-
1
-
-
35648992051
-
Pharmaceutical applications of hot-melt extrusion: part II
-
COI: 1:CAS:528:DC%2BD2sXht1WgtL%2FN, PID: 17963112
-
Repka MA et al. Pharmaceutical applications of hot-melt extrusion: part II. Drug Dev Ind Pharm. 2007;33(10):1043–57.
-
(2007)
Drug Dev Ind Pharm
, vol.33
, Issue.10
, pp. 1043-1057
-
-
Repka, M.A.1
-
2
-
-
34648812679
-
Pharmaceutical applications of hot-melt extrusion: part I
-
COI: 1:CAS:528:DC%2BD2sXhtVKqs7fF, PID: 17891577
-
Crowley MM et al. Pharmaceutical applications of hot-melt extrusion: part I. Drug Dev Ind Pharm. 2007;33(9):909–26.
-
(2007)
Drug Dev Ind Pharm
, vol.33
, Issue.9
, pp. 909-926
-
-
Crowley, M.M.1
-
3
-
-
84937814006
-
-
Repka MA et al. Applications of hot-melt extrusion for drug delivery. 2008.
-
Repka MA et al. Applications of hot-melt extrusion for drug delivery. 2008.
-
-
-
-
4
-
-
36549042006
-
Solid dispersions as strategy to improve oral bioavailability of poor water-soluble drugs
-
COI: 1:CAS:528:DC%2BD2sXhsVSmurnF, PID: 18061887
-
Vasconcelos T, Sarmento B, Costa P. Solid dispersions as strategy to improve oral bioavailability of poor water-soluble drugs. Drug Discov Today. 2007;12(23):1068–75.
-
(2007)
Drug Discov Today
, vol.12
, Issue.23
, pp. 1068-1075
-
-
Vasconcelos, T.1
Sarmento, B.2
Costa, P.3
-
5
-
-
84884137626
-
Development of amorphous solid dispersion formulations of a poorly water-soluble drug, MK-0364
-
COI: 1:CAS:528:DC%2BC3sXot1Oiurw%3D, PID: 23651642
-
Sotthivirat S et al. Development of amorphous solid dispersion formulations of a poorly water-soluble drug, MK-0364. Int J Pharm. 2013;452(1):73–81.
-
(2013)
Int J Pharm
, vol.452
, Issue.1
, pp. 73-81
-
-
Sotthivirat, S.1
-
6
-
-
84937817673
-
-
Formulating poorly water-soluble drugs: Springer
-
Williams RO, Watts AB, Miller DA. Formulating poorly water-soluble drugs 2012: Springer.
-
(2012)
Miller DA
-
-
Williams, R.O.1
Watts, A.B.2
-
7
-
-
84862304361
-
Improving the chemical stability of amorphous solid dispersion with cocrystal technique by hot melt extrusion
-
COI: 1:CAS:528:DC%2BC3MXhtleqsb%2FE, PID: 22009589
-
Liu X et al. Improving the chemical stability of amorphous solid dispersion with cocrystal technique by hot melt extrusion. Pharm Res. 2012;29(3):806–17.
-
(2012)
Pharm Res
, vol.29
, Issue.3
, pp. 806-817
-
-
Liu, X.1
-
8
-
-
84870201265
-
Stability and solubility enhancement of ellagic acid in cellulose ester solid dispersions
-
COI: 1:CAS:528:DC%2BC3sXisVSru7c%3D, PID: 23399175
-
Li B et al. Stability and solubility enhancement of ellagic acid in cellulose ester solid dispersions. Carbohydr Polym. 2013;92(2):1443–50.
-
(2013)
Carbohydr Polym
, vol.92
, Issue.2
, pp. 1443-1450
-
-
Li, B.1
-
9
-
-
0022537845
-
Clinical pharmacokinetics and pharmacological effects of carbamazepine and carbamazepine-10, 11-epoxide
-
COI: 1:STN:280:DyaL283nt12qsg%3D%3D, PID: 3524954
-
Bertilsson L, Tomson T. Clinical pharmacokinetics and pharmacological effects of carbamazepine and carbamazepine-10, 11-epoxide. Clin Pharmacokinet. 1986;11(3):177–98.
-
(1986)
Clin Pharmacokinet
, vol.11
, Issue.3
, pp. 177-198
-
-
Bertilsson, L.1
Tomson, T.2
-
10
-
-
3843097202
-
Classification of orally administered drugs on the World Health Organization model list of essential medicines according to the Biopharmaceutics Classification System
-
PID: 15296954
-
Lindenberg M, Kopp S, Dressman JB. Classification of orally administered drugs on the World Health Organization model list of essential medicines according to the Biopharmaceutics Classification System. Eur J Pharm Biopharm. 2004;58(2):265–78.
-
(2004)
Eur J Pharm Biopharm
, vol.58
, Issue.2
, pp. 265-278
-
-
Lindenberg, M.1
Kopp, S.2
Dressman, J.B.3
-
11
-
-
0041834829
-
Study of the solid state of carbamazepine after processing with gas anti-solvent technique
-
COI: 1:CAS:528:DC%2BD3sXmvFSjt78%3D, PID: 12957643
-
Moneghini M et al. Study of the solid state of carbamazepine after processing with gas anti-solvent technique. Eur J Pharm Biopharm. 2003;56(2):281–9.
-
(2003)
Eur J Pharm Biopharm
, vol.56
, Issue.2
, pp. 281-289
-
-
Moneghini, M.1
-
12
-
-
34250862709
-
Performance comparison of a co-crystal of carbamazepine with marketed product
-
COI: 1:CAS:528:DC%2BD2sXntF2mtbs%3D, PID: 17292592
-
Hickey MB et al. Performance comparison of a co-crystal of carbamazepine with marketed product. Eur J Pharm Biopharm. 2007;67(1):112–9.
-
(2007)
Eur J Pharm Biopharm
, vol.67
, Issue.1
, pp. 112-119
-
-
Hickey, M.B.1
-
13
-
-
0242322069
-
Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I
-
COI: 1:CAS:528:DC%2BD3sXovFCrsL4%3D, PID: 14603511
-
Grzesiak AL et al. Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I. J Pharm Sci. 2003;92(11):2260–71.
-
(2003)
J Pharm Sci
, vol.92
, Issue.11
, pp. 2260-2271
-
-
Grzesiak, A.L.1
-
14
-
-
77951538902
-
Combining HME & solubilization: Soluplus®—the solid solution
-
COI: 1:CAS:528:DC%2BC3cXlvVKjt7s%3D
-
Hardung H, Djuric D, Ali S. Combining HME & solubilization: Soluplus®—the solid solution. Drug Deliv Technol. 2010;10(3):20–7.
-
(2010)
Drug Deliv Technol
, vol.10
, Issue.3
, pp. 20-27
-
-
Hardung, H.1
Djuric, D.2
Ali, S.3
-
15
-
-
70449528319
-
Effects of extrusion process parameters on the dissolution behavior of indomethacin in Eudragit® E PO solid dispersions
-
COI: 1:CAS:528:DC%2BD1MXhsVCksr%2FP, PID: 19748557
-
Liu H et al. Effects of extrusion process parameters on the dissolution behavior of indomethacin in Eudragit® E PO solid dispersions. Int J Pharm. 2010;383(1):161–9.
-
(2010)
Int J Pharm
, vol.383
, Issue.1
, pp. 161-169
-
-
Liu, H.1
-
16
-
-
34447296485
-
Stabilization of hot-melt extrusion formulations containing solid solutions using polymer blends
-
Prodduturi S et al. Stabilization of hot-melt extrusion formulations containing solid solutions using polymer blends. AAPS PharmSciTech. 2007;8(2):E152–61.
-
(2007)
AAPS PharmSciTech
, vol.8
, Issue.2
, pp. E152-E161
-
-
Prodduturi, S.1
-
17
-
-
0030638567
-
Characteristics and significance of the amorphous state in pharmaceutical systems
-
COI: 1:CAS:528:DyaK28XntlOqt7k%3D, PID: 9002452
-
Hancock BC, Zografi G. Characteristics and significance of the amorphous state in pharmaceutical systems. J Pharm Sci. 1997;86(1):1–12.
-
(1997)
J Pharm Sci
, vol.86
, Issue.1
-
-
Hancock, B.C.1
Zografi, G.2
-
18
-
-
84880997550
-
Both solubility and chemical stability of curcumin are enhanced by solid dispersion in cellulose derivative matrices
-
COI: 1:CAS:528:DC%2BC3sXhtlOit7nL, PID: 23987452
-
Li B et al. Both solubility and chemical stability of curcumin are enhanced by solid dispersion in cellulose derivative matrices. Carbohydr Polym. 2013;98(1):1108–16.
-
(2013)
Carbohydr Polym
, vol.98
, Issue.1
, pp. 1108-1116
-
-
Li, B.1
-
19
-
-
75549091727
-
Evaluation of griseofulvin binary and ternary solid dispersions with HPMCAS
-
COI: 1:CAS:528:DC%2BC3cXovVGqsbs%3D, PID: 19842041
-
Al-Obaidi H, Buckton G. Evaluation of griseofulvin binary and ternary solid dispersions with HPMCAS. AAPS PharmSciTech. 2009;10(4):1172–7.
-
(2009)
AAPS PharmSciTech
, vol.10
, Issue.4
, pp. 1172-1177
-
-
Al-Obaidi, H.1
Buckton, G.2
-
21
-
-
1442348833
-
Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods
-
COI: 1:CAS:528:DC%2BD2cXhs1Giurw%3D, PID: 15019063
-
Sethia S, Squillante E. Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods. Int J Pharm. 2004;272(1):1–10.
-
(2004)
Int J Pharm
, vol.272
, Issue.1
-
-
Sethia, S.1
Squillante, E.2
-
22
-
-
0024382811
-
Effect of type and extent of crystalline order on chemical and physical stability of carbamazepine
-
COI: 1:CAS:528:DyaL1MXkvVCjsr4%3D
-
Krahn FU, Mielck JB. Effect of type and extent of crystalline order on chemical and physical stability of carbamazepine. Int J Pharm. 1989;53(1):25–34.
-
(1989)
Int J Pharm
, vol.53
, Issue.1
, pp. 25-34
-
-
Krahn, F.U.1
Mielck, J.B.2
-
23
-
-
84876933684
-
Preparation of carbamazepine–Soluplus® solid dispersions by hot-melt extrusion, and prediction of drug–polymer miscibility by thermodynamic model fitting
-
COI: 1:CAS:528:DC%2BC3sXisVKhsLk%3D, PID: 23333900
-
Djuris J et al. Preparation of carbamazepine–Soluplus® solid dispersions by hot-melt extrusion, and prediction of drug–polymer miscibility by thermodynamic model fitting. Eur J Pharm Biopharm. 2013;84(1):228–37.
-
(2013)
Eur J Pharm Biopharm
, vol.84
, Issue.1
, pp. 228-237
-
-
Djuris, J.1
-
24
-
-
1242298506
-
Evaluation of hypromellose acetate succinate (HPMCAS) as a carrier in solid dispersions
-
COI: 1:CAS:528:DC%2BD2cXpt1SgsA%3D%3D, PID: 15000425
-
Tanno F et al. Evaluation of hypromellose acetate succinate (HPMCAS) as a carrier in solid dispersions. Drug Dev Ind Pharm. 2004;30(1):9–17.
-
(2004)
Drug Dev Ind Pharm
, vol.30
, Issue.1
, pp. 9-17
-
-
Tanno, F.1
-
25
-
-
70449107051
-
Effects of polymer type and storage relative humidity on the kinetics of felodipine crystallization from amorphous solid dispersions
-
COI: 1:CAS:528:DC%2BD1MXhtlCrtb%2FE, PID: 19806435
-
Rumondor AC, Stanford LA, Taylor LS. Effects of polymer type and storage relative humidity on the kinetics of felodipine crystallization from amorphous solid dispersions. Pharm Res. 2009;26(12):2599–606.
-
(2009)
Pharm Res
, vol.26
, Issue.12
, pp. 2599-2606
-
-
Rumondor, A.C.1
Stanford, L.A.2
Taylor, L.S.3
-
26
-
-
84888382217
-
Inhibitory effect of hydroxypropyl methylcellulose acetate succinate on drug recrystallization from a supersaturated solution assessed using nuclear magnetic resonance measurements
-
COI: 1:CAS:528:DC%2BC3sXhsVWkurjK, PID: 24025080
-
Ueda K et al. Inhibitory effect of hydroxypropyl methylcellulose acetate succinate on drug recrystallization from a supersaturated solution assessed using nuclear magnetic resonance measurements. Mol Pharm. 2013;10(10):3801–11.
-
(2013)
Mol Pharm
, vol.10
, Issue.10
, pp. 3801-3811
-
-
Ueda, K.1
|