Properties of the flame retardant urea formaldehyde (UF) board made from saw dust fibers were investigated. Flame retardant chemicals that were evaluated include boric acid (BA) and borax (BX) which were incorporated with saw dust fibers to manufacture experimental panels. Three concentration levels, (0.5, 1, and 5%) of fire retardants and 10% urea formaldehyde resin based on oven dry fiber weight were used to manufacture experimental panels. Physical and mechanical properties including water absorption, modulus of rupture (MOR), and modulus of elasticity (MOE) were determined. The results showed that water absorption and bending strength decreased as the flame retardant increased. The highest concentration of (BA + BX) enhanced the fire retardant more than the lower ones. Scanning electron microscope and FTIR of composite panels were studied.
A novel class of 6-indolypyridine-3-carbonitrilile derivatives were synthesized and evaluated for antiproliferative activities to establish structure-activity relationship. The synthesis was carried out through one-pot multicomponent reaction of 3-acetylindole, aromatic aldehydes, ethyl cyanoacetate, and ammonium acetate in the presence of piperidine as a catalyst, using a microwave irradiation method or a traditional thermal method. This was followed by chlorination for compounds 13a–e and subsequent nucleophilic substitution of the chlorine group by ethylenediamine at C2 position of the pyridine ring. The antiproliferative activity of these new nicotinonitriles was evaluated against human ovarian adenocarcinoma (SK-OV-3), breast adenocarcinoma (MCF-7), and cervix adenocarcinoma (HeLa) cells. Among all compounds, 2-((2-aminoethyl)amino)-4-aryl-6-indolylnicotinonitriles series (15a, 15b, 15d, and 15e) exhibited higher antiproliferative activity cells with IC50 values of 4.1–13.4 μM.
The pulp black liquor waste (PBL), a byproduct from paper-making, is applied as a cement admixture in two types of cement, namely Ordinary Portland cement (OPC) and Portland limestone cement (LPC). The results showed that the water of consistency of cement pastes premixed with PBL was gradually increased with the concentration of PBL while the setting times (initial and final) were decreased. So, it can be used as an accelerator. The compressive strength increased slightly during the early ages of hydration but sharply during the later ages, particularly with those premixed with PBL. The combined water content and bulk density displayed the same trend as the compressive strength, whilst the apparent porosity decreased at all curing times. The IR spectra of cement pastes showed that the intensities of the different peaks of cement pastes with PBL are higher than those of the pure samples. The SEM images proved that the incorporation of PBL with cement did not affect the chemical composition of OPC or LPC hydrates, but it only affected the physical state, shape, size, morphology and crystallinity of the formed hydrates. The 2 wt. % of PBL is the optimum concentration.
Targeting cancer cells using integrin receptor is one of the promising targeting strategies in drug delivery. In this study, we conjugated an integrin-binding ligand (GGRGDSK) peptide to chitosan oligosaccharide (COS) using sulfo-SMCC as a bifunctional linker to afford COS-SMCC-GGRGDSK. The conjugated polymer was characterized by FT-IR, (1)H NMR, (13)C NMR, and SEM. COS-SMCC-GGRGDSK did not show cytotoxicity up to a concentration of 1mg/mL in the human leukemia cell line (CCRF-CEM). The conjugate was evaluated for its ability to enhance the cellular uptake of a cell-impermeable cargo (e.g., F'-G(pY)EEI phosphopeptide) in CCRF-CEM, and human ovarian carcinoma (SK-OV-3) cancer cell lines. Additionally, RGD modified and unmodified COS polymers were used to prepare nanoparticles by ionic gelation and showed particle size ranging from 187 to 338nm, and zeta potential of 12.2-18.3mV using dynamic light scattering. The efficiency of COS-NPs and COS-SMCC-RGDSK NPs was assayed for translocation of two synthetic cytotoxic agents ((2-(2-aminoethylamino)-4-(4-chlorophenyl)-6-(1H-indol-3-yl) nicotinonitrile (ACIN), and 2-(2-aminoethylamino)-6-(1H-indol-3-yl)-4-(4-methoxyphenyl)-nicotinonitrile (AMIN)) into CCRF-CEM and human prostate (DU-145) cancer cell lines. The results showed a dramatic reduction in the cell viability on their treatment with RGD targeted COS NPs in comparison to paclitaxel (PTX), free drug, and drug-loaded COS NPs.
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