Scholars Research Library. Study of the effect of Ampicillin Trihydrate on protein binding of Oseltamivir Phosphate

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

Biowaiver Study on Prednisolone Tablets 5 mg in Three Different Brands. Marketed in Sudan. Safaa Mohamed *, Tilal Elsaman

EFFECT OF GLUCOSE ON PROTEIN BINDING OF LOSARTAN POTASSIUM WITH BOVINE SERUM ALBUMIN

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

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

Scholars Research Library

STUDIES ON EFFECT OF BINDERS ON ETORICOXIB TABLET FORMULATIONS

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

Development and validation of stability indicating RP-LC method for estimation of calcium dobesilate in pharmaceutical formulations

Available Online through Research Article

Asian Journal of Pharmacy and Life Science ISSN Vol. 2 (2), July-Sept,2012

Formulation and Evaluation of Tinidazole Syrup Made by Mixed Solvency Concept Technique

Scholars Research Library

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

Comparative in-vitro evaluation of four different brands of metformin HCl available in Kanpur district, India

Experiment 3. Potentiometric Titration Using a ph Electrode. information necessary for both purposes by monitoring the ph of the solution as the

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

Bioequivalence Studies of Two Formulations of Famciclovir Tablets by HPLC Method

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

Β-FRUCTOFURANOSIDASE ENZYME

RP- HPLC and Visible Spectrophotometric methods for the Estimation of Meropenem in Pure and Pharmaceutical Formulations

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

This letter is to notify you of recent changes to the TAMIFLU product monograph. Please note, additions/changes have been highlighted in yellow.

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

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

Pelagia Research Library

Pelagia Research Library

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

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

ISSN: X CODEN: IJPTFI Available Online through Research Article

RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR CILOSTAZOL IN TABLET DOSAGE FORM

World Journal of Pharmaceutical Research

Experiment 3: Activity Determination

July-September JCPS Volume 7 Issue 3

Development and validation of related substances method for Varenicline and its impurities

A stability indicating RP-HPLC method for simultaneous estimation of darunavir and cobicistat in bulk and tablet dosage form

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

MOHAWK COLLEGE OF APPLIED ARTS AND TECHNOLOGY CHEMICAL AND ENVIRONMENTAL TECHNOLOGY DEPARTMENT. Lab Report ROOM NO: FE E309

Estimation of zolmitriptan by a new RP-HPLC method

Scholars Research Library

New RP - HPLC Method for the Determination of Valproic acid in Human Plasma

ENHANCEMENT OF SOLUBILITY OF BICALUTAMIDE DRUG USING SOLID DISPERSION TECHNIQUE

Available online at Scholars Research Library

Formulation and Evaluation of Acyclovir Liposomes

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

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

PHARMA SCIENCE MONITOR AN INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD ESTIMATION OF TOLVAPTAN IN BULK PHARMACEUTICAL FORMULATION

Method Development and Validation of Emtricitabine in Bulk by UV Spectroscopy

Reverse Phase HPLC Analysis of Atomoxetine in Pharmaceutical Dosage Forms

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

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

Scholars Research Library. Der Pharmacia Lettre, 2016, 8 (6): (

ANALYTICAL METHOD DEVELOPMENT AND VALIDATION CEFIXIME AND DICLOXACILLIN TABLETS

Vol-3, Issue-4, Suppl-1, Nov 2012 ISSN: Patel et al PHARMA SCIENCE MONITOR

International Journal of Research in Pharmaceutical and Nano Sciences Journal homepage:

Amudha S et al., Asian Journal of Pharmthiaceutical Technology & Innovation, 04 (21); 2016; Research Article

Pelagia Research Library

Scholars Research Library. Der Pharmacia Lettre, 2015, 7 (5):44-49 (

Research Article GALLIC ACID AND FLAVONOID ACTIVITIES OF AMARANTHUS GANGETICUS

International Journal of Pharma and Bio Sciences

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

Development, Estimation and Validation of Lisinopril in Bulk and its Pharmaceutical Formulation by HPLC Method

Journal of Chemical and Pharmaceutical Research

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

OUTLINE. ILVO Introduction Determination of HP Validation of method Conclusion

Spectrophotometric Estimation of Ganciclovir in Bulk Drug and its Formulation

DEVELOPMENT OF RP-HPLC METHOD FOR ESTIMATION OF DROTAVERINE HYDROCHLORIDE IN PHARMACEUTICAL FORMULATIONS

ISSN (Print)

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

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 ,

Scholars Research Library

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

DEVELOPMENT AND VALIDATION OF SPECTROPHOTOMETRIC METHOD FOR DETERMINATION OF METOPROLOL SUCCINATE

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

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

DEVELOPMENT AND VALIDATION OF NEW HPLC METHOD FOR THE ESTIMATION OF PALIPERIDONE IN PHARMACEUTICAL DOSAGE FORMS

Preparation and Characterization of Candesartan Cilexetil Solid Lipid Nanoparticulate Capsules

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

Global College of Pharmacy, Kahnpur Khui, Tehsil Anandpur Sahib, Distt.- Ropar, Punjab, India

HPLC-UV Determination of Abacavir Sulphate in Pharmaceutical Dosage Forms

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

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

Research and Reviews: Journal of Pharmacy and Pharmaceutical Sciences

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

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

Kinetics analysis of β-fructofuranosidase enzyme. 1-Effect of Time Incubation On The Rate Of An Enzymatic Reaction

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

Nitrate/Nitrite Assay Kit Manual Catalog #

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

Scholars Research Library. Formulation and evaluation of buccoadhesive tablet of Atenolol

The study the effect of polymer and surfactant concentration on characteristics of nanoparticle formulations

FACTORIAL STUDIES ON THE EFFECTS OF HYDROXY PROPYL β- CYCLODEXTRIN AND POLOXAMER 407 ON THE SOLUBILITY AND DISSOLUTION RATE OF BCS CLASS II DRUGS

Estimation of Zanamivir Drug present in Tablets using RP-HPLC Method

--> Buy True-PDF --> Auto-delivered in 0~10 minutes. GB Translated English of Chinese Standard: GB5009.

Simultaneous Estimation of Gemcitabine Hydrochloride and Capecitabine Hydrochloride in Combined Tablet Dosage Form by RP-HPLC Method

Journal of Chemical and Pharmaceutical Research, 2018, 10(3): Research Article

Available online Research Article

Method Development and Validation for the Estimation of Saroglitazar in Bulk and Pharmaceutical Dosage Form by RP-HPLC

Transcription:

Available online at www.scholarsresearchlibrary.com Der Pharmacia Lettre, 2011, 3(3): 320-324 (http://scholarsresearchlibrary.com/archive.html) ISSN 0975-5071 USA CODEN: DPLEB4 Study of the effect of Ampicillin Trihydrate on protein binding of Oseltamivir Phosphate S. Vijayaraj*, Divya. S, K. Guru Prasad Varma, V. Pavana Keerthi, R. Pragna and M. Venkatesh Department of Pharmaceutical Analysis, Sree Vidyanikethan College of Pharmacy, Sree Sainath Nagar, Tirupathi ABSTRACT Protein bound drugs are pharmacokinetically inactive where unbound drugs are pharmacologically active.highly protein bound drugs have reduced Pharmacological effect (invitro) with Albumin. Free drug concentration in the plasma is responsible for the observed pharmacological effect or therapeutic response. Oseltamivir phosphate is an antiviral drug used in the treatment and prophylaxis of both influenza virus A and influenza virus B. It is currently the drug of choice for the prevention of influenza virus infection. Invitro Protein binding study of oseltamivir phosphate was carried out for 200 mins and The percentage of bound drug was found to be 80% and percentage of free drug was found to be 20%.In co-administration of Oseltamivir phosphate with Ampicillin, The percentage of bound drug was found to be 68.6% and percentage of free drug was found to be 31.40% Increase in percentage of free drug was found to be 57%, shows beneficial drug interaction. Keywords: Oseltamivir phosphate, Ampicillin trihydrate, protein binding, Co-administration INTRODUCTION Oseltamivir phosphate is an antiviral drug used in the treatment and prophylaxis of both influenza virus A and influenza virus B. Fig 1 Fig 1 : Structure of Oseltamivir phosphate 320

Oseltamivir phosphate is readily absorbed and rapidly converted (half-life [t 1/2 ], 1 to 3 h) to its active carboxylate metabolite via hepatic esterases [1]. At least 75% of an oral dose reaches the systemic circulation as oseltamivir carboxylate, while less than 5% of an oral dose reaches the systemic circulation as oseltamivir phosphate. Once it is formed, oseltamivir carboxylate is minimally bound (3%) to human plasma proteins. It has a t 1/2 of 6 to 10 h and is eliminated by the kidney by a first-order process that includes glomerular filtration and tubular secretion by an anionic transporter system. [2] Ampicillin is a beta-lactam antibiotic that has been used extensively to treat bacterial infections. [3] Fig 2. Fig 2: Structure of Ampicillin trihydrate Co-administration of Oseltamivir phosphate with Ampicillin trihydrate shows beneficial drug interaction, thus increase bioavailability of oseltamivir phosphate. MATERIALS AND METHODS Equipment Shimadzu UV Pharma Spectrophotometer 1700, Elico L1613 ph Meter Shimadzu (ELB 300) Electronic balance, Shimadzu (BL 22OH) Electronic balance Reagents and solutions All employed chemicals were of analytical grade and high-purified water was used throughout. Oseltamivir phosphate pure sample was obtained as a gift sample from Hetero drugs, Hyderabad, India. The gift sample of pure drug Ampicillin trihydrate was received from Parabolic drugs. Ltd. Preparation of the standard graph of Oseltamivir Phosphate: 1) Preparation of primary stock solution: 10mg of oseltamivir phosphate taken in 100ml standard flask and make up the volume with 7.2 ph Phosphate buffer.this gives 100µg/ml.This is the primary stock solution. 2) Preparation of various concentrations of oseltamivir phosphate: From the primary stock solution the concentrations ranging from 15 µg/ml to 75µg/ml was prepared by diluting with phosphate buffer. A Standard graph was plotted by taking Time on X- axis and Absorbance on Y-axis. Fig 3 321

Fig-3: Standard graph of Oseltamivir phosphate Calibration curve for protein binding Absorbance 0.07 0.06 0.05 0.04 0.03 0.02 0.01 0 0 20 40 60 80 Concentration(mcg/ml) Preparation of 2.8 X 10-4 M Solution of Egg Albumin 0.315 g of egg albumin flakes is dissolved in 25 ml of distilled water. It is shaken well and is kept aside. Table-1: Protein binding studies of oseltamivir phosphate and ampicillin trihydrate Time(mins) Absorbance of 1.63 10-4 M Oseltamivir phosphate Absorbance of the mixture of Oseltamivir phosphate and Ampicillin 0 0.019 0.004 20 0.023 0.017 40 0.042 0.023 60 0.026 0.245 80 0.022 0.077 100 0.021 0.207 120 0.020 0.234 140 0.018 0.142 160 0.017 0.176 180 0.012 0.149 200 0.012 0.043 Studies on protein binding: 25 ml OF 1.63 X 10-4 M of oseltamivir phosphate is prepared using a buffer of ph 7.2. A boiling tube open on both sides is taken and a semipermeable membrane is tied on to the neck of the boiling tube. The egg albumin solution 10ml is taken inside the semipermeable membrane. The boiling tube is then immersed into the beaker containing the drug Oseltamivir phosphate 1.63 X 10-4 M. Immediately at zero time, 1ml of solution is pipetted out from the beaker and is replaced with 1ml of water. Readings are taken at 10, 20, 40, 60, 80, 100, 120 min and absorbance at 525 nm and is noted. Once equilibrium is reached there will be no further change in absorbance.so the constant value of absorbance is noted. From the absorbance, by using the standard graph, 322

determine the concentration in mcg/ml by extrapolation. From the concentration in mcg/ml determine the concentration in moles. [4] Table1 Preparation of 1.63 10-4 M solution of oseltamivir phosphate: 410.4 gms of drug dissolved in 1000ml of distilled water to obtain 1M.For 1.63 10-4 M solution 0.067gms of drug dissolved in 1000ml of distilled water. Procedure From the prepared oseltamivir phosphate solution 15ml solution was taken in a beaker and 15ml of albumin solution in boiling test separated by membrane.1ml of drug solution was taken from beaker for every 20mins and replaced with buffer immediately.1ml of solution was diluted to 10ml of buffer and absorbance was noted until a constant value by using UV spectrophotometer. Preparation of 32.68 10-4 M solution of Ampicillin trihydrate: 403.45 Gms of drug dissolved in 1000ml of distilled water to obtain 1M. For 32.68 10-4 M solution 1.3184gms of drug dissolved in 1000ml of distilled water. Table 2: Percentage of free drug of oseltamivir phosphate in presence of ampicillin trihydrate Drug oseltamivir phosphate oseltamivir phosphate and ampicillin % drug bound 80% 68.6% %drug free 20% 31.4% % increase in free drug 11.4% Fig 4 protein binding study of oseltamivir phosphate %DRUG 90% 80% 70% 60% 50% 40% 30% 20% 10% 0% 80% 20% oseltamivir phosphate 68.60% 31.40% oseltamivir phosphate and ampicillin CONDITION OF PROTEIN BINDING % drug bound %drug free Procedure for preparation of mixture of Oseltamivir Phosphate and Ampicillin trihydrate: The concentration of Oseltamivir phosphate and Ampicillin trihydrate in the mixture was chosen on the basis of the dose of Ampicillin that is co-administered with Oseltamivir Both the drug 323

solutions equal to 15 ml was taken into the beaker and 15ml of albumin solution in boiling test separated by membrane.1ml of drug solution was taken from beaker for every 20mins and replaced with buffer immediately.1ml of solution was diluted to 10ml of buffer and absorbance was noted until a constant value by using UV spectrophotometer. From the protein binding studies of mixture of Oseltamivir phosphate and Ampicillin trihydrate the effect of Ampicillin trihydrate on the protein binding of Oseltamivir phosphate was determined. Table2, Fig 4 RESULTS Protein binding study of oseltamivir phosphate was carried out for 200 mins. The percentage of bound drug was found to be 80% and percentage of free drug was found to be 20%. Protein binding of oseltamivir was determined in the presence of Ampicillin trihydrate for 200 mins. The percentage of bound was found to be 68.6%and percentage of free drug was found to be 31.40%.Thus co-administration of Oseltamivir phosphate with Ampicillin trihydrate shows 57% increase in free drug concentration. CONCLUSION Invitro protein binding studies of Oseltamvir phosphate shows increased bioavailability of Oseltamivir phosphate in co-administration with Ampicillin trihydrate, thus protein binding of Oseltamivir phosphate was found to be altered in presence of Ampicillin trihydrate REFERENCES [1] G, Massarella J, Ward P. Clin Pharmacokinet (1999), 37: 471 84 [2] Shargel, Leon. Applied Biopharmaceutics & Pharmacokinetics. New York: McGraw-Hill, Medical Pub. Division (2005). [3] Niklas Lindegardh et al., 2006, Antimicrobial Agents and Chemotherapy, September 2006, p. 3197-3199, Vol. 50, No. 9 [4] P. Vijayaraghavan, Judith Justin. Experimental Biopharmaceutics and pharmacokinetics. New century book house, 2006 324