PLLA封孔工艺对微弧氧化镁合金丝材性能的影响

目的提高微弧氧化镁合金丝材的强度和耐腐蚀性能。方法通过硅烷偶联及聚乳酸封孔处理对微弧氧化AZ31B镁合金丝材进行表面改性,采用扫描电子显微镜(SEM)、电子能谱仪(EDS)以及模拟胃液(SGF)浸泡实验、拉伸实验等设备和方法,研究了硅烷偶联工艺、聚乳酸封孔工艺对丝材综合性能的影响。结果微弧氧化镁合金丝材的耐腐蚀性能随偶联处理时间的延长先升高后降低,当处理时间为90 min时,丝材的耐腐蚀性能最佳。随封孔聚乳酸浓度的升高,丝材的耐腐蚀性能先升高后降低,强度增大;随提拉速度的增大,其耐腐蚀性能和强度均逐渐提高;随浸渍提拉次数的增多,丝材的耐腐蚀性能和强度逐渐降低。当聚乳酸质量浓度为0.14 g/m L、提拉速度为0.9 cm/s、浸渍提拉次数为1次时,硅烷偶联处理过的丝材的综合性能最佳。结论微弧氧化镁合金丝材的性能可以通过聚乳酸封孔处理改善,改善效果与聚乳酸浓度、提拉速度和浸渍提拉次数有关。微弧氧化镁合金丝材表面硅烷偶联处理能有效提高聚乳酸封孔效果。     

含生物功能基团磷脂胆碱的聚乳酸的合成反应

用天然甘油磷脂胆碱开环丙交酯,以获得具有仿生功能的生物降解聚乳酸.采用1H-NMR、FT-IR确证在聚合物结构中引入了生物功能基团磷脂胆碱.通过1H-NMR和GPC测定分子量及其分布,研究了反应时间和温度对聚合物分子量扣产率的影响,聚合物产率达80%以上.将磷脂引入聚乳酸链段中得到可全降解的、生物相容性好的磷脂高分子.这一新的思路可以用于合成一系列新型的药物载体和组织工程支架材料.     

Surface wetting phenomena of plasma polymer-coated sheets of poly(l-lactic acid)/poly(butylene succinate)

Water-repellent surfaces were fabricated on blend sheets of poly(l-lactic acid)/poly(butylene succinate) with various blending ratios by the successive processing; (1) plasma etching, followed by (2) the hydrophobic plasma polymer coating. Rough morphology was formed effectively on the mosaic structured surface of blend sheets via the oxidative etching, and advanced water repellency was achieved after the thin membrane coating was synthesized with a hydrophobic plasma polymer coating by use of hexamethyldisiloxane or hexamethyldisilazane. High water repellency is expressed through the columnar hair-like structured model, where the air-water surface interaction in the voids is taken into account.     

PLLA/CPC复合支架增强结构设计及制备

为制备用于负重部位骨缺损修复的人工植入体,提出了一种复合增强结构人工骨设计及制备方案,该方案采用聚左旋乳酸支架(PLLA)为增强结构,以自凝固磷酸钙骨水泥(CPC)为复合填充材料,制备了复合增强结构人工骨。研究了PLLA的棒材力学性能、支架设计和制作及其不同增强结构形式对人工骨力学性能的影响。力学试验结果表明,所制作的人工骨有效提高了承载能力,并且该复合结构能有效弥补金属骨无法降解的缺陷。     

镁合金支架材料AZ81表面PLGA(PTX)/PLLA/MAO涂层的研究

在AZ81镁合金表面制备了抗腐蚀和药物释放复合涂层,并对其耐蚀性、药物释放性能及生物相容性进行研究。DSC和红外光谱数据表明,紫杉醇均匀分散在PLGA体系中。药物释放数据表明30 d后,药物释放率在80%左右。SEM、电化学阻抗、极化及镁离子释放数据表明,PLLA涂层通过有效填充微弧氧化膜表面的微孔与裂缝提高了镁合金的耐腐蚀性。血液和细胞实验表明涂层镁合金血液相容性良好,无细胞毒性。     

In Vitro Characterizations of PLLA/β-TCP Porous Matrix Materials and RMSC-PLLA-β-TCP Composite Scaffolds

To develop a novel degradable poly (L-lactic acid)/β-tricalcium phosphate (PLLA/β-TCP) bioactive materials for bone tissue engineering, β-TCP powder was produced by a new wet process. Porous scaffolds were prepared by three steps, I.e. Solvent casting, compression molding and leaching stage. Factors influencing the compressive strength and the degradation behavior of the porous scaffold, e.g. Weight fraction of pore forming agent-sodium chloride (NaCl), weight ratio of PLLA: β-TCP, the particle size ofβ-TCP and the porosity, were discussed in details. Rat marrow stromal cells (RMSC) were incorporated into the composite by tissue engineering approach. Biological and osteogenesis potential of the composite scaffold were determined with MTT assay, alkaline phosphatase (ALP) activity and bone osteocalcin (OCN) content evaluation. Results show that PLLA/β-TCP bioactive porous scaffold has good mechanical and pore structure with adjustable compressive strength needed for surgery. RMSCs seeding on porous PLLA/β-TCP composite behaves good seeding efficacy, biocompatibility and osteoinductive potential. Osteoprogenitor cells could well penetrate into the material matrix and begin cell proliferation and osteogenic differentiation. Osseous matrix could be formed on the surface of the composite after culturing in vitro. It is expected that the PLLA/β-TCP porous composites are promising scaffolds for bone tissue engineering in prosthesis surgery.     

Preparation and in vitro release behavior of urapidil hydrochloride loading into microspheres based on poly(L‐lactide)

Microencapsulation of the antihypertensive drug urapidil hydrochloride was investigated as a means of controlling drug release and minimizing or eliminating local side effects. Poly(L ‐lactide) (PLLA) microspheres were prepared using an alternative oil‐in‐water (O/W) solvent‐evaporation method such as the O/W cosolvent solvent‐evaporation method and O/W with various electrolytes added to the aqueous phase method. The surface morphology and the size of the microspheres were observed by scanning electron microscope. Meanwhile, the drug loading efficiency of microspheres and the in vitro release of urapidil hydrochloride from microspheres were performed. The release study indicated that the urapidil hydrochloride‐PLLA microspheres exhibited better sustained release capacity, and the kinetics of urapidil hydrochloride‐PLLA microspheres in vitro release could be described by the Higuchi equation. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Supercritical CO2 precipitation of poly(l-lactic acid) in a wide range of miscibility

Polymer microparticles are useful for numerous applications such as stationary phases in chromatography, adsorbents and catalyst supports, as well as for drug delivery systems. In recent decades the application of supercritical fluids for microparticle precipitation has been developed to a point where it is an ideal alternative to conventional processes. In this work poly(l-lactic acid) (PLLA), a biodegradable and biocompatible thermoplastic aliphatic polyester, has been processed using supercritical fluids, particularly by rapid expansion of supercritical solutions (RESS) and supercritical antisolvent (SAS) processes over a wide miscibility range. Particle morphology was greatly improved from irregular blocks to spherical microparticles on applying the SAS process. The effects of changes in polymer concentration, liquid flow rate, nozzle diameter, solvent, pressure and temperature have also been evaluated on the particle size of PLLA in the SAS precipitation. A higher concentration of the initial solution led to a decrease in particle size. Dichloromethane was the best of the chlorinated solvents investigated. The nozzle diameter had a negligible effect on particle size and the highest liquid flow rate gave the largest particle size. A larger particle size was also obtained on increasing the operating temperature. In contrast, the particle size decreased on increasing the operating pressure.     

Combustion properties and transference behavior of ultrafine microencapsulated ammonium polyphosphate in ramie fabric‐reinforced poly(L‐lactic acid) biocomposites

Flame‐retardant biocomposites have attracted much attention in past decades. They can provide many advantages, such as total biodegradability and their abundant renewable sources. In the work reported, biocomposites based on poly(L ‐lactic acid) (PLLA), ramie fabric (FAB) and microencapsulated ammonium polyphosphate (MCAPP) were synthesized via hot press molding using the powder‐stacking procedure. The effects of transference behavior of the flame retardant on sustaining flame retardancy of the biocomposites were investigated. Thermogravimetric analysis shows that the improved flame retardancy is due to an increased char residue at high temperature. Field emission scanning electron microscopy images and wide‐angle X‐ray diffraction data were used to investigate the hydrolysis reaction and transference behavior of ammonium polyphosphate in the biocomposites. UL‐94 testing and limiting oxygen index measurements show that the PLLA/FAB/MCAPP biocomposites retain their flame retardancy even after 21 days in UV‐irradiation hydrothermal aging tests. The good sustained flame retardancy of the PLLA/FAB/MCAPP biocomposites is attributed to the docking interactions and good distribution of MCAPP in the biocomposites. Copyright © 2010 Society of Chemical Industry     

Glass transition and mechanical properties of PLLA and PDLLA‐PGA copolymer blends

The change of the glass transition temperatures (T_g) in the blend of poly(L ‐lactic acid) (PLLA) and the copolymers of poly(D,L ‐lactic acid) and poly(glycolic acid) (PDLLA‐PGA) with different D,L ‐lactic acid and glycolic acid composition ratio (50 : 50, 65 : 35, and 75 : 25) was studied by DSC. Dynamic mechanical measurement and tensile testing were performed at various temperatures around T_g of the blend. In the blend of PLLA and PDLLA‐PGA50 (composition ratio of PDLLA and PGA 50 : 50), T_g decreased from that of PLLA (about 58°C) to that of PDLLA‐PGA50 (about 30°C). A single step decrease was observed in the DSC curve around T_g between the weight fraction of PLLA (W(PLLA)) 1.0 and 0.7 (about 52°C) but two‐step changes in the curve are observed between W(PLLA) = 0.6 and 0.3. The T_g change between that of PLLA and that of PDLLA‐PGA and the appearance of two T_gs suggest the existence of PLLA rich amorphous region and PDLLA‐PGA copolymer rich amorphous region in the blend. A single step decrease of E′ occurs at around T_g of the pure PLLA but the two‐step decrease was observed at W(PLLA) = 0.6 and 0.4, supporting the existence of the PLLA rich region and PDLLA‐PGA rich region. Tensile testing for various blends at elevated temperature showed that the extension without yielding occurred above T_g of the blend. Partial miscibility is suggested for PLLA and PDLLA‐PGA copolymer blends. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2164–2173, 2004