This paper presents a study on the synthesis and characterization of hydroxyapatite that can be used to produce dental implants or serves as a replacement for other body hard tissues. The bioceramic material (hydroxyapatite) was derived from bovine bone samples after they were de-fatted and processed to produce particles measuring less than 250 μm. Processed bone powders were calcinated at 750℃ to obtain calcium phosphate compound (hydroxyapatite). This indicated complete elimination of the organic phase of the bone. The synthesized hydroxyapatite was physicochemically characterized using Fourier transform infrared spectroscopy (FTIR), an optical microscope and scanning electron microscopy (SEM). Hydroxyapatite powder was sintered into a block and then characterized mechanically by measuring its hardness using a Rockwell hardness testing machine. The hydrophilicity and hydrophobicity of the sintered blocked specimens were studied. The average wettability of the substrate, which was a characteristic of the contact angle, was found to be approximately 31.73 degrees. This contact angle value is a measure of the material hydrophilicity. The biostability/corrosive resistance of the sintered samples was simulated in vitro in phosphate buffered saline solution (pH 7.4) by incubating in an optical incubator shaker (set at 60 revolutions per minute) to mimic physiological conditions. The results showed that hydroxyapatite can be extracted economically from a natural source such as bovine bone and can be employed as a restorative biomaterial for dental implants and hard tissue replacement.

This paper presents in vitro studies of the sustained release of Annona muricata leaf extracts (AME) from hybrid electrospun fibers for breast cancer treatment.Electrospun hybrid scaffolds were fabricated from crude AME extracts, poly(lacticco-glycolic acid)/gelatin (PLGA/Ge) and pluronic F127. The physicochemical properties of the AME extract and scaffolds were studied. The antiproliferative effects of the scaffolds were also assessed on breast cancer (MCF-7 and MDA-MB-231) and non-tumorigenic breast (MCF10A) cell lines. Scanning electron microscope micrographs revealed a random network of micro-and submicron fibers. In vitro drug release profiles, governed by quasi-Fickian diffusion at pH 7.

This article presents silica nanoparticles for the sustained release of AMACR antibody-conjugated and free doxorubicin (DOX) for the inhibition of prostate cancer cell growth. Inorganic MCM-41 silica nanoparticles were synthesized, functionalized with phenylboronic acid groups (MCM-B), and capped with dextran (MCM-B-D). The nanoparticles were then characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, zeta potential analysis, nitrogen sorption, X-ray diffraction, and thermogravimetric analysis, before exploring their potential for drug loading and controlled drug release. This was done using a model prostate cancer drug, DOX, and a targeted prostate cancer drug, α-Methyl Acyl-CoA racemase (AMACR) antibody-conjugated DOX, which attaches specifically to AMACR proteins that are overexpressed on the surfaces of prostate cancer cells. The kinetics of sustained drug release over 30 days was then studied using zeroth order, first order, second order, Higuchi, and the Korsmeyer-Peppas models, while the thermodynamics of drug release was elucidated by determining the entropy and enthalpy changes. The flux of the released DOX was also simulated using the COMSOL Multiphysics software package. Generally, the AMACR antibodyconjugated DOX drug-loaded nanoparticles were more effective than the free DOX drug-loaded formulations in inhibiting the growth of prostate cancer cells in vitro over a 96 h period. The implications of the results are then discussed for the development of drug-eluting structures for the localized and targeted treatment of prostate cancer.

This paper presents a recent study on recycling poly-ethylene-tetraphylate (PET), known as plastic waste material in Ghana, to wealth. Composites were produced by heating aggregates together with shredded PET plastic waste material, while bitumen was added to the plastic-coated aggregates. The composites produced were reinforced with 4.5 wt%, 9.0 wt%, 13.6 wt%, and 18.0 wt% PET. Mechanical properties of the fabricated composite samples were studied with a Universal testing machine for optimization. The work demonstrated that shredded PET plastic waste material acts as a strong binding agent for bitumen that can improve on the shelf life of the asphalt. From the results, 13.6 wt% concentration of PET was shown to experience the maximum compressive strength and flexural strength. Besides, water resistance was shown to increase with PET concentrations/weight fraction. From the data characterized 13.6 wt% of PET plastic gives the optimum plastic concentration that enhances the rheological properties of bitumen. The implications of the result are therefore discussed for the use of 13.6 wt% PET in road construction.