中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
12期
1831-1838
,共8页
王鹏%皮斌%王金宁%朱雪松%杨惠林
王鵬%皮斌%王金寧%硃雪鬆%楊惠林
왕붕%피빈%왕금저%주설송%양혜림
生物材料%骨生物材料%硫酸钙%骨水泥%微球%壳聚糖%丝素%力学强度%理化特性%国家自然科学基金
生物材料%骨生物材料%硫痠鈣%骨水泥%微毬%殼聚糖%絲素%力學彊度%理化特性%國傢自然科學基金
생물재료%골생물재료%류산개%골수니%미구%각취당%사소%역학강도%이화특성%국가자연과학기금
biocompatible materials%calcium sulfate%chitosan%silk
背景:脊柱成形和脊柱后凸成形治疗中采用的硫酸钙骨水泥理化性质好,对人体无毒性作用,同时具有降解性能,但单独使用降解较快。<br> 目的:研制具有载药缓释功能的壳聚糖微球丝素基硫酸钙骨水泥。<br> 方法:采用三聚磷酸钠乳化交联法制备壳聚糖微球。采用浓度分别为3%,6%,9%的丝素溶液与CaSO4?0.5H 2 O混合,通过万能力学试验机确定骨水泥力学性能最佳时的丝素浓度,在此浓度下,按壳聚糖微球占CaSO 4?0.5H 2 O的质量比分别为0.5%,1%,5%的比例制备壳聚糖微球丝素基硫酸钙骨水泥,测定其抗压强度,并通过X射线多晶衍射仪及傅里叶红外光谱明确达到最佳抗压强度组的骨水泥成分,电镜观察复合骨水泥中壳聚糖微球的形态。<br> 结果与结论:当丝素溶液浓度为6%,壳聚糖微球含量为0.5%时,复合骨水泥的抗压强度最大,为(39.17±1.96) MPa,此时复合骨水泥的初凝时间为(12.99±1.63) min,终凝时间为(21.55±0.54) min;骨水泥中主要晶相组成为硫酸钙,傅里叶红外光谱结果证实复合骨水泥中含有丝素及壳聚糖;复合骨水泥中的微球表面稍有皱缩,但球形仍然完整,未见明显破坏,可见在制备复合骨水泥的过程中微球能保持稳定而不被破坏。
揹景:脊柱成形和脊柱後凸成形治療中採用的硫痠鈣骨水泥理化性質好,對人體無毒性作用,同時具有降解性能,但單獨使用降解較快。<br> 目的:研製具有載藥緩釋功能的殼聚糖微毬絲素基硫痠鈣骨水泥。<br> 方法:採用三聚燐痠鈉乳化交聯法製備殼聚糖微毬。採用濃度分彆為3%,6%,9%的絲素溶液與CaSO4?0.5H 2 O混閤,通過萬能力學試驗機確定骨水泥力學性能最佳時的絲素濃度,在此濃度下,按殼聚糖微毬佔CaSO 4?0.5H 2 O的質量比分彆為0.5%,1%,5%的比例製備殼聚糖微毬絲素基硫痠鈣骨水泥,測定其抗壓彊度,併通過X射線多晶衍射儀及傅裏葉紅外光譜明確達到最佳抗壓彊度組的骨水泥成分,電鏡觀察複閤骨水泥中殼聚糖微毬的形態。<br> 結果與結論:噹絲素溶液濃度為6%,殼聚糖微毬含量為0.5%時,複閤骨水泥的抗壓彊度最大,為(39.17±1.96) MPa,此時複閤骨水泥的初凝時間為(12.99±1.63) min,終凝時間為(21.55±0.54) min;骨水泥中主要晶相組成為硫痠鈣,傅裏葉紅外光譜結果證實複閤骨水泥中含有絲素及殼聚糖;複閤骨水泥中的微毬錶麵稍有皺縮,但毬形仍然完整,未見明顯破壞,可見在製備複閤骨水泥的過程中微毬能保持穩定而不被破壞。
배경:척주성형화척주후철성형치료중채용적류산개골수니이화성질호,대인체무독성작용,동시구유강해성능,단단독사용강해교쾌。<br> 목적:연제구유재약완석공능적각취당미구사소기류산개골수니。<br> 방법:채용삼취린산납유화교련법제비각취당미구。채용농도분별위3%,6%,9%적사소용액여CaSO4?0.5H 2 O혼합,통과만능역학시험궤학정골수니역학성능최가시적사소농도,재차농도하,안각취당미구점CaSO 4?0.5H 2 O적질량비분별위0.5%,1%,5%적비례제비각취당미구사소기류산개골수니,측정기항압강도,병통과X사선다정연사의급부리협홍외광보명학체도최가항압강도조적골수니성분,전경관찰복합골수니중각취당미구적형태。<br> 결과여결론:당사소용액농도위6%,각취당미구함량위0.5%시,복합골수니적항압강도최대,위(39.17±1.96) MPa,차시복합골수니적초응시간위(12.99±1.63) min,종응시간위(21.55±0.54) min;골수니중주요정상조성위류산개,부리협홍외광보결과증실복합골수니중함유사소급각취당;복합골수니중적미구표면초유추축,단구형잉연완정,미견명현파배,가견재제비복합골수니적과정중미구능보지은정이불피파배。
BACKGROUND:Calcium sulfate used in kyphoplasty and vertebrolplasty has good physical and chemical properties, exerts no toxic effects on human body and has the degradation performance. But its main drawback is rapid degradation. <br> OBJECTIVE:To develop a chitosan microsphere with silk fibroin/calcium sulfate cement to prepare drug carrier system. <br> METHODS:Chitosan microspheres were prepared by the emulsion method. Scanning electron microscopy, particle size analysis and swel ing rate were used to study the properties of the microspheres. Different silk concentrations (3%, 6%and 9%) and weight rates (0.5%,1%and 5%) of chitosan microspheres were used to determine the best formula which has the strongest mechanical properties. The composition of this composite bone cement was detected by using X-ray diffraction and Fourier transform infrared spectroscopy. <br> RESULTS AND CONCLUSION:When the concentration of silk fibroin was 6%and weight rate of chitosan microspheres was 0.5%, we could obtain the maximum compressive strength, which was (39.17±1.96) MPa. With this composition, the initial setting time was (12.99±1.63) minutes and the final setting time was (21.55±0.54) minutes. The results from X-ray diffraction and Fourier transform infrared spectroscopy demonstrated that the main phase composition was calcium sulfate, and silk and chitosan were also included. The composite chitosan microspheres exhibited a slightly wrinkled surface, but were stil intact in spherical shape, indicating the preparation of chitosan microspheres/silk fibroin/calcium sulfate cement was reliable and the product had good structures and properties.