-
2
-
-
0021289102
-
A clinical and pharmacokinetics basis for the selection and use of slow release theophylline products
-
2. L. Hendeles, R. P. Iafrate, and M. Weinberger. A clinical and pharmacokinetics basis for the selection and use of slow release theophylline products. Clin. Pharmacokin. 9:95-135 (1984).
-
(1984)
Clin. Pharmacokin.
, vol.9
, pp. 95-135
-
-
Hendeles, L.1
Iafrate, R.P.2
Weinberger, M.3
-
3
-
-
0013481751
-
-
L. F. Prescott and W. S. Nimmo (Ed.), Churehill Livingstone, Edinburgh
-
3. R. G. Shanks. In rate control in drug therapy. L. F. Prescott and W. S. Nimmo (Ed.), Churehill Livingstone, Edinburgh (1985).
-
(1985)
In Rate Control in Drug Therapy
-
-
Shanks, R.G.1
-
5
-
-
0016830071
-
Elementary osmotic pump
-
5. F. Theeuwes. Elementary osmotic pump. J. Pharm. Sci. 64: 1987-1991 (1975).
-
(1975)
J. Pharm. Sci.
, vol.64
, pp. 1987-1991
-
-
Theeuwes, F.1
-
6
-
-
0019495863
-
Osmotically actuated dosage forms for rate-controlled drug delivery
-
6. B. Eckenhoff, F. Theeuwes, and J. Urquhart. Osmotically actuated dosage forms for rate-controlled drug delivery. Pharm. Techn. 5:35-44 (1981).
-
(1981)
Pharm. Techn.
, vol.5
, pp. 35-44
-
-
Eckenhoff, B.1
Theeuwes, F.2
Urquhart, J.3
-
7
-
-
0022408524
-
Osmotic flow through controlled porosity films: An approach to delivery of water soluble compounds
-
7. G. M. Zentner, G. S. Rork, and K. J. Himmelstein. Osmotic flow through controlled porosity films: An approach to delivery of water soluble compounds. J. Contr. Rel. 2:217-229 (1985).
-
(1985)
J. Contr. Rel.
, vol.2
, pp. 217-229
-
-
Zentner, G.M.1
Rork, G.S.2
Himmelstein, K.J.3
-
11
-
-
0030874214
-
Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. II. Improved in vitro-in vivo correlation usinga two-phase dissolution test
-
11. J. S. Grundy, K. E. Anderson, J. A. Rogers, and R. T. Foster. Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. II. Improved in vitro-in vivo correlation usinga two-phase dissolution test. J. Contr. Rel. 48:9-17 (1997).
-
(1997)
J. Contr. Rel.
, vol.48
, pp. 9-17
-
-
Grundy, J.S.1
Anderson, K.E.2
Rogers, J.A.3
Foster, R.T.4
-
12
-
-
0343216466
-
-
U.S. Patent 3, 845, 770, November 5, 1974
-
12. F. Theeuwes and T. Higuchi. Osmotic dispersing device for releasing beneficial agent. U.S. Patent 3, 845, 770, November 5, 1974.
-
Osmotic Dispersing Device for Releasing Beneficial Agent
-
-
Theeuwes, F.1
Higuchi, T.2
-
13
-
-
0020452096
-
Comparison of the pharmacodynamic and pharmacokinetic profiles of single and multiple doses of a commercial slow-release metoprolol formulation with a new Oros® delivery systen
-
13. M. J. Kendall, D. B. Jack, K. L. Woods, S. J. Laugher, C. P. Quaterman, and V. A. John. Comparison of the pharmacodynamic and pharmacokinetic profiles of single and multiple doses of a commercial slow-release metoprolol formulation with a new Oros® delivery systen. Br. J. Clin. Pharmacol. 13:393-398 (1982).
-
(1982)
Br. J. Clin. Pharmacol.
, vol.13
, pp. 393-398
-
-
Kendall, M.J.1
Jack, D.B.2
Woods, K.L.3
Laugher, S.J.4
Quaterman, C.P.5
John, V.A.6
-
14
-
-
0025809463
-
Controlled porosity solubility-and resin-modulated osmotic drug delivery systems for release of diltiazem hydrochloride
-
14. G. M. Zentner, G. A. McClelland, and S. C. Sutton. Controlled porosity solubility-and resin-modulated osmotic drug delivery systems for release of diltiazem hydrochloride. J. Contr. Rel. 16:237-244 (1991).
-
(1991)
J. Contr. Rel.
, vol.16
, pp. 237-244
-
-
Zentner, G.M.1
McClelland, G.A.2
Sutton, S.C.3
-
15
-
-
0025135014
-
Theophylline tablets coated with aqueous latexes containing dispersed pore formers
-
15. R. Bodmeier and O. Paeratakul. Theophylline tablets coated with aqueous latexes containing dispersed pore formers. J. Pharm. Sci. 79:925-928 (1990).
-
(1990)
J. Pharm. Sci.
, vol.79
, pp. 925-928
-
-
Bodmeier, R.1
Paeratakul, O.2
-
17
-
-
0343883243
-
-
U.S. Patent 5, 134, 127, July 18, 1992
-
17. V. J. Stella and R. A. Rajewski. Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the pharmaceutical use thereof. U.S. Patent 5, 134, 127, July 18, 1992.
-
Derivatives of Cyclodextrins Exhibiting Enhanced Aqueous Solubility and the Pharmaceutical Use Thereof.
-
-
Stella, V.J.1
Rajewski, R.A.2
-
18
-
-
0030053698
-
The interaction of charged and uncharged drugs with neutral (HP-β-CD) and anionically charged (SBE7-β-CD) β-cyclodextrins
-
18. K. Okimoto, R. A. Rajewski, K. Uekama, J. A. Jona, and V. J. Stella. The interaction of charged and uncharged drugs with neutral (HP-β-CD) and anionically charged (SBE7-β-CD) β-cyclodextrins. Pharm. Res. 13:256-264 (1996).
-
(1996)
Pharm. Res.
, vol.13
, pp. 256-264
-
-
Okimoto, K.1
Rajewski, R.A.2
Uekama, K.3
Jona, J.A.4
Stella, V.J.5
-
19
-
-
0031048971
-
Effect of alkyl chain length and degree of substitution on the complexation of sulfoalkyl ether β-cyclodextrins with steroids
-
19. V. Zia, R. A. Rajewski, E. R. Bornancini, E. A. Luna, and V. J. Stella. Effect of alkyl chain length and degree of substitution on the complexation of sulfoalkyl ether β-cyclodextrins with steroids. J. Pharm. Sci. 86:220-224 (1997).
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 220-224
-
-
Zia, V.1
Rajewski, R.A.2
Bornancini, E.R.3
Luna, E.A.4
Stella, V.J.5
-
20
-
-
0000817098
-
Phase-solubility techniques
-
C. N. Reilly (Ed.), Interscience, New York
-
20. T. Higuchi and K. Connors. Phase-solubility techniques, in: C. N. Reilly (Ed.), Advances in Analytical Chemistry and Instrumentation, Interscience, New York, 1965, pp. 117-212.
-
(1965)
Advances in Analytical Chemistry and Instrumentation
, pp. 117-212
-
-
Higuchi, T.1
Connors, K.2
-
21
-
-
1842465678
-
-
J. R. Robinson and V. H. Lee (Ed.), Marcel Dekker Inc., New York
-
21. J. P. Skelly. Controlled drug delivery. J. R. Robinson and V. H. Lee (Ed.), Marcel Dekker Inc., New York, 294 (1987).
-
(1987)
Controlled Drug Delivery
, pp. 294
-
-
Skelly, J.P.1
-
22
-
-
0019952486
-
Serious bioavalability problems with a generic prolonged-release quinidine gluconate product
-
22. M. C. Meyer, A. B. Straughn, P. Lieberman, and J. Jacob. Serious bioavalability problems with a generic prolonged-release quinidine gluconate product. J. Clin. Pharmacol. 22:131-134 (1982).
-
(1982)
J. Clin. Pharmacol.
, vol.22
, pp. 131-134
-
-
Meyer, M.C.1
Straughn, A.B.2
Lieberman, P.3
Jacob, J.4
-
23
-
-
0021933962
-
Bioavailability of indomethacin capsules in humans (1): Bioavailability and effects of gastric acidity
-
23. N. Aoyagi, H. Ogata, N. Kaniwa, and A. Ejima. Bioavailability of indomethacin capsules in humans (1): Bioavailability and effects of gastric acidity. Int. J. Clin. Pharmacol. Ther. Toxicol. 23:496-474 (1985).
-
(1985)
Int. J. Clin. Pharmacol. Ther. Toxicol.
, vol.23
, pp. 496-1474
-
-
Aoyagi, N.1
Ogata, H.2
Kaniwa, N.3
Ejima, A.4
-
24
-
-
0025147050
-
In vitro and in vivo testing and correlation for oral controlled/modified-release dosage forms
-
24. J. P. Skelly, G. L. Amidon, W. H. Barr, L. Z. Benet, J. R. Carter, J. R. Robinson, V. P. Shah, and A. Yacobi. In vitro and in vivo testing and correlation for oral controlled/modified-release dosage forms. Pharm. Res. 7:975-982 (1990).
-
(1990)
Pharm. Res.
, vol.7
, pp. 975-982
-
-
Skelly, J.P.1
Amidon, G.L.2
Barr, W.H.3
Benet, L.Z.4
Carter, J.R.5
Robinson, J.R.6
Shah, V.P.7
Yacobi, A.8
-
25
-
-
0016689286
-
Application of the Loo-Riegelman absorption method
-
25. J. G. Wagner. Application of the Loo-Riegelman absorption method. J. Pharmacokin. Biopharm. 3:51 (1975).
-
(1975)
J. Pharmacokin. Biopharm.
, vol.3
, pp. 51
-
-
Wagner, J.G.1
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