-
1
-
-
33750263327
-
Milk thistle: Silybum marianum
-
Pepping J. Milk thistle: silybum marianum. Am J Health Syst Pharm. 1999;56:1195-7.
-
(1999)
Am. J. Health Syst. Pharm.
, vol.56
, pp. 1195-1197
-
-
Pepping, J.1
-
2
-
-
0025645646
-
Pharmacokinetic studies on IdB 1016, a silybin-phosphatidylcholine complex, in healthy human subjects
-
Barzaghi N, Crema F, Gatti G, Pifferi G, Perucca E. Pharmacokinetic studies on IdB 1016, a silybin-phosphatidylcholine complex, in healthy human subjects. Eur J Drug Metab Pharmacokinet. 1990;15:333-8.
-
(1990)
Eur. J. Drug Metab. Pharmacokinet.
, vol.15
, pp. 333-338
-
-
Barzaghi, N.1
Crema, F.2
Gatti, G.3
Pifferi, G.4
Perucca, E.5
-
3
-
-
0026776782
-
Pharmacokinetics of silybin in bile following administration of silipide and silymarin in cholecystectomy patients
-
Schandalik R, Gatti G, Perucca E. Pharmacokinetics of silybin in bile following administration of silipide and silymarin in cholecystectomy patients. Arzneimittelforschung. 1992;42:964-8.
-
(1992)
Arzneimittelforschung
, vol.42
, pp. 964-968
-
-
Schandalik, R.1
Gatti, G.2
Perucca, E.3
-
4
-
-
33646844410
-
Optimized preparation of silymarin dripping pills by a central composite design-response surface method
-
Chen W, Xia H, Wu W. Optimized preparation of silymarin dripping pills by a central composite design-response surface method. Chin Trad Herb Drug. 2005;36:679-83.
-
(2005)
Chin. Trad Herb Drug
, vol.36
, pp. 679-683
-
-
Chen, W.1
Xia, H.2
Wu, W.3
-
5
-
-
33745891184
-
Preparation of silymarin proliposome: A new way to increase oral bioavailability of silymarin in beagle dogs
-
Xiao YY, Song YM, Chen ZP, Ping QN. Preparation of silymarin proliposome: a new way to increase oral bioavailability of silymarin in beagle dogs. Int J Pharm. 2006;319:162-8.
-
(2006)
Int. J. Pharm.
, vol.319
, pp. 162-168
-
-
Xiao, Y.Y.1
Song, Y.M.2
Chen, Z.P.3
Ping, Q.N.4
-
6
-
-
33846839082
-
Formulation and biopharmaceutical evaluation of silymarin using SMEDDS
-
Woo JS, Kim TS, Park JH, Chi SC. Formulation and biopharmaceutical evaluation of silymarin using SMEDDS. Arch Pharm Res. 2007;30:82-9.
-
(2007)
Arch. Pharm. Res.
, vol.30
, pp. 82-89
-
-
Woo, J.S.1
Kim, T.S.2
Park, J.H.3
Chi, S.C.4
-
7
-
-
33646854907
-
Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system
-
Wu W, Wang Y, Que L. Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system. Eur J Pharm Biopharm. 2006;63:288-94.
-
(2006)
Eur. J. Pharm. Biopharm.
, vol.63
, pp. 288-294
-
-
Wu, W.1
Wang, Y.2
Que, L.3
-
8
-
-
0026522216
-
Study on doselinearity of the pharmacokinetics of silibinin diastereomers using a new stereospecific assay
-
Weyhenmeyer R, Mascher H, Birkmayer J. Study on doselinearity of the pharmacokinetics of silibinin diastereomers using a new stereospecific assay. Int J Clin Pharmacol Ther Toxicol. 1992;30:134-8.
-
(1992)
Int. J. Clin. Pharmacol. Ther. Toxicol.
, vol.30
, pp. 134-138
-
-
Weyhenmeyer, R.1
Mascher, H.2
Birkmayer, J.3
-
9
-
-
0029123169
-
The solubility and bioequivalence of silymarin preparations
-
Schulz HU, Schurer M, Krumbiegel G, Wachter W, Weyhenmeyer R, Seidel G. The solubility and bioequivalence of silymarin preparations. Arzneimittelforschung. 1995;45:61-4.
-
(1995)
Arzneimittelforschung
, vol.45
, pp. 61-64
-
-
Schulz, H.U.1
Schurer, M.2
Krumbiegel, G.3
Wachter, W.4
Weyhenmeyer, R.5
Seidel, G.6
-
10
-
-
0343487750
-
Formulation of self-emulsifying drug delivery systems
-
Pouton CW. Formulation of self-emulsifying drug delivery systems. Adv Drug Deliv Rev. 1997;25:47-58.
-
(1997)
Adv. Drug Deliv. Rev.
, vol.25
, pp. 47-58
-
-
Pouton, C.W.1
-
11
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine
-
Khoo SM, Humberstone AJ, Porter C J H, Edwards GA, Charman WN. Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine. Int J Pharm. 1998;167:155-64.
-
(1998)
Int. J. Pharm.
, vol.167
, pp. 155-164
-
-
Khoo, S.M.1
Humberstone, A.J.2
Porter, C.J.H.3
Edwards, G.A.4
Charman, W.N.5
-
12
-
-
0343673791
-
Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone
-
Kim HJ, Yoon KA, Hahn M, Park ES, Chi SC. Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone. Drug Dev Ind Pharm. 2000;26:523-9.
-
(2000)
Drug Dev. Ind. Pharm.
, vol.26
, pp. 523-529
-
-
Kim, H.J.1
Yoon, K.A.2
Hahn, M.3
Park, E.S.4
Chi, S.C.5
-
13
-
-
0033805858
-
Lipid formulation for oral administration of drugs: Non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
-
Pouton CW. Lipid formulation for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems. Eur J Pharm Sci. 2000;11: S93-8.
-
(2000)
Eur. J. Pharm. Sci.
, vol.11
-
-
Pouton, C.W.1
-
14
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: Formulation development and bioavailability assessment
-
Kommuru TR, Gurley B, Khan MA, Reddy IK. Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment. Int J Pharm. 2001;212:233-46.
-
(2001)
Int. J. Pharm.
, vol.212
, pp. 233-246
-
-
Kommuru, T.R.1
Gurley, B.2
Khan, M.A.3
Reddy, I.K.4
-
15
-
-
0037057347
-
Improvement of physicochemical properties of N-4472 Part II: Characterization of N-4472 microemulsion and the enhanced oral absorption
-
Itoh K, Matsui S, Tozuka Y, Oguchi T, Yamamoto K. Improvement of physicochemical properties of N-4472 Part II: characterization of N-4472 microemulsion and the enhanced oral absorption. Int J Pharm. 2002;246:75-83.
-
(2002)
Int. J. Pharm.
, vol.246
, pp. 75-83
-
-
Itoh, K.1
Matsui, S.2
Tozuka, Y.3
Oguchi, T.4
Yamamoto, K.5
-
16
-
-
0041331755
-
Examination of oral absorption and lymphatic transport of halofantrine in triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides
-
Holm R, Porter C J H, Edwards GA, Müllertz A, Kristensen HG, Charman WN. Examination of oral absorption and lymphatic transport of halofantrine in triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides. Eur J Pharm Sci. 2003;20:91-7.
-
(2003)
Eur. J. Pharm. Sci.
, vol.20
, pp. 91-97
-
-
Holm, R.1
Porter, C.J.H.2
Edwards, G.A.3
Müllertz, A.4
Kristensen, H.G.5
Charman, W.N.6
-
17
-
-
33646813333
-
Bioavailability of seocalcitol II: Development and characterisation of selfmicroemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides
-
Grove M, Müllertz A, Nielsen JL, Pedersen GP. Bioavailability of seocalcitol II: development and characterisation of selfmicroemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides. Eur J Pharm Sci. 2006;28:233-42.
-
(2006)
Eur. J. Pharm. Sci.
, vol.28
, pp. 233-242
-
-
Grove, M.1
Müllertz, A.2
Nielsen, J.L.3
Pedersen, G.P.4
-
18
-
-
34447333390
-
Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems
-
Cirri M, Mura P, Corvi Mora P. Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems. Int J Pharm. 2007;340:84-91.
-
(2007)
Int. J. Pharm.
, vol.340
, pp. 84-91
-
-
Cirri, M.1
Mura, P.2
Mora, P.C.3
-
19
-
-
1842609789
-
Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs
-
Kang BK, Lee JS, Chon SK, Jeong SY, Yuk SH, Khang G et al. Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int J Pharm. 2004;274:65-73.
-
(2004)
Int. J. Pharm.
, vol.274
, pp. 65-73
-
-
Kang, B.K.1
Lee, J.S.2
Chon, S.K.3
Jeong, S.Y.4
Yuk, S.H.5
Khang, G.6
-
21
-
-
0028234686
-
Targeting lymphatic transport and modified systemic distribution of CI-976, a lipophilic lipid-regulator drug, via a formulation approach
-
Haus DJ, Mehta SC, Radebaugh GW. Targeting lymphatic transport and modified systemic distribution of CI-976, a lipophilic lipid-regulator drug, via a formulation approach. Int J Pharm. 1994;108:85-93.
-
(1994)
Int. J. Pharm.
, vol.108
, pp. 85-93
-
-
Haus, D.J.1
Mehta, S.C.2
Radebaugh, G.W.3
-
22
-
-
0342617694
-
Lipid-based vehicles for the oral delivery of poorly water soluble drugs
-
Humberstone AJ, Charman WN. Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv Drug Deliv Rev. 1997;25:103-28.
-
(1997)
Adv. Drug Deliv. Rev.
, vol.25
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
23
-
-
0035984949
-
Lipid-based formulations for intestinal lymphatic delivery
-
O'Driscoll CM. Lipid-based formulations for intestinal lymphatic delivery. Eur J Pharm Sci. 2002;15:405-15.
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 405-415
-
-
O'Driscoll, C.M.1
-
24
-
-
0346494420
-
Polymer-drug compatibility: A guide to the development of delivery systems for the anticancer agent, ellipticine
-
Liu JB, Xiao YH, Allen C. Polymer-drug compatibility: a guide to the development of delivery systems for the anticancer agent, ellipticine. J Pharm Sci. 2004;93:132-43.
-
(2004)
J. Pharm. Sci.
, vol.93
, pp. 132-143
-
-
Liu, J.B.1
Xiao, Y.H.2
Allen, C.3
-
25
-
-
0343375906
-
Micelles and X-rays
-
Philipoff W. Micelles and X-rays. J Colloid Sci. 1950;5:169-91.
-
(1950)
J. Colloid Sci.
, vol.5
, pp. 169-191
-
-
Philipoff, W.1
-
26
-
-
49749170869
-
The ultraviolet absorption spectrum as a criterion of the type of solubilization
-
Riegelman S, Allawala NA, Hrenoff MK, Srait LA. The ultraviolet absorption spectrum as a criterion of the type of solubilization. J Colloid Sci. 1958;13:208-17.
-
(1958)
J. Colloid Sci.
, vol.13
, pp. 208-217
-
-
Riegelman, S.1
Allawala, N.A.2
Hrenoff, M.K.3
Srait, L.A.4
-
27
-
-
0001765888
-
Properties of high-performance concrete containing shrinkage-reducing admixture
-
Folliad KJ, Berke NS. Properties of high-performance concrete containing shrinkage-reducing admixture. Cem Concr Res. 1997;27:1357-64.
-
(1997)
Cem Concr Res.
, vol.27
, pp. 1357-1364
-
-
Folliad, K.J.1
Berke, N.S.2
-
28
-
-
0034601204
-
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
-
Gershanik T, Benita S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. Eur J Pharm Biopharm. 2000;50:179-88.
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 179-188
-
-
Gershanik, T.1
Benita, S.2
-
29
-
-
10644266732
-
The absorption kinetics of silymarin microemulsion in rat intestine
-
Yuan Q, Li XR, Wang HJ, Li XY, Liu Y. The absorption kinetics of silymarin microemulsion in rat intestine. Acta Pharm Sin. 2004;39:631-4.
-
(2004)
Acta Pharm. Sin.
, vol.39
, pp. 631-634
-
-
Yuan, Q.1
Li, X.R.2
Wang, H.J.3
Li, X.Y.4
Liu, Y.5
-
30
-
-
0026191737
-
Transport of lipophilic molecules by the intestinal lymphatic system
-
Charman WN, Stella VJ. Transport of lipophilic molecules by the intestinal lymphatic system. Adv Drug Deliv Rev. 1991;7:1-14.
-
(1991)
Adv. Drug Deliv. Rev.
, vol.7
, pp. 1-14
-
-
Charman, W.N.1
Stella, V.J.2
-
31
-
-
15244353232
-
Effect of selfmicroemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells
-
Sha XY, Yan GJ, Wu YJ, Li JC, Fang XL. Effect of selfmicroemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells. Eur J Pharm Sci. 2005;24:477-86.
-
(2005)
Eur. J. Pharm. Sci.
, vol.24
, pp. 477-486
-
-
Sha, X.Y.1
Yan, G.J.2
Wu, Y.J.3
Li, J.C.4
Fang, X.L.5
|