-
1
-
-
32644443823
-
Phase solubility and inclusion complex of itraconazole with β-cyclodextrin using supercritical carbon dioxide
-
10.1002/jps.20535
-
Al-Marzouqui, A.; I. Shehatta, B. Jobe, and A. Dowaidar. 2006. Phase solubility and inclusion complex of itraconazole with β-cyclodextrin using supercritical carbon dioxide. Journal of Pharmaceutical Sciences 95: 292-304.
-
(2006)
Journal of Pharmaceutical Sciences
, vol.95
, pp. 292-304
-
-
Al-Marzouqui, A.1
Shehatta, I.2
Jobe, B.3
Dowaidar, A.4
-
2
-
-
0018140749
-
Dissolution rates of hydrocortisone and prednisone utilizing sugar solid dispersion systems in tablet form
-
660521 10.1002/jps.2600670729 1:CAS:528:DyaE1MXht1ajtQ%3D%3D
-
Allen, L.V.; R.S. Levinson, and D. De Martono. 1978. Dissolution rates of hydrocortisone and prednisone utilizing sugar solid dispersion systems in tablet form. Journal of Pharmaceutical Sciences 67: 979-981.
-
(1978)
Journal of Pharmaceutical Sciences
, vol.67
, pp. 979-981
-
-
Allen, L.V.1
Levinson, R.S.2
De Martono, D.3
-
3
-
-
78651272645
-
Solubilizing the Insoluble
-
Arnum, P.V. 2010. Solubilizing the Insoluble. Pharmaceutical Technology 35: 50-56.
-
(2010)
Pharmaceutical Technology
, vol.35
, pp. 50-56
-
-
Arnum, P.V.1
-
4
-
-
42149127078
-
Predicting drug absorption and the effects of food on oral bioavailability
-
Benet, L.Z.; C. Wu, and J.M. Custodio. 2006. Predicting drug absorption and the effects of food on oral bioavailability. Bulletin Technology Gattefosse 99: 9-16.
-
(2006)
Bulletin Technology Gattefosse
, vol.99
, pp. 9-16
-
-
Benet, L.Z.1
Wu, C.2
Custodio, J.M.3
-
5
-
-
33144477406
-
Research strategies for safety evaluation of nanomaterials, part V: Role of dissolution in biological fate and effects of nanoscale particles
-
10.1093/toxsci/kfj084 1:CAS:528:DC%2BD28XhtlOntLk%3D
-
Borm, P.; F. Klaessig, T. Landry, and E. Al. 2006. Research strategies for safety evaluation of nanomaterials, part V: Role of dissolution in biological fate and effects of nanoscale particles. Toxicol Science 90: 23-32.
-
(2006)
Toxicol Science
, vol.90
, pp. 23-32
-
-
Borm, P.1
Klaessig, F.2
Landry, T.3
-
6
-
-
27744575591
-
Cyclodextrins in drug delivery: An updated review
-
16353992 10.1208/pt060243
-
Challa, R.; A. Ahuja, J. Ali, and R.K. Khar. 2005. Cyclodextrins in drug delivery: An updated review. AAPS PharmSciTech 6: E329-E357.
-
(2005)
AAPS PharmSciTech
, vol.6
-
-
Challa, R.1
Ahuja, A.2
Ali, J.3
Khar, R.K.4
-
7
-
-
79953685905
-
Nanonization strategies for poorly water-soluble drugs
-
20206289 10.1016/j.drudis.2010.02.009 1:CAS:528:DC%2BC3MXksFemtr8%3D
-
Chen, H.; C. Khemtong, X. Yang, X. Chang, and J. Gao. 2011. Nanonization strategies for poorly water-soluble drugs. Drug Discovery Today 16: 354-360.
-
(2011)
Drug Discovery Today
, vol.16
, pp. 354-360
-
-
Chen, H.1
Khemtong, C.2
Yang, X.3
Chang, X.4
Gao, J.5
-
8
-
-
0001647951
-
Study of different crystalline forms of mannitol: Comparative behaviour under compression
-
10.3109/03639048709068679 1:CAS:528:DyaL2sXmt1eitbw%3D
-
Debord, B.; C. Lefebvre, A.M. Guyot-Hermann, J. Hubert, R. Bouche, and J.C. Cuyot. 1987. Study of different crystalline forms of mannitol: Comparative behaviour under compression. Drug Development and Industrial Pharmacy 13: 1533-1546.
-
(1987)
Drug Development and Industrial Pharmacy
, vol.13
, pp. 1533-1546
-
-
Debord, B.1
Lefebvre, C.2
Guyot-Hermann, A.M.3
Hubert, J.4
Bouche, R.5
Cuyot, J.C.6
-
9
-
-
34547864243
-
Drug delivery strategies for poorly water-soluble drugs
-
17683253 10.1517/17425247.4.4.403 1:CAS:528:DC%2BD2sXos1ansL4%3D
-
Fahr, A.; and X. Liu. 2007. Drug delivery strategies for poorly water-soluble drugs. Expert Opinion on Drug Delivery 4: 403-416.
-
(2007)
Expert Opinion on Drug Delivery
, vol.4
, pp. 403-416
-
-
Fahr, A.1
Liu, X.2
-
10
-
-
0344305532
-
Processing pharmaceutical compounds using dense gas technology
-
10.1021/ie030219x 1:CAS:528:DC%2BD3sXns1Ogt7Y%3D
-
Foster, N.; R. Mammucari, F. Dehghani, A. Barrett, K. Bezanehtak, E. Coen, G. Combes, L. Meure, A. Ng, and H.L. Regtop. 2003. Processing pharmaceutical compounds using dense gas technology. Industrial and Engineering Chemistry Research 42: 6476-6493.
-
(2003)
Industrial and Engineering Chemistry Research
, vol.42
, pp. 6476-6493
-
-
Foster, N.1
Mammucari, R.2
Dehghani, F.3
Barrett, A.4
Bezanehtak, K.5
Coen, E.6
Combes, G.7
Meure, L.8
Ng, A.9
Regtop, H.L.10
-
11
-
-
0035292910
-
Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract
-
11259834 10.1016/S0169-409X(00)00130-7 1:CAS:528:DC%2BD3MXitVOhs7Y%3D
-
Horter, D.; and J.B. Dressman. 2001. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. Advanced Drug Delivery Reviews 46: 75-87.
-
(2001)
Advanced Drug Delivery Reviews
, vol.46
, pp. 75-87
-
-
Horter, D.1
Dressman, J.B.2
-
12
-
-
0034306609
-
Drug-excipient interactions and their affect on absorption
-
11050458 10.1016/S1461-5347(00)00301-1 1:CAS:528:DC%2BD3cXotlymsb4%3D
-
Jackson, K.; D. Young, and S. Pant. 2000. Drug-excipient interactions and their affect on absorption. Pharmaceutical Science and Technology Today 3: 336-345.
-
(2000)
Pharmaceutical Science and Technology Today
, vol.3
, pp. 336-345
-
-
Jackson, K.1
Young, D.2
Pant, S.3
-
13
-
-
80054697161
-
Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications
-
10.1016/j.ijpharm.2011.08.032 1:CAS:528:DC%2BC3MXhtlWmtrfI
-
Kawabata, Y.; K. Wada, M. Nakatani, S. Yamada, and S. Onoue. 2011. Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications. International Journal of Pharmacy 420: 1-10.
-
(2011)
International Journal of Pharmacy
, vol.420
, pp. 1-10
-
-
Kawabata, Y.1
Wada, K.2
Nakatani, M.3
Yamada, S.4
Onoue, S.5
-
14
-
-
28444461830
-
Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation
-
16129588 10.1016/j.ejpb.2005.05.009 1:CAS:528:DC%2BD2MXht1Ontb7E
-
Keck, C.M.; and R.H. Muller. 2006. Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation. European Journal of Pharmaceutics and Biopharmaceutics 62: 3-16.
-
(2006)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.62
, pp. 3-16
-
-
Keck, C.M.1
Muller, R.H.2
-
15
-
-
34548049483
-
Nanosizing-oral formulation development and biopharmaceutical evaluation
-
17601629 10.1016/j.addr.2007.05.003 1:CAS:528:DC%2BD2sXpsFGks7o%3D
-
Kesisoglou, F.; S. Panmai, and Y. Wu. 2007. Nanosizing-oral formulation development and biopharmaceutical evaluation. Advanced Drug Delivery Reviews 59: 631-644.
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, pp. 631-644
-
-
Kesisoglou, F.1
Panmai, S.2
Wu, Y.3
-
18
-
-
84868090406
-
Solid dispersions as a drug delivery system
-
10.4333/KPS.2011.41.3.125 1:CAS:528:DC%2BC3MXpvVOju7c%3D
-
Kim, K.T.; J.Y. Lee, M.Y. Lee, C.K. Song, J. Choi, and D-.D. Kim. 2011. Solid dispersions as a drug delivery system. Journal of Pharmaceutical Investigation 41: 125-142.
-
(2011)
Journal of Pharmaceutical Investigation
, vol.41
, pp. 125-142
-
-
Kim, K.T.1
Lee, J.Y.2
Lee, M.Y.3
Song, C.K.4
Choi, J.5
Kim, D.-D.6
-
19
-
-
5344234787
-
The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs
-
15454302 10.1016/j.ijpharm.2004.07.019 1:CAS:528:DC%2BD2cXnvVCjurw%3D
-
Kipp, J.E. 2004. The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs. International Journal of Pharmaceutics 284: 109-122.
-
(2004)
International Journal of Pharmaceutics
, vol.284
, pp. 109-122
-
-
Kipp, J.E.1
-
20
-
-
84859998651
-
A biopharmaceutical classification-based Right-First-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from First-In-Human to clinical Proof-Of-Concept
-
21121705 10.3109/10837450.2010.535826 1:CAS:528:DC%2BC38Xls1Wgsbk%3D
-
Ku, M.S.; and W. Dulin. 2012. A biopharmaceutical classification-based Right-First-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from First-In-Human to clinical Proof-Of-Concept. Pharmaceutical Development and Technology 17: 285-302.
-
(2012)
Pharmaceutical Development and Technology
, vol.17
, pp. 285-302
-
-
Ku, M.S.1
Dulin, W.2
-
21
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
-
10840189 10.1016/S0939-6411(00)00091-6
-
Löbenberg, R.; and G.L. Amidon. 2000. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. European Journal of Pharmaceutics and Biopharmaceutics 50: 3-12.
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.50
, pp. 3-12
-
-
Löbenberg, R.1
Amidon, G.L.2
-
22
-
-
84863149904
-
Characterization of nano oxaliplatin prepared by novel Fat Employing Supercritical Nano System, the FESNS(R)
-
21073400 10.3109/10837450.2010.531735 1:CAS:528:DC%2BC38Xit1Oltbo%3D
-
Lee, S.J.; Y.H. Kim, S.H. Lee, and M. Hahn. 2012. Characterization of nano oxaliplatin prepared by novel Fat Employing Supercritical Nano System, the FESNS(R). Pharmaceutical Development and Technology 17: 212-218.
-
(2012)
Pharmaceutical Development and Technology
, vol.17
, pp. 212-218
-
-
Lee, S.J.1
Kim, Y.H.2
Lee, S.H.3
Hahn, M.4
-
23
-
-
3843097202
-
Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system
-
15296954 10.1016/j.ejpb.2004.03.001
-
Lindenberg, M.; S. Kopp, and J.B. Dressman. 2004. Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system. European Journal of Pharmaceutics and Biopharmaceutics 58: 265-278.
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.58
, pp. 265-278
-
-
Lindenberg, M.1
Kopp, S.2
Dressman, J.B.3
-
24
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
11274893 10.1016/S1056-8719(00)00107-6 1:CAS:528:DC%2BD3MXitF2ksrc%3D
-
Lipinski, C.A. 2000. Drug-like properties and the causes of poor solubility and poor permeability. Journal of Pharmacological and Toxicological Methods 44: 235-249.
-
(2000)
Journal of Pharmacological and Toxicological Methods
, vol.44
, pp. 235-249
-
-
Lipinski, C.A.1
-
25
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
11259830 10.1016/S0169-409X(00)00129-0 1:CAS:528:DC%2BD3MXitVOhs7o%3D
-
Lipinski, C.A.; F. Lombardo, B.W. Dominy, and P.J. Feeney. 2001. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Advanced Drug Delivery Reviews 46: 3-26.
-
(2001)
Advanced Drug Delivery Reviews
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
27
-
-
0342897023
-
Nanosuspensions for the formulation of poorly water soluble drugs. I. Preparation by a size reduction technique
-
10.1016/S0378-5173(97)00311-6 1:CAS:528:DyaK1cXot12iuw%3D%3D
-
Muller, R.H.; and K. Peters. 1998. Nanosuspensions for the formulation of poorly water soluble drugs. I. Preparation by a size reduction technique. International Journal of Pharmaceutics 160: 229-237.
-
(1998)
International Journal of Pharmaceutics
, vol.160
, pp. 229-237
-
-
Muller, R.H.1
Peters, K.2
-
28
-
-
33947487639
-
The rate of solution of solid substances in their own solution
-
10.1021/ja02086a003
-
Noyes, A.A.; and W.R. Whitney. 1897. The rate of solution of solid substances in their own solution. Journal of the American Chemical Society 19: 930-934.
-
(1897)
Journal of the American Chemical Society
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
29
-
-
38949207528
-
Supercritical fluid technologies: An innovative approach for manipulating the solid-state of pharmaceuticals
-
17964684 10.1016/j.addr.2007.08.030 1:CAS:528:DC%2BD1cXitVaqtrg%3D
-
Pasquali, I.; R. Bettini, and F. Giordano. 2008. Supercritical fluid technologies: An innovative approach for manipulating the solid-state of pharmaceuticals. Advanced Drug Delivery Reviews 60: 399-410.
-
(2008)
Advanced Drug Delivery Reviews
, vol.60
, pp. 399-410
-
-
Pasquali, I.1
Bettini, R.2
Giordano, F.3
-
30
-
-
0000122370
-
Applications of small-molecule combinatorial chemistry to drug discovery
-
10.1016/1359-6446(96)89062-3 1:CAS:528:DyaK28XlvVaju7c%3D
-
Patel, D.V.; and E.M. Gordon. 1996. Applications of small-molecule combinatorial chemistry to drug discovery. Drug Discovery Today 1: 134-144.
-
(1996)
Drug Discovery Today
, vol.1
, pp. 134-144
-
-
Patel, D.V.1
Gordon, E.M.2
-
31
-
-
4544383493
-
Nanosuspensions in drug delivery
-
15340388 10.1038/nrd1494 1:CAS:528:DC%2BD2cXntFCns7o%3D
-
Rabinow, B.E. 2004. Nanosuspensions in drug delivery. Nat Rev Drug Discov 3: 785-796.
-
(2004)
Nat Rev Drug Discov
, vol.3
, pp. 785-796
-
-
Rabinow, B.E.1
-
32
-
-
0038493711
-
Itraconazole formulation studies of the melt-extrusion process with mixture design
-
12889782 10.1081/DDC-120021313 1:CAS:528:DC%2BD3sXls1Kqtr0%3D
-
Rambali, B.; G. Verreck, L. Baert, and D.L. Massart. 2003. Itraconazole formulation studies of the melt-extrusion process with mixture design. Drug Development and Industrial Pharmacy 29: 641-652.
-
(2003)
Drug Development and Industrial Pharmacy
, vol.29
, pp. 641-652
-
-
Rambali, B.1
Verreck, G.2
Baert, L.3
Massart, D.L.4
-
33
-
-
0034176470
-
Recent technological advances in oral drug delivery-a review
-
10754543 10.1016/S1461-5347(00)00247-9 1:CAS:528:DC%2BD3cXisFKisr4%3D
-
Sastry, S.; J. Nyshadham, and J. Fix. 2000. Recent technological advances in oral drug delivery-a review. Pharmaceutical Science and Technology Today 3: 138-145.
-
(2000)
Pharmaceutical Science and Technology Today
, vol.3
, pp. 138-145
-
-
Sastry, S.1
Nyshadham, J.2
Fix, J.3
-
34
-
-
67049169036
-
Developability assessment in pharmaceutical industry: An integrated group approach for selecting developable candidates
-
18855914 10.1002/jps.21592 1:CAS:528:DC%2BD1MXltlelu7g%3D
-
Saxena, V.; R. Panicucci, Y. Joshi, and S. Garad. 2009. Developability assessment in pharmaceutical industry: An integrated group approach for selecting developable candidates. Journal of Pharmaceutical Sciences 98: 1962-1979.
-
(2009)
Journal of Pharmaceutical Sciences
, vol.98
, pp. 1962-1979
-
-
Saxena, V.1
Panicucci, R.2
Joshi, Y.3
Garad, S.4
-
35
-
-
77953433925
-
Supercritical fluid technology: An overview of pharmaceutical applications
-
1:CAS:528:DC%2BC3cXht1eitLk%3D
-
Sekhon, B.S. 2010. Supercritical fluid technology: An overview of pharmaceutical applications. International Journal of PharmTech Research 2: 810-826.
-
(2010)
International Journal of PharmTech Research
, vol.2
, pp. 810-826
-
-
Sekhon, B.S.1
-
36
-
-
34548032742
-
Salt formation to improve drug solubility
-
17619064 10.1016/j.addr.2007.05.010 1:CAS:528:DC%2BD2sXpsFGksrc%3D
-
Serajuddin, A.T.M. 2007. Salt formation to improve drug solubility. Advanced Drug Delivery Reviews 59: 603-616.
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, pp. 603-616
-
-
Serajuddin, A.T.M.1
-
37
-
-
69549107526
-
Effect of wet milling process on the solid state of indomethacin and simvastatin
-
19576976 10.1016/j.ijpharm.2009.06.029 1:CAS:528:DC%2BD1MXhtV2hsb3E
-
Sharma, P.; W.A. Denny, and S. Garg. 2009. Effect of wet milling process on the solid state of indomethacin and simvastatin. International Journal of Pharmaceutics 380: 40-48.
-
(2009)
International Journal of Pharmaceutics
, vol.380
, pp. 40-48
-
-
Sharma, P.1
Denny, W.A.2
Garg, S.3
-
38
-
-
34548024418
-
Prodrug strategies to overcome poor water solubility
-
17628203 10.1016/j.addr.2007.05.013 1:CAS:528:DC%2BD2sXpsFGksL8%3D
-
Stella, V.J.; and K.W. Nti-Addae. 2007. Prodrug strategies to overcome poor water solubility. Advanced Drug Delivery Reviews 59: 677-694.
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, pp. 677-694
-
-
Stella, V.J.1
Nti-Addae, K.W.2
-
39
-
-
78751508035
-
Shape-specific polymeric nanomedicine: Emerging opportunities and challenges
-
10.1258/ebm.2010.010243 1:CAS:528:DC%2BC3MXivVKru70%3D
-
Tao, L.; W. Hu, Y. Liu, G. Huang, B. Sumer, and J. Gao. 2011. Shape-specific polymeric nanomedicine: Emerging opportunities and challenges. Experimental Medicine and Biology 236: 20-29.
-
(2011)
Experimental Medicine and Biology
, vol.236
, pp. 20-29
-
-
Tao, L.1
Hu, W.2
Liu, Y.3
Huang, G.4
Sumer, B.5
Gao, J.6
-
40
-
-
33845388144
-
Micellar nanocarriers: Pharmaceutical perspectives
-
17109211 10.1007/s11095-006-9132-0 1:CAS:528:DC%2BD28Xht1yis7rM
-
Torchilin, V. 2007. Micellar nanocarriers: Pharmaceutical perspectives. Pharmaceutical Research 24: 1-16.
-
(2007)
Pharmaceutical Research
, vol.24
, pp. 1-16
-
-
Torchilin, V.1
-
41
-
-
1842611878
-
Physicochemical characterization of solid dispersions of indomethacin with PEG 6000, Myrj 52, lactose, sorbitol, dextrin, and Eudragit E100
-
15109030 10.1081/DDC-120030426 1:CAS:528:DC%2BD2cXhvF2lt7w%3D
-
Valizadeh, H.; A. Nokhodchi, N. Qarakhani, P. Zakeri-Milani, S. Azarmi, D. Hassanzadeh, and R. Lobenberg. 2004. Physicochemical characterization of solid dispersions of indomethacin with PEG 6000, Myrj 52, lactose, sorbitol, dextrin, and Eudragit E100. Drug Development and Industrial Pharmacy 30: 303-317.
-
(2004)
Drug Development and Industrial Pharmacy
, vol.30
, pp. 303-317
-
-
Valizadeh, H.1
Nokhodchi, A.2
Qarakhani, N.3
Zakeri-Milani, P.4
Azarmi, S.5
Hassanzadeh, D.6
Lobenberg, R.7
-
42
-
-
53949092998
-
Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products
-
18721869 10.1016/j.ijpharm.2008.07.023
-
Van Eerdenbrugh, B.; G. Van Den Mooter, and P. Augustijns. 2008. Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products. International Journal of Pharmaceutics 364: 64-75.
-
(2008)
International Journal of Pharmaceutics
, vol.364
, pp. 64-75
-
-
Van Eerdenbrugh, B.1
Van Den Mooter, G.2
Augustijns, P.3
-
43
-
-
77954540200
-
Combined use of ordered mesoporous silica and precipitation inhibitors for improved oral absorption of the poorly soluble weak base itraconazole
-
20420905 10.1016/j.ejpb.2010.04.009
-
Van Speybroeck, M.; R. Mols, R. Mellaerts, T.D. Thi, J.A. Martens, J.V. Humbeeck, P. Annaert, G.V.D. Mooter, and P. Augustijns. 2010. Combined use of ordered mesoporous silica and precipitation inhibitors for improved oral absorption of the poorly soluble weak base itraconazole. European Journal of Pharmaceutics and Biopharmaceutics 75: 354-365.
-
(2010)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.75
, pp. 354-365
-
-
Van Speybroeck, M.1
Mols, R.2
Mellaerts, R.3
Thi, T.D.4
Martens, J.A.5
Humbeeck, J.V.6
Annaert, P.7
Mooter, G.V.D.8
Augustijns, P.9
-
44
-
-
0030866983
-
Physicochemical characterization of lipid nanoparticles and evaluation of their drug loading capacity and sustained release potential
-
10.1016/S0168-3659(97)00046-1 1:CAS:528:DyaK2sXmtlOmsbs%3D
-
Westesen, K.; H. Bunjes, and M.H.J. Koch. 1997. Physicochemical characterization of lipid nanoparticles and evaluation of their drug loading capacity and sustained release potential. Journal of Controlled Release 48: 223-236.
-
(1997)
Journal of Controlled Release
, vol.48
, pp. 223-236
-
-
Westesen, K.1
Bunjes, H.2
Koch, M.H.J.3
|