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Biomedical subjects

Zhiyun Chen

Publications and source records attributed to Zhiyun Chen.

5 recordsLinked to original sources

Regiochemical functionalization of a nanoscale cage-like structure: robust core-shell nanostructures crafted as vessels for selective uptake and release of small and large guests.

As synthetic methods evolve toward the preparation of increasingly complex nanostructured materials inspired from biological nano-objects, the ability to tailor the three-dimensional architecture and the placement of functional groups at well-defined positions within those frameworks is advancing. In this report, we demonstrate the ability to functionalize selectively internal and external sites (regiochemically) within polymer nanocages, to advance their development as synthetic analogs of viral capsids. Nanocages, possessing carbonyl groups on their internal surfaces and acrylic acid residues throughout their structure were prepared and functionalized, through either Schiff-base chemistry, to attach covalently phosphatidylethanolamine-based lipids within the nanocage, or carbodiimide-mediated coupling, to attach covalently the lipids throughout the shell. The resulting nanostructures were altered by the insertion of molecules within and on the structure, including, for the Schiff base functionalized nanostructure, an enhanced response to pH and increased uptake of hydrophobic guests. Additionally, the use of phosphatidylethanolamine lipids labeled with 7-nitrobenz-2-oxa-1,3-diazole (NBD) allowed for determination of the environmental polarities of the lipid domains within the lipid-nanocage constructs.

Acrylates↗

Disk morphology and disk-to-cylinder tunability of poly(acrylic acid)-b-poly(methyl acrylate)-b-polystyrene triblock copolymer solution-state assemblies.

Disk and cylindrical micellar assemblies were formed through self-organization of poly(acrylic acid)-b-poly(methyl acrylate)-b-polystyrene (PAA-b-PMA-b-PS) amphiphilic triblock copolymers with organic diamines as counterions in water/ tetrahydrofuran (THF) solvent mixtures. The system was investigated by means of transmission electron microscopy and cryogenic transmission electron microscopy. It was found that the assembled-state morphologies could be modified by alteration of the type and concentration of cationic diamine counterion undergoing interaction with the negatively charged, polyelectrolyte PAA corona block, the relative amount of water in the water/THF mixture, and the hydrophobic block chain length. Multivalency of the organic amine counterion was critical for disk formation. It was further demonstrated that a single block copolymer underwent disc-to-cylindrical micellar transitions reversibly with variation in the relative water/THF ratio. The ability to form disks beginning from either THF-rich or water-rich solutions indicated that the disk morphology was thermodynamically stable and that THF was important in keeping the micellar structure from becoming kinetically frozen. The nanoassemblies were produced having low size dispersities and were stable for at least one month. Intermediate structures between disks and cylinders were also observed, indicating two distinct kinetic pathways between the two micelle structures.

Journal Article↗

Unique toroidal morphology from composition and sequence control of triblock copolymers.

The mechanism by which the unique toroidal supramolecular assemblies were formed for triblock copolymers of acrylic acid (AA), methyl acrylate (MA), and styrene (S), PAA99-b-PMA73-b-PS66, was probed in this study by investigating the influences of the block copolymer compositions and sequences. Two triblock copolymers, PAA99-b-PMA73-b-PS66 and PAA99-b-PS76-b-PMA62, and two diblock copolymers, PAA99-b-PMA155 and PAA99-b-PS133, were studied under experimental solution-state conditions that involved a range of solvent/nonsolvent (tetrahydrofuran/water) compositions, each in the presence of 2,2'-(ethylenedioxy)bis(ethylamine). The resulting morphologies were determined by transmission electron microscopy. The failures to afford toroidal supramolecular assemblies from both diblock copolymers having comparable lengths of the total hydrophobic chain segment, either entirely PMA or entirely PS, and from the triblock copolymer having a reversed connection sequence for the hydrophobic (PMA and PS) segments demonstrate the unique self-assembly behaviors of triblock copolymers and the importance of the block copolymer sequence.

Acrylic Resins↗

Toroidal triblock copolymer assemblies.

A stable phase of toroidal, or ringlike, supramolecular assemblies was formed by combining dilute solution characteristics critical for both bundling of like-charged biopolymers and block copolymer micelle formation. The key to toroid versus classic cylinder micelle formation is the interaction of the negatively charged hydrophilic block of an amphiphilic triblock copolymer with a positively charged divalent organic counterion. This produces a self-attraction of cylindrical micelles that leads to toroid formation, a mechanism akin to the toroidal bundling of semiflexible charged biopolymers such as DNA. The toroids can be kinetically trapped or chemically cross-linked. Insight into the mechanism of toroid formation can be gained by observation of intermediate structures kinetically trapped during film casting.

Acrylates↗

Enhancement of radiation-induced apoptosis by preirradiation with low-dose X-rays in human leukemia MOLT-4 cells.

The effects of low-dose preirradiation on the process of radiation-induced cell death were investigated in human leukemic MOLT-4 cells. By 0.2 Gy of X-rays given 12 h prior to a challenge dose of 5 Gy, the process of apoptosis was accelerated. The acceleration was associated with a certain increase in caspase 3 activity, a disruption of the mitochondrial transmembrane potential, and an accumulation of p53 proteins. This finding is in contrast to the radiation adaptive responses in which a small dose of preirradiation would induce certain radiation resistance and decrease the cell death after irradiation with higher doses.

Adaptation, Physiological↗