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Tytuł:
CYTOTOXIC ACTIVITY OF VARTHEMIA IPHIONOIDES ESSENTIAL OIL AGAINST VARIOUS HUMAN CANCER CELL LINES
Autorzy:
Abbas, Manal M.
Abbas, Manal A.
Kandil, Yasser I.
Powiązania:
https://bibliotekanauki.pl/articles/895451.pdf
Data publikacji:
2019-08-30
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
apoptosis
cytotoxicity
anticancer
varthemia iphionoides
Opis:
Varthemia iphionoides is a perennial plant that belongs to Asteraceae family. This study investigates the cytotoxic effect of V. iphionoides essential oil on breast (MCF7), prostate (PC3), and chronic myelogenous leukemia (K562) and normal human fibroblast cell lines using MTT assay and flow cytometric analysis. In addition, GC-MS of the oil was carried out. The IC50 values for PC3, MCF7, K562 and fibroblast were 145.3, 188.8, 87.88 and 173.3 µg/ml, respectively. V. iphionoides essential oil was most effective against K562. Flow cytometric results for IC50 dose of V. iphionoides oil on K562 cells showed 32.2 % apoptosis in 24 h. GC-MS analysis resulted in the identification of 25 compounds. 1,8-Cineole, borneol, and α-cadinol were the major constituents of V. iphionoides volatile oil. In conclusion, this study reveals for the first time the cytotoxic activity of V. iphionoides essential oil on K562 cell line which may occur through apoptosis induction.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2019, 76, 4; 701-706
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
DESIGN, SYNTHESIS AND ANTICANCER ACTIVITY EVALUATION OF NEW QUINAZOLINE DERIVATIVES LINKED TO THIAZOLIDINONE, AZETIDINONE OR OXADIAZOL MOIETIES
Autorzy:
Ahmed, Marwa
Magdy, Naja
Powiązania:
https://bibliotekanauki.pl/articles/895415.pdf
Data publikacji:
2018-12-31
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
cytotoxicity
MCF-7
quinazoline
CASP3
Opis:
Novel series of 4-substituted 6,8-dibromo-2-(4-chloro-phenyl)-quinazoline have been designed and synthesized. All new derivatives were tested in vitro against MCF-7. Compounds Xc and XIb exerted powerful cytotoxic activity with low IC50 (6.3 and 6.9 µM) compared to doxorubicin 7.72 µM. Compounds Xa, IXb and IXc showed moderate cytotoxic effects with IC50 range (10.0 – 16.7) µM, respectively. Compounds IXa, XIc, XIa, VIIb, VIIIc, Xb and VIIIa showed promising cytotoxic effects with IC50 range (20.3 – 40 µM, respectively. ). Exploring their apoptotic effect; all compounds activated apoptotic cascade in MCF-7. Compounds Xc and XIb increased CASP3 activity more than doxorubicin.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 6; 1321-1328
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Design, synthesis and biological evaluation of some novel substituted quinazoline derivatives as antitumor agents.
Autorzy:
Ahmed, Marwa
Magdy, Naja
Powiązania:
https://bibliotekanauki.pl/articles/895417.pdf
Data publikacji:
2018-06-30
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
cytotoxicity
quinazoline
Tyrosine kinases
Opis:
New series of 6,8-dibromo-2-(4-chlorophenyl)quinazolin-4-yloxy derivatives were synthesized and their cytotoxic activity on MCF7, HEPG2 and HCT116 cell lines were evaluated. Compound XI and XIIIb were two times more active than doxorubicin on MCF7 cancer cell line. Compound VIIIa was 3 times more active than doxorubicin on HEPG2 cancer cell line. While compounds XII, XIIIa and XIIIb were more potent than doxorubicin on HCT116 cancer cell line. IC50 of all newly synthesized compounds were evaluated in vitro for thier inhibition to EGFR tyrosine kinase. All compound show good inhibitory activity on EGFR tyrosine kinase with IC50 range (6.19-19.87) µM.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 3
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
PREPARATION AND CHARACTERIZATION OF SELF-MICROEMUSIFYING DRUG DELIVERY SYSTEM (SMEDDS) OF CISPLATIN FOR ORAL USE IN OVARIAN CANCER TREATMENT
Autorzy:
Akartas, Irfan
Karasulu, Hatice Yeşim
Powiązania:
https://bibliotekanauki.pl/articles/895344.pdf
Data publikacji:
2020-02-29
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
cytotoxicity
ovarian cancer
cisplatin
SMEDDS
in vitro release
Opis:
Cisplatin is an antineoplastic drug, used for the treatment of ovarian cancer. SMEDDS has many advantages such as enhanced bioavailability, lymphatic targeting and ease of manufacture. The main objective of this study was to prepare and characterize Cisplatin loaded SMEDDS formulation and to evaluate antitumoral activity with cell viability studies. Cisplatin SMEDDS formulation was prepared and characterized physicochemically. In vitro release studies and cell viability studies were performed and evaluated. The mean droplet size of Cisplatin SMEDDS was measured as 25,4±1,9 nm and PDI was 0,241±0,018. Refractive index of the formulation was measured as 1,471±0,001. pH values of Cisplatin SMEDDS (dilution ratio 1:10 w) were measured as 5,84±0,09 and (dilution ratio 1:10 pH 6,8 PBS) 6,51±0,14. Viscosity of formulation was measured as 284 mPa. According to in vitro release studies, %78,17 of Cisplatin were released from Cisplatin SMEDDS. The formulation performed cytotoxic effect to A2780 cells; vitality was found 20,26% at 0,02 µg/mL. It was concluded that, Cisplatin SMEDDS could be beneficial for the treatment of ovarian cancer and it could be promising alternative due to its enhanced bioavailability.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2020, 77, 1; 183-193
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Modulation of Doxorubicin Cytotoxicity by Isoliquiritin and Cynarin Combination on Different Cancer Cell Lines
Autorzy:
Al-AdamI, Salat G.
Al-Khateeb, EKBAL H.
NUMAN, NAWFAL A.
ABBAS, Mannal M.
Tawfiq, FATIMA A.
Shakya, Ashok K.
Powiązania:
https://bibliotekanauki.pl/articles/895633.pdf
Data publikacji:
2020-06-29
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
cytotoxicity
doxorubicin
cancer cells
Modulation
Cynarin
Isoliquiritin
Opis:
Natural polyphenolic compounds produced by plant exhibit many pharmacological effects including antioxidant, chemopreventive as well as anticancer properties. This study was conducted to investigate the effect of cynarin ( from Artichoke, Cynara scolymus) and isoliquiritin (from Licorice, Glycyrrhiza uralensis) on doxorubicin (positive control) cytotoxicity in different cell lines including normal (Fibroblasts MCR-5 and Myoblasts H9c2) and cancer (colorectal HCT-116 and hepatocellular HEP-G2) cell lines. The cytotoxic effect of doxorubicin, isoliquiritin and cynarin alone or in different combination was studied on cancer cell lines as well as normal cell lines. The results obtained indicated that both cynarin and isoliquiritin enhance the cytotoxicity of doxorubicin. Both cynarin and isoliquiritin also reduce the cardiotoxicity of doxorubicin on normal cardiac cell lines. The combination of the three compounds (cynarin, isoliquiritin and doxorubicin) result in decrease the cytotoxicity of doxorubicin, which may indicate the presence of interaction and/or antagonism effect between cynarin and isoliquiritin. Cynarin was found to enhance the growth of (HCT-116 and HEP-G2) this might suggest avoiding use of Artichoke in subjects’ susceptibility for these cancers. All results were evaluated using statistical path and showed significant findings. The mechanism of enhanced doxorubicin’s cytotoxicity by cynarin or isoliquiritin also require further investigation to explain the increasing and/or the decreasing effect of these polyphenolic compounds on cytotoxicity of doxorubicin. The current finding can help to start with safe minimum dose of two or three combination of compounds in the context of clinical trials and practice.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2020, 77, 3; 475-484
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Anti-tumor agents: Design, Synthesis, and Biological study of N-Substituted-7-hydroxy-1-azacoumarin-3-carboxamide derivatives as potent cytotoxic agents
Autorzy:
Bakare, Safyah B.
Powiązania:
https://bibliotekanauki.pl/articles/1849341.pdf
Data publikacji:
2021
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
azacoumarin-3-carboxamide
cytotoxicity
1H
13C-NMR
spectraMCF-7
Opis:
Synthesis of ethyl 7-hydroxy-1-azacoumarin-3-carboxylate (3) was developed using ethyl-7-hydroxy coumarin-3-carboxylate and ammonium solution as the key synthons. Condensation of ethyl 7-hydroxy-1-azacoumarin-3-carboxylate with ammonium acetate and aniline to give N-substituted-7-hydroxy-1-azacoumarin-3-carboxamides (7-Hydroxy -1-azacoumarin-3-carboxamide (4) and N-phenyl 7-Hydroxy-1-azacoumarin-3-carboxamide (5)). Bromo derivative (N-phenyl 6, 8-dibromo-7-hydroxy-1-azacoumarin-3-carboxamide (6)) was obtained from halogenation of compound N-phenyl 7-Hydroxy-1-azacoumarin-3-carboxamide (5) with bromine in glacial acetic acid. N-phenyl-2,5-diacetoxy-6, 8-disubstituted-Quinoline-3-carboxamides (N-phenyl 2,7-diacetoxy-Quinoline-3-carboxamide (7) and N-phenyl 2,7-diacetoxy-6,8-dibromo-Quinoline-3-carboxamide (8)) were prepared via the acetylation of compounds 5 and 6 with acetic anhydride. Five compounds 4–8 were evaluated in vitro against more than one human tumor cell lines. Among the selected compounds, 6 showed the best in vitro cytotoxicity against the human cancer cell line; MCF-7 (with IC50 = 10.12 μM). In addition, cell cycle analysis of compound 6 demonstrated cell cycle arrest at G2/M phase and Pre-G1 apoptosis.
Źródło:
Polish Journal of Chemical Technology; 2021, 23, 1; 53-59
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Validation of a flow cytometry-based assay for monitoring complement-dependent cytotoxicity of an anti-CD20 biosimilar candidate antibody
Autorzy:
Blanco-Santana, R.
Cedeno-Arias, M.
Garcia-Perez, Z.
Columbie-Gilbert, D.
Portillo-Vaquer, A.
Rengifo-Calzado, E.
Powiązania:
https://bibliotekanauki.pl/articles/80888.pdf
Data publikacji:
2014
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
flow cytometry
validation
complement-dependent cytotoxicity
monoclonal antibody
CD20 antigen
biological activity
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2014, 95, 1
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Influence of G arrest on the cytotoxicity of DNA topoisomerase inhibitors toward human carcinoma cells with different p53 status.
Autorzy:
Bozko, Przemyslaw
Larsen, Annette
Raymond, Eric
Skladanowski, Andrzej
Powiązania:
https://bibliotekanauki.pl/articles/1043815.pdf
Data publikacji:
2002
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
cytotoxicity
UCN-01
p53
DNA topoisomerase inhibitors
G2 arrest
Opis:
We here report the influence of the cell cycle abrogator UCN-01 on RKO human colon carcinoma cells differing in p53 status following exposure to two DNA damaging agents, the topoisomerase inhibitors etoposide and camptothecin. Cells were treated with the two drugs at the IC90 concentration for 24 h followed by post-incubation in drug-free medium. RKO cells expressing wild-type, functional p53 arrested the cell cycle progression in both the G1 and G2 phases of the cell cycle whereas the RKO/E6 cells, which lack functional p53, only arrested in the G2 phase. Growth-arrested cells did not resume proliferation even after prolonged incubation in drug-free medium (up to 96 h). To evaluate the importance of the cell cycle arrest on cellular survival, a non-toxic dose of UCN-01 (100 nM) was added to the growth-arrested cells. The addition of UCN-01 was accompanied by mitotic entry as revealed by the appearance of condensed chromatin and the MPM-2 phosphoepitope, which is characteristic for mitotic cells. G2 exit and mitotic transit was accompanied by a rapid activation of caspase-3 and apoptotic cell death. The influence of UCN-01 on the long-term cytotoxic effects of the two drugs was also determined. Unexpectedly, abrogation of the G2 arrest had no influence on the overall cytotoxicity of either drug. In contrast, addition of UCN-01 to cisplatin-treated RKO and RKO/E6 cells greatly increased the cytotoxic effects of the alkylating agent. These results strongly suggest that even prolonged cell cycle arrest in the G2 phase of the cell cycle is not necessarily coupled to efficient DNA repair and enhanced cellular survival as generally believed.
Źródło:
Acta Biochimica Polonica; 2002, 49, 1; 109-119
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Stimulatory effects of single low-level irradiations with X-rays on functions of murine peritoneal macrophages
Autorzy:
Cheda, A.
Wrembel-Wargocka, J.
Nowosielska, E.
Janiak, M.
Powiązania:
https://bibliotekanauki.pl/articles/147798.pdf
Data publikacji:
2005
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
low doses
X-rays
macrophages
nitric oxide
cytotoxicity
TNF-alfa
Opis:
A number of epidemiological and experimental data indicate that exposures to low doses of low-LET ionising radiation may trigger the activity of natural anti-tumour immune mechanisms and inhibit tumour growth. In the present study, we assessed the cytotoxic activity and production of nitric oxide, superoxide anions, and tumour necrosis factor-alfa in peritoneal macrophages collected from BALB/c mice exposed to single whole-body irradiations with 0.1, 0.2, or 1.0 Gy X-rays. The results indicate that all the tested parameters were significantly up-regulated in macrophages obtained from mice exposed to 0.1 or 0.2 Gy X-rays but not in those collected from the sham-irradiated and 1.0 Gy-exposed animals.
Źródło:
Nukleonika; 2005, 50,suppl.2; 13-16
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
In vitro assay of the biological activity of bisphosphonates
Autorzy:
Chmielewska, E.
Miszczyk, P.
Kafarski, P.
Kempińska, K.
Wietrzyk, J.
Powiązania:
https://bibliotekanauki.pl/articles/1190037.pdf
Data publikacji:
2015
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
bisfosfoniany
cytotoksyczność
in vitro
aktywność biologiczna
inhibitor
bisphosphonates
cytotoxicity
biological activity
Opis:
Nowadays, the use of bisphosphonates are the gold standard of treatment of bone diseases. Due to the high utility of these compounds, scientists still search for better and better structures, with a variety of substituents at carbon’s atom and create new libraries or improve methods of their synthesis. To determine the potential effect of newly discovered bisphosphonates, for example antiosteoporotic activity, there are in vitro tests which allow to determine the half maximal inhibitory concentrations (IC50) of cells. This paper describes in detail the methodology for test the biological activity of bisphosphonates. Shows the results of biological activity for synthesized bisphosphonates in relation to the commercial-incadronate and zoledronate.
Źródło:
Interdisciplinary Journal of Engineering Sciences; 2014, 2, 1; 13--16
2300-5874
Pojawia się w:
Interdisciplinary Journal of Engineering Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bioeffects of silver nanoparticles (AgNPs) synthesized by producer of biosurfactant Bacillus subtilis strain : in vitro cytotoxicity, antioxidant properties and metabolic activities of mammalian cells
Autorzy:
Chojniak-Gronek, Joanna Małgorzata
Jałowiecki, Łukasz
Płaza, Grażyna Anna
Powiązania:
https://bibliotekanauki.pl/articles/2203138.pdf
Data publikacji:
2022
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
green synthesis
bio-AgNPs
in vitro cytotoxicity
antioxidant properties
PM-Ms
Biolog system
Opis:
The present study is focused on the evaluation of bioeffects of silver nanoparticles (AgNPs) synthesized by Bacillus subtilis strain I’-1a, the producer of iturin A lipopeptide biosurfactant. The following properties of biologically synthesized silver nanoparticles (bio-AgNPs) were evaluated: in vitro cytotoxicity, antioxidant properties, and metabolic activities of mammalian cells. As a control, chemically synthesized silver nanoparticles (chem-AgNPs) were used. In vitro, antioxidant activity of bio-AgNPs showed a significant effect on the scavenging of free radicals. Bio-AgNPs can be potent natural antioxidants and can be essential for health preservation against oxidative stress-related degenerative diseases, such as cancer. The cell viability of human skin fibroblasts NHDF was remarkably inhibited in the presence of both AgNPs. However, bio-AgNPs were more active than chem-AgNPs. In our experiment, microarrays PM-M1–PM-M4 were used to evaluate the growth of NHDF fibroblast cells in the presence of bio-AgNPs and chem-AgNPs. The NHDF fibroblast cells were more active in the presence of bio-AgNPs than in chem-AgNPs. Probably, the presence of biosurfactant produced by Bacillus subtilis I’-1a significantly increased the stability of biogenic AgNPs and enhanced their biological activities and specific interaction with human DNA. Furthermore, the evaluated biological activities were enhanced for the biosurfactant-based AgNPs.
Źródło:
Archives of Environmental Protection; 2022, 48, 4; 45--52
2083-4772
2083-4810
Pojawia się w:
Archives of Environmental Protection
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Material Production and the Effect of the System on Biocompatibility in the Modified Metal Injection Method
Autorzy:
Çiçek, Bünyamin
Sun, Yavuz
Powiązania:
https://bibliotekanauki.pl/articles/2203740.pdf
Data publikacji:
2023
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
metal injection molding
stainless steel
polymer
biomaterial
cytotoxicity
Opis:
In this study, the bio state of the alloy produced in the modified metal injection system was monitored after sintering. A new system operating with high gas pressure, far from the traditional injection model, has been established for material production. In this system, 316L stainless steel powders were molded using a PEG/PMMA/SA polymer recipe. During molding, approximately 60% 316L and 40% binder by volume were used. The samples obtained were sintered at different temperatures (1100-1300°C) after de-binding. Density measurement (Archimedes) and hardness tests (HV1) of the samples were measured as 6.74 g/cm3 and ~285 HV1, respectively. A potentiodynamic corrosion test was applied to monitor the effect of the amount of oxide in the structure of the 316L stainless steel produced. Corrosion tests were carried out in artificial body solutions. The corrosion rate was measured at the level of 17.08×10-3 mm/y. In terms of biocompatibility, a cytotoxicity test was applied to the samples and the life course of the bacteria was monitored. For the 316L alloys produced, the % vitality reached approximately 103%.
Źródło:
Archives of Metallurgy and Materials; 2023, 68, 1; 195--204
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Ocena cytotoksyczności kopolimeru glikolidu z laktydem (PLGA) w warunkach in vitro
Cytotoxicity of polylactide-co-glycolide (PLGA) - evaluation in vitro
Autorzy:
Cieślik, M.
Król, W.
Mertas, A.
Morawska-Chochół, A.
Ziąbka, M.
Chłopek, J.
Powiązania:
https://bibliotekanauki.pl/articles/284968.pdf
Data publikacji:
2008
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
biomateriały
kopolimer PLGA
cytotoksyczność
test MTT
test LDH
osteoblasty ludzkie
badania biologiczne
biomaterials
copolymer PLGA
cytotoxicity
MTT assay
LDH assay
human osteoblasts
biological evaluations
Opis:
Celem pracy była ocena in vitro cytotoksycznego działania bioresorbowalnego kopolimeru glikolidu z laktydem (PLGA) na ludzkie osteoblasty linii hFOB 1.19 poprzez pomiar aktywności dehydrogenazy mitochondrialnej (test MTT) oraz dehydrogenazy mleczanowej (test LDH). Do badań użyto ekstrakt uzyskany po 8 dniach inkubacji kopolimeru PLGA w medium wykorzystywanym do hodowli osteoblastów. Ekstrakt ten następnie kontaktowano przez 24 oraz 48 godziny z zaadherowanymi do dna naczynia hodowlanego osteoblastami. Po upływie założonego czasu inkubacji zarówno test MTT, jak i test LDH nie wykazał cytotoksycznego działania kopolimeru PLGA na ludzkie komórki kościotwórcze.
The aim of the work was to evaluate in vitro the cytotoxic effect of bioresorbable polylactide-co-glycolide (PLGA) on the hFOB 1.19 human osteoblastic cell line by measuring the activity of mitochondrial dehydrogenase (MTT test) and lactate dehydrogenase (LDH test). The research made use of an extract obtained after 8 days of PLGA incubation in a medium used for osteoblast culturing. The extract was then brought into contact with osteoblasts adhered to the bottom of the culture vessel for 24 and 48 hours. After the set incubation time neither the MTT test nor the LDH test showed a cytotoxic effect of PLGA on human osteogenic cells.
Źródło:
Engineering of Biomaterials; 2008, 11, no. 81-84; 35-39
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Pozaustrojowe badania nad toksycznym oddziaływaniem kopolimeru PLGA z dodatkiem hydroksyapatytu na ludzkie osteoblasty linii hFOB 1.19
In vitro examinations of toxic influence of PLGA co-polymer mixed with hydroxyapatite upon human osteoblasts line hFOB 1.19
Autorzy:
Cieślik, M.
Mertas, A.
Morawska-Chochół, A.
Orlicki, R.
Owczarek, A.
Król, W.
Powiązania:
https://bibliotekanauki.pl/articles/286207.pdf
Data publikacji:
2009
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
kompozyt
kopolimer glikolidu z laktydem
hydroksyapatyt
cytotoksyczność
test MTT
test LDH
osteoblasty ludzkie
badania in vitro
composite
lactide-glycolide co-polymer
hydroxyapatite
cytotoxicity
MTT test
LDH test
human osteoblasts
in vitro examinations
Opis:
W celu biologicznej oceny w warunkach in vitro kopolimeru glikolidu z laktydem z dodatkiem hydroksyapatytu (PLGA+HA) dokonano oceny stopnia jego cytotoksyczności względem ludzkich osteoblastów linii hFOB 1.19. Wykonano pomiar aktywności dehydrogenazy mitochondrialnej (test MTT) oraz dehydrogenazy mleczanowej (test LDH) po 24 i 48 godzinach kontaktu komórek z ekstraktem uzyskanym poprzez 8-dniową inkubację kompozytu w medium do hodowli osteoblastów. Kontaktowano ponadto badany materiał bezpośrednio z komórkami kościotwórczymi, a stopień cytotoksyczności oceniano po 24, 48 i 72 godzinach stosując w tym celu test LDH. W obu metodach badany materiał nie wpływał w sposób toksyczny na ludzkie osteoblasty.
In order to evaluate lactide-glycolide co-polymer with admixture of hydroxyapatite (PLGA+HA) from biological point of view in vitro conditions, its level of toxicity for human osteoblasts line hFOB 1.19 was assessed. The activity of mitochondrial dehydrogenase and lactate dehydrogenase was measured (MTT test and LDH test respectively) after 24 and 48 hours of the cells’ contact with the extract obtained through 8-day incubation of the composite in osteoblasts cultivation medium. Apart from that the material examined was contacted with bone-forming cells and its degree of toxicity was assessed after 24, 48 and 72 hours using LDH test. In both methods the material under examination did not have any toxic influence upon human osteoblasts.
Źródło:
Engineering of Biomaterials; 2009, 12, no. 89-91; 98-102
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Wpływ wzmocnionego włóknami węglowymi kopolimeru glokolidu z laktydem na odpowiedź komórkową
The impact of polylactide-co-glycolide reinforced with carbon fibres on cellular response
Autorzy:
Cieślik, M.
Król, W.
Mertas, A.
Morawska-Chochół, A.
Ziąbka, M.
Chłopek, J.
Powiązania:
https://bibliotekanauki.pl/articles/285677.pdf
Data publikacji:
2008
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
biomateriały
kopolimer PLGA
włókna węglowe
cytotoksyczność
test MTT
test LDH
osteoblasty ludzkie
badania biologiczne
biomaterials
copolymer PLGA
carbon fibres
cytotoxicity
MTT assay
LDH assay
human osteoblasts
biological evaluations
Opis:
W pracy dokonano oceny cytotoksycznego wpływu wzmocnionego włóknami węglowymi kopolimeru glikolidu z laktydem (PLGA+CF) na ludzkie osteoblasty linii hFOB 1.19. Przeprowadzono w tym celu pomiar aktywności dehydrogenazy mitochondrialnej metodą MTT oraz dehydrogenazy mleczanowej (test LDH) w warunkach in vitro. Oba testy nie wykazały toksycznego działania badanego kompozytu na ludzkie komórki kościotwórcze.
This work evaluates the cytotoxic impact of poly-lactide-co-glycolide reinforced with carbon fibres (PLGA+CF) on the hFOB 1.19 human osteoblastic cell line. To this end the levels of miochondrial dehydrogenase (MTT method) and lactate dehydrogenase (LDH test) were measured in vitro. Neither test showed a toxic effect of the studied composite on the human osteogenic cells.
Źródło:
Engineering of Biomaterials; 2008, 11, no. 81-84; 40-44
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Wyświetlanie 1-15 z 114

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