Suitable Solvent System Research Articles

Comparative Study of Amino Acids in the Life Stages of Silkworm (Bombyx mori L.)

The silkworm (Bombyx mori L.) undergoes distinct life stages, including egg, larva (caterpillar), pupa (chrysalis), and adult moth(imago), each with specific physiological requirements. Amino acids are essential for the growth and development of the silkworm. In this study, we work in paper chromatography to compare the amino acid profiles in different life stages of the silkworm. Samples were collected from eggs, larvae, pupae, and adult moths. Amino acids were extracted and separated on chromatographic paper using a suitable solvent system. The developed chromatograms were analyzed to determine the relative concentrations of specific amino acids. Our results revealed variations in the amino acid composition across the life stages. The amino acids such as glycine, methionine, leucine, and aspartic acid were common in all life stages of silkworms. These differences may be attributed to the physiological changes associated with metamorphosis and reproduction in adult silkworms. Overall, this study provides valuable insights into the dynamic changes in amino acid profiles during the life stages of silkworms, highlighting the importance of amino acids in their growth, development, and silk production. And, this study demonstrates the utility of paper chromatography as a cost-effective and reliable method for analyzing amino acid composition in complex biological samples, providing valuable insights into the nutritional dynamics of the silkworm lifecycle.

Solvent screening for the purification of monoterpenoids by countercurrent and centrifugal partition chromatography

AbstractBACKGROUNDCountercurrent chromatography (CCC) and centrifugal partition chromatography (CPC) are efficient techniques to purify terpenoids from essential oils. These methods require suitable solvent systems for the partition between the two immiscible liquid phases. In this study, using the analytical shake‐flask method, we measured the partition coefficients of three model monoterpenoids, namely carvone, eucalyptol and thymol, in 11 biphasic solvent systems, at 298.2 K. Moreover, the predictive COSMO‐RS model was applied to represent the partition coefficients of data measured in this work and retrieved from the literature, the liquid–liquid equilibrium (LLE) data of three solvent families suitable for CCC/CPC separations (i.e., Arizona, Modified Arizona and Green Arizona) and the solute's partition coefficients in the three solvent families.RESULTSThe partition coefficients obtained for thymol and eucalyptol are the first partition data available in the literature. The obtained root mean square deviations (RMSDs) between the experimental and predicted partition coefficients (log basis) varied between 0.28 and 0.49. For LLE, RMSDs of 0.040 and 0.048 were achieved for the Arizona and Green Arizona families, respectively.CONCLUSIONThe predictive COSMO‐RS model describes the monoterpenoid partition coefficients and the LLE data of the solvent families well. The most favorable solvent systems to perform the separations were identified, showing that systems with low and intermediate‐to‐low polarities are the most promising options for separating the selected monoterpenoids from their natural matrices by CCC/CPC techniques. © 2024 Society of Chemical Industry (SCI).

Research on the effect of DES properties on the preparation of h-BN nanosheets by electrochemical-liquid phase exfoliation method

Hexagonal boron nitride (h-BN) with a large specific surface area and unique optoelectronic properties has good application prospects in many fields. The liquid phase exfoliation method is considered the most promising method for achieving controllable preparation of boron nitride nanosheets (BNNSs), but the low-cost, relatively environmentally friendly and efficient liquid phase exfoliation is still difficult to achieve. Choosing a suitable solvent system is the key to achieving efficient exfoliation. Deep eutectic solvents (DESs) have the advantages of simple synthesis, low cost, high thermal and chemical stability and strong biocompatibility and are expected to be green solvents for preparation of BNNSs. In this paper, it was found that the properties of DESs and its interaction with h-BN had a significant impact on the electrochemical exfoliation of h-BN. The intercalation effect of DES and the compatibility between DES and h-BN were the main factors affecting the yield, while the quality of BNNSs mainly depended on the decomposition and expansion effect of DES. This rule also can be applied to prepare highly conductive and hydrophilic two-dimensional material Ti-MXene. This research explores the structure–activity relationship between two-dimensional materials and DESs, and provides a theoretical basis for the environmentally friendly and efficient preparation of two-dimensional materials using DESs as exfoliation solvents.

A Novel Process for Improving the Drug Loading of Highly Water-Soluble High-Dose Drug in FDM 3D Printed Tablets

ABSTRACTBackground: 3D printing technologies, also known as additive manufacturing technologies, are gaining importance in pharmaceutical research and manufacturing. These technologies are widely used in automobile, plastic, and material fabrication industries. In the recent past, pharmaceutical industries are actively working to increase the applicability of these technologies in commercial manufacturing. On the other hand, clinics and hospitals are ready to adopt these technologies due to their versatility such as flexibility, individual customization, and low-cost investment. FDM 3D printing technology is one of the widely used technologies for the manufacturing of finished products. However, this technology has limitations such as drug loading, scale-up issues, and regulatory requirements. The present study focused on developing a suitable solvent system along with a drug-loading method to increase the industrial applicability of this technology. Methods: Metformin, a high-dose, highly soluble drug, was selected as a model. Solvents such as water, ethanol, and methanol and their combinations were explored. Saturation solubility and drug loading in both PVA filaments and printed tablets were tested for drug loading. The solvent ratio of ethanol/methanol/water (8:1:1) was selected. The different infills of 10, 25, 50, 75, and 100% were printed using PVA filaments and were subjected to drug loading using soaking and solvent curing methods. Results: The soaking method has resulted in poor drug loading as well as layer separation and swelling of the polymer. The solvent curing method has a maximum drug loading of 91.9% w/w without physical deformities of the tablets. Moreover, the solvent curing method is a scalable process with less process time, and hence this method could be useful for both large-scale commercial manufacturing as well as customized formulations for personalized therapies. Conclusion: This method could be used for manufacturing thermoliable drug products and moderate-dose drug substances. Based on the research outcomes, we propose a novel, scalable, and rapid solvent-curing method for drug loading in the FDM 3D printing technique.

Evaluating solvent efficiency for carbon capture: Comparative analysis of temperature, concentration and diffusivity effects

In the pursuit of efficient carbon capture technologies, the selection and design of solvents play a pivotal role, directly impacting various crucial factors such as CO2 absorption capacity, equipment size, and regeneration energy requirements. The primary focus is on optimizing solvent systems through a comprehensive analysis of intermolecular interaction intensity, diffusion coefficient, and intra-molecular interaction intensity. This study employs a molecular dynamics simulation model to identify the most suitable solvent system by assessing the effect of operating variables like temperature, concentration, interaction intensity, and diffusivity of various single and blended amine systems. The assessment utilizes the radial distribution function and mean square displacement analysis. The results indicate that intermolecular interactions with CO2 are most significant in 30 wt% 2EAE, 40 wt% 2DMAE and 10% DMCA with 20% MCA ratio concentrations. TMPAD, in particular, stands out for its high repulsive interaction and low energy requirement for breaking the carbamate/bicarbonate ion. Diffusion behavior in various observed solvent systems is as follows: EAE > MEA > DMAE > MAE-DEAB > MAE-DMA2P > EAE-TMPAD > AMP-PZ > EAE-DEAB > MAE-TMPAD > EAE-DMA2P > MAE-DMAE > EAE-DMAE > TMPAD > MEA-AMP > DMA2P > DMCA-MCA > DEAB > MEA-PZ. Moreover, elevated temperatures facilitate enhanced diffusivity, leading to accelerated mass transfer rates. This implies the possibility of reducing the size of absorber units and lowering energy consumption. Further studies on heat of absorption and kinetic characteristics of solvent blends are necessary to ensure their practical applicability in carbon capture and industrial operations.

Enhancing growth speed of 3C–SiC using solution growth method by a new low temperature Mn-based cosolvent

Solution growth is a promising method for rapidly and stably preparing high-quality silicon carbide (SiC) single crystals. However, the coexistence of polycrystalline parasitism and solid inclusions during the growth of SiC in high-temperature solutions above 1800 °C still poses a serious threat to the quality of single crystals. Herein, we introduce an innovative Mn-based cosolvent for controlling the stable and fast growth of cubic-type silicon carbide (3C–SiC) single crystals at low temperatures. Firstly, our thermodynamic analysis reveals that SiC is the only stable solid compound in the low-temperature solution (1500–1600 °C) of the Si–Mn–C system, which is an important condition for the stable growth of crystals. Compared to typical solvents like Si–Cr, Si–Ti, and Si–Fe, the Si–Mn solvent exhibits the highest solubility and supersaturation for carbon. Secondly, our solubility calculations of SiC in the solvent show that the Mn-rich solvent can significantly increase the solubility of SiC. Thirdly, we successfully grew 3C–SiC single crystals from Si–Mn solution at 1500 °C without other SiC polymorphs produced. Rapid growth of SiC crystals in Mn-rich solution was achieved by modulating the content of Mn. Our work highlights the superiority of Si–Mn cosolvents in facilitating rapid growth of 3C–SiC single crystals at low temperatures. It introduces a novel approach by applying phase diagram calculation techniques to design suitable solvent systems for the solution growth of SiC single crystals.

A novel and high-efficient method for the preparation of heat-stable antifungal factor from Lysobacter enzymogenes by high-speed counter-current chromatography.

Heat-stable antifungal factor (HSAF) produced by the biocontrol bacterium Lysobacter enzymogenes shows considerable antifungal activity and has broad application potential in the agricultural and medical fields. There is a great demand for pure HSAF compounds in academic or industrial studies. However, an efficient preparation method that produces a high yield and high purity of HSAF is lacking, limiting the development of HSAF as a new drug. In the present study, high-speed counter-current chromatography (HSCCC) combined with column chromatography was successfully developed for the separation and preparation of HSAF from the crude extract of L. enzymogenes OH11. The crude extract was obtained by macroporous resin adsorption and desorption, and the main impurities were partly removed by ultraviolet light (254 nm) and gel filtration (Sephadex LH-20). In the HSCCC procedure, the selected suitable two-phase solvent system (n-hexane/ethyl acetate/methanol/water = 3:5:4:5, v/v, the lower phase added with 0.1% TFA) with a flow rate of 2.0 mL/min and a sample loading size of 100 mg was optimized for the separation. As a result, a total of 42 mg HSAF with a purity of 97.6% and recovery of 91.7% was yielded in one separation. The structure elucidation based on HR-TOF-MS, 1H and 13C NMR, and antifungal activities revealed that the isolated compound was unambiguously identified as HSAF. These results are helpful for separating and producing HSAF at an industrial scale, and they further demonstrate that HSCCC is a useful tool for isolating bioactive constituents from beneficial microorganisms.

Development of a general separation strategy by countercurrent chromatography using sanshools from Zanthoxylum bungeanum oleoresin as a case study.

Three kinds of sanshools were separated from Zanthoxylum bungeanum oleoresin by the high-speed countercurrent chromatography. Sanshools are a series of amide compounds extracted from the Zanthoxylum bungeanum. Due to similar structures, polarities, and dissociation constants, it was challenging to select an appropriate solvent system for their complete separation by countercurrent chromatography. To address this challenge, a solvent-system-selection strategy was proposed to identify a relatively suitable solvent system. Additionally, a separation procedure incorporating multi-elution modes selection was established to separate similar compounds in a logical order. Ultimately, a solvent system comprising n-hexane:ethyl acetate:methanol:water in a ratio of 19:1:1:5.67 was selected. Three amide compounds with high purity were obtained through the use of recycling elution mode to improve separation resolution: hydroxy-ε-sanshool (8.4 mg; purity: 90.64%), hydroxy-α-sanshool (326.4 mg; purity: 98.96%), and hydroxy-β-sanshool (71.8 mg; purity: 98.26%) were obtained from 600 mg sanshool crude extract. The summarized solvent-system-selection strategy and separation procedure incorporating multi-elution modes may instruct countercurrent chromatography users, particularly novices, seeking to separate compounds with highly similar chemical properties. This article is protected by copyright. All rights reserved.

Characterization of crude saponins from stem bark extract of Parinari curatellifolia and evaluation of its antioxidant and antibacterial activities

Abstract Saponins are surface active glycosides which occur in plants as one of the secondary products of primary metabolism. Saponins have been reported to demonstrate antimicrobial, antioxidant and other biological activities. This study was designed to characterize the crude saponins extracted from stem bark of Parinari curatellifolia and to study the antibacterial and antioxidant activities. The saponin was extracted using standard protocol and was subjected to physicochemical characterization. Foaming and haemolysis tests as wells as determination of foaming index were conducted to confirm the presence of saponins. The solubility of the crude saponins was tested in various organic solvents at room temperature. The nature of the aglycone moiety was identified using Salkowski’s and Liebermann–Burchard’s tests. The glycone moiety was identified using Fehling’s test. Fluorescence test was conducted using UV light at 254 and 366 nm. The TLC separation profile was determined in suitable solvent system. The saponin was subjected to UV and FTIR finger printings using standard methods. Silver nanoparticles were synthesized and characterized using standard method. The saponins were evaluated for antioxidant and antibacterial activities using standard procedures. The foaming index was found to be 1666.6. The crude saponin showed different degrees of solubility in the solvents tested and was found to be highly soluble in methanol, ethanol and DMSO. Generally, the saponins were found to be insoluble in non-polar solvents. The aglycone moiety was found to be triterpenoidal in nature and the glycone was found to be a reducing sugar. The crude saponin produced fluorescence at 254 nm which indicated the presence of some chromophores. The TLC showed the presence of some metabolites with varying Rf values. The UV analysis revealed two absorption peaks at 480 nm and 580 nm. The FTIR finger printing showed absorptions characteristic of some functional groups at different frequencies. The crude saponin and silver nanoparticles demonstrated free radical activity against DPPH free radical with IC50 of 5.878 mg/mL and IC50 0.2477 mg/mL, respectively while the H2O2 radical had IC50 of 5.750 mg/mL. The saponin inhibited the growth of Staphylococcus aureus with zone diameter of inhibition between 2 and 3 mm. The saponins are triterpenoidal in nature and demonstrated antioxidant and antibacterial activity.

Isolation and characterization of novel naturally occurring sophorolipid glycerides

Sophorolipids are promising glycolipid biosurfactants as they are readily produced and functional. Lactonic and acidic sophorolipids are well-known. Here, we used chromatography and suitable solvent systems to find and characterize novel, naturally occurring sophorolipid-glyceride derivatives from a Starmerella bombicola product. The sophorolipid-tri-glyceride and -di-glyceride are highly water soluble; they are more bulky and have a higher molecular weight than typical sophorolipids. Furthermore, the surface tension of the purified tri- and di-glyceride aqueous solutions decreases to approximately 40 mN/m, similar to that of conventional acidic sophorolipids. The tri-glyceride of the two sophorolipids and a fatty acid is more lipophilic, with oily properties and little surface activity. These sophorolipid-glycerides are the third-most abundant component after the well-known sophorolipids in S. bombicola products (the lactone:acid:glyceride component ratio in our samples was 49.2:33.5:17.3), and synergistic effects are expected when these sophorolipids are mixed.

Terbinafine HCl Film-Forming Spray for the Treatment of Topical Fungal Infections

Abstract: Terbinafine HCl is an allylamine used to treat fungal infections. It has substantial side effects that can be mitigated by using a topical semisolid dose form. The objective of this study was to develop a 1% Terbinafine HCl film-forming spray formulation to treat topical fungal infections. The formulation was developed by combining polymers, penetration enhancer, plasticizer, and a suitable solvent system. The central composite design with 3 independent variables and 2 dependent variables is implemented to optimize the formulation. The film-forming spray was put through its tests to assess formulation and container-related parameters such as pH, spray angle, spray pattern, density, volume delivered for one actuation and evaporation time. From the study, it was observed that the concentration of ethyl cellulose and Eudragit RSPO has a greater influence on the viscosity of the spray solution, whereas the eutectic mixture has a greater influence on the drug permeation followed by the polymers. It also tested with various fungi, and it was found that formulation showed better fungicidal activity than the marketed product achieved by triple action. The stability studies have shown that the optimized formulation was stable with temperature of 25 ± 2°C and RH 60 ± 5(six months) on the pH, viscosity and visual appearance of the formulation. The study has concluded that the formulated film-forming spray formulation is highly efficient in treating topical and transdermal fungal infections when compared to the traditional dosage forms. Keywords: Terbinafine HCl, Formulation, Fungal infection, Solid dosage forms, Ethyl cellulose.

Countercurrent chromatography as a frontier tool to discover new mechanical roles in liquid-liquid phase separation of cellular biomolecules.

The development of countercurrent chromatography (CCC) technology enabled us to achieve higher peak resolutions and more shortened separation times even for protein separation using aqueous two-phase solvent systems composed of polyethylene glycol and inorganic salts (or dextrans). By eliminating the solid support matrix, all analytes can be recovered from the coiled column after the separation is completed. Recently, it has been found that droplets of biomolecules formed by liquid-liquid phase separation in cells closely relate to the transcription, regulation of signal transduction, and formation of amyloids. Meanwhile, although CCC is a separation technique based on liquid-liquid partitioning of analytes between two immiscible phases, the mechanism of separation could suggest some idea concerning the formation of biomolecule droplets in cells. This article describes the recent advances in the CCC apparatus, the coiled separation column, the choice of a suitable two-phase solvent system, and the application to separation and purification of bioactive macromolecules such as proteins and enzymes, and also discusses the possibility of CCC as a tool to reveal new mechanical roles of biomolecule droplets in the cellular environments.

Unveiling the potential of deep eutectic solvents to improve the conformational and colloidal stability of immunoglobulin G antibodies

Deep Eutectic solvent as a suitable solvent system to design a final pharmaceutical formulation of immunoglobulin G antibodies.

Synthesis and Characterization of Newly Designed and Highly Solvatochromic Double Squaraine Dye for Sensitive and Selective Recognition towards Cu2.

Synthesis and characterization of a novel and zwitterionic double squaraine dye (DSQ) with a unique D-A-A-D structure is being reported. Contrary to the conventional mono and bis-squaraine dyes with D-A-D and D-A-D-A molecular frameworks reported so far, DSQ dye demonstrated strong solvatochromism allowing for the multiple ion sensing using a single probe by judicious selection of the suitable solvent system. The DSQ dye exhibited a large solvatochromic shift of about 200 nm with color changes from the visible to NIR region with metal ion sensitivity. Utilization of a binary solvent consisted of dimethylformamide and acetonitrile (1:99, v/v), highly selective detection of Cu2+ ions with the linearity range from 50 μM to 1 nM and a detection limit of 6.5 × 10−10 M has been successfully demonstrated. Results of the Benesi–Hildebrand and Jobs plot analysis revealed that DSQ and Cu2+ ions interact in the 2:1 molecular stoichiometry with appreciably good association constant of 2.32 × 104 M−1. Considering the allowed limit of Cu2+ ions intake by human body as recommended by WHO to be 30 μM, the proposed dye can be conveniently used for the simple and naked eye colorimetric monitoring of the drinking water quality.

Slot-Die Coated Triple-Halide Perovskites for Efficient and Scalable Perovskite/Silicon Tandem Solar Cells.

Wide bandgap halide perovskite materials show promising potential to pair with silicon bottom cells. To date, most efficient wide bandgap perovskites layers are fabricated by spin-coating, which is difficult to scale up. Here, we report on slot-die coating for an efficient, 1.68 eV wide bandgap triple-halide (3halide) perovskite absorber, (Cs0.22FA0.78)Pb(I0.85Br0.15)3 + 5 mol % MAPbCl3. A suitable solvent system is designed specifically for the slot-die coating technique. We demonstrate that our fabrication route is suitable for tandem solar cells without phase segregation. The slot-die coated wet halide perovskite is dried by a “nitrogen (N2)-knife” with high reproducibility and avoiding antisolvents. We explore varying annealing conditions and identify parameters allowing crystallization of the perovskite film into large grains reducing charge collection losses and enabling higher current density. At 150 °C, an optimized trade-off between crystallization and the PbI2 aggregates on the film’s top surface is found. Thus, we improve the cell stability and performance of both single-junction cells and tandems. Combining the 3halide top cells with a 120 μm thin saw damage etched commercial Czochralski industrial wafer, a 2-terminal monolithic tandem solar cell with a PCE of 25.2% on a 1 cm2 active area is demonstrated with fully scalable processes.

Synthesis, crystal structure and DFT of 6-chloro-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione

In this study, 6-chloro-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione was successfully synthesized and its structure was characterized via spectroscopic techniques, including 1H NMR, 13C NMR, FT-IR, and HRMS. Single crystals of this compound were grown in a suitable solvent system and optimized using single - crystal X-ray diffraction and density functional theory (DFT). The theoretical and experimental values were in good agreement, as indicated by the diffraction values. DFT was used to investing ate the physicochemical properties of the compounds by analyzing their frontier molecular orbitals and molecular electrostatic potentials.

Development and Validation of UV-spectrophotometric Method for Estimation of Gallic Acid in Acalypha indica Leaf Extract and its Cellulose Nanoparticle Formulation

Abstract: Aim/Background: Quantification of Gallic acid in the hydro-alcoholic extract of Acalypha indica and extract loaded cellulose nanoparticles is a characteristic parameter to assess the entrapment efficiency of nanoparticles. Gallic acid is one of the major phenolic acids identified in leaf extract of Acalypha Indica; hence, it was chosen to be estimated. Materials and Methods: A UV spectrophotometric method was developed using distilled water as a suitable solvent system to estimate Gallic acid. The method was validated for parameters such as linearity, precision, robustness and accuracy according to the ICH guidelines. The λmax of 256nm was observed for both Gallic acid and Acalypha indica extract, which indicated specificity of the method for further analysis. Results: Linearity was established between the concentration range of 5-30 μg/ml with a regression coefficient of 0.999 signifying good correlation between the concentration and absorbance. Average percent recovery of 97.6% demonstrated the accuracy of the method. The recorded RSD of <2% in precision validation indicated the correctness of the method. Ruggedness and robustness of the method were established with RSD of <2% suggesting that the analysis is unaffected with change in analyst and wavelength. The detectable and quantifiable limits of Gallic acid were found be 0.045 μg/ml and 0.119 μg/ml respectively, which demonstrated the sensitivity of the method as well. Conclusion: From the above results, it was concluded that the UV-spectrophotometric method can be employed to estimate Gallic acid in both leaf extract and extract loaded pharmaceutical formulations. Keywords: Gallic acid, UV spectrophotometer, Acalypha indica, Cellulose nanoparticles, Method validation, Leaf extract.

Separation and purification of nootkatone from fermentation broth of Yarrowia lipolytica with high-speed counter-current chromatography.

Nootkatone is an important functional sesquiterpene, which can be obtained by the biotransformation of valencene. It is increasingly important because of its pleasant citrus aroma and physiological effects. Yarrowia lipolytica is beneficial for biotechnology applications and has ability to transform valencene to nootkatone. High-speed counter-current chromatography (HSCCC) was used to isolate and purify the product of nootkatone in this study. The suitable two-phase solvent system was selected and the optimum separation conditions were determined. The partition coefficients of nootkatone and the separation factor between nootkatone and valencene were considered as the indexes. The results showed that there were numerous products during the transformation of valencene by Yarrowia lipolytica, and the content of nootkatone was 13.75%. The obtained nootkatone was separated by HSCCC with a solvent system n-hexane/methanol/water (5/4/1, v/v). The final purity of nootkatone was 91.61 ± 0.20% and the elution time was 290-310min. The structure of nootkatone was identified by gas chromatography-mass spectrometry (GC-MS), infrared spectrum and nuclear magnetic resonance hydrogen spectroscopy (1H NMR). This was the first report on the separation of nootkatone from the fermentation broth by HSCCC. This study proved that HSCCC could be used as an effective method to separate and purify the nootkatone from valencene transformed by Yarrowia lipolytica with n-hexane/methanol/water (5/4/1, v/v).

Citrus limon as an Abundant Source of Phytochemicals their Evaluation and Antioxidant Analysis with Bacterial Endophytes

Citrus limon (Lemon) belongs to Family Rutaceae, is commonly known as Kagdi Limbu or Lime. The peel is a leathery exocarp, or skin of the fruit containing numerous oil glands. Lime peel tea was traditionally used as an appetite stimulant, for cold and cough, for sore throat and as a digestive stimulant. It can also be used as an astringent for skin. Lime peel essential oil is use as an aroma and flavour enhancer. The goal of this study was to determine the phytochemical analyses of endophytes isolated from several parts of the Citrus limon plant, including the leaf, steam, root, seed, and peel. The presence of various phytochemical compounds was determined through qualitative analysis. This study will provide referential information for the correct identification of the bioactive compounds and suitable solvent system for separation of those compounds from the isolates of Citrus limon. The quantitative analysis of the phytochemical compounds allows, by using standard analytical technique, the determination of chemical groups, or compounds in aqueous extracts from different plants. For the determination of the antioxidant activity of the isolate is detected by DPPH, and FRAP method. DPPH gave the idea about % scavenging activity of the isolate.

UV Spectrophotometric Method for Quantification of Rivastigmine Tartrate in Simulated Nasal Fluid: Development and Validation

Background: Rivastigmine Tartrate belongs to the class of cholinesterase inhibitors in Anti-alzheimer’s disease with optimum therapeutic efficacy. Till now no validated method of its quantification has been reported in simulated nasal fluid. Objective: The current research investigation aims to develop a rapid, simple, and reliable UV spectrophotometric method for the quantitative determination of the pure form of Rivastigmine Tartrate in SNF. Method: A suitable method was developed by using double beam UV spectrophotometer and selection of a suitable solvent system for estimation of Rivastigmine Tartrate at absorbance maxima 263nm in SNF. The method was validated for various parameters like including accuracy, linearity and precision as per the International Conference on Harmonization guidelines. Results: The method developed by selecting simulated nasal fluid as the solvent system satisfied the optimum condition of the good quality peak at the selected wavelength. The results proposed the developed method for Rivastigmine Tartrate quantification in the simulated nasal fluid to be linear in the working concentration range of 5-60 µg/ml with a co-relation coefficient of 0.998. The % accuracy was found to be 99.8 -100.57. The % RSD values were &lt; 2 while LOD &amp; LOQ values were detected to be 0.316 and 1.053 respectively. Conclusion: The stated method was analyzed to be rapid, accurate, reliable, and precise. Further, it can be used in checking the quality control parameters of the Rivastigmine Tartrate in routine analysis.