A simple method to controlled synthesis of nano hydroxyapatite in different particle size

2018 ◽  
Vol 217 ◽  
pp. 177-180 ◽  
Author(s):  
Wei Liu ◽  
Gongming Qian ◽  
Lulu Liu ◽  
Bo Zhang ◽  
Xianyuan Fan
2020 ◽  
Vol 10 (3) ◽  
pp. 306-315
Author(s):  
Rupa Mazumder ◽  
Swarnali Das Paul

Background: Atenolol is a commonly used antihypertensive drug of class III BCS category. It suffers from the problem of poor intestinal absorption or permeability thus low bioavailability. The objective of the present study was to enhance the permeability of atenolol by using a suitable technique, which is economical and devoid of using any organic solvent. Methods: The nanocrystal technology by high-pressure homogenization was chosen for this purpose, which is a less expensive and simple method. In this technique, no organic solvent was used. The study was further aimed to characterize prepared nanocrystals in the solid state by Fourier Transform Infrared Spectroscopy (FTIR), Powder X-Ray Diffraction (PXRD) patterns, particle size, zeta potential, %yield and drug permeation study through isolated goat’s intestine. An in-vivo study was carried out to determine the pharmacokinetic property in comparison to pure drug powder using rats as experimental animals. The formulation design was optimized by a 3(2) factorial design. In these designs, two factors namely surfactant amount (X1) and speed of homogenizer (X2) were evaluated on three dependent variables namely particle size (y1), zeta potential (y2) and production yield (y3). Results: PXRD study indicated the presence of high crystal content in the prepared formulation. These nanocrystal formulations were found with a narrow size range from 125 nm to 652 nm and positive zeta potential of 16-18 mV. Optimized formulations showed almost 90% production yield. Permeability study revealed 90.88% drug release for optimized formulation in comparison to the pure drug (31.22%). The FTIR study also exposed that there was no disturbance in the principal peaks of the pure drug atenolol. This confirmed the integrity of the pure drug and its compatibility with the excipients used. A significant increase in the area under the concentration-time curve Cpmax and MRT for nanocrystals was observed in comparison to the pure drug. The higher values of the determination coefficient (R2) of all three parameters indicated the goodness of fit of the 3(2) factorial model. The factorial analysis also revealed that speed of homogenizer had a bigger effect on particle size (-0.2812), zeta potential (-0.0004) and production yield (0.0192) whereas amount of surfactant had a lesser effect on production yield (-370.4401), zeta potential (-43.3651) as well as particle size (-6169.2601). Conclusion: It is concluded that the selected method of nanocrystal formation and its further optimization by factorial design was effective to increase the solubility, as well as permeability of atenolol. Further, the systematic approach of factorial design provides rational evaluation and prediction of nanocrystals formulation on the selected limited number of smart experimentation.


2019 ◽  
Vol 7 (17) ◽  
pp. 4981-4987 ◽  
Author(s):  
Ruiyu Bao ◽  
Chen Chen ◽  
Jianxin Xia ◽  
Huiying Chen ◽  
Hua Li

The surface morphology and particle size of materials can be controlled using DEP technology.


1955 ◽  
Vol 76 (4) ◽  
pp. 466-468 ◽  
Author(s):  
Isamu Sano ◽  
Yoshiyasu Fujitani ◽  
Ken Sugiyama
Keyword(s):  

ROTOR ◽  
2017 ◽  
Vol 10 (1) ◽  
pp. 17
Author(s):  
Havid Arifian Rochman ◽  
Arief Ginanjar Dirgantara ◽  
Salahudin Junus ◽  
Imam Sholahuddin ◽  
Aris Zainul Muttaqin

The synthesis of nanoparticles using thermal DC plasma method is a simple method for ease of installation and high efficiency is due to the rate of precursor that can be controlled. Micro-sized aluminum powder is synthesized using thermal DC plasma undergoing a process of evaporation as it passes through high temperature plasma flame, where kemuadian oxidized aluminum particles which evaporates the particles are split and binds with oxygen to form aluminum oxide or also known as alumina (Al2O3). In this experiment, the flow rate of oxygen plasma parameters at 35 SCFH (Standard Cubic Feet per Hour) and 20 amperes flows with precursors rate variation of 1.16 g / min, 3.19 g / min, and 3.5 g / min. Precursors used is 88 micro sized aluminum powder. To determine the morphology of nanoparticles of alumina testing scanning electron microscopy (SEM), the morphology form of nanosphere. Results of the analysis showed that the rate of precursor low causing agglomeration level slightly while the higher rate of precursor agglomeration rate also increased. At the rate of precursor 1.16 g / min, nanoparikel undergo agglomeration with an average particle size of 36.55 nm, and then at a rate of 3.19 gr precursor / mnt an average particle size of 46.49 nm, and at a rate of 3.5 gr / mnt an average particle size of 46.49 nm. The powder nanoparticles were then characterized using X-ray defraksi (XRD) where all alumina nanoparticles were synthesized showed alumina phase that is formed is a phase δ-Al2O3. Keywords: Alumina nanoparticles, DC Thermal Plasma, morphology, precursor rate, nanoparticles size, SEM, XRD.


2004 ◽  
Vol 449-452 ◽  
pp. 1237-1240 ◽  
Author(s):  
Hwan Pil Park ◽  
Yoon Chung ◽  
Chong Seung Yoon ◽  
Sung Su Jo ◽  
Young Ho Kim

We developed a simple method of producing metal oxide nanoparticles by reacting a polyamic acid (PAA) with Cu or Sn metal films. Respective particle size, distribution, and morphology were characterized by transmission electron microscopy (TEM). The morphology of metal oxides dispersed in the polyimide is different in Cu and Sn metal films. The Cu2O particles were formed by the dissolution reaction between the polyamic acid and the Cu films. During curing, PAA dehydrates and converts to polyimide, accompanied by precipitation of Cu2O particles. The synthesized Cu2O particles were randomly dispersed within the polyimide. And their particle size was relatively uniform, having a narrow distribution. Mostly nanosize Cu2O particles were formed in the specimen made from 10 nm thick Cu film and the mixture of nanosize particles and Cu layers were observed in the 30 nm thick Cu film. On the other hands, the Sn film undergoes surface reaction with the polyamic acid. Therefore, the synthesized SnO2 particles existed only at the surface of the substrate. SnO2 particle size distribution was not uniform in the polyimide. Although particles were not distributed uniformly in the polyimide, they were confined in a monolayer. The different particle distributions were attributed to the reactivity difference of PAA with Cu and Sn films.


2001 ◽  
Vol 635 ◽  
Author(s):  
Young-wook Jun ◽  
Jong-Il Park ◽  
Jinwoo Cheon

AbstractOur study describes a convenient one-step synthesis of ZnSe and ZnTe nanocrystals (NC) whose sizes and shapes are precisely tuned by varing the growth temperature or stabilizing surfactants. We utilized molecular precursors, bis(phenylselenolate or phenyltellurolato)zinc -N,N,N',N'-tetramethylethylenediamine (TMEDA), which effectively produce 0-dimensional sphere or 1-dimensional nanorods of ZnSe or ZnTe, respectively. Nanocrystals are highly monodispersed and luminescent; the emission wavelength varies over a wide range depending on the particle size. This study constitutes a nice demonstration of direct size and shape controlled synthesis of semiconductor nanocrystals and this method can be extended to the synthesis of nanocrystals of other materials.


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