scholarly journals Electrospun Structural Hybrids of Acyclovir-Polyacrylonitrile at Acyclovir for Modifying Drug Release

Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4286
Author(s):  
He Lv ◽  
Shiri Guo ◽  
Gaoyi Zhang ◽  
Wanli He ◽  
Yonghui Wu ◽  
...  

In traditional pharmaceutics, drug–crystalline nanoparticles and drug–polymer composites are frequently explored for their ability to modify drug release profiles. In this study, a novel sort of hybrid with a coating of acyclovir crystalline nanoparticles on acyclovir-polyacrylonitrile composites was fabricated using modified, coaxial electrospinning processes. The developed acyclovir-polyacrylonitrile at the acyclovir nanohybrids was loaded with various amounts of acyclovir, which could be realized simply by adjusting the sheath fluid flow rates. Compared with the electrospun composite nanofibers from a single-fluid blending process, the nanohybrids showed advantages of modifying the acyclovir release profiles in the following aspects: (1) the initial release amount was more accurately and intentionally controlled; (2) the later sustained release was nearer to a zero-order kinetic process; and (3) the release amounts at different stages could be easily allocated by the sheath fluid flow rate. X-ray diffraction results verified that the acyclovir nanoparticles were in a crystalline state, and Fourier-transform infrared spectra verified that the drug acyclovir and the polymer polyacrylonitrile had a good compatibility. The protocols reported here could pave the way for developing new types of functional nanostructures.

2019 ◽  
Vol 2019 ◽  
pp. 1-13
Author(s):  
Rai Muhammad Sarfraz ◽  
Muhammad Rouf Akram ◽  
Muhammad Rizwan Ali ◽  
Asif Mahmood ◽  
Muhammad Usman Khan ◽  
...  

Current research work was carried out for gastro-protective delivery of naproxen sodium. Polyethylene glycol-g-poly (methacrylic acid) nanogels was developed through free radical polymerization technique. Formulation was characterized for swelling behaviour, entrapment efficiency, Fourier transform infrared (FTIR) spectroscopy, Differential scanning calorimetry (DSC), and Thermal Gravimetric Analysis (TGA), Powder X-ray diffraction (PXRD), Zeta size distribution, and Zeta potential measurements, and in-vitro drug release. pH dependent swelling was observed with maximum drug release at higher pH. PXRD studies confirmed the conversion of loaded drug from crystalline to amorphous form while Zeta size measurement showed size reduction. On the basis of these results it was concluded that prepared nanogels proved an effective tool for gastro-protective delivery of naproxen sodium.


Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.


2012 ◽  
Vol 268-270 ◽  
pp. 580-583 ◽  
Author(s):  
Yong Tang Jia ◽  
Cui Wu ◽  
Feng Chun Dong ◽  
Gang Huang ◽  
Xian Hua Zeng

The composite nanofiber membranes of poly (ε-caprolactone)/poly(vinyl pyrrolidone) (PCL/PVP) containing silver nanoparticles were prepared by electrospinning method. The morphology of composite nanofibers was characterized by scanning electron microscopy (SEM). The silver nanoparticles on the electrospun fibers were characterized by X-Ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The contact angle and water uptake of PCL/PVP/Ag nanofiber membranes were measured. The SEM photos indicated that the average diameter of the fibers was significantly decreased with the addition of silver nanoparticles. The X-Ray images showed that Ag nanoparticles were distributed on the surface of nanofiber membranes. When the PVP mole ratio was higher than 15%, the nanofiber membranes showed good hydrophilic property. The PCL/PVP/Ag nanofiber membranes could be applied to prepare wound dressing.


2011 ◽  
Vol 332-334 ◽  
pp. 317-320 ◽  
Author(s):  
Hui Qin Zhang

In this study, composite nanofibers of polyaniline doped with dodecylbenzene sulfonic acid (PANI-DBSA) and Poly(lactic acid) (PLA) were prepared via an electrospinning process. The surface morphology, thermal properties and crystal structure of PLA/PANI-DBSA nanofibers are characterized using Fourier transform infrared spectroscopy (FT-IR), wide-angle x-ray diffraction (WAXD) and scanning electron microscopy (SEM). SEM images showed that the morphology and diameter of the nanofibers were affected by the weight ratio of blend solution.


2017 ◽  
Vol 18 (4) ◽  
pp. 1406-1419
Author(s):  
F. Elmi ◽  
R. Chenarian Nakhaei ◽  
H. Alinezhad

Abstract This study is the first report of its type demonstrating the synthesis of mHAP on the basis of magnetic functionalization with nHAP, which were synthesized using Rutilus frisii kutum fish scale as a benign fishery waste by-product. The mHAP was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray diffraction (EDX), and Fourier transform infrared (FT-IR) spectroscopic techniques. The XRD pattern confirmed the formation of a single-phase nHAP without any extra steady phases. It was also found that the pseudo-second-order kinetic model gave a satisfactory fit to the experimental data (R2 = 0.99). The maximum removal percentages of Cu and Zn ions in optimal conditions (adsorbent dosage at 0.1 g, 30 min contact time at 25 ± 1 °C and pH = 5 ± 0.1) by mHAP were 97.1% and 93.8%, respectively. Results also demonstrated that mHAP could be recycled for up to five cycles in the case of copper and zinc. The Langmuir isotherm was proved to have a better correlation compared with that of the Freundlich isotherm. The thermodynamic parameters indicated that it was a spontaneously endothermic reaction. In conclusion, mHAP could be regarded as a powerful candidate for efficient biosorbent, capable of adsorbing heavy metals from aqueous solutions.


2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Wei Xiong ◽  
Yue-kun Shen ◽  
Peng Dong ◽  
Ying Xiao ◽  
Xiong-qing Huang ◽  
...  

Sustained release of anesthesia has shown great promise in the treatment of chronic pain in patients. In this research, we used neutralized ropivacaine as an anesthesia and poly(ε-caprolactone) (PCL) with different architectures to systematically study how these architectures affect the release of ropivacaine. After optimizing the parameters of the preparation of microspheres, ropivacaine-loaded 1-PCL microspheres and 4-PCL microspheres were obtained. Fourier Transform infrared spectra (FT-IR) and X-ray diffraction spectra (XRD) confirmed that ropivacaine was encapsulated within the microsphere rather than inserted on the surface of the microsphere. Ropivacaine was found to be buried deeper in the 1-PCL microsphere than in the 4-PCL microsphere. In vitro release assay revealed that small crystalline grains interfered with ropivacaine release in 4-PCL microspheres during the initial release period, but then two kinds of microspheres showed a similar ropivacaine release rate. We basically proved that the architecture of PCL has a negligible effect on ropivacaine release. Cell proliferation test revealed that the release of products from the microspheres resulted in insignificant toxicity towards mammalian cells.


2017 ◽  
Vol 17 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Dawei Gao ◽  
Lili Wang ◽  
Chunxia Wang ◽  
Yuping Chang ◽  
Pibo Ma

Abstract Polyacrylonitrile (PAN)/Co(OAc)2/carbon nanotubes (CNTs) composite nanofibers were fabricated via electrospinning with N,N-dimethylformamide (DMF) as solvent, and by carbonization and activation of the above precursor nanofibers, porous carbon composite nanofibers were successfully obtained. Scanning electron microscope, X-ray diffraction, ASAP 2020, and Solartron 1470 were used to characterize the surface morphology, the phase composition, specific surface area, and electrochemical property of the nanofibers, respectively. The result showed that some of the fibers were broken after sintering, and the surface area and pore volume of the porous C/Cu/CNTs were 771 m2/g and 0.347 cm3/g, respectively. The specific capacitance of the composite nanofibers reached up to 210 F/g at the current density of 1.0 A/g. Its energy density and power density were 3.1 Wh/Kg and 2,337 W/Kg, respectively, at the current of 0.5 and 5 mA.


2011 ◽  
Vol 175-176 ◽  
pp. 341-344 ◽  
Author(s):  
Byoung Suhk Kim ◽  
Kyu Oh Kim ◽  
Ick Soo Kim

We report the electrospun poly(L-lactide) (PLA) nanofibers incorporating polyhedral oligosilsesquioxane (POSS)-modified multiwalled carbon nanotubes (MWNTs). FT-IR, transmission electron microscopy (TEM) and Raman analysis confirmed the existence of POSS macromers bonded to the MWNTs as an extra phase. The thermal and microstructure properties of the PLA hybrid nanofibers with POSS-modified MWNTs were investigated by thermogravimetric analysis (TGA) and Wide-angle X-ray diffraction (WAXD).


2020 ◽  
Vol 8 (4) ◽  
pp. 1258-1267

The objective of this work was the physicochemical characterization of a Moroccan natural clay from the Jorf Arfoud region (Lampert Coodinates: x = 595610, y = 101578) and its valorization in the elimination of organic pollutants (methyl orange MO and methylene blue MB) from aqueous solutions, with the adsorption technique on raw and calcined clay at 500°C. The clay was characterized by chemical analysis such as X-ray fluorescence (XRF), X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron microscopy (SEM). Crude and purified clays, consisting essentially of silica and alumina, are a characteristic property of phyllosilicates and also contain amounts of quartz, kaolinite and calcite as associated minerals. The experiments were performed after optimization of the parameters influencing the system, such as pH, adsorbent mass, initial dye concentration and temperature. The clays used absorb better the MB than MO, for an initial concentration of 10 mg/L and 20 mg/L respectively. Langmuir and Freundlich models of adsorption isotherms were applied to fit experimental equilibrium data. Results have showed that the adsorption of MB and MO followed very well the second order kinetic model on raw clay. The adsorption process was found to be exothermic in the case of MB. However, the adsorption of MO was endothermic.


2020 ◽  
Vol 20 (5) ◽  
pp. 2878-2886
Author(s):  
Jia Liu ◽  
Guo-Dong Su ◽  
Zhou Wang

Magnetic Ni0.3Mg0.3Zn0.4Fe2O4 nanoparticles were synthesized by the absolute alcohol combustion method. The morphology, microstructure, and composition of as-prepared Ni0.3Mg0.3Zn0.4Fe2O4 nanoparticles were characterized by several techniques: the vibrating sample magnetometer (VSM), the scanning electron microscopy (SEM), the X-ray diffraction (XRD), and the energy dispersive spectroscopy (EDS). The experimental results showed that the calcination temperature and the solvent volume were the crucial factors for the synthesis of the magnetic Ni0.3Mg0.3Zn0.4Fe2O4 nanoparticles. The adsorption performance of Ni0.3Mg0.3Zn0.4Fe2O4 nanoparticles for congo red (CR) was investigated. The model of pseudo-second-order kinetic was optimal matching for obtaining the parameters of adsorption CR in the initial range of 100–400 mg/L−1, while, the isotherm data of CR onto Ni0.3Mg0.3Zn0.4Fe2O4 nanoparticles could conform to the Temkin model owing to the values of the square deviations, which revealed that the adsorption of CR onto Ni0.3Mg0.3Zn0.4Fe2O4 nanoparticles at room temperature was the monolayer and multilayer adsorption mechanism.


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