International Journal of Innovative Pharmaceutical Sciences and Research

Similar documents
MEDAK DIST. ANDHRA PRADESH STATE, INDIA. Research Article RECEIVED ON ACCEPTED ON

UV SPECTROPHOTOMETRIC METHOD DEVELOPMENT AND VALIDATION FOR THE DETERMINATION OF ATENOLOL AND LOSARTAN POTASSIUM BY Q-ANALYSIS

pharmaceutical formulations. Anagliptin shows absorption maximum at 246 nm and obeys beer s law in the

Development and validation of spectrophotometric method for simultaneous estimation of Sumatriptan and Naproxen sodium in tablet dosage form

Journal of Chemical and Pharmaceutical Research

210 J App Pharm Vol. 6; Issue 2: ; April, 2014 Mustafa et al, 2014

Development and Validation of Area Under Curve Method for Simultaneous Estimation of Thiocolchicoside and Lornoxicam in Tablet Dosage Form

IJRPC 2011, 1(4) Rohan et al. ISSN: INTERNATIONAL JOURNAL OF RESEARCH IN PHARMACY AND CHEMISTRY

Simultaneous UV Spectrophotometric Method For Estimation Of Ebastine And Montelukast Sodium In Tablet Dosage Form By Q-Ratio Method

Research Article Derivative Spectrophotometric Method for Estimation of Metformin Hydrochloride in Bulk Drug and Dosage Form

PHARMA SCIENCE MONITOR AN INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES

Method Development and Validation of Emtricitabine in Bulk by UV Spectroscopy

for Methotrexate. The result of analysis has been validated statistically and recovery studies confirmed the accuracy of

International Journal of PharmTech Research CODEN (USA): IJPRIF, ISSN: Vol.7, No.2, pp ,

Validated UV Spectrophotometric Method Development And Stability Studies Of Acamprosate Calcium In Bulk And Tablet Dosage Form

Validated Spectrophotometric Method for Simultaneous Estimation of Atorvastatin and Nicotinic acid in Combined Pharmaceutical dosage form

Development And Validation Of UV Spectrophotometric Method For Simultaneous Estimation Of Rutin And Gallic Acid In Hydroalcoholic Extract Of

Available Online through Research Article

Development and validation of UV spectrophotometric estimation of lisinopril dihydrate in bulk and tablet dosage form using area under curve method

Development and validation of UV-visible spectrophotometric method for estimation of rifapentine in bulk and dosage form

DEVELOPMENT AND VALIDATION OF SPECTROPHOTOMETRIC METHOD FOR DETERMINATION OF METOPROLOL SUCCINATE

The present manuscript describes simple, sensitive, rapid, accurate, precise and cost effective First derivative

Development and validation of UV Spectrophotometric method for simultaneous estimation of Lamivudine and Efavirenz in the Pharmaceutical dosage form

M. SASIKALA* 1, M. TEJA DEEPTHI 2, K. VINOD KUMAR 3, NAGA MALLIKARJUNA RAJA B. 4 ABSTRACT KEYWORDS

Journal of Chemical and Pharmaceutical Research, 2018, 10(2): Research Article

Development and validation of analytical methods for estimation of imatinib mesylate in bulk and solid dosage forms by UV spectroscopy

Research and Reviews: Journal of Pharmacy and Pharmaceutical Sciences

J Pharm Sci Bioscientific Res (4): ISSN NO

UV Spectrophotometric Estimation of Alprazolam by Area Under Curve And First Order Derivative Methods in Bulk and Pharmaceutical Dosage Form

Pelagia Research Library

Available online Research Article

Scholars Research Library. Der Pharmacia Lettre, 2016, 8 (3): (

Pelagia Research Library. Spectrophotometric method for simultaneous estimation of Valsartan and Hydrochlorothiazide in combined tablet dosage form

International Journal of Innovative Pharmaceutical Sciences and Research

IJRPC 2013, 3(1) Gandhi et al ISSN: INTERNATIONAL JOURNAL OF RESEARCH IN PHARMACY AND CHEMISTRY

Int. J. Pharm. Sci. Rev. Res., 31(1), March April 2015; Article No. 46, Pages:

UV VISIBLE SPECTROPHOTOMETRIC METHOD FOR THE SIMULTANEOUS ESTIMATION OF SERRATIOPEPTIDASE AND DICLOFENAC SODIUM IN THEIR BULK AND COMBINED DOSAGE FORM

International Journal of ChemTech Research CODEN( USA): IJCRGG ISSN : Vol.4, No.2, pp , April-June 2012

Comparative study of analytical method development of fluconazole in tablets and capsule by ultraviolet spectrophotometric method

DEVELOPMENT AND VALIDATION OF COLORIMETRIC METHODS FOR THE DETERMINATION OF RITONAVIR IN TABLETS

Development and Validation of a UV-Spectrophotometric Method for Quantification of Atorvastatin in Tablets

Asian Journal of Pharmacy and Life Science ISSN Vol.4 (2), April-June, 2014

International Journal of Drug Research and Technology

RP-HPLC Analysis of Temozolomide in Pharmaceutical Dosage Forms

Spectrophotometric Method for Simultaneous Estimation of Lopinavir and Ritonavir in bulk and tablet dosage form

Spectrophotometric Method for Estimation of Sitagliptin Phosphate in Bulk...

Scholars Research Library

36 J App Pharm Vol. 6; Issue 1: 36-42; January, 2014 Rao et al., 2014

Quantitative estimation of Rosuvastatin in bulk and tablet dosage form by using area under curve method

International Journal of ChemTech Research CODEN( USA): IJCRGG ISSN : Vol.4, No.2, pp , April-June 2012

UV-Visible Spectrophotometric Method for the Estimation of Rilpivirine Hydrochloride in Pharmaceutical Dosage Form by Using Multivariate Technique

International Journal of Pharma and Bio Sciences DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE ESTIMATION OF STRONTIUM RANELATE IN SACHET

Pelagia Research Library

International Journal of Advances in Pharmacy and Biotechnology Vol.3, Issue-1, 2017, 1-7 Research Article Open Access.

IJPAR Vol.3 Issue 4 Oct-Dec-2014 Journal Home page:

Absorption Correction Method for Simultaneous Estimation of Phenazopyridine HCl and Ciprofloxacin HCl in Combined Tablet Dosage Form

Development and Validation of A Spectrophotometric Method for Quantification and Dissolution Studies of Glimepiride in Tablets

International Journal of Pharmaceutical Research & Analysis

Simultaneous estimation of amlodipine and losartan by UV-method in bulk drug and tablet dosage formulation

INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH AND BIO-SCIENCE

JPSBR: Volume 4, Issue 6: 2014 ( ) ISSN NO

RP-HPLC Method Development and Validation of Abacavir Sulphate in Bulk and Tablet Dosage Form

IJPRD, 2011; Vol 4(06): August-2012 ( ) International Standard Serial Number

Research Article. Method Development of Antihypertensive Agent Using Official Dissolution Media

Validation of UV Spectrophotometric and HPLC Methods for Quantitative determination of Iloperidone in Pharmaceutical Dosage Form


First Order Derivative Spectrophotometric Method for Estimation of Melatonin in Bulk and Pharmaceutical Dosage Form

Department Of Quality Assurance Techniques, Modern College of Pharmacy Nigdi, Pune Maharashtra, India

Available Online through (or) IJPBS Volume 2 Issue 4 OCT-DEC Research Article Pharmaceutical Sciences

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR ASSAY AND DISSOLUTION OF METOPROLOL SUCCINATE EXTENDED RELEASE TABLETS

Development and Validation of a New Uv Method for the Analysis of Rebamipide

VALIDATED RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF DEXAMETHASONE AND GRANISETRON IN COMBINED DOSAGE FORMS

UV-Spectrophotometric methods for estimation of Valsartan in bulk and tablet dosage form

DEVELOPMENT OF UV SPECTROPHOTOMETRIC METHOD FOR THE ESTIMATION OF EZETIMIBE FROM TABLET FORMULATION

Journal of Chemical and Pharmaceutical Research, 2013, 5(1): Research Article

S. G. Talele, D. V. Derle. Department of Pharmaceutics, N.D.M.V.P. College of Pharmacy, Nashik, Maharashtra, India

UV-visible derivative spectroscopic method for simultaneous estimation of cefoperazone and tazobactam in injection dosage form

Stability indicating RP-HPLC method development and validation of Etizolam and Propranolol hydrochloride in pharmaceutical dosage form

Available online Research Article

Method Development and validation of Levosalbutamol sulphate by Derivative Spectroscopy Nyola Narendra* 1, 2, Govinda Samy Jeyabalan 1

Development and validation of UV and RP-HPLC method for estimation of Nepafenac in bulk drug and opthalmic formulation

IJPRD, 2011; Vol 3(11): January-2012 ( ) International Standard Serial Number

Development and Validation of Stability Indicating HPTLC Method for Estimation of Seratrodast

Observed amount of compound in sample % recovery = 100 Amount of all compound present in sample. The recovery values are summarized in Table 4.

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR QUANTITATIVE ANALYSIS TOLBUTAMIDE IN PURE AND PHARMACEUTICAL FORMULATIONS

DEVELOPMENT AND VALIDATION OF AN UV- SPECTROPHOTOMETRIC METHOD FOR THE ESTIMATION OF FLUOXETINE IN PURE AND TABLET DOSAGE FORMS

Asian Journal of Pharmaceutical Analysis and Medicinal Chemistry Journal home page:

Simultaneous determination of Prasugrel and Aspirin by. second order and ratio first order derivative ultraviolet

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF ETORICOXIB AND THIOCOLCHICOSIDE IN PHARMACEUTICAL DOSAGE FORMS

HPTLC Determination of Atomoxetine Hydrochloride from its Bulk Drug and Pharmaceutical Preparations

Development of a Validated RP-HPLC Method for the Analysis of Citicoline Sodium in Pharmaceutical Dosage Form using Internal Standard Method

World Journal of Pharmaceutical Research

Impact factor: 3.958/ICV: 4.10 ISSN:

THE PHARMA INNOVATION - JOURNAL. Difference Spectrophotometric Method for the Determination of Risperidone in Bulk and Tablet Dosage Form

July-September JCPS Volume 7 Issue 3

ISSN (Print)

Method Development and Validation for Simultaneous Estimation of Atorvastatin and Ezetimibe in Pharmaceutical Dosage Form by HPLC

Tulluri Chandrashekar. et al. / International Journal of Biopharmaceutics. 2010; 1(2): International Journal of Biopharmaceutics

Pankti M. Shah et al, Asian Journal of Pharmaceutical Technology & Innovation, 04 (17); 2016; 07-16

Spectrophotometric method development and validation for estimation of Tizanidine and Aceclofenac in Bulk Drug & Tablet formulation

Transcription:

International Journal of Innovative Pharmaceutical Sciences and Research www.ijipsr.com SIMULTANEOUS ESTIMATION OF PARACETAMOL AND IBUPROFEN IN BULK AND PHARMACEUTICAL DOSAGE FORM BY USING UV SPECTROPHOTOMETRIC METHOD 1 S.Harshini*, 2 G. Priyanka, 3 K.Swathi, 4 V.Roja Kumari, 5 M.Akiful Haque, 6 V V L N Prasad Department of Pharmaceutical Analysis and Quality assurance, School of Pharmacy, Anurag group of Institutions, Venkatapur (V),Ghatkesar (M), Rangareddy (D).INDIA Abstract A simple, specific, accurate and precise UV spectrophotometric method has been developed for the simultaneous estimation of paracetamol and ibuprofen in pharmaceutical dosage form. The absorption maxima of the paracetamol and ibuprofen were found to be 240 nm and 220nm respectively using Ethanol as solvent. This method obeys Beer s law in the employed concentration range of 1-15µg/ml and 2-20µg/ml for Paracetamol and ibuprofen respectively. Different analytical performance parameters such as linearity, precision, accuracy, limit of detection (LOD) and limit of quantification (LOQ) were determined according to ICH guidelines [1,2,3]. The accuracy of the method was confirmed by recovery studies of tablet dosage form and was found to be 98.41% and 99.25% for paracetamol and ibuprofen respectively. The LOD of paracetamol and ibuprofen was found to be 0.214µg/ml and 0.6µg/ml respectively and LOQ of paracetamol and ibuprofen was found to be 0.649 µg/ml and 0.82µg/ml respectively. The developed method was free from interferences due to excipients present in formulation and it can be used for routine quality control analysis. Keywords: UV; validation. Corresponding Author: S.Harshini Department of Pharmaceutical Analysis and Quality assurance, School of pharmacy, Anurag group of Institutions, Ghatkesar (M), Hyderabad, Andhra Pradesh, INDIA Email: harshinisirige27@gmail.com Phone: +91-9014297287 Available online: www.ijipsr.com January Issue 1854

INTRODUCTION Ibuprofen (IBU) chemically known as 2-[4-(2-methylpropyl) phenyl] propanoic acid (Figure 1), is an Anti-Inflammatory agent. Its pharmacological effects are believed to be due to inhibition of cyclooxygenase-2 (COX-2) which decreases the synthesis of prostaglandins involved in mediating inflammation, pain, fever and swelling [4,5]. Paracetamol (PAR) chemically known as N-(4-hydroxyphenyl)acetamide (Figure 2). It is an Analgesic and Antipyretic agent. It acts primarily in the CNS, increasing the pain threshold by inhibiting both isoforms of cyclooxygenase, COX-1, COX-2, and COX-3 enzymes involved in prostaglandin synthesis. The antipyretic properties of Paracetamol are likely due to direct effects on the heat-regulating centers of the hypothalamus resulting in peripheral vasodilatation, sweating and hence heat dissipation [6,7]. Fig. 1: Ibuprofen Fig. 2: Paracetamol The combination of Ibuprofen and Paracetamol is prescribed by physician for the treatment of pain, fever and inflammation associated with musculoskeletal and joint disorders. Literature survey reveals several methods that have been used for the quantitative determination of these two drugs individually and in combination with other drugs. The objective of the work is to develop a new UV spectrophotometric method for the simultaneous estimation of Ibuprofen and Paracetamol in pharmaceutical dosage form [8-13]. MATERIALS AND METHOD Ibuprofen and Paracetamol pure powder were gift samples supplied from Dr.Reddy s Laboratories Private Limited, Hyderabad, India. Formulation, Flexon (Label claim: Ibuprofen 400 mg and Paracetamol 500mg) was manufactured by ARISTO Pharmaceuticals Pvt. Ltd. and purchased from local pharmacy in Hyderabad, India. Shimadzu UV Visible spectrophotometer (model UV-1800) was employed with a spectral band width of 1 nm and a wavelength accuracy of 0.3 nm (with automatic wavelength correction with a pair of 1 cm matched quartz cells). Available online: www.ijipsr.com January Issue 1855

METHOD: SELECTION OF SOLVENT AND WAVELENGTH: Solubility of Ibuprofen and Paracetamol was checked in solvents like ethanol, water and methanol. UV spectrum of the two drugs in these solutions was recorded. The absorbance of the three drugs was found maximum in ethanol solvent compared to other solvents and three wavelengths 220 and 240nm (Figure 3) were selected which are the λmax of Ibuprofen and Paracetamol respectively. Fig. 3: Overlay spectra of Ibuprofen and Paracetamol showing selected wavelength Preparation standard stock solutions: Ibuprofen and Paracetamol (10 mg each) was separately weighed and transferred to 100 ml volumetric flask and all the three drugs were dissolved in ethanol to get a concentration of 100 μg/ml. Linearity: Calibration graph was found to be linear that is adherence to the system of Beer s law which was found over the concentration range of 2-20 μg/ml for Ibuprofen(Figure 4) and 1-15 μg/ml for Paracetamol (Figure 5). Absorbance and concentration was subjected to least square linear regression analysis to calculate the calibration equation and correlation coefficients. The regression data as given in Table 1, showed a good linear relationship. Table 1: Linearity Parameters Ibuprofen Paracetamol Linearity range 2-20 μg ml-1 1-15 μg ml-1 Correlation coefficient 0.997 0.998 Slope 0.046 0.094 Intercept 0.0209 0.016 Available online: www.ijipsr.com January Issue 1856

Fig. 4: Overlay spectra of standard ibuprofen (2-20 mg/ml) Fig. 5: Overlay spectra of standard paracetamol (1-15 mg/ml) Precision To check the degree of repeatability of the method, suitable statistical evaluation was carried out. The concentrations of two drugs were measured three times on the same day at intervals of 1hr and on three different days for intra and inter day study, respectively. The Relative Standard Deviation (% RSD) was found to be less than 2. The results were shown in Table 2. Table 2: Precision Studies Intraday precision % Interday precision % Drug Concentration (μg/ml) *RSD *RSD Ibuprofen 10 1.12 1.41 Paracetamol 11 0.31 0.16 * mean of three observations Limit of Detection (LOD) & Limit of Quantitation (LOQ) LOD and LOQ of Paracetamol and Ibuprofen were calculated mathematically. The LOD of Paracetamol and Ibuprofen were found to be 0.214µg/ml and 0.6µg/ml respectively. The LOQ of Paracetamol and Ibuprofen were found to be 0.649µg/ml and 0.82µg/ml respectively. Available online: www.ijipsr.com January Issue 1857

Accuracy In order to ensure the suitable and reliability of proposed method, recovery studies were carried out. To an equivalent quantity of formulation powder, a known quantity of standard Paracetamol and Ibuprofen were added at 50%, 100% level and the content were re-analyzed by the proposed method. The % recovery and % RSD were calculated. Table 3 summarizes the values. Table 3: Recovery Studies Data of Paracetamol And Ibuprofen Level %Recovery %RSD Paracetamol Ibuprofen Paracetamol Ibuprofen 50% 98.33 98.5 0.1 0.27 100% 98.41 99.25 0.39 0.23 Analysis of formulation For the analysis, 20 tablets each containing 40mg of paracetamol and ibuprofen were weighed and the average weight was dissolved in ethanol and the volume was made upto get the required concentrations absorbance were noted at 240nm and 220nm (Figure 6). Table 4 summarizes the absorbance values. The amounts of paracetamol and ibuprofen were calculated using the simultaneous equation given below. A1 = Absorbance of formulation at 240 nm A2 = Absorbance of the formulation at 220 nm ax1 = Absorptivity of Paracetamol at 240 nm ax2 = Absorptivity of Paracetamol at 220 nm ay1 = Absorptivity of Ibuprofen at 240 nm ay2 = Absorptivity of Ibuprofen at 220 nm Cx =concentration of Paracetamol Cy =Concentration of Ibuprofen Available online: www.ijipsr.com January Issue 1858

Table 4: Analysis of Formulation Drug Amount (mg/tablet) %label claim Labeled Estimated % RSD Paracetamol 500 499.5 99.9 0.53 Ibuprofen 400 402.05 100.51 0.95 Fig. 6: Formulation Spectra of Paracetamol and Ibuprofen RESULTS AND DISCUSSION Estimation of paracetamol and ibuprofen was achieved by simultaneous equation method by using UV spectrophotometer. The linearity was checked in different concentrations and Beers law obeyed in the concentration range of 1-15µg/ml and 2-20µg/ml for both paracetamol and ibuprofen. The slope, intercept and correlation coefficient values of paracetamol at 240nm are 0.094, 0.016 and 0.998. The slope, intercept and correlation coefficient values of Ibuprofen at 220nm are 0.046, 0.0209 and 0.997. The recovery studies were carried out to ensure the reproducibility and reliability of the method by adding known amount of standard drugs and analysis was carried out as per formulation procedure. CONCLUSION The developed UV spectrophotometric method is simple, precise, accurate, linear, reproducible and repeatable for the estimation of Ibuprofen and Paracetamol in pharmaceutical dosage forms without any interference from the excipients. It can be successfully applied for the routine analysis of both the two drugs in pharmaceutical dosage forms. REFERENCES 1. FDA Guidance for industry, Analytical procedures and methods Validation (draft guidance), august 2000. Available online: www.ijipsr.com January Issue 1859

2. ICH Guidelines Q1A (R2). Stability testing of new drug substances and products (revision 2), November 2003. 3. ICH Guidelines Q2 (R1). Validation of analytical procedures: Text and Methodology. International conference on Harmonization of technical requirements for the registration of pharmaceutical for human use, Geneva, Switzerland. 2005. 4. http://www.drugbank.ca/drugs/db01050 (Ibuprofen). 5. www.wikipedia.org/ibuprofen 6. http://www.drugbank.ca/drugs/db00316 (Paracetamol). 7. www.wikipedia.org/paracetamol 8. Yousry M. Issa, Sayed I.M. Zayed, Ibrahim H.I. Habib. Simultaneous determination of ibuprofen and paracetamol using derivatives of the ratio spectra method. Arabian J. Chem2011, vol 4, Pg no 259 263. 9. Tapan Kumar Giri, Dulal Krishna Tripathi. Simultaneous Equation Method for Simultaneous Estimation of Paracetamol and Ibuprofen in Combined Dosage Form. Int. J Pharm Boil Arc 2010, 1(2), Pg no 189 192. 10. Riddhi Gondalia, Rajashree Mashru, Pankaj Savaliya. Development and Validation of Spectrophotometric Methods for Simultaneous Estimation of IBUPROFEN and PARACETAMOL in Soft gelatin capsule by Simultaneous Equation Method. Int. J ChemTech Res 2010, Vol.2, Pg no 1881-1885. 11. Wafaa S. Hassan. Determination of Ibuprofen and Paracetamol in Binary Mixture Using Chemometric-Assisted Spectrophotometric Methods. Am. J. App Sci 2008, Pg no 1005-1012. 12. Rupali S. Joshi, Nilima S. Pawar, Sameer S. Katiyar, Devendra B. Zope and Amol T. Shinde. Development and validation of UV spectrophotometric methods for simultaneous estimation of Paracetamol and Ibuprofen in pure and tablet dosage form. Pelagia Research Library Der Pharmacia Sinica, 2011, Pg no 164-171. 13. Vu Dang Hoang, Dong Thi Ha Ly, Nguyen Huu Tho and Hue Minh Thi Nguyen. UV Spectrophotometric Simultaneous Determination of Paracetamol and Ibuprofen in Combined Tablets by Derivative and Wavelet Transform. The Scientific World Journal, 2014. Available online: www.ijipsr.com January Issue 1860