Different solvents and organic modifiers for the control of crystallographic parameters in nano-crystallite hydroxyapatite for amplification of photocatalytic activity.

In this research, HAp nanocrystals were synthesized using conventional wet chemical precipitation methods using various organic modifiers, including urea, palmitic acid, and naphthalene. Ethanol and isopropyl alcohol (IPA) were used as solvents in this process. Different characterization techniques, namely X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-vis absorption spectroscopy, were employed to ascertain the formation of HAp nanocrystals. Numerous structural parameters, including lattice parameters, unit cell size, volume of the unit cell, specific surface area, degree of crystallinity, dislocation density, macrostrain, and crystallinity index, were assessed using XRD data. The linear straight-line method of Scherrer's equation, Monshi-Scherrer's method, the Williamson-Hall method, the size-strain plot method, the Halder-Wagner method, and Sahadat-Scherrer's model were applied to compute the crystallite size of the synthesized HAp samples. All the synthesized HAp has crystalline structures within the permissible range of 1-150 nm which were estimated from the XRD data using the mentioned models. However, the values for strain (from -3 × 10-4 to 6.4 × 10-3), strain (from -9.599 × 104 to 7 × 1010 N m-2), and energy density (from -11 × 1011 to 2 × 107 J m-3) were also calculated for the synthesized samples. In addition, the optical band gap energy of the synthesized HAp was computed (5.89 to 6.19 eV). The synthesis media have a control on the crystallographic planes, e.g. in the case of the ethanol medium, the (110) plane exhibited significant intensity (which could potentially serve as a driving force for enhancing photocatalytic activity). The use of 100% ethanol HAp yields the most favorable outcome regarding both the degradation percentage (91.79%) and degradation capacity (7%) for the Congo red dye.

Synthesis of different types of nano-hydroxyapatites for efficient photocatalytic degradation of textile dye (Congo red): a crystallographic characterization.

The textile industry, a vital economic force in developing nations, faces significant challenges including the release of undesired dye effluents, posing potential health and environmental risks which need to be minimized with the aid of sustainable materials. This study focuses on the photocatalytic potential of hydroxyapatite together with different dopants like titanium-di-oxide (TiO2) and zinc oxide (ZnO). Here, we synthesized hydroxyapatite (HAp) using different calcium sources (calcium hydroxide, calcium carbonate) and phosphorous sources (phosphoric acid, diammonium hydrogen phosphate) precursors through a wet chemical precipitation technique. Pure and doped HAp were characterized via different technologies, which consist of X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), as well as UV-vis spectroscopy. The effectiveness of the synthesized photocatalyst was evaluated by its interactivity with synthetic azo dyes (Congo red). The photodegradation of Ca(OH)2_HAp, CaCO3_HAp, ZnO-doped HAp as well as TiO2-doped HAp, were obtained as 89%, 91%, 86%, and 91%, respectively. Furthermore, at neutral pH, TiO2-doped HAp shows the highest degradation (86%), whereas ZnO-doped HAp possesses the lowest degradation (73%). Additionally, various XRD models (Monshi-Scherrer's, Williamson-Hall, and Halder-Wagner methods) were employed to study crystallite dimension.

Fabrication and Characterization of a Bioscaffold Using Hydroxyapatite and Unsaturated Polyester Resin.

Outstanding biodegradability and biocompatibility are attributes associated with particular polyester substances that make this group useful in specific biomedical fields. To assess the potential as a biomaterial, a novel composite consisting of hydroxyapatite (HAp) and unsaturated polyester resin (UPR) was developed in this work. Using a hand-lay-up technique, various percentages (50, 40, 30, 20, and 10%) of HAp were reinforced into the UPR matrix to fabricate composite materials out of glass sheets. Prior to processing of the composite samples, hydroxyapatite was chemically synthesized in a wet chemical manner. Using a universal testing machine (UTM), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and thermo-gravimetric analysis (TGA), the fabricated samples were characterized. The crystallographic parameters of synthesized hydroxyapatite (HAp) were also estimated through a range of formulas. The optimal amount for hydroxyapatite was 40% according to the findings of the tensile strength (TS), tensile modulus (TM), percentage of elongation at break (EB), bending strength (BS), and bending modulus (BM). Improvements in TS, TM, BS, and BM for the ideal combination were 39.39, 9.21, 912.05, and 259.96%, in each case, over the controlled one. Thermogravimetric analysis (TGA) has been implemented to determine the degradation temperature of the fabricated composites up to 600 °C.

Amplification of photocatalytic degradation of antibiotics (amoxicillin, ciprofloxacin) by sodium doping in nano-crystallite hydroxyapatite.

In this research, we explain the production of sodium-doped hydroxyapatite (Na_HAp) via wet chemical precipitation, followed by crystal modification. To enhance its photocatalytic activity different % of (0.25, 0.5, 1, and 2) sodium doped into HAp crystal. It has been demonstrated that doping is an effective method for modifying the properties of nanomaterials, such as their optical performance and chemical reactivity. Several instrumental approaches were used to characterize this newly synthesized sodium-doped HAp (Na_HAp), e.g. scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and UV-vis spectrometry were used to analyze the morphology, elemental composition, crystal structure, and optical bandgap, respectively. Under sunlight irradiation, the new Na_HAp photocatalyst was put to use in the process of degrading pharmaceutical pollutants such as antibiotics (amoxicillin and ciprofloxacin). It was found that using a 0.1 g dose of 1% Na_HAp under specified conditions, such as a pH of 7 and 120 minutes of sunlight irradiation, resulted in degradation percentages of 60% and 41.59% for amoxicillin and ciprofloxacin, respectively. Different radical scavengers were utilized to determine the reaction mechanism for the photochemical degradation of antibiotics. Additionally, the ability to be reused and the stability of 1% Na_HAp, a newly developed photocatalyst, were assessed. Therefore, this research adds to our understanding of how to optimize redox capacity for the rapid breakdown of a variety of antibiotics when exposed to sunlight.

Synthesis of pure and doped nano-calcium phosphates using different conventional methods for biomedical applications: a review.

The applications of calcium phosphates (hydroxyapatite, tetracalcium phosphate, tricalcium phosphate (alpha and beta), fluorapatite, di-calcium phosphate anhydrous, and amorphous calcium-phosphate) are increasing day by day. Calcium hydroxyapatite, commonly known as hydroxyapatite (HAp), represents a mineral form of calcium apatite. Owing to its close molecular resemblance to the mineral constituents of bones, teeth, and hard tissues, HAp is often employed in the biomedical domain. In addition, it is extensively employed in various sectors such as the remediation of water, air, and soil pollution. The key advantage of HAp lies in its potential to accommodate a wide variety of anionic and cationic substitutions. Nevertheless, HAp and tricalcium phosphate (TCP) syntheses typically involve the use of chemical precursors containing calcium and phosphorus sources and employ diverse techniques, such as solid-state, wet, and thermal methods or a combination of these processes. Researchers are increasingly favoring natural sources such as bio-waste (eggshells, oyster shells, animal bones, fish scales, etc.) as viable options for synthesizing HAp. Interestingly, the synthesis route significantly influences the morphology, size, and crystalline phase of calcium phosphates. In this review paper, we highlight both dry and wet methods, which include six commonly used synthesis methods (i.e. solid-state, mechano-chemical, wet-chemical precipitation, hydrolysis, sol-gel, and hydrothermal methods) coupled with the variation in source materials and their influence in modifying the structural morphology from a bulky state to nanoscale to explore the applications of multifunctional calcium phosphates in different formats.

Enhancement of antimicrobial properties by metals doping in nano-crystalline hydroxyapatite for efficient biomedical applications.

In this study, we have introduced a method for the synthesis of various metal-doped nano-crystalline hydroxyapatites (HAp) using a standard wet chemical precipitation technique. Both divalent (Ni and Zn) and trivalent (Al and Fe) metals were selected for the doping process. Additional research work was also conducted to assess the antimicrobial efficacy of these doped-HAps against a range of gram-positive and gram-negative microorganisms. All the synthesized metal-doped hydroxyapatite (HAp) exhibited notable antibacterial characteristics against gram-negative bacterial strains, namely Escherichia coli (E. coli) and Salmonella typhi (S. typhi), outperforming the pure HAp. The inhibition zone observed for the metal-doped HAp ranged from 14 to 16 mm. The Fe ion displayed a notable inhibitory zone measuring 16 mm, proving to be the most expansive among all tested ions against both E. coli and S. typhi bacterial strains. The Zn-HAp exhibited a comparable inhibitory zone size of 14 mm against both S. typhi and E. coli. Additional characterization methods, such as X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, and Scanning electron microscopy (SEM), were used to validate the structural properties of the synthesized metal-doped hydroxyapatite (HAp) samples. The biocompatibility assessment of metal-doped hydroxyapatite (HAp) samples was carried out by haemolysis tests, which revealed that all synthesized hydroxyapatite (HAp) samples have the potential to serve as reliable biomaterials.

Synthesis of nano-hydroxyapatite using emulsion, pyrolysis, combustion, and sonochemical methods and biogenic sources: a review.

Hydroxyapatite (HAp) is comparable to materials in bone because its chemical components are similar to those contained in animal bone, and thus, its bioactive and biocompatible properties are similar. There are applications for HAp and relevant calcium phosphate in the medical and industrial sectors, and due to the rising demand for HAp nanoparticles, considerable work has been performed to develop a variety of synthetic pathways that incorporate scientifically and practically novel aspects. Numerous studies have been conducted to examine how changes in reaction parameters will successfully influence crucial HAp features. HAp can also be synthesized from biogenic sources such as HAp-rich fish scales or animal bones as an alternative to chemical precursors. Various preparation techniques produce crystals with varying sizes, but it has been found that nano-sized HAp exhibits a greater number of bioactive properties as compared to micron-sized HAp. Rather than considering conventional methods, this review focuses on alternative approaches such as emulsion, pyrolysis, combustion, and sonochemical methods along with waste bio-sources (biogenic sources) to obtain HAp. We summarize the currently accessible information pertaining to each synthesis process, while also focusing on their benefits and drawbacks.

ß-tricalcium phosphate synthesized in organic medium for controlled release drug delivery application in bio-scaffolds.

ß-tricalcium phosphate (ß-TCP) was synthesized in an organic medium (acetone) to obtain a single-phase product while calcium carbonate (CaCO3) and ortho-phosphoric acid (H3PO4) were the sources of Ca, and P, respectively. The synthesized ß-TCP was characterized by employing a number of sophisticated techniques vis. XRD, FTIR, FESEM, VSM and UV-Vis-NIR spectrometry. On the other hand, cytotoxicity, hemolysis, and antimicrobial activity for Gram-negative as well as Gram-positive (E. coli and S. aureus) bacteria were explored using this synthesized sample in powder format. However, to assess the drug loading and releasing profile, these powdered samples were first compressed into disks followed by sintering at 900 °C. Prior to loading the drug, porosity, density, and water absorbance characteristics of the scaffolds were examined in deionized water. Both loading and releasing profiles of the antibiotic (ciprofloxacin) were looked over at various selected time intervals which were continued up to 28 days. The observed results revealed that 2.87% of ciprofloxacin was loaded while 37% of this loaded drug was released within the selected time frame as set in this study. The scaffold was also immersed in SBF solution maintaining identical interim periods for the bioactivity evaluation. Furthermore, all three types of samples (e.g. drug-loaded, drug-released, and SBF-soaked) were characterized by FESEM and EDX while antimicrobial activity (against E. coli, S. typhi, and S. aureus) and efficacy to prevent hemolysis were also investigated. The drug-loaded scaffold presented a larger inhibition zone than the standard for all three types of microbes. Although powdered ß-TCP was inactive in killing the Gram-negative bacteria, surprisingly the drug-released scaffold showed an inhibition zone.

FTIR spectrum analysis to predict the crystalline and amorphous phases of hydroxyapatite: a comparison of vibrational motion to reflection.

Hydroxyapatites were synthesized from calcium carbonate and ortho-phosphoric acid in amorphous and crystalline phases by varying sintering temperature from 300 to 1100 °C maintaining an increment of 200 °C. The asymmetric and symmetric stretching, and bending vibrations of phosphate and hydroxyl groups were explored in Fourier transformation infrared (FTIR) spectra. Although the FTIR spectra revealed identical peaks in the full range (400-4000 cm-1 wavenumber), the narrow spectra exerted variations by splitting peaks and intensity. The intensities of peaks at 563, 599, 630, 962, 1026, and 1087 cm-1 wavenumbers were intensified gradually with the augmentation of sintering temperature, and the relation between the relative peak intensity and sintering temperature was correlated with the aid of the good linear regression coefficient. Peak separations were also found in the case of 962 and 1087 cm-1 wavenumbers when the sintering temperature was equal to or exceeded 700 °C. The conventional X-ray diffraction (XRD) technique was also employed to explore the crystalline and amorphous phases of synthesized hydroxyapatites.

Exploring the biomedical competency of gamma-radiation aided hydroxyapatite and its composite fabricated with nano-cellulose and chitosan.

The well-known biomaterial Ca-hydroxyapatite (Hap) in its pristine form holds the top ranking position in the field of biomedical research and extensive investigation is continuing across the globe to enhance its competency. Hence, having the intention to introduce superior physiognomies (e.g. cytotoxicity, haemocompatibility, and bioactivity coupled with antimicrobial and antioxidant activity) in Hap, in this research work, we exposed Hap to 200 kGy γ-radiation. As a result, γ-radiated Hap exhibited extreme antimicrobial (more than 98%) and moderate (∼34%) antioxidant properties. On the other hand, cytotoxicity and haemocompatibility of γ-radiated Hap were in good agreement with the ISO 10993-5 and ISO 10993-4 standards respectively. Since, bone and joint infections as well as degenerative disorders e.g. osteoarthritis, osteomyelitis, bone injury, and spinal problems have emerged as serious issues and urge a remedial way out, application of γ-radiated Hap could be a promising solution in this regard.

Synthesis and characterization of nano crystallite plaster of Paris prepared from waste eggshells and exploration of cytotoxicity, hemolysis and antimicrobial properties.

Plaster of Paris, a well-known biomaterial, was synthesized from waste eggshells, which were chosen as an available bio-source of calcium. The produced plaster of Paris was characterized by X-ray diffraction (XRD), Fourier Transform Infrared (FTIR), Raman spectroscopy, UV-Vis spectroscopy, and SEM images along with a few crystallographic parameters such as crystallite size (Scherrer equation and different model equations), lattice parameters, crystallinity index, the volume of the unit cell, microstrain, dislocation density, growth preference, and residual stress from the XRD-sin2 Ψ technique. The biomedical competency of the prepared plaster of Paris was evaluated utilizing the cytotoxicity, hemolysis, and antimicrobial activity of E. coli and S. aureus. The cytotoxicity assessment has revealed that the percentages of viable cells were 93-98% and a highly hemocompatible nature (<5%) was exerted by the sample. The plaster of Paris only revealed antimicrobial properties against Gram-positive bacteria (S. aureus), and no effect was noticed for Gram-negative bacteria (E. coli).

Effect of dye and temperature on the physico-mechanical properties of jute/PP and jute/LLDPE based composites.

Jute fabrics and unidirectional jute fiber reinforced polypropylene (PP) and linear low density polyethylene (LLDPE) based composites were prepared successfully by compression molding technique. The unidirectional jute fiber was treated with Reactive Orange HB® and Deep Blue LW® dye to investigate physico-mechanical properties. The Reactive Orange HB® treated composites showed relatively better mechanical properties than the Deep Blue LW® treated composites. The jute fiber-based composites showed higher mechanical properties than that of jute-based fabrics. The polypropylene-based composites showed better mechanical properties than that of LLDPE. The variations of mechanical properties were also observed. The highest mechanical properties were at -18 °C and lowest at 50 °C. Water absorbent, SEM and FT-IR analysis of the composite was also carried out.