Universiti Putra Malaysia, Faculty of Food Science and Technology, 43400 Serdang, Selangor, Malaysia.
Universiti Putra Malaysia, Faculty of Food Science and Technology, 43400 Serdang, Selangor, Malaysia.
J Control Release. 2018 Mar 28;274:93-101. doi: 10.1016/j.jconrel.2017.10.011. Epub 2017 Oct 12.
Cell impurities are an emerging nucleating molecular barriers having the capability in disordering the metabolic chain reactions of proteolysis, glycolysis and lipolysis. Their massive effects induced by copolymer crystal growth in compaction with metal and mineral transients are extended as well as in damaging DNA and mRNA structure motif and other molecular assembly e.g. histones structure unites. Their polycrystalline packing modes, polydispersity and their tendency to surface and interface adhesion prompted us in structuring scaffold biomaterials enriched with biopeptides, layered by phospho-glycerides ester-forms. The interface tension of the formed map is flexible and dependent to the surface exposure and its collapse modes to the surrounding molecular ligands. Thus, the attempts in increasing surface exposure e.g. the viscoelastic of structured lipopeptides and types of formed network structures interplays an extra- conjugating biomolecules having a least cytotoxicity effects to cells constituents. Disulfides molecules are selected to be the key regulatory element in rejoining both lipidic and proteic moieties by disordering atoms status via chemical ionization using organic catalyst. The insertion of methionine based peptidic chain at the lateral surfaces of scaffold biomaterials enhances the electron-meta-static motions by raising a molecular disordering status at distinct regions of the map e.g. epimerization into a nonpolar side that helps the chemical conjunction of disulfide groups with the esterified phosphoglycerides mono-layers. These effects in turn are accomplished by the formation of meso-sphere nonpolar- vesicles. The oxidation of disulfide group would alter the ordering of initial molecules by raising a newly molecular disorders to the map with high polarity to surface regions. In the same time indicates a continuation in the crystallization growth factor via a low chemical lesions between the impurities and a supersaturation in the intra-atomic distances with maximum cross linking to the deformed ligand with scaffold biomaterials.
细胞杂质是新兴的成核分子障碍,具有扰乱蛋白水解、糖酵解和脂肪分解代谢链反应的能力。它们在与金属和矿物质瞬变的共晶晶体生长中引起的大量影响得到了扩展,同时也破坏了 DNA 和 mRNA 结构基序以及其他分子组装,如组蛋白结构单元。它们的多晶体堆积模式、多分散性以及它们表面和界面附着的趋势促使我们构建富含生物肽的支架生物材料,这些生物肽由磷酸甘油酯酯形式分层。形成的图谱的界面张力是灵活的,取决于表面暴露及其向周围分子配体的坍塌模式。因此,增加表面暴露的尝试,例如结构脂肽的粘弹性和形成的网络结构类型的相互作用,会对细胞成分产生最小细胞毒性的额外共轭生物分子。二硫化物分子被选择为通过使用有机催化剂通过化学离子化扰乱原子状态来重新连接脂质和蛋白质部分的关键调节元件。在支架生物材料的侧表面插入基于蛋氨酸的肽链,通过在图谱的不同区域提高分子无序状态,例如外消旋化为非极性侧,从而增强电子静电力运动,从而有助于二硫化物基团与酯化的磷酸甘油酯单层的化学结合。这些效应反过来又通过形成中间球体非极性囊泡来实现。二硫化物基团的氧化会通过向具有高极性的图谱表面区域引入新的分子无序来改变初始分子的有序性。同时,它还表明在杂质之间存在低化学损伤以及原子内距离的过饱和度,从而与支架生物材料的变形配体进行最大交联,从而继续进行结晶生长因子。