中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
12期
2273-2276
,共4页
李楠%王雪明%齐宏旭%翟俊山%王艳%胡平%朱建华
李楠%王雪明%齊宏旭%翟俊山%王豔%鬍平%硃建華
리남%왕설명%제굉욱%적준산%왕염%호평%주건화
聚乳酸%聚3羟基丁酸酯共聚4羟基丁酸酯%聚碳酸酯%电纺丝%亲水性
聚乳痠%聚3羥基丁痠酯共聚4羥基丁痠酯%聚碳痠酯%電紡絲%親水性
취유산%취3간기정산지공취4간기정산지%취탄산지%전방사%친수성
背景:近年来聚乳酸、羟基磷灰石类复合材料支架具有良好的生物降解性和生物相容性而被广泛的研究,但是这类复合材料在增强材料界面的结合、调节材料的降解速率、改善材料的强度等方面仍不能满足理想的组织工程支架材料的要求.目的:探讨电纺丝法制备纳米纤维的结构形态及表面亲水性.方法:分别将聚乳酸、聚3羟基丁酸酯共聚4羟基丁酸酯和聚碳酸亚丙酯通过静电纺丝法制备纳米纤维膜,扫描电镜对纤维膜的结构形态进行分析,并观察在人体环境相近的磷酸盐缓冲溶液(37℃,pH 7.4)中浸泡不同时间的表面亲水性.结果与结论:通过静电纺丝技术可以将聚乳酸、聚3羟基丁酸酯共聚4羟基丁酸酯和聚碳酸亚丙酯3种材料制各成微纳米纤维结构,控制制备参数可以获得不同直径的纤维,样品随着在培养液中的浸泡时间延长,总体显示出接触角比初始降低,亲水性增强.
揹景:近年來聚乳痠、羥基燐灰石類複閤材料支架具有良好的生物降解性和生物相容性而被廣汎的研究,但是這類複閤材料在增彊材料界麵的結閤、調節材料的降解速率、改善材料的彊度等方麵仍不能滿足理想的組織工程支架材料的要求.目的:探討電紡絲法製備納米纖維的結構形態及錶麵親水性.方法:分彆將聚乳痠、聚3羥基丁痠酯共聚4羥基丁痠酯和聚碳痠亞丙酯通過靜電紡絲法製備納米纖維膜,掃描電鏡對纖維膜的結構形態進行分析,併觀察在人體環境相近的燐痠鹽緩遲溶液(37℃,pH 7.4)中浸泡不同時間的錶麵親水性.結果與結論:通過靜電紡絲技術可以將聚乳痠、聚3羥基丁痠酯共聚4羥基丁痠酯和聚碳痠亞丙酯3種材料製各成微納米纖維結構,控製製備參數可以穫得不同直徑的纖維,樣品隨著在培養液中的浸泡時間延長,總體顯示齣接觸角比初始降低,親水性增彊.
배경:근년래취유산、간기린회석류복합재료지가구유량호적생물강해성화생물상용성이피엄범적연구,단시저류복합재료재증강재료계면적결합、조절재료적강해속솔、개선재료적강도등방면잉불능만족이상적조직공정지가재료적요구.목적:탐토전방사법제비납미섬유적결구형태급표면친수성.방법:분별장취유산、취3간기정산지공취4간기정산지화취탄산아병지통과정전방사법제비납미섬유막,소묘전경대섬유막적결구형태진행분석,병관찰재인체배경상근적린산염완충용액(37℃,pH 7.4)중침포불동시간적표면친수성.결과여결론:통과정전방사기술가이장취유산、취3간기정산지공취4간기정산지화취탄산아병지3충재료제각성미납미섬유결구,공제제비삼수가이획득불동직경적섬유,양품수착재배양액중적침포시간연장,총체현시출접촉각비초시강저,친수성증강.
BACKGROUND: Recently, poly (lactic acid)/hydroxyapatite composite scaffolds have been widely used due to good biodegradation and biocompatibility. But poly (lactic acid)/hydroxyapatite composite material can not satisfy the requirements of ideal tissue-engineered scaffold materials owing to drawbacks in some aspects including enhancing material surface binding,adjusting material degradation velocity, and improving material intensity.OBJECTIVE: To investigate the structural morphology and surface hydrophilicity of nanometer fiber membrane prepared by electrospinning.METHODS: Poly(lactic acid), poly (3-hydroxybutyrate-co-4-hydroxybutyrate), and poly(propylene carbonate) nanometer fiber membranes were respectively prepared by electrospinning. The structural morphology of these three nanometer fiber membranes,as well as the surface hydrophilicity after soaking in phosphate buffered saline (37 ℃, pH 7.4) similar to human body environment
for different time periods, was observed through the use of scanning electron microscope.RESULTS AND CONCLUSION: Poly(lactic acid), poly(3-hydroxybutyrate-co-4-hydroxybutyrate), and polypropylene carbonate) could be prepared into micro- and nano-sized fiber structure by electrospinning. Different fiber diameters of nanometer fiber membranes could be produced by controlling preparation parameters. With the prolonged soaking time in culture medium, the contact angle of three fiber members was reduced greatly and surface hydrophilicity was gradually enhanced.