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Quantitative determination of Piroxicam in pharmaceutical dosage using reversed-phase high performance liquid chromatographic method
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Mô tả chi tiết
Journal of Science and Technology, Vol. 39A, 2019
© 2019 Industrial University of Ho Chi Minh City
QUANTITATIVE DETERMINATION OF PIROXICAM IN
PHARMACEUTICAL DOSAGE USING REVERSED-PHASE HIGH
PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD
NGUYEN QUOC THANG
Chemical engineering faculty - Industrial University of Ho Chi Minh City,
Abstract. Piroxicam is a well known and very effective anti-inflammatory drug. Piroxicam can be
determined by various methods. Here, we introduced a reversed-phase high-performance liquid
chromatographic (RP-HPLC) method for the determination of piroxicam in tablets. A Hypersil BDSC18 column (4.0 mm x 125 mm), 5 μm particle size and Diode Array Detector at wavelength 334 nm
were used for separation and detection of piroxicam. The mobile phase was a mixture of MeOH and
0.03M potassium phosphate buffer in a ratio 80:20; v/v, set at a flow rate of 0.3 mL/min. Total
chromatographic analysis time per sample was approximately 7 min with piroxicam eluting with
retention times of 4.694 min. The linear range was collected from 20 to 80 mg/mL, with linear
regression S = 0.0878C - 0.0927, correlation coefficient R2
= 0.9994. The limit of detection (LOD) and
limit of quantification (LOQ) were 109 ng/mL and 363 ng/mL, respectively. The recovery was from
99.0% to 101.8%. This method is simple, precise and rapid for quantitative determination of piroxicam
in tablets.
Key words: Piroxicam, reversed-phase high-performance liquid chromatography, pharmaceutical
dosage.
1. INTRODUCTION
Piroxicam was (4-hydroxy-2-methyl-N-2-(pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide,
(Fig. 1). It was a well known and very effective antiinflammatory drug [1]. Piroxicam is a
cyclooxygenase inhibiting, non-steroidal anti-inflammatory drug (NSAID) which exhibited antiinflammatory, analgesic, and antipyretic activities in animal models [2]. It was used for musculoskeletal
disorders, dysmenorrhea, and postoperative pain and its long half-life enables it to be administered once
daily.
Figure 1: Chemical structures of piroxicam.
Piroxicam has been examined by various methods: spectrophotometric procedures,
spectrofluorometric methods, HPLC method and FT-IR spectrometry. A spectrophotometric method for
the determination of piroxicam in drug is based on the reaction of piroxicam and alizarin (I) or alizarin
red S (II) or alizarin yellow G (III) or quinalizarin (IV) which can be measured at the optimum
wavelength [3]. Another to determination of piroxicam based on the reduction of ferric ferricyanide into
ferro-ferricyanide (Prussian Blue), with maximum of absorbance at 760 nm [4]. Piroxicam can also be
determined by spectrofluorometric methods, the method is based on the oxidation of piroxicam with