-
1
-
-
0033787026
-
Swelling-controlled release system for the vaginal delivery of miconazole
-
Mandal TK. (2000). Swelling-controlled release system for the vaginal delivery of miconazole. Eur J Pharm Biopharm, 50: 337-43.
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 337-343
-
-
Mandal, T.K.1
-
2
-
-
31144437775
-
Sustained- and controlledrelease drug-delivery systems
-
Banker GS, Rhodes CT, eds, New York: Marcel Dekker, Inc.
-
Jantzen GM, Robinson JR. (2002). Sustained- and controlledrelease drug-delivery systems. In: Banker GS, Rhodes CT, eds. Modern pharmaceutics. New York: Marcel Dekker, Inc., 501-28.
-
(2002)
Modern Pharmaceutics
, pp. 501-528
-
-
Jantzen, G.M.1
Robinson, J.R.2
-
3
-
-
33745453488
-
Modified release peroral dosage form
-
Aulton ME, ed, Edinburgh: Churchill Livingstone
-
Collet J, Moreton C. (2002). Modified release peroral dosage form. In: Aulton ME, ed. Pharmaceutics the science of dosage form design. Edinburgh: Churchill Livingstone, 289-306.
-
(2002)
Pharmaceutics the Science of Dosage Form Design
, pp. 289-306
-
-
Collet, J.1
Moreton, C.2
-
4
-
-
0034212876
-
Swellable matrices for controlled drug delivery: Gel-layer behaviour, mechanisms and optimal performance
-
Colombo P, Bettini R, Santi P, Peppas NA. (2000). Swellable matrices for controlled drug delivery: Gel-layer behaviour, mechanisms and optimal performance. Pharm Sci Technol Today, 3: 198-204.
-
(2000)
Pharm. Sci. Technol. Today
, vol.3
, pp. 198-204
-
-
Colombo, P.1
Bettini, R.2
Santi, P.3
Peppas, N.A.4
-
5
-
-
33645038541
-
Development of a controlled release low dose class II drug-Glipizide
-
Jamzad S, Fassihi R. (2006). Development of a controlled release low dose class II drug-Glipizide. Int J Pharm, 312: 24-32.
-
(2006)
Int. J. Pharm.
, vol.312
, pp. 24-32
-
-
Jamzad, S.1
Fassihi, R.2
-
6
-
-
0027626506
-
Swelling-controlled release in hydrogel matrices for oral route
-
Colombo P. (1993). Swelling-controlled release in hydrogel matrices for oral route. Adv Drug Deliv Rev, 11: 37-57. (Pubitemid 23257482)
-
(1993)
Advanced Drug Delivery Reviews
, vol.11
, Issue.1-2
, pp. 37-57
-
-
Colombo, P.1
-
7
-
-
0035844738
-
Modeling of drug release from delivery systems based on hydroxylpropyl methylcellulose (HPMC)
-
Siepmann J, Peppas NA. (2001). Modeling of drug release from delivery systems based on hydroxylpropyl methylcellulose (HPMC). Adv Drug Deliv Rev, 48: 139-57.
-
(2001)
Adv. Drug. Deliv. Rev.
, vol.48
, pp. 139-157
-
-
Siepmann, J.1
Peppas, N.A.2
-
8
-
-
0023555525
-
Importance of drug type, tablet shape and added diluents on drug release kinetics from hydroxylpropyl methylcellulose matrix tablets
-
Ford JL, Rubinstein MH, McCaul F, Hogan JE, Edgar PJ. (1987). Importance of drug type, tablet shape and added diluents on drug release kinetics from hydroxylpropyl methylcellulose matrix tablets. Int J Pharm, 40: 223-34.
-
(1987)
Int. J. Pharm.
, vol.40
, pp. 223-234
-
-
Ford, J.L.1
Rubinstein, M.H.2
McCaul, F.3
Hogan, J.E.4
Edgar, P.J.5
-
9
-
-
0025278818
-
Influence of molecular size and water solubility of the solute on its release from swelling and erosion controlled polymeric matrices
-
Rao K V R, Padmalatha Devi K, Buri P. (1990). Influence of molecular size and water solubility of the solute on its release from swelling and erosion controlled polymeric matrices. J Control Release, 12: 133-41.
-
(1990)
J. Control Release
, vol.12
, pp. 133-141
-
-
Rao, K.V.R.1
Devi, K.P.2
Buri, P.3
-
10
-
-
0029077990
-
Overall mechanism behind matrix sustained release (SR) tablets prepared with hydroxylpropylmethylcellulose 2910
-
Tahara K, Yamamoto K, Nishihata T. (1995). Overall mechanism behind matrix sustained release (SR) tablets prepared with hydroxylpropylmethylcellulose 2910. J Control Release, 35: 59-66.
-
(1995)
J. Control Release
, vol.35
, pp. 59-66
-
-
Tahara, K.1
Yamamoto, K.2
Nishihata, T.3
-
11
-
-
0031657420
-
Polymer erosion and drug release characterization of hydroxylpropyl methylcellulose matrices
-
Reynolds TD, Gehrke SH, Hussain AS, Shenouda LS. (1998). Polymer erosion and drug release characterization of hydroxylpropyl methylcellulose matrices. J Pharm Sci, 87: 1115-23.
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 1115-1123
-
-
Reynolds, T.D.1
Gehrke, S.H.2
Hussain, A.S.3
Shenouda, L.S.4
-
12
-
-
0032708697
-
HPMC matrices for controlled drug delivery: A new model combining diffusion, swelling and dissolution mechanisms and predicting the release kinetics
-
Siepmann J, Kranz H, Bodmeier R, Peppas NA. (1999). HPMC matrices for controlled drug delivery: A new model combining diffusion, swelling and dissolution mechanisms and predicting the release kinetics. Pharm Res, 16: 1748-56.
-
(1999)
Pharm. Res.
, vol.16
, pp. 1748-1756
-
-
Siepmann, J.1
Kranz, H.2
Bodmeier, R.3
Peppas, N.A.4
-
13
-
-
0027624286
-
Preparation, structure and diffusion behaviour of hydrogels in controlled release
-
Peppas NA, Khare AR. (1993). Preparation, structure and diffusion behaviour of hydrogels in controlled release. Adv Drug Deliv Rev, 11: 1-35.
-
(1993)
Adv. Drug. Deliv. Rev.
, vol.11
, pp. 1-35
-
-
Peppas, N.A.1
Khare, A.R.2
-
14
-
-
0346094228
-
Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications
-
DOI 10.1016/S0939-6411(03)00161-9
-
Berger J, Reist M, Mayer JM, Felt O, Peppas NA, Gurny R. (2004). Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur J Pharm Biopharm, 57: 19-34. (Pubitemid 38058801)
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.57
, Issue.1
, pp. 19-34
-
-
Berger, J.1
Reist, M.2
Mayer, J.M.3
Felt, O.4
Peppas, N.A.5
Gurny, R.6
-
15
-
-
5644302940
-
The characteristics of spontaneously forming physically cross-linked hydrogels composed of two water-soluble phospholipid polymers for oral drug delivery carrier I: Hydrogel dissolution and insulin release under neutral pH condition
-
Nam K, Watanabe J, Ishihara K. (2004). The characteristics of spontaneously forming physically cross-linked hydrogels composed of two water-soluble phospholipid polymers for oral drug delivery carrier I: Hydrogel dissolution and insulin release under neutral pH condition. Eur J Pharm Sci, 23: 261-70.
-
(2004)
Eur. J. Pharm. Sci.
, vol.23
, pp. 261-270
-
-
Nam, K.1
Watanabe, J.2
Ishihara, K.3
-
16
-
-
13844250268
-
Characteristics of interpolyelectrolyte complexes of Eudragit E100 with Eudragit L100
-
DOI 10.1016/j.jconrel.2004.11.031, PII S016836590400598X
-
Moustafine RI, Kabanova TV, Kemenova VA, Van den Mooter G. (2005). Characteristics of interpolyelectrolyte complexes of Eudragit E100 with Eudragit L100. J Control Release, 103: 191-8. (Pubitemid 40248571)
-
(2005)
Journal of Controlled Release
, vol.103
, Issue.1
, pp. 191-198
-
-
Moustafine, R.I.1
Kabanova, T.V.2
Kemenova, V.A.3
Van Den Mooter, G.4
-
17
-
-
0034005095
-
Chitosan, a drug carrier for the 21st century: A review
-
Paul W, Sharma CP. (2000). Chitosan, a drug carrier for the 21st century: A review. STP Pharm Sci, 10: 5-22.
-
(2000)
STP Pharm. Sci.
, vol.10
, pp. 5-22
-
-
Paul, W.1
Sharma, C.P.2
-
18
-
-
0032482180
-
Inclusion and release of proteins from polysaccharide-based polyion complexes
-
Dumitriu S, Chornet E. (1998). Inclusion and release of proteins from polysaccharide-based polyion complexes. Adv Drug Deliv Rev, 31: 223-46.
-
(1998)
Adv. Drug. Deliv. Rev.
, vol.31
, pp. 223-246
-
-
Dumitriu, S.1
Chornet, E.2
-
20
-
-
33845928305
-
Reversed chitosan-alginate polyelectrolyte complex for stability improvement of alpha-amylase: Optimization and physicochemical characterization
-
Sankalia MG, Mashru RC, Sankalia JM, Sutariya VB. (2007). Reversed chitosan-alginate polyelectrolyte complex for stability improvement of alpha-amylase: Optimization and physicochemical characterization. Eur J Pharm Biopharm, 65: 215-32.
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.65
, pp. 215-232
-
-
Sankalia, M.G.1
Mashru, R.C.2
Sankalia, J.M.3
Sutariya, V.B.4
-
21
-
-
35148872627
-
Chitosan-polycarbophil complexes in swellable matrix systems for controlled drug release
-
Lu Z, Chen W, Hamman JH. (2007). Chitosan-polycarbophil complexes in swellable matrix systems for controlled drug release. Curr Drug Deliv, 4: 257-63.
-
(2007)
Curr. Drug. Deliv.
, vol.4
, pp. 257-263
-
-
Lu, Z.1
Chen, W.2
Hamman, J.H.3
-
22
-
-
39749125471
-
Matrix polymeric excipients: Comparing a novel interpolyelectrolyte complex with hydroxypropylmethylcellulose
-
Lu Z, Chen W, Olivier EI, Hamman JH. (2008). Matrix polymeric excipients: Comparing a novel interpolyelectrolyte complex with hydroxypropylmethylcellulose. Drug Deliv, 15: 87-96.
-
(2008)
Drug. Deliv.
, vol.15
, pp. 87-96
-
-
Lu, Z.1
Chen, W.2
Olivier, E.I.3
Hamman, J.H.4
-
23
-
-
39749188663
-
Chitosanpolycarbophil interpolyelectrolyte complex as an excipient for bioadhesive matrix systems to control macromolecular drug delivery
-
Lu Z, Chen W, Hamman JH, Ni J, Zhai X. (2008). Chitosanpolycarbophil interpolyelectrolyte complex as an excipient for bioadhesive matrix systems to control macromolecular drug delivery. Pharm Dev Technol, 13: 37-47.
-
(2008)
Pharm. Dev. Technol.
, vol.13
, pp. 37-47
-
-
Lu, Z.1
Chen, W.2
Hamman, J.H.3
Ni, J.4
Zhai, X.5
-
24
-
-
77952618991
-
-
Rockville: United States Pharmacopeial Convention, Inc
-
United States Pharmacopoeia 29 (USP). (2006). Rockville: United States Pharmacopeial Convention, Inc.
-
(2006)
United States Pharmacopoeia 29 (USP)
-
-
-
25
-
-
0023196815
-
A simple equation for description of solute release. II Fickian and anomalous release from swellable devices
-
Ritger PL, Peppas NA. (1987). A simple equation for description of solute release. II Fickian and anomalous release from swellable devices. J Control Release, 5: 37-42.
-
(1987)
J. Control Release
, vol.5
, pp. 37-42
-
-
Ritger, P.L.1
Peppas, N.A.2
-
26
-
-
0033051406
-
A new method for dissolution studies of lipid filled capsules employing nifedipine as a model drug
-
Pillay V, Fassihi R. (1999). A new method for dissolution studies of lipid filled capsules employing nifedipine as a model drug. Pharm Res, 16: 333-8.
-
(1999)
Pharm. Res.
, vol.16
, pp. 333-338
-
-
Pillay, V.1
Fassihi, R.2
-
27
-
-
0021904208
-
Analysis of Fickian and non-Fickian drug release from polymers
-
Peppas NA. (1985). Analysis of Fickian and non-Fickian drug release from polymers. Pharm Acta Helv, 60: 110-1.
-
(1985)
Pharm. Acta Helv.
, vol.60
, pp. 110-111
-
-
Peppas, N.A.1
-
28
-
-
85056934683
-
Analysis of drug dissolution data
-
Dressman JB, Lennernäs H, eds, New York: Marcel Dekker, Inc.
-
Reppas C, Nicolaides E. (2000). Analysis of drug dissolution data. In: Dressman JB, Lennernäs H, eds. Oral drug absorption prediction and assessment. New York: Marcel Dekker, Inc., 229-54.
-
(2000)
Oral. Drug. Absorption Prediction and Assessment
, pp. 229-254
-
-
Reppas, C.1
Nicolaides, E.2
-
29
-
-
0037148652
-
The influence of core materials and film coating on the drug release from coated pellets
-
DOI 10.1016/S0378-5173(01)00921-8, PII S0378517301009218
-
Sousa JJ, Sousa A, Moura MJ, Podczeck F, Nowton JM. (2002). The influence of core materials and film coating on the drug release from coated pellets. Int J Pharm, 233: 111-22. (Pubitemid 34230423)
-
(2002)
International Journal of Pharmaceutics
, vol.233
, Issue.1-2
, pp. 111-122
-
-
Sousa, J.J.1
Sousa, A.2
Moura, M.J.3
Podczeck, F.4
Newton, J.M.5
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