Gene and drug delivery systems need crucial update in the issue of nanocarriers. Layered double hydroxides (LDHs) are known as biocompatible inorganic lamellar nanomaterials with versatile properties. In the present study, Zn/Al-LDH nanoparticle was synthesized and characterized by FTIR, XRD, SEM, TEM and Zeta potential tests and then intercalated with valproate and methyldopa by co-precipitation and ion exchange methods. These nanocarriers were applied as high activity nanolayers-based delivery systems. On the other hand, Zn/Al-LDH þ plasmid/gene (pCEP4/Cdk9) evaluated on C2C12 myoblast cells. Cooperation loading indicated high efficiency of sorting and release of drugs. Additionally, the Real-Time PCR and Western blotting results for plasmid-gene (pCEP4/Cdk9) delivery showed that Zn/Al-LDH nanoparticles can be used as an effective carrier in cellular uptake and release of genes for gene therapy. Easy and cost-effective production of Zn/Al-LDH nanoparticles proposed them as potential alternatives for the traditional routs of drug/gene delivery.

A metal-organic framework/periodic mesoporous silica (MOF-5@SBA-15) hybrid material has been prepared by using SBA-15 as a matrix. The prepared MOF-5@SBA-15 hybrid material was then deposited on a stainless-steel wire to obtain the fiber for the solid-phase microextraction of phenolic compounds. Modifications in the metal-organic framework structure have proven to improve the extraction performance of MOF/SBA-15 hybrid materials, compared to pure MOF-5 and SBA-15. Optimum conditions include an extraction temperature of 75°C, a desorption temperature of 260°C, and a salt concentration of 20% w/v. The dynamic linear range and limit of detection range from 0.1-500 and from 0.01-3.12 ng/mL, respectively. The repeatability for one fiber (n = 3), expressed as relative standard deviation, is between 4.3 and 9.6%. The method offers the advantage of being simple to use, rapid, and low cost, the thermal stability of the fiber, and high relative recovery (compared to conventional methods) represent additional attractive features.

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Highly porous polyaniline/hexagonally ordered silica sorbent was used for fabrication of the inside needle capillary adsorption trap (INCAT) device. Polyaniline/SBA-15 nanocomposite was synthesized via chemical polymerization technique. The fabricated INCAT device was evaluated to the extraction of some polycyclic aromatic hydrocarbons (PAHs) from aqueous sample solutions in combination with gas chromatography (GC)-mass spectrometry (MS). A one at-the-time optimization strategy was applied for optimizing the important extraction parameters such as extraction temperature, extraction time, ionic strength, sampling flow rate, desorption time, and desorption temperature. In optimum conditions (extraction temperature 55 °C, extraction time 20 min, ionic strength 20% (w/v), flow rate 4.5 mL min(-1), desorption temperature 270 °C, desorption time 3 min) the repeatability for one INCAT device (n = 4), expressed as relative standard deviation, was between 4.2 and 10.2% for the tested compounds. The quantitation limits for the studied compounds were between 1 and 5 pg mL(-1). The developed method was successfully applied to spring water sample which was spiked with PAHs with the relative recovery percentages of 87.3-109.1%. The developed method offers the advantage of being simple to use, with shorter analysis times, lower cost of equipment, and thermal stability.

In this research, a carbon nanotube/layered double hydroxide nanocomposite was synthesized by an in situ growth route by electrostatic force. The prepared carbon nanotube/layered double hydroxide nanocomposite was successfully prepared and deposited on a stainless-steel wire for the fabrication of the solid-phase microextraction fiber. The fiber was evaluated for the extraction of phenolic compounds from water samples. Analytical merits of the method, under optimum conditions (extraction temperature: 75°C, extraction time: 30 min, desorption time: 2 min, desorption temperature 260°C, salt concentration: 10% w/v) are 0.01-300 ng/mL for the linear dynamic range and 0.005-0.08 for the limit of detection. In optimum conditions, the repeatability for one fiber (n = 3), expressed as relative standard deviation, was between 6.5 and 9.9% for the phenolic compounds.

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A highly porous fiber-coated SBA-15/polyaniline material was prepared for solid-phase microextraction (SPME). The SBA-15/polyaniline nanocomposite was synthesized via chemical polymerization. The prepared SBA-15/polyaniline particles were analyzed by scanning electron microscopy analysis. The prepared nanomaterial was immobilized onto a stainless steel wire for fabrication of the SPME fiber. The fiber was evaluated for the extraction of some polycyclic aromatic hydrocarbons (PAHs) from aqueous sample solutions in combination with gas chromatography-mass spectrometry (GC-MS). In optimum conditions (extraction temperature 60°C, extraction time 40 min, ionic strength 20%, stirring rate: 500 rpm, desorption temperature 260°C, desorption time 2 min), the repeatability for one fiber (n=3), expressed as relative standard deviation (RSD%), was between 5.3 and 8.6% for the test compounds. For deionized water, spiked with selected PAHs, the detection limits for the studied compounds were between 2 and 20 pg/mL.