Synthesis and Characterization of Hydroxyapatite Powder from Natural Gypsum Rock

2014 ◽  
Vol 893 ◽  
pp. 56-59 ◽  
Author(s):  
Eko Pujiyanto ◽  
Pringgo Widyo Laksono ◽  
Joko Triyono
Keyword(s):  
Crystal Size ◽  
Vero Cells ◽  
Bone Substitutes ◽  
In Vitro Cytotoxicity ◽  
Mtt Method ◽  
Hydroxyapatite Powder ◽  
Gypsum Rock ◽  
Xrd Patterns

This study prepared hydroxyapatite powder that synthesized from natural gypsum rock and find out physicalchemical and cytotoxicity properties. The synthesis realized by reacting natural gypsum powder with 1M of (NH4)2HPO4 solutions using a microwave. Characterizations of natural gypsum powder and hydroxyapatite powder were conducted by XRD, XRF and SEM. In vitro cytotoxicity testings of hydroxyapatite powder were conducted by MTT method using vero cells. XRD patterns of gypsum powder closed to JCPDF 33-0311 (gypsum standard). Characteristics of gypsum powder i.e. contained 41.72% CaO, level of purity 91,6 % and crystal size 7,147 nm. Charateristic of hydroxyapatite powder that synthesized from natural gypsum powder i.e. contained 46.91% CaO and 40.20% P2O5, XRD patern closed to JCPDF 09-432 (hydroxyapatite standard), level of purity 99 % and crystal size 1.243 nm. There were not significantly difference in cytotoxicity properties of hydroxyapatite powder that synthesized from natural gypsum rock and commercial hydroxyapatite powder (p= 0.086). These results indicated hydroxyapatite powder that synthesized from natural gypsum rock possible to be used as bone substitutes.

scholarly journals In vitro cytotoxicity of Aspilia pluriseta Schweinf. extract fractions

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Sospeter N. Njeru ◽  
Jackson M. Muema
Keyword(s):  
Biological Activities ◽  
Vero Cells ◽  
In Vitro Cytotoxicity ◽  
Root Extract ◽  
Lack Of Information ◽  
Information Gap ◽  
Diphenyltetrazolium Bromide ◽  
Potential Use

Abstract Objectives We and others have shown that Aspilia pluriseta is associated with various biological activities. However, there is a lack of information on its cytotoxicity. This has created an information gap about the safety of A. pluriseta extracts. As an extension to our recent publication on the antimicrobial activity and the phytochemical characterization of A. pluriseta root extracts, here we report on cytotoxicity of tested solvent fractions. We evaluated the potential cytotoxicity of these root extract fractions on Vero cell lines by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Results We show that all solvent extract fractions (except methanolic solvent fractions) had cytotoxic concentration values that killed 50% of the Vero cells (CC50) greater than 20 µg/mL and selectivity index (SI) greater than 1.0. Taken together, we demonstrate that, A. pluriseta extract fractions’ earlier reported bioactivities are within the acceptable cytotoxicity and selective index limits. This finding scientifically validates the potential use of A. pluriseta in the discovery of safe therapeutics agents.

scholarly journals In Vitro Cytotoxicity of Aspilia Pluriseta Schweinf. Extract Fractions

2020 ◽  
Author(s):  
Sospeter Ngoci Njeru ◽  
Jackson Mbithi Muema
Keyword(s):  
Biological Activities ◽  
Vero Cells ◽  
In Vitro Cytotoxicity ◽  
Root Extracts ◽  
Lack Of Information ◽  
Information Gap ◽  
Diphenyltetrazolium Bromide ◽  
Potential Use

Abstract Objectives: We and others have shown that Aspilia pluriseta is associated with various biological activities. However, there is a lack of information on A. pluriseta cytotoxicity. This has created an information gap about the safety of A. pluriseta extracts. As an extension to our recent publication on the antimicrobial activity and the phytochemicals characterization of A. pluriseta root extracts, here we report the missing data on cytotoxicity of tested extracts. We evaluated the potential cytotoxicity of the root extracts on Vero cell lines by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Results: We show that all solvent extracts (except methanolic solvent fractions) had cytotoxic concentration values that killed 50% of the Vero cells (CC50) greater than 20 µg/mL and selectivity index (SI) of greater than 1.0. Taken together, we demonstrate that, A. pluriseta extract fractions’ earlier reported bioactivity are within the acceptable cytotoxicity and selective index limits. This scientifically validates the potential use of A. pluriseta in the discovery of safe therapeutics agents.

Up-conversion emission and in vitro cytotoxicity characterization of blue emitting, biocompatible SrTiO3 nanoparticles activated with Tm3+ and Yb3+ ions

RSC Advances ◽  
2016 ◽  
Vol 6 (45) ◽  
pp. 39469-39479 ◽  
Author(s):  
R. Pazik ◽  
A. Zięcina ◽  
B. Poźniak ◽  
M. Malecka ◽  
L. Marciniak ◽  
...  
Keyword(s):  
Particle Size ◽  
Cytotoxic Effect ◽  
In Vitro Cytotoxicity ◽  
Ion Release ◽  
Size Dependent ◽  
U2os Cells

Blue emitting, up-converting NP's of SrTiO3:Tm3+/Yb3+ synthesized using the citric route are biocompatible towards J774.E whereas the cytotoxic effect to U2OS cells is not particle size dependent but most probably is related to Sr2+ ion release.

Chitosan nanoparticles for tamoxifen delivery and cytotoxicity to MCF-7 and Vero cells

2011 ◽  
Vol 83 (11) ◽  
pp. 2027-2040 ◽  
Author(s):  
Neralakere Ramanna Ravikumara ◽  
Basavaraj Madhusudhan
Keyword(s):  
Particle Size ◽  
Chitosan Nanoparticles ◽  
Vero Cells ◽  
In Vitro Cytotoxicity ◽  
Correlation Spectroscopy ◽  
Scanning Calorimetry ◽  
Ζ Potential ◽  
Human Red Blood Cells ◽  
Tamoxifen Citrate

In this study, tamoxifen citrate-loaded chitosan nanoparticles (tamoxcL-ChtNPs) and tamoxifen citrate-free chitosan nanoparticles (tamoxcF-ChtNPs) were prepared by an ionic gelation (IG) method. The physicochemical properties of the nanoparticles were analyzed for particle size, zeta (ζ) potential, and other characteristics using photon correlation spectroscopy (PCS), zeta phase analysis light scattering (PALS), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), and differential scanning calorimetry (DSC). The variation in particle size was assessed by changing the concentration of chitosan, pentasodium tripolyphosphate (TPP), and the pH of the solution. The optimized tamoxcL-ChtNPs showed mean diameter of 187 nm, polydispersity of 0.125, and ζ-potential of +19.1 mV. The encapsulation efficiency (EE) of tamoxifen citrate (tamoxc) increased at higher concentrations, and release of tamoxc from the chitosan matrix displayed controlled biphasic behavior. Those tamoxcL-ChtNPs tested for chemosensitivity showed dose- and time-dependent antiproliferative activity of tamoxc. Further, tamoxcL-ChtNPs were found to be hemocompatible with human red blood cells (RBCs) and safe by in vitro cytotoxicity tests, suggesting that they offer promise as drug delivery systems in therapy.

scholarly journals Preparation and Characterization of Chitosan obtained from Pacific White Shrimp Shells and its in vitro Antifungal Activity

2020 ◽  
Vol 32 (10) ◽  
pp. 2515-2519
Author(s):  
Arnannit Kuyyogsuy
Keyword(s):  
Pacific White Shrimp ◽  
White Shrimp ◽  
X Ray Diffraction ◽  
Vitro Assay ◽  
Shrimp Shells ◽  
Xrd Patterns ◽  
Two Peaks ◽  
In Vitro Antifungal Activity

In this article, a method for the processing of chitosan from Pacific white shrimp shells is developed which involves three steps viz. demineralization, deproteinization, and deacetylation. The samples of chitosan with more than 90% degree of deacetylation (DD%) were obtained by FTIR. This indicated that the current processing method of shrimp shells was beneficial for chitosan production. The morphology of chitosan sample was determined using scanning electron microscopy (SEM). X-ray diffraction (XRD) patterns exhibited two peaks of crystalline character approximately at 10º and 20º (2θ). The effect of 0.1% (w/v) of chitosan on the growth of Penicillium digitatum was tested by an in vitro assay and the results showed an almost complete inhibition (98% ± 0.56).

Isolation and characterization of toxoplasma exo-antigens from In vitro culture in MRC5 and vero cells

1987 ◽  
Vol 17 (3) ◽  
pp. 829-834 ◽  
Author(s):  
Bernabe Chumpitazi ◽  
Pierre Ambroise-Thomas ◽  
Maryvonne Cagnard ◽  
Jean M. Autheman
Keyword(s):  
In Vitro Culture ◽  
Vero Cells ◽  
Isolation And Characterization

scholarly journals Plasmodium falciparum: In Vitro Cytotoxicity Testing Using MTT

1998 ◽  
Vol 3 (1) ◽  
pp. 49-53 ◽  
Author(s):  
J. Enrico Lazaro ◽  
Frederick Gay
Keyword(s):  
Plasmodium Falciparum ◽  
Culture System ◽  
Inhibitory Concentration ◽  
In Vitro Cytotoxicity ◽  
Mtt Method ◽  
Diphenyltetrazolium Bromide ◽  
Wide Range ◽  
In Vitro Culture System ◽  
Comparative Results

The microculture tetrazolium assay using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) was used to estimate the 50% inhibitory concentration of chloroquine, quinine, artemisinin, and atovaquone using a Plasmodium falciparum in vitro culture system. The MTT assay was compared to the standard tritiated hypoxan-thine assay and to a previously described method, the 2,2′-di-p-nitrophenyl-5,5′-diphenyl-3,3′-[3,3′-dimethoxy-4,4′-diphenylenel-ditetrazolium chloride (NBT) assay. In general, the results show that the three assays generate comparative results. The results of this study suggest that the MTT method is able to give a profile of cytotoxic dose response effects over a wide range of concentrations of a drug. The method may be used in work that does not require extreme pre-cision and sensitivity, for instance, as a portable rapid screen to assay natural products for in vitro cytotoxic ac-tivity against Plasmodium falciparum.

3D Microtomography Characterization of Dental Implantology Bone Substitutes Used In Vivo

2013 ◽  
Vol 541 ◽  
pp. 97-113 ◽  
Author(s):  
Rossella Bedini ◽  
Deborah Meleo ◽  
Raffaella Pecci
Keyword(s):  
Bone Substitute ◽  
Histological Analysis ◽  
Research Work ◽  
Bone Substitutes ◽  
Human Bone ◽  
Histological Techniques ◽  
In Vitro Characterization

After a short introduction to bone substitute biomaterials and X-ray microtomography, this article describes a research work carried out for in-vitro characterization of bone substitute biomaterials as well as for in-vivo investigation of human bone grafted with biomaterials. Three different bone substitute biomaterials have been analyzed in-vitro by means of 3D microtomographic technique, while human bone samples grafted with bone substitute biomaterials are investigated by 3D microtomography and histological techniques. 3D images of bone substitutes and human bone samples with biomaterials have been obtained, together with morphometric parameters, by microtomography . 2D histological images have also been obtained by traditional technique only for human bone samples with biomaterials. Compared to traditional histological analysis, 3D microtomography shows better results for investigating bone tissue and bone substitute biomaterial, and in a short time. Nevertheless, histological analysis remains the best technique for the observation of soft tissue and blood vessels.

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