ABSTRACT
We present an efficient and effective method for preparing a novel self-assembled nanostructured material with high toughness and impact strength from a blend of di-glycidyl ether of bisphenol-A (DGEBA) and epoxidized poly(styrene-block-butadiene-block-styrene) (eSBS55) tri-block copolymer. The field emission scanning electron microscopy and transmission electron microscope results show the nanostructured morphological characteristics of the blends. This study achieved the highest fracture toughness, with a fracture toughness in the form of critical stress intensity factors (KIC) value of 2.54 MPa m1/2, in epoxy/block copolymer blends compared to previous works in the field. The impact strength also increased by 116% compared to neat epoxy. This is a major advancement in epoxy toughening due to the use of a single secondary phase. The resulting highly tough and impact-resistant material is a promising candidate for coating applications in industries such as flooring, building, aerospace, and automobiles.
ABSTRACT
CuInS2 (CIS) quantum dots (QDs) are known to be ideal fluorophores based on their low toxicity and tunable emission. However, due to low quantum yield (QY) and photostability, the surface is usually passivated by a higher bandgap shell (e.g. ZnS). This always resulted in a blue-shifted emission position which is not usually favourable for biological imaging. To address this problem, we herein report the passivation of green synthesized near infra-red emitting glutathione (GSH) capped CuInS2 QDs using different concentration of sodium alginate (SA) at different temperatures. The as-synthesized QDs are small (~ 3.2 nm), highly crystalline and emitted in the near infra-red region. The optical results showed a 36% increase in photostability and a 2-fold increase in quantum yield at ratio 1:8 (SA: CIS) which is suitable for prolonged biological imaging applications. Transmission electron microscope and X-ray diffraction (XRD) analyses showed that the materials are highly crystalline without any change in shape and size after passivation with the biopolymer. Graphical Abstract.
Subject(s)
Alginates/chemistry , Copper/chemistry , Fluorescent Dyes/chemistry , Fluorescent Dyes/chemical synthesis , Indium/chemistry , Quantum Dots/chemistry , Chemistry Techniques, Synthetic , Glutathione/chemistry , Green Chemistry Technology , TemperatureABSTRACT
The toxicity of heavy metals present in binary semiconductor nanoparticles also known as quantum dots (QDs) has hindered their wide applications hence the advent of non-toxic ternary quantum dots. These new group of quantum dots have been shown to possess some therapeutic action against cancer cell lines but not significant enough to be referred to as an ideal therapeutic agent. In this report, we address this problem by conjugating red emitting CuInS/ZnS QDs to a 5,10,15,20-tetrakis(3-hydroxyphenyl)porphyrin -photosensitizer for improved bioactivities. The glutathione capped CuInS/ZnS QDs were synthesized in an aqueous medium using a kitchen pressure cooker at different Cu: In ratios (1:4 and 1:8) and at varied temperatures (95 °C, 190 °C and 235 °C). Optical properties show that the as-synthesized CuInS/ZnS QDs become red-shifted compared to the core (CuInS) after passivation with emission in the red region while the cytotoxicity study revealed excellent cell viability against normal kidney fibroblasts (BHK21). The highly fluorescent, water-soluble QDs were conjugated to 5,10,15,20-tetrakis(3-hydroxyphenyl)porphyrin (mTHPP) via esterification reactions at room temperature. The resultant water-soluble conjugate was then used for the cytotoxicity, fluorescent imaging and gene expression study against human monocytic leukemia cells (THP-1). Our result showed that the conjugate possessed high cytotoxicity against THP-1 cells with enhanced localized cell uptake compared to the bare QDs. In addition, the gene expression study revealed that the conjugate induced inflammation compared to the QDs as NFKB gene was over-expressed upon cell inflammation while the singlet oxygen (1O2) study showed the conjugate possessed large amount of 1O2, three times than the bare porphyrin. Thus, the as-synthesized conjugate looks promising as a therapeutic agent for cancer therapy.
Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Metal Nanoparticles , Porphyrins , Quantum Dots/adverse effects , Sulfides , Zinc Compounds , Cell Line, Tumor , Humans , Leukemia, Myeloid/genetics , Leukemia, Myeloid/metabolism , Metal Nanoparticles/chemistry , Microscopy, Confocal , Spectrum Analysis , Sulfides/chemistry , Theranostic Nanomedicine , Zinc Compounds/chemistryABSTRACT
We herein report the synthesis of MFe2O4 (Mâ¯=â¯Mn, Mg)/reduced graphene oxide (MFe2O4/RGO) through a simple and novel pressure cooker assisted solvothermal method. The structure and morphology of the as-prepared materials were investigated using X-ray diffraction (XRD), transmission electron microscopic (TEM) and X-ray photoelectron spectroscopy (XPS). The antimicrobial study revealed that the as-synthesized materials displayed good antibacterial effect against E. coli and S. aureus bacteria. In addition, due to the small particle size of MnFe2O4, MnFe2O4/RGO nanocomposite show better antibacterial activity than MgFe2O4/RGO nanocomposite.
