-
1
-
-
0029618438
-
Solid dispersions of nimodipine: Physico-chemical and dissolution rate studies
-
K. P. R. Chowdary, K. V. R. Murthy and C. D. S. Prasad, Solid dispersions of nimodipine: Physico-chemical and dissolution rate studies, Indian Drugs 32 (1995) 537-542.
-
(1995)
Indian Drugs
, vol.32
, pp. 537-542
-
-
Chowdary, K.P.R.1
Murthy, K.V.R.2
Prasad, C.D.S.3
-
2
-
-
0344541110
-
Alternative solvent-free preparation methods for felodipine surface solid dispersions
-
J. Kerc, S. Srcic and B. Kofler, Alternative solvent-free preparation methods for felodipine surface solid dispersions, Drug Dev. Ind. Pharm. 24 (1998) 359-363.
-
(1998)
Drug Dev. Ind. Pharm.
, vol.24
, pp. 359-363
-
-
Kerc, J.1
Srcic, S.2
Kofler, B.3
-
3
-
-
0017599519
-
The influence of the additive on the presentation of a drug in hard gelatin capsules
-
J. M. Newton and F. N. Razzo, The influence of the additive on the presentation of a drug in hard gelatin capsules, J. Pharm. Pharmacol. 29 (1997) 294-297.
-
(1997)
J. Pharm. Pharmacol.
, vol.29
, pp. 294-297
-
-
Newton, J.M.1
Razzo, F.N.2
-
4
-
-
0017745871
-
In-vivo evaluation of the effect of five disintegrants on the biovailability of furosemide from tablets
-
M. H. Rubinstein and E. J. Price, In-vivo evaluation of the effect of five disintegrants on the biovailability of furosemide from tablets, J. Pharm. Pharmacol. 29 (1997) 5P.
-
(1997)
J. Pharm. Pharmacol.
, vol.29
-
-
Rubinstein, M.H.1
Price, E.J.2
-
5
-
-
0023696371
-
Influence of sodium lauryl sulphate on indomethacin release pattern from zinc-indomethacin complex and indomethacin capsules
-
A. K. Singla and D. K. Mediratta, Influence of sodium lauryl sulphate on indomethacin release pattern from zinc-indomethacin complex and indomethacin capsules, Drug Dev. Ind. Pharm. 14 (1998) 1883-1888.
-
(1998)
Drug Dev. Ind. Pharm.
, vol.14
, pp. 1883-1888
-
-
Singla, A.K.1
Mediratta, D.K.2
-
6
-
-
0033997669
-
Dissolution of ionizable water-soluble drugs: The combined effect of pH and surfactant
-
G. L. Amidon, Jinno and J. R. Crison, Dissolution of ionizable water-soluble drugs: The combined effect of pH and surfactant, J. Pharm. Sci. 89 (2000) 268-274.
-
(2000)
J. Pharm. Sci.
, vol.89
, pp. 268-274
-
-
Amidon, G.L.1
Jinno2
Crison, J.R.3
-
7
-
-
85176846159
-
Fast analgesic activity from recrystallized nimesulide and its solid dispersion
-
S. Mutalik, Venkatesh and N. Udupa, Fast analgesic activity from recrystallized nimesulide and its solid dispersion, Indian J. Physiol. Pharmacol. 46 (2000) 115-116.
-
(2000)
Indian J. Physiol. Pharmacol.
, vol.46
, pp. 115-116
-
-
Mutalik, S.1
Venkatesh2
Udupa, N.3
-
8
-
-
0021364844
-
The role of disintegrants in hard gelatin capsules
-
J. S. Botzolakis and L. L. Augsburger, The role of disintegrants in hard gelatin capsules, J. Pharm. Pharmacol. 36 (1984) 77-84.
-
(1984)
J. Pharm. Pharmacol.
, vol.36
, pp. 77-84
-
-
Botzolakis, J.S.1
Augsburger, L.L.2
-
9
-
-
0023873176
-
Disintegrating agents in hard gelatin capsules. Part I: Mechanism of action
-
J. S. Botzolakis and L. L. Augsburger, Disintegrating agents in hard gelatin capsules. Part I: Mechanism of action, Drug Dev. Ind. Pharm. 14 (1998) 29-41.
-
(1998)
Drug Dev. Ind. Pharm.
, vol.14
, pp. 29-41
-
-
Botzolakis, J.S.1
Augsburger, L.L.2
-
10
-
-
0023726047
-
Disintegrating agents in hard gelatine capsules. Part II: Swelling efficiency
-
J. S. Botzolakis and L. L. Augsburger, Disintegrating agents in hard gelatine capsules. Part II: Swelling efficiency, Drug Dev. Ind. Pharm. 14 (1988) 1235-1248.
-
(1988)
Drug Dev. Ind. Pharm.
, vol.14
, pp. 1235-1248
-
-
Botzolakis, J.S.1
Augsburger, L.L.2
-
11
-
-
0023786759
-
Calculation of disintegrant critical concentration in order to optimize tablets disintegration
-
J. Ringard and A. M. Guyot-Hermann, Calculation of disintegrant critical concentration in order to optimize tablets disintegration, Drug Dev. Ind. Pharm. 14 (1998) 2321-2339.
-
(1998)
Drug Dev. Ind. Pharm.
, vol.14
, pp. 2321-2339
-
-
Ringard, J.1
Guyot-Hermann, A.M.2
-
12
-
-
0025058625
-
Improving dissolution rates griseofulvin by dispositon on disintegrants
-
S. L. Law and C. H. Chiang, Improving dissolution rates griseofulvin by dispositon on disintegrants, Drug Dev. Ind. Pharm. 16 (1990) 137-147.
-
(1990)
Drug Dev. Ind. Pharm.
, vol.16
, pp. 137-147
-
-
Law, S.L.1
Chiang, C.H.2
-
13
-
-
0013302526
-
Evaluation pregelatinised starch as tablet excipients for improving dissolution rate and efficiency of nimodipine
-
K. P. R. Chowdary and N. Rama Rao, Evaluation pregelatinised starch as tablet excipients for improving dissolution rate and efficiency of nimodipine, Int. J. Pharm. Excip. 1 (1999) 20-24.
-
(1999)
Int. J. Pharm. Excip.
, vol.1
, pp. 20-24
-
-
Chowdary, K.P.R.1
Rama Rao, N.2
-
14
-
-
0019456715
-
Carboxymethyl cellulose: Effect of degree of polymerization and substitution of tablet disintegration and dissolution
-
N. H. Shah, J. H. Lazarus, P. R. Sheth and C. I. Jaworski, Carboxymethyl cellulose: Effect of degree of polymerization and substitution of tablet disintegration and dissolution, J. Pharm. Sci. 70 (1981) 611-613.
-
(1981)
J. Pharm. Sci.
, vol.70
, pp. 611-613
-
-
Shah, N.H.1
Lazarus, J.H.2
Sheth, P.R.3
Jaworski, C.I.4
-
15
-
-
84907034443
-
Evaluation of croscarmellose as a tablet disintegrant in direct compression systems
-
E. A. Gorman, C. T. Rhodes and E. M. Rudnic, Evaluation of croscarmellose as a tablet disintegrant in direct compression systems, Drug Dev. Ind. Pharm. 8 (1982) 397-410.
-
(1982)
Drug Dev. Ind. Pharm.
, vol.8
, pp. 397-410
-
-
Gorman, E.A.1
Rhodes, C.T.2
Rudnic, E.M.3
-
17
-
-
0015535580
-
New tablet disintegrating agent: Cross-linked polyvinylpyrrolidone
-
A. S. Kornblum and S. B. Stoopak, New tablet disintegrating agent: Cross-linked polyvinylpyrrolidone, J. Pharm. Sci. 62 (1973) 43-49.
-
(1973)
J. Pharm. Sci.
, vol.62
, pp. 43-49
-
-
Kornblum, A.S.1
Stoopak, S.B.2
-
18
-
-
0001959892
-
Tablets
-
(Eds. L. Lachman, H. A. Liberman, and J. L. Kanig), Verghese Publishing House, Bombay
-
G. S. Bankar and H. R. Anderson, Tablets, in The Theory and Practice of Industrial Pharmacy, Fourth Indian Edition (Eds. L. Lachman, H. A. Liberman, and J. L. Kanig), Verghese Publishing House, Bombay 1991, pp. 328.
-
(1991)
The Theory and Practice of Industrial Pharmacy, Fourth Indian Edition
, pp. 328
-
-
Bankar, G.S.1
Anderson, H.R.2
-
19
-
-
0001776320
-
Colloidal silicon dioxide
-
(Eds: A. Wade and J. W. Paul), American Pharmaceutical Association/The Pharmaceutical Press, Washington DC/London
-
D. Harpaz, Colloidal Silicon Dioxide, in Handbook of Pharmaceutical Excipients, Second Edition (Eds: A. Wade and J. W. Paul), American Pharmaceutical Association/The Pharmaceutical Press, Washington DC/London 1994, pp. 424.
-
(1994)
Handbook of Pharmaceutical Excipients, Second Edition
, pp. 424
-
-
Harpaz, D.1
-
20
-
-
0030910347
-
Study of the influence of both cyclodextrin and L-lysine on the aqeous solubility of nimesulide; isolation and characterization of nimesulide-L-lysine-cyclodextrine complexes
-
G. Piel, B. Pirotte, I. Delneuville, P. Neven, G. Llabres, J. Delarge and L. Delattre, Study of the influence of both cyclodextrin and L-lysine on the aqeous solubility of nimesulide; isolation and characterization of nimesulide-L-lysine-cyclodextrine complexes, J. Pharm. Sci. 86 (1997) 475-480.
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 475-480
-
-
Piel, G.1
Pirotte, B.2
Delneuville, I.3
Neven, P.4
Llabres, G.5
Delarge, J.6
Delattre, L.7
-
21
-
-
0033755142
-
Improvement of Nimesulide dissolution by co-grinding method using surfactants
-
M. C. Gohel and L. D. Patel, Improvement of Nimesulide dissolution by co-grinding method using surfactants, Pharm. Pharmacol. Commun. 6 (2000) 433-440.
-
(2000)
Pharm. Pharmacol. Commun.
, vol.6
, pp. 433-440
-
-
Gohel, M.C.1
Patel, L.D.2
-
22
-
-
85176846173
-
Processing of nimesulide-PEG 400-PG-PVP solid dispersions: Preparation, characterization and in-vitro dissolution
-
in press
-
M. C. Gohel and L. D. Patel, Processing of Nimesulide-PEG 400-PG-PVP Solid Dispersions: Preparation, Characterization and in-vitro Dissolution, Drug Dev. Ind. Pharm., in press.
-
Drug Dev. Ind. Pharm.
-
-
Gohel, M.C.1
Patel, L.D.2
-
23
-
-
0019908451
-
Effect of particle size on the compaction mechanism tensile strength of tablets
-
A. McKenna and D. F. McCafferty, Effect of particle size on the compaction mechanism tensile strength of tablets, J. Pharm. Pharmacol. 34 (1982) 347-351.
-
(1982)
J. Pharm. Pharmacol.
, vol.34
, pp. 347-351
-
-
McKenna, A.1
McCafferty, D.F.2
-
24
-
-
85176861640
-
-
Rockville
-
United States Pharmacopoea 23/National Formulary 18, United States Pharmacopeial Convention, Rockville 1995, pp. 1791.
-
(1995)
United States Pharmacopeial Convention
, pp. 1791
-
-
-
25
-
-
0032908384
-
Development of multiple w / o / w emulsions showing prolonged anti-inflammatory activity of nimesulide
-
P. Tandon and R. Mishra, Development of multiple w / o / w emulsions showing prolonged anti-inflammatory activity of nimesulide, Acta Pharm. Turcia 41 (1999) 15-18.
-
(1999)
Acta Pharm. Turcia
, vol.41
, pp. 15-18
-
-
Tandon, P.1
Mishra, R.2
-
26
-
-
0023813783
-
An attempt at bringing to light a »Phase inversion« in a binary mixture of two dimensional rounded particles
-
C. Lefebvre, A. M. Barthelemy and G. Hermann, An attempt at bringing to light a »Phase inversion« in a binary mixture of two dimensional rounded particles, Drug Dev. Ind. Pharm. 14 (1988) 2443-2465.
-
(1988)
Drug Dev. Ind. Pharm.
, vol.14
, pp. 2443-2465
-
-
Lefebvre, C.1
Barthelemy, A.M.2
Hermann, G.3
-
27
-
-
0034050926
-
The influence of crystallization conditions on the morphology of lactose intended for use as a carrier for dry powder aerosols
-
X. M. Zeng, G. P. Martin, C. Marriott and J. Pritchard, The influence of crystallization conditions on the morphology of lactose intended for use as a carrier for dry powder aerosols, J. Pharm. Pharmacol. 52 (2000) 633-643.
-
(2000)
J. Pharm. Pharmacol.
, vol.52
, pp. 633-643
-
-
Zeng, X.M.1
Martin, G.P.2
Marriott, C.3
Pritchard, J.4
-
28
-
-
1142303337
-
What is the true solubility advantage for amorphous pharmaceuticals?
-
B. C. Hancock and M. Parks, What is the true solubility advantage for amorphous pharmaceuticals? Pharm. Res. 17 (2000) 397-404.
-
(2000)
Pharm. Res.
, vol.17
, pp. 397-404
-
-
Hancock, B.C.1
Parks, M.2
-
29
-
-
0016422844
-
The concept of dissolution efficiency
-
K. A. Khan, The concept of dissolution efficiency, J. Pharm. Pharmacol. 27 (1975) 48-49.
-
(1975)
J. Pharm. Pharmacol.
, vol.27
, pp. 48-49
-
-
Khan, K.A.1
-
30
-
-
2342652446
-
Mathematical comparison of dissolution profiles
-
J. W. Moore and H. H. Flanner, Mathematical comparison of dissolution profiles, Pharm. Technol. 20 (1996) 64-74.
-
(1996)
Pharm. Technol.
, vol.20
, pp. 64-74
-
-
Moore, J.W.1
Flanner, H.H.2
-
31
-
-
0023856181
-
Grinding effect on some pharmaceutical properties of drugs by adding β-cyclodextrine
-
S. Y. Lin, Y. H. Kao and J. C. Yang, Grinding effect on some pharmaceutical properties of drugs by adding β-cyclodextrine, Drug Dev. Ind. Pharm. 14 (1988) 99-118.
-
(1988)
Drug Dev. Ind. Pharm.
, vol.14
, pp. 99-118
-
-
Lin, S.Y.1
Kao, Y.H.2
Yang, J.C.3
-
32
-
-
0032768725
-
Solid-state of drug-cyclodextrine inclusion complexes in PEG 6000 prepared by a new method
-
M. Wulff and M. Alden, Solid-state of drug-cyclodextrine inclusion complexes in PEG 6000 prepared by a new method, Eur. J. Pharm. Sci. 8 (1999) 269-281.
-
(1999)
Eur. J. Pharm. Sci.
, vol.8
, pp. 269-281
-
-
Wulff, M.1
Alden, M.2
|