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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/123456789/78199
完整後設資料紀錄
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dc.contributor.advisor楊台鴻(Tai-Horng Young)
dc.contributor.authorShen Yangen
dc.contributor.author楊森zh_TW
dc.date.accessioned2021-07-11T14:45:40Z-
dc.date.available2026-12-31
dc.date.copyright2016-10-14
dc.date.issued2016
dc.date.submitted2016-07-25
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[13] Yang Y-Y, Chia H-H, Chung T-S. Effect of preparation temperature on the characteristics and release profiles of PLGA microspheres containing protein fabricated by double-emulsion solvent extraction/evaporation method. Journal of Controlled Release. 2000;69:81-96.
[14] O'Donnell PB, McGinity JW. Preparation of microspheres by the solvent evaporation technique. Advanced drug delivery reviews. 1997;28:25-42.
[15] Allemann E, Gurny R, Doelker E. Preparation of aqueous polymeric nanodispersions by a reversible salting-out process: influence of process parameters on particle size. International Journal of Pharmaceutics. 1992;87:247-53.
[16] Barichello JM, Morishita M, Takayama K, Nagai T. Encapsulation of hydrophilic and lipophilic drugs in PLGA nanoparticles by the nanoprecipitation method. Drug development and industrial pharmacy. 1999;25:471-6.
[17] Huang Y-Y, Chung T-W, Tzeng T-w. Drug release from PLA/PEG microparticulates. International Journal of pharmaceutics. 1997;156:9-15.
[18] Iqbal K, Khan A, Khattak MMAK. Biological significance of ascorbic acid (Vitamin C) in human health–a review. Pakistan Journal of Nutrition. 2004;3:5-13.
[19] Chojkier M, Houglum K, Solis-Herruzo J, Brenner D. Stimulation of collagen gene expression by ascorbic acid in cultured human fibroblasts. A role for lipid peroxidation? Journal of Biological Chemistry. 1989;264:16957-62.
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[26] Falcone SJ, DOERFLER AM, BERG RA. Novel synthetic dermal fillers based on sodium carboxymethylcellulose: comparison with crosslinked hyaluronic acid–based dermal fillers. Dermatologic Surgery. 2007;33:S136-S43.
[27] Piacquadio D, Jarcho M, Goltz R. Evaluation of hylan b gel as a soft-tissue augmentation implant material. Journal of the American Academy of Dermatology. 1997;36:544-9.
[28] Sasaki M, Miyazaki T, Nakamura T, Takahashi T, Miyauchi S, Iwata H. Immunogenicity of hylan gf 20 in Guinea pigs and mice. The Journal of rheumatology. 2004;31:943-50.
[29] Robson MC, Del Beccaro EJ, Heggers JP. The effect of prostaglandins on the dermal microcirculation after burning, and the inhibition of the effect by specific pharmacological agents. Plastic and reconstructive surgery. 1979;63:781-7.
[30] Hoffman AS. Hydrogels for biomedical applications. Annals of the New York Academy of Sciences. 2001;944:62-73.
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[32] Wallace DG, Rosenblatt J. Collagen gel systems for sustained delivery and tissue engineering. Advanced drug delivery reviews. 2003;55:1631-49.
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[34] Metreveli NO, Jariashvili KK, Namicheishvili LO, Svintradze DV, Chikvaidze EN, Sionkowska A, et al. UV–vis and FT-IR spectra of ultraviolet irradiated collagen in the presence of antioxidant ascorbic acid. Ecotoxicology and environmental safety. 2010;73:448-55.
[35] Darr D, Combs S, Pinnell S. Ascorbic acid and collagen synthesis: Rethinking a role for lipid peroxidation. Archives of biochemistry and biophysics. 1993;307:331-5.
[36] Geesin J, Hendricks L, Falkenstein P, Gordon J, Berg R. Regulation of collagen synthesis by ascorbic acid: characterization of the role of ascorbate-stimulated lipid peroxidation. Archives of biochemistry and biophysics. 1991;290:127-32.
[37] Geesin JC, Brown LJ, Gordon JS, Berg RA. Regulation of collagen synthesis in human dermal fibroblasts in contracted collagen gels by ascorbic acid, growth factors, and inhibitors of lipid peroxidation. Experimental cell research. 1993;206:283-90.
[38] Gould BS, WOESSNKER J. Biosynthesis of collagen. The influence of ascorbic acid on the proline, hydroxyproline, glycine and collagen content of regenerating guinea pig skin. Journal of Biological Chemistry. 1957;226:289-300.
[39] Murad S, Grove D, Lindberg K, Reynolds G, Sivarajah A, Pinnell S. Regulation of collagen synthesis by ascorbic acid. Proceedings of the National Academy of Sciences. 1981;78:2879-82.
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[41] Stone N, Meister A. Function of ascorbic acid in the conversion of proline to collagen hydroxyproline. Nature. 1962;194:555-7.
[42] Gillbro J, Olsson M. The melanogenesis and mechanisms of skin‐lightening agents–existing and new approaches. International journal of cosmetic science. 2011;33:210-21.
[43] Smith WP. The effects of topical L (+) lactic acid and ascorbic acid on skin whitening. International journal of cosmetic science. 1999;21:33-40.
[44] Marionnet C, Vioux‐Chagnoleau C, Pierrard C, Sok J, Asselineau D, Bernerd F. Morphogenesis of dermal–epidermal junction in a model of reconstructed skin: beneficial effects of vitamin C. Experimental dermatology. 2006;15:625-33.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78199-
dc.description.abstract注射式皮膚填充物是近年來常被應用在醫學美容的生醫材料,藉由具生物相容性與生物降解性生醫材料來製備,而膠原蛋白為其中一種常見的填充物材料,膠原蛋白具有良好生物相容性、生物可降解性且具有許多蛋白質鍵結區域可供細胞貼附近而促進細胞增生,而聚乳酸聚乙醇酸共聚物為一種生物可降解性高分子,藉由乳化法可以製作藥物載體並且提供持續釋放的效果。
抗壞血酸,又通稱維他命C,為一種水溶性的抗氧化劑,其參與人體許多的生理反應,如膠原蛋白生成、細胞增生、氧化還原反應、與免疫系統的反應……等等。因在本研究中,我們利用乳化法揮發法將抗壞血酸包覆於聚乳酸聚乙醇酸共聚物奈米粒子中,並包覆於膠原蛋白水膠中,製造一種可以持續釋放抗壞血酸約14天之皮下填充物,藉由聚乳酸聚乙醇酸共聚物微米粒子保護易氧化的抗壞血酸,而這樣的材料在細胞實驗中確實可以增加纖維細胞膠原蛋白的生成量與細胞活性 ,而在天竺鼠的動物實驗中也可以確實增加真皮層的厚度,相較於控制組約有百分之七的增加量,希望藉由此材料提供填充物一個更有效的生醫材料。
zh_TW
dc.description.abstractInjectable filler is widely used in facial and bone rejuvenation, in this research, we combining the PLGA drug delivery system, l-ascorbic acid and collagen hydrogel into injectable filler. The PLGA polymers were widely in drug delivery system. Because of its remarkable biocompatibility and biodegradability. The collagen hydrogel can extend the drug releasing time and widely used in dermatology which has abilities of biocompatible, degradable and its great cellular interactions. The l-ascorbic acid can enhance cell viability and increase the secretion of collagen by fibroblast.
We proposed that when the filler degrade slowly the ascorbic acid also released and the drug will stimulate the fibroblast to proliferation and secreting the collagen. And the secreted collagen and cell proliferation can enhance the facial rejuvenation ability of the filler.
This research showed that the filler combining to l-ascorbic acid could successfully increase the cell viability and secretion of collagen by fibroblast. We hope this material could provide a better choice for cosmetic surgery.
en
dc.description.provenanceMade available in DSpace on 2021-07-11T14:45:40Z (GMT). No. of bitstreams: 1
ntu-105-R03548012-1.pdf: 2737554 bytes, checksum: 50cd47e2dbbd0d5a0f4dc7e52d9cc199 (MD5)
Previous issue date: 2016
en
dc.description.tableofcontents致謝 i
中文摘要 ii
Abstract iii
Content iv
List of Tables vii
List of Figures viii
Chapter 1 Introduction 1
1.1 Dermal Filler 1
1.2 Fibroblast 2
1.3 Collagen 3
1.4 PLGA 4
1.5 L-Ascorbic acid 5
1.6 The Aim 6
Chapter 2 Materials and Methods 7
2.1 Biological and Chemical Reagents 7
2.2 Instruments 8
2.3 Culture Medium Preparation 9
2.4 Collagen Solution preparation 9
2.5 Cell Culture 9
2.6 L-Ascorbic acid Loaded PLGA Particle Preparation 10
2.7 In Vitro Drug Release 10
2.8 Cell Viability Assay 10
2.9 Collagen Assay 11
2.10 Western blot 12
2.11 Animal Experiment 12
Chapter 3 Results 14
3.1 Particles Structure Analysis 14
3.2 Drug Release Profile 15
3.3 Cell Morphologies and Cell Viability After Treatment 16
3.4 Collagen Assay 17
3.5 Histology 19
Chapter 4 Discussion 20
Chapter 5 Conclusion and Perspective 23
Figures 24
Tables 39
References 40
dc.language.isoen
dc.subject聚乳酸聚乙醇酸共聚物zh_TW
dc.subject皮膚填充物zh_TW
dc.subject抗壞血酸zh_TW
dc.subject膠原蛋白zh_TW
dc.subjectl-ascorbic aciden
dc.subjectinjection filleren
dc.subjectcollagenen
dc.subjectPLGAen
dc.title膠原蛋白水膠包覆含抗壞血酸之聚乳酸聚乙醇酸共聚物粒子之應用zh_TW
dc.titleApplication of collagen hydrogel containing l-ascorbic acid loaded PLGA particlesen
dc.typeThesis
dc.date.schoolyear104-2
dc.description.degree碩士
dc.contributor.oralexamcommittee林頌然(Sung-Jan Lin),王大銘(Da-Ming Wang),賴君義(Juin-Yih Lai)
dc.subject.keyword皮膚填充物,膠原蛋白,聚乳酸聚乙醇酸共聚物,抗壞血酸,zh_TW
dc.subject.keywordinjection filler,collagen,PLGA,l-ascorbic acid,en
dc.relation.page46
dc.identifier.doi10.6342/NTU201601035
dc.rights.note有償授權
dc.date.accepted2016-07-25
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-lift2026-12-31-
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