-
1
-
-
0032103736
-
Crystallisation of partially amorphous griseofulvin in water vapour: determination of kinetic parameters using isothermal heat conduction microcalorimetry
-
Ahmed H., Buckton G., and Rawlins D.A. Crystallisation of partially amorphous griseofulvin in water vapour: determination of kinetic parameters using isothermal heat conduction microcalorimetry. Int. J. Pharm. 167 (1998) 139-145
-
(1998)
Int. J. Pharm.
, vol.167
, pp. 139-145
-
-
Ahmed, H.1
Buckton, G.2
Rawlins, D.A.3
-
2
-
-
59349117713
-
-
Auweter, H., Bohn, H., Heger, R., Horn, D., Siegel, B., Siemensmeyer, K., 2002. Precipitated water-insoluble colorants in colloid disperse form. United States Patent 6,494,924.
-
Auweter, H., Bohn, H., Heger, R., Horn, D., Siegel, B., Siemensmeyer, K., 2002. Precipitated water-insoluble colorants in colloid disperse form. United States Patent 6,494,924.
-
-
-
-
3
-
-
0026735598
-
The relationship between particle size and solubility
-
Buckton G., and Beezer A.E. The relationship between particle size and solubility. Int. J. Pharm. 82 (1992) R7-R10
-
(1992)
Int. J. Pharm.
, vol.82
-
-
Buckton, G.1
Beezer, A.E.2
-
4
-
-
19944394500
-
The rutin/beta-cyclodextrin interactions in fully aqueous solution: spectroscopic studies and biological assays
-
Calabro M.L., Tommasini S., Donato P., Stancanelli R., Raneri D., Catania S., Costa C., Villari V., Ficarra P., and Ficarra R. The rutin/beta-cyclodextrin interactions in fully aqueous solution: spectroscopic studies and biological assays. J. Pharm. Biomed. Anal. 36 (2005) 1019-1027
-
(2005)
J. Pharm. Biomed. Anal.
, vol.36
, pp. 1019-1027
-
-
Calabro, M.L.1
Tommasini, S.2
Donato, P.3
Stancanelli, R.4
Raneri, D.5
Catania, S.6
Costa, C.7
Villari, V.8
Ficarra, P.9
Ficarra, R.10
-
5
-
-
0033865338
-
Naturally occurring polyphenolic antioxidants modulate IgE-mediated mast cell activation
-
Chen S., Gong J., Liu F., and Mohammed U. Naturally occurring polyphenolic antioxidants modulate IgE-mediated mast cell activation. Immunology 100 (2000) 471-480
-
(2000)
Immunology
, vol.100
, pp. 471-480
-
-
Chen, S.1
Gong, J.2
Liu, F.3
Mohammed, U.4
-
6
-
-
0034817206
-
Biomarkers for exposure to dietary flavonoids: a review of the current evidence for identification of quercetin glycosides in plasma
-
Day A.J., and Williamson G. Biomarkers for exposure to dietary flavonoids: a review of the current evidence for identification of quercetin glycosides in plasma. Br. J. Nutr. 86 Suppl 1 (2001) S105-S110
-
(2001)
Br. J. Nutr.
, vol.86
, Issue.SUPPL. 1
-
-
Day, A.J.1
Williamson, G.2
-
7
-
-
0025885064
-
Quercetin and rutin as inhibitors of azoxymethanol-induced colonic neoplasia
-
Deschner E.E., Ruperto J., Wong G., and Newmark H.L. Quercetin and rutin as inhibitors of azoxymethanol-induced colonic neoplasia. Carcinogenesis 12 (1991) 1193-1196
-
(1991)
Carcinogenesis
, vol.12
, pp. 1193-1196
-
-
Deschner, E.E.1
Ruperto, J.2
Wong, G.3
Newmark, H.L.4
-
8
-
-
0028977190
-
Micellar solubility and micelle/water partitioning of polychlorinated biphenyls in solutions of sodium dodecyl sulfate
-
Dulfer W.J., Bakker M.W.C., and Govers H.A.J. Micellar solubility and micelle/water partitioning of polychlorinated biphenyls in solutions of sodium dodecyl sulfate. Environ. Sci. Technol. 29 (1995) 985-992
-
(1995)
Environ. Sci. Technol.
, vol.29
, pp. 985-992
-
-
Dulfer, W.J.1
Bakker, M.W.C.2
Govers, H.A.J.3
-
9
-
-
17744396286
-
Pharmacokinetics and bioavailability of quercetin glycosides in humans
-
Graefe E.U., Wittig J., Mueller S., Riethling A.K., Uehleke B., Drewelow B., Pforte H., Jacobasch G., Derendorf H., and Veit M. Pharmacokinetics and bioavailability of quercetin glycosides in humans. J. Clin. Pharmacol. 41 (2001) 492-499
-
(2001)
J. Clin. Pharmacol.
, vol.41
, pp. 492-499
-
-
Graefe, E.U.1
Wittig, J.2
Mueller, S.3
Riethling, A.K.4
Uehleke, B.5
Drewelow, B.6
Pforte, H.7
Jacobasch, G.8
Derendorf, H.9
Veit, M.10
-
10
-
-
0242303641
-
Preparation and spectral investigation on inclusion complex of beta-cyclodextrin with rutin
-
Haiyun D., Jianbin C., Guomei Z., Shaomin S., and Jinhao P. Preparation and spectral investigation on inclusion complex of beta-cyclodextrin with rutin. Spectrochim. Acta A: Mol. Biomol. Spectrosc. 59 (2003) 3421-3429
-
(2003)
Spectrochim. Acta A: Mol. Biomol. Spectrosc.
, vol.59
, pp. 3421-3429
-
-
Haiyun, D.1
Jianbin, C.2
Guomei, Z.3
Shaomin, S.4
Jinhao, P.5
-
11
-
-
21844461846
-
Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine
-
Hecq J., Deleers M., Fanara D., Vranckx H., and Amighi K. Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine. Int. J. Pharm. 299 (2005) 167-177
-
(2005)
Int. J. Pharm.
, vol.299
, pp. 167-177
-
-
Hecq, J.1
Deleers, M.2
Fanara, D.3
Vranckx, H.4
Amighi, K.5
-
12
-
-
1842559836
-
Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs
-
Hu J., Johnston K.P., and Williams R.O. Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs. Drug Dev. Ind. Pharm. 30 (2004) 233-245
-
(2004)
Drug Dev. Ind. Pharm.
, vol.30
, pp. 233-245
-
-
Hu, J.1
Johnston, K.P.2
Williams, R.O.3
-
13
-
-
0029785036
-
Leg oedema protection from a buckwheat herb tea in patients with chronic venous insufficiency: a single-centre, randomised, double-blind, placebo-controlled clinical trial
-
Ihme N., Kiesewetter H., Jung F., Hoffmann K.H., Birk A., Muller A., and Grutzner K.I. Leg oedema protection from a buckwheat herb tea in patients with chronic venous insufficiency: a single-centre, randomised, double-blind, placebo-controlled clinical trial. Eur. J. Clin. Pharmacol. 50 (1996) 443-447
-
(1996)
Eur. J. Clin. Pharmacol.
, vol.50
, pp. 443-447
-
-
Ihme, N.1
Kiesewetter, H.2
Jung, F.3
Hoffmann, K.H.4
Birk, A.5
Muller, A.6
Grutzner, K.I.7
-
14
-
-
33344478634
-
Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs
-
Jinno J., Kamada N., Miyake M., Yamada K., Mukai T., Odomi M., Toguchi H., Liversidge G.G., Higaki K., and Kimura T. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J. Control Release 111 (2006) 56-64
-
(2006)
J. Control Release
, vol.111
, pp. 56-64
-
-
Jinno, J.1
Kamada, N.2
Miyake, M.3
Yamada, K.4
Mukai, T.5
Odomi, M.6
Toguchi, H.7
Liversidge, G.G.8
Higaki, K.9
Kimura, T.10
-
15
-
-
33846626309
-
In silico prediction of drug solubility in water-dioxane mixtures using the Jouyban-Acree model
-
Jouyban A. In silico prediction of drug solubility in water-dioxane mixtures using the Jouyban-Acree model. Pharmazie 62 (2007) 46-50
-
(2007)
Pharmazie
, vol.62
, pp. 46-50
-
-
Jouyban, A.1
-
16
-
-
33749475086
-
Dissolution enhancement of flavonoids by solid dispersion in PVP and PEG matrixes: a comparative study
-
Kanaze F.I., Kokkalou E., Niopas I., Georgarakis M., Stergiou A., and Bikiaris D. Dissolution enhancement of flavonoids by solid dispersion in PVP and PEG matrixes: a comparative study. J. Appl. Polym. Sci. 102 (2006) 460-471
-
(2006)
J. Appl. Polym. Sci.
, vol.102
, pp. 460-471
-
-
Kanaze, F.I.1
Kokkalou, E.2
Niopas, I.3
Georgarakis, M.4
Stergiou, A.5
Bikiaris, D.6
-
17
-
-
59349116244
-
-
Kipp, J. E., Wong, J. C. T., Doty, M. J., Rebbeck, C. L., 2003. Microprecipitation method for preparing submicron suspensions. United States Patent 6,607,784.
-
Kipp, J. E., Wong, J. C. T., Doty, M. J., Rebbeck, C. L., 2003. Microprecipitation method for preparing submicron suspensions. United States Patent 6,607,784.
-
-
-
-
18
-
-
59349106634
-
-
Kipp, J. E., Wong, J. C. T., Doty, M. J., Werling, J., Rebbeck, C. L., Brynjelsen, S., 2005. Method for preparing submicron particle suspensions. United States Patent 6,884,436.
-
Kipp, J. E., Wong, J. C. T., Doty, M. J., Werling, J., Rebbeck, C. L., Brynjelsen, S., 2005. Method for preparing submicron particle suspensions. United States Patent 6,884,436.
-
-
-
-
19
-
-
35348905544
-
Solubility of nanoparticles: nonextensive thermodynamics approach
-
Letellier P., Mayaffre A., and Turmine M. Solubility of nanoparticles: nonextensive thermodynamics approach. J. Phys.: Condens. Matter 19 (2007) 436229-436238
-
(2007)
J. Phys.: Condens. Matter
, vol.19
, pp. 436229-436238
-
-
Letellier, P.1
Mayaffre, A.2
Turmine, M.3
-
20
-
-
0032746334
-
Preparation and dissolution property of ipriflavone solid dispersion
-
Li Y.P., Zhang X.Y., Zhou J.J., and Pei Y.Y. Preparation and dissolution property of ipriflavone solid dispersion. Zhongguo Yao Li Xue Bao 20 (1999) 957-960
-
(1999)
Zhongguo Yao Li Xue Bao
, vol.20
, pp. 957-960
-
-
Li, Y.P.1
Zhang, X.Y.2
Zhou, J.J.3
Pei, Y.Y.4
-
21
-
-
0002510887
-
Avoiding investment in doomed drugs, is poor solubility an industry wide problem?
-
Lipinski C.A. Avoiding investment in doomed drugs, is poor solubility an industry wide problem?. Curr. Drug Dis. 1 (2001) 17-19
-
(2001)
Curr. Drug Dis.
, vol.1
, pp. 17-19
-
-
Lipinski, C.A.1
-
22
-
-
0036742053
-
Poor aqueous solubility-an industry wide problem in drug discovery
-
Lipinski C.A. Poor aqueous solubility-an industry wide problem in drug discovery. Am. Pharm. Rev. 5 (2002) 82-85
-
(2002)
Am. Pharm. Rev.
, vol.5
, pp. 82-85
-
-
Lipinski, C.A.1
-
23
-
-
59349107746
-
-
List, M., Sucker, H., 1988. Pharmaceutical colloidal hydrosols for injection. GB Patent 2,200,048.
-
List, M., Sucker, H., 1988. Pharmaceutical colloidal hydrosols for injection. GB Patent 2,200,048.
-
-
-
-
24
-
-
0028824401
-
Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats
-
Liversidge G.G., and Conzentino P. Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats. Int. J. Pharm. 125 (1995) 309-313
-
(1995)
Int. J. Pharm.
, vol.125
, pp. 309-313
-
-
Liversidge, G.G.1
Conzentino, P.2
-
25
-
-
0029080002
-
Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs.
-
Liversidge G.G., and Cundy K.C. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. Int. J. Pharm. 125 (1995) 91-97
-
(1995)
Int. J. Pharm.
, vol.125
, pp. 91-97
-
-
Liversidge, G.G.1
Cundy, K.C.2
-
26
-
-
59349095473
-
-
Liversidge, G.G., Cundy, K.C., Bishop, J. F., Czekai, D. A., 1992. Surface modified drug nanoparticles. United States Patent 5,145,684.
-
Liversidge, G.G., Cundy, K.C., Bishop, J. F., Czekai, D. A., 1992. Surface modified drug nanoparticles. United States Patent 5,145,684.
-
-
-
-
27
-
-
59349098536
-
-
Liversidge, G. G., Phillips, C. P., Cundy, K. C., 1994. Method to reduce particle size growth during lyophilization. United States Patent 5,302,401.
-
Liversidge, G. G., Phillips, C. P., Cundy, K. C., 1994. Method to reduce particle size growth during lyophilization. United States Patent 5,302,401.
-
-
-
-
28
-
-
11044221846
-
Role of Cyclodextrins in Improving Oral Drug Delivery
-
Loftsson T., Brewster M., and Másson M. Role of Cyclodextrins in Improving Oral Drug Delivery. Am. J. Drug. Deliv. 2 (2004) 261-275
-
(2004)
Am. J. Drug. Deliv.
, vol.2
, pp. 261-275
-
-
Loftsson, T.1
Brewster, M.2
Másson, M.3
-
29
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins 1. Drug solubilization and stabilization
-
Loftsson T., and Brewster M.E. Pharmaceutical applications of cyclodextrins 1. Drug solubilization and stabilization. J. Pharm. Sci. 85 (1996) 1017-1025
-
(1996)
J. Pharm. Sci.
, vol.85
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
30
-
-
0032562766
-
Quercetin is recovered in human plasma as conjugated derivatives which retain antioxidant properties
-
Manach C., Morand C., Crespy V., Demigné C., Texier O., Régérat F., and Rémésy C. Quercetin is recovered in human plasma as conjugated derivatives which retain antioxidant properties. FEBS Lett. 426 (1998) 331-336
-
(1998)
FEBS Lett.
, vol.426
, pp. 331-336
-
-
Manach, C.1
Morand, C.2
Crespy, V.3
Demigné, C.4
Texier, O.5
Régérat, F.6
Rémésy, C.7
-
31
-
-
0033637140
-
The effects of plant flavonoids on mammalian cells:implications for inflammation, heart disease, and cancer
-
Middleton E., Kandaswami C., and Theoharides T.C. The effects of plant flavonoids on mammalian cells:implications for inflammation, heart disease, and cancer. Pharm. Rev. 52 (2000) 673-751
-
(2000)
Pharm. Rev.
, vol.52
, pp. 673-751
-
-
Middleton, E.1
Kandaswami, C.2
Theoharides, T.C.3
-
32
-
-
34547874107
-
Drug nanocrystals of poorly soluble drugs
-
Nalwa H.S. (Ed), American Scientific Publishers
-
Müller R.H., and Akkar A. Drug nanocrystals of poorly soluble drugs. In: Nalwa H.S. (Ed). Encyclopedia of Nanoscience and Nanotechnology. (2004), American Scientific Publishers 627-638
-
(2004)
Encyclopedia of Nanoscience and Nanotechnology.
, pp. 627-638
-
-
Müller, R.H.1
Akkar, A.2
-
33
-
-
59349114918
-
-
Müller, R. H., Becker, R., Kruss, B., Peters, K., 1999. Pharmaceutical nanosuspensions for medicament administration as systems with increased saturation solubility and rate of solution. United States Patent 5,858,410.
-
Müller, R. H., Becker, R., Kruss, B., Peters, K., 1999. Pharmaceutical nanosuspensions for medicament administration as systems with increased saturation solubility and rate of solution. United States Patent 5,858,410.
-
-
-
-
34
-
-
0000451513
-
Emulsions and nanosuspensions for the formulation of poorly soluble drugs
-
Müller R.H., Benita S., and Böhm B. Emulsions and nanosuspensions for the formulation of poorly soluble drugs. Medpharm. Stuttgart (1998)
-
(1998)
Medpharm. Stuttgart
-
-
Müller, R.H.1
Benita, S.2
Böhm, B.3
-
35
-
-
0002819692
-
Nanosuspensions for the formulation of poorly soluble drugs
-
Nielloud F., and Marti-Mestres G. (Eds), Marcel Dekker
-
Müller R.H., Jacobs C., and Kayser O. Nanosuspensions for the formulation of poorly soluble drugs. In: Nielloud F., and Marti-Mestres G. (Eds). Pharmaceutical Emulsions and Suspensions. (2000), Marcel Dekker 383-407
-
(2000)
Pharmaceutical Emulsions and Suspensions.
, pp. 383-407
-
-
Müller, R.H.1
Jacobs, C.2
Kayser, O.3
-
36
-
-
0035937599
-
Nanosuspensions as particulate drug formulations in therapy: rationale for development and what we can expect for the future
-
Müller R.H., Jacobs C., and Kayser O. Nanosuspensions as particulate drug formulations in therapy: rationale for development and what we can expect for the future. Adv. Drug Deliv. Rev. 47 (2001) 3-19
-
(2001)
Adv. Drug Deliv. Rev.
, vol.47
, pp. 3-19
-
-
Müller, R.H.1
Jacobs, C.2
Kayser, O.3
-
37
-
-
6344237328
-
DissoCubes - a novel formulation for poorly soluble and poorly bioavailable drugs
-
Rathbone M.J., Hadgraft J., and Roberts M.S. (Eds), Marcel Dekker
-
Müller R.H., Jacobs C., and Kayser O. DissoCubes - a novel formulation for poorly soluble and poorly bioavailable drugs. In: Rathbone M.J., Hadgraft J., and Roberts M.S. (Eds). Modified-Release Drug Delivery Systems (2003), Marcel Dekker 135-149
-
(2003)
Modified-Release Drug Delivery Systems
, pp. 135-149
-
-
Müller, R.H.1
Jacobs, C.2
Kayser, O.3
-
39
-
-
59349109018
-
-
Müller, R. H., Mäder, K., Krause, K., 2000b. Verfahren zur schonenden Herstellung von hochfeinen Micro-/Nanopartikeln. PCT Application PCT/EP00/06535.
-
Müller, R. H., Mäder, K., Krause, K., 2000b. Verfahren zur schonenden Herstellung von hochfeinen Micro-/Nanopartikeln. PCT Application PCT/EP00/06535.
-
-
-
-
40
-
-
0029164807
-
-
22 nd International Symposium of Controlled Release of Bioactive Materials, Washington DC
-
Müller R.H., Peters K., Becker R., and Kruss B. Nanosuspensions for the i.v. administration of poorly soluble drugs-stability during sterilization and long-term storage (1995), 22 nd International Symposium of Controlled Release of Bioactive Materials, Washington DC 574-575
-
(1995)
Nanosuspensions for the i.v. administration of poorly soluble drugs-stability during sterilization and long-term storage
, pp. 574-575
-
-
Müller, R.H.1
Peters, K.2
Becker, R.3
Kruss, B.4
-
41
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes A.A., and 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
-
42
-
-
59349094289
-
-
O'Neil, M. J., 2006. The Merck index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 14th Edition. Merck.
-
O'Neil, M. J., 2006. The Merck index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 14th Edition. Merck.
-
-
-
-
43
-
-
0033402974
-
Evaluation of solubility parameter to predict apparent solubility of amorphous and crystalline cefditoren pivoxil
-
Ohta M., Oguch T., and Yamamoto K. Evaluation of solubility parameter to predict apparent solubility of amorphous and crystalline cefditoren pivoxil. Pharm. Acta Helv. 74 (1999) 59-64
-
(1999)
Pharm. Acta Helv.
, vol.74
, pp. 59-64
-
-
Ohta, M.1
Oguch, T.2
Yamamoto, K.3
-
44
-
-
0024839118
-
Influence of flavonoids on combined experimental infections with EMC virus and Staphylococcus aureus in mice
-
Panasiak W., Wleklik M., Oraczewska A., and Luczak M. Influence of flavonoids on combined experimental infections with EMC virus and Staphylococcus aureus in mice. Acta Microbiol. Pol. 38 (1989) 185-188
-
(1989)
Acta Microbiol. Pol.
, vol.38
, pp. 185-188
-
-
Panasiak, W.1
Wleklik, M.2
Oraczewska, A.3
Luczak, M.4
-
45
-
-
0017857869
-
Quantitative crystallinity determinations for beta-lactam antibiotics by solution calorimetry: correlations with stability
-
Pikal M.J., Lukes A.L., Lang J.E., and Gaines K. Quantitative crystallinity determinations for beta-lactam antibiotics by solution calorimetry: correlations with stability. J. Pharm. Sci. 67 (1978) 767-773
-
(1978)
J. Pharm. Sci.
, vol.67
, pp. 767-773
-
-
Pikal, M.J.1
Lukes, A.L.2
Lang, J.E.3
Gaines, K.4
-
46
-
-
0010259723
-
Nanopure™ pure drug nanoparticles for the formulation of porly soluble drugs
-
Radtke M. Nanopure™ pure drug nanoparticles for the formulation of porly soluble drugs. NewDrugs 3 (2001) 62-68
-
(2001)
NewDrugs
, vol.3
, pp. 62-68
-
-
Radtke, M.1
-
47
-
-
41949130280
-
Formulation of nanosuspensions of albendazole for oral administration
-
Rao M.Y., Kumar M., and Apte S. Formulation of nanosuspensions of albendazole for oral administration. Curr. Nanosci. 4 (2008) 53-58
-
(2008)
Curr. Nanosci.
, vol.4
, pp. 53-58
-
-
Rao, M.Y.1
Kumar, M.2
Apte, S.3
-
48
-
-
34447536520
-
When poor solubility becomes an issue: from early stage to proof of concept
-
Stegemann S., Leveiller F., Franchi D., de Jong H., and Linden H. When poor solubility becomes an issue: from early stage to proof of concept. Eur. J. Pharm. Sci. 31 (2007) 249-261
-
(2007)
Eur. J. Pharm. Sci.
, vol.31
, pp. 249-261
-
-
Stegemann, S.1
Leveiller, F.2
Franchi, D.3
de Jong, H.4
Linden, H.5
-
49
-
-
25444531236
-
Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of 4-chloro-3-nitrobenzoic acid and 2-chloro-5-nitrobenzoic acid solubilities with the Abraham solvation parameter model
-
Stovall D.M., Givens C., Keown S., Hoover K.R., Barnes R., Harris C., Lozano J., Nguyen M., Rodriguez E., Acree J.W.E., and Abraham M.H. Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of 4-chloro-3-nitrobenzoic acid and 2-chloro-5-nitrobenzoic acid solubilities with the Abraham solvation parameter model. Phys. Chem. Liq. 43 (2005) 351-360
-
(2005)
Phys. Chem. Liq.
, vol.43
, pp. 351-360
-
-
Stovall, D.M.1
Givens, C.2
Keown, S.3
Hoover, K.R.4
Barnes, R.5
Harris, C.6
Lozano, J.7
Nguyen, M.8
Rodriguez, E.9
Acree, J.W.E.10
Abraham, M.H.11
-
50
-
-
59349089729
-
-
Sucker, H., Gassmann, P., 1994. Improvements in pharmaceutical compositions. European Patent 0,580,690.
-
Sucker, H., Gassmann, P., 1994. Improvements in pharmaceutical compositions. European Patent 0,580,690.
-
-
-
-
51
-
-
33646275041
-
Rutin
-
Florey K. (Ed), Academic Press Inc., London
-
Taha I.K., Favid J.M., and Mahmoud M.A. Rutin. In: Florey K. (Ed). Analytical Profiles of Drug Substances (1983), Academic Press Inc., London 623-681
-
(1983)
Analytical Profiles of Drug Substances
, pp. 623-681
-
-
Taha, I.K.1
Favid, J.M.2
Mahmoud, M.A.3
-
52
-
-
59349116245
-
-
TCI, 2007. Strategies for bioavailability enhancement of poorly soluble or poorly permeable drugs. Technology Catalysts International (TCI), Falls Church.
-
TCI, 2007. Strategies for bioavailability enhancement of poorly soluble or poorly permeable drugs. Technology Catalysts International (TCI), Falls Church.
-
-
-
-
53
-
-
0025755129
-
Particle formation with supercritical fluids-a review
-
Tom J.W., and Debenedetti P.G. Particle formation with supercritical fluids-a review. J. Aerosol. Sci. 22 (1991) 555-584
-
(1991)
J. Aerosol. Sci.
, vol.22
, pp. 555-584
-
-
Tom, J.W.1
Debenedetti, P.G.2
-
54
-
-
32344452100
-
Preparation of hydrophobic drugs cyclodextrin complex by lyophilization monophase solution
-
Wang Z., Deng Y., Sun S., and Zhang X. Preparation of hydrophobic drugs cyclodextrin complex by lyophilization monophase solution. Drug. Dev. Ind. Pharm. 32 (2006) 73-83
-
(2006)
Drug. Dev. Ind. Pharm.
, vol.32
, pp. 73-83
-
-
Wang, Z.1
Deng, Y.2
Sun, S.3
Zhang, X.4
-
55
-
-
0032399926
-
A new understanding of the relationship between solubility and particle size
-
Wenju W., and Nancollas G.H. A new understanding of the relationship between solubility and particle size. J. Solution Chem. 27 (1998) 521-531
-
(1998)
J. Solution Chem.
, vol.27
, pp. 521-531
-
-
Wenju, W.1
Nancollas, G.H.2
-
56
-
-
36048934038
-
Preparation, physicochemical characterization, and antioxidant effects of quercetin nanoparticles
-
Wu T.H., Yen F.L., Lin L.T., Tsai T.R., Lin C.C., and Cham T.M. Preparation, physicochemical characterization, and antioxidant effects of quercetin nanoparticles. Int. J. Pharm. 346 (2008) 160-168
-
(2008)
Int. J. Pharm.
, vol.346
, pp. 160-168
-
-
Wu, T.H.1
Yen, F.L.2
Lin, L.T.3
Tsai, T.R.4
Lin, C.C.5
Cham, T.M.6
-
57
-
-
0033062735
-
Physicochemical properties of amorphous clarithromycin obtained by grinding and spray drying
-
Yonemochi E., Kitahara S., Maeda S., Yamamura S., Oguchi T., and Yamamoto K. Physicochemical properties of amorphous clarithromycin obtained by grinding and spray drying. Eur. J. Pharm. Sci. 7 (1999) 331-338
-
(1999)
Eur. J. Pharm. Sci.
, vol.7
, pp. 331-338
-
-
Yonemochi, E.1
Kitahara, S.2
Maeda, S.3
Yamamura, S.4
Oguchi, T.5
Yamamoto, K.6
-
58
-
-
0034042048
-
Rapid expansion from supercritical to aqueous solution to produce submicron suspensions of water-insoluble drugs
-
Young T.J., Mawson S., Johnston K.P., Henriksen I.B., Pace G.W., and Mishra A.K. Rapid expansion from supercritical to aqueous solution to produce submicron suspensions of water-insoluble drugs. Biotechnol. Prog. 16 (2000) 402-407
-
(2000)
Biotechnol. Prog.
, vol.16
, pp. 402-407
-
-
Young, T.J.1
Mawson, S.2
Johnston, K.P.3
Henriksen, I.B.4
Pace, G.W.5
Mishra, A.K.6
|