| 研究生: |
陳旻 Chen, Min |
|---|---|
| 論文名稱: |
內視鏡治療術中有機纖維溶液對組織抬升之效應 Effects of Organic Fiber Solutions on Tissue Elevation in Endoscopic Treatment |
| 指導教授: |
王覺寬
Wang, Muh-Rong |
| 學位類別: |
碩士 Master |
| 系所名稱: |
工學院 - 航空太空工程學系 Department of Aeronautics & Astronautics |
| 論文出版年: | 2011 |
| 畢業學年度: | 99 |
| 語文別: | 中文 |
| 論文頁數: | 79 |
| 中文關鍵詞: | 無針式噴注 、組織抬升 、HPMC 、有機纖維溶液 |
| 外文關鍵詞: | needle-free injection, tissue elevation, HPMC, organic fiber solution |
| 相關次數: | 點閱:77 下載:1 |
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本研究乃利用自製之內視鏡用無針式注射系統,以HPMC(羥丙基甲基纖維素)、MC(甲基纖維素)、甘油、褐藻膠為工作流體進行生物體之組織抬升,實驗乃是以內視鏡用無針式注射器緊貼待抬升之組織表面進行生物體組織噴注及抬升之作用,並利用數位相機記錄組織抬升及其消散之過程,以探討不同的工作流體進行組織抬升後液體消散之情形及無針式之噴注及注射特性。使用之生物體組織為足齡約六個月大之豬胃,主要之參數包含噴注量、速度、功率、注射位置、組織抬升高度、抬升消散時間等。為使組織成功抬升,第一步驟為穿透胃黏膜層,第二步驟為將抬升溶液順利注入,使用1650mm長的內視鏡管做體外動物實驗,在不同噴注壓力、不同噴注時間下成功穿透豬胃黏膜層的條件為噴注壓力最小為80bar,相當於最小噴注功率2.8w。另外,比較內視鏡工作流體輸送管長度1650mm與2350mm之兩種應用實例,結果顯示2350mm管長之實例所需噴注功率遠低於1650mm之實例,故之工作流體在系統中的能量損失,主要消耗於輸送管的部分。組織抬升之第二步驟需將抬升溶液注入次黏膜層,實驗結果發現,羥丙基甲基纖維素黏滯性越高時,抬升時間越長,當羥丙基甲基纖維素濃度大於0.5%(wt%)時,初始高度為10.6mm,其半衰期大於60分鐘,此時間足夠醫護人員操作手術。使用相同黏滯係數(20cP)的不同溶液,包括羥丙基甲基纖維素、褐藻膠、甘油等做為抬升溶液,初始抬升高度無顯著差異,但羥丙基甲基纖維素的半衰期為最長(超過60分鐘)。將抬升後的豬胃組織浸於福馬林使其硬化固定,再以H&E染色,證實無針式噴注之位置深達生物體組織之次黏膜層,故可以將組織之黏膜層抬升,使病灶與正常組織有效分離,以利後續內視鏡醫療手術之順利進行。
This paper investigates the characteristics of endoscopic needle-free injection and the performance of tissue elevation by an endoscopic needle-free injection system. We choose the stomach of six-months-old pig as the test material, with HPMC, MC, glycerin and alginate as the working fluid. The parameters include the injection mass, average power of injection, and the height of tissue elevation, and the evolution of tissue elevation. Longer duration of tissue elevation of the submucosal layer is maintained under the pressure of 90bar and the concentration of HPMC at 0.5%. The tissue elevation is 10.6mm suitable for medical surgery with the higher injection pressure under the same concentration of the working fluid because of the increased injection power. Analysis on the evolution of tissue elevation found that duration time is more than 60 minute under higher concentration of HPMC. The duration of tissue elevation is longer for higher concentration of the working fluid because the higher viscosity under high concentration would result in the elongation of the elevation time. A clear separation of the mucosal layer from the muscle layer is achieved by injecting HPMC in the samples with formalin-fixed and paraffin-embedded sections stained with H&E. Results of the experiments would provide the data base for endoscopic surgery in order to assure a successful operation.
[1] Y. Nir, et al., "Fear of injections in young adults: prevalence and associations," Am J Trop Med Hyg, vol. 68, pp. 341-4, Mar 2003.
[2] M. Dicko, et al., "Safety of immunization injections in Africa: not simply a problem of logistics," Bull World Health Organ, vol. 78, pp. 163-9, 2000.
[3] D. U. Ekwueme, et al., "Model-based estimates of risks of disease transmission and economic costs of seven injection devices in sub-Saharan Africa," Bull World Health Organ, vol. 80, pp. 859-70, 2002.
[4] M. M. Levine, New Generation Vaccines, 4 ed., 2004.
[5] M. A. Miller and E. Pisani, "The cost of unsafe injections," Bull World Health Organ, vol. 77, pp. 808-11, 1999.
[6] L. Simonsen, et al., "Unsafe injections in the developing world and transmission of bloodborne pathogens: a review," Bull World Health Organ, vol. 77, pp. 789-800, 1999.
[7] R. M. Jacobson, et al., "Making vaccines more acceptable--methods to prevent and minimize pain and other common adverse events associated with vaccines," Vaccine, vol. 19, pp. 2418-27, Mar 21 2001.
[8] J. V. Bennett, et al., "Aerosolized measles and measles-rubella vaccines induce better measles antibody booster responses than injected vaccines: randomized trials in Mexican schoolchildren," Bull World Health Organ, vol. 80, pp. 806-12, 2002.
[9] C. B. Bridges, et al., "Prevention and control of influenza. Recommendations of the Advisory Committee on Immunization Practices (ACIP)," MMWR Recomm Rep, vol. 52, pp. 1-34; quiz CE1-4, Apr 25 2003.
[10] G. M. Glenn, et al., "Transcutaneous immunization and immunostimulant strategies," Immunol Allergy Clin North Am, vol. 23, pp. 787-813, Nov 2003.
[11] E. H. Moylett and I. C. Hanson, "Mechanistic actions of the risks and adverse events associated with vaccine administration," J Allergy Clin Immunol, vol. 114, pp. 1010-20; quiz 1021, Nov 2004.
[12] P. E. Fine, "Poliomyelitis: very small risks and very large risks," Lancet Neurol, vol. 3, p. 703, Dec 2004.
[13] Y. Roth, et al., "Feasibility of aerosol vaccination in humans," Ann Otol Rhinol Laryngol, vol. 112, pp. 264-70, Mar 2003.
[14] J. Baxter and S. Mitragotri, "Jet-induced skin puncture and its impact on needle-free jet injections: experimental studies and a predictive model," J Control Release, vol. 106, pp. 361-73, Sep 2 2005.
[15] N. J. Quinlan, et al., "Investigations of gas and particle dynamics in first generation needle-free drug delivery devices," Shock Waves, vol. 10, pp. 395-404, 2001.
[16] Y. Liu and M. A. F. Kendall, "Numerical study of a transient gas and particle flow in a high-speed needle-free ballistic particulate vaccine delivery system " Journal of Mechanics in Medicine and Biology, vol. 4, p. 20, 2004.
[17] M. Kendall, "Engineering of needle-free physical methods to target epidermal cells for DNA vaccination," Vaccine, vol. 24, pp. 4651-6, May 22 2006.
[18] E. L. Giudice and J. D. Campbell, "Needle-free vaccine delivery," Adv Drug Deliv Rev, vol. 58, pp. 68-89, Apr 20 2006.
[19] S. Mitragotri, "Current status and future prospects of needle-free liquid jet injectors," Nat Rev Drug Discov, vol. 5, pp. 543-8, Jul 2006.
[20] S. Mitragotri, "Immunization without needles," Nat Rev Immunol, vol. 5, pp. 905-916, 2005.
[21] 黃博偉, 2007醫療器材工業年鑑: 工業技術研究院產業經濟與趨勢研究中心, 2008.
[22] S.-e. Kudo, et al., "Endoscopic Diagnosis and Treatment of Early Colorectal Cancer," World Journal of Surgery, vol. 21, pp. 694-701, 1997.
[23] S. H. Makuuchi Hiroyasu "Endoscopic mucosal resection for early esophageal cancer," Surgical Therapy, vol. 90, p. 2004, 1996.
[24] T. Nakajima, "Gastric cancer treatment guidelines in Japan," Gastric Cancer, vol. 5, pp. 1-5, 2002.
[25] H. Ono, et al., "Endoscopic mucosal resection for treatment of early gastric cancer," Gut, vol. 48, pp. 225-9, Feb 2001.
[26] V. I. Egorov, et al., "Mechanical properties of the human gastrointestinal tract," Journal of Biomechanics, vol. 35, pp. 1417-1425, 2002.
[27] J. Zhao, et al., "Stomach stress and strain depend on location, direction and the layered structure," J Biomech, vol. 41, pp. 3441-7, Dec 5 2008.
[28] G. F. Kaehler, et al., "Selective fluid cushion in the submucosal layer by water jet: advantage for endoscopic mucosal resection," Eur Surg Res, vol. 39, pp. 93-7, 2007.
[29] M. Fujishiro, et al., "Comparison of various submucosal injection solutions for maintaining mucosal elevation during endoscopic mucosal resection," Endoscopy, vol. 36, pp. 579-83, Jul 2004.
[30] M. Fujishiro, et al., "Different mixtures of sodium hyaluronate and their ability to create submucosal fluid cushions for endoscopic mucosal resection," Endoscopy, vol. 36, pp. 584-9, Jul 2004.
[31] J. Rosen, et al., "Biomechanical properties of abdominal organs in vivo and postmortem under compression loads," J Biomech Eng, vol. 130, p. 021020, Apr 2008.
[32] M. Ohkuwa, et al., "New endoscopic treatment for intramucosal gastric tumors using an insulated-tip diathermic knife," Endoscopy, vol. 33, pp. 221-6, Mar 2001.
[33] N. Rosenberg, "Submucosal saline wheal as safety factor in fulguration or rectal and sigmoidal polypi," AMA Arch Surg, vol. 70, pp. 120-2, Jan 1955.
[34] S. V. Kantsevoy, et al., "Endoscopic mucosal resection and endoscopic submucosal dissection," Gastrointest Endosc, vol. 68, pp. 11-8, Jul 2008.
[35] M. Fujishiro, et al., "Tissue damage of different submucosal injection solutions for EMR," Gastrointest Endosc, vol. 62, pp. 933-42, Dec 2005.
[36] J. J. Hyun, et al., "Comparison of the characteristics of submucosal injection solutions used in endoscopic mucosal resection," Scand J Gastroenterol, vol. 41, pp. 488-92, Apr 2006.
[37] D. Polymeros, et al., "Comparative performance of novel solutions for submucosal injection in porcine stomachs: An ex vivo study," Dig Liver Dis, vol. 42, pp. 226-9, Mar 2010.
[38] A. B. Feitoza, et al., "Hydroxypropyl methylcellulose: A better submucosal fluid cushion for endoscopic mucosal resection," Gastrointestinal Endoscopy, vol. 57, pp. 41-47, 2003.
[39] J. L. Alio, et al., "Phacoemulsification in the anterior chamber," J Cataract Refract Surg, vol. 28, pp. 67-75, Jan 2002.
[40] T. J. Liesegang, et al., "The use of hydroxypropyl methylcellulose in extracapsular cataract extraction with intraocular lens implantation," Am J Ophthalmol, vol. 102, pp. 723-6, Dec 15 1986.
[41] A. Storr-Paulsen and M. Larsen, "Long-term results of extracapsular cataract extraction with posterior chamber lens implantation: sodium hyaluronate 1% vs hydroxypropyl methylcellulose 2%," Acta Ophthalmol (Copenh), vol. 69, pp. 766-9, Dec 1991.
[42] J. Siepmann and N. A. Peppas, "Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC)," Advanced Drug Delivery Reviews, vol. 48, pp. 139-157, 2001.
[43] N. Sarkar, "Thermal gelation properties of methyl and hydroxypropyl methylcellulose," Journal of Applied Polymer Science, vol. 24, pp. 1073-1087, 1979.
[44] O. A. Shergold and N. A. Fleck, "Mechanisms of deep penetration of soft solids, with application to the injection and wounding of skin," Proceedings of the Royal Society of London Series a-Mathematical Physical and Engineering Sciences, vol. 460, pp. 3037-3058, Oct 2004.
[45] 陶托拉, 解剖學原理與實用: 合記出版社, 1996.