scholarly journals The Promising Role of Chitosan–Poloxamer 188 Nanocrystals in Improving Diosmin Dissolution and Therapeutic Efficacy against Ferrous Sulfate-Induced Hepatic Injury in Rats

Pharmaceutics ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2087
Author(s):  
Neamet S. Lotfy ◽  
Thanaa M. Borg ◽  
Elham A. Mohamed

Diosmin (DSN) exhibits poor water solubility and low bioavailability. Although nanocrystals (NCs) are successful for improving drug solubility, they may undergo crystal growth. Therefore, DSN NCs were prepared, employing sonoprecipitation utilizing different stabilizers. The optimum stabilizer was combined with chitosan (CS) as an electrostatic stabilizer. NCs based on 0.15% w/v poloxamer 188 (PLX188) as a steric stabilizer and 0.04% w/v CS were selected because they showed the smallest diameter (368.93 ± 0.47 nm) and the highest ζ-potential (+40.43 ± 0.15 mV). Mannitol (1% w/v) hindered NC enlargement on lyophilization. FT-IR negated the chemical interaction of NC components. DSC and XRD were performed to verify the crystalline state. DSN dissolution enhancement was attributed to the nanometric rod-shaped NCs, the high surface area, and the improved wettability. CS insolubility and its diffusion layer may explain controlled DSN release from CS-PLX188 NCs. CS-PLX188 NCs were more stable than PLX188 NCs, suggesting the significance of the combined electrostatic and steric stabilization strategies. The superiority of CS-PLX188 NCs was indicated by the significantly regulated biomarkers, pathological alterations, and inducible nitric oxide synthase (iNOS) expression of the hepatic tissue compared to DSN suspension and PLX188 NCs. Permeation, mucoadhesion, and cellular uptake enhancement by CS may explain this superiority.

2021 ◽  
Author(s):  
Ayat Nuri ◽  
Abolfazl Bezaatpour ◽  
Mandana Amiri ◽  
Nemanja Vucetic ◽  
Jyri-Pekka Mikkola ◽  
...  

AbstractMesoporous SBA-15 silicate with a high surface area was prepared by a hydrothermal method, successively modified by organic melamine ligands and then used for deposition of Pd nanoparticles onto it. The synthesized materials were characterized with infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), nitrogen physisorption, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP-OES). The catalyst was effectively used in the Mizoroki–Heck coupling reaction of various reactants in the presence of an organic base giving the desired products in a short reaction time and with small catalysts loadings. The reaction parameters such as the base type, amounts of catalyst, solvents, and the temperature were optimized. The catalyst was easily recovered and reused at least seven times without significant activity losses. Graphic Abstract


RSC Advances ◽  
2019 ◽  
Vol 9 (42) ◽  
pp. 24368-24376 ◽  
Author(s):  
Ajay Kumar Adepu ◽  
Srinath Goskula ◽  
Suman Chirra ◽  
Suresh Siliveri ◽  
Sripal Reddy Gujjula ◽  
...  

In the present study, we synthesized several high-surface area V2O5/TiO2–SiO2 catalysts (vanado titanium silicate, VTS). The synthesized materials are characterized by PXRD, FE-SEM/EDAX, TEM, BET-surface area, FT-IR, UV-Vis, XPS, fluorescence and photocatalytic studies.


NANO ◽  
2015 ◽  
Vol 10 (02) ◽  
pp. 1550023 ◽  
Author(s):  
Chunnian Chen ◽  
Xuwang Fu ◽  
Wei Fan ◽  
Ting Ma

This paper reports a new graphene oxide (GO)/acenaphthenequinone composite as efficient electrode in electrochemical supercapacitors. The nanosheets of GO provide high surface area and conductivity. The microneedle-like acenaphthenequinone contributes convincible specific capacitance. The structure and morphology of GO/acenaphthenequinone composite have been characterized by field-emission scanning electron microscopy (FESEM), Fourier transform infrared (FT-IR) spectra and Raman spectra. According to the cyclic voltammetry (CV), galvanostatic charge/discharge, impedance spectra and cycling life analyses, the GO/acenaphthenequinone composite exhibits brilliant supercapacitors performance with a specific capacitance of 248.7 F g-1 at a scan rate of 1 mV s-1 and enhanced stability of about 82% (147.5 F g-1) of initial capacitance (179.8 F g-1) after 500 cycles at a current density of 1 A g-1.


2014 ◽  
Vol 91 ◽  
pp. 79-81
Author(s):  
Abina M. Crean ◽  
Robert J. Ahern ◽  
Rakesh Dontireddy ◽  
Walid Faisil ◽  
John P. Hanrahan ◽  
...  

Low drug water-solubility is a major challenge to overcome in the development of tablet or capsule dosage forms for a large number of promising drug candidates. Strategies to improve drug solubility and dissolution involve chemical, physical and formulation approaches. An emerging formulation approach to increase drug dissolution and solubility involves the creation of solid dispersions of drug molecules on to a high surface area inorganic carrier, such as porous silica. The combined benefits of a hydrophilic inorganic substrate, increased drug surface area and a high-energy drug form facilitate rapid drug dissolution into aqueous based media and can create supersaturated drug solutions. The work presented provides a brief overview of the silica grades investigated, processes employed to load drugs onto the silica substrates, provide some examples of the ability of silica to enhance drug dissolution and highlight some of the challenges in the development of these novel drug delivery systems.


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Sana Ahmad ◽  
Anam Nazir ◽  
Tousif Hussain

Titanium dioxide nanoparticles were prepared by a modified sol-gel route. Titanium butoxide was used as precursor and nebulizer was used for a fine spray of particles. The prepared powders were characterized by FT-IR, SEM, XRD, and TGA-DTA methods. The results indicated that nanoparticles with small size and high surface area were synthesized. XRD result indicated that TiO2 nanoparticles were obtained in pure anatase crystalline form with a crystallite size of 40 nm. The catalytic activity of as-synthesized nanoparticles was tested for the degradation of formic acid and toluene.


2009 ◽  
Vol 12 (3) ◽  
pp. 250 ◽  
Author(s):  
Roya Talari ◽  
Ali Nokhodchi ◽  
Seyed Abolfazl Mostafavi ◽  
Jaleh Varshosaz

Purpose: The micronization using milling process to enhance dissolution rate is extremely inefficient due to a high energy input, and disruptions in the crystal lattice which can cause physical or chemical instability. Therefore, the aim of the present study is to use in situ micronization process through pH change method to produce micron-size gliclazide particles for fast dissolution hence better bioavailability. Methods: Gliclazide was recrystallized in presence of 12 different stabilizers and the effects of each stabilizer on micromeritic behaviors, morphology of microcrystals, dissolution rate and solid state of recrystallized drug particles were investigated. Results: The results showed that recrystallized samples showed faster dissolution rate than untreated gliclazide particles and the fastest dissolution rate was observed for the samples recrystallized in presence of PEG 1500. Some of the recrystallized drug samples in presence of stabilizers dissolved 100% within the first 5 min showing at least 10 times greater dissolution rate than the dissolution rate of untreated gliclazide powders. Micromeritic studies showed that in situ micronization technique via pH change method is able to produce smaller particle size with a high surface area. The results also showed that the type of stabilizer had significant impact on morphology of recrystallized drug particles. The untreated gliclazide is rod or rectangular shape, whereas the crystals produced in presence of stabilizers, depending on the type of stabilizer, were very fine particles with irregular, cubic, rectangular, granular and spherical/modular shape. The results showed that crystallization of gliclazide in presence of stabilizers reduced the crystallinity of the samples as confirmed by XRPD and DSC results. Conclusion: In situ micronization of gliclazide through pH change method can successfully be used to produce micron-sized drug particles to enhance dissolution rate.


2018 ◽  
Vol 4 (5) ◽  
pp. 555-559
Author(s):  
K.V. Divya Lakshmi ◽  
T. Siva Rao

Nickel and sulfur co-doped TiO2 photocatalyst were prepared by using sol-gel method with dopants precursors of nickel nitrate and thiourea. Prepared samples were characterized by XRD, UV-Vis-DRS, TEM, BET, FT-IR and SEM-EDX. These characterization and experimental results revealed that there is a formation of anatase phase, decreased band gap 2.62 eV for NIST-2, small particle size 7.3 nm and high surface area 142.62 m2/g. The FT-IR frequency shift for Ti-O-Ti was observed from 569 cm-1 to 460-560 cm-1 for co-doped TiO2. The efficiency of photocatalytic and antibacterial was evaluated by degradation of Orange-II dye and Escherichia coli (MTCC-443) respectively. The complete degradation of Orange-II was achieved in 120 min at optimum reaction parameters for NIST-2 at pH-3, catalyst dosage-100 mg/L and initial dye concentration at 10 mg/L.


Molecules ◽  
2021 ◽  
Vol 26 (21) ◽  
pp. 6569
Author(s):  
Maryam Afsharpour ◽  
Mehdi Elyasi ◽  
Hamedreza Javadian

This paper reports the synthesis of a new nitrogen-doped porous bio-graphene (NPBG) with a specific biomorphic structure, using Pistacia lentiscus as a natural carbon source containing nitrogen that also acts as a bio-template. The obtained NPBG demonstrated the unique feature of doped nitrogen with a 3D nanoporous structure. Next, a WO3/N-doped porous bio-graphene nanocomposite (WO3/NPBG-NC) was synthesized, and the products were characterized using XPS, SEM, TEM, FT-IR, EDX, XRD, and Raman analyses. The presence of nitrogen doped in the structure of the bio-graphene (BG) was confirmed to be pyridinic-N and pyrrolic-N with N1 peaks at 398.3 eV and 400.5 eV, respectively. The photocatalytic degradation of the anionic azo dyes and drugs was investigated, and the results indicated that the obtained NPBG with a high surface area (151.98 m2/g), unique electronic properties, and modified surface improved the adsorption and photocatalytic properties in combination with WO3 nanoparticles (WO3-NPs) as an effective visible-light-driven photocatalyst. The synthesized WO3/NPBG-NC with a surface area of 226.92 m2/g displayed lower bandgap and higher electron transfer compared with blank WO3-NPs, leading to an increase in the photocatalytic performance through the enhancement of the separation of charge and a reduction in the recombination rate. At the optimum conditions of 0.015 g of the nanocomposite, a contact time of 15 min, and 100 mg/L of dyes, the removal percentages were 100%, 99.8%, and 98% for methyl red (MR), Congo red (CR), and methyl orange (MO), respectively. In the case of the drugs, 99% and 87% of tetracycline and acetaminophen, respectively, at a concentration of 10 mg/L, were removed after 20 min.


Author(s):  
Idongesit Justina Mbonu ◽  
Olusegun Kehinde Abiola

Adsorption of N2 on mixed ligand benzoic acid and 1, 10-phenanthroline ligands of Mn(II) metal-organic framework (MOF)–nanoparticles were demonstrated. The adsorption capacity and pore size distribution of the synthesized MOF were conducted experimentally by measuring the N2 adsorption isotherm at 77.3 K. The resulting data were fitted to Brunauer-Emmett-Teller (BET), de Boer, Dubinin-Redusbkevich (DR), Banet-Joyner-Halenda (BJH), Horvath-Kawazoe (HK) and Density Functional Theory (DFT) models to describe the adsorptive behaviour of the synthesized nanoparticles. The DSC analysis shows the high chemical stability of this compound. The FT-IR measurement reports present the abundant of highly coordinated functional groups. And the adsorption properties evaluated by different adsorption models compared with existing adsorbent materials suggest Mn-MOF with good thermal stability, high surface area and pore openings, is a promising material for storing gases and energy because at low or high pressures, it can adsorb nitrogen gas due to its large openings.


Pharmaceutics ◽  
2022 ◽  
Vol 14 (1) ◽  
pp. 110
Author(s):  
Avelino Corma ◽  
Pablo Botella ◽  
Eva Rivero-Buceta

The administration of cytotoxic drugs in classical chemotherapy is frequently limited by water solubility, low plasmatic stability, and a myriad of secondary effects associated with their diffusion to healthy tissue. In this sense, novel pharmaceutical forms able to deliver selectively these drugs to the malign cells, and imposing a space-time precise control of their discharge, are needed. In the last two decades, silica nanoparticles have been proposed as safe vehicles for antitumor molecules due to their stability in physiological medium, high surface area and easy functionalization, and good biocompatibility. In this review, we focus on silica-based nanomedicines provided with specific mechanisms for intracellular drug release. According to silica nature (amorphous, mesostructured, and hybrids) nanocarriers responding to a variety of stimuli endogenously (e.g., pH, redox potential, and enzyme activity) or exogenously (e.g., magnetic field, light, temperature, and ultrasound) are proposed. Furthermore, the incorporation of targeting molecules (e.g., monoclonal antibodies) that interact with specific cell membrane receptors allows a selective delivery to cancer cells to be carried out. Eventually, we present some remarks on the most important formulations in the pipeline for clinical approval, and we discuss the most difficult tasks to tackle in the near future, in order to extend the use of these nanomedicines to real patients.


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