Stability, biofunctional, and antimicrobial characteristics of cannabidiol isolate for the design of topical formulations.

Cannabidiol (CBD) is a high-value natural compound of Cannabis Sativa plant. It is a non-psychotropic phytocannabinoid, attracting significant attention as a multifunctional active ingredient for topical applications. Although it is demonstrated that CBD can be used for specific dermatological ailments, reliable data on functionalities are limited. The present study aimed to investigate the structural stability, biofunctionality, and antimicrobial characteristics of CBD isolate to assist in the design of various topical formulations. The stability of CBD in solid and solubilized states was assessed to establish storage and formulation conditions. The performance of CBD solubilized in organic and aqueous media was evaluated for free radical scavenging, tyrosinase, and collagenase enzyme inhibition, which showed good prospects for the ingredient. The antimicrobial activity of solubilized CBD was evaluated against Gram-negative (E. coli, P. aeruginosa), Gram-positive bacterial strains (S. aureus, S. epidermidis, C. acnes), and fungal strains (C. albicans, M. furfur) using agar well diffusion and broth microdilution methods. Due to the presence of surfactants in CBD aqueous solution, it displayed a lack of antimicrobial activity against all the tested microorganisms. CBD solubilized in an organic medium showed no activity against Gram-negative bacterial strains but higher activity against tested Gram-positive bacterial and fungal strains.

Application of Layered Double Hydroxides as a Slow-Release Phosphate Source: A Comparison of Hydroponic and Soil Systems.

The utilization of slow-release fertilizer materials capable of responding to their environment and releasing nutrient ions efficiently over a prolonged period is an emerging research area in agricultural materials sciences. In this study, two-dimensional layered materials were prepared to release phosphor ions (P) slowly into the soil as well as in the hydroponic system. Various P-intercalated layered double hydroxides (LDHs) (Mg/Al, Zn/Al, and Mg-Zn/Al-LDHs) with a molar ratio of 2:1 were synthesized using an ion-exchange method from corresponding LDHs containing NO3 - ions within the layers. Sodium alginate (SA) was used to encapsulate P-intercalated Mg/Al-LDH to produce bionanocomposite beads (LB) to check the effect of the biopolymer matrix on the release characteristics. The prepared materials were characterized by XRD and FTIR to confirm the incorporation of P in LDHs. TGA, SEM, and elemental analysis were also performed to study the thermal decomposition pattern, surface morphology, and chemical composition of synthesized materials. The P-release experiments were conducted in a soil solution. The performance of the prepared materials was investigated in soil as well as in a hydroponic system for tomato plants under a controlled atmosphere of humidity, temperature, and light. The fertilization ability of the prepared materials was compared with that of a soluble P source (KH2PO4), commercial hydroponic fertilizer (Nutrifeed), and a commercial soil slow-release fertilizer (Wonder plant starter). The prepared materials demonstrated a slow release of P in the soil solution. P-intercalated LDHs were not very effective under hydroponic conditions; however, the LDHs were more effective in the soil system in terms of dry matter production and P content in dry matter. Furthermore, LDHs were able to increase the soil pH value over time.

A Comparison of Nitrate Release from Zn/Al-, Mg/Al-, and Mg-Zn/Al Layered Double Hydroxides and Composite Beads: Utilization as Slow-Release Fertilizers.

Nitrate-loaded Zn/Al, Mg/Al, and Mg-Zn/Al layered double hydroxides (LDHs) were synthesized using the coprecipitation method. The slow-release properties of LDHs were measured in powder form at various pH conditions. Sodium alginate was used to encapsulate Mg/Al LDH to produce composite beads (LB) to further slow down the release of nitrate ions. The prepared LDH samples and LB were characterized by X-ray diffraction, attenuated total reflectance Fourier transform infrared spectroscopy, thermogravimetric analysis, and inductively coupled plasma optical emission spectroscopy. The surface morphologies of LDHs and LB were obtained from scanning electron microscopy analysis. The slow-release properties of the materials were evaluated using a kinetic study of nitrate release in tap water, soil solution, as well as plant growth experiments using coriander (Coriandrum sativum). The nitrate release ability of LDHs and LB was compared with a soluble nitrate source. The plant growth experiments showed that all three LDHs were able to supply an adequate amount of nitrate to the plant similar to the soluble fertilizer while maintaining the availability of nitrate over extended periods. The ability of LDHs to increase soil pH was also demonstrated.

Development of hemp seed oil nanoemulsions loaded with ascorbyl palmitate: Effect of operational parameters, emulsifiers, and wall materials.

The perceived health properties of hemp seed oil, as one of the few plant-basedsources of omega-3 and omega-6 fatty acids with an ideal ratio of 1:3, suggest its incorporation in food-grade emulsions to improve its water solubility and oxidative stability. The current research's main aim was nanoemulsification of hemp seed oil using the oil-in-water emulsification method followed by ultrasonication. The entrapment efficiency of the nanoemulsions for antioxidant ascorbyl palmitate and its impact on oxidative stability of the oil was also evaluated. Gum arabic: maltodextrin in 75:25 ratio could result in nanoemulsion with entrapment efficiency of 97.10 % for ascorbyl palmitate and radical scavenging activity of oil-soluble bioactives of 92.13 %. Moreover, incorporation of ascorbyl palmitate could effectively retard the oxidation, specifically in nanoemulsions containing gum Arabic. The optimum formulation of nanoemulsion having an average droplet size of 293 nm can be applied as an ideal vegetarian source of omega-3 fatty acids.

Layered Double Hydroxides for Sustainable Agriculture and Environment: An Overview.

Agricultural practices in modern society have a detrimental impact on the health of the ecosystem, environment, and consumers. The significantly high usage rate of chemicals causes serious harm, and the sector demands the development of innovative materials that can foster improved food production and lessen ecological impacts. The majority of layered double hydroxides (LDH) are synthetic. At the same time, some of them occur in the form of natural minerals (hydrotalcite), which have recently emerged as favorable materials and provided advanced and ingenious frontiers in various fields of agriculture through practical application possibilities that can replace conventional agricultural systems. LDH can exchange anions intercalated between the layers in the interlayer structure, and there is evidence that atmospheric carbon dioxide and moisture can completely break down LDH over time. Due to certain unique properties such as tunable structure, specific intercalation chemistry, pH-dependent stability, as well as retention of the guest molecules within interlayers and their subsequent controlled release, LDHs are increasingly investigated as materials to enhance yield, quality of crops, and soil in recent times. This review aims to present the current research progress in the design and development of LDH-based materials as nanoscale agrochemicals to illustrate its relevance in making agro-practices more sustainable and efficient. Specific emphasis is given to the functionality of these materials as effective materials for the slow release of fertilizers and plant growth factors as well as adsorption of toxic agrochemical residues and contaminants. Relevant research efforts have been briefly reviewed, and the potential of LDH as new generation green materials to provide solutions to agricultural problems for improving food productivity and security has been summarized.

Chitosan molecular weights affect anthracnose incidence and elicitation of defence-related enzymes in avocado (Persea americana) cultivar 'Fuerte'.

Anthracnose decay is one of the major causes of postharvest losses of avocados (Persea americana), during marketing. Currently, Prochloraz® fungicide is used to control anthracnose at postharvest stage which poses threat to consumer safety. Therefore, this study evaluated the effects of high and low molecular weight chitosan on the control of avocado anthracnose and fruit defence mechanism. In curative inoculation, avocados '(Fuerte') were inoculated via the wounds with C. gloeosporioides spore suspension (20 µL, 1 × 106 spores mL-1). Thereafter coated with different concentrations (0.5%, 1% and 1.5%) of low (LMWC) and high molecular weight (HMWC) chitosan and fruits were held at 25 °C for 5 days. The % anthracnose incidence in avocado fruits was recorded on day 5. During preventative inoculation, wounded fruits were dipped in different concentrations of LMWC or HMWC solutions, and subsequently inoculated with C. gloeosporioides suspension. Preventatively inoculated fruits were stored for 28 days at 6.5 °C, 85% RH and thereafter for 5 days at 25 °C and 75% RH to simulated market shelf condition. The % anthracnose incidence was recorded on day 5. Fruit treated with Prochloraz® and water were included as controls for both curative and preventative infected fruits. Promising chitosan coatings with the lowest anthracnose incidence and the controls were investigated for skin epicatechin content, defence-related genes; phenylalanine ammonia lyase (PAL), lipoxygenase (LOX), fatty acid elongase (avael) and desaturase (avfad 12-3), chalcone synthase (CHS) and flavonol synthase (FLS) using RT- qPCR method. The zeta potential of selected chitosan coatings was done following standard procedures. Percentage of anthracnose incidence were lowest in 1.5% LMWC (18%, 3 mm) compared to Prochloraz® (23%, 5 mm) and the untreated fruit (90%, 24 mm). The 1.5% LMWC had the highest up-regulation of PAL, avfael, avfad 12-3, CHS, FLS genes and down-regulation of LOX gene with concomitant increase in epicatechin content (340 mg kg-1) relative to other chitosan treatments, untreated and Prochloraz® treated fruits. The superior positive zeta potential of LMWC 1.5% coating corroborates its effectiveness in controlling avocado anthracnose than HMWC 1.5%. It is possible that the interaction between the positively charged chitosan amino group (-NH3+) and the negatively charged microbial cell membrane is responsible for the enhanced antifungal activity. In late season naturally infected fruits dipped in 1.5% LMWC, anthracnose incidence dropped to 28% while Prochloraz® treated fruits showed anthracnose incidence of 82% on day 8 at the market shelf. LMWC 1.5% can replace the currently used Prochloraz®.

Cannabidiol-Mediated Green Synthesis, Characterization, and Cytotoxicity of Metal Nanoparticles in Human Keratinocyte Cells.

This study investigated a unique one-pot microwave-assisted green synthesis method of gold (Au) and silver (Ag) nanoparticles (NPs) using cannabidiol (CBD) as a capping and reducing agent. Furthermore, Au and Ag NPs were also chemically synthesized using poly(vinyl pyrrolidone), which functioned as reference materials when comparing the size, shape, and cytotoxicity of NPs. Synthesis parameters such as reaction time, temperature, and precursor molar ratio were optimized to control the size and shape of the biosynthesized NPs. Various characterization techniques such as transmission electron microscopy, ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy, and X-ray diffraction were used to confirm the formation and properties of Au and Ag NPs. Both biosynthesized metal NPs were spherical and monodispersed, with average particle sizes of 8.4 nm (Au-CBD) and 4.8 nm (Ag-CBD). This study also explored the potential cytotoxicity of CBD-capped NPs in human keratinocyte cells, which was observed to be of minimal concern. The novel synthesis approach presented in this study is free from harsh chemical reagents; therefore, these NPs can be used in a wide array of applications, including the pharmaceutical and biomedical fields.

Pathogenesis of Keratinocyte Carcinomas and the Therapeutic Potential of Medicinal Plants and Phytochemicals.

Keratinocyte carcinoma (KC) is a form of skin cancer that develops in keratinocytes, which are the predominant cells present in the epidermis layer of the skin. Keratinocyte carcinoma comprises two sub-types, namely basal cell carcinoma (BCC) and squamous cell carcinoma (SCC). This review provides a holistic literature assessment of the origin, diagnosis methods, contributing factors, and current topical treatments of KC. Additionally, it explores the increase in KC cases that occurred globally over the past ten years. One of the principal concepts highlighted in this article is the adverse effects linked to conventional treatment methods of KC and how novel treatment strategies that combine phytochemistry and transdermal drug delivery systems offer an alternative approach for treatment. However, more in vitro and in vivo studies are required to fully assess the efficacy, mechanism of action, and safety profile of these phytochemical based transdermal chemotherapeutics.

Materials Science Challenges in Skin UV Protection: A Review.

UV radiation is one of the critical environmental stress factors for human skin, which can trigger various problems such as pruritus, burning, erythema, premature skin aging and skin cancer. Hence, UV protection has become an indispensable daily routine and the use of topical sunscreen products is rapidly increasing. However, there are emerging concerns over the efficiency and safety of existing chemical and physical UV filters used in consumer products. Furthermore, there is no universally approved method for assessing sun protection efficiency regardless of the immediate end user need to develop safer sunscreen products that afford broad-spectrum photoprotection. It is evident that the current organic and inorganic UV filters have significant unfavorable impacts on human, environmental, and marine safety. Therefore, effective alternative UV filters should be established. This article comprehensively reviews the properties, safety, health and ecological concerns of various UV filters including TiO2 and ZnO nanoparticles as well as the limitations of the testing protocols and guidelines provided by major regulatory bodies. The photoreactivity of UV filters used in sunscreen remains a major challenge, and it is crucial to develop new sunscreen ingredients, which not only protect the consumer, but also the environment.

Layered Double Hydroxide-Based Functional Nanohybrids as Controlled Release Carriers of Pharmaceutically Active Ingredients.

The chemical stability, degradation and penetration ability of pharmaceutically active ingredients in topical formulations are the greatest challenges because of problems with the protection of actives for long times and with delivery. Therefore, the development of unique and efficient substrate material is vital for their protection and controlled drug release. Layered double hydroxides (LDHs) known as hydrotalcite like compounds possess positive charges due to isomorphic substitutions, which are counterbalanced by hydrated exchangeable anions located in the interlayer region. Some of the active ingredient molecules can be intercalated into the inner region of the LDHs through ionic bonding, hydrogen bonding or van der Waals interaction to form nanohybrids, which are more potent for their protection and controlled-release. This account focuses on our recent research efforts and key scientific and technical challenges in the development of LDH based nanohybrids for commercial use in advanced controlled release carriers of active ingredients in topical formulations.

Oxidative Coupling of 1-Naphthols over Noble and Base Metal Catalysts.

Bismuth-promoted platinum catalysts were tested for the oxidative coupling of 2- and 4-substituted 1-naphthols at different temperatures and ambient pressure. The principal final products are the 3,3'-substituted 1,1'-binaphthalenylidene-4,4'-diones and the 4,4'-substituted 2,2'-binaphthalenylidene-1,1'-diones, respectively. Hydrogen peroxide was used as the oxidant. Only naphthols with electron-donating substituents reacted. The corresponding binaphthalenyl diols can be considered as reaction intermediates. Yields of up to 99 % were obtained from 2-methyl-1-naphthol as the starting material within 20 minutes. Probably for steric reasons, the diol is the final product obtained from 2-ethyl-1-naphthol. For 4-methoxy-1-naphthol the outcome is determined by the reaction temperature. At 25 °C the expected 1,1'-dione is the major product, whereas at 60 °C 1'-hydroxy-4'-methoxy-2,2'-binaphthalenyl-1,4-dione is formed; the loss of one methoxy unit and the preservation of the hydroxy group can be explained by the competitive cleavage of one of the two OMe bonds at higher temperature. Unpromoted platinum and a range of other metallic catalysts, including gold and Raney nickel, were also found to be active. The products obtained are brightly colored solids that could be used as dyes. The method described is truly catalytic and environmentally benign. The potential of the technique justifies further research to expand on the applicability of this novel method.

Influence of citric acid on SnO2 nanoparticles synthesized by wet chemical processes.

Tin oxide (SnO2) nanoparticles with size range of 19 to 100 nm were successfully synthesized using wet chemical process (i.e., chemical precipitation and sol-gel processes). The samples were analysed by X-Ray diffraction, Scanning electron microscopy, Energy dispersive X-ray spectroscopy, Raman and FTIR spectroscopy, BET surface area and Thermogravimetric analyses. The results showed that variation of citric acid concentration directly influences the particle size and the BET specific surface area. The XRD analysis revealed that nanoparticles were phase pure and that all materials exhibited a tetragonal rutile structure of SnO2. Characterisation of the materials was carried out using techniques such as scanning electron microscopy, X-ray diffraction, Fourier Transform Infrared spectroscopy, Thermogravimetric and BET analyses.

CoS-carbon nanotube heterostructure: one-step synthesis and optical properties.

This article reports on the synthesis, characterization, and optical properties of a cobalt sulphide (CoS) quantum dot (QD)-decorated multi-walled carbon nanotube (MWCNT) heterostructure. A novel one-pot chemical-solution route has been used for the in situ synthesis of a CoS-decorated MWCNT heterostructure without disturbing the inherent structure of the MWCNTs. The synthesized heterostructure has been extensively characterized by scanning electron microscopy, scanning transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and Fourier transform infrared spectrometry. The UV-absorption and fluorescence spectral properties of pristine MWCNTs are significantly improved after heterostructure formation with CoS-QDs.

A comparison of purification procedures for multi-walled carbon nanotubes produced by chemical vapour deposition.

A comparison of three different purification procedures for multi-walled carbon nanotubes (MWCNTs) produced by chemical vapour deposition (CVD) has been presented. The methods involved gas-phase oxidation by calcination, liquid-phase oxidation by H2O2, hydrothermal treatment and acid refluxing in HCl. Sample purity was documented with the Raman spectroscopy, Transmission electron microscopy (TEM), Scanning electron microscopy (SEM) and thermo gravimetric analysis (TGA). The Raman spectroscopy, SEM and TEM results showed that the liquid phase oxidation-acid refluxing route successfully eliminated most of the impurities without damaging the nanotube structure. TGA analysis showed in increase in density of MWCNTs with better oxidation resistance after purification and the metal content was reduced from 23.8 wt% to 5.4 wt%.

The effect of calcination on multi-walled carbon nanotubes produced by dc-arc discharge.

Multi-walled carbon nanotubes were synthesized by dc-arc discharge in helium atmosphere and the effect of calcination at different temperatures ranging from 300-600 degrees C was studied in detail. The degree of degradation to the structural integrity of the multi-walled carbon nanotubes during the thermal process was studied by Raman spectroscopy, Scanning electron microscopy and High resolution transmission electron microscopy. The thermal behaviour of the as prepared and calcined samples was investigated by thermogravimetric analysis. Calcination in air at 400 degrees C for 2 hours was found to be an efficient and simple method to eliminate carbonaceous impurities from the nanotube bundles with minimal damage to the tube walls and length. The impurities were oxidized at a faster rate when compared to the nanotubes and gave good yield of about 50%. The nanotubes were observed to be damaged at temperature higher than 450 degrees C. The results show that this method is less destructive when compared liquid phase oxidation with 5 M HNO3.

Purification of multi-walled carbon nanotubes.

The discovery of carbon nanotubes (CNTs) has stimulated intensive research to characterize their structure and to determine their physical properties, both by direct measurement and through predictive methods. Many of the fundamental and remarkable properties of CNTs are now well-known, and their exploitation in a wide range of applications forms a large part of research currently in progress. However, the absence of a reliable, large-volume production capacity, simple and efficient purification methods, the high cost of carbon nanotubes and the fact that there is little selectivity in controlling the properties of the product are factors that have principally inhibited the commercialization of CNT technologies. Ever since CNTs were detected, considerable efforts have been directed at their synthesis, characterization and functionalization. Nevertheless, the CNT sample obtained by different techniques has the disadvantage of containing non-CNT impurities, such as graphitic particles, fullerenes, residual catalyst particles and amorphous carbon, which degrade the intrinsic properties of these materials. If the carbon nanotube is ever to accomplish its promise as an industrial material, large and high-quality aliquots, will be required. A number of purification methods involving elimination processes, such as physical separation, gas-phase and liquid-phase oxidation, in combination with chemical treatments, have been developed for nanotube materials. Though the quantitative determination of purity remains controversial, reported yields are best regarded with an appropriate level of scepticism on the method of assay. This review highlights the past and recent developments in the purification of multi-walled carbon nanotubes.

Purification of laser synthesized SWCNTs by different methods: a comparative study.

A comparison of different purification procedures for single walled carbon nanotubes (SWCNTs) synthesized by laser-vapourization has been presented. The methods involved gas-phase oxidation by calcination, liquid-phase oxidation by H2O2, hydrothermal treatment and acid refluxing in HCI. Sample purity is documented with Raman spectroscopy, Transmission electron microscopy, Scanning electron microscopy and thermogravimetric analysis. Multi-spot analyses were done to check the homogeneity of the purified samples. Different purification processes produced SWCNT material with purity in the range of 48-78%. Raman and TEM results suggested that prolonged calcination results in selective etching of larger diameter nanotubes. SEM and TGA analyses showed increase in density of SWCNTs with better oxidation resistance after purification.

Purification of single-walled carbon nanotubes.

The discovery of carbon nanotubes (CNTs) created much excitement and stimulated extensive research into the properties of nanometer-scale cylindrical networks. From then on, various methods for the synthesis and characterization of aligned CNTs-both single-walled (SWCNTs) and multi-walled (MWCNTs) by different methods have been hotly pursued. Unfortunately, most methods currently in use produce raw multi component solid products, only a small fraction of which contains carbon nanotubes. The balance of the material is composed of residual catalyst particles (some of which are encased in concentric graphitic shells), fullerenes, other graphitic materials and amorphous carbon. These impurities cause a serious impediment for their detailed characterization and applications. If the carbon nanotube is ever to fulfill its promise as an engineering material, large, high quality aliquots will be required. A number of purification methods involving elimination processes such as physical separation, gas phase and liquid phase oxidation in combination with chemical treatments have been developed for nanotube materials. Though the quantitative determination of purity remains controversial, reported yields are best regarded with an appropriate level of skepticism on the method of assay. In this article, a review is given on the past and recent advances in purification of SWCNTs.