1. 2. 3. 4. 5. 6. © Chemometric Optimization Of A SIA Promethazine Hydrochloride Assay Method...

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1. 2. 3. 4. 5. 6. © Chemometric Optimization Of A SIA Promethazine Hydrochloride Assay Method Idris, AM; Assubaie, FN; Sultan, SM ELSEVIER SCIENCE BV, MICROCHEMICAL JOURNAL; pp: 7-13; Vol: 83 King Fahd University of Petroleum & Minerals http://www.kfupm.edu.sa Summary quential injection analysis (SIA) method for the assay of promethaz chloride, based on its oxidation by acidified cerium(W), was optimized. Three metric approaches were applied: (i) factorial design (3(3) applied to surface and 2(3) applied to effect factor) for screening the potential interacting va univariant for optimizing insignificantly interacting variables and (iii) sim izing potentially interacting variables. The optimum experimental conditio 30 mu l of 0.38 mol/l sulphuric acid, 30 mu l of 3.99 x 10(-3) mol/l cerium(I l of promethazine hydrochloride and 20 mu l/s flow rate. The detection limit .032 x 10(-5) mol/l and the calibration curve was linear up to 1.563 mol/l wi lation coefficient 0.9998, accuracy range of 89.0-101.5%, relative st tion 1.1 % (n = 10) and sample frequency at least 20 samples/h. The method wa ed to tablet form and validated with the British Pharmacopoeia method. The oped SIA method is fully automated, reproducible, sensitive, rapid and reagen g, and therefore suitable for routine control in tablets form. (c) 2006 Elsev ll rights reserved. References: *BRIT PHARM, E COP CD VER 6 0 *GRAB SOL, 2000, MULTISIMPLEX US GUID *US PHARM, 2003, E COP CD VER 26 NF 2 ALWARTHAN AA, 1993, ANAL CHIM ACTA, V282, P169 AMAN T, 2003, ANAL LETT, V36, P2961, DOI 10.1081/AL-120026414 BASAVAIAH K, 1998, TALANTA, V47, P59 Copyright: King Fahd University of Petroleum & Minerals; http://www.kfupm.edu.sa

Transcript of 1. 2. 3. 4. 5. 6. © Chemometric Optimization Of A SIA Promethazine Hydrochloride Assay Method...

Page 1: 1. 2. 3. 4. 5. 6. © Chemometric Optimization Of A SIA Promethazine Hydrochloride Assay Method Idris, AM; Assubaie, FN; Sultan, SM ELSEVIER SCIENCE BV,

1.2.3.4.5.6.

©

Chemometric Optimization Of A SIA Promethazine

Hydrochloride Assay

Method

Idris, AM; Assubaie, FN; Sultan, SM

ELSEVIER SCIENCE BV, MICROCHEMICAL JOURNAL; pp: 7-13; Vol: 83

King Fahd University of Petroleum & Minerals

http://www.kfupm.edu.sa

Summary

A sequential injection analysis (SIA) method for the assay of promethazine

hydrochloride, based on its oxidation by acidified cerium(W), was optimized. Three

chemometric approaches were applied: (i) factorial design (3(3) applied to surface

plot and 2(3) applied to effect factor) for screening the potential interacting variables,

(ii) univariant for optimizing insignificantly interacting variables and (iii) simplex for

optimizing potentially interacting variables. The optimum experimental conditions

were 30 mu l of 0.38 mol/l sulphuric acid, 30 mu l of 3.99 x 10(-3) mol/l cerium(IV),

20 mu l of promethazine hydrochloride and 20 mu l/s flow rate. The detection limit

was 7.032 x 10(-5) mol/l and the calibration curve was linear up to 1.563 mol/l with a

correlation coefficient 0.9998, accuracy range of 89.0-101.5%, relative standard

deviation 1.1 % (n = 10) and sample frequency at least 20 samples/h. The method was

applied to tablet form and validated with the British Pharmacopoeia method. The

developed SIA method is fully automated, reproducible, sensitive, rapid and reagent-

saving, and therefore suitable for routine control in tablets form. (c) 2006 Elsevier

B.V All rights reserved.

References:*BRIT PHARM, E COP CD VER 6 0*GRAB SOL, 2000, MULTISIMPLEX US GUID*US PHARM, 2003, E COP CD VER 26 NF 2ALWARTHAN AA, 1993, ANAL CHIM ACTA, V282, P169AMAN T, 2003, ANAL LETT, V36, P2961, DOI 10.1081/AL-120026414BASAVAIAH K, 1998, TALANTA, V47, P59

Copyright: King Fahd University of Petroleum & Minerals;http://www.kfupm.edu.sa

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7.8.9.10.11.12.13.14.15.16.17.18.19.20.21.22.23.24.25.26.27.28.29.30.31.

©

BASAVAIAH K, 2000, FARMACO, V55, P87BASAVAIAH K, 2001, ANAL SCI, V17, P963BASAVAIAH K, 2001, FARMACO, V56, P579BASAVAIAH K, 2002, TURK J CHEM, V26, P551BASAVAIAH K, 2003, INDIAN J CHEM TECHN, V10, P356BASAVAIAH K, 2004, FARMACO, V59, P315BAXTER RI, 1984, ANAL CHIM ACTA, V164, P171CALATAYUD JM, 1992, ANAL CHIM ACTA, V264, P283CALATAYUD JM, 1992, J PHARMACEUT BIOMED, V10, P37CALATAYUD JM, 1992, MICROCHEM J, V45, P129CHEN D, 1991, TALANTA, V38, P1227DANIEL D, 2003, ANAL CHIM ACTA, V494, P215, DOI10.1016/S0003-2670(03)00903-6DEORSI D, 1996, J PHARMACEUT BIOMED, V14, P1635DIAZ AN, 1991, ANAL CHIM ACTA, V255, P297FARHADI K, 2003, ACTA CHIM SLOV, V50, P395FEHER Z, 1988, ANAL BIOMED CHEM, V32, P345GOLABI SM, 1991, TALANTA, V38, P1253GOWDA HS, 1978, ANAL CHIM ACTA, V99, P343HOMYAK I, 1997, BIOMED CHROMATOGR, V11, P99ISSA AS, 1984, TALANTA, V31, P287ISSA YM, 2000, MIKROCHIM ACTA, V134, P9KERDWAY MM, 1992, MIKROCHIM ACTA, V108, P323KUZMICKA L, 1988, PHARMAZIE, V43, P288LARA FJ, 2005, ANAL CHIM ACTA, V535, P101, DOI

10.1016/j.aca.2004.11.08132. LIMA JLFC, 1997, J PHARM SCI, V86, P123433. MISIUK W, 1996, PHARMAZIE, V51, P6234. MOHAMED FA, 1995, ANAL LETT, V28, P249135. MUIJSELAAR PGHM, 1996, J CHROMATOGR A, V735, P39536. NAGARAJA P, 2000, ANAL SCI, V16, P112737. NI YN, 2001, ANAL CHIM ACTA, V439, P15938. PENA L, 1993, J PHARM BIOMED ANAL, V11, P89339. PUZANOWSKATARAS.H, 1989, PHARMAZIE, V44, P3540. RAMA MJR, 2004, J PHARMACEUT BIOMED, V35, P1027, DOI41. 10.1016/j/jphs.2004.03.01042. REGULSKA E, 2002, J PHARMACEUT BIOMED, V27, P33543. ROMERO AM, 1992, ANAL LETT, V7, P128944. SAIF MJ, 2005, TALANTA, V67, P869, DOI 10.1016/j.talanta.2005.03.03445. SHAMSIPUR M, 2002, J AOAC INT, V85, P55546. SULTAN SM, 1993, TALANTA, V40, P68147. SULTAN SM, 1995, ANALYST, V120, P56148. SULTAN SM, 2003, TALANTA, V59, P1073, DOI 10.1016/S0039-

9140(03)00016-X49. TAHA AM, 1983, ANALYST, V108, P1500

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USLU B, 1996, TURK J CHEM, V20, P323WALSH MI, 1983, ANALYST, V108, P626WALSH MI, 1988, TALANTA, V35, P320WANG RY, 1999, J CHROMATOGR B, V721, P327WANG RY, 2001, J SEP SCI, V24, P658ZHANG Q, 2005, INT J PHARM, V302, P10, DOI

10.1016/j.ijpharm.2005.05.043

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