聚乙二醇修饰的树枝状聚合物(Dendrimer)用于药物传递的分子动力学研究课件

,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,MSC 2007,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,1,聚乙二醇修饰的树枝状聚合物,(Dendrimer),用于药物传递的分子动力学研究,李有勇,苏州大学 功能纳米与软物质研究院,中国化学会第二十七届年会,2010,厦门,1聚乙二醇修饰的树枝状聚合物(Dendrimer)用于药物传,2,生物材料用于人体组织和器官的诊断、修复或增进其功能的一类高技术材料,药物传递系统也是一类生物材料，,主要包括口服缓控释系统、透皮给药系统和靶向给药系统。,每年被数千万的人群所使用。（目前美国市场是每年,200,亿美元的销售额。）,生物材料和药物传递系统,药物传递对大分子药物（如蛋白质）和基因治疗尤为重要。,药物传递的根本目的是获得高效低毒的药物治疗，即药物能集中在靶部位，在某时释放一定量并维持一定时间。为使药物发挥最大的效力，,必须掌握药物传递的基本原理，即药物如何在体内传递，如何获得理想的药物传递系统及其研究方法。,通过精确控制药物在体内的位置，可以减少药物的副作用，减少药物的剂量并可以发展新的疗法。,2生物材料用于人体组织和器官的诊断、修复或增进其功能的一类高,3,EPR,效应,Enhanced Permeability and Retention effect,正常组织中的微血管内皮间隙致密、结构完整,大分子和脂质颗粒不易透过血管壁,而实体瘤组织中血管丰富、血管壁间隙较宽、结构完整性差,淋巴回流缺失,造 成大分子类物质和脂质颗粒具有选择性高通透性和滞留性,这种现象被称作实体瘤组织的高通透性和滞留效应,简称,EPR,效应。,EPR,效应促进了大分子类物质在肿瘤组织的选择性分布,可以增加药效并减少系统副作用。,3EPR 效应 Enhanced Permeability,4,药物的靶向传递举例,4药物的靶向传递举例,5,Non-ideal properties of drugs, their therapeutic implications, and the effects of DDS (Drug Delivery System),药物传递系统解决的问题,5Non-ideal properties of drugs,6,The bullet points summarize the major develop-ability factors examined at different stages.,药物传递是药物研发中的重要一环,6The bullet points summarize t,7,药物传递系统的分类,liposome,polymer micelle,dendrimer,The drug molecules are illustrated in,red balls,Carbon nanotubes,7药物传递系统的分类liposomepolymer mice,8,Dendrimers,highly branched, globular macromolecules with many arms emanating from a central core,a new class of macromolecular architecture and precise construction modules,precise and designable architecture,tunable solubility,efficient membrane transport,high loading capacity,high uniformity and purity,low toxicity and immunogenicity, and bioattachment capability,8Dendrimers highly branched, g,9,Dendrimer,作为载体的协同作用,Starpharma,药物小分子直接和受体进行相互作用,Dendrimer,可以扩展药物小分子的作用模式，如同时和受体的四个作用靶点进行作用，提高药物的活性；同时和多个受体进行作用；可以使得不同受体之间通过,Dendrimer,进行桥梁作用。,9Dendrimer作为载体的协同作用Starpharma药,10,The advantages of dendrimer as the host for drug delivery:,表面功能基团的调控,10The advantages of dendrimer,11,Dendrimers modified by PEG on the surface,Hydrophilic PEG increases solubility,Hydrophilic PEG also increases biocompatibility,pH, ion strength, temperature, and solvent will affect the structure and functions of the dendrimer,11Dendrimers modified by PEG o,12,理论模拟需要解决的问题,How the drug molecules interact with the host and where the drug molecules locates in the host (e.g. in the core of the dendrimer or the modified shell).,How to redesign the load to make the drug release become slower and more efficient with maximum drug loading;,pH effect, which varies in different cells in the body and affects the shape of the dendrimer as well as the interaction between dendrimer and drug molecules.,Temperature, ion strength, and solvent have similar effects as pH effect.,How the generation number and architecture of the dendrimer affect the delivery efficiency.,12理论模拟需要解决的问题,13,3D structure of PPI-5 after equibration,3D structure of PPI-5 covered by 3,4,5-tris(tetraethyleneoxy) benzoyl units with PEG polymers are connected,With protonation, counter-ions, and explicit solvent,PPI Dendrimer,的结构预测,(CCBTX Monte Carlo,方法）,133D structure of PPI-5 after,14,CCBTX Monte Carlo,方法,CCBTX,蒙特卡洛方法是一种高效的通用的蒙特卡洛方法，可以对蛋白质,loop,区，聚合物，树枝状聚合物进行高效构象采样，并能对体系的系宗进行热力学统计。,Protein loop prediction:,Y. Li, et al.,J. Am. Chem. Soc.,2007, 129, 10720;,Y. Li, et al. Curr. Med. Chem. 2010, 17, 1167;,Goddard, et al. ChemMedChem, 2010, in press;,Goddard, et al. J. Struct. Biol., 2010, in press;,Polymer and Dendrimer:,Y. Li, et al.,J. Am. Chem. Soc. 2004, 126, 1872-1885.,Y. Li, et al. J. Phys. Chem. B. 2006, 110, 18134-18137.,Maiti, et al. J. Chem. Phys. 2009, 130, 144902.,14CCBTX Monte Carlo方法CCBTX蒙特卡洛,15,The location of the guest molecule,15The location of the guest mo,16,Hierdock method for docking the ligands,16Hierdock method for docking,17,Location of the guest molecules in the dendrimer,4 guest molecules stay in the core region of the dendrimer and are stable during the dynamics,12 guest molecules stay in the core region of the dendrimer and are stable during the dynamics,32 guest molecules stay not only in the core region of the dendrimer but also in the PEG region on the surface. They are stable during the dynamics,17Location of the guest molecu,18,Radius gyration of the guest molecules in the dendrimer,Radius gyration evolution,Radius gyration decreases as more guest molecules filled in.,The guest molecules filled the core region first, then the surface region.,This agrees with SAXS experiments, which measure the radius of gyration.,18Radius gyration of the guest,19,-,0.01,0,0.01,0.02,0.03,0.04,0.05,0.06,0.07,-,5,5,15,25,35,45,55,Radial density,Radial Distance (,),Radial density distribution of PPI5-PEG,with Bengal Rose,BR 0ns,water 0ns,BR 1ns,water 1ns,Favorable interaction between PEG and water,19-0.0100.010.020.030.040.050.,20,The PEG tail on the surface is important for encapsulate guest molecules too,withPEG,Without PEG tail, guest molecule diffuses readily,The cavity of the dendrimer core cannot host all of the guest molecules,withoutPEG,PEG,修饰的平行对比,20The PEG tail on the surface,21,The distance of each guest molecule to the host dendrimer,These guest molecules are stable during 1ns MD and are distributed in different locations of the host molecules.,有,PEG,修饰,21The distance of each guest m,22,PEG,修饰的平行对比,Without PEG tails, the dendrimer cannot hold 32 BR molecules strongly.,BR in dendrimer without PEG,D = 0.097 x 10,-5,cm2/s,BR in “Compact PEG”,D = 0.039 x 10,-5,cm2/s,MSD for Bengal Rose molecules in “Compact PEG” (red) and PPI-5 dendrimer without PEG modification (black). We can see that Bengal Rose diffuses quickly for dendrimer without PEG and PEG plays role to encapsulate the guest molecules.,22PEG修饰的平行对比Without PEG tails,23,It is straightforward to use simulation to implement the new ideas to improve the efficiency of dendrimer for drug delivery (optimal loading and slow releasing),药物传递体系设计思路和实现,23It is straightforward to use,24,Computational simulation and rational design of dendrimer for drug delivery,We successfully sample the structure of dendrimer with Monte Carlo program (CCBTX) and use molecule dynamics to illustrate the interaction between the dendrimer and guest molecules in the solvent.,The guest molecules fill into the core of the dendrimer first, then into the surface region. The radius gyration decreases as guest molecules filled in. This agrees with the radius gyration measured by SAXS.,The PEG tail on the surface not only increases hydrophilic and biocompatibility of the dendrimer, but also plays role in hosting the guest molecules.,It is necessary to use computational simulation to study pH, ion strength, temperature, and solvent effects (affecting both structure and functions of the host dendrimer molecule).,总结,24Computational simulation and,25,Thank you all for the attention!,25Thank you all for the attent,