Dual-wavelength Method Research Articles

Application of spectrophotometry in novel simultaneous dissolution profiling of a single pill triple therapy of amlodipine, perindopril and indapamide; whiteness evaluation

Simple, diverse univariate spectrophotometric methods were developed and validated for the determination of amlodipine besylate (AM), perindopril arginine (PE), and indapamide (ID). The first method involved direct measurement of AM absorbance at 365 nm within a concentration range of 2.00–40.00 µg/mL, where PE and ID exhibited no spectral interference. To eliminate the contribution of AM from the ternary mixture, its spectrum was divided by a reference spectrum of AM (12 µg/mL), followed by mathematical subtraction of the resulting constant. The spectrum was then multiplied by the AM divisor to yield a corrected spectrum of the PE and ID binary mixture, allowing their quantification. Various approaches were used to quantify both drugs, including measurement of their second (2DD) and first derivative (1DD) spectra at 231.30 nm and 251.00 nm, respectively. Additionally, the ratio difference (RD) technique and dual wavelength (DW) method were employed. The concentration ranges for PE and ID were 5.00–100.00 µg/mL and 1.00–20.00 µg/mL, respectively. Among these methods, the DW technique was the simplest, so it was chosen for dissolution monitoring of PE and ID. These methods were successfully applied to determine AM, PE, and ID in bulk powder, as well as in Triplixam® tablets, without interference from excipients and in different used dissolution media. The whiteness of the method was evaluated, demonstrating its excellent environmental, analytical and practical efficiency.

A leading error compensation method for weld seam tracking based on dual-sensing and dual-wavelength

Purpose Leading error in line laser weld seam tracking significantly affects tracking accuracy. This paper aims to propose an accurate and reliable compensation method without increasing system complexity for weld seam tracking to improve tracking precision. Design/methodology/approach Based on the line laser seam tracking method, the seam image is simultaneously captured to obtain the angle offset of the seam relative to the sensor direction, which is then combined with the leading distance to calculate the leading error. The two sensing methods use different wavelengths and are captured simultaneously by a color industrial camera. The images of the two different wavelengths can be separated by extracting the RGB components, and the compensated tracking results are obtained after image processing. Findings The results of static positioning experiment indicate that the average absolute error in weld seam positioning is reduced to 0.099 mm after compensation. The real-time tracking experiments demonstrate that the proposed method preserves tracking accuracy even with changes in the sensor’s angle of deviation during welding, with the average absolute error being 0.248 mm. This method effectively enhances the precision of line laser weld seam tracking when the sensor exhibits a deviation relative to the welding direction. Originality/value By using the dual-sensing and dual-wavelength method for leading error compensation, the method effectively addresses the leading error issue while maintaining the advantages of the line laser seam tracking method.

Dual-wavelength synchronous control method for liquid crystal optical phased array

The liquid crystal optical phased array (LCOPA), as a key beam steering device, has gained increasing significance in the field of space laser communication. With the rapid advancement of space laser communication technology, the demand for precise synchronous control of multi-wavelength beams has significantly increased, particularly in ensuring reliable communication links through synchronized control of signal and beacon beams. The signal beam is primarily utilized for data transmission, while the beacon beam is responsible for path calibration and real-time tracking. However, due to the limitations of natural dispersion effects, conventional LCOPA control methods struggle to achieve synchronized manipulation of beams at different wavelengths, resulting in error accumulation and response delays in communication links, thereby compromising the accuracy and efficiency of information transmission. To address this challenge, this study proposes and validates a dual-wavelength synchronous control method based on LCOPA. The method establishes a phase optimization principle centered on minimizing the least-squares error of complex amplitudes and expands the phase modulation capability of LCOPA hardware, thereby overcoming the natural dispersion governed by the grating equation. Simulation and experimental results demonstrate that this method achieves exceptionally high beam pointing accuracy, meeting the demands of high-precision information transmission in multi-wavelength laser communication. This study provides an innovative technical pathway for the application of LCOPA in multi-wavelength laser communication and establishes a solid theoretical foundation for future experimental research on multi-wavelength control.

Stability-indicating spectrophotometric quantification of safinamide in the presence of its possible degradation product.

In recent times, a truly exquisite pharmaceutical marvel has graced the world of medicine, known as Safinamide (SAF). This opulent creation has been specifically tailored to cater to the needs of individuals afflicted with Parkinson's disease (PD), an esteemed neurological condition renowned for its regal ability to impede motor skills, coordination, and equilibrium. It is highly improbable that degradation products of pharmaceutical components would significantly compromise efficiency and safety of a drug during its shelf life. Pharmaceutical analysis requires a variety of stability tests to be conducted under distinct conditions. As a result, there was an increased need for the development of an analytical methodology capable of reliably separating and quantifying degradants and impurities that might be found in pharmaceuticals. In this study, we have developed two efficient and straightforward spectrophotometric methodologies for the concurrent estimation of SAF and its degradation product (SAF DEG), which is the main acid hydrolysis product. The confirmation of degradation product build-up by the use of several analytical techniques, including infrared spectroscopy (IR), and mass spectrometry (MS) investigations. The present methodologies have been validated for linearity within the concentration range of 5-30µg/ml for SAF, and 5-15µg/mL, 2-15µg/ml for SAF DEG for fourier self-deconvolution (FSD) and dual wavelength (DW) methods, respectively. The originality of these techniques lies in their status as the first stability-indicating spectrophotometric procedures that are both environmentally friendly. Moreover, the process of obtaining pure SAF DEG offers substantial economic benefits by obviating the need to acquire a costly constituent. The use of intelligent techniques was employed to analyze the pharmaceutical dosage form, potentially offering significant advantages to the pharmaceutical industry.

Temperature distribution measurement of solid propellant combustion based on dual-wavelength imaging method

Temperature distribution measurement of solid propellant combustion based on dual-wavelength imaging method

Wide-area topography using reflection phase microscopy for surface inspection.

In this study, we demonstrated an inspection system utilizing reflection phase microscopy to enhance both depth range and field of view (FOV). By implementing a dual-wavelength method, we achieved a maximum expected depth range of 7.7 µm. The amplified phase due to the dual-wavelength approach was effectively mitigated by utilizing the configuration of successive accumulation of interferograms. In addition, the error correction algorithms further enhanced image quality, yielding a precision of 1.30 nm. Furthermore, we employed sophisticated image stitching techniques to attain a FOV of approximately 11 × 11 mm2. This system enabled us to perform precise, wide-area inspections of hole structures fabricated on a silicon wafer, demonstrating its efficacy and potential for high-resolution, large-scale industrial applications.

A high-quality fluorescence elimination dual-wavelength Raman method for biological detection and its application in cancer diagnosis

Raman-based methods offer a promising approach for in vivo biological detection. However, the fluorescence of biological samples will significantly affect Raman measurement accuracy. Moreover, due to the existence of excitation wavelength-dependent fluorescent molecules in biological tissues, especially porphyrin molecules, the fluorescence also exhibits significant wavelength dependence. To achieve high-quality Raman spectra of biological tissue, in this work we proposed a dual-wavelength Raman method. Two lasers with different wavelengths were used to excite optical signals in the same region, and the ordinary fluorescence and additional wavelength-dependent fluorescence in the biological samples could be eliminated by two-step normalization calibration; thus, the accuracy of Raman measurement was significantly enhanced. We applied this method to early cancer diagnosis and identified several molecules and structures worthy of attention in carcinogenesis for esophageal tissue, such as phenylalanine and the CC bonds of porphyrins. Normal, precancerous, and early cancer samples were successfully identified by the changes in biomolecules with associated degrees of malignancy. Thus, the imaging and diagnosis of indefinite tumors were realized, which verified the potential of the dual-wavelength Raman method in biological detection.

Study of the optical rotatory of potassium titanyl phosphate using the advanced dual-wavelength polarimetric method

A dual-wavelength high-accuracy universal polarimeter was applied to the circular birefringence and optical activity measurement in potassium titanyl phosphate (KTP) nonlinear crystal. The experimental setup used two single-mode He-Ne lasers with close wavelengths of 594 and 633 nm as light sources. Measurement has been carried out for two crystal settings in directions of a 45-degree relative angle to the [100] and [010] crystallographic axes. Multiple light reflections inside the crystal sample were considered when processing the results of the polarimetric measurements. The results have been analysed using the optical transmission function for the polariser-sample-analyser system, and 2D intensity contour maps made it possible to determine the phase parameters, systematic errors, and eigenwaves ellipticity. It was found that the gyration tensor component of the KTP crystal is equal to g12 = 1.4 ⋅ 10−5 which in terms of optical rotatory power corresponds to the very small magnitude of the rotation value of 2.3 deg/mm.

Seven-Core Fiber Composite Structures-Based Mach-Zehnder Interferometer for Bending and Temperature Measurement

In the paper, an optical fiber sensor based on a seven-core fiber composite structure is presented, which enables dual-parameter sensing of bending and temperature. The proposed structure is fabricated by combining the strongly-coupled seven-core fibers (SC-SCFs) and a weakly-coupled seven-core fiber (WC-SCF). The SC-SCF acts as a beam coupler and enhances the Mach-Zehnder interference, while the WC-SCF serves as the enhanced section of another Mach-Zehnder interference. Therefore, the spectrum response of the fiber structure mentioned above exhibits a superposition effect of two Mach-Zehnder interferometers (MZIs). Among them, two dips corresponding to different MZIs are used to measure bending and temperature. The experimental results show the bending sensitivity and temperature sensitivity of the two MZIs are −4.238 nm/m−1, −2.263 nm/m−1, 0.047 nm/°C, and 0.064 nm/°C, respectively. It proves that our sensor is very sensitive to bending. Through the dual-wavelength matrix method, the bending and temperature can be measured simultaneously. With the benefit of the composite structure, low cost, and ease of fabrication, the proposed sensor can be used in harsh environments.

Specialized greenness sustainability tools for evaluation of the spectrophotometric methodologies greenness: Spectral signal manipulation for resolving the interfering telmisartan and metoprolol succinate spectra in their bulk and pharmaceutical formulation

Hypertension is a leading cause of cardiovascular mortality, often accompanied by complications such as arrhythmia and stroke. This silent killer requires a multifaceted pharmacological approach for effective management. This article presents new, environmentally friendly spectrophotometric methods for simultaneous quantification of telmisartan (TER) and metoprolol succinate (MTR) in laboratory prepared mixtures and pharmaceutical formulations. The suggested methodologies include the following: area under the curve method (AUC) utilizing area at specific wavelength ranges 228–233 nm (λ1 – λ2) and 240–245 nm (λ3 – λ4) for each analyte and Fourier self-deconvolution method (FD) depending on built-in function to address spectral interferences. In addition, the induced dual wavelength method (IDWL) employing equality factors to obtain absorbance differences at designated wavelengths, ratio difference method (RD) utilizing divisor-based ratio spectra where the utilized divisors were TER 40 μg/mL and MTR 90 μg/mL, and ratio derivative method (RDV) generating spectra through first derivative application that was measured at 266 nm and 246 nm for TER and MTR, respectively. These methods offer green alternatives for the accurate and precise determination of TER and MTR with exceptional linearity of 3–45, and 15–200 μg/mL for TER and MTR, respectively. Furthermore, the methods showed a coefficient of determination exceeding 0.9995 and good detection and quantification levels. A comprehensive greenness assessment, employing five distinct evaluation tools, confirmed the reduced environmental impact of the proposed methods in terms of waste generation, chemical consumption, and instrument safety. Successful analysis of pharmaceutical formulations and laboratory prepared mixtures containing different TER and MTR ratios confirmed the validity of the proposed methods. Standard addition studies further supported these findings, and the statistical results were comparable to those obtained using a reference method.

Spectrophotometric determination of olanzapine, fluoxetine HCL and its impurity using univariate and chemometrics methods reinforced by latin hypercube sampling: Validation and eco-friendliness assessments

Novel univariate and chemometrics-aided UV spectrophotometric methods were tailored to undergo the fundamentals of green and white analytical chemistry for the simultaneous estimation of a ternary mixture of olanzapine (OLA), fluoxetine HCL (FLU), and its toxic impurity 4-(Trifluoromethyl) phenol (FMP) without any prior separation. The dual-wavelength ratio spectrum univariate method was used to determine OLA and FLU in the presence of FMP in the range of (4–20) and (5–50) μg/ml, respectively. In compliance with the International Conference on Harmonization (ICH) standards, the technique was validated and established Remarkable accuracy (98–102%) and precision (< 2%) with limits of quantification (LOQs) of 0.432 and 2.002 μg/ml, respectively. Partial least squares (PLS) and artificial neural networks (ANNs) are chemometric methodologies that have advantages over the univariate method and use significant innovations employing Latin hypercube sampling (LHS), allowing the generation of a reliable validation set to guarantee the effectiveness and sustainability of these models. The concentration ranges used were (2–20), (2–20), and (5–50) μg/ml; for PLS, the LOQs were 0.602, 0.508, and 1.429 μg/ml, and the root mean square errors of prediction (RMSEPs) were 0.087, 0.048, and 0.159 for OLA, FMP, and FLU, respectively; and for ANNs, the LOQs were 0.551, 0.465, and 0.965 μg/ml, with RMSEPs of 0.056, 0.047, and 0.087 for OLA, FMP, and FLU, respectively. The developed methods yield a greener National Environmental Methods Index (NEMI) with an eco-scale assessment (ESA) score of 90 and a complementary Green Analytical Procedure Index (complex GAPI) in quadrants with an analytical greenness metric (AGREE) score of 0.8. The Red‒Green–Blue 12 algorithm (RGB 12) scored 88.9, outperforming on reported methods and demonstrating widespread practical and environmental approval. Statistical analysis revealed no noteworthy differences (P > 0.05) among the proposed and published techniques. Both pure powders and pharmaceutical capsules were analyzed via these methods.

Dual-wavelength transmission based on liquid crystal tunable filter with high signal-to-noise ratio

Aiming at the problem of limited transmission energy of liquid crystal tunable filter (LCTF), a dual-wavelength transmission system with high signal-to-noise ratio (SNR) is proposed in this paper. The proposed transmission factor Qp is the main influence on the number and location of transmission wavelengths as well as the bandwidth of each transmission wavelength for dual-wavelength systems. Dual-wavelength LCTF can improve the effective transmission energy of the system by increasing the number of filtering channels, and the transmission energy can be increased by about 1.8 times and 70% at short and long wavelengths, respectively, which improves the signal-to-noise ratio (SNR) of the system. Moreover, the dual-wavelength LCTF system is even possible to increase the transmission energy by about 7% at a 33% increase in spectral resolution. Therefore, the dual-wavelength LCTF transmission method not only can improve the SNR of target detection with dual-wavelength response features, but also can effectively solve the problem of contradiction between spectral resolution and spectral transmission energy.

A Brief Review on Dual Wavelength Spectrophotometry: The Simultaneous Estimation Method and its Application

The dual wavelength spectrophotometry is developed and validated for simultaneous estimation of various combinations of two drugs. Dual wavelength method is used to eliminate interference due to absorbance of other drug at sampling wavelengths for one drug. Two wavelengths are selected for each drug in such a way that the difference in absorbance is zero for the second drug. The principle for dual wavelength method is the absorbance difference between two points on the mixture spectra is directly proportional to the concentration of the component of interest and independent of interfering component. The Following review article contains a brief regarding dual wavelength spectrophotometry introduction, principle, examples and application of different pharmaceutical, organic and inorganic compounds.

Sustainable and technically smart spectrophotometric determination of PAXLOVID: a comprehensive ecological and analytical performance rating

The Food and Drug Administration (FDA) authorized the administration of ritonavir (RIT)-boosted nirmatrelvir (NMV) on May 25, 2023, for the treatment of mild to moderate COVID-19 in patients who are at high risk of developing severe COVID-19. In accordance with sustainability and environmental friendliness, simple, eco-friendly, and sustainable spectrophotometric methods were established for concurrently estimating RIT and NMV in newly launched copackaged pills. The suggested solutions for resolving the spectral overlap between RIT and NMV involve the following mathematical methods: the first derivative method (1D), second derivative method (2D), and dual-wavelength zero-order method (DWZ). When ethanol was used as a green dilution solvent, the linearity range was adjusted (10–250 µg/mL) for both drugs. The procedures resulted in a high correlation coefficient (not less than 0.9996) and satisfactory levels of detection and quantification. Additionally, method validation was performed in accordance with International Council for Harmonization norms. Moreover, a detailed ecological and sustainability evaluation protocol was established to confirm the greenness and whiteness of the methods. Finally, the proposed method, along with previously reported methods for analysing NMV and RIT, were reviewed analytically and ecologically.

Implementation of an FPGA-Based 3D Shape Measurement System Using High-Level Synthesis

Three-dimensional(3D) shape measurement using point clouds has recently gained significant attention. Phase measuring profilometry (PMP) is widely preferred for its robustness against external lighting changes and high-precision results. However, PMP suffers from long computation times due to complex calculations and its high memory usage. It also faces a 2π ambiguity issue, as the measured phase is limited to the 2π range. This is typically resolved using dual-wavelength methods. However, these methods require separate measurements of phase changes at two wavelengths, increasing the data processing volume and computation times. Our study addresses these challenges by implementing a 3D shape measurement system on a System-on-Chip (SoC)-type Field-Programmable Gate Array (FPGA). We developed a PMP algorithm with dual-wavelength methods, accelerating it through high-level synthesis (HLS) on the FPGA. This hardware implementation significantly reduces computation time while maintaining measurement accuracy. The experimental results demonstrate that our system operates correctly on the SoC-type FPGA, achieving computation speeds approximately 11.55 times higher than those of conventional software implementations. Our approach offers a practical solution for real-time 3D shape measurement, potentially benefiting applications in fields such as quality control, robotics, and computer vision.

Simultaneous spectrophotometric and chromatographic determination of Ketorolac and Dexamethasone: Overall assessment regarding environmental Impact, Practicality, and functionality principles

Determination of a drug combination that contains a minor component that is also a poorly UV absorbing analyte represents greet challenges in drug analysis. A fixed-dose ophthalmic combination of ketorolac tromethamine (KET) and dexamethasone sodium phosphate (DEX) (in the ratio of 5:1) is used to relieve post-surgical inflammation and seasonal allergic conjunctivitis due to their analgesic and anti-inflammatory activity. Five spectrophotometric methods and a reversed phase chromatographic separation method were developed and validated for simultaneous determination of both drugs in lab-prepared eye drops. Direct spectrophotometric determination of KET (the major, highly UV absorbing analyte) was achieved from the zero-order UV absorption spectra at 323 nm while DEX (which is the minor, poorly UV absorbing analyte) was quantified after applying several spectrophotometric methods. Either fundamental zero-order spectra or ratio spectra were used, and measurements were done at either single or dual wavelengths. The developed methods were: isosbestic point method, absorption factor method, dual wavelength method, ratio difference UV spectrophotometric method, and simultaneous equation method. The developed spectrophotometric methods determine KET in the linearity range of 2.0–12.0 μg/mL and DEX in the range of 5.0 – 35.0 μg/mL. For accurate spectrophotometric determination of DEX in the ratio of the dosage form, multiple standard addition method was applied. HPLC technique was also applied for separation and quantification of both drugs. Chromatographic separation was attained by using Hypersil ODS-C18 (150 x 4.6 mm, 5 μm) column. The mobile phase was composed of 50 % methanol: 50 % phosphate buffer (pH 2.5). The column compartment was maintained at 25 °C. Flow rate was adjusted at 1.2 mL/min and detection was performed by DAD at 254 nm. The linearity of HPLC method was 5.0–100.0 μg/mL, and 5.0–50.0 μg/mL for KET and DEX, respectively. Simultaneous determination of both drugs was applied to lab-prepared eye drops that contain also benzalkonium chloride as inactive ingredient. The developed methods determined the cited drugs with good and acceptable % recovery. The results of the developed methods and a reported HPLC method were compared using one-way ANOVA test, F-test and student’s t-test at confidence level 95 %, and they show no significant statistical difference. Assessment of greenness of the developed methods in comparison with reported HPLC method was performed using different tools, including analytical eco-scale, GAPI and AGREE. HPLC-EAT was also performed to ensure greenness of developed HPLC method. Moreover, assessment of practicality, applicability, and functionality of developed and reported methods was evaluated by BAGI metric tool and WAC calculator, respectively. The developed methods allow simple, rapid, and accurate analysis of quality control samples that contain KET and DEX.

Simultaneously Estimation of Multicomponent Containing Formulation by using UV-Spectroscopy [Aspirin-Atorvastatin

The market is currently offering a wide range of combination dose forms, and the quantity is growing daily. Due to their improved potency, various actions, speedier relief, fewer side effects, and higher patient acceptability, these multicomponent formulations are becoming more and more popular. It is therefore intended that these formulations satisfy all requirements for their efficacy, safety, and quality. This is only feasible if many analytical methods are available to determine them. When doing a simultaneous multicomponent analysis, various UV spectrophotometric techniques are applied.These techniques rely on logging and processing absorption spectra computationally. The various techniques covered in this review include the use of simultaneous equations, derivative spectrophotometry, mean centring of the ratio spectra, absorption factor method, double divisor ratio spectra derivative method, successive ratio derivative spectra, Q-absorbance ratio method, isosbestic point method, absorpitivity factor method, dual wavelength method, mean centring of the ratio spectra, and multivariate methods. A synopsis of the theories and a few uses for these techniques are given.

In silico modified UV spectrophotometric approaches to resolve overlapped spectra for quality control of rosuvastatin and teneligliptin formulation

Abstract A binary blend of rosuvastatin (ROS) and teneligliptin (TEN) used for the management of cardiovascular complications require a simple, analytical process for the quality assurance of this formulation. UV absorption spectra of ROS and TEN showed overlapping spectra. Hence, the overlapped spectra of ROS and TEN were separated by ratio difference, ratio first derivative; constant extraction coupled with exponentiation with division spectrum, and induced dual-wavelength methods. The proposed methods were authenticated by following the international council for harmonization criteria. A good linear relationship was demonstrated by all four methods, in 2–15 and 2–30 µg/mL for ROS and TEN, respectively. The high percentage retrieval of 98.96–100.22 and 98.72–99.73% for ROS and TEN, respectively, with small relative error, assured the correctness of the techniques. The validated techniques were employed for concurrent evaluation of ROS and TEN from binary formulation and laboratory-prepared mixture. The standard addition process verified the reliability of the projected procedures. The developed methods showed same accuracy and precision when compared to the HPLC methods along with safer solvent. Finally, the environmental sustainability of the presented UV spectroscopic procedures was found to be better than the reported HPLC method. Hence, eco-friendly, simple, and accurate mathematically processed UV spectroscopic procedures can be employed for simultaneous quantification of ROS and TEN for routine quality control study.

Novel UV Spectrophotometric approaches for the concurrent determination of Teneligliptin and Metformin in Tablet Formulation

In the study simultaneous assessment of teneligliptin hydrobromide hydrate and metformin hydrochloride in tablets were developed and validated by four new UV spectroscopic approaches. The ratio difference approach was used to measure the variation in two selected amplitudes of ratio spectra, and the regression equation was employed to determine the amounts of pharmaceuticals. The second approach, known as the first derivative of ratio spectra approach, the UV spectra were transformed into their ratio spectra and corresponding first derivatives, and the first-derivative signal was gauged at 275 and 226.2 nm for metformin hydrochloride and teneligliptin hydrobromide hydrate, sequentially, making use of 2 nm as the wavelength interval (Δλ) and a factor of 1 as a scaling factor, respectively. Whereas absorbance subtraction method works with the principle of finding isosbestic point and calculating absorption factor. The fourth approach, known as the dual wavelength method, relies on computing the absorbance difference at two different wavelengths where the other drug has same absorbance. Linearity and range, specificity, accuracy, precision, limit of detection and quantification were among the criteria evaluated during validation of the new methods in agreement with ICH recommendations and found to be within the permitted limits. For both the medicines, a linear response was observed in all four methods over the concentration sequence of 2-12 µg/ml. Therefore, the proposed methodologies may be successfully used for the concurrent evaluation of teneligliptin hydrobromide hydrate and metformin hydrochloride in tablet form.

Utility of sustainable ratio derivative spectrophotometry for the concurrent assay of synergistic repurposed drugs for COVID-19 infections; Insilico pharmacokinetics proof

The cutting-edge combination of fluvoxamine (FVM) and ivermectin (IVM) has been presented as a proposed dosage form for the treatment of COVID-19 infections in early diagnosed patients. The main objective of this work is to develop simple, sensitive, and efficient methods for the synchronous quantification of FVM and IVM without any prior separation. Four green UV-methods were employed for the synchronous quantification, namely: Fourier functions convolution of absorption spectra, FFAS, Fourier functions convolution of derivative spectra of absorption curves, FFDS, Fourier function convolution of ratio spectra of absorption curves, FFRS and the dual-wavelength method, DWM. FFRS and DWM approaches can be able to reconcile the two components' significantly interfering spectrum presented in this commixture. Good linearity was checked in the range of 5–40, and 2.5–25 μg/mL for the FVM, and IVM, respectively. All approaches developed have been recommended in compliance with ICH principles. Furthermore, the approaches’ greenness was predestined by “National Environmental Method Index” (NEMI), “Analytical GREEnness metric (AGREE)”, the “Analytical Eco-Scale”, and the “Green Analytical Procedure Index” (GAPI). In addition, spider diagram was utilized for the assessment of the greenness index of the solvent used. Beside greenness, the sustainability of our methods was investigated using the HEXAGON tool. Continuing the constant pursuit of greenness, drug-drug interactions (DDIs) between FVM & IVM were predicted by insilico tools to ensure the safety of the suggested mixture as a preliminary step before invitro and in vivo studies. Because they were deemed sustainable, affordable, and successful, the suggested UV-methods may be used for routine quality control investigations of the indicated formulations FVM & IVM.