Simultaneous Determination of Artesunate and Amodiaquine in Fixed-Dose Combination by a RP-HPLC Method with Double UV Detection: Implementation in Interlaboratory Study Involving Seven African National Quality Control Laboratories

被引:14
|
作者
Le Vaillant, Y. [1 ,2 ]
Brenier, C. [2 ]
Grange, Y. [2 ]
Nicolas, A. [3 ]
Bonnet, P. A. [2 ]
Massing-Bias, L. R. [4 ]
Rakotomanga, P. [5 ]
Koumare, B. [6 ]
Mahly, A. [7 ]
Absi, M. [8 ]
Ciss, M. [9 ]
Loueslati, M. H. [10 ]
Chauvey, D. [2 ]
机构
[1] Agence Francaise Securite Sanit Prod Sante, Direct Lab & Controles, F-34748 Vendargues, France
[2] Agence Francaise Securite Sanit Prod Sante, Direct Lab & Controles, F-34740 Vendargues, France
[3] Agence Francaise Securite Sanit Prod Sante, Direct Lab & Controles, F-93285 St Denis, France
[4] Lab Natl Controle Qualite Medicaments & Expertise, Yaounde, Cameroon
[5] Agence Medicament Madagascar BP, Antananarivo 101, Madagascar
[6] Lab Natl Sante, Bamako, Mali
[7] Lab Natl Controle Qualite Medicaments, Rabat, Morocco
[8] Lab Natl Sante Publ & Expertise, Niamey, Niger
[9] Lab Natl Controle Qualite Medicaments, Dakar, Senegal
[10] Lab Natl Controle Qualite Medicaments, Tunis 1006, Tunisia
关键词
RP-HPLC-UV; Simultaneous determination; Artesunate and amodiaquine; Drug combination; EXTRACTION PROCEDURE; DRUG-COMBINATION; PEAK COMPRESSION; GRADIENT ELUTION; HUMAN PLASMA; LIQUID; DIHYDROARTEMISININ; ARTEMISININ; VALIDATION; MALARIA;
D O I
10.1007/s10337-012-2241-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The fixed-dose combination artesunate (AS)-amodiaquine (AQ) is one of the most widely used treatments for uncomplicated falciparum malaria. It is currently proposed to the inclusion in the model list of essential medicines of World Health Organization and has been recently prequalified. Until now, no satisfactory method for the simultaneous determination of the two active ingredients had been available. Thus, a reversed phase high performance liquid chromatography for the quantitative determination of AQ and AS was developed and validated. Chromatography was performed using an end-capped octadecylsilyl silica gel column (100 x 4.6 mm, 3 mu m) with a binary gradient using aqueous phase containing potassium dihydrogen phosphate (10 mM) and acetonitrile. Taking into consideration the physico-chemical characteristics of the two compounds related to their ionization, the use of a counter ion was necessary to ensure the retention of AQ in a reversed phase system simultaneously to AS. Thus, aqueous mobile phase was adjusted to pH 3.0 and the chosen counter ion was sodium 1-octanesulfonate (100 mM). In these conditions, the retention times were about 4 min for AQ and 10 min for AS with UV detection at 300 and 210 nm, respectively. Method was then validated according to ICH guideline (specificity/linearity/accuracy/precision) and potential interferences with excipients and degradation products were checked. It has also been used for an interlaboratory study involving seven African National Quality Control Laboratories and Afssaps (Agence fran double dagger aise de s,curit, sanitaire des produits de sant,) laboratory. The results demonstrate that this rapid and simple method can be easily used by official laboratories for routine control, market survey and for the detection of potential substandard medicines which are very frequent in African countries.
引用
收藏
页码:617 / 628
页数:12
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    Y. Le Vaillant
    C. Brenier
    Y. Grange
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    A. Mahly
    M. Absi
    M. Ciss
    M. H. Loueslati
    D. Chauvey
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