Effect of Surfactant Tail Structure on Phase Behavior of Branched and Linear Alkylbenzene Sulfonate in Water and Oil Ternary Systems

Systematic investigations into the phase behavior of a ternary system of linear alkyl benzene sulfonate (LAS) or branched alkyl benzene sulfonate (BAS) in oil (corn or olive oil) and water were carried out. The study showed that there is a relationship between the surfactants’ chemical structure, aggregation properties, and the formation of micelles. The aggregation properties were dramatically affected by small structural variations of the hydrophobic group at constant carbon number. Micelles formation was found to be correlated with the extent of chain branching by affecting oil-water interfacial tension, where the branched alkyl tail has significantly more ability to form micelles than the linear one. It was found possible to distinguish between LAS and BAS based on their phase behavior

Jordanian Kaolinite with TiO₂ for Improving Solar Light Harvesting Used in Dye Removal

TiO2-Kaolinite nanocomposite photocatalysts were synthesized using the sol-gel method, with titanium isopropoxide/HCl as reactants and Jordanian kaolinite clay as a support material. The samples’ TiO2 content ranged from 10% to 70% (m/m). TiO2-Kaolinite composites were characterized using FTIR, SEM, XRF, and XRD. According to XRD measurements of the nano-composite samples, the intensity of the anatase peaks increased as the TiO2 percentage of the composition increased. As the percentage of TiO2 increased, so did the peaks of Ti-O-Si in FTIR. The extent of photocatalytic degradation of Congo-red dye was used to evaluate the photocatalytic activity of the prepared nanocomposites. After four hours under the sun, the percentage of Congo-red degradation ranged from 27 to 99 percent depending on the TiO2 content of the used nanocomposite. Meanwhile, the concentration drop in the dark did not exceed 10%. Photodegradation outperforms traditional treatment methods in terms of target degradation. Using naturally abundant materials such as clay in conjunction with metal oxides is widely regarded as an effective method of modifying the photoresponse properties of TiO2 particles, thereby improving solar light harvesting for target degradation

Synthesis of Mono-Amino Substituted γ-CD: Host–Guest Complexation and In Vitro Cytotoxicity Investigation

Cyclodextrins (CDs) are cyclic oligosaccharides which can trap hydrophobic molecules and improve their chemical, physical, and biological properties. γ-CD showed the highest aqueous solubility with the largest cavity diameter among other CD types. The current study describes a direct and easy method for nucleophilic mono-aminos to be substituted with γ-CD and tested for their ability to host the guest curcumin (CUR) as a hydrophobic drug model. The mass spectrometry and NMR analyses showed the successful synthesis of three amino-modified γ-CDs: mono-6-amino-6-deoxy-cyclodextrine (γ-CD-NH2), mono-6-deoxy-6-ethanolamine-γ-cyclodextrine (γ-CD-NHCH2CH2OH), and mono-6-deoxy-6-aminoethylamino)-γ-cyclodextrin (γ-CD-NHCH2CH2NH2). These three amino-modified γ-CDs were proven to be able to host CUR as native γ-CDs with formation constants equal to 6.70 ± 1.02, 5.85 ± 0.80, and 8.98 ± 0.90 mM−1, respectively. Moreover, these amino-modified γ-CDs showed no significant toxicity against human dermal fibroblast cells. In conclusion, the current work describes a mono-substitution of amino-modified γ-CDs that can still host guests and showed low toxicity in human dermal fibroblasts cells. Therefore, the amino-modified γ-CDs can be used as a carrier host and be conjugated with a wide range of molecules for different biomedical applications, especially for active loading methods

Aptamers Chemistry: Chemical Modifications and Conjugation Strategies

Soon after they were first described in 1990, aptamers were largely recognized as a new class of biological ligands that can rival antibodies in various analytical, diagnostic, and therapeutic applications. Aptamers are short single-stranded RNA or DNA oligonucleotides capable of folding into complex 3D structures, enabling them to bind to a large variety of targets ranging from small ions to an entire organism. Their high binding specificity and affinity make them comparable to antibodies, but they are superior regarding a longer shelf life, simple production and chemical modification, in addition to low toxicity and immunogenicity. In the past three decades, aptamers have been used in a plethora of therapeutics and drug delivery systems that involve innovative delivery mechanisms and carrying various types of drug cargos. However, the successful translation of aptamer research from bench to bedside has been challenged by several limitations that slow down the realization of promising aptamer applications as therapeutics at the clinical level. The main limitations include the susceptibility to degradation by nucleases, fast renal clearance, low thermal stability, and the limited functional group diversity. The solution to overcome such limitations lies in the chemistry of aptamers. The current review will focus on the recent arts of aptamer chemistry that have been evolved to refine the pharmacological properties of aptamers. Moreover, this review will analyze the advantages and disadvantages of such chemical modifications and how they impact the pharmacological properties of aptamers. Finally, this review will summarize the conjugation strategies of aptamers to nanocarriers for developing targeted drug delivery systems

Recent advances in using liposomes for delivery of nucleic acid-based therapeutics

Nucleic acid therapeutics are rapidly expanding because of recent advancements in production and purification. This class of therapeutics may change the field of disease treatment and personalized medicine since it can cure diseases. However, drug delivery systems are crucial for these therapeutics to fulfill their potential. Liposomes have long been considered ideal platforms for systemic drugs delivery. Considering the development in cancer therapeutics, this work emphases on the current advancements in liposomes’ Nano-formulations, functionalization, and design and how it has been applied to nucleic acid therapeutics. Accordingly, this review covers the literature that deals with liposomes in nucleic acid therapy

Impact of nanoscale magnetite and zero valent iron on the batch-wise anaerobic co-digestion of food waste and waste-activated sludge

As a potential approach for enhanced energy generation fromanaerobic digestion, iron-based conductive nanoparticles have been proposed to enhance the methane production yield and rate. In this study, the impact of two different types of iron nanoparticles, namely the nano-zero-valent-iron particles (NZVIs) and magnetite (Fe3O4) nanoparticles (NPs) was investigated, using batch test under mesophilic conditions (35 °C). Magnetite NPs have been applied in doses of 25, 50 and 80 mg/L, corresponding to 13.1, 26.2 and 41.9 mg magnetite NPs/gTS of substrate, respectively. The results reveal that supplementing anaerobic batches with magnetite NPs at a dose of 25 mg/L induces an insignificant effect on hydrolysis and methane production. However, incubation with 50 and 80 mg/L magnetite NPs have instigated comparable positive impact with hydrolysis percentages reaching approximately 95% compared to 63% attained in control batches, in addition to a 50% enhancement in methane production yield. A biodegradability percentage of 94% was achieved with magnetite NP doses of 50 and 80 mg/L, compared to only 62.7% obtained with control incubation. NZVIs were applied in doses of 20, 40 and 60 mg/L, corresponding to 10.8, 21.5 and 32.2 mg NZVIs/gTS of substrate, respectively. The results have shown that supplementing anaerobic batches with NZVIs revealed insignificant impact, most probably due to the agglomeration of NZVI particles and consequently the reduction in available surface area, making the applied doses insufficient for measurable effect.Sanitary Engineerin

FAC scan histogram analysis of the Ep1 aptamer binding to selected cell lines NIH/3T3 and KATO III.

<p>The binding of Ep1 aptamer compared to unstained cells and nonspecific ssDNA sequence.</p