ABSTRACT
Voltammetric analysis at platinum and gold rotating disc electrode [RDE] in 0.1 mol 1[-1] sulphuric acid has been applied for the determination of the active ingredient in solid dosage form. Non zero intercept in the limiting current versus concentration plot was proportionally good to excellent for the solid dosage form and is free from interference from adsorption on the electrodes. All of the dosage forms proved amenable to rapid voltammetric determination with a means standard deviation of 1.2
Subject(s)
Platinum , Gold , Technology, Pharmaceutical/instrumentation , Sulfuric Acids/chemistry , Pharmaceutical Preparations/analysis , Equipment Design , Dosage Forms , Electrochemical TechniquesABSTRACT
The bone-biomaterial interface has been characterized by layers of afibrillar extracellular matrix (ECM) enriched in non collagenous proteins, including osteopontin (OPN), a multifunctional protein that in bone controls cell adhesion and ECM mineralization. Physical and chemical aspects of biomaterial surfaces have been demonstrated to affect cell-ECM-substrate interactions. The present paper described the ability of oxidative nanopatterning of titanium (Ti) surfaces to control extracellular OPN deposition in vitro. Ti discs were chemically treated by a mixture of H2SO4/H2O2 for either 30 min [Nano(30') Ti] or 4 h [Nano(4h) Ti]. Non-etched Ti discs were used as control. Primary osteogenic cells derived from newborn rat calvarial bone were plated on control and etched Ti and grown under osteogenic conditions up to 7 days. High resolution scanning electron microscopy revealed that treated Ti discs exhibited a nanoporous surface and that areas of larger nanopits were noticed only for Nano(4h) Ti. Large extracellular OPN accumulation were detectable only for Nano(4h) Ti, which was associated with OPN-positive cells with typical aspects of migrating cells. At day 3, quantitative results in terms of areas of OPN labeling were as follows: Nano(4h) Ti > Nano(30') Ti > Control Ti. In conclusion, chemically nanostructured Ti surfaces may support the enhancement of endogenous extracellular OPN deposition by osteogenic cells in vitro depending on the etching time, a finding that should be taken into consideration in strategies to biofunctionalize implant surfaces with molecules with cell adhesion capacity.
A interface osso-implante é caracterizada pela presença de uma camada de matriz extracellular (MEC) afibrilar rica em proteínas não-colágenas, incluindo osteopontina (OPN), cujas funções no tecido ósseo estão relacionadas à adesão celular e ao controle do processo de mineralização da MEC (crescimento de cristais). Aspectos físicos e químicos das superfícies de biomateriais podem afetar as interações célula-MEC-substrato. O objetivo do presente estudo foi demonstrar a capacidade de aspectos nanotopográficos de superfície de titânio (Ti) de controlar a deposição extracelular de OPN in vitro. Discos de Ti foram tratados quimicamente por solução de H2SO4/H2O2 durante 30 min [Nano(30') Ti] ou 4 h [Nano(4h) Ti]. Superfícies de Ti não tratadas foram usadas como controle. Células osteogênicas primárias derivadas de calvárias de ratos recém-nascidos foram plaqueadas sobre os discos de Ti e cultivadas em condições osteogênicas por até 7 dias. Microscopia eletrônica de varredura de alta resolução revelou que os discos de Ti tratados quimicamente exibiam superfície nanoporosa, com áreas de nanoporos maiores para Nano(4h) Ti. Apenas para esse grupo detectavam-se acúmulos extensos de OPN extracelular, os quais se distribuíam em áreas adjacentes a células OPN-positivas, com aspectos morfológicos típicos de células em migração. Em conclusão, a nanoestruturação química de superfície de Ti pode favorecer o aumento da deposição extracelular de OPN endógena por células osteogênicas in vitro, dependendo do tempo de condicionamento utilizado, o que deve ser considerado no desenvolvimento de estratégias para funcionalizar superfícies de implantes com moléculas com reconhecido efeito no processo de adesão celular.
Subject(s)
Animals , Rats , Biocompatible Materials/chemistry , Dental Materials/chemistry , Extracellular Matrix Proteins/pharmacokinetics , Nanoparticles/chemistry , Osteopontin/pharmacokinetics , Titanium/chemistry , Adsorption , Animals, Newborn , Acid Etching, Dental/methods , Cells, Cultured , Cell Adhesion/physiology , Cell Movement/physiology , Hydrogen Peroxide/chemistry , Materials Testing , Microscopy, Electron, Scanning , Nanotechnology , Oxidation-Reduction , Osteoblasts/metabolism , Osteoblasts/physiology , Osteogenesis/physiology , Rats, Wistar , Surface Properties , Sulfuric Acids/chemistry , Time FactorsABSTRACT
The aims of this study were to characterize the microstructure of a commercially pure titanium (cpTi) surface etched with HCl/H2SO4 (AE-cpTi) and to investigate its in vitro cytocompatibility compared to turned cpTi (T-cpTi). T-cpTi showed a grooved surface and AE-cpTi revealed a surface characterized by the presence of micropits. Surface parameters indicated that the AE-cpTi surface is more isotropic and present a greater area compared to T-cpTi. The oxide film thickness was similar between both surfaces; however, AE-cpTi presented more Ti and O and less C. Osteoblastic cell proliferation, alkaline phosphatase activity, and bone-like nodule formation were greater on T-cpTi than on AE-cpTi. These results show that acid etching treatment produced a surface with different topographical and chemical features compared to the turned one, and such surface modification affected negatively the in vitro cytocompatibility of cpTi as demonstrated by decreasing culture growth and expression of osteoblastic phenotype.
O objetivo deste estudo foi caracterizar a microestrutura de uma superfície de titânio comercialmente puro (cpTi) condicionada com HCl/H2SO4 (acid etched) (AE-cpTi) e investigar sua citocompatibilidade in vitro, comparada à do cpTi usinado (turned) (T-cpTi). O T-cpTi apresentou uma superfície com sulcos e o AE-cpTi exibiu uma superfície caracterizada pela presença de micro-vales. Os parâmetros de superfície indicaram que a superfície AE-cpTi é mais isotrópica e apresenta uma área maior quando comparada à superfície T-cpTi. A espessura da camada de óxido foi similar para as duas superfícies; no entanto, a AE-cpTi apresentou maiores quantidades de Ti e O e menor, de C. A proliferação de células osteoblásticas, a atividade de fosfatase alcalina e a formação de matriz mineralizada foram maiores na superfície T-cpTi que na AE-cpTi. Esses resultados mostram que o condicionamento ácido produziu uma superfície com características topográficas e químicas diferentes quando comparadas às da superfície usinada. Além disso, observou-se que essas modificações de superfície afetaram de forma negativa a citocompatibilidade in vitro do cpTi como demonstrado pela inibição da proliferação celular e da expressão do fenótipo osteoblástico.
Subject(s)
Humans , Acid Etching, Dental , Biocompatible Materials/pharmacology , Dental Materials/pharmacology , Osteoblasts/drug effects , Titanium/pharmacology , Alkaline Phosphatase/analysis , Alveolar Process/cytology , Biocompatible Materials/chemistry , Biomarkers/analysis , Cells, Cultured , Carbon/chemistry , Cell Adhesion/drug effects , Cell Division/drug effects , Cell Proliferation/drug effects , Cell Survival/drug effects , Dental Materials/chemistry , Hydrochloric Acid/chemistry , Interferometry , Materials Testing , Microscopy, Electron, Scanning , Osteogenesis/drug effects , Phenotype , Photoelectron Spectroscopy , Surface Properties , Sulfuric Acids/chemistry , Titanium/chemistryABSTRACT
To investigate the disposition and tissue distribution of ML12 after intravenous (iv) administration in rats, the compound in plasma or in tissue was extracted into ethyl acetate under basic condition and was determined by HPLC after extracted by dilute sulfuric acid. Excitation wavelength and emission wavelength of fluorescence detection were 278 nm and 307 nm, respectively. The data were processed with the software 3P97 to calculate the main pharmaceutical parameters of ML12. At dose of 5 and 10 mg/kg, the elimination of the drug from plasma was found to be kinetically linear, but when the dosage was 20 mg/kg, a non-linear feature was observed. The highest level of ML12 was found in the kidney. Distribution of ML12 after iv administration was extensive and the concentration-time profile was found to be fitted to an open two-compartment model.
Subject(s)
Antihypertensive Agents/pharmacokinetics , Biological Availability , Chromatography, High Pressure Liquid/methods , Kinetics , Pharmaceutical Preparations , Rats, Sprague-Dawley , Spectrometry, Fluorescence/methods , Sulfuric Acids/chemistry , Tissue DistributionABSTRACT
The conventional method of Fiske and Subba Row for the estimation of inorganic phosphate (Pi) is although rapid, but suffers from the disadvantage that the color is unstable and hence the optical density (OD) measurements have to be carried out within a short time span of 8-12 min. This poses a restriction on the number of samples, which can be handled in a batch. Although, modified procedures involving use of alternate reducing agents/or increasing the concentration of H2SO4 in conventional method have been subsequently developed, but the problem of color stability could not be solved. In addition, the use of higher concentrations H2SO4 has rendered the methods unsuitable in enzyme assays, especially if the acid labile phosphate containing substrates have been used. In the present study, attempts have been made to suitably modify the method to improve the stability of the color and sensitivity and also for its applicability in enzyme assays, especially when acid labile phosphate containing substrates such as ATP is used. We used the higher concentrations (0.625, 0.8 and 1.0 N) of H2SO4 rather than 0.5 N used in the conventional assay procedures. Under these conditions, the reagent blanks do not develop color for up to 24 h, whereas the intensity of the molybdenum blue color in the standard and/or experimental tubes increased with time reaching optimum value at 24 h. Simultaneously, the absorption maximum shifts from 660 nm to 820 nm. The highest concentration of H2SO4 (1.0 N) is found to be the most effective in the process of color development. The sensitivity of the method is from 1.7 to 2.1 times higher, as compared to the conventional Fiske and Subba Row method for the measurements carried out at the end of 15 min at 820 nm and with the highest concentration of H2SO4 (1.0 N); the sensitivity increased 4.8-fold at the end of 24 h. Presence of glucose and sucrose (1-10 mM), NaCl and KCI (5-100 mM), MgCl2 (1-10 mM) and BSA (10 to 500 microg per assay tube) do not interfere either with color development or with OD measurements. The extent of ATP hydrolysis is 1.6 to 3.4% for up to 1 hi, depending upon the concentration of H2SO4 used. Only negligible hydrolysis of G6P is observed under these conditions. These results suggest that the presently modified method is suitable for Pi analysis in the enzyme assays, in the presence of labile phosphate containing substrates.
Subject(s)
Adenosine Triphosphate/chemistry , Carbohydrates/chemistry , Chromogenic Compounds/chemistry , Glucose-6-Phosphate/analysis , Phosphates/analysis , Salts/chemistry , Serum Albumin, Bovine/chemistry , Sulfuric Acids/chemistryABSTRACT
In pickling industries, a lot of sludge is generated during the treatment of pickling effluent and there is severe problem of its disposal. Disposal of this sludge as per the Hazardous Waste (Management & Handling) Rules, 1989 is not easy. Its transportation and construction of lined disposal sites pose very severe problems. In the normal practice, the sludge is being disposed of at the sides of roads and railway tracks to fill low lying areas. This may cause serious health hazards. Considering these problems, a study has been undertaken to minimize the sludge generation during the treatment of pickling effluent by neutralizing it with lime, sodium hydroxide and combination of both. An attempt has been made to do an economic evaluation of the above process.
Subject(s)
Alum Compounds/chemistry , Calcium Compounds/chemistry , Hazardous Waste/prevention & control , Industrial Waste/prevention & control , Metallurgy , Oxides/chemistry , Sodium Hydroxide/chemistry , Steel , Sulfites/chemistry , Sulfuric Acids/chemistry , Waste Disposal, Fluid/methodsABSTRACT
OBJECTIVE@#A rapid color test for screening gamma-hydroxybutyric acid (GHB) and its precursor gamma-butyrolactone(GBL) was investigated in drink and urine samples.@*METHODS@#In an acidic solution, GHB was converted to GBL, which reacted with hydroxylamine hydrochloride in presence of sodium hydroxide, forming hydroxamate. A purple complex was formed when hydroxamate reacted with ferric chloride in acidic condition.@*RESULTS@#Detection limit concentrations of GHB in drinks were between 0.5-2 mg/mL, less than the popular abuse concentrations of GHB. This method was usable for urine, with detection limit concentration 0.5 mg/mL. Interferences of common organic solvents and narcotics and depressants were surveyed.@*CONCLUSION@#This method is simple, safe, and rapid; it facilitates rapid screening of GHB and GBL in clinic and forensic laboratories.
Subject(s)
Humans , 4-Butyrolactone/urine , Alcoholic Beverages/analysis , Anesthetics/urine , Beverages/analysis , Forensic Medicine/methods , Hydrogen-Ion Concentration , Hydroxybutyrates/urine , Solvents/chemistry , Sulfuric Acids/chemistryABSTRACT
Ante la creciente oferta de sistemas y marcas comerciales existentes actualmente en plaza, cada vez resulta más imprescindible la selección profesional jerarquizada para cada caso clínico en particular. Hay innumerable cantidad de clonaciones que muchas veces nada nuevo aportan y confunden cada día más el mercado. Calidad y servicio son factores a tener en cuenta en el momento de la elección. Resulta indudable que son las empresas que más aportan en investigación, las que marcan pautas a nivel mundial y ofrecen profuctos de avanzada. Ciertos parámetros a tener en cuenta en el momento de decidir qué implante colocar son: - Los hexágonos externos presentan excelentes soluciones estéticas y permiten una adecuada corrección de las angulaciones. Su mayor limitación suele ser el sistema de conexión y cierta tendencia al aflojamiento o pérdida de los tornillos, sobre todo en restauraciones unitarias. El uso de tornillos de oro y torque adecuada minimizan dicho problema. - Los de hexágono interno y cono tornillo presentan mayor estabilidad en el encastre y una adecuada solución cosmética aunque menos versátil. En estos últimos, implantes preangulados contribuyen a tal fin en casos clínicos que así lo requieran. - Los implantes de superficie tratada con ácido se indican expecialmente en huesos de baja y mala calidad por los excelentes reportes clínicos que auguran un índice de éxito a largo plazo, significativamente mayor. Sin embargo, es necesario un seguimiento durante lapsos más prolongados para corroborar lo expuesto. De la misma manera, en huesos de buena calidad se podrían acortar los tiempos de espera para la carga. - En huesos de poco espesor y/o calidad pobre sería de elección el implante de una sola fase quirúrgica y de superficie tratada para optimizar los resultados
Subject(s)
Dental Implantation, Endosseous/methods , Dental Implantation, Endosseous/trends , Hydrochloric Acid/chemistry , Sulfuric Acids/chemistry , Alveolar Process/anatomy & histology , Bone Density/physiology , Dental Abutments/trends , Dental Occlusion , Dental Stress Analysis , Durapatite/chemistry , Acid Etching, Dental/methods , Osseointegration/physiology , Patent , Surface Properties , Titanium/chemistryABSTRACT
Recentemente, tem tornado aparente que o sucesso do implante endosteal é largamente, se näo totalmente, determinado pela biocompatibilidade do material usado. Esta biocompatibilidade parece estar determinada näo somente pela natureza química do material, mas também pela propriedade micromorfológica da superfície do implante. Os resultados apresentam uma avaliaçäo histológica da cicatrizaçäo inicial da implantaçäo de discos de titânio c.p. com superfície porosa fixados endostealmente. Para testar esta avaliaçäo foram utilizados 12 coelhos machos com peso médio de 3,2 Kg., sendo que cada animal recebeu 2 discos de titânio c.p.. Em todos os animais, os discos de titânio foram utilizados para avaliaçäo histológica de crescimento ósseo...
Subject(s)
Animals , Male , Rabbits , Hydrofluoric Acid/pharmacology , Nitric Acid/pharmacology , Sulfuric Acids/pharmacology , Sulfuric Acids/chemistry , Sulfuric Acids/therapeutic use , Bone Development , Biocompatible Materials/chemistry , Biocompatible Materials/therapeutic use , Titanium/adverse effects , Hydrofluoric Acid/chemistry , Hydrofluoric Acid/therapeutic use , Nitric Acid/chemistry , Nitric Acid/therapeutic use , Microscopy, Atomic Force/methods , Bone Nails/adverse effects , Tibia/surgery , Tibia/transplantationABSTRACT
A natureza de superfície de um biomaterial determina os processos envolvidos na resposta biológica a um material implantado e pode ser descrita em termos de energia, química e morfologia superficial. O objetivo desta pesquisa foi analisar os efeitos de diferentes tratamentos preparatórios sobre as superfícies de Ti cp grau I utilizado na fabricaçäo de implantes odontológicos. Esta pesquisa faz parte de um projeto multidisciplinar cujo principal objetivo a longo prazo é definir as características superficiais que determinam uma interaçäo biológica ótima com implantes de Ti cp. Noventa discos de Ti cp grau I foram preparados metalograficamente com papel SiC de granulaçäo 200 e 600, polidos utilizando pontas de diamante de 6,3 e 1/4µ e submetidos a um protocolo de limpeza através de solventes e lavagens com água bidestilada e deionizada...