Development and Validation of Reversed-phase High-performance Liquid Chromatography Method for the Simultaneous Estimation of Benzoyl Peroxide and Resveratrol
A new, reliable, and sensitive reversed-phase high-performance liquid chromatography method has been developed and validated for simultaneous assay of benzoyl peroxide (BPO) and resveratrol. An isocratic separation of BPO and resveratrol was achieved on C18, 250 mm × 4.6 mm I.d., 5 μm particle size columns with a flow rate of 1.2 ml/min and using a UV detector to monitor the elute at 245 nm. The mobile phase consisted of an ammonium acetate (pH 4) and ethanol. Response was a linear function of drug concentration in the range of 10–100 mg/mL range with an R2 of 0.993 for BPO and 10–100 μg/mL range with an R2 of 0.995 for resveratrol, accuracy with percent relative standard deviation of 100.65 ± 0.23 (benzoic peroxide) and 100.48 ± 0.45 (resveratrol) and with a limit of detection and quantification for BPO and resveratrol, respectively. The result of analysis has been validated statistically and by recovery study. The accuracy ranged between 99.65 and 101.91%. The method was found to be precise, reproducible, and rapid.
Analytical method development and validation for the estimation of quinapril ...SriramNagarajan19
A simple and selective LC method is described for the determination of Quinapril and Tolcapone tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a Mixed Phosphate buffer (KH2PO4 +K2HPO4): Acetonitrile 40:60, with detection of 239 nm. Linearity was observed in the range 50 - 150 µg /ml for Quinapril (r2 =0.995) and 62.5- 187.5µg /ml for Tolcapone (r2 =0.999) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
An emerging way of estimation of Olmesartan medoxomil & Hydrochlorothiazide i...Priyanka Bose
An emerging way of estimation of Olmesartan medoxomil & Hydrochlorothiazide in Bulk & Combined tablet dosage form by Absorbance Correction Method using methanol as solvent system. It is cost effective, highly precised method for estimation.
Analytical method development and validation for the estimation of quinapril ...SriramNagarajan19
A simple and selective LC method is described for the determination of Quinapril and Tolcapone tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a Mixed Phosphate buffer (KH2PO4 +K2HPO4): Acetonitrile 40:60, with detection of 239 nm. Linearity was observed in the range 50 - 150 µg /ml for Quinapril (r2 =0.995) and 62.5- 187.5µg /ml for Tolcapone (r2 =0.999) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
An emerging way of estimation of Olmesartan medoxomil & Hydrochlorothiazide i...Priyanka Bose
An emerging way of estimation of Olmesartan medoxomil & Hydrochlorothiazide in Bulk & Combined tablet dosage form by Absorbance Correction Method using methanol as solvent system. It is cost effective, highly precised method for estimation.
Bioanalytical RP-HPLC Method Development and Validation for Estimation of Cur...Sagar Savale
The present study was aimed at developing a reversed phase high performance liquid chromatography (RPHPLC) method for determination of curcumin (CRM) in plasma and hydrochlorothiazide was used as an internal
standard. The separation was achieved by using C-18 column (Qualisil BDS C18, 250 mm x 4.6 mm I.D.)
coupled with a guard column of silica, mobile phase was consisting of acetonitrile: water with 0.1% formic acid
(40:60 v/v). The flow rate was 0.3 ml/min and the drug was detected using PDA detector at the wavelength of 423
nm. The experimental conditions, including the diluting solvent, mobile phase composition, column saturation
and flow rate, were optimised to provide high-resolution and reproducible peaks. The developed method was
validated in terms of linearity, recovery, precision, ruggedness, sensitivity (LOD and LOQ) and stability study
(short and long-term stabilities, Freeze/thaw stability and post-preparative).
A new analytical method development and validation for the simultaneus estima...SriramNagarajan19
A simple and selective LC method is described for the determination of Ibuprofen and Tramadol in tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a mixture of 60 volumes of Triethylamine buffer, 40 volumes of acetonitrile with detection of 227 nm. Linearity was observed in the range 50-150 µg/ml for Ibuprofen (r2 =0.983) and 50-150 µg /ml for Tramadol (r2 =0.985) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
A newly validated HPLC method development for simultaneous estimation of rito...SriramNagarajan19
The aim of the present work was to develop a isocratict RP-HPLC for simultaneous analysis of ritonavir and lopinavir in tablet dosage form. Method: chromatographic system was optimized using a Agilent XDB C18(150 x 4.6mm,5µm) column with potassium dihydrogen phosphate (pH 4.6) and acetonitrile in the ratio of 45;55, as a mobile phase, at a flow rate of 1.0 ml/min. detection was carried out at 215nm by a photodiode array detector. Result: ritonavir and lopinavir were eluted with retention times of 4.821 and 3.814mins respectively. Beer’s lambert’s law was obeyed over the concentration ranges of 12.5 to 50µg/ml and 50 to 200µg/ml for ritonavir and lopinavir, respectively. Conclusion: the high recovery and low coefficients of variation confirm the suitability of the method for simultaneous analysis of both drugs in a tablet dosage form. Statistical analysis proves that the method is sensitive and significant for the analysis of ritonavir and lopinavir in pure and in pharmaceutical dosage form without any interference from the excipients. The method was validated in accordance with ICH guidelines. Validation revealed the method is specific, rapid, accurate, precise, reliable, and reproducible.
A new analytical method development and validation for the simultaneus estima...SriramNagarajan19
A simple and selective LC method is described for the determination of Albuterol and Ipratropium Bromide in tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a mixture of 80 volumes of methanol and 20 volumes of water with detection of 239 nm. Linearity was observed in the range 36-84 µg /ml for Albuterol (r2 =0.996) and 6-14 µg /ml for Ipratropium Bromide (r2 =0.997) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
Aim: UV Spectrophotometric Method Development and Validation for quantitative estimation of
Diclofenac Sodium. Objective: U.V Spectrophotometric method have been widely employed for
determination of analyte in a mixture. Our aim is to develop spectroscopic method for estimation of the
diclofenac sodium in ternary mixture by using U.V spectrophotometry. Methodology: The method was
validated as per ICH guidelines. The recovery studies confirmed the accuracy and precision of the method.
Conclusion: It was successfully applied for the analysis of the drug in bulk and could be effectively used for
the routine analysis.
IOSR Journal of Pharmacy and Biological Sciences(IOSR-JPBS) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of Pharmacy and Biological Science. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Pharmacy and Biological Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
UV Spectrophotometric Method Development And Validation For Quantitative Esti...Sagar Savale
U.V Spectrophotometric method have been widely employed in determination of Halcinonide in a mixture or fixed dose combination. For the ternary mixture containing Halcinonide, no spectrophotometric method for evaluation has been reported so far. Thus our aim is to develop method for Halcinonide estimation in ternary mixture using U.V spectrophotometry.
The drug or drug combination may not be official in any pharmacopoeias.
A proper analytical procedure for the drug may not be available in the literature due to patent regulations.
Analytical methods may not be available for the drug in the form of a formulation due to the interference caused by the formulation excipients.
Analytical methods for the quantitation of the drug in biological fluids may not be available.
Analytical methods for a drug in combination with other drugs may not be available.
The existing analytical procedures may require expensive reagents and solvents. It may also involve cumbersome extraction and separation procedures and these may not be reliable.
Bioanalytical RP-HPLC Method Development and Validation for Estimation of Cur...Sagar Savale
The present study was aimed at developing a reversed phase high performance liquid chromatography (RPHPLC) method for determination of curcumin (CRM) in plasma and hydrochlorothiazide was used as an internal
standard. The separation was achieved by using C-18 column (Qualisil BDS C18, 250 mm x 4.6 mm I.D.)
coupled with a guard column of silica, mobile phase was consisting of acetonitrile: water with 0.1% formic acid
(40:60 v/v). The flow rate was 0.3 ml/min and the drug was detected using PDA detector at the wavelength of 423
nm. The experimental conditions, including the diluting solvent, mobile phase composition, column saturation
and flow rate, were optimised to provide high-resolution and reproducible peaks. The developed method was
validated in terms of linearity, recovery, precision, ruggedness, sensitivity (LOD and LOQ) and stability study
(short and long-term stabilities, Freeze/thaw stability and post-preparative).
A new analytical method development and validation for the simultaneus estima...SriramNagarajan19
A simple and selective LC method is described for the determination of Ibuprofen and Tramadol in tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a mixture of 60 volumes of Triethylamine buffer, 40 volumes of acetonitrile with detection of 227 nm. Linearity was observed in the range 50-150 µg/ml for Ibuprofen (r2 =0.983) and 50-150 µg /ml for Tramadol (r2 =0.985) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
A newly validated HPLC method development for simultaneous estimation of rito...SriramNagarajan19
The aim of the present work was to develop a isocratict RP-HPLC for simultaneous analysis of ritonavir and lopinavir in tablet dosage form. Method: chromatographic system was optimized using a Agilent XDB C18(150 x 4.6mm,5µm) column with potassium dihydrogen phosphate (pH 4.6) and acetonitrile in the ratio of 45;55, as a mobile phase, at a flow rate of 1.0 ml/min. detection was carried out at 215nm by a photodiode array detector. Result: ritonavir and lopinavir were eluted with retention times of 4.821 and 3.814mins respectively. Beer’s lambert’s law was obeyed over the concentration ranges of 12.5 to 50µg/ml and 50 to 200µg/ml for ritonavir and lopinavir, respectively. Conclusion: the high recovery and low coefficients of variation confirm the suitability of the method for simultaneous analysis of both drugs in a tablet dosage form. Statistical analysis proves that the method is sensitive and significant for the analysis of ritonavir and lopinavir in pure and in pharmaceutical dosage form without any interference from the excipients. The method was validated in accordance with ICH guidelines. Validation revealed the method is specific, rapid, accurate, precise, reliable, and reproducible.
A new analytical method development and validation for the simultaneus estima...SriramNagarajan19
A simple and selective LC method is described for the determination of Albuterol and Ipratropium Bromide in tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a mixture of 80 volumes of methanol and 20 volumes of water with detection of 239 nm. Linearity was observed in the range 36-84 µg /ml for Albuterol (r2 =0.996) and 6-14 µg /ml for Ipratropium Bromide (r2 =0.997) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
Aim: UV Spectrophotometric Method Development and Validation for quantitative estimation of
Diclofenac Sodium. Objective: U.V Spectrophotometric method have been widely employed for
determination of analyte in a mixture. Our aim is to develop spectroscopic method for estimation of the
diclofenac sodium in ternary mixture by using U.V spectrophotometry. Methodology: The method was
validated as per ICH guidelines. The recovery studies confirmed the accuracy and precision of the method.
Conclusion: It was successfully applied for the analysis of the drug in bulk and could be effectively used for
the routine analysis.
IOSR Journal of Pharmacy and Biological Sciences(IOSR-JPBS) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of Pharmacy and Biological Science. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Pharmacy and Biological Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
UV Spectrophotometric Method Development And Validation For Quantitative Esti...Sagar Savale
U.V Spectrophotometric method have been widely employed in determination of Halcinonide in a mixture or fixed dose combination. For the ternary mixture containing Halcinonide, no spectrophotometric method for evaluation has been reported so far. Thus our aim is to develop method for Halcinonide estimation in ternary mixture using U.V spectrophotometry.
The drug or drug combination may not be official in any pharmacopoeias.
A proper analytical procedure for the drug may not be available in the literature due to patent regulations.
Analytical methods may not be available for the drug in the form of a formulation due to the interference caused by the formulation excipients.
Analytical methods for the quantitation of the drug in biological fluids may not be available.
Analytical methods for a drug in combination with other drugs may not be available.
The existing analytical procedures may require expensive reagents and solvents. It may also involve cumbersome extraction and separation procedures and these may not be reliable.
Similar to Development and Validation of Reversed-phase High-performance Liquid Chromatography Method for the Simultaneous Estimation of Benzoyl Peroxide and Resveratrol
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
U.V Spectrophotometric method have been widely employed in determination of individual components in a mixture or fixed dose combination. Our aim is to develop spectroscopic method for estimation of the paracetamol in ternary mixture by using U.V spectrophotometry.
Stability indicating analytical method development and validation for estimat...SriramNagarajan18
Stability indicating analytical method development and validation for estimation of Ceftazidime and Avibactam in bulk and pharmaceutical dosage form using RP-HPLC
Analytical method development and validation for the estimation of aspirin an...SriramNagarajan19
A simple and selective LC method is described for the determination of Aspirin and Omeprazole in tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a mixture of 30 volumes of ammonium acetate buffer, 40 volumes of acetonitrile and 30 volumes of Methanol with detection of 233 nm. Linearity was observed in the range 18-42 µg/ml for Aspirin (r2 =0.983) and 6-14 µg /ml for Omeprazole (r2 =0.970) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim. The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
Stability Indicating RP HPLC Method Development and Validation of Everolimus ...ijtsrd
Everolimus is semisynthetic derivative of sirolimus, which is isolated from Streptomyces hygroscopicus. A novel reversed phase high performnce liquid chromatography HPLC method for determination of the everolimus in the presence of degradation product or pharmaceutical excipients. Seperation was carried out using Cosmosil C18 250mm x 4. 6ID , column having particle size 5 micron using acetonitrile and methanol mixture, and pH adjusted to 3, a flow rate of 1. 0 mL min, and ultraviolet detection at 285nm. A retention time nearly 3. 806 min was observed. The calibration curve for everolimus was linear from range of 5 25 µg mL with limit of detection and limit of quantitation of 0. 0817 and 0. 2478 µg mL, respectively. Analytical validation parameters such as selectivity, specificity, linearity, accuracy and precision were evaluated and relative standard deviation value for all the key parameters were less than 2. 0 . The stability indicating method was developed by exposing the drug to stress conditions of acid and base hydrolysis, oxidation, photodegradation, and thermal degradation the obtained degraded products were successfully seperated from the APIs. This method was validated in acceptance with ICH guidelines and results within the acceptance criteria. Rushikesh Mulay | Rishikesh Bachhav "Stability Indicating RP-HPLC Method Development and Validation of Everolimus in Bulk and Pharmaceutical Dosage Form" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, URL: https://www.ijtsrd.com/papers/ijtsrd46341.pdf Paper URL : https://www.ijtsrd.com/pharmacy/analytical-chemistry/46341/stability-indicating-rphplc-method-development-and-validation-of-everolimus-in-bulk-and-pharmaceutical-dosage-form/rushikesh-mulay
A new analytical method development and validation for the simultaneus estima...SriramNagarajan19
A simple and selective LC method is described for the determination of LEDIPASVIR and SOFOSBUVIR in tablet dosage forms. Chromatographic separation was achieved on a c18 column using mobile phase consisting of a mixture of Mixed Phosphate Buffer:ACN (55:45) with detection of 213 nm. Linearity was observed in the range 60-140 µg/ml for LEDIPASVIR oxalate (r2 =0.999) and 6-14 µg /ml for SOFOSBUVIR (r2 =0.996) for the amount of drugs estimated by the proposed methods was in good agreement with the label claim.
The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form.
Determination of Satranidazole through Ion-Associative Complex ReactionRatnakaram Venkata Nadh
A simple, selective, accurate and low-cost spectrophotometric method
has been described for determination of satranidazole in bulk and
pharmaceutical formulations. The developed method involves the
formation of chloroform extractable colored ion-association complex
of satranidazole with Tropaeolin OOO (TPooo). The extracted colored
complex showed absorbance maximum at wavelength 484 nm and
obeying Beer′s law in the concentration 4-20 μg mL-1 with the
correlation coeffiecent of 0.9998. The results of statistical analysis of
the proposed method reveals high accuracy and good precession. Thus,
the proposed method can be used commercially for the determination
of satranidazole in bulk and pharmaceutical formulations.
Determination of Satranidazole through Ion-Associative Complex ReactionRatnakaram Venkata Nadh
A simple, selective, accurate and low-cost spectrophotometric method
has been described for determination of satranidazole in bulk and
pharmaceutical formulations. The developed method involves the
formation of chloroform extractable colored ion-association complex
of satranidazole with Tropaeolin OOO (TPooo). The extracted colored
complex showed absorbance maximum at wavelength 484 nm and
obeying Beer′s law in the concentration 4-20 μg mL-1 with the
correlation coeffiecent of 0.9998. The results of statistical analysis of
the proposed method reveals high accuracy and good precession. Thus,
the proposed method can be used commercially for the determination
of satranidazole in bulk and pharmaceutical formulations.
Development and Validation of Reversed Phase-High-Performance Liquid Chromato...BRNSS Publication Hub
A simple, accurate, precise, and robust in vitro methods developed and validated for measurement of drug release in Aminocaproic Acid tablets. High-performance liquid chromatography (HPLC) method for quantification of drug in dissolution samples of Aminocaproic Acid tablet is developed and validated. 0.1 N Hydrochloric acid is used as dissolution medium and Basket (USP-I) as apparatus at 100 rpm. The sample was withdrawn after 60 min. The developed HPLC method was used for quantitative estimation of drug release in dissolution samples of Aminocaproic Acid tablet. Chromatogram was run through Inertsil ODS 3V, (250 × 4.6 mm), 5 μm. Mobile phase containing buffer solution and methanol in the pumped through column at a flow rate of 1 ml/min. Buffer used in this method was 13.3 g sodium dihydrogen phosphate monohydrate, 500 mg of Heptane-1-sulfonic acid sodium salt, and 1.0 mL of Triethylamine buffer with pH 2.20 adjusted by orthophosphoric acid. Optimized wavelength for Aminocaproic acid was 210 nm. Retention time of Aminocaproic acid was found about 4.0 min; linearity range was 132.605 μg/ml–828.787 μg/ml. The new method was evaluated according to ICH guideline and as far as validation results are concern correlation coefficient value was 0.9999 for the very compound, percentage recovery 100.0%, repeatability results relative standard deviation 0.9 for Aminocaproic acid. The developed HPLC method was found to be a simple and rapid one for regular analysis in professional laboratory.
International Journal of Pharmaceutical and Biological Archive
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Development and Validation of Reversed-phase High-performance Liquid Chromatography Method for the Simultaneous Estimation of Benzoyl Peroxide and Resveratrol
2. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 114
98.99% and 70.00%, respectively. Ammonium
acetate (RCI Lab Scan), ethanol (RCI Lab Scan),
and water (Milli-Q) used were of HPLC grade to
prepare the mobile phase and diluents.
Instrument and chromatographic condition
The instrument used: LC-2010, Shimadzu,
Japan,equipped with an UV-Visible detector and
a photodiode array detector (an auto-sampler,
Luna®)
Stationary Phase: C18, 250 × 4.6 mm, 5µ particle
size
Elution mode: Linear gradient elution [A:B
(20:80)v/v]
Mobile phase: A: Ammonium acetate pH 4.0
(20.0 mM of Ammonium acetate was prepared in
distilled water for 1000 ml volume and pH was
maintained up to 4.0 with glacial acetic acid)
B: Ethanol
Absorption maxima: 245 nm
Column Temperature: 40 ᵒC
Flow rate: 1.2 ml/min.
Injection volume: 10 µl
Diluent: Ethanol
Table 1: Retention time of drugs (resveratrol and benzoyl
peroxide)
Name of drug Retention time (min)
Resveratrol 2.361
Benzoyl peroxide 4.486
EXPERIMENTAL WORK
Standard stock solution preparation
Standard solution preparation
About 100 mg of drug was dissolved in 100 ml of
diluents (as mentioned above) to obtain a solution
of 1000 µg/ml as stock.
Standards mixture preparation
Standard solution of both the drugs was mixed in
the ratio of 1:1 to prepare a mixture solution.
HPLC chromatogram of mixture sample
On HPLC analysis of mixture of standards,
chromatogram was optimized in which retention
time of drugs [Tables 1-9].
Figure 2: Structure of benzoyl peroxide
Figure 1: Chemical structure of resveratrol
Figure 3: A linear curve was obtained in the range of 10–100
μg/ml with an equation of y=35905.x +69541 and R2=0.995
Figure 4: A linear curve was obtained in the range of
10–100 μg/ml with an equation of y=36545.x+66902 and
R2=0.993
3. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 115
Validation of HPLC method[6,7]
Linearity and range
The linearity of analytical method is its ability
to elicit test results that are directly proportional
to the concentration of analyte in sample within
a given range. The range of analytical method is
the interval between the upper and lower levels
of analyte that have been demonstrated to be
determined within a suitable level of precision,
accuracy, and linearity. Linearity range for
resveratrol and benzoyl peroxide was found to
be 10-100µg/ml. All the dilutions were filtered
through 0.22 µ filter and injected.
Accuracy
Accuracy of the method was determined in terms
of percentage recovery of standard. Recovery
studies were carried out by addition of standard
Table 2: Resveratrol linearity
Concentration (μg/ml) Retention time Mean ± SD Area Mean ± SD
10 2.361 2.360667 ± 0.000577 1056164 1054246 ± 6367.468
2.361 1059434
2.36 1047140
20 2.36 2.358667 ± 0.004163 1336893 1334957 ± 1682.97
2.354 1334135
2.362 1333843
40 2.361 2.363333 ± 0.002082 2198612 2194148 ± 5446.838
2.364 2195753
2.365 2188079
60 2.359 2.362333 ± 0.004933 2853813 2859021 ± 6842.789
2.368 2866771
2.36 2856479
80 2.358 2.36 ± 0.002 3651879 3676891 ± 22593.12
2.362 3695820
2.36 3682973
100 2.36 2.361 ± 0.001732 4178500 4183833 ± 12757.26
2.36 4174607
2.363 4198391
SD: Standard deviation
Table 3: Linearity of benzoyl peroxide
Concentration (μg/ml) Retention time Mean ± SD Area Mean ± SD
10 4.698 4.585667 ± 0.106566 1036331 1039717 ± 7506.454
4.486 1048320
4.573 1034500
20 4.547 4.546333 ± 0.001155 1534173 1540111 ± 5823.588
4.547 1540347
4.545 1545813
40 4.549 4.545667 ± 0.003512 2017205 2016893 ± 461.9679
4.542 2017111
4.546 2016362
60 4.545 4.542 ± 0.003 2774099 2758076 ± 32867.71
4.539 2720270
4.542 2779860
80 4.543 4.542667 ± 0.005508 3570584 3557502 ± 11400.87
4.537 3549688
4.548 3552233
100 4.541 4.538 ± 0.003606 4430887 4460296 ± 25675.68
4.534 4478254
4.539 4471746
SD: Standard deviation
4. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 116
Table 4: Data of accuracy study of resveratrol and benzoyl peroxide
% Concentration Concentration
(resveratrol and
benzoyl peroxide)
Resveratrol
(area)
Corresponding
conc.
% Amount
recovered
Mean ± SD %RSD
50% 200 (100 + 100) 3658744 99.963877 99.9638769 99.69056 ± 0.987024 0.990088
200 (100 + 100) 3678429 100.51213 100.5121292
200 (100 + 100) 3609619 98.595683 98.59568305
75% 300 (150 + 150) 5601450 154.07071 102.7138096 102.5966 ± 1.645966 1.604308
300 (150 + 150) 5503505 151.34282 100.8952142
300 (150 + 150) 5680463 156.27133 104.1808847
100% 400 (200 + 200) 7495021 206.80908 103.4045398 105.0732 ± 1.460639 1.390116
400 (200 + 200) 7690034 212.24044 106.12022
400 (200 + 200) 7659477 211.38939 105.6946943
SD: Standard deviation, RSD: Relative standard deviation
Table 5: Data of accuracy study of resveratrol and benzoyl peroxide
% Concentration Concentration
(resveratrol and
benzoyl peroxide)
Resveratrol
(area)
Corresponding
conc.
% Amount
recovered
Mean±SD %RSD
50% 200 (100+100) 3658744 99.963877 99.9638769 99.69056±0.987024 0.990088
200 (100+100) 3678429 100.51213 100.5121292
200 (100+100) 3609619 98.595683 98.59568305
75% 300 (150+150) 5601450 154.07071 102.7138096 102.5966±1.645966 1.604308
300 (150+150) 5503505 151.34282 100.8952142
% Concentration Concentration
(resveratrol and
benzoyl peroxide)
Benzoyl
peroxide
(area)
Corresponding
conc.
Amount
recovered
Mean±SD %RSD
50% 200 (100+100) 3889227 104.5923 104.5923 102.316±2.469858 2.413952
200 (100+100) 3710068 99.68986 99.68986
200 (100+100) 3818822 102.6658 102.6658
75% 300 (150+150) 6436533 174.2956 116.197 114.5104±1.74565 1.524447
300 (150+150) 6245447 169.0668 112.7112
300 (150+150) 6350241 171.9343 114.6229
100% 400 (200+200) 8618838 234.0111 117.0056 116.4403±0.516023 0.443166
400 (200+200) 8544935 231.9889 115.9944
400 (200+200) 8568799 232.6419 116.3209
SD: Standard deviation, RSD: Relative standard deviation
drug solution at the three concentration levels
50%, 75%, and 100% in pre-analyzed sample. In
this method, the known concentration of standard
drug was added to the assay sample.
Precision
The intraday and interday variation for the
determination of all the three drugs were
carried out with concentrations over three
levels in the same day and 3 consecutive
days where repeatability was determined with
lower concentration and injected 6
times and
percentage relative standard deviation (RSD)
was calculated.
Repeatability
a. Intraday (Day-1)
b. Interday (Day-2)
c. Interday (Day-3).
Limit of detection (LOD) and limit of quantification
(LOQ)
The LOD and LOQ of developed method were
studied as per ICH guidelines. Several approaches
for determining the LOD and LOQ are possible,
depending on the procedure, i.e.,
a non-
instrumental or instrumental. Among them, here,
employed method was as follows:
LOD=3.3σ/S and
LOQ=10σ/S
6. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 118
Table 7: LOD and LOQ
Sample name LOD LOQ
Resveratrol 1.1724 (µg/ml) 3.5529 (µg/ml)
Benzoyl peroxide 2.3184 (µg/ml) 7.0255 (µg/ml)
LOD: Limit of detection, LOQ: Limit of quantification
Where, σ=The standard deviation of response
S=The slope of calibration curve.
Robustness
The robustness was studied by analyzing the sample
of lower concentration with deliberate variation in
the method parameters.The change in the responses
of drugs was noted in terms of percentage RSD.
Robustness of the method was studied by change in
flow rate or change in mobile phase ratio.
Ruggedness
The ruggedness was studied by analyzing the
same samples of three drugs by changing analyst.
The change in the responses of drugs was noted in
terms of percentage RSD.
The percentage RSD should not be more than
2. The percentage RSD obtained for change of
Level (%) Concentration (resveratrol+benzoyl peroxide) μg/ml Resveratrol (area) Mean±SD %RSD
300 (150+150) 2791055
100% 400 (200+200) 3960252 3933132.33±56655.86 1.440477
400 (200+200) 3868014
400 (200+200) 3971131
Level (%) Concentration (resveratrol+benzoyl peroxide) μg/ml Benzoyl peroxide
(area)
Mean±SD %RSD
50% 200 (100+100) 2196213 2182203±12389.11 0.567734
200 (100+100) 2177704
200 (100+100) 2172692
75% 300 (150+150) 3260804 3251008.333±39763.96 1.223127
300 (150+150) 3207262
300 (150+150) 3284959
100% 400 (200+200) 4565591 4493090±71131.53 1.583132
400 (200+200) 4423412
400 (200+200) 4490267
Interday (Day-3)
Level (%) Concentration (resveratrol+benzoyl peroxide) μg/ml Resveratrol (area) Mean±SD %RSD
50% 200 (100+100) 2016975 2029919.67±22972.07 1.131674
200 (100+100) 2016341
200 (100+100) 2056443
75% 300 (150+150) 3109663 3090264±19739.38 0.63876
300 (150+150) 3090928
300 (150+150) 3070201
100% 400 (200+200) 4023902 4032820.33±23179.12 0.574762
400 (200+200) 4015425
400 (200+200) 4059134
Level (%) Concentration (resveratrol+benzoyl peroxide) μg/ml Benzoyl peroxide
(area)
Mean±SD %RSD
50% 200 (100+100) 1303259 1310352±23746.74 1.812241
200 (100+100) 1290960
200 (100+100) 1336837
75% 300 (150+150) 3332588 3281068±50522.45 1.539817
300 (150+150) 3279010
300 (150+150) 3231606
100% 400 (200+200) 4354741 4408520.667±46776.38 1.061045
400 (200+200) 4439751
400 (200+200) 4431070
SD: Standard deviation, RSD: Relative standard deviation
Table 6: (Continued)
7. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 119
analyst was found to be 2, which was within
the acceptance criteria. Hence, the method was
rugged.
Specificity
Specificity of the methods was achieved by
the analysis of different laboratory prepared
Table 8: Robustness data of resveratrol a and b
a. Robustness data of resveratrol and benzoyl peroxide with deliberate change in flow rate
Flow rate Concentration
(resveratrol + benzoyl peroxide)
μg/ml
Resveratrol (area) Mean±SD %RSD
1 100 (50 + 50) 1953117 1947541 ± 14368.74807 0.737789
100 (50 + 50) 1931220
100 (50 + 50) 1958286
1.2 100 (50 + 50) 1819267 1815792.3 ± 3009.788254 0.165756
100 (50 + 50) 1813993
100 (50 + 50) 1814117
1.4 100 (50 + 50) 685362 673528.67 ± 10253.87426 1.522411
100 (50 + 50) 667264
100 (50 + 50) 667960
Flow rate Concentration
(resveratrol + benzoyl peroxide)
μg/ml
Benzoyl
peroxide (area)
Mean±SD %RSD
1 100 (50 + 50) 1630083 1618465 ± 15330.09 0.947199
100 (50 + 50) 1624223
100 (50 + 50) 1601090
1.2 100 (50 + 50) 1635828 1625210 ± 9948.474 0.612135
100 (50 + 50) 1616104
100 (50 + 50) 1623699
1.4 100 (50 + 50) 679452 672858 ± 8730.604 1.29754
100 (50 + 50) 662957
100 (50 + 50) 676165
b. Robustness data of resveratrol and BPO with deliberate change in mobile phase ratio
Mobile phase
ratio (ethanol: buffer)
Concentration
(resveratrol + benzoyl
peroxide) μg/ml
Resveratrol (area) Mean±SD %RSD
78:22 100 (50 + 50) 1108670 1126952.3 ± 19597.20991 1.738956
100 (50 + 50) 1124545
100 (50 + 50) 1147642
80:20 100 (50 + 50) 772479 778712 ± 7062.016638 0.906884
100 (50 + 50) 777275
100 (50 + 50) 786382
82:18 100 (50 + 50) 1221815 1208931.3 ± 16808.75553 1.390381
100 (50 + 50) 1215061
100 (50 + 50) 1189918
Mobile phase
ratio (ethanol: buffer)
Concentration (resveratrol + benzoyl
peroxide) μg/ml
Benzoyl
peroxide (area)
Mean±SD %RSD
78:22 100 (50 + 50) 871441 864326 ± 9006.983 1.042082
100 (50 + 50) 867338
100 (50 + 50) 854199
80:20 100 (50 + 50) 883716 868564.3 ± 16300.26 1.876689
100 (50 + 50) 870659
100 (50 + 50) 851318
82:18 100 (50 + 50) 1319203 1324616 ± 5054.562 0.381587
100 (50 + 50) 1325431
100 (50 + 50) 1329213
SD: Standard deviation, RSD: Relative standard deviation
8. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 120
mixtures of resveratrol and BPO within the
linearity range.
RESULTS AND DISCUSSION
The results indicate that the recoveries are
well within the acceptance range of 99–116%,
indicating a good degree of sensitivity of the
method toward detection of analytes in sample.
Therefore, method is accurate, and it can be used
for the estimation of both drugs.
Precision
The method was found to be precise due to low
values of the percentage RSD.
LOD and LOQ
The LOD and LOQ of the method were calculated
based on standard deviation of the response and the
slope (s) of the calibration curve at approximate
levels of the LOD and LOQ. The results obtained
were within the limit.
Robustness
The percentage RSD should not be more than 2.
The percentage RSD obtained for change of flow
rate, change in mobile phase ratio was found to
be 2, which was within the acceptance criteria.
Hence, the method was robust.
Ruggedness
The ruggedness was studied by analyzing the
same samples of three drugs by changing analyst.
The change in the responses of drugs was noted in
terms of percentage RSD.
The percentage RSD should not be more than
2. The percentage RSD obtained for change of
analyst was found to be 2, which was within
the acceptance criteria. Hence, the method was
rugged.
CONCLUSION
The HPLC method was developed and validated
for the simultaneous analysis of BPO and RES.
The results together established that the method is
simple, accurate, precise, reproducible, rapid, and
sensitive.Themethodcouldbeappliedsuccessfully
and economically for the simultaneous estimation
of BPO and RES in laboratory samples for efficient
data generation and for combination formulations
of these two drugs in the future.
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Table 9: Analyst
Analyst‑I
Concentration
(resveratrol + benzoyl
peroxide) μg/ml
Resveratrol
(area)
Mean ± SD %RSD Benzoyl
peroxide (area)
Mean ± SD %RSD
100 (50 + 50) 1569155 1561248 ± 8852.24 0.566998 934788 932131.3 ± 15019.23 1.611278
100 (50 + 50) 1547757 947062
100 (50 + 50) 1568798 945648
100 (50 + 50) 1567420 935229
100 (50 + 50) 1560266 922800
100 (50 + 50) 1554091 907261
Analyst‑II
Concentration
(resveratrol + benzoyl
peroxide) μg/ml
Resveratrol
(area)
Mean ± SD %RSD Benzoyl
peroxide (area)
Mean ± SD %RSD
100 (50 + 50) 781047 788059.2 ± 5310.945 0.673927 906716 920431.2 ± 17438.57 1.894609
100 (50 + 50) 784247 900704
100 (50 + 50) 787597 941010
100 (50 + 50) 787056 936630
100 (50 + 50) 794747 929984
100 (50 + 50) 793661 907543
9. Kamra, et al.: Development and validation of RP-HPLC method for the simultaneous estimation of BPO and RES
IJPBA/Apr-Jun-2018/Vol 9/Issue 2 121
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