REZA FAJAR KURNIAWAN, 051411131069 (2018) VALIDASI METODE KCKT PADA UJI DISOLUSI TERBANDING TABLET PIROKSIKAM. Skripsi thesis, Universitas Airlangga.

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Abstract

The purpose of this study was to obtain a valid analysis method for in-vitro comparative dissolution test of piroxicam tablets using HPLC. The chromatographic separation was achieved using Lichrospher 100 RP-18 column (250 mm x 4 mm i.d., 5 μm particle size). The isocratic mobile phase was methanol: pH 4.0 phosphate buffer (45:55; v/v) at a flow rate of1,2 mL/min and column temperature of 40°C. The analysis determination were performed using UV-Vis detector at λ of353 nm. The simulated samples with three different dissolution media at pH of 1,2; 4,5 and 6,8. The sample volume injected was 20 μL. The method showed linear relationship with regression equation of y= 28765.95x-398058,3 with r = 0.9998, y = 31413.18x-310086.9 with r = 0.9990 and y = 25295.31x-385507.2 with r = 0.9990 at pH 1,2, pH4,5 and pH 6,8, respectively. The method showedprecision, with a relative standard deviation (RSD) smaller than 2%. The accuracy test by spiked placebo procedure obtained good recovery i.e. 100,21; 100,13 and 100,50 respectively. The HPLC condition in this study is suitable for determination of dissolution profiles of piroxicam in tablets.

Item Type:	Thesis (Skripsi)
Additional Information:	KKB KK-2 FF.KF. 37- 18 Kur v
Uncontrolled Keywords:	Method validation, HPLC, compartive dissolution, piroxicam
Subjects:	R Medicine > RS Pharmacy and materia medica > RS200-201 Pharmaceutical dosage forms
Divisions:	05. Fakultas Farmasi > Kimia Farmasi
Creators:	Creators NIM REZA FAJAR KURNIAWAN, 051411131069 UNSPECIFIED
Contributors:	Contribution Name NIDN / NIDK Thesis advisor Moch. Yuwono, Prof.Dr.rer.nat., MS., Apt. UNSPECIFIED Thesis advisor Asri Darmawati, Dr., MS., Apt. UNSPECIFIED
Depositing User:	Tatik Poedjijarti
Date Deposited:	13 Dec 2018 16:03
Last Modified:	13 Dec 2018 16:03
URI:	http://repository.unair.ac.id/id/eprint/76735
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