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68
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. . , , . . , - . , .
. . , .
Ь
IN VITRO
: , ,
є ( ) є ,
in vitro
in vivo. ,
in vitro, є .
:
,
. ,
.
(Higuchi) [1]:
(1)
:
(2)
Mt
– , t;
M0
– , ;
S – ;
D – є ;
C0
– ;
Cs
– ;
K – .
(Lapidus Lordi) (K)
, ’є (V) (S),
[2]:
(3)
є
’є (S/V) .
© . . , . . , 2013
,)2( 0
tCCCD
S
M
ss
t
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69
Є , S/V
,
[3–5].
є є S/V
in vitro
Kollidon SR, Methocel K 4M
. є (340 / ),
– є (20 / )
, є
( . 1).
– (TMZ∙2HCl, Sochinaz SA,
); (BASF SE, Ludwigshafen, ).
– (Granulac-200; Meggle AG, ). –
( , 450 000)
( , 50 000) 8:2 (Kollidon SR, BASF SE, );
( 2208 USP, Methocel K4M CR,
Colorcon, ), -CH3
- 19–24 %,
-CH2
CH(OH)CH3
- – 7–12%. – (Aerosil
200 Ph., Evonik AG, ). – (Pruv, JRS
Pharma, ).
•2HCl
TMZ•2HCl
• 2
. 1.
.
– TMZ∙2HCl Granulac-200 (17,5 31,3%)
(48,8%) (50,0%) (Turbula T2F, Willy A. Bachofen AG,
) 15 ,
0,5 ; (0,2%) (1,0%),
0,5 , 5 .
•
70
(D) 8, 9 10 ,
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(Korsch EK0, Korsch AG, ).
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(VanKel 7000, 7010, 7025, Varian Inc., ) : 900
pH 6,8 37±0,5 ° ,
100 / . 0,35
є .
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269 . TMZ∙2HCl
.
,
100%.
Kollidon SR, Methocel K4M -
. ,KollidonSRє , MethocelK4M–
. « »
,
Kollidon SR Methocel K4M.
8 9 10
200 300 400
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/ 3
( ).
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,
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9 300 0,84 15,5 0,82 20,4
10 400 0,74 14,8 0,74 18,6
Methocel K4M 8 200 0,94 38,8 0,93 49,7
9 300 0,83 34,6 0,82 43,7
10 400 0,74 33,5 0,75 40,8
S/V
Kollidon SR Methocel K4M
TMZ∙2HCl ( . 2, , 3, ) ( . 2, B, 3, B)
.
71
TMZ•2HCl
B
C D
. 2. Kollidon SR: A –
TMZ∙2HCl, B – ; : –
TMZ∙2HCl, D –
72
TMZ•2HCl
B
C D
. 3. Methocel K4M:
A – TMZ∙2HCl, B – ; :
– TMZ∙2HCl, D –
Mt
/S (2)
TMZ∙2HCl ( . 2, C, 3, C)
( . 2, D, 3, D).
(Mt
/S)/ S/V,
TMZ∙2HCl ( . 4) Ethocel-10,
KollidonSR,MethocelK4M, , TMZ∙2HCl
S/V,
.
73
. 4.
TMZ∙2HCl
, є є
in vitro
in vitro , , in vivo .
1. ’ , є
’є (S/V).
2. ,
Kollidon SR Methocel K4M ,
TMZ∙2HCl є
S/V
S/V, .
є
.
1. Siepmann J., Peppas N. A. Higuchi equation: Derivation, applications, use and misuse
// Inter. J. Pharmaceutics. – 2011. – V. 481, N 1. – P. 6–12.
2. Lapidus H., Lordi N. G. Drug Release from Compressed Hydrophilic Matrices // J.
Pharm. Sci. – 1968. – V. 57, N 8. – P. 1292–1301.
3. Raju P. N. et al. Effect of tablet surface area and surface area/volume on drug release
from lamivudine extend release matrix tablets // Inter. J. Pharmac. Sci. Nanotechnol. –
2010. – V. 3, N 1. – P. 872–876.
4. Reynolds T. D., Mitchell S. A., Balwinski K. M. Investigation of the Effect of Tablet
Surface Area/Volume on Drug Release from Hydroxypropylmethylcellulose Controlled-
Release Matrix Tablets // Drug Dev. Industr. Pharmacy. – 2002. – V. 28, N 4. – P. 457–466.
5. The Lubrizol Corporation. Drug Release from Carbomer Tablets As A Function of
Tablet Surface Area-To-Volume Ratio. Technical Data Sheet – 781. 2011 p.
02. 10. 2013.
74
. . , . .
. . ,
IN VITRO
: , ,
,
in vitro
in vivo. , ,
in vivo, .
in vitro
, .
,
(S/V).
,
Kollidon SR Methocel K4M
,
TMZ∙2HCl S/V
S/V,
.
V. V. Mohylyuk, L. L. Davtian
Shupyk National Medical Academy of Post-Graduate Education, Kyiv
EFFECT OF TABLET SIZE ON TRIMETAZIDINE DIHYDROCHLORIDE AND
CAFFEINE IN VITRO RELEASE FROM MATRIX TABLETS WITH DIFFERENT
MATRIX FORMERS
Key words: matrix former, matrix tablets, drug release
A B S T R A C T
Oral matrix tablet with extended release of active pharmaceutical ingredient (API) is
popular dosage forms that allow to achieve desirable in vitro drug release and correspondent
level of therapeutic concentration in vivo. That’s why, the research of factors that can to
influence on in vitro drug release is an actual task.
75
Effect of tablet size increasing with simultaneous tablet mass increasing on in vitro
release of trimetazidine dihydrochloride and caffeine from matrix tablets obtained by direct
compression method was discovered.
It was found that initial tablet surface area to volume ratio (S/V) was decreasing with
increasing of tablet size.
It was proved that diffusion release ofTMZ∙2HCl and caffeine decreased with decreasing
of initial tablet S/V and was close to linear dependence on initial tablet S/V according to
Lapidus and Lordi equation independently of matrix former and API solubility.
Results of this experiment are the basis of further investigation of matrix type effect on
API release from matrix tablets.
: Valentyn.mohylyuk@gmail.com
Вплив розміру таблеток на кінетику вивільнення in vitro триметазидину дигідрохлориду та кофеїну з матричних таблеток з різними матриксоутво

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Вплив розміру таблеток на кінетику вивільнення in vitro триметазидину дигідрохлориду та кофеїну з матричних таблеток з різними матриксоутво

  • 1. 68 615.45:615.012/014 . . , , . . , - . , . . . , . Ь IN VITRO : , , є ( ) є , in vitro in vivo. , in vitro, є . : , . , . (Higuchi) [1]: (1) : (2) Mt – , t; M0 – , ; S – ; D – є ; C0 – ; Cs – ; K – . (Lapidus Lordi) (K) , ’є (V) (S), [2]: (3) є ’є (S/V) . © . . , . . , 2013 ,)2( 0 tCCCD S M ss t 
  • 2. 69 Є , S/V , [3–5]. є є S/V in vitro Kollidon SR, Methocel K 4M . є (340 / ), – є (20 / ) , є ( . 1). – (TMZ∙2HCl, Sochinaz SA, ); (BASF SE, Ludwigshafen, ). – (Granulac-200; Meggle AG, ). – ( , 450 000) ( , 50 000) 8:2 (Kollidon SR, BASF SE, ); ( 2208 USP, Methocel K4M CR, Colorcon, ), -CH3 - 19–24 %, -CH2 CH(OH)CH3 - – 7–12%. – (Aerosil 200 Ph., Evonik AG, ). – (Pruv, JRS Pharma, ). •2HCl TMZ•2HCl • 2 . 1. . – TMZ∙2HCl Granulac-200 (17,5 31,3%) (48,8%) (50,0%) (Turbula T2F, Willy A. Bachofen AG, ) 15 , 0,5 ; (0,2%) (1,0%), 0,5 , 5 . •
  • 3. 70 (D) 8, 9 10 , 0,75 D 200, 300 400 (Korsch EK0, Korsch AG, ). « ». « » ( ) Apparatus (VanKel 7000, 7010, 7025, Varian Inc., ) : 900 pH 6,8 37±0,5 ° , 100 / . 0,35 є . - (UV-2101 PC, Shimadzu Scientific Instruments Inc., ) 269 . TMZ∙2HCl . , 100%. Kollidon SR, Methocel K4M - . ,KollidonSRє , MethocelK4M– . « » , Kollidon SR Methocel K4M. 8 9 10 200 300 400 S/V: 1,1 < 1,2 < 1,3 2 / 3 ( ). S/V є - , , TMZ∙2HCl S/V, 2 / 3 Mt=2 , %/ S/V, 2 / 3 Mt=2 , %/ Kollidon SR 8 200 0,94 18,1 0,93 23,0 9 300 0,84 15,5 0,82 20,4 10 400 0,74 14,8 0,74 18,6 Methocel K4M 8 200 0,94 38,8 0,93 49,7 9 300 0,83 34,6 0,82 43,7 10 400 0,74 33,5 0,75 40,8 S/V Kollidon SR Methocel K4M TMZ∙2HCl ( . 2, , 3, ) ( . 2, B, 3, B) .
  • 4. 71 TMZ•2HCl B C D . 2. Kollidon SR: A – TMZ∙2HCl, B – ; : – TMZ∙2HCl, D –
  • 5. 72 TMZ•2HCl B C D . 3. Methocel K4M: A – TMZ∙2HCl, B – ; : – TMZ∙2HCl, D – Mt /S (2) TMZ∙2HCl ( . 2, C, 3, C) ( . 2, D, 3, D). (Mt /S)/ S/V, TMZ∙2HCl ( . 4) Ethocel-10, KollidonSR,MethocelK4M, , TMZ∙2HCl S/V, .
  • 6. 73 . 4. TMZ∙2HCl , є є in vitro in vitro , , in vivo . 1. ’ , є ’є (S/V). 2. , Kollidon SR Methocel K4M , TMZ∙2HCl є S/V S/V, . є . 1. Siepmann J., Peppas N. A. Higuchi equation: Derivation, applications, use and misuse // Inter. J. Pharmaceutics. – 2011. – V. 481, N 1. – P. 6–12. 2. Lapidus H., Lordi N. G. Drug Release from Compressed Hydrophilic Matrices // J. Pharm. Sci. – 1968. – V. 57, N 8. – P. 1292–1301. 3. Raju P. N. et al. Effect of tablet surface area and surface area/volume on drug release from lamivudine extend release matrix tablets // Inter. J. Pharmac. Sci. Nanotechnol. – 2010. – V. 3, N 1. – P. 872–876. 4. Reynolds T. D., Mitchell S. A., Balwinski K. M. Investigation of the Effect of Tablet Surface Area/Volume on Drug Release from Hydroxypropylmethylcellulose Controlled- Release Matrix Tablets // Drug Dev. Industr. Pharmacy. – 2002. – V. 28, N 4. – P. 457–466. 5. The Lubrizol Corporation. Drug Release from Carbomer Tablets As A Function of Tablet Surface Area-To-Volume Ratio. Technical Data Sheet – 781. 2011 p. 02. 10. 2013.
  • 7. 74 . . , . . . . , IN VITRO : , , , in vitro in vivo. , , in vivo, . in vitro , . , (S/V). , Kollidon SR Methocel K4M , TMZ∙2HCl S/V S/V, . V. V. Mohylyuk, L. L. Davtian Shupyk National Medical Academy of Post-Graduate Education, Kyiv EFFECT OF TABLET SIZE ON TRIMETAZIDINE DIHYDROCHLORIDE AND CAFFEINE IN VITRO RELEASE FROM MATRIX TABLETS WITH DIFFERENT MATRIX FORMERS Key words: matrix former, matrix tablets, drug release A B S T R A C T Oral matrix tablet with extended release of active pharmaceutical ingredient (API) is popular dosage forms that allow to achieve desirable in vitro drug release and correspondent level of therapeutic concentration in vivo. That’s why, the research of factors that can to influence on in vitro drug release is an actual task.
  • 8. 75 Effect of tablet size increasing with simultaneous tablet mass increasing on in vitro release of trimetazidine dihydrochloride and caffeine from matrix tablets obtained by direct compression method was discovered. It was found that initial tablet surface area to volume ratio (S/V) was decreasing with increasing of tablet size. It was proved that diffusion release ofTMZ∙2HCl and caffeine decreased with decreasing of initial tablet S/V and was close to linear dependence on initial tablet S/V according to Lapidus and Lordi equation independently of matrix former and API solubility. Results of this experiment are the basis of further investigation of matrix type effect on API release from matrix tablets. : Valentyn.mohylyuk@gmail.com