Farklı tipteki aljinat dental ölçü maddelerinin sitotoksisite yönünden değerlendirilmesi

Purpose: The aim of this study was to assess the cytotoxicity of different types of alginate impression materials. Material and Method: Cavex CA37, A3KROM, ALGINPLUS FAST ve ORALGHINE alginate impression materials were used. According to the manufacturer’s instructions, alginates were mixed with serum physiological to obtain alginate specimens. Specimens were performed in sterile with ethylene oxide gas and then placed on to the L929 fibroblast cell culture. According to the 1999 ISO 10993-5 protochols, cytotoxicity were determined by means of agar overley test. Results: According to the lisis of the cells, ORALGH<NE and Cavex CA37; 4-4-4-5-5, ALGINPLUS and A3KROM; 2-3-3-3-2 were determined. Values of the cytotoxicity were determined 4,4 for ORALGH<NE and Cavex CA37, whereas 2,6 for ALGINPLUS and A3KROM. Conclusion: Cytotoxicity degree of the alginates were different because of the composition of the alginates. It was determined that ORALGHINE and Cavex CA37 were severely cytotoxic, ALGINPLUS and A3KROM were moderately cytotoxic. ÖZET Amaç: Bu in vitro çalışmanın amacı, farklı tipteki aljinat ölçü maddelerini sitotoksisite yönünden değerlendirmektir. Gereç ve Yöntem: Farklı tipteki dört aljinat, Cavex CA37, A3KROM, ALGINPLUS FAST ve ORALGHINE, üretici firmaların talimatlar doğrultusunda belirtilen oranlarda, serum fizyolojik ile karıştırılarak aljinat numuneleri hazırlandı. Hazırlanan numuneler etilen oksit gazıyla steril edildi ve L929 fibroblast hücre serisi kullanılarak elde edilen kültüre yerleştirildi. Agar overley testi kullanılarak sitotoksisitenin belirlenmesinde ISO 1999 yıl 10993-5 numaral protokolü takip edildi. Bulgular: Hücrelerin lizis miktarına göre yapılan puanlama değerleri ORALGHINE ve Cavex CA37 için; 4-4-4-5-5, ALGINPLUS ve A3KROM için; 2-3-3-3-2 olarak tespit edildi. Sitotoksisite değerleri de ORALGHINE ve Cavex CA37 için 4.4, ALGINPLUS ve A3KROM için ise 2.6 olarak bulundu. Sonuçlar: İçerik farklılığına bağlı olarak aljinatlarn sitotoksisite değerleri farklılık göstermiştir. ORALGHINE ve Cavex CA37’nin belirgin derecede sitotoksik olduğu, ALGINPLUS ve A3KROM’ un ise makul derecede sitotoksik olduğu belirlendi. Anahtar kelimeler: Sitotoksisite, aljinat

A nationwide multicentre study in Turkey for establishing reference intervals of haematological parameters with novel use of a panel of whole blood

IntroductionA nationwide multicentre study was conducted to establish well-defined reference intervals (RIs) of haematological parameters for the Turkish population in consideration of sources of variation in reference values (RVs). Materials and methodsK2-EDTA whole blood samples (total of 3363) were collected from 12 laboratories. Sera were also collected for measurements of iron, UIBC, TIBC, and ferritin for use in the latent abnormal values exclusion (LAVE) method. The blood samples were analysed within 2 hours in each laboratory using Cell Dyn and Ruby (Abbott), LH780 (Beckman Coulter), or XT-2000i (Sysmex). A panel of freshly prepared blood from 40 healthy volunteers was measured in common to assess any analyser-dependent bias in the measurements. The SD ratio (SDR) based on ANOVA was used to judge the need for partitioning RVs. RIs were computed by the parametric method with/without applying the LAVE method. ResultsAnalyser-dependent bias was found for basophils (Bas), MCHC, RDW and MPV from the panel test results and thus those RIs were derived for each manufacturer. RIs were determined from all volunteers’ results for WBC, neutrophils, lymphocytes, monocytes, eosinophils, MCV, MCH and platelets. Gender-specific RIs were required for RBC, haemoglobin, haematocrit, iron, UIBC and ferritin. Region-specific RIs were required for RBC, haemoglobin, haematocrit, UIBC, and TIBC. ConclusionsWith the novel use of a freshly prepared blood panel, manufacturer-specific RIs’ were derived for Bas, Bas%, MCHC, RDW and MPV. Regional differences in RIs were observed among the 7 regions of Turkey, which may be attributed to nutritional or environmental factors, including altitude

Cytotoxicity evaluation of methacrylate- and silorane-based composite resins

<p><strong>Objectives:</strong> The objective of this study was to investigate and compare the cytotoxic effects of four composite resin materials with different content.</p> <p><strong>Material and Methods: </strong>Two traditional methacrylate-based (Clearfil AP-X, RefleXions), as well as a self-adhering methacrylate-based (Vertise Flow) and a silorane-based (Filtek Silorane) composite resin were tested in the experiment. Ten cylindrical specimens were made of each material, using a mould (2mm. thick and 8 mm. in diameter). An agar diffusion method was employed, and cytotoxicity rankings were determined using lysis index scores. For statistical analysis, Kruskal-Wallis and Mann-Whitney U-tests were used.</p> <p><strong>Results:</strong> Amongst the composite resins, the silorane-based composite was found to be less cytotoxic than the methacrylate-based composite resins, which all had the same cytotoxicity ranking.</p> <p><strong>Conclusions:</strong> The silorane-based composite resin was considered more biocompatible than the methacrylate-based composite resins.</p&gt

Synthesis, characterization, and assessment of cytotoxic, antiproliferative, and antiangiogenic effects of a novel procainamide hydrochloride-poly (maleic anhydride-co-styrene) conjugate

Poly(maleic anhydride-co-styrene) (MAST) was synthesized by a free-radical polymerization reaction. A bioactive molecule, procainamide hydrochloride (PH), was then conjugated to MAST. The conjugation product was named as MAST/PH. Structural characterization of MAST and MAST/PH was carried out by Fourier Transform Infrared and Nuclear Magnetic Resonance spectroscopy. Their molecular weights were determined by size-exclusion chromatography. A mechanism was then suggested for the conjugation reaction. The results of the cytotoxicity assay, employing a mouse fibroblast cell line (L929), indicated that MAST/PH had no cytotoxicity at concentrations 662 μgmL 1 (p > 0.05). Antiproliferative activities of MAST/PH and PH were determined by the BrdU cell proliferation ELISA assay, using C6 and HeLa cell lines. In the experiment, two anticancer chemotherapy drugs, cisplatin and 5-fluorouracil, were included as positive control. Antiproliferative activity results demonstrated that MAST/PH yielded the highest suppression profile (approximately 42%) at 20 μg/ml, while free PH exerted the same activity at 100 μg/ml. Interestingly, both MAST/PH and PH suppressed the proliferation of only one of the cell lines, C6 cells. Both cisplatin and 5-fluorouracil yielded approximately 60% antiproliferative activity on C6 cells at 20 and 100 μg/ml concentrations. Antiangiogenic capacity of both MAST and MAST/PH was also investigated by using the chicken chorioallantoic membrane assay. Results obtained indicated that while MAST/PH could be included into the category of good antiangiogenic substances, the activity score of MAST was within the weak category

Cytotoxicity of three maleic anhydride copolymers and common solvents used for polymer solvation

Three maleic anhydride copolymers were synthesized by free-radical copolymerization. The synthesized products were named as follows: maleic anhydride-styrene (MAST); maleic anhydride-vinyl acetate (MAVA), and maleic anhydride-methyl methacrylate (MAMMA). Initiators used in the reactions were azobisisobutyronitrile (AIBN, 70 A degrees C, benzene) for MAST and benzoyl-peroxide [BPO, 80 A degrees C, methyl ethyl ketone (MEK)] for MAVA and MAMMA. Structural characterizations were carried out by Fourier transform infrared (FTIR) and nuclear magnetic resonance [H-1 NMR, C-13 NMR, and C-13-APT (attached-proton test)] spectrometry. Surface morphology was studied by scanning electron microscopy (SEM). Solubility of the copolymers was examined in water and in twelve different organic solvents. Cytotoxicity of the copolymers and the solvents was evaluated by using a mouse fibroblast cell line (L929), copolymers had almost no toxicity. Of the twelve organic solvents, acetone, MEK, and tetrahydrofuran (THF) produced the least toxicity. MEK was found to be the best solvent and used for the solvation of the copolymers