Amphoteric Compounds Research Articles

Synergistic modulation of hydrogen bond network reconstruction and pH buffering of electrolyte enables highly reversible Zn anode

Utilizing aqueous electrolytes offers zinc-ion batteries (ZIBs) with inherent safety, high ionic conductivity, and power density, which is promising for energy storage applications. While the H2O-induced problems including hydrogen evolution reaction (HER) and the accumulation of by-products hinder the electrochemical performance of ZIBs. Herein, proline is used as an electrolyte additive to solve the above issues. Density functional theory (DFT) calculation and experimental results confirm that abundant hydrogen bonds (HBs) are formed between proline and H2O, disrupting the original HB network to inhibit HER kinetics. Meanwhile, as an amphoteric compound, proline neutralizes the OH− generated by HER, preventing it to react with Zn2+ and SO42− to form insulating by-products. Consequently, the Zn||Zn symmetric cell reaches the cycle life of 5500 h at 1.0 mA cm−2, 1.0 mAh cm−2, and 660 h at 10 mA cm−2, 5.0 mAh cm−2. When matching with the VO2 cathode, the Zn||VO2 cell achieves a capacity retention of 68.25 % at 5.0 A g−1 after 6694 cycles. This work provides a novel perspective integrating the regulation of the HB network and pH buffer chemistry to develop advanced aqueous electrolytes.

Vibrational signatures of dynamic excess proton storage between primary amine and carboxylic acid groups.

Ammonium and carboxylic moieties play a central role in proton-mediated processes of molecular recognition, charge transfer or chemical change in (bio)materials. Whereas both chemical groups constitute acid-base pairs in organic salt-bridge structures, they may as well host excess protons in acidic environments. The binding of excess protons often precedes proton transfer reactions and it is therefore of fundamental interest, though challenging from a quantum chemical perspective. As a benchmark for this process, we investigate proton storage in the amphoteric compound 5-aminovaleric acid (AV), within an intramolecular proton bond shared by its primary amine and carboxylic acid terminal groups. Infrared ion spectroscopy is combined with abinitio Molecular Dynamics (AIMD) calculations to expose and rationalize the spectral signatures of protonated AV and its deuterated isotopologues. The dynamic character of the proton bond confers a fluxional structure to the molecular framework, leading to wide-ranging bands in the vibrational spectrum. These features are reproduced with remarkable accuracy by AIMD computations, which serves to lay out microscopic insights into the excess proton binding scenario.

Corrosion Mitigation in Molten Salt Environments.

The aim of this paper is to present methods for corrosion mitigation in molten salt environments. The corrosion of structural materials depends directly on the redox potential of the salt. When the redox potential of the salt is higher than the standard potentials of the elements constituting the structural materials, corrosion occurs. If the reverse is true, no corrosion is observed. Herein, a methodology for calculating the theoretical potential of a molten salt is provided and compared with experimental measurements. Three ways to mitigate corrosion by modifying the salt redox potential are proposed: (i) using a soluble/soluble redox system; (ii) using a potentiostatic method; and (iii) using an amphoteric compound such as UCl3, TiCl2, or TiCl3. Immersion tests were conducted under the above conditions to validate the methodology.

Phase Diagram of the MgF2–SrF2 System and Interactions of Magnesium and Strontium Fluorides with Other Fluorides

The phase diagram of the SrF2–MgF2 system has been studied by differential thermal analysis (DTA) and X-ray powder diffraction (XRD). The stability area of the compound SrMgF4 is very small, and its extent is about 20°С between 870 and 890°С. The formation of compounds by magnesium fluoride and strontium fluoride with other metal fluorides is considered in the M versus X coordinates, where M is the cumulative moment of the cation and X is the cation electronegativity. Two areas of compound formation were identified for each of the fluorides. Magnesium and strontium fluorides are amphoteric compounds in terms of the Lewis acid and base theory.

Synthesis of novobiocin derivatives and evaluation of their antigonococcal activity and pharmacokinetics

Gonorrhea has become a serious problem because the number of infected people is increasing and the multi-drug resistance of the causative bacteria, Neisseria gonorrhoeae, is progressing. To develop novel drugs against resistant N. gonorrhoeae, we focused on the antibiotic novobiocin (1). This natural product has a different mechanism of action from existing drugs for gonorrhea, which may make it effective against resistant strains. Actually, it was applied to resistant N. gonorrhoeae, and moderate antibacterial activity was confirmed. Based on this result, we investigated the development of an antigonococcal drug with 1 as the lead compound. The pharmacophore is thought to be the noviose sugar moiety, especially around the 3′-position, so we derivatized this part in order to improve antibacterial activity. As a result, we found that 5 with an methylpyrrole ester structure have a very potent antibacterial activity. This derivative also showed excellent antigonococcal activity against resistant strains in vitro, however it has poor water solubility and pharmacokinetics because it is the acidic lipid-soluble compound. Therefore, we considered introduction of a basic substituent into the molecule would result in an amphoteric compound with improved water solubility, and we investigated further derivatization. As a result of synthesizing various derivatives, we found 47 containing imidazole with strong antigonococcal activity and greatly improved water solubility. This derivative has also improved metabolism and blood concentration in vivo, and is expected to be orally absorbed. Based on these results, we believe that 47 is a very promising anti-gonococcal lead compound and has great potential for further development.

Enhancing the Performance of Perovskite Solar Cells by Introducing 4-(Trifluoromethyl)-1H-imidazole Passivation Agents.

Defects in perovskite films are one of the main factors that affect the efficiency and stability of halide perovskite solar cells (PSCs). Uncoordinated ions (such as Pb2+, I-) act as trap states, causing the undesirable non-radiative recombination of photogenerated carriers. The formation of Lewis acid-base adducts in perovskite directly involves the crystallization process, which can effectively passivate defects. In this work, 4-(trifluoromethyl)-1H-imidazole (THI) was introduced into the perovskite precursor solution as a passivation agent. THI is a typical amphoteric compound that exhibits a strong Lewis base property due to its lone pair electrons. It coordinates with Lewis acid Pb2+, leading to the reduction in defect density and increase in crystallinity of perovskite films. Finally, the power conversion efficiency (PCE) of PSC increased from 16.49% to 18.97% due to the simultaneous enhancement of open-circuit voltage (VOC), short circuit current density (JSC) and fill factor (FF). After 30 days of storage, the PCE of the 0.16 THI PSC was maintained at 61.9% of its initial value, which was 44.3% for the control device. The working mechanism of THI was investigated. This work provides an attractive alternative method to passivate the defects in perovskite.

Simultaneous effect of different chromatographic conditions on the chromatographic retention of pentapeptide derivatives (HGRFG and NPNPT).

Introduction: Oligopeptides exhibit great prospects for clinical application and its separation is of great importance in new drug development. Methods: To accurately predict the retention of pentapeptides with analogous structures in chromatography, the retention times of 57 pentapeptide derivatives in seven buffers at three temperatures and four mobile phase compositions were measured via reversed-phase high-performance liquid chromatography. The parameters ( , , and ) of the acid-base equilibrium were obtained by fitting the data corresponding to a sigmoidal function. We then studied the dependence of these parameters on the temperature (T), organic modifier composition (φ, methanol volume fraction), and polarity ( parameter). Finally, we proposed two six-parameter models with (1) pH and T and (2) pH and φ or as the independent variables. These models were validated for their prediction capacities by linearly fitting the predicted retention factor k-value and the experimental k-value. Results: The results showed that and exhibited linear relationships with , φ or for all pentapeptides, especially for the acid pentapeptides. In the model of pH and T, the correlation coefficient (R2) of the acid pentapeptides was 0.8603, suggesting a certain prediction capability of chromatographic retention. Moreover, in the model of pH and φ or , the R2 values of the acid and neutral pentapeptides were greater than 0.93, and the average root mean squared error was approximately 0.3, indicating that the k-values could be effectively predicted. Discussion: In summary, the two six-parameter models were appropriate to characterize the chromatographic retention of amphoteric compounds, especially the acid or neutral pentapeptides, and could predict the chromatographic retention of pentapeptide compounds.

Study on Thermodynamics and Kinetics of Cephalexin Enzymatic Hydrolysis and Its Process Development to Prepare 7-ADCA

Cephalosporin enzymatic hydrolysis technology is a green technology for recovering 7-amino-3-deacetoxycephalosporanic acid (7-ADCA) from cephalosporin mother liquor. Solubility is critical for the production and purification of 7-ADCA. In this paper, the solubility of 7-ADCA and phenylglycine was measured. Solubility-temperature correlation model and solubility-pH correlation model were investigated, and Akaike information criterion (AIC) analysis was performed. The kinetic parameters of the enzymatic hydrolysis reaction of cephalexin, cefradine, and cefadroxil were determined, and the reaction rates under different substrate concentrations were measured, and the Lineweaver–Burk double-reciprocal equation was used to draw a graph. The Michaelis constants Km/(mg/mL) were 73.98, 583.84, 38.66, Vmax/(mg/mL·min) 4.20, 16.00, 1.96, respectively. The experimental results show that amphoteric compounds and buffers can prompt the reaction, low concentration of methanol promotes the reaction, while high concentration of methanol inhibits the reaction, and ethanol, isopropanol, tetrahydrofuran (THF), dimethyl sulfoxide (DMSO), ethylene glycol (EG), 1,4-dioxane all have different degrees of inhibition on the reaction speed. Finally, based on thermodynamic and kinetic studies, a process technology for the preparation of 7-ADCA by hydrolysis catalyzed of cephalexin was developed. It was confirmed that the proposed process route of preferential removal of phenylglycine by elution and/or cooling crystallization was reasonable and effective. The 7-ADCA crystal products obtained by crystallization were characterized by PXRD, thermal analysis, infrared, electron microscope, and high-performance liquid chromatography (HPLC).

Development and Validation of a Strong Cation Exchange Chromatographic Column Coupled with High-Performance Liquid Chromatography Method for Meropenem and Evaluation of Its Stability in Human Plasma: Application to the Therapeutic Drug Monitoring.

Meropenem is a wide inter-individual variability in the pharmacokinetic, and standard dosing may not be adequate in critically ill patients. Therapeutic drug monitoring is a useful tool to optimize dosing. Meropenem is the amphoteric compound with an isoelectric point of 5.15. The secondary amino group of meropenem is positively charged when pH ≤ 5.4, thus we attempted to separate by strong cation exchange (SCX) column using acetonitrile/25-mM potassium dihydrogen phosphate (pH3.0; 60:40) as mobile phase, and good peak shape and effective separation obtained. Generally, meropenem were unstable in plasma. We try to investigate stability of plasma samples using the medium QC sample with or without 3-(N-morpholino) propanesulfonic acid (MOPS) as stabilizer solutions at possible conditions during handling and storage. Meropenem showed higher stability at -80°C, and addition of MOPS might increase the short-term and extracted samples stability. This method is suitable for the quantification of meropenem in human plasma from 0.5 to 100μg/mL. The accuracy was ranged from 96.53 to 101.11% with relative standard deviation ≤ 4.76%. The method has been used for determined 63 critically ill patients treated with meropenem. During the first measurement, 11 patients showed trough levels below the target ranges despite standard dosing. Through continuous or prolonged infusion, 8/11 patients (72.73%) led to adequate trough levels. The described SCX-high-performance liquid chromatography method for meropenem in human plasma is a powerful tool for therapeutic drug monitoring.

Materiality of Homeopathic Medicines. DynHom Research Program.

Background: Homeopathy is controversial because using highly dilute medicines (high homeopathic potencies, HHP) beyond the Avogadro/Loschmidt limit. Previous publications [1,2] using NMR relaxation revealed the involvement of nanobubbles and/or nanoparticles and/or nanometric superstructures in high potentizations. NTA demonstrated the presence of particles in HHPs [3,4]. With SEM-EDX [5] we observed an ionic diversity common to all preparations including HHPs and significant differences in the relative quantity of each ion between different homeopathic manufacturing lines and controls. FTIR spectroscopy [6] shows that the molecular composition is that of carbonates, primarily sodium bicarbonate.
 Methods: To observe the materiality of homeopathic medicines a multidisciplinary approach is necessary. In collaboration with several universities we are able to observe these medications with NMR, NTA, SEM-EDX, FTIR, pH and EPA.
 Results: The essential component of all already studied homeopathic medicines is sodium hydrogen carbonate modulated by some other elements in specific quantity, size and shape. The probability that the observed results could have occurred just by random chance can be rejected (especially above Avogadro limit) p < 0,001.
 Conclusions: The homeopathic medicines do contain material with a specific ionic composition even in HHPs diluted beyond the Avogadro/Loschmidt limit. This specificity can be attributed to the manufacturing process. These results demonstrate that the step-by-step process (dynamized or not) does not match the theoretical expectations in a dilution process. The starting material and dilution/dynamization method influences the nature of these NPs. The role of carbonates and sodium bicarbonate must be carefully studied in the future. Its aqueous solution is alkaline in nature but it is an amphoteric compound, which means that the compound has both acidic as well as alkaline character. The reaction with acids results in sodium salts and carbonic acid and reaction with basic solution produce carbonates and water. Specific electric fields are indeed detectable.

CONCEPTUAL DIFFICULTIES OF SECONDARY SCHOOL STUDENTS IN UNDERSTANDING ACID-BASE CHEMISTRY

The dissemination of scientific knowledge has enormous transformative potential. As a result, a nation's progress and growth can't get off the ground without a solid foundation in scientific literacy. From this perspective, the education of science is crucial to cultivating a scientific worldview and boosting students' scientific knowledge. The motivation for this study stems from researchers' previous observations of secondary school students' conceptual difficulties in acid-base chemistry. The study used a descriptive, quantitative research approach to investigate common misconceptions about acid-base chemistry held by high school pupils. A special test instrument labelled as test designed to measure the conceptual difficulties in acid-base chemistry (TCDAB) was developed to measure the conceptual difficulties of secondary school students in Acid-Base chemistry. The Punjab Text Book Board, Lahore, version January 2020, 10th chapter Chemistry Text Book was used as a reference for the creation of the test (TCDAB). A table of the specification was used and was delimited to the first three levels of the cognitive domain of Bloom’s taxonomy. TCDAB has been validated by well-known chemists and educators. Test re-tests method was used to determine the reliability and the correlation coefficient (r) was 0.92. The internal consistency of the instrument was also evaluated using SPSS, and the resulting Cronbach alpha coefficient was 0.83. All the students studying chemistry in public secondary school of the district Bahawalnagar of the Punjab, Pakistan were population of this study (Dist. BWN consist of five tehsils which having total 250 schools). To conduct the survey of this study, a sample of 500 students from twenty (20) secondary schools, four (4) secondary schools (2 boys and 2 girls) from each five tehsils was selected by using the convenient sampling technique due to covid-19 in district Bahawalnagar city. The results of the analysis of TCDAB indicated that 60% concept-based items in acid-base chemistry were difficult like Arrhenius concept, Lowry Bronsted concept and Lewis Concepts, amphoteric compounds, conjugate acids and bases, chemical properties of acids and bases, concentration of acid base chemistry, strength of acid base chemistry, Uses of acids and bases, PH scale, and indicators. Keywords: Acid-base chemistry, conceptual difficulties, table of specification, cognitive domain

An amphoteric betaine electrolyte additive enabling a stable Zn metal anode for aqueous batteries.

The corrosion and dendritic growth of the Zn anode limit its electrochemical performance in aqueous Zn batteries. Here, we present an amphoteric betaine additive for 5 m ZnCl2 aqueous electrolyte. The carboxyl group on betaine forms hydrogen bonds with water and reduces the water activity. The molecule also experiences preferential adsorption on the Zn surface and separates the interactions between Zn and water. Side reactions at the Zn electrode are thus inhibited. The regulated interface also ensures uniform Zn deposition. As a result, the electrolyte with betaine additive allows reversible Zn plating/stripping for over 1400 h at 0.5 mA cm-2. A capacity retention of 94% is obtained after 3000 cycles for a VO2 cathode.

System eigenmobilities in zone electrophoresis: A general moving-boundary approach.

System zones in capillary zone electrophoresis represent an important topic, very interesting from the theoretical point but also important for practice. This paper is aimed at contributing to the understanding of system zones as one of the very fundamental properties of electrophoretic systems, by developing an alternative approach to the so far used vector-matrix model of calculation of system mobilities (system eigenmobilities). The presented model is based on the solution of the differential form of the moving-boundary equation. The result for acid-base systems is a single algebraic equation valid universally for a zone comprising any number of constituents (mono- or polyhydric strong or weak acids or bases and/or amphoteric compounds). The value of the described solution against previous models consists in its explicit form, expressing the system eigenmobility of a homogeneous zone of given composition as a function of only known quantities. The obtained equation is shown to be the common source of various simplified equations obtained in the past for particular simple systems. The applicability of the simplified equations is discussed in terms of completeness of the results (number of output system eigenmobilities). For non-buffered systems, the occurrence of a previously unreported non-zero value of system eigenmobility is discussed that is equal to the arithmetic average of mobilities of the solvent ions.

Prediction of n-octanol/water partition coefficient of strongly ionized compounds by ion-pair reversed-phase liquid chromatography with silica-based stationary phase

反相液相色谱(RPLC)是测定正辛醇/水分配系数(log P)的有效方法,但由于缺少同类型模型化合物,RPLC在测定强离解化合物的log P时遇到挑战。该文在硅胶基质C18色谱柱上,采用离子抑制反相液相色谱(IS-RPLC)和离子对反相液相色谱(IP-RPLC)分别对中性化合物、酚酸、羧酸、磺酸及部分两性化合物的保留行为进行了系统研究。在IS-RPLC模式下,利用中性化合物、弱离解的酚酸和苯羧酸作为模型化合物,建立了表观正辛醇/水分配系数(log D)与纯水相保留因子对数值(log kw)的定量结构-保留行为关系(QSRR)模型,测定了19种离解化合物的log D值,作为后续IP-RPLC的模型化合物及验证化合物。在IP-RPLC模式下,将中性、弱离解和强离解化合物作为混合模型组,以溶质静电荷ne、氢键酸碱性参数A和B为桥梁,建立了线性良好的log D-log kw-IP模型,采用3种不同类型的离解化合物进行了外部验证实验,预测值误差低于10%,证实了模型的可靠性。在此基础上,预测了8种强离解化合物的log D7.0值(pH 7.0条件下的log D值)。研究表明,利用结构相关参数沟通不同类型的模型化合物,是实现IP-RPLC测定强离解化合物log D值的一种行之有效的方法。与聚乙烯醇基质色谱柱相比,通用型的硅胶基质色谱柱上尽管存在着更多的次级作用,但可以为强离解化合物log D的测定提供更灵活的选择。

Multiorgan Crystal Deposition of an Amphoteric Drug in Rats Due to Lysosomal Accumulation and Conversion to a Poorly Soluble Hydrochloride Salt.

Poor solubility of drug candidates mainly affects bioavailability, but poor solubility of drugs and metabolites can also lead to precipitation within tissues, particularly when high doses are tested. RO0728617 is an amphoteric compound bearing basic and acidic moieties that has previously demonstrated good solubility at physiological pH but underwent widespread crystal deposition in multiple tissues in rat toxicity studies. The aim of our investigation was to better characterize these findings and their underlying mechanism(s), and to identify possible screening methods in the drug development process. Main microscopic features observed in rat RO0728617 toxicity studies were extensive infiltrates of crystal-containing macrophages in multiple organs. Matrix-assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometry revealed that these crystals contained the orally administered parent compound, and locality was confirmed to be intracytoplasmic and partly intralysosomal by electron microscopic examination. Crystal formation was explained by lysosomal accumulation of the compound followed by precipitation of the hydrochloride salt under physiological conditions in the lysosomes, which have a lower pH and higher chloride concentration in comparison to the cytosol. This study demonstrates that risk of drug precipitation can be assessed by comparing the estimated lysosomal drug concentration at a given dose with the solubility of the compound at lysosomal conditions.

Influence of natural L-amino acids on the interfacial tension of an oil-water system and rock wettability alterations

The cost and environmental effects of most conventional surfactants have increased the search for a greener and cheaper alternative for enhanced oil recovery (EOR) applications. The natural L-amino acids are amphoteric compound with excellent surface properties that have found versatile applications in the pharmaceutical, cosmetic, and food industries. These amino acids exhibited amphipathic nature due to their hydrophobic alkyl chain and charged head. Hence, they could form contacts with both polar and non-polar surface ligands simultaneously. In this study, four amino acids, namely L-arginine, L-lysine, L-methionine, and L-tryptophan, were investigated to access their ability to reduce the interfacial tension (IFT) and alter the wettability of oil-wet sandstone rock. The pendant/rising drop and sessile drop method were employed in IFT and contact angle measurements. The stability of amino acids in brine and the compatibility with other EOR chemicals were tested through visual observation of the precipitates and cloudiness. With the exception of L-tryptophan, the compatibility and stability results revealed that all the amino acids have high salt tolerance above 25 wt% sodium chloride (NaCl). The solutions of amino acids and chemicals such as cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS), hydrolyzed polyacrylamide (HPAM), alkali, and alkali-polymer were transparent even at 80 °C.The IFT test results showed that the amino acids significantly reduced the crude oil-water IFT compared to the IFT of n-decane-water system. The IFT between deionized water and crude oil decreased by 76.61% and 55.24%, 24.79%, 45.23% in the presence of L-arginine, lysine, methionine, and tryptophan solutions, respectively. Addition of 0.01 wt% L-arginine, L-lysine and L-methionine to 0.1 wt% SDS reduced the IFT by 28.3%, 15.6%, and 10.97% respectively. The contact angle test showed that L-amino acids have great potential as wettability modifying agents. The contact angles reduced with the decreasing pH (potential of hydrogen) and with increasing brine concentrations from 1 to 4 wt%. Specifically, the contact angle reduced from 92.3°, 91.42°, 89.81° and 92.95 to 47.24°, 53.9°, 58.9° and 59.0° for L-arginine, L-lysine, L-methionine and L-tryptophan, respectively at a pH of about 3. The study suggests that the L-amino acids could be a potential EOR agent in a high saline environment, mainly as a wettability modifier, as well as additives to improve the surface activity of the conventional surfactant and EOR chemicals.

Characterization of pH Dependent-Charged Structures of Valine and Aspartic Acid Through Their Partitioning into Imidazolium-Based Ionic Liquids

Imidazolium-based ionic liquids 1-hexyl-3-methylimidazolium hexaflorophosphate, and 1-hexyl-3-methylimidazolium tetrafloroborate were used to determine pH dependent-ionic forms of Valine and Aspartic acid in aqueous solutions. For this purpose, the partitioning behaviors of both compounds between the aqueous phase with different pH values and ionic liquid phase were investigated. The results revealed that due to having different pH-dependent ionic forms, each compound showed different partitioning behavior. Partitioning behaviors of Valine and Aspartic acid depend strongly to aqueous solution acidity and chemical structures of ionic liquids. Water content of ionic liquid phase and charge density of anionic and cationic constituents of ionic liquids are effective parameters for extraction of studied amino acids into ionic liquid phase. This study was considered as a basis for introducing a green technique to realize the real ionic species of different amphoteric compounds such as amino acids in the aqueous solutions.

Development of a novel method for polar metabolite profiling by supercritical fluid chromatography/tandem mass spectrometry

Supercritical carbon dioxide (scCO2), the main fluid in the mobile phase for supercritical fluid chromatography (SFC), is non-polar. The majority of polar compounds are little soluble in scCO2, thereby rendering them poor candidates for achieving separation by carbon dioxide-based SFC. There is no reported method for the comprehensive analysis of hydrophilic metabolites by SFC with mobile phases comprising a high CO2 ratio. In this study, we investigated the effect of additives in the modifier for enabling the application of SFC to profile diverse polar compounds for metabolomics. Eleven types of columns were screened by using proteinogenic amino acids as the model compounds. The addition of water and acids (formic acid and trifluoroacetic acid (TFA)) to the modifier was also investigated to improve the solubility of the polar compounds and mitigate the unfavorable interaction between the stationary phase and the polar compounds. A significant improvement in the peak shapes of the amino acids was observed upon addition of TFA. The CO2/modifier ratio and TFA concentration in the mobile phases were investigated using the CROWNPAK CR-I (+) column, which showed the best performance during the column-screening. The CO2/methanol/water/TFA ratio of 70/27/3/0.15 (v/v/v/v) was determined as the optimized mobile phase composition. Furthermore, the applicability of the optimized analytical method to other polar compounds was examined; 100 cationic and amphoteric compounds with predicted logPow values that ranged from –5.9 to 1.7 could be simultaneously analyzed without derivatization. Anionic compounds such as organic acids, phosphates, and sugars were excluded from the target analytes. Most of the previously reported SFC methods for analyzing polar compounds employ a gradient elution and require the use of high modifier ratios at 40% or more. In the proposed method, the use of water and TFA enabled the rapid and simultaneous analysis under isocratic elution within 10 min, even with a high CO2 ratio of 70%. Additionally, a rat serum extract was analyzed using the optimized conditions, and 43 polar metabolites were successfully detected. This result demonstrates the applicability of the SFC/tandem mass spectrometry method to real samples.

Development and Validation of a Liquid Chromatographic Method for Concurrent Assay of Weakly Basic Drug Verapamil and Amphoteric Drug Trandolapril inPharmaceutical Formulations

The analysis of weakly basic drugs such as verapamil by reverse-phase liquid chromatography remains a problem, particularly when present in combination with other drugs such as amphoteric compounds like trandolapril. In this study, the simple, accurate, precise and fully validated RP-LC method for the simultaneous determination of verapamil and trandolapril in combined dosage forms has been developed. The LC method allowed quantitation over the ranges of 0.50-18.00 μg/mL and 0.05-1.00μg/mL for verapamil and trandolapril, respectively. The detection limits were found to be 0.008μg/mL and 0.018μg/mL for verapamil and trandolapril, respectively. Moreover, pKa values of verapamil and trandolapril were determined via the dependence of the retention factor on the pH of the mobile phase for ionizable substances. The effect of the mobile phase composition on the ionization constant was studied by measuring the pKa at different methanol-water mixtures, ranging 50-65% (v/v). It was shown that RP-HPLC was sllitab1e for the high throughput analysis of the combination of verapamil and trandolapril. The method also allows a number of cost and time saving benefits and can be readily employed for the analysis of pharmaceutical formulations. The method has been verified, without any interference from excipients, for the concurrent analysis of these compounds in tablets.

Photo Amphoteric Compound Generators for Environmentally-friendly Materials

Photo Amphoteric Compound Generators for Environmentally-friendly Materials