Open Access. Powered by Scholars. Published by Universities.®
Physical Sciences and Mathematics Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 14 of 14
Full-Text Articles in Physical Sciences and Mathematics
Ultrafiltration-Based Sample Preparation And Hplc-Uv Determination Of Diclofenac In Human Plasma Samples, Merve Nenni̇, Ayşegül Doğan, Mustafa Çelebi̇er, Murat Soyseven, Mustafa Si̇nan Kaynak, Hassan Y. Aboul-Enein, Göksel Arli̇
Ultrafiltration-Based Sample Preparation And Hplc-Uv Determination Of Diclofenac In Human Plasma Samples, Merve Nenni̇, Ayşegül Doğan, Mustafa Çelebi̇er, Murat Soyseven, Mustafa Si̇nan Kaynak, Hassan Y. Aboul-Enein, Göksel Arli̇
Turkish Journal of Chemistry
The sample preparation step is the initial step in pharmaceutical analysis. While ultrafiltration is a well-known technique used in the food and pharmaceutical industries, it has rarely been used to measure the plasma concentration of active pharmaceutical ingredients. This study aimed to analyze diclofenac sodium (DS) in human plasma samples using ultrafiltration-based sample preparation before high-performance liquid chromatography (HPLC) analysis. The advantages and limitations of ultrafiltration-based sample preparation in bioanalysis were evaluated by comparing the results with conventional methods. The precipitating agent was used before ultrafiltration. The analysis was carried on an HPLC-UV system with a C18 column (250 ×4.6 …
Chromatographic Profile Of Major Whey Proteins In Some Dairy Beverages Based On Milk Serum, Doina Prodan, Miuta Filip, Mihaela Vlassa, Marioara Moldovan, Rahela Carpa
Chromatographic Profile Of Major Whey Proteins In Some Dairy Beverages Based On Milk Serum, Doina Prodan, Miuta Filip, Mihaela Vlassa, Marioara Moldovan, Rahela Carpa
Turkish Journal of Chemistry
The aim of this study was the determination of chromatographic profiles of major whey proteins (WP): α-lactalbumin (α-La), β-lactoglobulin A and B, (β-Lg A and B), bovine serum albumin (BSA) in dairy beverages based on Zonar milk serum. The studied WP were separated by high-performance liquid chromatography (HPLC) on Aeris XB-C18 column using gradient elution with 0.1% trifluoroacetic acid (TFA) in water and 0.1% TFA in 80% acetonitrile, at 214 nm detection. The HPLC method was validated for system suitability, selectivity/specificity, linearity (R2 ≥ 0.996), precision (RSD% ≤ 2.01), trueness (recovery 96.29%-102.08%), sensitivity (limits of quantification (LOQ) 1.35-10.08 μg/mL), …
Development And Validation Of An Hplc Method For Determination Of Rofecoxib In Bovine Serum Albumin Microspheres, Esra Demi̇rtürk, Emi̇rhan Nemutlu, Selma Şahi̇n, Levent Öner
Development And Validation Of An Hplc Method For Determination Of Rofecoxib In Bovine Serum Albumin Microspheres, Esra Demi̇rtürk, Emi̇rhan Nemutlu, Selma Şahi̇n, Levent Öner
Turkish Journal of Chemistry
A simple and reliable HPLC method was developed and validated for determination of rofecoxib in bovine serum albumin microsphere. The analyses were performed on a C18 column (150 x 4.6 mm, 5 μm particle size) at room temperature with UV detection at 272 nm. The mobile phase was composed of acetonitrile-0.1% o-phosphoric acid solution in water (1:1, v/v) mixture, and flow rate was set to 1 mL/min. The method was validated according to the international guidelines with respect to stability, linearity range, limit of quantitation and detection, precision, accuracy, specificity, and robustness. The detection and quantification limit of the method …
Comparison Of Antioxidant Capacities And Antioxidant Components Of Commercial Bitter Melon (Momordica Charantia L.) Products, Esi̇n Akyüz, Sercan Türkoğlu, Kevser Sözgen Başkan, Esma Tütem, Mustafa Reşat Apak
Comparison Of Antioxidant Capacities And Antioxidant Components Of Commercial Bitter Melon (Momordica Charantia L.) Products, Esi̇n Akyüz, Sercan Türkoğlu, Kevser Sözgen Başkan, Esma Tütem, Mustafa Reşat Apak
Turkish Journal of Chemistry
In this study, the total phenolic contents and total antioxidant capacities of some commercial bitter melon products (powder, packaged powder, capsule, paste in olive oil), and of unripe and ripe fruits were determined by spectrophotometric and chromatographic methods. The total antioxidant capacities of unripe and ripe bitter melon samples, determined by using the CUPRAC (cupric reducing antioxidant capacity assay) and ABTS (2,2'-Azinobis-(3-Ethylbenzthiazolin-6-Sulfonic Acid)/HRP (horseradish peroxidase) methods, were 42.5 and 36.3 μmol TRE (Trolox equivalent) g-1, and 8.7 and 7.0 μmol TRE g-1, respectively. The TAC (total antioxidant capacity) order of the studied samples using the same 2 methods were determined …
Step-By-Step Optimization Of The Hilic Method For Simultaneous Determination Of Abacavir, Lamivudine, And Zidovudine From Dosage Form, Cem Erkmen, Mehmet Gümüştaş, Si̇bel Ayşil Özkan, Bengi̇ Uslu
Step-By-Step Optimization Of The Hilic Method For Simultaneous Determination Of Abacavir, Lamivudine, And Zidovudine From Dosage Form, Cem Erkmen, Mehmet Gümüştaş, Si̇bel Ayşil Özkan, Bengi̇ Uslu
Turkish Journal of Chemistry
Combined therapy for HIV treatment shows superior efficacy in comparison to single therapy. Furthermore, the separation and determination of the combined dosage forms hold a significant place in the pharmaceutical industry. Not only reverse phase high-performance liquid chromatography (HPLC) but also hydrophilic interaction liquid chromatography (HILIC) can be used for these purposes. Contrary to conventional RP systems, HILIC may be an alternative for the analysis of polar substances. The aim of this study was the step-by-step development of a simple, rapid, and reliable method for the simultaneous determination of antiviral compounds from their marketed formulation (Trizivir). In order to achieve …
Determination Of N-Acetylcysteine In The Presence Of Ciprofloxacin Or Levofloxacin In Microparticulate Dry Powder Inhalers, Yağmur Akdağ Çayli, Selma Şahi̇n, Emi̇rhan Nemutlu, Levent Öner
Determination Of N-Acetylcysteine In The Presence Of Ciprofloxacin Or Levofloxacin In Microparticulate Dry Powder Inhalers, Yağmur Akdağ Çayli, Selma Şahi̇n, Emi̇rhan Nemutlu, Levent Öner
Turkish Journal of Chemistry
A fast and easy method was validated for simultaneous determination of ciprofloxacin hydrochloride monohydrate (CP), levofloxacin hemihydrate (LV), and N-acetylcysteine (NAC) in samples. The analysis was performed on a C$_{18}$ column (250 x 4.6 mm, 5 μm) (Inertsil ODS-3V) using an isocratic elution method with a mobile phase composed of 25 mM KH$_{2}$PO$_{4}$ (pH 3.0) and methanol (72:28, v/v) at a flow rate of 1 mL/min. UV detection was performed at 214 nm for NAC and 293 nm for CP and LV. The method was validated for linearity, accuracy, precision (repeatability and reproducibility), specificity, sensitivity, and stability. The calibration study …
Ultrasound-Assisted Surfactant/Ionic Liquid Aqueous Two-Phase System Extraction Prior To High Performance Liquid Chromatography For The Determination Of Tetracyclines In Milk And Honey Samples, Hayri̇ye Mi̇ne Antep, Taşkin Mumcu, Kami̇l Bostanci, Serap Seyhan Bozkurt, Melek Merdi̇van
Ultrasound-Assisted Surfactant/Ionic Liquid Aqueous Two-Phase System Extraction Prior To High Performance Liquid Chromatography For The Determination Of Tetracyclines In Milk And Honey Samples, Hayri̇ye Mi̇ne Antep, Taşkin Mumcu, Kami̇l Bostanci, Serap Seyhan Bozkurt, Melek Merdi̇van
Turkish Journal of Chemistry
In this work, an ultrasonic-assisted surfactant/ionic liquid aqueous two-phase system (ATPS) extraction method was developed to extract six tetracycline antibiotics from food samples before their chromatographic determination using high performance liquid chromatography. The ATPS was formed with 1-allyl-3-methyl-imidazolium bromide, Triton X-100, and dipotassium hydrogen phosphate. The parameters including type and amount of surfactant, ionic liquid and salt, pH of sample solution, and sonication time were optimized. Under the optimized conditions, linear calibration curves of the six tetracyclines were obtained in the range of 10--500 $\mu $g L$^{-1}$ with $>$ r$^{2} =$ 0.990 (n $=$ 9). The proposed green analytical …
Hplc Fluorescence Determination Of Ochratoxin A Utilizing A Double Internal Standard And Its Application To Poultry Feed, Muzaffer Tunçel, Eli̇f Mi̇ne Öncü Kaya, Ülkü Di̇lek Uysal, Tufan Güray
Hplc Fluorescence Determination Of Ochratoxin A Utilizing A Double Internal Standard And Its Application To Poultry Feed, Muzaffer Tunçel, Eli̇f Mi̇ne Öncü Kaya, Ülkü Di̇lek Uysal, Tufan Güray
Turkish Journal of Chemistry
A validated liquid chromatography method employing a fluorescence detector for the determination of ochratoxin A (OTA) was developed with double internal standard and it was applied to ten different poultry feeds. The analysis was performed in an octadecyl silane column using a solvent system [ACN:water:formic acid (50:50:1.25, v/v/v)] by isocratic elution. The flow rate and injection volume were 1 mL min^{-1} and 12 \mu L, respectively. Signals were detected at 278(\lambda_{ex})/315(\lambda_{em}) and 330(\lambda_{ex})/450(\lambda_{em}) nm between 0 and 8, and 8.01 and 20.0 min, respectively. The method was validated with precision, linearity, accuracy, limit of detection, limit of quantification, robustness, and …
Determination Of Iridoid Glycosides From Four Turkish Lamium Species By Hplc-Esi/Ms, Funda Nuray Yalçin, Duygu Kaya, İhsan Çaliş, Tayfun Ersöz, Erhan Palaska
Determination Of Iridoid Glycosides From Four Turkish Lamium Species By Hplc-Esi/Ms, Funda Nuray Yalçin, Duygu Kaya, İhsan Çaliş, Tayfun Ersöz, Erhan Palaska
Turkish Journal of Chemistry
An HPLC-ESI/MS method that enables fast detection and identification of iridoid glycosides is described. Eleven iridoid glycosides known to occur in the genus Lamium-lamalbide, sesamoside, 6-\beta-OH ipolamiide, shanzhiside methyl ester, dehydropenstemoside, barlerin (= 8-O-acetylshanzhiside methyl ester), 6-O-syringyl-8-O- acetylshanzhiside methyl ester, lamerioside, lamiide, eriobioside, and ipolamiide, were identified by means of their retention time and ESI/MS data. This method was successfully applied to the identification of the iridoid composition of the n-butanol extracts of Lamium eriocephalum Bentham subsp. eriocephalum, L. garganicum L. subsp. pulchrum R. Mill, L. garganicum L. subsp. laevigatum Arcangeli, and L. purpureum L. var. purpureum from the Turkish …
Chromatographic Determination Of Phenolic Acids In The Snowdrop By Hplc, Mustafa Tüzen, Mustafa Özdemi̇r
Chromatographic Determination Of Phenolic Acids In The Snowdrop By Hplc, Mustafa Tüzen, Mustafa Özdemi̇r
Turkish Journal of Chemistry
Free and esterified phenolic acids of Galanthus elwesii (snowdrop) were extracted with petroleum ether and determined by HPLC. Cinnamic, ferulic, vanillic, p-coumaric, p-hydroxy benzoic, and caffeic acids were detected by a linear gradient elution with acetic acid/water (2:98 v/v) and acetic acid/acetonitrile/water (2:30:68 v/v) as the mobile phases in 30 min with a flow rate of 1.5 mL/min. Among the acids from snowdrop extracts, p-hydroxy benzoic was the major constituent followed by vanillic and ferulic acids.
Simultaneous Determination Of Fe(Ii) And Fe(Iii) In Pharmaceutical Samples By Post-Column Derivatization/Hplc, Hami̇de Z. Şenyuva, Deni̇z Yurtsever Sarica, Tuncel Özden
Simultaneous Determination Of Fe(Ii) And Fe(Iii) In Pharmaceutical Samples By Post-Column Derivatization/Hplc, Hami̇de Z. Şenyuva, Deni̇z Yurtsever Sarica, Tuncel Özden
Turkish Journal of Chemistry
A post-column derivatization HPLC method with visible absorbance detection at 521 nm was modified for the simultaneous determination of Fe(II) and Fe(III) in mixtures. The method was applied to pharmaceuticals marketed in Turkey. Iron species were separated on a post-column derivatization HPLC, IonPac CS5A (4x250 mm) analytical column using a pyridine-2,6-dicarboxylic acid based eluent. The determinations of Fe(II) and Fe(III) were also realized by the most common method of FAAS, total iron determination. Detection limits (3S) were found to be 0.109 \mu g/L for Fe(II) and 0.217 \mu g/L for Fe(III), respectively. The mean recovery of the HPLC and AAS …
Determination Of Linear Alkylbenzene Sulphonates And Their Biodegradation Intermediates By Isocratic Rp-Hplc, Mehmet Akyüz, David J. Roberts
Determination Of Linear Alkylbenzene Sulphonates And Their Biodegradation Intermediates By Isocratic Rp-Hplc, Mehmet Akyüz, David J. Roberts
Turkish Journal of Chemistry
An HPLC method was developed to determine linear alkylbenzene sulphonates (LASs) and their biotransformation products sulphophenyl carboxylates by isocratic chromatography using two C_{18} columns in series. Solid-phase extraction with a (C_{18}) cartridge was employed to isolate LAS from sediment and sewage effluent samples. Sodium perchlorate and ammonium perchlorate were used as ion pair agents. The recovery of the compounds was 94% \pm 2 and 98% \pm 2 respectively for sediment and sewage effluent. It was demonstrated that it is possible to separate LAS compounds and their isomers and homologues using this system.
Determination Of Hydrochlorothiazide And Enalapril Maleate In Tablet Formulations By Reversed-Phase Hplc, Idrees F. Al-Momani̇
Determination Of Hydrochlorothiazide And Enalapril Maleate In Tablet Formulations By Reversed-Phase Hplc, Idrees F. Al-Momani̇
Turkish Journal of Chemistry
A high-performance liquid chromatographic procedure is presented for the determination of hydrochlorothiazide (HCT) and enalapril maleate (EM) in pharmaceutical tablets. An aliquot of the sample is dissolved in 15% acetonitrile (ACN) containing thiophylline as an internal standard and chromatographed on a Supelcosil LC-8 (5 \mu m), (150 mm x 4.6 mm i.d.) column. The mobile phase was 3.0 mM tetrabutylammoniumhydrogen sulfate (TBAHS) in ACN/water/triethylamine (TEA), (14, 85.6, 6.4 V/V) adjusted to pH 4.1 by glacial acetic acid. The detection was at 220 nm. The method was tested for linearity, accuracy, recovery, and specificity.
High-Performance Liquid Chromatographic Determination Of Oxytetracycline Residue In Cured Meat Products, Hami̇de Z. Şenyuva, Tuncel Özden, Deni̇z Yurtsever Sarica
High-Performance Liquid Chromatographic Determination Of Oxytetracycline Residue In Cured Meat Products, Hami̇de Z. Şenyuva, Tuncel Özden, Deni̇z Yurtsever Sarica
Turkish Journal of Chemistry
The development of a sensitive automated method for residue control of oxytetracycline (OTC) in cured meat (soudjouk) is described. The principle steps involve the extraction of OTC from cured meat in the presence of citric acid with nitric acid, methanol and de-ionized water, and then the determination by HPLC. In HPLC, Hypersil BDC C18 column was used and OTC was separated at 24 ^{o}C using a mobile phase of H_2O (pH=2.10 with H_2SO_4): ACN (85:15, v/v) at a flow rate of 1.5 ml/min. A variable wavelength detector was set at 360 nm. The detection limit of the method was calculated …