scholarly journals KARAKTERISASI FISIKOKIMIA NANOKRISTAL EKSTRAK HERBA SELEDRI ( Apium graveolens L.) DENGAN PERBEDAAN KONSENTRASI POLOXAMER188

2020 ◽  
Vol 4 (1) ◽  
pp. 31-39
Author(s):  
Henni Rosaini ◽  
Rina Wahyuni ◽  
Boyke Panata Sinaga ◽  
Wahyu Margi Sidoretno
Keyword(s):  
Particle Size ◽  
Apium Graveolens ◽  
Poloxamer 188 ◽  
Marker Compound ◽  
Biopharmaceutics Classification System Class ◽  
Particle Size Analyzer ◽  
Ft Ir ◽  
Low Solubility ◽  
Grinding Time

Celery (Apium graveolens L) is a plant of Apiaceae family which contains flavonoids, saponins, tannins, essential oils, apiin, apigenin, choline, asparagine, vitamin A, B, C. Apigenin contained in celery included in the BCS (Biopharmaceutics Classification System)  class II, which has low solubility and high permeability drugs. One method for increasing solubility is the nanocrystal method. Where the purpose of this study was to see the effect of differences in the concentration of poloxamer 188 on the characterization of nanocrystal. The results of the particle size analyzer (PSA) showed particle size distribution in formula 1 the concentration of poloxamer 188 40% 6 hour grinding time of 1648.5 nm with a potential zeta value of -11.2. While the formula 2 concentration of poloxamer 188 50% and formula 3 the concentration of poloxamer 188 60% with a 5 hour grinding time of 1049.6 and 1483.2 with a potential zeta value of -12.5 and -8.9. From the FT-IR analysis shows the presence of clusters in formulas 1, 2, and 3 which are not found in apigenin which is a celery marker compound, on the contrary there are groups on apigenin which are not found in formulas 1, 2, and 3.

Isolasi Dan Karakterisasi Bentonit Alam Menjadi Nanopartikel Monmorillonit

2018 ◽  
Vol 3 (1) ◽  
pp. 12 ◽  
Author(s):  
Zaimahwati Zaimahwati ◽  
Yuniati Yuniati ◽  
Ramzi Jalal ◽  
Syahman Zhafiri ◽  
Yuli Yetri
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Particle Size ◽  
Surface Morphology ◽  
Average Diameter ◽  
Particle Size Analyzer ◽  
Ft Ir ◽  
Scanning Electron ◽  
Sedimentation Processes

<p>Pada penelitian ini telah dilakukan isolasi dan karakterisasi bentonit alam menjadi nanopartikel montmorillonit. Bentonit alam yang digunakan diambil dari desa Blangdalam, Kecamatan Nisam Kabupaten Aceh Utara.  Proses isolasi meliputi proses pelarutan dengan aquades, ultrasonic dan proses sedimentasi. Untuk mengetahui karakterisasi montmorillonit dilakukan uji FT-IR, X-RD dan uji morfologi permukaan dengan Scanning Electron Microscopy (SEM). Partikel size analyzer untuk menganalisis dan menentukan ukuran nanopartikel dari isolasi bentonit alam. Dari hasil penelitian didapat ukuran nanopartikel montmorillonit hasil isolasi dari bentonit alam diperoleh berdiameter rata-rata 82,15 nm.</p><p><em>In this research we have isolated and characterized natural bentonite into montmorillonite nanoparticles. Natural bentonite used was taken from Blangdalam village, Nisam sub-district, North Aceh district. The isolation process includes dissolving process with aquades, ultrasonic and sedimentation processes.  The characterization of montmorillonite, FT-IR, X-RD and surface morphology test by Scanning Electron Microscopy (SEM). Particle size analyzer to analyze and determine the size of nanoparticles from natural bentonite insulation. From the research results obtained the size of montmorillonite nanoparticles isolated from natural bentonite obtained an average diameter of 82.15 nm.</em></p>

Characterization of Well-Dispersed CeO2 Nanoparticles Prepared by a New Method of Reverse Microemulsion

2011 ◽  
Vol 194-196 ◽  
pp. 781-784
Author(s):  
Fa Mei Feng ◽  
Jia Qing Xie ◽  
Li Ke Zou ◽  
Bin Xie
Keyword(s):  
Particle Size ◽  
Fourier Transform ◽  
Ceo2 Nanoparticles ◽  
Size Distributions ◽  
X Ray ◽  
Transmission Electron ◽  
Particle Size Analyzer ◽  
Ft Ir ◽  
Cubic Structure

Well-dispersed CeO2 nanoparticles were successfully prepared in a simple system composed of sodium bis (2-ethylhexyl) sulfosuccinate (AOT)- octane-water (W/O) microemulsion in this paper. The morphology and microstructure of the products were characterized by the laser particle size analyzer, Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometer (XRD), differential scanning calorimeter (DSC) and transmission electron microscope (TEM). It was found that the CeO2nanoparticles obtained from this method have well-proportioned size distributions; the surfactant (AOT) molecule was adsorbed on the surface of CeO2nanoparticles precursor, which is favorable for the dispersion of CeO2nanoparticles; the CeO2nanoparticles calcined was a crystal of the cubic structure. In addition, the mechanism on the formation of the CeO2nanoparticles was also proposed in this paper.

ANALISIS KARAKTERISASI SERBUK BIOKERAMIK DARI CANGKANG TELUR AYAM BROILER

ROTOR ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 1
Author(s):  
Hendri Van Hoten
Keyword(s):  
Particle Size ◽  
Electron Microscope ◽  
Powder Size ◽  
Test Results ◽  
Optimum Parameters ◽  
Transmission Electron ◽  
Particle Size Analyzer ◽  
Average Size ◽  
Grinding Time

The research is about analysis of Nano Sized Bioceramic Characterization Using Particle Size Analyzer (PSA). In the previous research, optimization of the parameters of making nano powders on Ball Mill machines using the Taguchi and ANOVA methods. The optimum parameters of the Taguchi Design analysis were grinding rate, grinding time and Ball Powder Ratio respectively 250 rpm, 3 hours and 1: 6. After that the characterization of the powder use a Scanning Electron Microscope (SEM) and Transmission Electron Microscope (TEM). Powder size measurement use SEM tools obtained the smallest average size of 1.305 mm while using TEM tools showed the average size of the smallest powder between 50-100 nm. TEM test results were confirmed again using PSA. The results of the characterization using PSA showed that the particle size in the range 100-300 nm was approximately 80%

A Simple Dissolved Metals Mixing Route to Prepare Nanostructured Mg0.8Zn0.2TiO3 Solid Solution

2015 ◽  
Vol 1112 ◽  
pp. 47-52 ◽  
Author(s):  
Frida Ulfah Ermawati ◽  
Suasmoro Suasmoro ◽  
Suminar Pratapa
Keyword(s):  
Solid Solution ◽  
Particle Size ◽  
Rietveld Analysis ◽  
Dissolved Metals ◽  
Intermediate Phases ◽  
Particle Size Analyzer ◽  
Ft Ir ◽  
Xrd Patterns ◽  
Zn Ions

A study of liquid mixing route to synthesize high purity Mg0.8Zn0.2TiO3 nanopowder, a candidate dielectric ceramics, has been successfully performed. Formation of the phases on the dried powder was studied using TG/DTA, XRD and FT-IR data. Rietveld analysis on the collected XRD patterns confirmed the formation of solid solution in the system. Such solid solution can be obtained from the powder calcined at 500 °C, but calcination at 550 °C gave rise to the most optimum molar purity up to 98.5% without intermediate phases. The role of Zn ions on the formation of solid solution was also discussed. Homogeneity of particle size distribution and nano-crystallinity of the system was verified from the particle size analyzer data, TEM image and the Rietveld analysis output.

scholarly journals Optimization of nanostructured/nano sized rice husk ash preparation

2020 ◽  
Vol 17 (3(Suppl.)) ◽  
pp. 0953
Author(s):  
Medhat Mostafa ◽  
Hamdy Salah ◽  
Amro B. Saddek ◽  
Nabila Shehata
Keyword(s):  
Particle Size ◽  
Rice Husk ◽  
Amorphous Silica ◽  
Particle Shape ◽  
Rice Husk Ash ◽  
Loss On Ignition ◽  
Shape Distribution ◽  
Disk Mill ◽  
Grinding Time

The objective of the study is developing a procedure for production and characterization of rice husk ash (RHA). The effects of rice husk (RH) amount, burning/cooling conditions combined with stirring on producing of RHA with amorphous silica, highest SiO2, lowest loss on ignition (LOI), uniform particle shape distribution and nano structured size have been studied. It is concluded that the best amount is 20 g RH in 125 ml evaporating dish Porcelain with burning for 2 h at temperature 700 °C combined with cooling three times during burning to produce RHA with amorphous silica, SiO2 90.78% and LOI 1.73%. On the other hand, cooling and stirring times affect the variation of nano structured size and particle shape distribution. However, no crystalline phases were found in RHA in all cases. Results proved that the Attritor ball mill was more suitable than vibration disk mill for pulverizing nano structured RHA with 50% of particle size (D50) lower than 45 mm and 99 % of particle size (D99) lower than 144 mm to nanosized RHA with D50 lower than 36 nm and D99 lower than 57 nm by grinding time 8.16 min to every 1 g RHA without changes in morphousity of silica.

PREPARATION AND CHARACTERIZATION OF GLYCYRRHETINIC ACID-MODIFIED POLOXAMER 188/CHITOSAN NANOPARTICLES

NANO ◽  
2013 ◽  
Vol 08 (04) ◽  
pp. 1350042 ◽  
Author(s):  
JING WANG ◽  
LI GUO ◽  
LI FANG MA
Keyword(s):  
High Performance ◽  
Drug Loading ◽  
Chitosan Nanoparticles ◽  
Spherical Shape ◽  
Glycyrrhetinic Acid ◽  
Poloxamer 188 ◽  
H Nmr ◽  
Ft Ir

In this paper, we firstly synthesized glycyrrhetinic acid-modified double amino-terminated poloxamer 188 (GA–NH–POLO–NH–GA). The structure of the synthesized compound was confirmed by 1H-NMR and Fourier transform infrared (FT-IR) spectroscopy. Then the nanoparticles composed of GA–NH–POLO–NH–GA/chitosan (GA–NH–POLO–NH–GA/CTS) were prepared by an ionic gelation process. The characterization of the nanoparticles was measured by dynamic light scattering (DLS) and scanning electron microscope (SEM). The results showed that the nanoparticles were well dispersed with a spherical shape and the particle size was distributed between 100 nm and 300 nm. The cytotoxicity based on MTT assay against cells (QGY-7703 cells and L929 cells) showed that the nanoparticles had low toxicity and good biocompatibility. The encapsulation efficiency and drug loading of 5-fluorouracil-loaded nanoparticles (5-FU nanoparticles) were measured by high-performance liquid chromatography (HPLC) and fluorescence spectroscopy, ultraviolet-visible (UV-vis) absorbance. The encapsulation of 5-Fu-loaded CTS nanoparticles was 12.8% and the drug loading was 2.9%, while the encapsulation of 5-Fu-loaded GA–NH–POLO–NH–GA/CTS nanoparticles was 20.9% and the drug loading was 3.36%. The release profile showed that the GA–NH–POLO–NH–GA/CTS nanoparticles were available for sustained release of 5-Fu. The GA–NH–POLO–NH–GA/CTS nanoparticles have a higher affinity to the QGY-7703 cells, so indicated that the GA–NH–POLO–NH–GA/CTS nanoparticles have the capacity of liver-targeting in vitro.

Steroid Compounds Isolation from Carthamus tinctorius Linn as Antimalarial

2021 ◽  
pp. 5297-5304
Author(s):  
Rini Hamsidi ◽  
Wahyuni Wahyuni ◽  
Adryan Fristiohady ◽  
Muhammad Hajrul Malaka ◽  
Idin Sahidin ◽  
...  
Keyword(s):  
Antimalarial Activity ◽  
Carthamus Tinctorius ◽  
Spectroscopic Techniques ◽  
1H And 13C Nmr ◽  
Marker Compound ◽  
Ic50 Value ◽  
Ft Ir ◽  
Ir Spectroscopic

Carthamus tinctorius Linn, also known as safflower, is a plant with the potential of being used in the production of antimalarial drugs. The purpose of this study was to isolate and identify the steroid compounds in the safflower and determine its antimalarial activity in vitro. The isolation process was conducted through extraction and chromatography methods. Then, the characterization of the isolated compounds was conducted through spectroscopic techniques which include Fourier Transform Infrared Spectroscopy (FT-IR), NMR 1-D (1H and 13C-NMR), and NMR 2-D (HMQC, HMBC, and H-H COZY) as well as comparing data with the existing literatures. In addition, the tests conducted were with variations of isolate concentrations (10, 1, 0.1, 0.01, and 0.001 μg/mL) against 3D7 strain of Plasmodium falciparum. Based on the FT-IR spectroscopic data, the steroid compounds isolated from safflowers might be stigmasterols. In addition, the isolates had -OH functional group in the region of 3431 cm-1, C-O in the region of 1053 cm-1, and Csp3-H in regions of 2960, 2934, and 2865 cm-1. The NMR 1-D data showed presence of 29 carbon atoms, while the protons were 48 in number. Furthermore, the IC50 value of the compound was 34.03 μg/mL with a percentage inhibition of 43.92% against the growth of P. falciparum. Therefore, it was classified as inactive agent in inhibiting the growth of malaria parasites, however, it could be used as a marker compound in C. tinctorius Linn extract.

Effect of Process on the Dielectric Properties of BaTiO3-Based X9R Ceramics

2014 ◽  
Vol 906 ◽  
pp. 18-24 ◽  
Author(s):  
Bao Lin Zhang ◽  
Bin Bin Zhang ◽  
Ning Ning Wang ◽  
Jing Ming Fei
Keyword(s):  
Particle Size ◽  
Dielectric Properties ◽  
Milling Time ◽  
Sintering Temperature ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Sintered Ceramic ◽  
X Ray ◽  
Particle Size Analyzer

The effect of milling time and sintering process on the dielectric properties of BaTiO3-based X9R ceramics was investigated. The characterization of the raw powders and the sintered ceramic was carried out by X-ray diffraction and scanning electron microscopy. The particle size distribution of the mixed powders was examined by Laser Particle Size Analyzer. The results shown that with the milling time extended, the Cruie Peak was depressed, or even disappeared. Moreover, with the rise of sintering temperature, the dielectric constant of the ceramics increased and the dielectric loss decreased gradually. Eventually, by milling for 11h and sintering at 1090°Cfor 2h, good dielectric properties were obtained, which were ε25°C≥ 2526, εr/εr25°C≤± 12% (–55~200°C), tanδ≤1.12% (25°C).

Synthesis and Characterization of a Novel Folate-Conjugated Themoresponsive Micelles

2012 ◽  
Vol 529 ◽  
pp. 555-559 ◽  
Author(s):  
Jing Jin ◽  
Jian Peng Xue ◽  
Si Si Cui ◽  
Jie Cao ◽  
Dong Yin Zhang ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Amphiphilic Copolymer ◽  
Feed Ratio ◽  
Synthesis And Characterization ◽  
Amphiphilic Copolymers ◽  
Living Body ◽  
Particle Size Analyzer ◽  
Copolymer Poly

In this study, a amphiphilic copolymer, poly ((N-isopropylacrylamide)-co-acrylamide-co- (octadecylacrylate)-co-(Falate-(polyethyleneglycol)-(acrylicacid)))(P(NIPA-co-AAm-co-ODA-co-FPA)) micelles was synthesized by free radical random copolymerization. The obtained amphiphilic copolymers were self-assembled into micelles, which exhibited thermally sensitivity. LCST of the micelles was detected by uv-vis spectrophotometer. The diameter and morphology of micelles were determined by laser particle size analyzer (LPSA) and transmittance electron microscope (TEM), respectively. The micelle with a diameter of 60 nm and LCST of 40 oC was obtained by utilizing of ODA and the feed ratio of NIPA and AAm, respectively, which is satisfied for drug delivery in living body. The maximum DLC was achieved with the amount of ODA (180mg).

scholarly journals Synthesis of Silver Nanoparticles Using Muntingia Calabura L. Leaf Extract as Bioreductor and Applied as Glucose Nanosensor

2018 ◽  
Vol 34 (6) ◽  
pp. 3088-3094 ◽  
Author(s):  
Abdul Wahid Wahab ◽  
Abdul Karim ◽  
Nursiah La Nafie ◽  
Nurafni Nurafni ◽  
I. Wayan Sutapa
Keyword(s):  
Particle Size ◽  
Silver Nanoparticles ◽  
Reduction Method ◽  
Measurement Range ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Muntingia Calabura

Silver nanoparticles have been synthesized by reduction method using extract of Muntingia calabura L. leaf a bioreductor. The process of silver nanoparticles formation was monitored by UV-Vis method. The results showed that the absorbance values increased according to the increase of reaction time. Maximum absorption of silver nanoparticle was obtained at a wavelength of 41-421 nm. The size of silver nanoparticles was determined using a PSA (Particle Size Analyzer) with a particle size distribution of 97.04 nm. The functional groups compound that contribute in the synthesis was analyzed using Fourier Transform Infrared Spectroscopy (FTIR). Morphology of the silver nanoparticles was observed by an Scanning Electron Microscope instrument and the structure characterization of the compounds were analyzed using X-Ray Diffraction. The glucose nanosensor based on silver nanoparticles have the measurement range of 1 mM - 4 mM with the regretion (R2) is 0,9516, the detection limit of sensor is 3,2595 mM, the sensitivity of sensor is 2,0794 A. mM-1. mM-2.

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