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91.
The aim of this study was to optimize the formula of free blended coating membrane of ethyl cellulose (EC) and chitosan (CS), including their suitable ratio range and the best plasticizer used. The dry films were produced by a casting/solvent evaporation method, with different volume ratio of EC and CS solution plasticized by various plasticizers, respectively. The wet films were prepared by immersing dry films in pH 6.8 phosphate buffer saline (PBS) for 24 h. The promising ratio range of EC/CS was below 20/5 or 20/6 with various plasticizer, which was determined by comparing the viscosity of the blended solutions and the morphology of the blended films. The efficiency of plasticization was evaluated by measuring glass transition temperature (Tg). All the testing plasticizers have good compatibility with EC or CS and dibutyl phthalate (DBP) have the strongest efficiency inducing the lowest Tg (39.9°C) of the film. Mechanical properties were evaluated by the ratio of tensile strength (T) to elastic modulus (E). In the wet state, the films with DBP had the highest T/E value (1.2). The results of leaching of plasticizers also verified that DBP was the most stable plasticizer in the films. The release rates of tetramethylpyrazine phosphate (TMPP) through the pellets coated with the blended films of EC/CS (20 : 6 v/v) plasticized by various plasticizers showed that the more water‐soluble the plasticizer was, the more quickly TMPP dissolved from the coated pellets, which further indicated that the water‐insoluble plasticizers (such as DBP) could be more applicable to keep the sustained or controlled release property of the blended films in wet state. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1932–1939, 2006 相似文献
92.
J. L. Escobar D. García A. Valerino D. Zaldívar E. Hernez Issa Katime 《应用聚合物科学杂志》2004,91(6):3433-3437
Hydrogels are hydrophilic polymers that swell to an equilibrium volume in the presence of water, preserving their shape. The dynamic swelling behavior of poly(N‐isopropylacrylamide‐co‐N,N‐dimethylacrylamide) [poly(NIPA‐co‐DMA)] copolymers at 37°C was investigated. It was observed that the swelling degree in the copolymers decreases with the N‐isopropylacrylamide content. In addition, the liberation mechanism was found to be Fickian. Diffusion coefficients according to Fick′s law as a function of the N‐isopropylacrylamide concentration and results of the release process are reported. The kinetics of cephazoline sodium release from poly(NIPA‐co‐DMA) hydrogels with different compositions was studied. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3433–3437, 2004 相似文献
93.
A series of nanocomposite hydrogels were prepared from various ratios of N‐isopropylacrylamide (NIPAAm) and organic montmorillonite (MMT). The influence of the extent of MMT in the NIPAAm/MMT nanocomposite hydrogels on the physical properties and drug‐release behavior was the main purpose of this study. The microstructure and morphology were identified by X‐ray diffraction (XRD) and scanning electronic microscopy (SEM). The results showed that the swelling ratios for these nanocomposite hydrogels decreased with increase in the content of MMT. The gel strength and Young's modulus of the gels also increased with increase in the content of MMT. XRD results indicated that the exfoliation of MMT was achieved in the swollen state. Finally, the drug‐release behavior for the gels was also assessed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3652–3660, 2003 相似文献
94.
95.
P-糖蛋白基因疫苗的构建与鉴定 总被引:2,自引:0,他引:2
目的 制备P 糖蛋白基因疫苗。方法 利用PCR方法扩增编码人类P 糖蛋白多药耐药基因序列胞外区约 1kb片段 ,与真核表达载体pcDNA3进行定向重组 ,限制性内切酶BamHI和XhoI双酶切反应及测序鉴定该重组基因疫苗 ,磷酸钙共沉淀法转染人类K5 62红白血病细胞 ,经G418筛选后 ,免疫组化分析该重组基因疫苗表达产物的抗原特异性。结果 构建了pcDNA3 MDR1重组基因疫苗。限制性内切酶BamHI和XhoI双酶切分别显示 5 .4kb的载体片段及约 1kb的插入序列 ,测序 948个碱基中除 2个碱基突变外均与原序列排列相符。免疫组化方法证实细胞膜表面MDR1约 1kb片段的表达产物可被抗Pgp抗体识别。结论 构建的pcDNA3 MDR1重组基因疫苗可被市售的Pgp抗体特异性识别 ,具有Pgp抗原特异性 相似文献
96.
Preparation and characterization of chitosan-poly(acrylic acid) polymer magnetic microspheres 总被引:2,自引:0,他引:2
A modified method to prepare chitosan-poly(acrylic acid)(CS-PAA) polymer magnetic microspheres was reported in this paper. First, via self-assembly of positively charged CS and negatively charged Fe3O4 nanoparticles, magnetic CS cores with a large amount of Fe3O4 nanoparticles were successfully prepared. Subsequently, the AA monomers were polymerized on the magetic CS cores based on the reaction system of water-soluble polymer-monomer pairs. These polymer magnetic microspheres had a high Fe3O4 loading content, and showed unique pH-dependent behaviors on the size and zeta potential. From the magnetometer measurements data, the CS-PAA polymer magnetic microspheres also had superparamagnetic property as well as fast magnetic response. A continuous release of the entrapped ammonium glycyrrhizinate in such polymer magnetic microspheres occurred, which confirmed the potential applications of these microspheres for the targeted delivery of drugs. 相似文献
97.
高校规模的不断扩大,教学改革的不断深化与有限教学资源的矛盾日益突出,现有的课程管理和服务无法满足学校快速发展的需求。流程重组通过分析和改进组织过程,可以更好地实现业务目标,该文将ESIA方法应用于业务流程再造,使用ESIA中的清除、简化、整合、自动化策略对排课流程中的问题进行优化,通过统一发布教学任务、集中排课、减少中间沟通环节等方法提升排课流程的效率和便捷性,极大地提高了师生的满意度、提升管理质量、为高校排课流程优化提供参考。 相似文献
98.
该文介绍了在大数据时代背景下针对药品安全网络舆情监测现状,梳理分析了药品安全网络舆情监测系统需求,根据需求和网络舆情监测的特点,提出了药品安全网络舆情监测系统的软件设计框架,介绍了实现该系统所需的主要舆情监测处理技术。该系统设计该设计集监测、预警、分析、报告于一体,合理融合了大数据处理与自然语言处理技术,同时提出了用传统统计分析和深度学习方法来解决舆情分析中“文本分类和情感分析”等关键技术问题。最后,从用户交互的层面给出了药品安全网络舆情监测系统的可视化方案,为药品安全行业网络舆情监测提供了一种实现途径。 相似文献
99.
S期激酶相关蛋白2(S-phase kinase-associated protein 2,Skp2)与Skp1形成的蛋白质聚合物在调控癌细胞生长周期中发挥着重要作用,而苯并吡喃酮类抑制剂(简称BPC)可有效抑制Skp1-Skp2的形成,但其分子识别机制尚不明确.通过生物信息学统计分析已报道的Skp1-Skp2晶体结构,确定模拟体系后,首先用同源模建对其模拟体系缺失的结构进行补全;然后用分子对接方法获得Skp1-Skp2-BPC复合物模型并用于后续分子动力学模拟.计算结果表明:疏水相互作用是促使BPC特异性结合在由Skp2 W109、D110、L117、I120、R138和W139所构成口袋中的主要驱动力,自由能计算值与实验数据吻合较好.Skp2结合BPC后,结合口袋周围的氢键网络有所加强,口袋附近的溶剂化水分子数量明显减少,导致Skp1-Skp2的体系稳定性下降.体系构象成簇与运动性分析显示,Skp1-Skp2在结合BPC抑制剂后,Skp1的运动更加剧烈,这可能是BPC主要的抑制机理. 相似文献
100.
采用紫外-可见分光光度法测定了柿叶总黄酮缓释微丸在人工胃液和磷酸盐缓冲液(pH=6.8)中的累积释药率,并分别对其释药模型进行拟合.结果显示缓释微丸在磷酸盐缓冲液中12h的累积释药率为83.22%,释药模型符合Higuchi方程;在人工胃液中12h的累积释药率为55.42%,释药模型为Higuchi方程.相较于人工胃液,柿叶总黄酮缓释微丸在磷酸盐缓冲液中具有良好的释药性能. 相似文献