVblocking monomer is selected from a group consisting of 2-(2-hydroxy--methacryloxyethylphenyl)-2H-benzotriazole, 2-(2-hydroxy--methacryloxyethylphenyl)-2H-6-chloro-benzotriazole, 2-(2-hydroxy--methacryloxyethylphenyl)-2H- 6- methoxybenzotriazole, 2-[3 -t-butyl- -(3"-dimethylvinylsilylpropoxy)-2 -hydroxyphenyl]--methoxybenzo triazole, 2-[3 - t-butyl- - (3"-methacryloylozypropyl)phenyl]--chlorobenzotriazole and 2-[2 -hydroxy- -(γ-methacryloyloxypropoxy)-3 - tert-butylphenyl]--methoxy-2h-benzotriazole. [00] In various embodiments of the present disclosure, the hydrogel composition further includes a hydrophobic monomer in a range from 1 to parts by weight. The hydrophobic monomer is selected from a group consisting of methyl methacrylate, butyl methacrylte, n-hexyl methacrylate and isobornyl methacrylate. [006] In various embodiments of the present disclosure, the hydrogel composition further includes an organic solvent in a range from 1 to parts by weight. The organic solvent is selected from a group consisting of glycerol, n-butanol, t-butanol, t-amyl alcohol and n-hexanol. [007] The hydrogel composition stated above was filled into and between two polypropylene molds, and cured under visible light to fabricate a hydrogel contact lens. The hydrogel contact lens was subsequently dry-released from molds and extracted with hot water. After being extracted with hot water, the hydrogel contact lens was placed in the polypropylene blister package filled with borate buffered saline. The polypropylene blister package was sealed with aluminum foil and autoclaved at 1 C for minutes. [008] The hydrogel contact lens made by the manufacturing method stated above has a water content in a range of 38 80%, preferably 70%, and can also block % blue light which is characterized by a wavelength of nanometers (nm). [009] The following hydrogel compositions are only exemplary, but not intended to limit the present disclosure. Specifically, each of the hydrogel compositions 1 8 includes 2-hydroxyethyl methacrylate (HEMA) 9 parts by weight, methacrylic acid 1.9 parts by weight, ethylene glycol dimethacrylate 0.8 part by weight, 1,1,1-trimethylolpropane trimethacrylate 0.1 part by weight, bis(2,4,6-trimethylbenzoyl)phenyl phosphine oxide 0. part by weight, 2-(2-hydroxy-- methacryloxyethylphenyl)-2h-benzotriazole 1.0 part by weight, a reactive blue dye 19 (RB19) 0.03 part by weight and a yellow dye with different structures and amount as shown in Table 3. Table 3 shows the transmittance of blue light ( nm) of the hydrogel contact lenses made of the hydrogel compositions 1 8. Table 3 Hydrogel compositions 1 (Control) Yellow dye with structure 1 (parts by weight) Yellow dye with structure 2 (parts by weight) Yellow dye with structure 4 (parts by weight) Yellow dye with structure (parts by weight) Transmittance of blue light (%) 98% 60% 4% 80% % 8% 7% 0% Blockage of blue light (%) 0 % % % 4% 1% 2% 0% 4 0 [0060] As shown in Table 3, when the yellow dye of the hydrogel compositions is in a range from 0.02 to 0.1 part by weight, the transmittance of blue light of the hydrogel contact lenses made of the hydrogel compositions 1 8 are 4 8%. In other words, the hydrogel contact lenses can block 1 % blue light. Accordingly, users can prevent their eyes from the damage of blue light and have a clear vision, even during the evening, while wearing the hydrogel contact lenses made of the hydrogel compositions 1 8. [0061] Then, visual acuity and contract sensitivity of the comprehensive tests were performed. The quantity of letters which can be correctly identified by the subjects under different environmental conditions (sun light, regular room light and dim light) and contrast were also measured [0062] The above tests were performed by subjects who are between 2 years old. The visual acuity of the subjects was /2 while wearing their habitual contact lenses, in which the "/2" means that ordinary people can see a visual target at 2 feet, but the subjects can only see the visual target at feet. First, subjects respectively wore hydrogel contact lenses (experimental contact lenses) and normal contact lenses (control contact lenses), in which the hydrogel contact lenses (experimental contact lenses) were made of the hydrogel composition 7 stated above were with 2% blockage of blue light. In contrast, the normal contact lenses (control contact lenses) could not block the blue light. Furthermore, the experimental contact lenses and the control contact lenses both had the same base curve and diameter. Next, the subjects were evaluated for visual acuity and contrast sensitivity by identifying 60 test letters at 4-meter distance 12

13 under the different environmental conditions (sun light, regular room light and dim light) and the different contrast levels about the colors of letters and background. The quantity of letters that could be correctly identified reflects the visual acuity and the contrast sensitivity of the subjects, and the results (p < 0.0) are shown in Table Table 4 Sun light (^8,000 Lux) Experimental contact lens (with 2% blockage of blue light) Control contact lens High contrast (0%) Medium contrast (%) Low contrast (2.%) Regular room light (190 6 Lux) Experimental contact lens (with 2% blockage of blue light) Control contact lens High contrast (0%) Medium contrast (%) Low contrast (2.%) Dim light ( Lux) Experimental contact lens (with 2% blockage of blue light) Control contact lens High contrast (0%) Medium contrast (%) Low contrast (2.%) [0063] As a result, no matter under sun light, regular room light or dim light, and high contrast, medium contrast or low contrast, the experimental contact lenses with 2% blockage of blue light does not affect the subjects to correctly identify letters. Further, while wearing the experimental contact lenses, the subjects can correctly identify more quantity of letters than wearing the control contact lenses, and have better visual acuity and contrast sensitivity. Even wearing the experimental contact lenses in the dim light environment, the subjects still have better visual acuity and contrast sensitivity. [0064] The embodiments of the present disclosure discussed above have advantages over existing contact lens, and the advantages are summarized below. The hydrogel contact lens made of the hydrogel composition in the present disclosure can block % blue light to protect eyes from exposing to the harmful blue light, and further prevent eye diseases such as cataract and macular degeneration. In addition, the hydrogel contact lens made of the hydrogel composition of the present disclosure do not affect but even improve the visual acuity and the contract sensitivity of the users. Therefore, the users wearing the hydrogel contact lens provided by the present disclosure can have a good vision even under the dim light. [006] Although the present invention has been described in considerable detail with reference to certain embodiments thereof, other embodiments are possible. Therefore, the spirit and scope of the appended claims should not be limited to the description of the embodiments contained herein. [0066] It will be apparent to those skilled in the art that various modifications and variations can be made to the structure of the present invention without departing from the scope or spirit of the invention. In view of the foregoing, it is intended that the present invention cover modifications and variations of this invention provided they fall within the scope of the following claims. 0 Claims 1. A hydrogel composition for manufacturing a hygrogel contact lens, the hydrogel composition comprising: a hydrophilic monomer in a range from to parts by weight; a blue light-blocking monomer in a range from 0.02 to 0. part by weight and having a yellow dye; a crosslinker in a range from 0.1 to 1 part by weight; and 13

14 an initiator in a range from 0.2 to 2 parts by weight. 2. The hydrogel composition of claim 1, wherein the hydrophilic monomer is in a range from 96. to parts by weight. 3. The hydrogel composition of Claim 1, further comprising a silicone component selected from a group consisting of a silicone monomer, a silicone macromer and a silicone prepolymer, and wherein the silicon component is in a range from to 9 parts by weight, and the hydrophilic monomer is in a range from to 60 parts by weight. 4. The hydrogel composition of claim 3, wherein the silicone monomer has a structure of formula (1): 1 2 wherein V 1 is or 3 L 1 is a C3 C7 alkylene group or 4 0 and R 1 is a methyl group or 14

15 wherein * is a linkage position of V 1, L 1 and R 1 in the structure of formula (1).. The hydrogel composition of claim 3, wherein the silicone macromer has a structure of formula (2): 1 wherein L 2 is a C3 C alkylene group, 2 3 and S 2 is 4 wherein R 2 is C3 C alkyl group, n is an integer from 2 to 4, and * is a linkage position of V 2 and S 2 in the structure of formula (2). 6. The hydrogel composition of claim 3, wherein the silicone prepolymer has a structure of formula (3): 0 wherein V 3 is 1

16 or 1 L 3 is a C2 C alkylene group, and m is an integer from to 0, wherein * is a linkage position of V 3 in the structure of formula (3). 7. The hydrogel composition of claim 1, wherein the yellow dye has a structure of formula (4): 2 wherein R 3 is -OH or -CH 3, and R 4 is -O- or -CH 2 CH 2 NH-. 8. The hydrogel composition of claim 7, wherein when R 3 is -OH and R 4 is -CH 2 CH 2 NH- in the structure of formula (4), the yellow dye has a structure of formula (): The hydrogel composition of claim 7, wherein when R 3 is -CH 3 and R 4 is -O- in the structure of formula (4), the yellow dye has a structure of formula (6): 0 16

17 1. The hydrogel composition of claim 1, wherein the yellow dye has a sulfonyl group or a sulfonate group. 11. The hydrogel composition of claim, wherein when the yellow dye has the sulfonyl group, the yellow dye has a structure of formula (7): The hydrogel composition of claim, wherein when the yellow dye has the sulfonate group, the yellow dye has a structure of formula (8): The hydrogel composition of claim 1, wherein the yellow dye has an amide group. 14. The hydrogel composition of claim 13, wherein when the yellow dye has the amide group, the yellow dye has a 17

18 structure of formula (9): The hydrogel composition of claim 1, wherein the hydrophilic monomer is selected from a group consisting of N- vinyl pyrrolidone (NVP), 2-hydroxyethyl methacrylate (HEMA), glyceryl methacrylate (GM), methacrylic acid, acrylic acid, N,N-dimethyl acrylamide (DMA), N,N-dimethyl methacrylamide and N-vinyl-N-methyl acetamide. 16. The hydrogel composition of claim 1, wherein the crosslinker is selected from a group consisting of ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, ally dimethacrylate, ethylene glycol dially ether, triethylene glycol dially ether, tetraethylene glycol dially ether, triallyl-s-triazine-2,4,6(1h,3h,h)-trione and 1,1,1 -trimethylolpropane trimethacrylate. 17. The hydrogel composition of claim 1, wherein the initiator is a photoinitiator. 18. The hydrogel composition of claim 17, wherein the photoinitiator is a phosphine-oxide-based initiator, a titanium metallocene-based initiator or a combination thereof. 19. The hydrogel composition of claim 18, wherein the phosphine-oxide-based initiator is selected from a group consisting of diphenyl (2,4,6-triphenyl)phosphine oxide, bis(2,4,6-trimethylbenzoyl)phenyl phosphine oxide and bis(2,6-dimethoxylbenzoyl)(2,4,4-trimethylpentyl) phosphine oxide. 3. The hydrogel composition of claim 18, wherein the titanium metallocene-based initiator comprises dicyclopentadienyl bis[2,4-difluoro-3-(1-pyrrolyl) phenyl] titanium. 21. The hydrogel composition of claim 1, further comprising an UV-blocking monomer in a range from 0. to 2 parts by weight. 22. The hydrogel composition of claim 21, wherein the UV-blocking monomer has benzophenone, benzotriazole or a combination thereof The hydrogel composition of claim 22, wherein when the UV-blocking monomer has benzophenone, the UV-blocking monomer is selected from a group consisting of 4-methacryloxy-2-hydroxy benzophenone and 4-(2-acryloxyethoxy- 2-hydroxy benzophenone The hydrogel composition of claim 22, wherein when the UV-blocking monomer has benzotriazole, the UV-blocking monomer is selected from a group consisting of 2-(2-hydroxy--methacryloxyethylphenyl)-2H-benzotriazole, 2-(2- hydroxy--methacryloxyethylphenyl)-2h-6-chloro-benzotriazole, 2-(2-hydroxy--methacryloxyethylphenyl)-2H- 6- methoxybenzotriazole, 2-[3 -t-butyl- -(3"-dimethylvinylsilylpropoxy)-2 -hydroxyphenyl]--methoxybenzo triazole, 2-[3 -t-butyl- - (3"-methacryloylozypropyl)phenyl]--chlorobenzotriazole and 2-[2 -hydroxy- -(γ-methacryloyloxypropoxy)-3 -tert-butylphenyl]--methoxy-2h-benzotriazole. 2. The hydrogel composition of claim 1, further comprising a hydrophobic monomer in a range from 1 to parts by weight. 26. The hydrogel composition of claim 2, wherein the hydrophobic monomer is selected from a group consisting of methyl methacrylate, butyl methacrylte, n-hexyl methacrylate and isobornyl methacrylate. 18

19 27. The hydrogel composition of claim 1, further comprising an organic solvent in a range from 1 to parts by weight. 28. The hydrogel composition of claim 27, wherein the organic solvent is selected from a group consisting of glycerol, n-butanol, t-butanol, t-amyl alcohol and n-hexanol. 29. A hydrogel contact lens, comprising: a contact lens body made of the hydrogel composition of any of claim 1 to

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