ABSTRACT

Two distinct pathways for cell death exist. Compared 10 necrotic death. physiological or apoptoticcell death is an active suicidal process that consists of a cascade of well-regulated synthetic events, Participation of specific genes in apoptosis. and ils possible molecular regulation. are considered in order to investigate the mechanism ofccii death induced by some cancer chemotherapeutic agems.

Polypropylene (PP)/maleic anhydride grafted poly(styrene-b-ethylene-co-butylene-b-styrene) triblock copolymer (SEBS-g-MA)/halloysite nanotube (HNT) ternary nanocomposites were prepared by two methods: onestep simultaneous melt mixing (SM) of all components; and masterbatch-based melt mixing (MB) involving revolution/rotation-type high shear mixing of a concentrated solution of HNT and SEBS-g-MA, followed by melt blending with PP. Organically modified HNTs (Org-HNTs) with cetyltrimethyl ammonium bromide were prepared via a special cryoscopic expansion/modification technique (C-XP/M). The morphological structures and mechanical properties of the composites, as well as the amount of reinforcer/toughener-compatibilizer (HNT/SEBS-g-MA) at a ratio of 1/3, were discussed as a function of SM and MB techniques. Morphological studies showed that the SM technique revealed microcomposite structures with large aggregates of Org-HNTs in the matrix. In contrast, the MB technique, with the help of elastomeric phase encapsulation, resulted in the best HNT dispersion in the PP matrix, leading to improved mechanical properties. In particular, the PP-based ternary nanocomposite with 3 wt % Org-HNT and 9 wt % SEBS-g-MA prepared by the MB method exhibited 200% higher impact strength compared with PP, attributed to well dispersed, encapsulated, and compatibilized HNTs in the matrix, which created a good balance between stiffness and toughness. POLYM. COMPOS., 00:000-000,

Summary: In situ synthesis of poly(methyl methacrylate) (PMMA) nanocomposites by photopolymerization using organophilic montmorillonite (MMT) as the layered clay is reported. MMT clay was ion exchanged with N‐phenacyl, N,N‐dimethylanilinium hexafluoro phosphate (PDA) which acts as both suitable intercalant‐ and photo‐initiator. These modified clays were then dispersed in methyl methacrylate (MMA) monomer in different loading degrees to carry out the in situ photopolymerization. Intercalation ability of the photoinitiator and exfoliated nanocomposite structure were evidenced by both X‐ray diffraction (XRD) spectroscopy and transmission electron microscopy (TEM). Thermal properties and morphologies of the resultant nanocomposites were also studied.Schematic representation of clay‐PMMA nanocomposites by photoinitiated radical polymerization.imageSchematic representation of clay‐PMMA nanocomposites by photoinitiated radical polymerization.

Programmed cell death or apoptosis occurs under physiological conditions as a result of physiological effectors. It is a relatively slower process and requires active participation of the cell in the suicidal mechanism. Apoptosis is controlled by precise intrinsic genetic programme and may be induced by almost all those stimuli causing necrosis. The role played by the intensity in determining the death process and the underlying mechanism is imperfectly understood. Morphologically apoptotic cells appear as small condensed body. The chromatin is dense and fragmented, packed into compact membrane-bound bodies together with randomly distributed cell organelles. The plasma membrane loses its characteristic architecture and shows extensive blebbing. It buds off projections so that the whole cell may split into several membrane-bound apoptotic bodies. Significant chemical changes take place in the plasma membrane. This helps in recognition of the apoptotic bodies by phagocytes. At this moment it is unclear if all cells can undergo apoptosis or it is a characteristic of only some tissues which are predisposed to apoptotic death being directly under the control of hormones or growth factors. Experimental studies aimed at comparison of induction of apoptosis in cells of different origin are warranted to elucidate this point. Biochemically a pre-commitment step for induction of death programmation through macromolecular synthesis is essential for most systems. The double-stranded linker DNA between nucleosomes is cleaved at regular inter-nucleosomal sites through the action of a Ca2+, Mg(2+)-sensitive neutral endonuclease. Zinc is a potent inhibitor of the enzyme. Calcium probably plays a key controlling role in activation of the enzyme since prevention of Ca2+ increase prevents endonuclease activation. It is becoming evident that signal transduction through appropriate receptors control the Ca2+ flux in the cells. Most apoptotic cells require synthesis of RNA and proteins. Delay or abrogation of apoptosis by inhibition of macromolecular synthesis is well known. The dying cells show high mRNA levels for several enzymes. Several degradative enzymes become active. Regulatory proteins maintain control over the apoptotic cascade. At the molecular level, search has been initiated for the mammalian equivalents of the cell death (ced) gene. Activation of several specific genes is indicated. Specific expression of cell death-associated gene products (e.g. TRPM-2/SGP-2) has been reported in several unrelated apoptotic cell systems. Sequential induction of c-fos, c-myc and 70 kDa heat shock protein is reported. Studies demonstrate that certain genes must remain in a transcriptionally active demethylated state during programmed cell death. Recent evidences clearly indicate that apoptosis may be positively or negatively modulated by certain genes.(ABSTRACT TRUNCATED AT 400 WORDS)

Polypropylene (PP)/maleic anhydride grafted polystyrene-b-poly (ethylene/butylene)-b-polystyrene (SEBS-g-MA)/organophilic halloysite nanotube clay ternary nanocomposites were produced by using HNT/SEBS-g-MA masterbatches at different nanotube loadings (1 wt%, 3 wt%, and 5 wt%). The masterbatches with different ratios of HNT/SEBS-g-MA (1/1, 1/2, and 1/3) were prepared via a revolution/rotation type mixing-assisted masterbatch process. All nanocomposites showed higher storage moduli and damping at low temperatures as compared to neat polypropylene. The nanocomposites having HNT/SEBS-g-MA ratio of 1/3 were found to act as effective dampers with their relatively higher damping values. In terms of short-term creep performance, 1 wt% and 3 wt% organophilic halloysite nanotube loaded systems with low amount of SEBS-g-MA (<9 wt%) enhanced dimensional stability of polypropylene with their lower creep strain and permanent deformation values. More specifically, among the nanocomposites, 3 wt% organophilic halloysite nanotube loaded nanocomposite with HNT/SEBS-g-MA ratio of 1/3 and co-continuous like morphology not only exhibited an effective damping over a wide range of temperature (from −70℃ to 50℃) but also showed relatively higher storage moduli at low temperature region together with lower permanent creep deformation as compared to neat polypropylene. As a result, the HNT/SEBS-g-MA masterbatch in 1/3 ratio was found to be the most suitable in polypropylene blend nanocomposites. It may be advantageous for polypropylene nanocomposite based applications where high damping/toughness at low temperature conditions and high dimensional stability under load are desired.

A series of polypropylene (PP)/poly(ethylene- co-vinyl acetate) (EVA) blend nanocomposites was produced by utilizing different amounts of organophilic halloysite nanotube (Org-HNT) and EVA-based compatibilizers/tougheners. They were prepared by using either only EVA elastomer or using EVA with the compatibilizers which are maleic anhydride grafted EVA (EVA-g-MA) and poly(ethylene-vinyl acetate-carbon monoxide) (EVACO) as well as maleic anhydride grafted PP (PP-g-MA). The morphology–mechanical property relationship was investigated as a function of nature of the compatibilizer and the amount of aluminosilicate nanotube/compatibilizer. The composites prepared without using the EVA-based compatibilizers in all nanotube loading degrees (1%, 3%, 5%) exhibited nanotube aggregates as evidenced by scanning electron microscope analyses. On the other hand, EVA-g-MA and EVACO provided a good dispersion of HNTs at both PP–EVA interface and in the PP matrix. The use of compatibilizers together with 3% Org-HNT resulted in PP/EVA blend nanocomposites with higher tensile modulus and toughness when compared to PP/EVA blend. Particularly, EVACO compatibilizer having highly polar carbonyl group at its backbone provided the highest toughness and Young’s modulus as well as impact resistance for the 3% Org-HNT loaded nanocomposite while retaining the yield strength as an indication of a good balance between stiffness/toughness.

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