Development of a green HPLC method for the analysis of artesunate and amodiaquine impurities using Quality by Design.

Abstract:

:Greening analytical methods has become of great interest in the field of pharmaceutical analysis to protect both the operators' health and the environment. In this work, an innovative methodology combining Quality-by-Design (QbD) and Green Chemistry principles was followed to develop a single, green and robust RP-HPLC method for the quantitative analysis of impurities of both artesunate and amodiaquine drugs. Ethanol was selected as the best ecofriendly alternative solvent in substitution to the commonly used organic solvents such as acetonitrile and methanol. To achieve method objectives, resolutions between the 10 peaks were chosen as critical method attributes (CMAs) to be optimized through QbD approach. Based on a quality risk assessment, pH, temperature, and gradient slope were then selected as critical method parameters (CMPs) and a three level full factorial design was used to model the CMAs as function of the CMPs. Response surface methodology associated to Monte Carlo simulations allowed to determine the method operable domain region (MODR), i.e., the multidimensional combination of CMPs where CMAs simultaneously satisfied specifications (Rs ≥ 1.5) with a probability at least equal to 95 %. Inside the MODR, the working point was chosen based on green criteria, involving a mobile phase composed of ethanol and 10 mM acetic acid only as pH modifier. The method was successfully validated for all impurities using accuracy profile methodology, which was fully compliant with the ICH Q2(R1) requirements. Finally, the method was applied to the analysis of amodiaquine and artesunate impurities in raw materials and formulations.

journal_name

J Pharm Biomed Anal

authors

Yabré M,Ferey L,Somé TI,Sivadier G,Gaudin K

doi

10.1016/j.jpba.2020.113507

subject

Has Abstract

pub_date

2020-10-25 00:00:00

pages

113507

eissn

0731-7085

issn

1873-264X

pii

S0731-7085(20)31393-5

journal_volume

190

pub_type

杂志文章
  • Determination of nimodipine in human plasma by ultra performance liquid chromatography-tandem mass spectrometry and pharmacokinetic application.

    abstract::A fast and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for the determination and pharmacokinetic study of nimodipine in human plasma. With nitrendipine as the internal standard, sample pretreatment involved one-step extraction with diethyl ether of 0.5 m...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2007.10.035

    authors: Qin F,Ma Y,Wang Y,Chen L,Wang D,Li F

    更新日期:2008-02-13 00:00:00

  • Qualitative and quantitative analyses of Compound Danshen extract based on 1H NMR method and its application for quality control.

    abstract::In this study, a new approach using 1H NMR spectroscopy combined with chemometrics method was developed for qualitative and quantitative analyses of extracts of Compound Danshen Dripping Pills (CDDP). For the qualitative analysis, some metabolites presented in Compound Danshen extract (CDE, extraction intermediate of ...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2016.08.017

    authors: Yan KJ,Chu Y,Huang JH,Jiang MM,Li W,Wang YF,Huang HY,Qin YH,Ma XH,Zhou SP,Sun H,Wang W

    更新日期:2016-11-30 00:00:00

  • Interactions of oxyphenbutazone with different cyclodextrins in aqueous medium and in the solid state.

    abstract::The interactions between a nonsteroidal anti-inflammatory drugs, oxyphenbutazone (OPB), with two cyclodextrins, beta-cyclodextrin (beta-CD) and gamma-cyclodextrin (gamma-CD), have been studied in an aqueous medium and in the solid state. Differential scanning calorimetry, hot stage microscopy, thermogravimetric analys...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(02)00042-0

    authors: Veiga MD,Merino M

    更新日期:2002-06-01 00:00:00

  • LC separation of calcipotriol from its photodegradation products and protection possibilities using adjuvants.

    abstract::Mobile phase optimization and reversed-phase column characteristics were used to separate photodegradation products from the parent compound, 24-cyclopropyl-9-,10-secochola-5,7,10(19),22-tetraene-1alpha,3beta,24-triol (calcipotriol). Separation between calcipotriol and its degradation products was obtained with an ace...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(01)00390-9

    authors: Cirunay JJ,Vander Heyden Y,Plaizier-Vercammen J

    更新日期:2001-08-01 00:00:00

  • Determination of morphine and codeine in urine by gas chromatography-mass spectrometry.

    abstract::GC-MS is one of the recommended analytical techniques for the identification and confirmation of opiates in urine. A method for the qualitative detection and quantitation of codeine and morphine in urine samples by this technique has been developed. This method is also suitable for the detection of their main metaboli...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/0731-7085(90)80140-k

    authors: Solans A,de la Torre R,Segura J

    更新日期:1990-01-01 00:00:00

  • A new approach to evaluate stability of amodiaquine and its metabolite in blood and plasma.

    abstract::A stability study for amodiaquine (AQ) and desethylamodiaquine (AQm) in whole blood and plasma is reported. AQ, AQm and chloroquine (CQ) were simultaneously analysed and the ratios AQ/CQ and AQm/CQ were used to ensure correct interpretation of the stability results. CQ was stable in whole blood and plasma at all teste...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2005.10.018

    authors: Blessborn D,Neamin G,Bergqvist Y,Lindegårdh N

    更新日期:2006-04-11 00:00:00

  • Characterization of a new illicit phosphodiesterase-type-5 inhibitor identified in the softgel shell of a dietary supplement.

    abstract::A new sildenafil analog has been identified in the softgel shell of a dietary supplement. The compound was investigated by UV spectroscopy and high-resolution MS analysis, leading to the proposed structure 1-methyl-5-{5-[2-(4-methylpiperazin-1-yl)acetyl]-2-propoxyphenyl}-3-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidi...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2018.08.031

    authors: Doi T,Takahashi K,Yamazaki M,Asada A,Takeda A,Kiyota K,Tagami T,Sawabe Y,Yamano T

    更新日期:2018-11-30 00:00:00

  • Liquid chromatography-tandem mass spectrometry for simultaneous measurement of thromboxane B2 and 12(S)-hydroxyeicosatetraenoic acid in serum.

    abstract::Arachidonic acid (AA) is metabolized in human platelets by two main pathways: via cyclooxygenase (COX-1) to prostaglandins and thromboxane (TX)A2 and via 12-lipoxygenase (12-LOX) to 12(S)-hydroxyeicosatetraenoic acid (12(S)-HETE). While COX products are known to regulate platelet reactivity, the role of 12-LOX metabol...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 临床试验,杂志文章

    doi:10.1016/j.jpba.2014.04.004

    authors: Squellerio I,Porro B,Songia P,Veglia F,Caruso D,Tremoli E,Cavalca V

    更新日期:2014-08-05 00:00:00

  • Screening of NOS activity and selectivity of newly synthesized acetamidines using RP-HPLC.

    abstract::Nitric Oxide Synthase (NOS) inhibitors could play a powerful role in inflammatory and neurodegenerative diseases. In this work, novel acetamidine derivatives of NOS were synthesized and the inhibitor activity was evalued. To screen the activity and selectivity, the l-citrulline residue, after the enzymatic NOS assay, ...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2015.11.045

    authors: Fantacuzzi M,Maccallini C,Di Matteo M,Ammazzalorso A,Bruno I,De Filippis B,Giampietro L,Mollica A,Amoroso R

    更新日期:2016-02-20 00:00:00

  • Free-radical degradation of high-molecular-weight hyaluronan induced by ascorbate plus cupric ions. Testing of bucillamine and its SA981-metabolite as antioxidants.

    abstract::High-molecular-weight hyaluronan (HA) samples were exposed to free-radical chain-degradation reactions induced by ascorbate in the presence of Cu(II) ions - the so-called Weissberger's oxidative system. The concentrations of both reactants [ascorbate, Cu(II)] were comparable to those that may occur during an early sta...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2011.06.015

    authors: Valachová K,Hrabárová E,Priesolová E,Nagy M,Baňasová M,Juránek I,Soltés L

    更新日期:2011-11-01 00:00:00

  • Simultaneous HPLC determination of multiple components in a commercial cosmetic cream.

    abstract::A high-performance liquid chromatographic method for the simultaneous determination of magnesium ascorbyl phosphate (I), imidazolidinylurea (II), a mixture of methyl-(III), ethyl-(IV), propyl-(V), butyl-(VI) parabens dissolved in phenoxyethanol, and ascorbyl palmitate (VII), was studied by using a cyano-propyl column ...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(98)00173-3

    authors: Sottofattori E,Anzaldi M,Balbi A,Tonello G

    更新日期:1998-10-01 00:00:00

  • Detection of sibutramine in adulterated dietary supplements using attenuated total reflectance-infrared spectroscopy.

    abstract::Sibutramine is one of the most occurring adulterants encountered in dietary supplements with slimming as indication. These adulterated dietary supplements often contain a herbal matrix. When customs intercept these kind of supplements it is almost impossible to discriminate between the legal products and the adulterat...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2014.08.009

    authors: Deconinck E,Cauwenbergh T,Bothy JL,Custers D,Courselle P,De Beer JO

    更新日期:2014-11-01 00:00:00

  • Synthesis and LC characterization of clenbuterol molecularly imprinted polymers.

    abstract::Highly selective non-covalent clenbuterol (CL) imprinted polymers were prepared using methacrylic acid as monomer and ethylene glycol dimethacrylate as cross-linking agent. HPLC experiments with columns packed with this material showed that CL are selectively recognised with respect to all other adrenergic substances ...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(00)00477-5

    authors: Masci G,Casati G,Crescenzi V

    更新日期:2001-05-01 00:00:00

  • An optimized reverse-phase high performance liquid chromatographic method for evaluating percutaneous absorption of glucosamine hydrochloride.

    abstract::A relatively simple, selective, precise and accurate high performance liquid chromatography (HPLC) method based on a reaction of phenylisothiocyanate (PITC) with glucosamine (GL) in alkaline media was developed and validated to determine glucosamine hydrochloride permeating through human skin in vitro. It is usually p...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2005.11.044

    authors: Tekko IA,Bonner MC,Williams AC

    更新日期:2006-05-03 00:00:00

  • Evaluation of the content and stability of the constituents of mother tinctures and tinctures: the case of Crataegus oxyacantha L. and Hieracium pilosella L.

    abstract::As a part of our investigations on the content and stability of herbal drug preparations, we evaluated the content and stability of tinctures and mother tinctures of Hawthorn leaves and flowers and Hawkweed. Hawthorn preparations are mainly used by patients with cardiac diseases; Hawkweed is employed for the treatment...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2007.01.046

    authors: Bilia AR,Eterno F,Bergonzi MC,Mazzi G,Vincieri FF

    更新日期:2007-05-09 00:00:00

  • Simultaneous isolation of Rutin and Esculin from plant material and drugs using solid-phase extraction.

    abstract::Simultaneous isolation of Rutin and Esculin from pharmaceutical materials (plant--Flos hippocastani and drugs--Venescin, Venacorn) using solid-phase extraction (SPE) have been made. For this investigation the Bakerbond SPE columns with different unpolar and polar chemically bonded phases were used. On the basis of iso...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/0731-7085(93)80199-b

    authors: Buszewski B,Kawka S,Suprynowicz Z,Wolski T

    更新日期:1993-03-01 00:00:00

  • Clinical analysis of sampatrilat, a combined renal endopeptidase and angiotensin-converting enzyme inhibitor II: assay in the plasma and urine of human volunteers by dissociation enhanced lanthanide fluorescence immunoassay (DELFIA).

    abstract::Sampatrilat is a dual inhibitor of angiotensin converting enzyme (ACE) and neutral endopeptidase (NEP) under development for the treatment of hypertension and congestive heart failure. In order to support the early clinical development (with oral administration and an expected low bioavailability), a sensitive and sel...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(97)00127-1

    authors: Venn RF,Barnard G,Kaye B,Macrae PV,Saunders KC

    更新日期:1998-01-01 00:00:00

  • Simultaneous determination of naringin, hesperidin, neohesperidin, naringenin and hesperetin of Fractus aurantii extract in rat plasma by liquid chromatography tandem mass spectrometry.

    abstract::A liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed for the simultaneous determination of naringin, hesperidin, neohesperidin, naringenin and hesperetin in rat plasma, using liquiritin as the internal standard. Plasma samples extracted with a solid-phase extraction procedure were separated...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2011.05.001

    authors: Tong L,Zhou D,Gao J,Zhu Y,Sun H,Bi K

    更新日期:2012-01-25 00:00:00

  • Development of SPME-LC-MS method for screening of eight beta-blockers and bronchodilators in plasma and urine samples.

    abstract::The current work describes the development and validation of a simple, efficient, and fast method using solid phase microextraction coupled to liquid chromatography-tandem mass spectrometry (SPME-LC-MS/MS) for the concomitant measurement of eight beta-blockers and bronchodilators in plasma and urine. The presented ass...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2016.03.001

    authors: Goryński K,Kiedrowicz A,Bojko B

    更新日期:2016-08-05 00:00:00

  • Fluorescence determination of sulphobutylether-beta-cyclodextrin in human plasma by size exclusion chromatography with inclusion complex formation.

    abstract::A selective method for the determination of sulphobutylether-beta-cyclodextrin (SBECD) in human plasma has been developed and validated over the range 4-200 microg ml(-1). SBECD is extracted from plasma using end-capped cyclohexyl solid phase extraction cartridges. This is followed by high performance size exclusion c...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(99)00283-6

    authors: Gage R,Venn RF,Bayliss MA,Edgington AM,Roffey SJ,Sorrell B

    更新日期:2000-06-01 00:00:00

  • Validation of a simple HPLC-UV method for rifampicin determination in plasma: Application to the study of rifampicin arteriovenous concentration gradient.

    abstract::In clinical practice, rifampicin exposure is estimated from its concentration in venous blood samples. In this study, we hypothesized that differences in rifampicin concentration may exist between arterial and venous plasma. An HPLC-UV method for determining rifampicin concentration in plasma using rifapentine as an i...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2016.02.013

    authors: Goutal S,Auvity S,Legrand T,Hauquier F,Cisternino S,Chapy H,Saba W,Tournier N

    更新日期:2016-05-10 00:00:00

  • A rapid and sensitive method for simultaneous determination of insulin and A21-desamido insulin by high-performance liquid chromatography.

    abstract::A reversed-phase high-performance liquid chromatography (RP-HPLC) method with UV-detection at room temperature has been developed for the analysis of insulin and its main degradation product, A21-desamido insulin. Octadecylsilica was used as stationary phase and a mixture of water and acetonitrile containing tetramety...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(03)00336-4

    authors: Moslemi P,Najafabadi AR,Tajerzadeh H

    更新日期:2003-09-15 00:00:00

  • Electrochemical investigation of interaction between mitomycin C and DNA in a novel drug-delivery system.

    abstract::A novel drug-delivery system was developed by loading the anticancer drug, mitomycin C (MC) into an oil/water system with the aim of investigation by electrochemical sensing the interaction between the drug and DNA in microemulsion phase. The physical and physicochemical properties (droplet size, pH, viscosity, conduc...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2007.05.005

    authors: Karadeniz H,Alparslan L,Erdem A,Karasulu E

    更新日期:2007-10-18 00:00:00

  • LC and LC-MS study of stress decomposition behaviour of isoniazid and establishment of validated stability-indicating assay method.

    abstract::Isoniazid was subjected to different ICH prescribed stress conditions of thermal stress, hydrolysis, oxidation and photolysis. The drug was stable to dry heat (50 and 60 degrees C). It showed extensive decomposition under hydrolytic conditions, while it was only moderately sensitive to oxidation stress. The solid drug...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2006.10.013

    authors: Bhutani H,Singh S,Vir S,Bhutani KK,Kumar R,Chakraborti AK,Jindal KC

    更新日期:2007-03-12 00:00:00

  • High-performance liquid chromatographic assay and erythrocyte partitioning of fleroxacin, a new fluoroquinolone antibiotic.

    abstract::A rapid technique for sample preparation and HPLC was developed to study in vitro the erythrocyte binding and plasma protein binding of fleroxacin in the concentration range 0.2-15 micrograms ml-1. The red blood cell partition coefficient of fleroxacin was 1.45 +/- 0.18 at 25 degrees C and was independent of concentra...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/0731-7085(90)80008-d

    authors: Brunt E,Limberg J,Derendorf H

    更新日期:1990-01-01 00:00:00

  • Relationship between retention characteristics and physicochemical parameters of solutes on porous graphitized carbon column.

    abstract::The retention of 44 barbituric acid derivatives was determined on porous graphitized carbon (PGC) column using dioxane water mixtures as eluents. Linear correlations were calculated between the logarithm of the capacity factor and the dioxane concentration in the eluent. Free Wilson analysis combined with stepwise reg...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(98)00205-2

    authors: Forgács E,Cserháti T

    更新日期:1998-12-01 00:00:00

  • Determination of sulphathiazole and sulphanilamide by photochemically induced fluorescence and first-derivative fluorescence.

    abstract::This manuscript reports the usefulness of the determination of sulphathiazole (ST) using photochemically induced fluorescence (RTPF) and RTPF coupling with first derivative (D1-RTPF), and the determination of sulphanilamide (SAN) by meaning first derivative of the emission spectrum. By irradiating 5 min, with intense ...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2004.12.024

    authors: García MC,Diez NM,Gil DB,López FS

    更新日期:2005-06-15 00:00:00

  • Impurity profiling of anticancer preclinical candidate, IIIM-290.

    abstract::IIIM-290, an orally bioavailable preclinical candidate is effective in human xenograft models of leukemia, colon and pancreatic cancer. The promising preclinical data of this lead candidate has shown its potential for clinical development. As a part of its preclinical development, impurity profiling of pilot scale bat...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2018.12.027

    authors: Kumar V,Bhurta D,Sharma A,Kumar P,Bharate SB,Vishwakarma RA,Bharate SS

    更新日期:2019-03-20 00:00:00

  • Determination of lovastatin and simvastatin in pharmaceutical dosage forms by MEKC.

    abstract::A micellar electrokinetic chromatographic (MEKC) method was developed for the quantification of lovastatin and simvastatin, cholesterol lowering agents in pharmaceutical dosage forms. Lovastatin and simvastatin were separated using an electrolyte system consisting of 12% acetonitrile (v/v) in 25 mM sodium borate buffe...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/s0731-7085(02)00128-0

    authors: Srinivasu MK,Raju AN,Reddy GO

    更新日期:2002-07-20 00:00:00

  • Impurity profiling of l-asparagine monohydrate by ion pair chromatography applying low wavelength UV detection.

    abstract::l-asparagine is a non-essential amino acid being used for a variety of pharmaceutical applications. The compound may be produced following synthetic or fermentative pathways leading to the formation of distinct impurities such as organic acids, other amino acids, dipeptides, or cyclic amino acid derivatives. Analysis ...

    journal_title:Journal of pharmaceutical and biomedical analysis

    pub_type: 杂志文章

    doi:10.1016/j.jpba.2016.08.035

    authors: Schilling K,Amstalden MC,Meinel L,Holzgrabe U

    更新日期:2016-11-30 00:00:00