• Je něco špatně v tomto záznamu ?

Effect of solvent selection on drug loading and amorphisation in mesoporous silica particles

M. Šoltys, P. Kovačík, O. Dammer, J. Beránek, F. Štěpánek,

. 2019 ; 555 (-) : 19-27. [pub] 20181103

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc19028112

Increasing the dissolution rate of poorly water-soluble active pharmaceutical ingredients (APIs) is a key strategy used for improving their oral bioavailability. One of the formulation approaches is API loading to mesoporous carrier particles, which can increase the dissolution rate through the combination of improved powder wettability and dispersion, higher surface area, and API conversion from crystalline to the amorphous state. From the formulation process point of view, the maximum achievable drug loading is a crucial parameter, which depends on the loading method. Drug loading by sorption from a solution is a technologically attractive approach, since it involves familiar unit operations (mixing, filtration, drying). However, the success of the equilibrium sorption approach depends on the choice of the solvent. In this work we present an experimental study of loading efficiency to mesoporous silica particles, based on a set of 10 APIs combined with 6 different solvents at a range of concentrations. We show that due to the competitive nature of the adsorption process, the solvent with the highest API solubility is not necessarily the best candidate for maximising the API loading. Based on the investigated drug-solvent combinations, we show that the dielectric constant of the solvent is a good predictor of loading efficiency and can be used as a general guideline for solvent selection. On the other hand, we did not find any systematic correlation between commonly measured API properties such as logP and their loading efficiency.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc19028112
003      
CZ-PrNML
005      
20230703090304.0
007      
ta
008      
190813s2019 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.ijpharm.2018.10.075 $2 doi
035    __
$a (PubMed)30395956
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Šoltys, Marek $u Department of Chemical Engineering, University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic.
245    10
$a Effect of solvent selection on drug loading and amorphisation in mesoporous silica particles / $c M. Šoltys, P. Kovačík, O. Dammer, J. Beránek, F. Štěpánek,
520    9_
$a Increasing the dissolution rate of poorly water-soluble active pharmaceutical ingredients (APIs) is a key strategy used for improving their oral bioavailability. One of the formulation approaches is API loading to mesoporous carrier particles, which can increase the dissolution rate through the combination of improved powder wettability and dispersion, higher surface area, and API conversion from crystalline to the amorphous state. From the formulation process point of view, the maximum achievable drug loading is a crucial parameter, which depends on the loading method. Drug loading by sorption from a solution is a technologically attractive approach, since it involves familiar unit operations (mixing, filtration, drying). However, the success of the equilibrium sorption approach depends on the choice of the solvent. In this work we present an experimental study of loading efficiency to mesoporous silica particles, based on a set of 10 APIs combined with 6 different solvents at a range of concentrations. We show that due to the competitive nature of the adsorption process, the solvent with the highest API solubility is not necessarily the best candidate for maximising the API loading. Based on the investigated drug-solvent combinations, we show that the dielectric constant of the solvent is a good predictor of loading efficiency and can be used as a general guideline for solvent selection. On the other hand, we did not find any systematic correlation between commonly measured API properties such as logP and their loading efficiency.
650    _2
$a adsorpce $7 D000327
650    _2
$a farmaceutická chemie $x metody $7 D002626
650    _2
$a krystalizace $7 D003460
650    _2
$a nosiče léků $x chemie $7 D004337
650    _2
$a léčivé přípravky $x aplikace a dávkování $x chemie $7 D004364
650    _2
$a poréznost $7 D016062
650    _2
$a oxid křemičitý $x chemie $7 D012822
650    _2
$a rozpustnost $7 D012995
650    _2
$a rozpouštědla $x chemie $7 D012997
650    _2
$a farmaceutická technologie $x metody $7 D013678
655    _2
$a časopisecké články $7 D016428
700    1_
$a Kovačík, Pavel $u Zentiva, k.s., U Kabelovny 130, 102 00 Praha 10, Czech Republic.
700    1_
$a Dammer, Ondřej $u Zentiva, k.s., U Kabelovny 130, 102 00 Praha 10, Czech Republic. $7 xx0303489
700    1_
$a Beránek, Josef $u Zentiva, k.s., U Kabelovny 130, 102 00 Praha 10, Czech Republic.
700    1_
$a Štěpánek, František $u Department of Chemical Engineering, University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic. Electronic address: Frantisek.Stepanek@vscht.cz.
773    0_
$w MED00002359 $t International journal of pharmaceutics $x 1873-3476 $g Roč. 555, č. - (2019), s. 19-27
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30395956 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20190813 $b ABA008
991    __
$a 20230703090303 $b ABA008
999    __
$a ok $b bmc $g 1433261 $s 1066572
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2019 $b 555 $c - $d 19-27 $e 20181103 $i 1873-3476 $m International journal of pharmaceutics $n Int. j. pharm. $x MED00002359
LZP    __
$a Pubmed-20190813

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...