Effects of poly(2-hydroxyethyl methacrylate) and poly(vinyl-pyrrolidone) hydrogel implants on myopic and normal chick sclera

Experimental Eye Research

Volumn 88, Issue 3, 2009, Pages 445-457

  Su, James ^a   Iomdina, Elena ^b   Tarutta, Elena ^b   Ward, Brian ^c   Song, Jie ^d   Wildsoet, Christine F ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b MOSCOW HELMHOLTZ RESEARCH INSTITUTE OF EYE DISEASES   (Russian Federation)

^c STANFORD UNIVERSITY MEDICAL CENTER   (United States)

^d UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

chick sclera; hydrogel; myopia; poly(2 hydroxyethyl methacrylate); poly(vinyl pyrrolidone); scleral remodeling

Indexed keywords

POLYMACON; POVIDONE;

A SCAN; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CARTILAGE CELL; CELL PROLIFERATION; CHICK; CONTROLLED STUDY; EXTRACELLULAR MATRIX; EYE INFLAMMATION; HYDROGEL; MYOPIA; NONHUMAN; PRIORITY JOURNAL; SCLERA;

ANIMALS; BIOCOMPATIBLE MATERIALS; CHICKENS; CHONDROCYTES; DISEASE MODELS, ANIMAL; EYE; HYDROGEL; MYOPIA; POLYHYDROXYETHYL METHACRYLATE; POVIDONE; PROSTHESES AND IMPLANTS; SCLERA;

EID: 61549132007     PISSN: 00144835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.exer.2008.10.029     Document Type: Article

References (54)

1. Abramoff M.D., Magelhaes P.J., and Ram S.J. Image processing with image-j. Biophoton. Int. 11 7 (2004) 36-42
2. Avetisov E.S., Savitskaya N.F., Vinetskaya M.I., and Iomdina E.N. A study of biochemical and biomechanical qualities of normal and myopic eye sclera in humans of different age groups. Metab. Pediatr. Syst. Ophthalmol. 7 4 (1983) 183-188
3. Avetisov E.S., Tarutta E.P., Iomdina E.N., Vinetskaya M.I., and Andreyeva L.D. Nonsurgical and surgical methods of sclera reinforcement in progressive myopia. Acta. Ophthalmol. Scand. 75 6 (1997) 618-623
4. Choh V., Lew M.Y., Nadel M.W., and Wildsoet C.F. Effects of interchanging hyperopic defocus and form deprivation stimuli in normal and optic nerve-sectioned chicks. Vis. Res. 46 6-7 (2006) 1070-1079
5. Curtin B.J., Iwamoto T., and Renaldo D.P. Normal and staphylomatous sclera of high myopia: an electron microscopic study. Arch. Ophthalmol. 97 5 (1979) 912-915
6. D'Hermies F., Korobelnik J.-F., Caputo G., Mashhour B., Chauvaud D., Pouliquen Y., and Renard G. Encapsulation of scleral buckling materials: a study of sixty specimens. Ophthalmology 105 6 (1998) 1079-1086
7. Fan D.S.P., Lam D.S.C., Chan C.K.M., Fan A.H., Cheung E.Y.Y., and Rao S.K. Topical atropine in retarding myopic progression and axial length growth in children with moderate to severe myopia: a pilot study. Jpn. J. Ophthalmol. 51 1 (2007) 27-33
8. Friedman B. Stress upon the ocular coats: effects of scleral curvature, scleral thickness, and intraocular pressure. Eye Ear Nose Throat Mon. 45 9 (1966) 59-66
9. Gilmartin B. Myopia: precedents for research in the twenty-first century. Clin. Experiment. Ophthalmol. 32 3 (2004) 305-324
10. Gottlieb M.D., Joshi H.B., and Nickla D.L. Scleral changes in chicks with form-deprivation myopia. Curr. Eye Res. 9 12 (1990) 1157-1165
11. Hayes A.J., MacPherson S., Morrison H., Dowthwaite G., and Archer C.W. The development of articular cartilage: evidence for an appositional growth mechanism. Anat. Embryol. 203 6 (2001) 469-479
12. Ihanamaki T., Pelliniemi L.J., and Vuorio E. Collagens and collagen-related matrix components in the human and mouse eye. Prog. Retin. Eye Res. 23 4 (2004) 403-434
13. Jacob J.T., Gebhardt B.M., and Lewando J. Synthetic scleral reinforcement materials. II. Collagen types in the fibrous capsule. J. Biomed. Mater. Res. 32 2 (1996) 181-186
14. Jacob J.T., Lin J.J., and Mikal S.P. Synthetic scleral reinforcement materials. III. Changes in surface and bulk physical properties. J. Biomed. Mater. Res. 37 4 (1997) 525-533
15. Kee C.-S., Marzani D., and Wallman J. Differences in time course and visual requirements of ocular responses to lenses and diffusers. Invest. Ophthalmol. Vis. Sci. 42 3 (2001) 575-583
16. Kermis H.R., Rao G., and Barbari T.A. Transport properties of phema membranes for optical glucose affinity sensors. J. Memb. Sci. 212 1-2 (2003) 75-86
17. Kidane A., Szabocsik J.M., and Park K. Accelerated study on lysozyme deposition on poly(hema) contact lenses. Biomaterials 19 22 (1998) 2051-2055
18. Kusakari T., Sato T., and Tokoro T. Regional scleral changes in form-deprivation myopia in chicks. Exp. Eye Res. 64 3 (1997) 465-476
19. Kusakari T., Sato T., and Tokoro T. Visual deprivation stimulates the exchange of the fibrous sclera into the cartilaginous sclera in chicks. Exp. Eye Res. 73 4 (2001) 533-546
20. Marzani D., and Wallman J. Growth of the two layers of the chick sclera is modulated reciprocally by visual conditions. Invest. Ophthalmol. Vis. Sci. 38 9 (1997) 1726-1739
21. McBrien N.A., Cornell L.M., and Gentle A. Structural and ultrastructural changes to the sclera in a mammalian model of high myopia. Invest. Ophthalmol. Vis. Sci. 42 10 (2001) 2179-2187
22. McBrien N.A., and Gentle A. Role of the sclera in the development and pathological complications of myopia. Prog. Retin. Eye Res. 22 3 (2003) 307-338
23. Merrett K., Griffith C.M., Deslandes Y., Pleizier G., and Sheardown H. Adhesion of corneal epithelial cells to cell adhesion peptide modified phema surfaces. J. Biomater. Sci. Polym. Ed. 12 (2001) 647-671
24. Morgan I., and Rose K. How genetic is school myopia?. Prog. Retin. Eye Res. 24 1 (2005) 1-38
25. Nickla D., Rada J., and Wallman J. Isolated chick sclera shows a circadian rhythm in proteoglycan synthesis perhaps associated with the rhythm in ocular elongation. J. Comp. Physiol. A 185 (1999) 81-90
26. Nickla D.L., Wildsoet C., and Wallman J. Visual influences on diurnal rhythms in ocular length and choroidal thickness in chick eyes. Exp. Eye Res. 66 2 (1998) 163-181
27. Norton. Animal models of myopia: learning how vision controls the size of the eye. Inst. Lab. Anim. Res. J. 40 2 (1999) 59-77
28. Norton T.T., and Rada J.A. Reduced extracellular matrix in mammalian sclera with induced myopia. Vis. Res. 35 9 (1995) 1271-1281
29. Paik D.C., Wen Q., Airiani S., Braunstein R.E., and Trokel S.L. Aliphatic [beta]-nitro alcohols for non-enzymatic collagen cross-linking of scleral tissue. Exp Eye Res. 87 3 (2008) 279-285
30. Phillips J.R., Khalaj M., and McBrien N.A. Induced myopia associated with increased scleral creep in chick and tree shrew eyes. Invest. Ophthalmol. Vis. Sci. 41 8 (2000) 2028-2034
31. Phillips J.R., and McBrien N.A. Pressure-induced changes in axial eye length of chick and tree shrew: significance of myofibroblasts in the sclera. Invest. Ophthalmol. Vis. Sci. 45 3 (2004) 758-763
32. Pijls R.T., Cruysberg L.P.J., Nuijts R.M.M.A., Dias A.A., and Koole L.H. Capacity and tolerance of a new device for ocular drug delivery. Int. J. Pharm. 341 1-2 (2007) 152-161
33. Rada J.A., Achen V.R., and Rada K.G. Proteoglycan turnover in the sclera of normal and experimentally myopic chick eyes. Invest. Ophthalmol. Vis. Sci. 39 11 (1998) 1990-2002
34. Rada J.A., Matthews A.L., and Brenza H. Regional proteoglycan synthesis in the sclera of experimentally myopic chicks. Exp. Eye Res. 59 6 (1994) 747-760
35. Rada J.A., Nickla D.L., and Troilo D. Decreased proteoglycan synthesis associated with form deprivation myopia in mature primate eyes. Invest. Ophthalmol. Vis. Sci. 41 8 (2000) 2050-2058
36. Rymer J., and Wildsoet C.F. The role of the retinal pigment epithelium in eye growth regulation and myopia: a review. Vis. Neurosci. 22 (2005) 251-261
37. Saw S. A synopsis of the prevalence rates and environmental risk factors for myopia. Clin. Exp. Optom. 86 5 (2003) 289-294
38. Schippert R., Brand C., Schaeffel F., and Feldkaemper M.P. Changes in scleral mmp-2, timp-2 and tgfβ-2 mrna expression after imposed myopic and hyperopic defocus in chickens. Exp. Eye Res. 82 4 (2006) 710-719
39. Schmid G.F., Papastergiou G.I., Nickla D.L., Riva C.E., Lin T., Stone R.A., and Laties A.M. Validation of laser Doppler interferometric measurements in vivo of axial eye length and thickness of fundus layers in chicks. Curr. Eye Res. 15 6 (1996) 691-696
40. Shih Y.-F., Hsiao C.K., Chen C.-J., Chang C.-W., Hung P.T., and Lin L.L.K. An intervention trial on efficacy of atropine and multi-focal glasses in controlling myopic progression. Acta. Ophthalmol. Scand. 79 3 (2001) 233-236
41. Siegwart J.T., and Norton T.T. Regulation of the mechanical properties of tree shrew sclera by the visual environment. Vis. Res. 39 2 (1999) 387-407
42. Song J., Malathong V., and Bertozzi C.R. Mineralization of synthetic polymer scaffolds: a bottom-up approach for the development of artificial bone. J. Am. Chem. Soc. 127 10 (2005) 3366-3372
43. Song J., Saiz E., and Bertozzi C.R. A new approach to mineralization of biocompatible hydrogel scaffolds: an efficient process toward 3-dimensional bonelike composites. J. Am. Chem. Soc. 125 5 (2003) 1236-1243
44. Tarutta E.P., Andreeva L.D., Markosian G.A., Iomdina E.N., Lazuk A.V., and Kruzhkova G.V. Reinforcement of the sclera with new types of synthetic materials in progressive myopia. Vestn. Oftalmol. 115 5 (1999) 8-10
45. Tarutta E.P., Iomdina E.N., Shamkhalova E.S., Andreeva L.D., and Maksimova M.V. Scleral fortification in children at high risk of progressive myopia. Vestn. Oftalmol. 108 2 (1992) 14-17
46. Thompson F.B. A simplified scleral reinforcement technique. Am. J. Ophthalmol. 86 6 (1978) 782-790
47. Tortora G.J., and Grabowski S.R. Principles of Anatomy and Physiology. seventh ed. (1992), HarperCollins College Publishers, New York
48. Vacanti F.X. Phema as a fibrous capsule-resistant breast prosthesis. Plast. Reconstr. Surg. 113 3 (2004) 949-952
49. Wildsoet C. Neural pathways subserving negative lens-induced emmetropization in chicks - insights from selective lesions of the optic nerve and ciliary nerve. Curr. Eye Res. 27 6 (2003) 371-385
50. Wildsoet C., and Wallman J. Choroidal and scleral mechanisms of compensation for spectacle lenses in chicks. Vis. Res. 35 9 (1995) 1175-1194
51. Wollensak G., Iomdina E., Dittert D.-D., Salamatina O., and Stoltenburg G. Cross-linking of scleral collagen in the rabbit using riboflavin and UVA. Acta. Ophthalmol. Scand. 83 (2005) 477-482
52. Wollensak G., and Spoerl E. Collagen crosslinking of human and porcine sclera. J. Cataract. Refract. Surg. 30 3 (2004) 689-695
53. Yasuda H. Biocompatibility of nanofilm-encapsulated silicone and silicone-hydrogel contact lenses. Macromol Biosci 6 2 (2006) 121-138
54. Yew, K.-L. Is lens-induced myopia another type of form-deprivation myopia? Evidence from chicks using optical, lighting, and surgical manipulations. M.S. thesis, Vision Science, School of Optometry, University of California, Berkeley; 2004.