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  1. NTU Theses and Dissertations Repository
  2. 工學院
  3. 醫學工程學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78239
完整後設資料紀錄
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dc.contributor.advisor林峯輝(Feng-Huei Lin)
dc.contributor.authorYi-Ning Chenen
dc.contributor.author陳誼寧zh_TW
dc.date.accessioned2021-07-11T14:47:20Z-
dc.date.available2025-08-14
dc.date.copyright2020-08-25
dc.date.issued2020
dc.date.submitted2020-08-14
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32. Naik, P., et al., Multidrug-Resistant Pseudomonas aeruginosa Evokes Differential Inflammatory Responses in Human Microglial and Retinal Pigment Epithelial Cells. Microorganisms, 2020. 8(5): p. 735.
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34. Suo, L.-g., et al., Anti-inflammatory TIPE2 inhibits angiogenic VEGF in retinal pigment epithelium. Molecular immunology, 2016. 73: p. 46-52.
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36. Chen, C., D. Guo, and G. Lu, Wogonin protects human retinal pigment epithelium cells from LPS-induced barrier dysfunction and inflammatory responses by regulating the TLR4/NF-κB signaling pathway. Molecular medicine reports, 2017. 15(4): p. 2289-2295.
37. Anderson, O.A., A. Finkelstein, and D.T. Shima, A2E induces IL-1ss production in retinal pigment epithelial cells via the NLRP3 inflammasome. PloS one, 2013. 8(6).
38. Peter, B., S. Bosze, and R. Horvath, Biophysical characteristics of proteins and living cells exposed to the green tea polyphenol epigallocatechin-3-gallate (EGCg): review of recent advances from molecular mechanisms to nanomedicine and clinical trials. European Biophysics Journal, 2017. 46(1): p. 1-24.
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40. Santangelo, C., et al., Polyphenols, intracellular signalling and inflammation. Annali-istituto superiore di sanita, 2007. 43(4): p. 394.
41. Tseng, C.-L., et al., Synergistic effect of artificial tears containing epigallocatechin gallate and hyaluronic acid for the treatment of rabbits with dry eye syndrome. PLoS One, 2016. 11(6).
42. Cavet, M.E., et al., Anti-inflammatory and anti-oxidative effects of the green tea polyphenol epigallocatechin gallate in human corneal epithelial cells. Molecular vision, 2011. 17: p. 533.
43. Thichanpiang, P. and K. Wongprasert, Green tea polyphenol epigallocatechin-3-gallate attenuates TNF-α-induced intercellular adhesion molecule-1 expression and monocyte adhesion to retinal pigment epithelial cells. The American journal of Chinese medicine, 2015. 43(01): p. 103-119.
44. Chan, C.-M., et al., Effects of (-)-epigallocatechin gallate on RPE cell migration and adhesion. Molecular vision, 2010. 16: p. 586.
45. Schanté, C.E., et al., Chemical modifications of hyaluronic acid for the synthesis of derivatives for a broad range of biomedical applications. Carbohydrate polymers, 2011. 85(3): p. 469-489.
46. De Boulle, K., et al., A review of the metabolism of 1, 4‐Butanediol Diglycidyl ether–crosslinked hyaluronic acid dermal fillers. Dermatologic Surgery, 2013. 39(12): p. 1758-1766.
47. Ji, G.Y., et al., Efficacy and safety of sodium hyaluronate with 1, 4-butanediol diglycidyl ether compared to sodium carboxymethylcellulose in preventing adhesion formation after lumbar discectomy. Korean Journal of Spine, 2015. 12(2): p. 41.
48. Falcone, S.J. and R.A. Berg, Crosslinked hyaluronic acid dermal fillers: a comparison of rheological properties. Journal of Biomedical Materials Research Part A: An Official Journal of The Society for Biomaterials, The Japanese Society for Biomaterials, and The Australian Society for Biomaterials and the Korean Society for Biomaterials, 2008. 87(1): p. 264-271.
49. Barth, H., et al., A cross-linked hyaluronic acid hydrogel (Healaflow®) as a novel vitreous substitute. Graefe's Archive for Clinical and Experimental Ophthalmology, 2016. 254(4): p. 697-703.
50. Zhang, J.N., et al., Development of a BDDE-crosslinked hyaluronic acid based microneedles patch as a dermal filler for anti-ageing treatment. Journal of industrial and engineering chemistry, 2018. 65: p. 363-369.
51. Zhang, J., et al., Synthesis and characterization of hyaluronic acid/human-like collagen hydrogels. Materials Science and Engineering: C, 2014. 43: p. 547-554.
52. Lin, Y.-K., K.-H. Chen, and C.-Y. Kuan, The synthesis and characterization of a thermally responsive hyaluronic acid/Pluronic copolymer and an evaluation of its potential as an artificial vitreous substitute. Journal of Bioactive and Compatible Polymers, 2013. 28(4): p. 355-367.
53. Organization, I.S., ISO 10993‐5: 2009. Biological evaluation of medical devices–Part 5: Tests for in vitro cytotoxicity. 2009.
54. Mateos, M.V., et al., The phospholipase D pathway mediates the inflammatory response of the retinal pigment epithelium. The international journal of biochemistry cell biology, 2014. 55: p. 119-128.
55. Codeluppi, S., et al., Influence of rat substrain and growth conditions on the characteristics of primary cultures of adult rat spinal cord astrocytes. Journal of neuroscience methods, 2011. 197(1): p. 118-127.
56. Pirkmajer, S. and A.V. Chibalin, Serum starvation: caveat emptor. American Journal of Physiology-Cell Physiology, 2011. 301(2): p. C272-C279.
57. Lin, Y.-L. and J.-K. Lin, (−)-Epigallocatechin-3-gallate blocks the induction of nitric oxide synthase by down-regulating lipopolysaccharide-induced activity of transcription factor nuclear factor-κB. Molecular pharmacology, 1997. 52(3): p. 465-472.
58. Friedrich, S., Y.-L. Cheng, and B. Saville, Finite element modeling of drug distribution in the vitreous humor of the rabbit eye. Annals of biomedical engineering, 1997. 25(2): p. 303-314.
59. Kleinberg, T.T., et al., Vitreous substitutes: a comprehensive review. Survey of ophthalmology, 2011. 56(4): p. 300-323.
60. Edsman, K., et al., Gel properties of hyaluronic acid dermal fillers. Dermatologic Surgery, 2012. 38(7pt2): p. 1170-1179.
61. Lai, J.Y., The role of bloom index of gelatin on the interaction with retinal pigment epithelial cells. International journal of molecular sciences, 2009. 10(8): p. 3442-3456.
62. Dinarello, C.A., Interleukin 1 and interleukin 18 as mediators of inflammation and the aging process. The American journal of clinical nutrition, 2006. 83(2): p. 447S-455S.
63. Witte, K.K. and A.L. Clark, Nutritional abnormalities contributing to cachexia in chronic illness. International journal of cardiology, 2002. 85(1): p. 23-31.
64. Kaur, C., et al., Microglia-derived proinflammatory cytokines tumor necrosis factor-alpha and interleukin-1beta induce Purkinje neuronal apoptosis via their receptors in hypoxic neonatal rat brain. Brain Structure and Function, 2014. 219(1): p. 151-170.
65. Durand, M.L., Bacterial and fungal endophthalmitis. Clinical Microbiology Reviews, 2017. 30(3): p. 597-613.
66. Watanabe, A., et al., Changes in corneal thickness following vitreous surgery. Clinical Ophthalmology (Auckland, NZ), 2012. 6: p. 1293.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78239-
dc.description.abstract許多與玻璃體視網膜病變相關的眼睛疾病,像是視網膜剝離、黃斑部病變等,都可能需要玻璃體切除術來改善視力,藉由灌注替代物填充切除後的玻璃體腔室,然而手術後容易引起發炎反應,造成手術失敗產生其他眼睛疾病副作用,或是替代物的降解。因此本研究在替代物中添加表沒食子兒茶素沒食子酸酯(EGCG),其為天然的茶葉萃取物並有許多研究指出具有抗發炎特性,並且以1,4-丁二醇二縮水甘油醚(BDDE)交聯透明質酸(HA)製備玻璃體替代物,此材料已經通過測試具有良好生物安全性,期望能夠模擬原生玻璃體性質且減少發炎反應的產生。
本研究以 FTIR 和 1H-NMR 檢驗交聯官能基的改變與交聯程度,檢測交聯劑 BDDE 的殘餘量,再鑑定折射率、黏彈性質以及滲透壓,以酵素模擬體外降解,測定降解速率;細胞實驗部分,使用 WST-1 測定材料細胞毒性,Live/Dead 染色觀察細胞活性,而後同時給予細胞脂多醣(LPS)以及本實驗材料觀察誘導發炎情況以及材料抗發炎效果,利用即時定量反轉錄聚合酶連鎖反應(RT-qPCR)測定細胞發炎基因表現變化;動物實驗部分,進行玻璃體切除術並注入本實驗替代物,測量眼壓與角膜厚度,以及視網膜電流圖進行視網膜功能性檢驗,未來將以眼球組織切片染色觀察眼睛結構與發炎現象。
本實驗成功製備出透明易注射之膠體溶液,BDDE 殘餘量符合安全標準,材料的物化性質也與原生玻璃體極為相似,具有較長的降解時間能在術後維持填充效果;體外實驗則證實材料具有良好生物相容性,添加 50 μM EGCG 具有抑制發炎作用;動物實驗選用 50 μM EGCG 為基準而調動低、中、高三種的濃度劑量,藉此讓注射後被未切除完全玻璃體液稀釋的 EGCG 能夠發揮抗發炎作用,結果顯示注射含有 100 μM EGCG 之替代物具有較佳的替代效果,術後眼壓和角膜厚度沒有顯著變化,視網膜電訊號振幅強度也與術前無顯著差異。
zh_TW
dc.description.abstractA range of vitreoretinopathy complications such as retinal detachment and macular degeneration can be treated with vitrectomy. After surgery, vitreous substitutes should be injected to maintain properties and structure. However, high incidence rate of postoperative inflammation, which cause the failure of surgery and the early degradation of substitute, has been reported following surgery. To alleviate this condition, EGCG, which is present in green tea extract with anti-oxidant and anti-inflammatory properties, was added into our substitute materials. We investigated BDDE-crosslinked HA for a vitreous substitute and expected to mimic the properties of the vitreous humor and reduce the postoperative inflammatory response. We successfully developed a transparent and injectable gel solution. The results of FTIR and 1H-NMR confirmed the cross-linking reaction between BDDE and HA. BDDE residue in the materials was lower than 2 ppm. The refractive index, dynamic viscosity, and osmolality were similar to the vitreous humor. The materials underwent gradual degradation and the complete degradation occurred after one month. For the in vitro study, the cytotoxicity was evaluated by WST-1 assay and Live/Dead stain. High biocompatibility were presented in both test. In the anti-inflammation study, we used LPS to induce inflammation co-treated with our materials and assessed cytokines mRNA expression by RT-qPCR. Substitutes with 50 μM EGCG inhibited the expression of inflammatory cytokines significantly. To avoid dilution of EGCG of injected substitutes by remaining vitreous humor after surgery and the aqueous humor circulation in vivo, we proposed to use three dosages of EGCG based on the in vitro study. The results showed that no significant change in intraocular pressure and cornea thickness of operated eyes of the substitutes with 100 μM EGCG. The amplitudes of electrical signal on electroretinograms also remained normal compared with preoperative signal.en
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Previous issue date: 2020
en
dc.description.tableofcontents誌謝 I
中文摘要 II
Abstract III
目錄 V
圖目錄 VIII
表目錄 X
縮寫目錄 XI
公式目錄 XIII
第一章 緒論 ... 1
1.1 前言 ... 1
1.2 眼睛構造與功能 ... 1
1.3 眼科疾病以及玻璃體切除術 ... 2
1.4 玻璃體替代物 ... 3
1.5 理想的替代物選擇 ... 5
1.6 研究目的 ... 6
第二章 文獻回顧 ... 7
2.1 玻璃體切除術(vitrectomy) ... 7
2.2 眼科手術後發炎反應(postoperative inflammation) ... 7
2.2.1 眼睛的發炎(intraocular inflammation) ... 7
2.2.2 治療方法 ... 8
2.2.3 術後發炎反應體外誘導模型以及細胞發炎因子 ... 9
2.3 表沒食子兒茶素沒食子酸酯(epigallocatechin-gallate, EGCG) ... 12
2.4 1, 4-丁二醇二縮水甘油醚(BDDE)交聯透明質酸(HA) ... 16
第三章 材料與方法 ... 18
3.1 實驗藥品 ... 18
3.2 實驗儀器 ... 20
3.3 實驗架構 ... 21
3.4 材料製備與分析 ... 22
3.4.1 製備交聯透明質酸混合兒茶素 ... 22
3.4.2 交聯官能基以及交聯程度鑑定 ... 22
3.4.3 1,4-丁二醇二縮水甘油醚 (BDDE)殘餘量檢測 ... 23
3.4.4 折射率檢測 ... 23
3.4.5 黏彈性質檢測 ... 23
3.4.6 滲透壓檢測 ... 24
3.4.7 降解速率 ... 24
3.5 In vitro 體外實驗 ... 25
3.5.1 細胞株及培養液 ... 25
3.5.2 WST-1 細胞增殖測試 ... 25
3.5.3 Live and Dead 細胞活性測試 ... 26
3.5.4 LPS 誘導發炎之毒性測試 ... 26
3.5.5 細胞發炎反應基因表現檢測 ... 27
3.6 In vivo 動物實驗 ... 28
3.6.1 玻璃體切除術(vitrectomy) ... 28
3.6.2 眼壓與角膜厚度量測 ... 29
3.6.3 視網膜電流圖(electroretinogram, ERG) ... 30
3.7 統計分析 ... 31
第四章 結果與討論 ... 32
4.1 交聯透明質酸添加EGCG 之材料分析 ... 32
4.1.1 傅立葉轉換顯微紅外光譜(FTIR) ... 32
4.1.2 核磁共振氫譜(1H-NMR) ... 33
4.1.3 1, 4-丁二醇二縮水甘油醚 (BDDE)殘餘量 ... 34
4.1.4 折射率 ... 35
4.1.5 黏彈性質 ... 35
4.1.6 滲透壓 ... 36
4.1.7 降解速率 ... 37
4.2 In vitro 體外細胞實驗 ... 37
4.2.1 WST-1 細胞增殖測試 ... 37
4.2.2 Live/Dead 細胞活性測試 ... 38
4.2.3 LPS 誘導發炎之毒性測試 ... 39
4.2.4 EGCG 抗發炎作用檢驗 ... 40
4.3 In vivo 動物實驗 ... 41
4.3.1 術後眼睛外觀觀察以及眼壓、角膜厚度量測 ... 41
4.3.2 ERG 檢測玻璃體切除術後對視力之影響 ... 44
第五章 結論 ... 46
參考文獻 ... 47
dc.language.isozh-TW
dc.subject表沒食子兒茶素沒食子酸酯zh_TW
dc.subject玻璃體切除術zh_TW
dc.subject術後發炎zh_TW
dc.subject4-丁二醇二 縮水甘油醚zh_TW
dc.subject透明質酸zh_TW
dc.subjectpostoperative inflammationen
dc.subjectvitrectomyen
dc.subjectEGCGen
dc.subjectBDDEen
dc.subjectHAen
dc.title合成可注射交聯透明質酸添加兒茶素作為人工玻璃體之研究zh_TW
dc.titleThe Synthesis and Evaluation of Injectable Crosslinked Hyaluronic Acid Gel with Epigallocatechin Gallate as Vitreous Substitutesen
dc.typeThesis
dc.date.schoolyear108-2
dc.description.degree碩士
dc.contributor.coadvisor曾靖孋(Ching-Li Tseng)
dc.contributor.oralexamcommittee黃義侑(Yi-You Huang)
dc.subject.keyword玻璃體切除術,術後發炎,表沒食子兒茶素沒食子酸酯,1,4-丁二醇二 縮水甘油醚,透明質酸,zh_TW
dc.subject.keywordvitrectomy,postoperative inflammation,EGCG,BDDE,HA,en
dc.relation.page51
dc.identifier.doi10.6342/NTU202003222
dc.rights.note有償授權
dc.date.accepted2020-08-17
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept醫學工程學研究所zh_TW
dc.date.embargo-lift2025-08-14-
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