-
1
-
-
34248535178
-
Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers
-
Ahuja, N., Katare, O.P., Singh, B., Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers. Eur. J. Pharm. Biopharm. 65 (2007), 26–38.
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.65
, pp. 26-38
-
-
Ahuja, N.1
Katare, O.P.2
Singh, B.3
-
2
-
-
75549091727
-
Evaluation of griseofulvin binary and ternary solid dispersions with HPMCAS
-
Al-Obaidi, H., Buckton, G., Evaluation of griseofulvin binary and ternary solid dispersions with HPMCAS. AAPS PharmSciTech 10 (2009), 1172–1177.
-
(2009)
AAPS PharmSciTech
, vol.10
, pp. 1172-1177
-
-
Al-Obaidi, H.1
Buckton, G.2
-
3
-
-
0030816152
-
Improvement of the biological performance of oral anticoagulant drugs. 1
-
Ammar, H., Ghorab, M., El-Nahhas, S., Makram, T., Improvement of the biological performance of oral anticoagulant drugs. 1. Warfarin. Die Pharmazie 52 (1997), 627–631.
-
(1997)
Warfarin. Die Pharmazie
, vol.52
, pp. 627-631
-
-
Ammar, H.1
Ghorab, M.2
El-Nahhas, S.3
Makram, T.4
-
4
-
-
77951498256
-
Characterization and stability of solid dispersions based on PEG/polymer blends
-
Bley, H., Fussnegger, B., Bodmeier, R., Characterization and stability of solid dispersions based on PEG/polymer blends. Int. J. Pharm. 390 (2010), 165–173.
-
(2010)
Int. J. Pharm.
, vol.390
, pp. 165-173
-
-
Bley, H.1
Fussnegger, B.2
Bodmeier, R.3
-
5
-
-
33745329492
-
Analytical techniques used to characterize drug-polyvinylpyrrolidone systems in solid and liquid states – an overview
-
Chadha, R., Kapoor, V., Kumar, A., Analytical techniques used to characterize drug-polyvinylpyrrolidone systems in solid and liquid states – an overview. J. Sci. Ind. Res., 65, 2006, 459.
-
(2006)
J. Sci. Ind. Res.
, vol.65
, pp. 459
-
-
Chadha, R.1
Kapoor, V.2
Kumar, A.3
-
6
-
-
84892687255
-
Development of novel fast-dissolving tacrolimus solid dispersion-loaded prolonged release tablet
-
Cho, J.H., Kim, Y.-I., Kim, D.-W., Yousaf, A.M., Kim, J.O., Woo, J.S., Yong, C.S., Choi, H.-G., Development of novel fast-dissolving tacrolimus solid dispersion-loaded prolonged release tablet. Eur. J. Pharm. Sci. 54 (2014), 1–7.
-
(2014)
Eur. J. Pharm. Sci.
, vol.54
, pp. 1-7
-
-
Cho, J.H.1
Kim, Y.-I.2
Kim, D.-W.3
Yousaf, A.M.4
Kim, J.O.5
Woo, J.S.6
Yong, C.S.7
Choi, H.-G.8
-
7
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
Craig, D.Q., The mechanisms of drug release from solid dispersions in water-soluble polymers. Int. J. Pharm. 231 (2002), 131–144.
-
(2002)
Int. J. Pharm.
, vol.231
, pp. 131-144
-
-
Craig, D.Q.1
-
8
-
-
84883716320
-
To evaluate the change in release from solid dispersion using sodium lauryl sulfate and model drug sulfathiazole
-
Dave, R.H., Patel, H.H., Donahue, E., Patel, A.D., To evaluate the change in release from solid dispersion using sodium lauryl sulfate and model drug sulfathiazole. Drug Dev. Ind. Pharm. 39 (2013), 1562–1572.
-
(2013)
Drug Dev. Ind. Pharm.
, vol.39
, pp. 1562-1572
-
-
Dave, R.H.1
Patel, H.H.2
Donahue, E.3
Patel, A.D.4
-
9
-
-
0006519197
-
Dissolution properties of praziquantel–PVP systems
-
El-Arini, S.K., Leuenberger, H., Dissolution properties of praziquantel–PVP systems. Pharm. Acta Helv. 73 (1998), 89–94.
-
(1998)
Pharm. Acta Helv.
, vol.73
, pp. 89-94
-
-
El-Arini, S.K.1
Leuenberger, H.2
-
10
-
-
0022650603
-
The current status of solid dispersions
-
Ford, J.L., The current status of solid dispersions. Pharm. Acta Helv. 61 (1985), 69–88.
-
(1985)
Pharm. Acta Helv.
, vol.61
, pp. 69-88
-
-
Ford, J.L.1
-
11
-
-
0035964448
-
Dissolution properties and anticonvulsant activity of phenytoin-polyethylene glycol 6000 and-polyvinylpyrrolidone K-30 solid dispersions
-
Franco, M., Trapani, G., Latrofa, A., Tullio, C., Provenzano, M., Serra, M., Muggironi, M., Biggio, G., Liso, G., Dissolution properties and anticonvulsant activity of phenytoin-polyethylene glycol 6000 and-polyvinylpyrrolidone K-30 solid dispersions. Int. J. Pharm. 225 (2001), 63–73.
-
(2001)
Int. J. Pharm.
, vol.225
, pp. 63-73
-
-
Franco, M.1
Trapani, G.2
Latrofa, A.3
Tullio, C.4
Provenzano, M.5
Serra, M.6
Muggironi, M.7
Biggio, G.8
Liso, G.9
-
12
-
-
31344476101
-
Dissolution rate improvement of poorly water-soluble drugs obtained by adsorbing solutions of drugs in hydrophilic solvents onto high surface area carriers
-
Friedrich, H., Fussnegger, B., Kolter, K., Bodmeier, R., Dissolution rate improvement of poorly water-soluble drugs obtained by adsorbing solutions of drugs in hydrophilic solvents onto high surface area carriers. Eur. J. Pharm. Biopharm. 62 (2006), 171–177.
-
(2006)
Eur. J. Pharm. Biopharm.
, vol.62
, pp. 171-177
-
-
Friedrich, H.1
Fussnegger, B.2
Kolter, K.3
Bodmeier, R.4
-
13
-
-
25444433702
-
Improvement of solubility and stability of poorly soluble drugs
-
Freie Univerisitat Berlin Berlin, Germany
-
Friedrich, H., Improvement of solubility and stability of poorly soluble drugs. Ph.D. Disseration, 2004, Freie Univerisitat Berlin, Berlin, Germany.
-
(2004)
Ph.D. Disseration
-
-
Friedrich, H.1
-
14
-
-
84863093376
-
Formulation and in-vitro-evaluation of isotretinoin tablets
-
Ghorab, M.M., Babiker, M.E.A., Formulation and in-vitro-evaluation of isotretinoin tablets. J. Chem. Pharm. Res. 4 (2012), 2817–2831.
-
(2012)
J. Chem. Pharm. Res.
, vol.4
, pp. 2817-2831
-
-
Ghorab, M.M.1
Babiker, M.E.A.2
-
15
-
-
1642546963
-
Homogentisic acid derivatives from Miliusa balansae
-
Huong, D.T., Kamperdick, C., Sung, T.V., Homogentisic acid derivatives from Miliusa balansae. J. Nat. Prod. 67 (2004), 445–447.
-
(2004)
J. Nat. Prod.
, vol.67
, pp. 445-447
-
-
Huong, D.T.1
Kamperdick, C.2
Sung, T.V.3
-
16
-
-
23844493377
-
A new flavone and cytotoxic activity of flavonoid constituents isolated from Miliusa balansae (Annonaceae)
-
Huong, D., Luong, D., Thao, T., Sung, T., A new flavone and cytotoxic activity of flavonoid constituents isolated from Miliusa balansae (Annonaceae). Pharmazie 60 (2005), 627–629.
-
(2005)
Pharmazie
, vol.60
, pp. 627-629
-
-
Huong, D.1
Luong, D.2
Thao, T.3
Sung, T.4
-
17
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner, C., Dressman, J., Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 50 (2000), 47–60.
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
18
-
-
84871549340
-
Solid dispersion of quercetin in cellulose derivative matrices influences both solubility and stability
-
Li, B., Konecke, S., Harich, K., Wegiel, L., Taylor, L.S., Edgar, K.J., Solid dispersion of quercetin in cellulose derivative matrices influences both solubility and stability. Carbohydr. Polym. 92 (2013), 2033–2040.
-
(2013)
Carbohydr. Polym.
, vol.92
, pp. 2033-2040
-
-
Li, B.1
Konecke, S.2
Harich, K.3
Wegiel, L.4
Taylor, L.S.5
Edgar, K.J.6
-
19
-
-
0029971327
-
Effect of particle size on the available surface area of nifedipine from nifedipine-polyethylene glycol 6000 solid dispersions
-
Lin, C.-W., Cham, T.-M., Effect of particle size on the available surface area of nifedipine from nifedipine-polyethylene glycol 6000 solid dispersions. Int. J. Pharm. 127 (1996), 261–272.
-
(1996)
Int. J. Pharm.
, vol.127
, pp. 261-272
-
-
Lin, C.-W.1
Cham, T.-M.2
-
20
-
-
28844465151
-
Characteristics of rofecoxib-polyethylene glycol 4000 solid dispersions and tablets based on solid dispersions
-
Liu, C., Desai, K.G.H., Characteristics of rofecoxib-polyethylene glycol 4000 solid dispersions and tablets based on solid dispersions. Pharm. Dev. Technol. 10 (2005), 467–477.
-
(2005)
Pharm. Dev. Technol.
, vol.10
, pp. 467-477
-
-
Liu, C.1
Desai, K.G.H.2
-
21
-
-
84942333290
-
Supercritical impregnation of polymer matrices spatially confined in microcontainers for oral drug delivery: effect of temperature, pressure and time
-
Marizza, P., Pontoni, L., Rindzevicius, T., Alopaeus, J., Su, K., Zeitler, J.A., Keller, S., Kikic, I., Moneghini, M., De Zordi, N., Supercritical impregnation of polymer matrices spatially confined in microcontainers for oral drug delivery: effect of temperature, pressure and time. J. Supercrit. Fluids 107 (2016), 145–152.
-
(2016)
J. Supercrit. Fluids
, vol.107
, pp. 145-152
-
-
Marizza, P.1
Pontoni, L.2
Rindzevicius, T.3
Alopaeus, J.4
Su, K.5
Zeitler, J.A.6
Keller, S.7
Kikic, I.8
Moneghini, M.9
De Zordi, N.10
-
22
-
-
34548270616
-
Preparation, characterization and in vivo evaluation of ibuprofen binary solid dispersions with poloxamer 188
-
Newa, M., Bhandari, K.H., Li, D.X., Kwon, T.-H., Kim, J.A., Yoo, B.K., Woo, J.S., Lyoo, W.S., Yong, C.S., Choi, H.G., Preparation, characterization and in vivo evaluation of ibuprofen binary solid dispersions with poloxamer 188. Int. J. Pharm. 343 (2007), 228–237.
-
(2007)
Int. J. Pharm.
, vol.343
, pp. 228-237
-
-
Newa, M.1
Bhandari, K.H.2
Li, D.X.3
Kwon, T.-H.4
Kim, J.A.5
Yoo, B.K.6
Woo, J.S.7
Lyoo, W.S.8
Yong, C.S.9
Choi, H.G.10
-
23
-
-
33745080296
-
Dissolution improvement of high drug-loaded solid dispersion
-
Okonogi, S., Puttipipatkhachorn, S., Dissolution improvement of high drug-loaded solid dispersion. AAPS PharmSciTech 7 (2006), E148–E153.
-
(2006)
AAPS PharmSciTech
, vol.7
, pp. E148-E153
-
-
Okonogi, S.1
Puttipipatkhachorn, S.2
-
24
-
-
0036166898
-
Preparation and characterisation of ibuprofen–poloxamer 188 granules obtained by melt granulation
-
Passerini, N., Albertini, B., González-Rodrı́guez, M.L., Cavallari, C., Rodriguez, L., Preparation and characterisation of ibuprofen–poloxamer 188 granules obtained by melt granulation. Eur. J. Pharm Sci. 15 (2002), 71–78.
-
(2002)
Eur. J. Pharm Sci.
, vol.15
, pp. 71-78
-
-
Passerini, N.1
Albertini, B.2
González-Rodrı́guez, M.L.3
Cavallari, C.4
Rodriguez, L.5
-
25
-
-
84884184043
-
HPMC as a potential enhancer of nimodipine biopharmaceutical properties via ball-milled solid dispersions
-
Riekes, M.K., Kuminek, G., Rauber, G.S., de Campos, C.E.M., Bortoluzzi, A.J., Stulzer, H.K., HPMC as a potential enhancer of nimodipine biopharmaceutical properties via ball-milled solid dispersions. Carbohydr. Polym. 99 (2014), 474–482.
-
(2014)
Carbohydr. Polym.
, vol.99
, pp. 474-482
-
-
Riekes, M.K.1
Kuminek, G.2
Rauber, G.S.3
de Campos, C.E.M.4
Bortoluzzi, A.J.5
Stulzer, H.K.6
-
26
-
-
0032692607
-
Antiviral flavonoid from Pterocaulon sphacelatum, an Australian aboring medicine
-
Semple, S.J., Nobbs, S.F., Pyke, S.M., Reynolds, G.D., Flower, R.L., Antiviral flavonoid from Pterocaulon sphacelatum, an Australian aboring medicine. J. Ethnolpharmacol. 68 (1999), 283–288.
-
(1999)
J. Ethnolpharmacol.
, vol.68
, pp. 283-288
-
-
Semple, S.J.1
Nobbs, S.F.2
Pyke, S.M.3
Reynolds, G.D.4
Flower, R.L.5
-
27
-
-
0037685267
-
The preparation of agglomerates containing solid dispersions of diazepam by melt agglomeration in a high shear mixer
-
Seo, A., Holm, P., Kristensen, H.G., Schæfer, T., The preparation of agglomerates containing solid dispersions of diazepam by melt agglomeration in a high shear mixer. Int. J. Pharm. 259 (2003), 161–171.
-
(2003)
Int. J. Pharm.
, vol.259
, pp. 161-171
-
-
Seo, A.1
Holm, P.2
Kristensen, H.G.3
Schæfer, T.4
-
28
-
-
0032885450
-
Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs
-
Serajuddin, A., Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J. Pharm. Sci. 88 (1999), 1058–1066.
-
(1999)
J. Pharm. Sci.
, vol.88
, pp. 1058-1066
-
-
Serajuddin, A.1
-
29
-
-
79951550017
-
Chrysosplenol C increases contraction in rat ventricular myocytes
-
Son, M.-J., Kim, H.K., Kim, Y.H., Van Sung, T., Cuong, N.M., Woo, S.-H., Chrysosplenol C increases contraction in rat ventricular myocytes. J. Cardiovasc. Pharmacol. 57 (2011), 259–262.
-
(2011)
J. Cardiovasc. Pharmacol.
, vol.57
, pp. 259-262
-
-
Son, M.-J.1
Kim, H.K.2
Kim, Y.H.3
Van Sung, T.4
Cuong, N.M.5
Woo, S.-H.6
-
30
-
-
84930625148
-
Preparation and characterization of solid dispersion using a novel amphiphilic copolymer to enhance dissolution and oral bioavailability of sorafenib
-
Truong, D.H., Tran, T.H., Ramasamy, T., Choi, J.Y., Choi, H.-G., Yong, C.S., Kim, J.O., Preparation and characterization of solid dispersion using a novel amphiphilic copolymer to enhance dissolution and oral bioavailability of sorafenib. Powder Technol. 283 (2015), 260–265.
-
(2015)
Powder Technol.
, vol.283
, pp. 260-265
-
-
Truong, D.H.1
Tran, T.H.2
Ramasamy, T.3
Choi, J.Y.4
Choi, H.-G.5
Yong, C.S.6
Kim, J.O.7
-
31
-
-
0022394475
-
Antiviral acitivity of natural occuring flavonoids in vitro
-
Tsuchiya, Y., Shimizu, M., Hiyama, Y., Itoh, K., Hashimoto, Y., Nakayama, M., Horie, T., Morita, N., Antiviral acitivity of natural occuring flavonoids in vitro. Chem. Pharm. Bull. (Tokyo) 33 (1985), 3881–3886.
-
(1985)
Chem. Pharm. Bull. (Tokyo)
, vol.33
, pp. 3881-3886
-
-
Tsuchiya, Y.1
Shimizu, M.2
Hiyama, Y.3
Itoh, K.4
Hashimoto, Y.5
Nakayama, M.6
Horie, T.7
Morita, N.8
-
32
-
-
9644254099
-
Solid dispersions of nimodipine and polyethylene glycol 2000: dissolution properties and physico-chemical characterisation
-
Urbanetz, N.A., Lippold, B.C., Solid dispersions of nimodipine and polyethylene glycol 2000: dissolution properties and physico-chemical characterisation. Eur. J. Pharm. Biopharm. 59 (2005), 107–118.
-
(2005)
Eur. J. Pharm. Biopharm.
, vol.59
, pp. 107-118
-
-
Urbanetz, N.A.1
Lippold, B.C.2
-
33
-
-
84936867849
-
Exploration of pharmacophore in chrysosplenol C as activator in ventricular myocyte contraction
-
Venkateswararao, E., Son, M.-J., Sharma, N., Manickam, M., Boggu, P., Kim, Y.H., Woo, S.-H., Jung, S.-H., Exploration of pharmacophore in chrysosplenol C as activator in ventricular myocyte contraction. ACS Med. Chem. Lett. 6 (2015), 758–763.
-
(2015)
ACS Med. Chem. Lett.
, vol.6
, pp. 758-763
-
-
Venkateswararao, E.1
Son, M.-J.2
Sharma, N.3
Manickam, M.4
Boggu, P.5
Kim, Y.H.6
Woo, S.-H.7
Jung, S.-H.8
-
34
-
-
67650178803
-
Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent
-
Wu, K., Li, J., Wang, W., Winstead, D.A., Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent. J. Pharm. Sci. 98 (2009), 2422–2431.
-
(2009)
J. Pharm. Sci.
, vol.98
, pp. 2422-2431
-
-
Wu, K.1
Li, J.2
Wang, W.3
Winstead, D.A.4
-
35
-
-
84655164813
-
Novel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changes
-
Yan, Y.-D., Sung, J.H., Kim, K.K., Kim, D.W., Kim, J.O., Lee, B.-J., Yong, C.S., Choi, H.-G., Novel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changes. Int. J. Pharm. 422 (2012), 202–210.
-
(2012)
Int. J. Pharm.
, vol.422
, pp. 202-210
-
-
Yan, Y.-D.1
Sung, J.H.2
Kim, K.K.3
Kim, D.W.4
Kim, J.O.5
Lee, B.-J.6
Yong, C.S.7
Choi, H.-G.8
|