-
1
-
-
0021828631
-
Psychopharmacological effects of vinpocetine in normal healthy volunteers
-
Subhan Z, Hindmarch I. 1985. Psychopharmacological effects of vinpocetine in normal healthy volunteers. Eur J Clin Pharmacol 28:567-571.
-
(1985)
Eur J Clin Pharmacol
, vol.28
, pp. 567-571
-
-
Subhan, Z.1
Hindmarch, I.2
-
2
-
-
0036258772
-
Vinpocetine increases blood flow oxygenation in stroke patients: A near infrared spectroscopy and transcranial doppler study
-
Bonoczk P, Panczel G, Nagy Z. 2002. Vinpocetine increases blood flow oxygenation in stroke patients: A near infrared spectroscopy and transcranial doppler study. Eur J Ultrasound 15:85-91.
-
(2002)
Eur J Ultrasound
, vol.15
, pp. 85-91
-
-
Bonoczk, P.1
Panczel, G.2
Nagy, Z.3
-
3
-
-
0035122035
-
Vinpocetine treatment in acute ischaemic stoke: A pilot single-blind randomized clinical trial
-
Feigin VL, Doronin BM, Popova TF, Gribatcheva EV, Tchernov DV. 2001. Vinpocetine treatment in acute ischaemic stoke: A pilot single-blind randomized clinical trial. Eur J Neurol 8:81-85.
-
(2001)
Eur J Neurol
, vol.8
, pp. 81-85
-
-
Feigin, V.L.1
Doronin, B.M.2
Popova, T.F.3
Gribatcheva, E.V.4
Tchernov, D.V.5
-
7
-
-
1042269559
-
Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine
-
Kostewicz ES, Wunderlich M, Brauns U, Becker R, Bock T, Dressman JB. 2004. Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine. J Pharm Pharmacol 56:43-51.
-
(2004)
J Pharm Pharmacol
, vol.56
, pp. 43-51
-
-
Kostewicz, E.S.1
Wunderlich, M.2
Brauns, U.3
Becker, R.4
Bock, T.5
Dressman, J.B.6
-
9
-
-
0344673395
-
Methods to enhance the complexation efficiency of cyclodextrins
-
Loftsson T, Másson M, Sirgurjónsdottir JF. 1999. Methods to enhance the complexation efficiency of cyclodextrins. STP Pharma Sci 9:237-242.
-
(1999)
STP Pharma Sci
, vol.9
, pp. 237-242
-
-
Loftsson, T.1
Másson, M.2
Sirgurjónsdottir, J.F.3
-
11
-
-
0033951798
-
Drug/cyclodextrin/hydroxy acid multicomponent systems. Properties and pharmaceutical applications
-
Redenti E, Szente L, Szejtli J. 2000. Drug/cyclodextrin/hydroxy acid multicomponent systems. Properties and pharmaceutical applications. J Pharm Sci 89:1-8.
-
(2000)
J Pharm Sci
, vol.89
, pp. 1-8
-
-
Redenti, E.1
Szente, L.2
Szejtli, J.3
-
12
-
-
0242334093
-
Physicochemical investigation of the effects of water-soluble polymers on vinpocetine complexation with β-cyclodextrin and its sulfobutyl ether derivative in solution and solid state
-
Ribeiro L, Ferreira D, Veiga F. 2003. Physicochemical investigation of the effects of water-soluble polymers on vinpocetine complexation with β-cyclodextrin and its sulfobutyl ether derivative in solution and solid state. Eur J Pharm Sci 20:253-266.
-
(2003)
Eur J Pharm Sci
, vol.20
, pp. 253-266
-
-
Ribeiro, L.1
Ferreira, D.2
Veiga, F.3
-
13
-
-
11144224538
-
Multicomponent complex formation between vinpocetine, cyclodextrins, tartaric acid, and water-soluble polymers monitored by NMR and solubility studies
-
Ribeiro L, Carvalho RA, Ferreira DC, Veiga FJB. 2005. Multicomponent complex formation between vinpocetine, cyclodextrins, tartaric acid, and water-soluble polymers monitored by NMR and solubility studies. Eur J Pharm Sci 24:1-13.
-
(2005)
Eur J Pharm Sci
, vol.24
, pp. 1-13
-
-
Ribeiro, L.1
Carvalho, R.A.2
Ferreira, D.C.3
Veiga, F.J.B.4
-
14
-
-
0025690410
-
A new method for the preparation of drug containing polylactic acid microparticles without using organic solvents
-
Wichert B, Rohdewald P. 1990. A new method for the preparation of drug containing polylactic acid microparticles without using organic solvents. J Controlled Release 14:269-283.
-
(1990)
J Controlled Release
, vol.14
, pp. 269-283
-
-
Wichert, B.1
Rohdewald, P.2
-
15
-
-
0032550372
-
Improved dissolution and bioavaibility of phenytoin by sulfobutylether-β- cyclodextrin [(SBE)-β-CD] and hydroxypropyl-β-cyclodextrin
-
Savolainen J, Jarvinen K, Matilainen L, Jarvinen T. 1998. Improved dissolution and bioavaibility of phenytoin by sulfobutylether-β- cyclodextrin [(SBE)-β-CD] and hydroxypropyl-β-cyclodextrin. Int J Pharm 165:69-78.
-
(1998)
Int J Pharm
, vol.165
, pp. 69-78
-
-
Savolainen, J.1
Jarvinen, K.2
Matilainen, L.3
Jarvinen, T.4
-
17
-
-
0030614844
-
Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH
-
Charman WN, Porter CJH, Mithani S, Dressman JB. 1997. Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH. J Pharm Sci 86:269-282.
-
(1997)
J Pharm Sci
, vol.86
, pp. 269-282
-
-
Charman, W.N.1
Porter, C.J.H.2
Mithani, S.3
Dressman, J.B.4
-
18
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs
-
Galia E, Nicolaides E, Horter D, Lobenberg R, Reppas C, Dressman JB. 1998. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm Res 15:698-705.
-
(1998)
Pharm Res
, vol.15
, pp. 698-705
-
-
Galia, E.1
Nicolaides, E.2
Horter, D.3
Lobenberg, R.4
Reppas, C.5
Dressman, J.B.6
-
19
-
-
0033452575
-
Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data
-
Nicolaides E, Galia E, Efthymiopoulos C, Dressman JB, Reppas C. 1999. Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data. Pharm Res 16:1876-1882.
-
(1999)
Pharm Res
, vol.16
, pp. 1876-1882
-
-
Nicolaides, E.1
Galia, E.2
Efthymiopoulos, C.3
Dressman, J.B.4
Reppas, C.5
-
20
-
-
0036195307
-
Forecasting the oral absorption behavior of poorly soluble weak bases using solubility and dissolution studies in biorelevant media
-
Kostewicz ES, Brauns U, Becker P, Dressman JB. 2002. Forecasting the oral absorption behavior of poorly soluble weak bases using solubility and dissolution studies in biorelevant media. Pharm Res 19:345-349.
-
(2002)
Pharm Res
, vol.19
, pp. 345-349
-
-
Kostewicz, E.S.1
Brauns, U.2
Becker, P.3
Dressman, J.B.4
-
22
-
-
2342652446
-
Mathematical comparison of curves with an emphasis on in vitro dissolution profiles
-
Moore JW, Flanner HH. 1996. Mathematical comparison of curves with an emphasis on in vitro dissolution profiles. Pharm Technol 20:64-74.
-
(1996)
Pharm Technol
, vol.20
, pp. 64-74
-
-
Moore, J.W.1
Flanner, H.H.2
-
23
-
-
0028340366
-
Estimation and correlation of drug water solubility with pharmacological parameters required for biological activity
-
Morelock MM, Choi LL, Bell GL, Wright JL. 1994. Estimation and correlation of drug water solubility with pharmacological parameters required for biological activity. J Pharm Sci 83:948-952.
-
(1994)
J Pharm Sci
, vol.83
, pp. 948-952
-
-
Morelock, M.M.1
Choi, L.L.2
Bell, G.L.3
Wright, J.L.4
-
24
-
-
0037452410
-
Design of pH-independent controlled release matrix tablets for acidic drugs
-
Rao VM, Engh K, Qiu Y. 2003. Design of pH-independent controlled release matrix tablets for acidic drugs. Int J Pharm 252:81-86.
-
(2003)
Int J Pharm
, vol.252
, pp. 81-86
-
-
Rao, V.M.1
Engh, K.2
Qiu, Y.3
-
25
-
-
0000655208
-
FIP guidelines for dissolution testing of solid oral products (final drafts, 1995)
-
FIP
-
FIP. 1996. FIP guidelines for dissolution testing of solid oral products (final drafts, 1995). Drug Inf J 30:1071-1084.
-
(1996)
Drug Inf J
, vol.30
, pp. 1071-1084
-
-
-
26
-
-
0034002639
-
Mechanism by which cyclodextrins modify drug release from polymeric drug delivery systems
-
Bibby DC, Davies NM, Tucker IG. 2000. Mechanism by which cyclodextrins modify drug release from polymeric drug delivery systems. Int J Pharm 197:1-11.
-
(2000)
Int J Pharm
, vol.197
, pp. 1-11
-
-
Bibby, D.C.1
Davies, N.M.2
Tucker, I.G.3
-
27
-
-
2142756811
-
Investigation and physicochemical characterization of vinpocetine-sulfobutyl ether β-cyclodextrin binary and ternary complexes
-
Ribeiro L, Loftsson T, Ferreira D, Veiga F. 2003. Investigation and physicochemical characterization of vinpocetine-sulfobutyl ether β-cyclodextrin binary and ternary complexes. Chem Pharm Bull 51:914-922.
-
(2003)
Chem Pharm Bull
, vol.51
, pp. 914-922
-
-
Ribeiro, L.1
Loftsson, T.2
Ferreira, D.3
Veiga, F.4
-
28
-
-
0036891949
-
Preliminary pharmacokinetic study of different preparations of acyclovir with β-cyclodextrin
-
Luengo J, Aránguiz T, Sepúlveda J, Hernández L, Von Plessing C. 2002. Preliminary pharmacokinetic study of different preparations of acyclovir with β-cyclodextrin. J Pharm Sci 91:2593-2598.
-
(2002)
J Pharm Sci
, vol.91
, pp. 2593-2598
-
-
Luengo, J.1
Aránguiz, T.2
Sepúlveda, J.3
Hernández, L.4
Von Plessing, C.5
-
29
-
-
0038738049
-
Assessment of a controlled release hydrophilic matrix formulation for metoclopramide HCl
-
Hasan EI, Amro BI, Arafat T, Badwan AA. 2003. Assessment of a controlled release hydrophilic matrix formulation for metoclopramide HCl. Eur J Pharm Biopharm 55:339-344.
-
(2003)
Eur J Pharm Biopharm
, vol.55
, pp. 339-344
-
-
Hasan, E.I.1
Amro, B.I.2
Arafat, T.3
Badwan, A.A.4
-
30
-
-
0031786697
-
Co-administration of a water-soluble polymer increases the usefulness of cyclodextrins in solid oral dosage forms
-
Savolainen J, Jarvinen K, Taipale H, Jarho P, Loftsson T, Jarvinen T. 1998. Co-administration of a water-soluble polymer increases the usefulness of cyclodextrins in solid oral dosage forms. Pharm Res 15:1696-1701.
-
(1998)
Pharm Res
, vol.15
, pp. 1696-1701
-
-
Savolainen, J.1
Jarvinen, K.2
Taipale, H.3
Jarho, P.4
Loftsson, T.5
Jarvinen, T.6
-
31
-
-
0034713284
-
Biopharmaceutics and pharmacokinetics in drug research
-
Panchagnula R, Thomas NS. 2000. Biopharmaceutics and pharmacokinetics in drug research. Int J Pharm 201:131-150.
-
(2000)
Int J Pharm
, vol.201
, pp. 131-150
-
-
Panchagnula, R.1
Thomas, N.S.2
-
32
-
-
0030816899
-
Bioavailability of different artemisinin tablet formulation in rabbit plasma: Correlation with results obtained by an in vitro dissolution method
-
Ngo TH, Quintens I, Roets E, Declerck PJ, Hoogmartens J. 1997. Bioavailability of different artemisinin tablet formulation in rabbit plasma: Correlation with results obtained by an in vitro dissolution method. J Pharm Biomed Anal 16:185-189.
-
(1997)
J Pharm Biomed Anal
, vol.16
, pp. 185-189
-
-
Ngo, T.H.1
Quintens, I.2
Roets, E.3
Declerck, P.J.4
Hoogmartens, J.5
-
33
-
-
0041667788
-
Spray-dried redispersible oil-in-water emulsion to improve oral bioavailability of poorly soluble drugs
-
Dollo G, Le Corre P, Guerin A, Chevanne F, Burgot JL, Leverge R. 2003. Spray-dried redispersible oil-in-water emulsion to improve oral bioavailability of poorly soluble drugs. Eur J Pharm Sci 19:273-280.
-
(2003)
Eur J Pharm Sci
, vol.19
, pp. 273-280
-
-
Dollo, G.1
Le Corre, P.2
Guerin, A.3
Chevanne, F.4
Burgot, J.L.5
Leverge, R.6
-
34
-
-
0037436015
-
Hydrophilic and hydrophobic cyclodextrin in a new sustained release oral formulation of nicardipine: In vitro evaluation and bioavailability studies in rabbits
-
Fernandes C, Ramos P, Falcão AC, Veiga F. 2003. Hydrophilic and hydrophobic cyclodextrin in a new sustained release oral formulation of nicardipine: In vitro evaluation and bioavailability studies in rabbits. J Controlled Release 88:127-134.
-
(2003)
J Controlled Release
, vol.88
, pp. 127-134
-
-
Fernandes, C.1
Ramos, P.2
Falcão, A.C.3
Veiga, F.4
-
35
-
-
24644465873
-
Anatomical and physiological differences between various species used in studies on the pharmacokinetics and toxicology of xenobiotics. Bilthoven
-
623860610, pp
-
Zwart LL, Rompelberg CJM, Sips AJAM, Van Engelen JGM. 1999. Anatomical and physiological differences between various species used in studies on the pharmacokinetics and toxicology of xenobiotics. Bilthoven: RIVM Report 623860610, pp 1-100.
-
(1999)
RIVM Report
, pp. 1-100
-
-
Zwart, L.L.1
Rompelberg, C.J.M.2
Sips, A.J.A.M.3
Van Engelen, J.G.M.4
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