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Robust mixed-mode chromatography method development using Analytical Quality by Design approach for analysis of selected drugs

Robustan razvoj metode multimodalne hromatografije primenom principa ugrađivanja kvaliteta kroz dizajn za analizu odabarnih lekova

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2022
Robust_mixed_mode_pub_2022.pdf (224.5Kb)
Authors
Svrkota, Bojana
Krmar, Jovana
Protić, Ana
Otašević, Biljana
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Abstract
Mixed-Mode Liquid Chromatography (MMLC) includes several separation mechanisms in a single column, which is why MMLC can analyze compounds in a broad range of polarities and ionization potentials in a single run (1). Acclaim Mixed-Mode WCX-1 column with the ability to expose hydrophobic and weak cation exchange interactions was thus selected to analyse a challenging mixture of neutral and cationic forms: ergotamine, mecloxamine, camylofin, caffeine and propyphenazone, used as a fixed combination. MMLC method was developed in line with Analytical Quality by Design (AQbD) approach implying the scientifically-based understanding of process properties and risk-based management of the method life cycle. AQbD refers to pre-definition of the method’s Analytical Target Profile (ATP) by means of baseline separations within the shortest possible time, as well as definition of Critical Method Attributes (CMAs) as a measure of method quality and Critical Method Parameters (CMPs) affecti...ng CMAs (2). Acetonitrile content, pH and acetate buffer concentration were selected as CMPs since retention mechanism expression in MMLC strongly depends on the mobile phase characteristics. The dependence of CMAs on CMPs was revealed following a face-centred central composition design plan of experiments and accompanying mathematical models, coefficients and standard error values. Design Space in which ATP is achieved with a high level of reliability (π = 90%), was determined by Monte Carlo simulations taking error distribution into account. Its margins pointed out to the working point that assures proper method robustness (pH 5.2, 90 mM acetate buffer solution and 48% (v/v) of acetonitrile).

Multimodalna tečna hromatografija (Mixed‐Mode Liquid Chromatography – MMLC) uključuje nekoliko mehanizama razdvajanja u jednoj koloni, zbog čega se ova tehnika može koristiti za simultanu analizu jedinjenja širokog opsega polarnosti i jonizacionog potencijala (1). Acclaim Mixed‐Mode WCX‐1 kolona sa sposobnošću ekspresije hidrofobnih i interakcija slabe katjonske izmene, je odabrana za analizu izazovne smeše neutralnih i katjonskih oblika analita: ergotamina, mekloksamina, kamilofina, kofeina i propifenazona, koji se primenjuju u fiksnoj kombinaciji. MMLC metoda je razvijena u skladu sa pristupom ugradnje kvaliteta kroz dizajn (Analytical Quality by Design – AQbD) koji podrazumeva naučno zasnovano razumevanje svojstava procesa i upravljanje životnim ciklusom metode prema riziku. AQbD se odnosi na unapred definisanje analitičkog ciljanog profila metode (Analytical Target Profile - ATP) odnosno razdvajanje na baznoj liniji za što kraće vreme, kao i na definisanje kritičnih osob...ina metode (Critical Method Attributes - CMA) kao mere kvaliteta metode i kritičnih parametara metode (Critical Method Parameters - CMP) koji utiču na CMA (2). Sadržaj acetonitrila, pH i koncentracija acetatnog pufera izabrani su kao CMP, pošto ekspresija MMLC retencionih mehanizma zavisi od karakteristika mobilne faze. Zavisnost CMA od CMP definisana je pomoću plana eksperimenata usklađenim sa centralnim kompozicionim dizajnom, ka centru orijentisanim i pratećim matematičkim modelima, koeficijentima i vrednostima standardne greške. Prostor dizajna u kome se ATP postiže sa visokim nivoom pouzdanosti (π = 90%) određen je Monte Karlo simulacijama uzimajuć i u obzir distribuciju grešaka. Njegov okvir ukazuje na radnu tačku koja obezbeđuje odgovarajuć u robusnost metode (pH 5,2, 90 mM rastvor acetatnog pufera i 48% (v/v) acetonitrila).

Source:
Arhiv za farmaciju, 2022, 72, 4 suplement, S243-S244
Publisher:
  • Savez farmaceutskih udruženja Srbije (SFUS)
Note:
  • VIII Kongres farmaceuta Srbije sa međunarodnim učešćem, 12-15.10.2022. Beograd

ISSN: 0004-1963

[ Google Scholar ]
Handle
https://hdl.handle.net/21.15107/rcub_farfar_4524
URI
https://farfar.pharmacy.bg.ac.rs/handle/123456789/4524
Collections
  • Radovi istraživača / Researchers’ publications
Institution/Community
Pharmacy
TY  - CONF
AU  - Svrkota, Bojana
AU  - Krmar, Jovana
AU  - Protić, Ana
AU  - Otašević, Biljana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4524
AB  - Mixed-Mode Liquid Chromatography (MMLC) includes several separation
mechanisms in a single column, which is why MMLC can analyze compounds in a broad
range of polarities and ionization potentials in a single run (1). Acclaim Mixed-Mode WCX-1
column with the ability to expose hydrophobic and weak cation exchange interactions was
thus selected to analyse a challenging mixture of neutral and cationic forms: ergotamine,
mecloxamine, camylofin, caffeine and propyphenazone, used as a fixed combination. MMLC
method was developed in line with Analytical Quality by Design (AQbD) approach implying
the scientifically-based understanding of process properties and risk-based management of
the method life cycle. AQbD refers to pre-definition of the method’s Analytical Target Profile
(ATP) by means of baseline separations within the shortest possible time, as well as
definition of Critical Method Attributes (CMAs) as a measure of method quality and Critical
Method Parameters (CMPs) affecting CMAs (2). Acetonitrile content, pH and acetate buffer
concentration were selected as CMPs since retention mechanism expression in MMLC
strongly depends on the mobile phase characteristics. The dependence of CMAs on CMPs was
revealed following a face-centred central composition design plan of experiments and
accompanying mathematical models, coefficients and standard error values. Design Space in
which ATP is achieved with a high level of reliability (π = 90%), was determined by Monte
Carlo simulations taking error distribution into account. Its margins pointed out to the
working point that assures proper method robustness (pH 5.2, 90 mM acetate buffer solution
and 48% (v/v) of acetonitrile).
AB  - Multimodalna tečna hromatografija (Mixed‐Mode Liquid Chromatography – MMLC)
uključuje nekoliko mehanizama razdvajanja u jednoj koloni, zbog čega se ova tehnika može
koristiti za simultanu analizu jedinjenja širokog opsega polarnosti i jonizacionog potencijala
(1). Acclaim Mixed‐Mode WCX‐1 kolona sa sposobnošću ekspresije hidrofobnih i interakcija
slabe katjonske izmene, je odabrana za analizu izazovne smeše neutralnih i katjonskih oblika
analita: ergotamina, mekloksamina, kamilofina, kofeina i propifenazona, koji se primenjuju u
fiksnoj kombinaciji. MMLC metoda je razvijena u skladu sa pristupom ugradnje kvaliteta kroz
dizajn (Analytical Quality by Design – AQbD) koji podrazumeva naučno zasnovano
razumevanje svojstava procesa i upravljanje životnim ciklusom metode prema riziku. AQbD
se odnosi na unapred definisanje analitičkog ciljanog profila metode (Analytical Target
Profile - ATP) odnosno razdvajanje na baznoj liniji za što kraće vreme, kao i na definisanje
kritičnih osobina metode (Critical Method Attributes - CMA) kao mere kvaliteta metode i
kritičnih parametara metode (Critical Method Parameters - CMP) koji utiču na CMA (2).
Sadržaj acetonitrila, pH i koncentracija acetatnog pufera izabrani su kao CMP, pošto
ekspresija MMLC retencionih mehanizma zavisi od karakteristika mobilne faze. Zavisnost
CMA od CMP definisana je pomoću plana eksperimenata usklađenim sa centralnim
kompozicionim dizajnom, ka centru orijentisanim i pratećim matematičkim modelima,
koeficijentima i vrednostima standardne greške. Prostor dizajna u kome se ATP postiže sa
visokim nivoom pouzdanosti (π = 90%) određen je Monte Karlo simulacijama uzimajuć i u
obzir distribuciju grešaka. Njegov okvir ukazuje na radnu tačku koja obezbeđuje
odgovarajuć u robusnost metode (pH 5,2, 90 mM rastvor acetatnog pufera i 48% (v/v)
acetonitrila).
PB  - Savez farmaceutskih udruženja Srbije (SFUS)
C3  - Arhiv za farmaciju
T1  - Robust mixed-mode chromatography method development using Analytical Quality by Design approach for analysis of selected drugs
T1  - Robustan razvoj metode multimodalne hromatografije primenom principa ugrađivanja kvaliteta kroz dizajn za analizu odabarnih lekova
VL  - 72
IS  - 4 suplement
SP  - S243
EP  - S244
UR  - https://hdl.handle.net/21.15107/rcub_farfar_4524
ER  - 
@conference{
author = "Svrkota, Bojana and Krmar, Jovana and Protić, Ana and Otašević, Biljana",
year = "2022",
abstract = "Mixed-Mode Liquid Chromatography (MMLC) includes several separation
mechanisms in a single column, which is why MMLC can analyze compounds in a broad
range of polarities and ionization potentials in a single run (1). Acclaim Mixed-Mode WCX-1
column with the ability to expose hydrophobic and weak cation exchange interactions was
thus selected to analyse a challenging mixture of neutral and cationic forms: ergotamine,
mecloxamine, camylofin, caffeine and propyphenazone, used as a fixed combination. MMLC
method was developed in line with Analytical Quality by Design (AQbD) approach implying
the scientifically-based understanding of process properties and risk-based management of
the method life cycle. AQbD refers to pre-definition of the method’s Analytical Target Profile
(ATP) by means of baseline separations within the shortest possible time, as well as
definition of Critical Method Attributes (CMAs) as a measure of method quality and Critical
Method Parameters (CMPs) affecting CMAs (2). Acetonitrile content, pH and acetate buffer
concentration were selected as CMPs since retention mechanism expression in MMLC
strongly depends on the mobile phase characteristics. The dependence of CMAs on CMPs was
revealed following a face-centred central composition design plan of experiments and
accompanying mathematical models, coefficients and standard error values. Design Space in
which ATP is achieved with a high level of reliability (π = 90%), was determined by Monte
Carlo simulations taking error distribution into account. Its margins pointed out to the
working point that assures proper method robustness (pH 5.2, 90 mM acetate buffer solution
and 48% (v/v) of acetonitrile)., Multimodalna tečna hromatografija (Mixed‐Mode Liquid Chromatography – MMLC)
uključuje nekoliko mehanizama razdvajanja u jednoj koloni, zbog čega se ova tehnika može
koristiti za simultanu analizu jedinjenja širokog opsega polarnosti i jonizacionog potencijala
(1). Acclaim Mixed‐Mode WCX‐1 kolona sa sposobnošću ekspresije hidrofobnih i interakcija
slabe katjonske izmene, je odabrana za analizu izazovne smeše neutralnih i katjonskih oblika
analita: ergotamina, mekloksamina, kamilofina, kofeina i propifenazona, koji se primenjuju u
fiksnoj kombinaciji. MMLC metoda je razvijena u skladu sa pristupom ugradnje kvaliteta kroz
dizajn (Analytical Quality by Design – AQbD) koji podrazumeva naučno zasnovano
razumevanje svojstava procesa i upravljanje životnim ciklusom metode prema riziku. AQbD
se odnosi na unapred definisanje analitičkog ciljanog profila metode (Analytical Target
Profile - ATP) odnosno razdvajanje na baznoj liniji za što kraće vreme, kao i na definisanje
kritičnih osobina metode (Critical Method Attributes - CMA) kao mere kvaliteta metode i
kritičnih parametara metode (Critical Method Parameters - CMP) koji utiču na CMA (2).
Sadržaj acetonitrila, pH i koncentracija acetatnog pufera izabrani su kao CMP, pošto
ekspresija MMLC retencionih mehanizma zavisi od karakteristika mobilne faze. Zavisnost
CMA od CMP definisana je pomoću plana eksperimenata usklađenim sa centralnim
kompozicionim dizajnom, ka centru orijentisanim i pratećim matematičkim modelima,
koeficijentima i vrednostima standardne greške. Prostor dizajna u kome se ATP postiže sa
visokim nivoom pouzdanosti (π = 90%) određen je Monte Karlo simulacijama uzimajuć i u
obzir distribuciju grešaka. Njegov okvir ukazuje na radnu tačku koja obezbeđuje
odgovarajuć u robusnost metode (pH 5,2, 90 mM rastvor acetatnog pufera i 48% (v/v)
acetonitrila).",
publisher = "Savez farmaceutskih udruženja Srbije (SFUS)",
journal = "Arhiv za farmaciju",
title = "Robust mixed-mode chromatography method development using Analytical Quality by Design approach for analysis of selected drugs, Robustan razvoj metode multimodalne hromatografije primenom principa ugrađivanja kvaliteta kroz dizajn za analizu odabarnih lekova",
volume = "72",
number = "4 suplement",
pages = "S243-S244",
url = "https://hdl.handle.net/21.15107/rcub_farfar_4524"
}
Svrkota, B., Krmar, J., Protić, A.,& Otašević, B.. (2022). Robust mixed-mode chromatography method development using Analytical Quality by Design approach for analysis of selected drugs. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije (SFUS)., 72(4 suplement), S243-S244.
https://hdl.handle.net/21.15107/rcub_farfar_4524
Svrkota B, Krmar J, Protić A, Otašević B. Robust mixed-mode chromatography method development using Analytical Quality by Design approach for analysis of selected drugs. in Arhiv za farmaciju. 2022;72(4 suplement):S243-S244.
https://hdl.handle.net/21.15107/rcub_farfar_4524 .
Svrkota, Bojana, Krmar, Jovana, Protić, Ana, Otašević, Biljana, "Robust mixed-mode chromatography method development using Analytical Quality by Design approach for analysis of selected drugs" in Arhiv za farmaciju, 72, no. 4 suplement (2022):S243-S244,
https://hdl.handle.net/21.15107/rcub_farfar_4524 .

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