-
1
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes A.A., Whitney W.R. The rate of solution of solid substances in their own solutions. J. Am. Chem. Soc. 19:1897;930-934.
-
(1897)
J. Am. Chem. Soc.
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
2
-
-
0002642747
-
Theorie der Reaktionsgeschwindigkeit in heterogenen Systemen
-
Nernst W. Theorie der Reaktionsgeschwindigkeit in heterogenen Systemen. Zeitschrift f. Physik. Chemie. 47:1904;52-55.
-
(1904)
Zeitschrift F. Physik. Chemie
, vol.47
, pp. 52-55
-
-
Nernst, W.1
-
3
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs
-
Galia E., Nicolaides E., Hörter D., Löbenberg R., Reppas C., Dressman J.B. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm. Res. 15:1998;698-705.
-
(1998)
Pharm. Res.
, vol.15
, pp. 698-705
-
-
Galia, E.1
Nicolaides, E.2
Hörter, D.3
Löbenberg, R.4
Reppas, C.5
Dressman, J.B.6
-
5
-
-
0030638567
-
Characteristics and significance of the amorphous state in pharmaceutical systems (review)
-
Hancock B.C., Zografi G. Characteristics and significance of the amorphous state in pharmaceutical systems (review). J. Pharm. Sci. 86:1997;1-12.
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 1-12
-
-
Hancock, B.C.1
Zografi, G.2
-
6
-
-
0038768850
-
Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract (review)
-
Hoerter D., Dressman J.B. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract (review). Adv. Drug Delivery Rev. 25:1997;3-14.
-
(1997)
Adv. Drug Delivery Rev.
, vol.25
, pp. 3-14
-
-
Hoerter, D.1
Dressman, J.B.2
-
7
-
-
0029819323
-
Pharmaceutical application of cyclodextrins. 1. Drug solubilisation and stabilization (review)
-
Loftsson T., Brewster M.E. Pharmaceutical application of cyclodextrins. 1. Drug solubilisation and stabilization (review). J. Pharm. Sci. 85:1996;1017-1025.
-
(1996)
J. Pharm. Sci.
, vol.85
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
8
-
-
0003466960
-
-
Menlo Park, CA: Addison-Wesley
-
Castellan G.W. Physical Chemistry. 1983;324-336 Addison-Wesley, Menlo Park, CA.
-
(1983)
Physical Chemistry
, pp. 324-336
-
-
Castellan, G.W.1
-
9
-
-
85008071016
-
Studies on absorption of eutectic mixtures. I. A comparison of the behavior of eutectic mixtures of sulphathiazole and that of ordinary sulphathiazole in man
-
Sekiguchi K., Obi N. Studies on absorption of eutectic mixtures. I. A comparison of the behavior of eutectic mixtures of sulphathiazole and that of ordinary sulphathiazole in man. Chem. Pharm. Bull. 9:1961;866-872.
-
(1961)
Chem. Pharm. Bull.
, vol.9
, pp. 866-872
-
-
Sekiguchi, K.1
Obi, N.2
-
10
-
-
84984082270
-
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures II - experimental evaluation of a eutectic mixture: Urea-acetaminophen system
-
Goldberg A.H., Gibaldi M., Kanig J.L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures II - experimental evaluation of a eutectic mixture: urea-acetaminophen system. J. Pharm. Sci. 55:1966;482-487.
-
(1966)
J. Pharm. Sci.
, vol.55
, pp. 482-487
-
-
Goldberg, A.H.1
Gibaldi, M.2
Kanig, J.L.3
-
11
-
-
0013795160
-
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures I - theoretical considerations and discussion of the literature
-
Goldberg A.H., Gibaldi M., Kanig J.L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures I - theoretical considerations and discussion of the literature. J. Pharm. Sci. 54:1965;1145-1148.
-
(1965)
J. Pharm. Sci.
, vol.54
, pp. 1145-1148
-
-
Goldberg, A.H.1
Gibaldi, M.2
Kanig, J.L.3
-
13
-
-
0015124656
-
Pharmaceutical applications of solid dispersion systems
-
Chiou W.L., Riegelman S. Pharmaceutical applications of solid dispersion systems. J. Pharm. Sci. 60:1971;1281-1302.
-
(1971)
J. Pharm. Sci.
, vol.60
, pp. 1281-1302
-
-
Chiou, W.L.1
Riegelman, S.2
-
15
-
-
0343217013
-
Feste Dispersionen
-
J. Kreuter, Herzfeldt C.-D. Frankfurt am Main: Springer
-
Kreuter J. Feste Dispersionen. Kreuter J., Herzfeldt C.-D. Grundlagen der Arzneiformenlehre Galenik. 2:1999;262-274 Springer, Frankfurt am Main.
-
(1999)
Grundlagen der Arzneiformenlehre Galenik
, vol.2
, pp. 262-274
-
-
Kreuter, J.1
-
16
-
-
0014628768
-
Preparation and dissolution characteristics of several fast-release solid dispersions of griseofulvin
-
Chiou W.L., Riegelman S. Preparation and dissolution characteristics of several fast-release solid dispersions of griseofulvin. J. Pharm. Sci. 58:1969;1505-1510.
-
(1969)
J. Pharm. Sci.
, vol.58
, pp. 1505-1510
-
-
Chiou, W.L.1
Riegelman, S.2
-
17
-
-
0001368366
-
Studies on absorption of eutectic mixtures. II. Absorption of fused conglomerates of chloramphenicol and urea in rabbits
-
Sekiguchi K., Obi N., Ueda Y. Studies on absorption of eutectic mixtures. II. Absorption of fused conglomerates of chloramphenicol and urea in rabbits. Chem. Pharm. Bull. 12:1964;134-144.
-
(1964)
Chem. Pharm. Bull.
, vol.12
, pp. 134-144
-
-
Sekiguchi, K.1
Obi, N.2
Ueda, Y.3
-
18
-
-
0002846475
-
Effect of particle size on dissolution and gastrointestinal absorption rates of pharmaceuticals
-
Levy G. Effect of particle size on dissolution and gastrointestinal absorption rates of pharmaceuticals. Am. J. Pharm. 135:1963;78-92.
-
(1963)
Am. J. Pharm.
, vol.135
, pp. 78-92
-
-
Levy, G.1
-
19
-
-
0000538772
-
Properties of fused mannitol in compressed tablets
-
Kanig J.L. Properties of fused mannitol in compressed tablets. J. Pharm. Sci. 53:1964;188-192.
-
(1964)
J. Pharm. Sci.
, vol.53
, pp. 188-192
-
-
Kanig, J.L.1
-
20
-
-
84984085031
-
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures III - experimental evaluation of griseofulvin-succinic acid solid solution
-
Goldberg A.H., Gibaldi M., Kanig J.L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures III - experimental evaluation of griseofulvin-succinic acid solid solution. J. Pharm. Sci. 55:1966;487-492.
-
(1966)
J. Pharm. Sci.
, vol.55
, pp. 487-492
-
-
Goldberg, A.H.1
Gibaldi, M.2
Kanig, J.L.3
-
21
-
-
0013920636
-
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures IV - chloramphenicol-urea system
-
Goldberg A.H., Gibaldi M., Kanig J.L., Mayersohn M. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures IV - chloramphenicol-urea system. J. Pharm. Sci. 55:1966;581-583.
-
(1966)
J. Pharm. Sci.
, vol.55
, pp. 581-583
-
-
Goldberg, A.H.1
Gibaldi, M.2
Kanig, J.L.3
Mayersohn, M.4
-
22
-
-
0031423468
-
Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions
-
Taylor L.S., Zografi G. Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. Pharm. Res. 14:1997;1691-1698.
-
(1997)
Pharm. Res.
, vol.14
, pp. 1691-1698
-
-
Taylor, L.S.1
Zografi, G.2
-
23
-
-
0017235421
-
Dissolution rates of high energy sulfathiazole-povidone coprecipitates II: Characterization of form of drug controlling its dissolution rate via solubility studies
-
Simonelli A.P., Mehta S.C., Higuchi W.I. Dissolution rates of high energy sulfathiazole-povidone coprecipitates II: characterization of form of drug controlling its dissolution rate via solubility studies. J. Pharm. Sci. 65:1976;355-361.
-
(1976)
J. Pharm. Sci.
, vol.65
, pp. 355-361
-
-
Simonelli, A.P.1
Mehta, S.C.2
Higuchi, W.I.3
-
24
-
-
0022544509
-
The effect of wetting agents on the dissolution of indomethacin solid dispersion systems
-
Hilton J.E., Summers M.P. The effect of wetting agents on the dissolution of indomethacin solid dispersion systems. Int. J. Pharm. 31:1986;157-164.
-
(1986)
Int. J. Pharm.
, vol.31
, pp. 157-164
-
-
Hilton, J.E.1
Summers, M.P.2
-
25
-
-
0030805738
-
Inhibitory effects of water-soluble polymers on precipitation of RS-8359
-
Usui F., Maeda K., Kusai A., Ikeda M., Nishimura K., Yamamoto K. Inhibitory effects of water-soluble polymers on precipitation of RS-8359. Int. J. Pharm. 154:1997;59-66.
-
(1997)
Int. J. Pharm.
, vol.154
, pp. 59-66
-
-
Usui, F.1
Maeda, K.2
Kusai, A.3
Ikeda, M.4
Nishimura, K.5
Yamamoto, K.6
-
26
-
-
0018229451
-
Phase equilibria and dissolution rates of indomethacin-polyethylene glycol 6000 solid dispersions
-
Ford J.L., Rubinstein M.H. Phase equilibria and dissolution rates of indomethacin-polyethylene glycol 6000 solid dispersions. Pharm. Acta Helv. 53:1978;327-332.
-
(1978)
Pharm. Acta Helv.
, vol.53
, pp. 327-332
-
-
Ford, J.L.1
Rubinstein, M.H.2
-
27
-
-
0014642572
-
Some physical factors affecting the enhanced blepharototic activity of orally administered reserpine-cholanic acid coprecipitates
-
Stoll R.T., Bates T.R., Nieforth K.A., Swarbrick J. Some physical factors affecting the enhanced blepharototic activity of orally administered reserpine-cholanic acid coprecipitates. J. Pharm. Sci. 58:1969;1457-1459.
-
(1969)
J. Pharm. Sci.
, vol.58
, pp. 1457-1459
-
-
Stoll, R.T.1
Bates, T.R.2
Nieforth, K.A.3
Swarbrick, J.4
-
28
-
-
0017665599
-
Surface tension lowering and dissolution rate of hydrocortisone from solid solutions of selected n-acyle esters of cholesterol
-
Kim K.H., Jarowski C.I. Surface tension lowering and dissolution rate of hydrocortisone from solid solutions of selected n-acyle esters of cholesterol. J. Pharm. Sci. 66:1977;1536-1540.
-
(1977)
J. Pharm. Sci.
, vol.66
, pp. 1536-1540
-
-
Kim, K.H.1
Jarowski, C.I.2
-
29
-
-
0029921142
-
Characterization and dissolution behavior of nifedipine and phosphatidylcholine binary systems
-
Yamamura S., Rogers J.A. Characterization and dissolution behavior of nifedipine and phosphatidylcholine binary systems. Int. J. Pharm. 130:1996;65-73.
-
(1996)
Int. J. Pharm.
, vol.130
, pp. 65-73
-
-
Yamamura, S.1
Rogers, J.A.2
-
30
-
-
0023130237
-
Dissolution rates of partially water-soluble drugs from solid dispersion systems. I. Prednisolone
-
Jachowicz R. Dissolution rates of partially water-soluble drugs from solid dispersion systems. I. Prednisolone. Int. J. Pharm. 35:1987;1-5.
-
(1987)
Int. J. Pharm.
, vol.35
, pp. 1-5
-
-
Jachowicz, R.1
-
31
-
-
0029586490
-
Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques
-
Betageri G.V., Makarla K.R. Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques. Int. J. Pharm. 126:1995;155-160.
-
(1995)
Int. J. Pharm.
, vol.126
, pp. 155-160
-
-
Betageri, G.V.1
Makarla, K.R.2
-
32
-
-
0025883345
-
Injection molding as a suitable process for manufacturing solid dispersions or solutions
-
Wacker S., Soliva M., Speiser P. Injection molding as a suitable process for manufacturing solid dispersions or solutions. Pharmazeutische Industrie. 53:1991;853-856.
-
(1991)
Pharmazeutische Industrie
, vol.53
, pp. 853-856
-
-
Wacker, S.1
Soliva, M.2
Speiser, P.3
-
33
-
-
0028830177
-
Extrusion-spheronisation - A literature review (review)
-
Vervaet C., Baert L., Remon J.P. Extrusion-spheronisation - a literature review (review). Int. J. Pharm. 116:1995;131-146.
-
(1995)
Int. J. Pharm.
, vol.116
, pp. 131-146
-
-
Vervaet, C.1
Baert, L.2
Remon, J.P.3
-
34
-
-
0013915842
-
Galenische Aspekte der Arzneimittelwirkung
-
Speiser P. Galenische Aspekte der Arzneimittelwirkung. Pharm. Acta Helv. 41:1966;321-342.
-
(1966)
Pharm. Acta Helv.
, vol.41
, pp. 321-342
-
-
Speiser, P.1
-
36
-
-
0016066608
-
Spritzgießverfahren zur Herstellung peroraler Retardpräperate
-
Hüttenrauch R. Spritzgießverfahren zur Herstellung peroraler Retardpräperate. Pharmazie. 29:1974;297-302.
-
(1974)
Pharmazie
, vol.29
, pp. 297-302
-
-
Hüttenrauch, R.1
-
38
-
-
0028945577
-
Hot spin mixing: A new technology to manufacture solid dispersions - part 1: Testosterone
-
Dittgen M., Fricke S., Gerecke H., Osterwald H. Hot spin mixing: a new technology to manufacture solid dispersions - part 1: testosterone. Pharmazie. 50:1995;225-226.
-
(1995)
Pharmazie
, vol.50
, pp. 225-226
-
-
Dittgen, M.1
Fricke, S.2
Gerecke, H.3
Osterwald, H.4
-
39
-
-
0029031081
-
Hot spin mixing: A new technology to manufacture solid dispersions - part 3: Progesterone
-
Dittgen M., Fricke S., Gerecke H., Osterwald H. Hot spin mixing: a new technology to manufacture solid dispersions - part 3: progesterone. Pharmazie. 50:1995;507-508.
-
(1995)
Pharmazie
, vol.50
, pp. 507-508
-
-
Dittgen, M.1
Fricke, S.2
Gerecke, H.3
Osterwald, H.4
-
40
-
-
0029002345
-
Hot spin mixing: A new technology to manufacture solid dispersions - part 2: Dienogest
-
Dittgen M., Gräser T., Kaufmann G., Gerecke H., Osterwald H., Oettel M. Hot spin mixing: a new technology to manufacture solid dispersions - part 2: dienogest. Pharmazie. 50:1995;50-51.
-
(1995)
Pharmazie
, vol.50
, pp. 50-51
-
-
Dittgen, M.1
Gräser, T.2
Kaufmann, G.3
Gerecke, H.4
Osterwald, H.5
Oettel, M.6
-
41
-
-
0001732876
-
A method for preparing an aqueous colloidal dispersion of organic materials by using water-soluble polymers: Dispersion of beta-carotene by polyvinylpyrrolidone
-
Tachibana T., Nakamura A. A method for preparing an aqueous colloidal dispersion of organic materials by using water-soluble polymers: dispersion of beta-carotene by polyvinylpyrrolidone. Kolloid-Z. Polym. 203:1965;130-133.
-
(1965)
Kolloid-Z. Polym.
, vol.203
, pp. 130-133
-
-
Tachibana, T.1
Nakamura, A.2
-
42
-
-
0013966747
-
New method of solid-state dispersion for increasing dissolution rates
-
Mayersohn M., Gibaldi M. New method of solid-state dispersion for increasing dissolution rates. J. Pharm. Sci. 55:1966;1323-1324.
-
(1966)
J. Pharm. Sci.
, vol.55
, pp. 1323-1324
-
-
Mayersohn, M.1
Gibaldi, M.2
-
43
-
-
0014592643
-
Dissolution characteristics of reserpine-polyvinylpyrrolidone co-precipitates
-
Bates T.R. Dissolution characteristics of reserpine-polyvinylpyrrolidone co-precipitates. J. Pharm. Pharmacol. 21:1969;710-712.
-
(1969)
J. Pharm. Pharmacol.
, vol.21
, pp. 710-712
-
-
Bates, T.R.1
-
44
-
-
0014515660
-
Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates
-
Simonelli A.P., Metha S.C., Higuchi W.I. Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates. J. Pharm. Sci. 58:1969;538-549.
-
(1969)
J. Pharm. Sci.
, vol.58
, pp. 538-549
-
-
Simonelli, A.P.1
Metha, S.C.2
Higuchi, W.I.3
-
45
-
-
0028326530
-
Effect of polyvinylpyrrolidone on the crystallinity and dissolution rate of solid dispersions of the antiinflammatory Ci-987
-
Kearney A.S., Gabriel D.L., Mehta S.C., Radebaugh G.W. Effect of polyvinylpyrrolidone on the crystallinity and dissolution rate of solid dispersions of the antiinflammatory Ci-987. Int. J. Pharm. 104:1994;169-174.
-
(1994)
Int. J. Pharm.
, vol.104
, pp. 169-174
-
-
Kearney, A.S.1
Gabriel, D.L.2
Mehta, S.C.3
Radebaugh, G.W.4
-
46
-
-
0032526833
-
Enhancement of carbamazepine dissolution - In vitro and in vivo evaluation
-
El-Zein H., Riad L., Elbary A.A. Enhancement of carbamazepine dissolution - in vitro and in vivo evaluation. Int. J. Pharm. 168:1998;209-220.
-
(1998)
Int. J. Pharm.
, vol.168
, pp. 209-220
-
-
El-Zein, H.1
Riad, L.2
Elbary, A.A.3
-
47
-
-
0029915651
-
Dissolution behavior of griseofulvin solid dispersions using polyethylene glycol, talc, and their combination as dispersion carriers
-
Lo W.Y., Law S.L. Dissolution behavior of griseofulvin solid dispersions using polyethylene glycol, talc, and their combination as dispersion carriers. Drug Dev. Ind. Pharm. 22:1996;231-236.
-
(1996)
Drug Dev. Ind. Pharm.
, vol.22
, pp. 231-236
-
-
Lo, W.Y.1
Law, S.L.2
-
48
-
-
0002488303
-
Polyethylene glycol
-
A. Wade, & P.J. Weller. Washington, DC/London: American Pharmaceutical Association/The Pharmaceutical Press
-
Price J.C. Polyethylene glycol. Wade A., Weller P.J. Handbook of Pharmaceutical Excipients. 1994;355-361 American Pharmaceutical Association/The Pharmaceutical Press, Washington, DC/London.
-
(1994)
Handbook of Pharmaceutical Excipients
, pp. 355-361
-
-
Price, J.C.1
-
49
-
-
0016539272
-
Dissolution of acetylsalicylic acid from acetylsalicylic acid-polyethylene glycol 6000 coprecipitates
-
Asker A.F., Whitworth C.W. Dissolution of acetylsalicylic acid from acetylsalicylic acid-polyethylene glycol 6000 coprecipitates. Pharmazie. 30:1975;530-531.
-
(1975)
Pharmazie
, vol.30
, pp. 530-531
-
-
Asker, A.F.1
Whitworth, C.W.2
-
50
-
-
0028961183
-
Preformulation study of etoposide. 2. Increased solubility and dissolution rate by solid-solid dispersions
-
Shah J.C., Chen J.R., Chow D. Preformulation study of etoposide. 2. Increased solubility and dissolution rate by solid-solid dispersions. Int. J. Pharm. 113:1995;103-111.
-
(1995)
Int. J. Pharm.
, vol.113
, pp. 103-111
-
-
Shah, J.C.1
Chen, J.R.2
Chow, D.3
-
51
-
-
0031725929
-
Investigation of formulation approaches to improve the dissolution of SB-210661, a poorly water soluble 5-lipoxygenase inhibitor
-
Perng C.Y., Kearney A.S., Patel K., Palepu N.R., Zuber G. Investigation of formulation approaches to improve the dissolution of SB-210661, a poorly water soluble 5-lipoxygenase inhibitor. Int. J. Pharm. 176:1998;31-38.
-
(1998)
Int. J. Pharm.
, vol.176
, pp. 31-38
-
-
Perng, C.Y.1
Kearney, A.S.2
Patel, K.3
Palepu, N.R.4
Zuber, G.5
-
52
-
-
0031748005
-
Preparation, characterization, and dissolution studies of ibuprofen solid dispersions using polyethylene glycol (peg), talc, and peg-talc as dispersion carriers
-
Khan G.M., Zhu J.B. Preparation, characterization, and dissolution studies of ibuprofen solid dispersions using polyethylene glycol (peg), talc, and peg-talc as dispersion carriers. Drug Dev. Ind. Pharm. 24:1998;455-462.
-
(1998)
Drug Dev. Ind. Pharm.
, vol.24
, pp. 455-462
-
-
Khan, G.M.1
Zhu, J.B.2
-
53
-
-
0021801507
-
Similarities in the release rates of different drugs from polyethylene glycol 6000 solid dispersions
-
Dubois J.L., Ford J.L. Similarities in the release rates of different drugs from polyethylene glycol 6000 solid dispersions. J. Pharm. Pharmacol. 37:1985;494-495.
-
(1985)
J. Pharm. Pharmacol.
, vol.37
, pp. 494-495
-
-
Dubois, J.L.1
Ford, J.L.2
-
54
-
-
0022630799
-
The properties of solid dispersions of indomethacin or phenylbutazone in polyethylene glycol
-
Ford J.L., Stewart A.F., Dubois J.-L. The properties of solid dispersions of indomethacin or phenylbutazone in polyethylene glycol. Int. J. Pharm. 28:1986;11-22.
-
(1986)
Int. J. Pharm.
, vol.28
, pp. 11-22
-
-
Ford, J.L.1
Stewart, A.F.2
Dubois, J.-L.3
-
56
-
-
0033020439
-
Thermal behavior and dissolution properties of naproxen from binary and ternary solid dispersions
-
Mura P., Faucci M.T., Manderioli A., Bramanti G., Parrini P. Thermal behavior and dissolution properties of naproxen from binary and ternary solid dispersions. Drug Dev. Ind. Pharm. 25:1999;257-264.
-
(1999)
Drug Dev. Ind. Pharm.
, vol.25
, pp. 257-264
-
-
Mura, P.1
Faucci, M.T.2
Manderioli, A.3
Bramanti, G.4
Parrini, P.5
-
57
-
-
0029971327
-
Effect of particle size on the available surface area of nifedipine from nifedipine-polyethylene glycol 6000 solid dispersions
-
Lin C.W., Cham T.M. Effect of particle size on the available surface area of nifedipine from nifedipine-polyethylene glycol 6000 solid dispersions. Int. J. Pharm. 127:1996;261-272.
-
(1996)
Int. J. Pharm.
, vol.127
, pp. 261-272
-
-
Lin, C.W.1
Cham, T.M.2
-
58
-
-
0026502791
-
Physicochemical aspects of drug release. XIV. The effects of some ionic and non-ionic surfactants on properties of a sparingly soluble drug in solid dispersions
-
Sjökvist E., Nyström C., Aldén M., Caram-Lelham N. Physicochemical aspects of drug release. XIV. The effects of some ionic and non-ionic surfactants on properties of a sparingly soluble drug in solid dispersions. Int. J. Pharm. 79:1992;123-133.
-
(1992)
Int. J. Pharm.
, vol.79
, pp. 123-133
-
-
Sjökvist, E.1
Nyström, C.2
Aldén, M.3
Caram-Lelham, N.4
-
59
-
-
0030575733
-
Thermal investigation of crystallization of polyethylene glycols in solid dispersions containing oxazepam
-
Gines J.M., Arias M.J., Moyano J.R., Sanchezsoto P.J. Thermal investigation of crystallization of polyethylene glycols in solid dispersions containing oxazepam. Int. J. Pharm. 143:1996;247-253.
-
(1996)
Int. J. Pharm.
, vol.143
, pp. 247-253
-
-
Gines, J.M.1
Arias, M.J.2
Moyano, J.R.3
Sanchezsoto, P.J.4
-
60
-
-
0027264653
-
Dissolution kinetics of piroxicam in solid dispersions with polyethylene glycol-4000
-
Fernandez M., Margarit M.V., Rodriguez I.C., Cerezo A. Dissolution kinetics of piroxicam in solid dispersions with polyethylene glycol-4000. Int. J. Pharm. 98:1993;29-35.
-
(1993)
Int. J. Pharm.
, vol.98
, pp. 29-35
-
-
Fernandez, M.1
Margarit, M.V.2
Rodriguez, I.C.3
Cerezo, A.4
-
61
-
-
0033021347
-
Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000
-
Trapani G., Franco M., Latrofa A., Pantaleo M.R., Provenzano M.R., Sanna E., Maciocco E., Liso G. Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000. Int. J. Pharm. 184:1999;121-130.
-
(1999)
Int. J. Pharm.
, vol.184
, pp. 121-130
-
-
Trapani, G.1
Franco, M.2
Latrofa, A.3
Pantaleo, M.R.4
Provenzano, M.R.5
Sanna, E.6
MacIocco, E.7
Liso, G.8
-
62
-
-
0028568102
-
Improvement of the diuretic effect of triamterene via solid dispersion technique with PEG 4000
-
Arias M.J., Gines J.M., Moyano J.R., Perez-Barrales M.J., Vela M.T., Rabasco A.M. Improvement of the diuretic effect of triamterene via solid dispersion technique with PEG 4000. Eur. J. Drug Metab. Pharmacokinet. 19:1994;295-302.
-
(1994)
Eur. J. Drug Metab. Pharmacokinet.
, vol.19
, pp. 295-302
-
-
Arias, M.J.1
Gines, J.M.2
Moyano, J.R.3
Perez-Barrales, M.J.4
Vela, M.T.5
Rabasco, A.M.6
-
63
-
-
0021265072
-
Absorption and dissolution of nitrofurantoin from different experimental formulations
-
Ali A.A., Gorashi A.S. Absorption and dissolution of nitrofurantoin from different experimental formulations. Int. J. Pharm. 19:1984;297-306.
-
(1984)
Int. J. Pharm.
, vol.19
, pp. 297-306
-
-
Ali, A.A.1
Gorashi, A.S.2
-
64
-
-
0030014394
-
Bioavailability of norfloxacin from PEG 6000 solid dispersion and cyclodextrin inclusion complexes in rabbits
-
Fawaz F., Bonini F., Guyot M., Bildet J., Maury M., Lagueny A.M. Bioavailability of norfloxacin from PEG 6000 solid dispersion and cyclodextrin inclusion complexes in rabbits. Int. J. Pharm. 132:1996;271-275.
-
(1996)
Int. J. Pharm.
, vol.132
, pp. 271-275
-
-
Fawaz, F.1
Bonini, F.2
Guyot, M.3
Bildet, J.4
Maury, M.5
Lagueny, A.M.6
-
65
-
-
0029096616
-
Improvement of the dissolution kinetics of SR 33557 by means of solid dispersions containing PEG 6000
-
Lheritier J., Chauvet A., Abramovici B., Masse J. Improvement of the dissolution kinetics of SR 33557 by means of solid dispersions containing PEG 6000. Int. J. Pharm. 123:1995;273-279.
-
(1995)
Int. J. Pharm.
, vol.123
, pp. 273-279
-
-
Lheritier, J.1
Chauvet, A.2
Abramovici, B.3
Masse, J.4
-
66
-
-
0028340095
-
Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000
-
Margarit M.V., Rodriguez I.C., Cerezo A. Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000. Int. J. Pharm. 108:1994;101-107.
-
(1994)
Int. J. Pharm.
, vol.108
, pp. 101-107
-
-
Margarit, M.V.1
Rodriguez, I.C.2
Cerezo, A.3
-
68
-
-
0030668791
-
Comparison of nicotinamide, ethylurea and polyethylene glycol as carriers for nifedipine solid dispersion systems
-
Suzuki H., Sunada H. Comparison of nicotinamide, ethylurea and polyethylene glycol as carriers for nifedipine solid dispersion systems. Chem. Pharm. Bull. 45:1997;1688-1693.
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 1688-1693
-
-
Suzuki, H.1
Sunada, H.2
-
69
-
-
0023117244
-
Dissolution rates of partially water-soluble drugs from solid dispersion systems. II. Phenytoin
-
Jachowicz R. Dissolution rates of partially water-soluble drugs from solid dispersion systems. II. Phenytoin. Int. J. Pharm. 35:1987;7-12.
-
(1987)
Int. J. Pharm.
, vol.35
, pp. 7-12
-
-
Jachowicz, R.1
-
70
-
-
0030659145
-
Enhanced dissolution of ursodeoxycholic acid from the solid dispersion
-
Okonogi S., Yonemochi E., Oguchi T., Puttipipatkhachorn S., Yamamoto K. Enhanced dissolution of ursodeoxycholic acid from the solid dispersion. Drug Dev. Ind. Pharm. 23:1997;1115-1121.
-
(1997)
Drug Dev. Ind. Pharm.
, vol.23
, pp. 1115-1121
-
-
Okonogi, S.1
Yonemochi, E.2
Oguchi, T.3
Puttipipatkhachorn, S.4
Yamamoto, K.5
-
71
-
-
0028127826
-
Characterization and dissolution of fenofibrate solid dispersion systems
-
Sheu M.T., Yeh C.M., Sokoloski T.D. Characterization and dissolution of fenofibrate solid dispersion systems. Int. J. Pharm. 103:1994;137-146.
-
(1994)
Int. J. Pharm.
, vol.103
, pp. 137-146
-
-
Sheu, M.T.1
Yeh, C.M.2
Sokoloski, T.D.3
-
72
-
-
0005108843
-
Povidone
-
A. Wade, & P.J. Weller. Washington, DC/London: American Pharmaceutical Association/The Pharmaceutical Press
-
Walking W.D. Povidone. Wade A., Weller P.J. Handbook of Pharmaceutical Excipitients. 1994;392-399 American Pharmaceutical Association/The Pharmaceutical Press, Washington, DC/London.
-
(1994)
Handbook of Pharmaceutical Excipitients
, pp. 392-399
-
-
Walking, W.D.1
-
74
-
-
0022409189
-
Influence of wetting factors on the dissolution behavior of flufenamic acid
-
Itai S., Nemoto M., Kouchiwa S., Murayama H., Nagai T. Influence of wetting factors on the dissolution behavior of flufenamic acid. Chem. Pharm. Bull. 33:1985;5464-5473.
-
(1985)
Chem. Pharm. Bull.
, vol.33
, pp. 5464-5473
-
-
Itai, S.1
Nemoto, M.2
Kouchiwa, S.3
Murayama, H.4
Nagai, T.5
-
75
-
-
0030062860
-
Dissolution behavior of probucol from solid dispersion systems of probucol-polyvinylpyrrolidone
-
Yagi N., Terashima Y., Kenmotsu H., Sekikawa H., Takada M. Dissolution behavior of probucol from solid dispersion systems of probucol-polyvinylpyrrolidone. Chem. Pharm. Bull. 44:1996;241-244.
-
(1996)
Chem. Pharm. Bull.
, vol.44
, pp. 241-244
-
-
Yagi, N.1
Terashima, Y.2
Kenmotsu, H.3
Sekikawa, H.4
Takada, M.5
-
76
-
-
0030606846
-
Preparation, dissolution and characterization of albendazole solid dispersions
-
Torrado S., Torrado S., Torrado J.J., Cadorniga R. Preparation, dissolution and characterization of albendazole solid dispersions. Int. J. Pharm. 140:1996;247-250.
-
(1996)
Int. J. Pharm.
, vol.140
, pp. 247-250
-
-
Torrado, S.1
Torrado, S.2
Torrado, J.J.3
Cadorniga, R.4
-
77
-
-
0024604891
-
The in-vitro pH-dissolution dependence and in-vivo bioavailability of frusemide-PVP solid dispersions
-
Doherty C., York P. The in-vitro pH-dissolution dependence and in-vivo bioavailability of frusemide-PVP solid dispersions. J. Pharm. Pharmacol. 41:1989;73-78.
-
(1989)
J. Pharm. Pharmacol.
, vol.41
, pp. 73-78
-
-
Doherty, C.1
York, P.2
-
79
-
-
0017101027
-
The influence of polyvinylpyrrolidone on the dissolution and bioavailability of hydrochlorothiazide
-
Corrigan O.I., Timoney R.F., Whelan M.J. The influence of polyvinylpyrrolidone on the dissolution and bioavailability of hydrochlorothiazide. J. Pharm. Pharmacol. 28:1976;703-706.
-
(1976)
J. Pharm. Pharmacol.
, vol.28
, pp. 703-706
-
-
Corrigan, O.I.1
Timoney, R.F.2
Whelan, M.J.3
-
81
-
-
0023195131
-
Bioavailability and erosive activity of solid dispersions of some non-steroidal anti-inflammatory drugs
-
Ramadan E.M., Abd El-Gawad A.H., Nouh A.T. Bioavailability and erosive activity of solid dispersions of some non-steroidal anti-inflammatory drugs. Pharm. Ind. 49:1987;508-513.
-
(1987)
Pharm. Ind.
, vol.49
, pp. 508-513
-
-
Ramadan, E.M.1
Abd El-Gawad, A.H.2
Nouh, A.T.3
-
82
-
-
0032528994
-
Dissolution improvement of RS-8359 by the solid dispersion prepared by the solvent method
-
Usui F., Maeda K., Kusai A., Ikeda M., Nishimura K., Yamamoto K. Dissolution improvement of RS-8359 by the solid dispersion prepared by the solvent method. Int. J. Pharm. 170:1998;247-256.
-
(1998)
Int. J. Pharm.
, vol.170
, pp. 247-256
-
-
Usui, F.1
Maeda, K.2
Kusai, A.3
Ikeda, M.4
Nishimura, K.5
Yamamoto, K.6
-
83
-
-
0029912865
-
Solid dispersions of benidipine hydrochloride. 1. Preparations using different solvent systems and dissolution properties
-
Suzuki H., Miyamoto N., Masada T., Hayakawa E., Ito K. Solid dispersions of benidipine hydrochloride. 1. Preparations using different solvent systems and dissolution properties. Chem. Pharm. Bull. 44:1996;364-371.
-
(1996)
Chem. Pharm. Bull.
, vol.44
, pp. 364-371
-
-
Suzuki, H.1
Miyamoto, N.2
Masada, T.3
Hayakawa, E.4
Ito, K.5
-
85
-
-
0031958399
-
Influence of water-soluble polymers on the dissolution of nifedipine solid dispersions with combined carriers
-
Suzuki H., Sunada H. Influence of water-soluble polymers on the dissolution of nifedipine solid dispersions with combined carriers. Chem. Pharm. Bull. 46:1998;482-487.
-
(1998)
Chem. Pharm. Bull.
, vol.46
, pp. 482-487
-
-
Suzuki, H.1
Sunada, H.2
-
86
-
-
0028337031
-
Improved oral absorption of enteric coprecipitates of a poorly soluble drug
-
Kondo N., Iwao T., Hirai K., Fukuda M., Yamanouchi K., Yokoyama K., Miyaji M., Ishihara Y., Kon K., Ogawa Y., Mayumi T. Improved oral absorption of enteric coprecipitates of a poorly soluble drug. J. Pharm. Sci. 83:1994;566-570.
-
(1994)
J. Pharm. Sci.
, vol.83
, pp. 566-570
-
-
Kondo, N.1
Iwao, T.2
Hirai, K.3
Fukuda, M.4
Yamanouchi, K.5
Yokoyama, K.6
Miyaji, M.7
Ishihara, Y.8
Kon, K.9
Ogawa, Y.10
Mayumi, T.11
-
87
-
-
0028267604
-
Release of carbamazepine from solid dispersions with polyvinylpyrrolidone/vinylacetate copolymer (PVP/VA)
-
Zingone G., Rubessa F. Release of carbamazepine from solid dispersions with polyvinylpyrrolidone/vinylacetate copolymer (PVP/VA). S.T.P. Pharm. Sci. 4:1994;122-127.
-
(1994)
S.T.P. Pharm. Sci.
, vol.4
, pp. 122-127
-
-
Zingone, G.1
Rubessa, F.2
-
88
-
-
0031791549
-
Enhanced dissolution of furosemide by coprecipitating or cogrinding with crospovidone
-
Shin S., Oh I., Lee Y., Choi H., Choi J. Enhanced dissolution of furosemide by coprecipitating or cogrinding with crospovidone. Int. J. Pharm. 175:1998;17-24.
-
(1998)
Int. J. Pharm.
, vol.175
, pp. 17-24
-
-
Shin, S.1
Oh, I.2
Lee, Y.3
Choi, H.4
Choi, J.5
-
89
-
-
0141653520
-
Hydroxypropylmethylcellulose
-
A. Wade, & P.J. Weller. Washington, DC/London: American Pharmaceutical Association/The Pharmaceutical Press
-
Harwood R.J., Johnson J.L. Hydroxypropylmethylcellulose. Wade A., Weller P.J. Handbook of Pharmaceutical Excipients. 1994;229-232 American Pharmaceutical Association/The Pharmaceutical Press, Washington, DC/London.
-
(1994)
Handbook of Pharmaceutical Excipients
, pp. 229-232
-
-
Harwood, R.J.1
Johnson, J.L.2
-
90
-
-
0032997934
-
Improving the oral bioavailability of albendazole in rabbits by the solid dispersion technique
-
Kohri N., Yamayoshi Y., Xin H., Iseki K., Sato N., Todo S., Miyazaki K. Improving the oral bioavailability of albendazole in rabbits by the solid dispersion technique. J. Pharm. Pharmacol. 51:1999;159-164.
-
(1999)
J. Pharm. Pharmacol.
, vol.51
, pp. 159-164
-
-
Kohri, N.1
Yamayoshi, Y.2
Xin, H.3
Iseki, K.4
Sato, N.5
Todo, S.6
Miyazaki, K.7
-
91
-
-
0031573912
-
Dissolution mechanism and rate of solid dispersion particles of nilvadipine with hydroxypropylmethylcellulose
-
Okimoto K., Miyake M., Ibuki R., Yasumura M., Ohnishi N., Nakai T. Dissolution mechanism and rate of solid dispersion particles of nilvadipine with hydroxypropylmethylcellulose. Int. J. Pharm. 159:1997;85-93.
-
(1997)
Int. J. Pharm.
, vol.159
, pp. 85-93
-
-
Okimoto, K.1
Miyake, M.2
Ibuki, R.3
Yasumura, M.4
Ohnishi, N.5
Nakai, T.6
-
92
-
-
0141653520
-
Hydroxypropylcellulose
-
A. Wade, & P.J. Weller. Washington, DC/London: American Pharmaceutical Association/The Pharmaceutical Press
-
Harwood R.J., Johnson J.L. Hydroxypropylcellulose. Wade A., Weller P.J. Handbook of Pharmaceutical Excipients. 1994;223-228 American Pharmaceutical Association/The Pharmaceutical Press, Washington, DC/London.
-
(1994)
Handbook of Pharmaceutical Excipients
, pp. 223-228
-
-
Harwood, R.J.1
Johnson, J.L.2
-
93
-
-
0028227032
-
Application of the solid dispersion method to the controlled release of medicine. 6. Release mechanism of a slightly water soluble medicine and interaction between flurbiprofen and hydroxypropyl cellulose in solid dispersion
-
Yuasa H., Ozeki T., Takahashi H., Kanaya Y., Ueno M. Application of the solid dispersion method to the controlled release of medicine. 6. Release mechanism of a slightly water soluble medicine and interaction between flurbiprofen and hydroxypropyl cellulose in solid dispersion. Chem. Pharm. Bull. 42:1994;354-358.
-
(1994)
Chem. Pharm. Bull.
, vol.42
, pp. 354-358
-
-
Yuasa, H.1
Ozeki, T.2
Takahashi, H.3
Kanaya, Y.4
Ueno, M.5
-
94
-
-
0022402243
-
Physical properties of solid dispersions of poorly water-soluble drugs with enteric coating agents
-
Hasegawa A., Kawamura R., Nakagawa H., Sugimoto I. Physical properties of solid dispersions of poorly water-soluble drugs with enteric coating agents. Chem. Pharm. Bull. 33:1985;3429-3435.
-
(1985)
Chem. Pharm. Bull.
, vol.33
, pp. 3429-3435
-
-
Hasegawa, A.1
Kawamura, R.2
Nakagawa, H.3
Sugimoto, I.4
-
95
-
-
0029928882
-
Oral absorption improvement of poorly soluble drug using solid dispersion technique
-
Kai T., Akiyama Y., Nomura S., Sato M. Oral absorption improvement of poorly soluble drug using solid dispersion technique. Chem. Pharm. Bull. 44:1996;568-571.
-
(1996)
Chem. Pharm. Bull.
, vol.44
, pp. 568-571
-
-
Kai, T.1
Akiyama, Y.2
Nomura, S.3
Sato, M.4
-
96
-
-
0342782456
-
Hydroxypropyl methylcellulose phthalate
-
A. Wade, & P.J. Weller. Washington, DC/London: American Pharmaceutical Association/The Pharmaceutical Press
-
Lee J.C. Hydroxypropyl methylcellulose phthalate. Wade A., Weller P.J. Handbook of Pharmaceutical Excipients. 1994;233-237 American Pharmaceutical Association/The Pharmaceutical Press, Washington, DC/London.
-
(1994)
Handbook of Pharmaceutical Excipients
, pp. 233-237
-
-
Lee, J.C.1
-
97
-
-
0004697352
-
Polymethacrylates
-
A. Wade, & P.J. Weller. Washington, DC/London: American Pharmaceutical Association/The Pharmaceutical Press
-
Shukla A.J. Polymethacrylates. Wade A., Weller P.J. Handbook of Pharmaceutical Excipitients. 1994;362-366 American Pharmaceutical Association/The Pharmaceutical Press, Washington, DC/London.
-
(1994)
Handbook of Pharmaceutical Excipitients
, pp. 362-366
-
-
Shukla, A.J.1
-
98
-
-
0030767342
-
Improved dissolution of ofloxacin via solid dispersion
-
Okonogi S., Oguchi T., Yonemochi E., Puttipipatkhachorn S., Yamamoto K. Improved dissolution of ofloxacin via solid dispersion. Int. J. Pharm. 156:1997;175-180.
-
(1997)
Int. J. Pharm.
, vol.156
, pp. 175-180
-
-
Okonogi, S.1
Oguchi, T.2
Yonemochi, E.3
Puttipipatkhachorn, S.4
Yamamoto, K.5
-
99
-
-
0345195980
-
Effect of chitosan and chitosan glutamate enhancing the dissolution properties of the poorly water soluble drug nifedipine
-
Portero A., Remunanlopez C., Vilajato J.L. Effect of chitosan and chitosan glutamate enhancing the dissolution properties of the poorly water soluble drug nifedipine. Int. J. Pharm. 175:1998;75-84.
-
(1998)
Int. J. Pharm.
, vol.175
, pp. 75-84
-
-
Portero, A.1
Remunanlopez, C.2
Vilajato, J.L.3
-
100
-
-
0030580116
-
An investigation into the critical surfactant concentration for solid solubility of hydrophobic drug in different polyethylene glycols
-
Wulff M., Alden M., Craig D.Q.M. An investigation into the critical surfactant concentration for solid solubility of hydrophobic drug in different polyethylene glycols. Int. J. Pharm. 142:1996;189-198.
-
(1996)
Int. J. Pharm.
, vol.142
, pp. 189-198
-
-
Wulff, M.1
Alden, M.2
Craig, D.Q.M.3
-
101
-
-
0345267209
-
Enhanced release of oxazepam from tablets containing solid dispersions
-
Jachowicz R., Nürnberg E. Enhanced release of oxazepam from tablets containing solid dispersions. Int. J. Pharm. 159:1997;149-158.
-
(1997)
Int. J. Pharm.
, vol.159
, pp. 149-158
-
-
Jachowicz, R.1
Nürnberg, E.2
|