-
1
-
-
6944253961
-
Transformation of ginseng saponins to ginsenoside Rh2 by acids and human intestinal bacteria and biological activities of their transformants
-
Bae EA, Han MJ, Kim EJ, Kim DH. Transformation of ginseng saponins to ginsenoside Rh2 by acids and human intestinal bacteria and biological activities of their transformants. Arch Pharm Res. 2004;27(1):61-67.
-
(2004)
Arch Pharm Res
, vol.27
, Issue.1
, pp. 61-67
-
-
Bae, E.A.1
Han, M.J.2
Kim, E.J.3
Kim, D.H.4
-
2
-
-
0042526129
-
Degradation of ginsenosides in humans after oral administration
-
Tawab MA, Bahr U, Karas M, Wurglics M, Schubert-Zsilavecz M. Degradation of ginsenosides in humans after oral administration. Drug Metab Dispos. 2003;31(8):1065-1071.
-
(2003)
Drug Metab Dispos
, vol.31
, Issue.8
, pp. 1065-1071
-
-
Tawab, M.A.1
Bahr, U.2
Karas, M.3
Wurglics, M.4
Schubert-Zsilavecz, M.5
-
3
-
-
20044364935
-
High performance liquid chromatographic-mass spectrometric determination of ginsenoside Rg3 and its metabolites in rat plasma using solid-phase extraction for pharmacokinetic studies
-
Xie HT, Wang GJ, Sun JG, et al. High performance liquid chromatographic-mass spectrometric determination of ginsenoside Rg3 and its metabolites in rat plasma using solid-phase extraction for pharmacokinetic studies. J Chromatogr B Analyt Technol Biomed Life Sci. 2005;818(2):167-173.
-
(2005)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.818
, Issue.2
, pp. 167-173
-
-
Xie, H.T.1
Wang, G.J.2
Sun, J.G.3
-
4
-
-
84555188034
-
The in vitro structure-related anti-cancer activity of ginsenosides and their derivatives
-
Dong H, Bai LP, Wong VK, et al. The in vitro structure-related anti-cancer activity of ginsenosides and their derivatives. Molecules. 2011;16(12):10619-10630.
-
(2011)
Molecules
, vol.16
, Issue.12
, pp. 10619-10630
-
-
Dong, H.1
Bai, L.P.2
Wong, V.K.3
-
5
-
-
33646734515
-
Ginsenoside 20(S)-protopanaxadiol inhibits the proliferation and invasion of human fibrosarcoma HT1080 cells
-
Li G, Wang Z, Sun Y, Liu K, Wang Z. Ginsenoside 20(S)-protopanaxadiol inhibits the proliferation and invasion of human fibrosarcoma HT1080 cells. Basic Clin Pharmacol Toxicol. 2006;98(6):588-592.
-
(2006)
Basic Clin Pharmacol Toxicol
, vol.98
, Issue.6
, pp. 588-592
-
-
Li, G.1
Wang, Z.2
Sun, Y.3
Liu, K.4
Wang, Z.5
-
6
-
-
33947394746
-
20S-protopanaxadiol-induced programmed cell death in glioma cells through caspase-dependent and -independent pathways
-
Liu GY, Bu X, Yan H, Jia WW. 20S-protopanaxadiol-induced programmed cell death in glioma cells through caspase-dependent and -independent pathways. J Nat Prod. 2007;70(2):259-264.
-
(2007)
J Nat Prod
, vol.70
, Issue.2
, pp. 259-264
-
-
Liu, G.Y.1
Bu, X.2
Yan, H.3
Jia, W.W.4
-
7
-
-
80052064898
-
20(S)-Protopanaxadiol, a metabolite of ginsenosides, induced cell apoptosis through endoplasmic reticulum stress in human hepatocarcinoma HepG2 cells
-
Zhu GY, Li YW, Tse AK, et al. 20(S)-Protopanaxadiol, a metabolite of ginsenosides, induced cell apoptosis through endoplasmic reticulum stress in human hepatocarcinoma HepG2 cells. Eur J Pharmacol. 2011;668(1-2):88-98.
-
(2011)
Eur J Pharmacol
, vol.668
, Issue.1-2
, pp. 88-98
-
-
Zhu, G.Y.1
Li, Y.W.2
Tse, A.K.3
-
8
-
-
0036403187
-
Structure-function relationship exists for ginsenosides in reducing cell proliferation and inducing apoptosis in the human leukemia (THP-1) cell line
-
Popovich DG, Kitts DD. Structure-function relationship exists for ginsenosides in reducing cell proliferation and inducing apoptosis in the human leukemia (THP-1) cell line. Arch Biochem Biophys. 2002;406(1): 1-8.
-
(2002)
Arch Biochem Biophys
, vol.406
, Issue.1
, pp. 1-8
-
-
Popovich, D.G.1
Kitts, D.D.2
-
9
-
-
42249110033
-
20(S)-protopanaxadiol and 20(S)-protopanaxatriol as antiangiogenic agents and total assignment of 1H NMR spectra
-
Usami Y, Liu YN, Lin AS, et al. 20(S)-protopanaxadiol and 20(S)-protopanaxatriol as antiangiogenic agents and total assignment of 1H NMR spectra. J Nat Prod. 2008;71(3):478-481.
-
(2008)
J Nat Prod
, vol.71
, Issue.3
, pp. 478-481
-
-
Usami, Y.1
Liu, Y.N.2
Lin, A.S.3
-
10
-
-
33847104559
-
In vitro anti-cancer activity and structure-activity relationships of natural products isolated from fruits of Panax ginseng
-
Wang W, Zhao Y, Rayburn ER, Hill DL, Wang H, Zhang R. In vitro anti-cancer activity and structure-activity relationships of natural products isolated from fruits of Panax ginseng. Cancer Chemother Pharmacol. 2007;59(5):589-601.
-
(2007)
Cancer Chemother Pharmacol
, vol.59
, Issue.5
, pp. 589-601
-
-
Wang, W.1
Zhao, Y.2
Rayburn, E.R.3
Hill, D.L.4
Wang, H.5
Zhang, R.6
-
11
-
-
34249008148
-
Antiestrogenic effect of 20S-protopanax-adiol and its synergy with tamoxifen on breast cancer cells
-
Yu Y, Zhou O, Hang Y, Bu X, Jia W. Antiestrogenic effect of 20S-protopanax-adiol and its synergy with tamoxifen on breast cancer cells. Cancer. 2007;109(11):2374-2382.
-
(2007)
Cancer
, vol.109
, Issue.11
, pp. 2374-2382
-
-
Yu, Y.1
Zhou, O.2
Hang, Y.3
Bu, X.4
Jia, W.5
-
12
-
-
79951933277
-
Identification of 20(S)-protopanaxadiol metabolites in human liver microsomes and human hepatocytes
-
Li L, Chen X, Li D, Zhong D. Identification of 20(S)-protopanaxadiol metabolites in human liver microsomes and human hepatocytes. Drug Metab Dispos. 2011;39(3):472-483.
-
(2011)
Drug Metab Dispos
, vol.39
, Issue.3
, pp. 472-483
-
-
Li, L.1
Chen, X.2
Li, D.3
Zhong, D.4
-
13
-
-
77955739067
-
Development of a UPLC-ESI-MS/MS assay for 20(S)-Protopanaxadiol and pharmacokinetic application of its two formulations in rats
-
Han MH, Chen J, Chen S, Wang X. Development of a UPLC-ESI-MS/MS assay for 20(S)-Protopanaxadiol and pharmacokinetic application of its two formulations in rats. Anal Sci. 2010;26(7):749-753.
-
(2010)
Anal Sci
, vol.26
, Issue.7
, pp. 749-753
-
-
Han, M.H.1
Chen, J.2
Chen, S.3
Wang, X.4
-
14
-
-
78649647329
-
Controlled crystallization of the lipophilic drug fenofibrate during freeze-drying: Elucidation of the mechanism by in-line raman spectroscopy
-
de Waard H, De Beer T, Hinrichs WL, Vervaet C, Remon JP, Frijlink HW. Controlled crystallization of the lipophilic drug fenofibrate during freeze-drying: elucidation of the mechanism by in-line raman spectroscopy. APPS J. 2010;12(4):569-575.
-
(2010)
APPS J
, vol.12
, Issue.4
, pp. 569-575
-
-
de Waard, H.1
de Beer, T.2
Hinrichs, W.L.3
Vervaet, C.4
Remon, J.P.5
Frijlink, H.W.6
-
15
-
-
77951189574
-
Pharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticles
-
Lai J, Lu Y, Yin Z, Hu F, Wu W. Pharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticles. Int J Nanomedicine. 2010;5:13-23.
-
(2010)
Int J Nanomedicine
, vol.5
, pp. 13-23
-
-
Lai, J.1
Lu, Y.2
Yin, Z.3
Hu, F.4
Wu, W.5
-
17
-
-
78649629451
-
Lyotropic liquid crystal systems in drug delivery
-
Guo C, Wang J, Cao F, Lee RJ, Zhai G. Lyotropic liquid crystal systems in drug delivery. Drug Discov Today. 2010;15(23-24):1032-1040.
-
(2010)
Drug Discov Today
, vol.15
, Issue.23-24
, pp. 1032-1040
-
-
Guo, C.1
Wang, J.2
Cao, F.3
Lee, R.J.4
Zhai, G.5
-
18
-
-
84870367372
-
Lipid-based liquid crystalline nanoparticles as oral drug delivery vehicles for poorly water-soluble drugs: Cellular interaction and in vivo absorption
-
Zeng N, Gao X, Hu Q, et al. Lipid-based liquid crystalline nanoparticles as oral drug delivery vehicles for poorly water-soluble drugs: cellular interaction and in vivo absorption. Int J Nanomed. 2012;7:3703-3718.
-
(2012)
Int J Nanomed
, vol.7
, pp. 3703-3718
-
-
Zeng, N.1
Gao, X.2
Hu, Q.3
-
19
-
-
0037026284
-
Preparation and structural investigations of colloidal dispersions prepared from cubic monoglyceride-water phases
-
Siekmann B, Bunjes H, Koch MH, Westesen K. Preparation and structural investigations of colloidal dispersions prepared from cubic monoglyceride-water phases. Int J Pharm. 2002;244(1-2):33-43.
-
(2002)
Int J Pharm
, vol.244
, Issue.1-2
, pp. 33-43
-
-
Siekmann, B.1
Bunjes, H.2
Koch, M.H.3
Westesen, K.4
-
20
-
-
0347300807
-
Lipid-based supramolecular systems for topical application: A preformulatory study
-
Esposito E, Eblovi N, Rasi S, et al. Lipid-based supramolecular systems for topical application: a preformulatory study. AAPS Pharm Sci. 2003;5(4):E30.
-
(2003)
AAPS Pharm Sci
, vol.5
, Issue.4
-
-
Esposito, E.1
Eblovi, N.2
Rasi, S.3
-
21
-
-
67349089022
-
Chemopreventive potential of piperine in 7,12-dimethylbenz[a]anthracene-induced skin carcinogenesis in Swiss albino mice
-
Vellaichamy L, Balakrishnan S, Panjamurthy K, Manoharan S, Alias LM. Chemopreventive potential of piperine in 7,12-dimethylbenz[a]anthracene-induced skin carcinogenesis in Swiss albino mice. Environ Toxicol Pharmacol. 2009;28(1):11-18.
-
(2009)
Environ Toxicol Pharmacol
, vol.28
, Issue.1
, pp. 11-18
-
-
Vellaichamy, L.1
Balakrishnan, S.2
Panjamurthy, K.3
Manoharan, S.4
Alias, L.M.5
-
22
-
-
8644238077
-
Piperine is a potent inhibitor of nuclear factor-kappaB (NF-kappaB), c-Fos, CREB, ATF-2 and proinflammatory cytokine gene expression in B16F-10 melanoma cells
-
Pradeep CR, Kuttan G. Piperine is a potent inhibitor of nuclear factor-kappaB (NF-kappaB), c-Fos, CREB, ATF-2 and proinflammatory cytokine gene expression in B16F-10 melanoma cells. Int Immunopharmacol. 2004;4(14):1795-1803.
-
(2004)
Int Immunopharmacol
, vol.4
, Issue.14
, pp. 1795-1803
-
-
Pradeep, C.R.1
Kuttan, G.2
-
23
-
-
79954645941
-
Suppression of phorbol-12-myristate-13-acetate-induced tumor cell invasion by piperine via the inhibition of PKCα/ERK1/2-dependent matrix metalloproteinase-9 expression
-
Hwang YP, Yun HJ, Kim HG, et al. Suppression of phorbol-12-myristate-13-acetate-induced tumor cell invasion by piperine via the inhibition of PKCα/ERK1/2-dependent matrix metalloproteinase-9 expression. Toxicol Lett. 2011;203(1):9-19.
-
(2011)
Toxicol Lett
, vol.203
, Issue.1
, pp. 9-19
-
-
Hwang, Y.P.1
Yun, H.J.2
Kim, H.G.3
-
24
-
-
0036070626
-
Piperine, a major constituent of black pepper, inhibits human P-glycoprotein and CYP3A4
-
Bhardwaj RK, Glaeser H, Becquemont L, Klotz U, Gupta SK, Fromm MF. Piperine, a major constituent of black pepper, inhibits human P-glycoprotein and CYP3A4. J Pharmacol Exp Ther. 2002;302(2): 645-650.
-
(2002)
J Pharmacol Exp Ther
, vol.302
, Issue.2
, pp. 645-650
-
-
Bhardwaj, R.K.1
Glaeser, H.2
Becquemont, L.3
Klotz, U.4
Gupta, S.K.5
Fromm, M.F.6
-
25
-
-
47949101818
-
Curcuminoids inhibit multiple human cytochromes P450, UDP-glucuronosyltransferase,andsulfotransferase enzymes, whereas piperine is a relatively selective CYP3A4 inhibitor
-
Volak LP, Ghirmai S, Cashman JR, Court MH. Curcuminoids inhibit multiple human cytochromes P450, UDP-glucuronosyltransferase,andsulfotransferase enzymes, whereas piperine is a relatively selective CYP3A4 inhibitor. Drug Metab Dispos. 2008;36(8):1594-1605.
-
(2008)
Drug Metab Dispos
, vol.36
, Issue.8
, pp. 1594-1605
-
-
Volak, L.P.1
Ghirmai, S.2
Cashman, J.R.3
Court, M.H.4
-
26
-
-
0028796713
-
Characterisation of a newly isolated Caco-2 clone (TC-7), as a model of transport processes and biotransformation of drugs
-
Caro I, Boulenc X, Rousset M, et al. Characterisation of a newly isolated Caco-2 clone (TC-7), as a model of transport processes and biotransformation of drugs. Int J Pharm. 1995;116(2):147-158.
-
(1995)
Int J Pharm
, vol.116
, Issue.2
, pp. 147-158
-
-
Caro, I.1
Boulenc, X.2
Rousset, M.3
-
27
-
-
0037371414
-
Metabolism of flavonoids via entericrecycling: Role of intestinal disposition
-
Chen J, Lin H, Hu M. Metabolism of flavonoids via entericrecycling: role of intestinal disposition. J Pharmacol Exp Ther. 2003;304(3):1228-1235.
-
(2003)
J Pharmacol Exp Ther
, vol.304
, Issue.3
, pp. 1228-1235
-
-
Chen, J.1
Lin, H.2
Hu, M.3
-
28
-
-
4243139494
-
Disposition of flavonoids via enteric recycling: Enzyme-transporter coupling affects metabolism of biochanin A and formononetin and excretion of their phase II conjugates
-
Jia XB, Chen J, Lin H, Hu M. Disposition of flavonoids via enteric recycling: enzyme-transporter coupling affects metabolism of biochanin A and formononetin and excretion of their phase II conjugates. J Pharmacol Exp Ther. 2004;310(3):1103-1113.
-
(2004)
J Pharmacol Exp Ther
, vol.310
, Issue.3
, pp. 1103-1113
-
-
Jia, X.B.1
Chen, J.2
Lin, H.3
Hu, M.4
-
29
-
-
84870387426
-
Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: In vitro and in vivo studies
-
Lv LZ, Tong CQ, Lv Q, et al. Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies. Int J Nanomedicine. 2012;7:4099-4107.
-
(2012)
Int J Nanomedicine
, vol.7
, pp. 4099-4107
-
-
Lv, L.Z.1
Tong, C.Q.2
Lv, Q.3
-
30
-
-
84870342662
-
Uptake and transport of a novel anticancer drug-delivery system: Lactosyl-norcantharidin-associated N-trimethyl chitosan nanoparticles across intestinal Caco-2 cell monolayers
-
Guan M, Zhu QL, Liu Y, et al. Uptake and transport of a novel anticancer drug-delivery system: lactosyl-norcantharidin-associated N-trimethyl chitosan nanoparticles across intestinal Caco-2 cell monolayers. Int J Nanomedicine. 2012;7:1921-1930.
-
(2012)
Int J Nanomedicine
, vol.7
, pp. 1921-1930
-
-
Guan, M.1
Zhu, Q.L.2
Liu, Y.3
-
31
-
-
77955049646
-
Self-assembled liquid crystalline nanoparticles as a novel ophthalmic delivery system for dexamethasone: Improving preocular retention and ocular bioavailability
-
Gan L, Han S, Shen J, et al. Self-assembled liquid crystalline nanoparticles as a novel ophthalmic delivery system for dexamethasone: Improving preocular retention and ocular bioavailability. Int J Pharm. 2010;396:179-187.
-
(2010)
Int J Pharm
, vol.396
, pp. 179-187
-
-
Gan, L.1
Han, S.2
Shen, J.3
-
32
-
-
84867883989
-
Functionalized carbon nanomaterials: Exploring the interactions with Caco-2 cells for potential oral drug delivery
-
Coyuco JC, Liu Y, Tan BJ, Chiu GN. Functionalized carbon nanomaterials: exploring the interactions with Caco-2 cells for potential oral drug delivery. Int J Nanomedicine. 2011;6:2253-2263.
-
(2011)
Int J Nanomedicine
, vol.6
, pp. 2253-2263
-
-
Coyuco, J.C.1
Liu, Y.2
Tan, B.J.3
Chiu, G.N.4
-
33
-
-
79551514621
-
Identification of permeability-related hurdles in oral delivery of curcumin using the Caco-2 cell model
-
Wahlang B, Pawar YB, Bansal AK. Identification of permeability-related hurdles in oral delivery of curcumin using the Caco-2 cell model. Eur J Pharm Biopharm. 2011;77(2):275-282.
-
(2011)
Eur J Pharm Biopharm
, vol.77
, Issue.2
, pp. 275-282
-
-
Wahlang, B.1
Pawar, Y.B.2
Bansal, A.K.3
-
34
-
-
79960078025
-
Nanostructured liquid crystalline particles provide long duration sustained-release effect for a poorly water soluble drug after oral administration
-
Nguyen TH, Hanley T, Porter CJ, Boyd BJ. Nanostructured liquid crystalline particles provide long duration sustained-release effect for a poorly water soluble drug after oral administration. J Control Release. 2011;153(2):180-186.
-
(2011)
J Control Release
, vol.153
, Issue.2
, pp. 180-186
-
-
Nguyen, T.H.1
Hanley, T.2
Porter, C.J.3
Boyd, B.J.4
-
35
-
-
34447265979
-
A lipid-based liquid crystalline matrix that provides sustained release and enhanced oral bioavailability for a model poorly water soluble drug in rats
-
Boyd BJ, Khoo SM, Whittaker DV, Davey G, Porter CJ. A lipid-based liquid crystalline matrix that provides sustained release and enhanced oral bioavailability for a model poorly water soluble drug in rats. Int J Pharm. 2007;340(1-2):52-60.
-
(2007)
Int J Pharm
, vol.340
, Issue.1-2
, pp. 52-60
-
-
Boyd, B.J.1
Khoo, S.M.2
Whittaker, D.V.3
Davey, G.4
Porter, C.J.5
-
36
-
-
0031372220
-
Submicron particles of reversed lipid phases in water stabilized by a nonionic amphiphilic polymer
-
Gustafsson J, Ljusberg-Wahren H, Almgren M, Larsson K. Submicron particles of reversed lipid phases in water stabilized by a nonionic amphiphilic polymer. Langmuir. 1997;13(26):6964-6971.
-
(1997)
Langmuir
, vol.13
, Issue.26
, pp. 6964-6971
-
-
Gustafsson, J.1
Ljusberg-Wahren, H.2
Almgren, M.3
Larsson, K.4
-
37
-
-
57149105903
-
Evaluation of nanosuspensions for absorption enhancement of poorly soluble drugs: In vitro transport studies across intestinal epithelial monolayers
-
Lenhardt T, Vergnault G, Grenier P, Scherer D, Langguth P. Evaluation of nanosuspensions for absorption enhancement of poorly soluble drugs: in vitro transport studies across intestinal epithelial monolayers. APPS J. 2008;10(3):435-438.
-
(2008)
APPS J
, vol.10
, Issue.3
, pp. 435-438
-
-
Lenhardt, T.1
Vergnault, G.2
Grenier, P.3
Scherer, D.4
Langguth, P.5
-
38
-
-
0027142277
-
Lipid absorption: Passing through the unstirred layers, brush-border membrane, and beyond
-
Thomson AB, Schoeller C, Keelan M, Smith L, Clandinin MT. Lipid absorption: passing through the unstirred layers, brush-border membrane, and beyond. Can J Physiol Pharmacol. 1993;71(8):531-555.
-
(1993)
Can J Physiol Pharmacol
, vol.71
, Issue.8
, pp. 531-555
-
-
Thomson, A.B.1
Schoeller, C.2
Keelan, M.3
Smith, L.4
Clandinin, M.T.5
-
39
-
-
52949093858
-
An evaluation of the relative roles of the unstirred water layer and receptor sink in limiting the in-vitro intestinal permeability of drug compounds of varying lipophilicity
-
Katneni K, Charman SA, Porter CJ. An evaluation of the relative roles of the unstirred water layer and receptor sink in limiting the in-vitro intestinal permeability of drug compounds of varying lipophilicity. J Pharm Pharmacol. 2008;60(10):1311-1319.
-
(2008)
J Pharm Pharmacol
, vol.60
, Issue.10
, pp. 1311-1319
-
-
Katneni, K.1
Charman, S.A.2
Porter, C.J.3
-
40
-
-
71649100500
-
Analysis of unstirred water layer in in vitro permeability experiments
-
Korjamo T, Heikkinen AT, Mönkkönen J. Analysis of unstirred water layer in in vitro permeability experiments. J Pharm Sci. 2009;98(12): 4469-4479.
-
(2009)
J Pharm Sci
, vol.98
, Issue.12
, pp. 4469-4479
-
-
Korjamo, T.1
Heikkinen, A.T.2
Mönkkönen, J.3
-
41
-
-
33646581362
-
Detailed structure of diamond-type lipid cubic nanoparticles
-
Angelov B, Angelova A, Papahadjopoulos-Sternberg B, et al. Detailed structure of diamond-type lipid cubic nanoparticles. J Am Chem Soc. 2006;128(17):5813-5817.
-
(2006)
J Am Chem Soc
, vol.128
, Issue.17
, pp. 5813-5817
-
-
Angelov, B.1
Angelova, A.2
Papahadjopoulos-Sternberg, B.3
-
42
-
-
18544366270
-
Proteocubosomes: Nanoporous vehicles with tertiary organized fluid interfaces
-
Angelova A, Angelov B, Papahadjopoulos-Sternberg B, Ollivon M, Bourgaux C. Proteocubosomes: nanoporous vehicles with tertiary organized fluid interfaces. Langmuir. 2005;21(9):4138-4143.
-
(2005)
Langmuir
, vol.21
, Issue.9
, pp. 4138-4143
-
-
Angelova, A.1
Angelov, B.2
Papahadjopoulos-Sternberg, B.3
Ollivon, M.4
Bourgaux, C.5
-
43
-
-
84863607199
-
Protein-containing PEGylated cubosomic particles: Freeze-fracture electron microscopy and synchrotron radiation circular dichroism study
-
Angelov B, Angelova A, Papahadjopoulos-Sternberg B, Hoffmann SV, Nicolas V, Lesieur S. Protein-containing PEGylated cubosomic particles: Freeze-fracture electron microscopy and synchrotron radiation circular dichroism study. J Phys Chem B. 2012;116(26):7676-7686.
-
(2012)
J Phys Chem B
, vol.116
, Issue.26
, pp. 7676-7686
-
-
Angelov, B.1
Angelova, A.2
Papahadjopoulos-Sternberg, B.3
Hoffmann, S.V.4
Nicolas, V.5
Lesieur, S.6
-
44
-
-
79951487610
-
SAXS investigation of a cubic to a sponge (L3) phase transition in self-assembled lipid nanocarriers
-
Angelov B, Angelova A, Mutafchieva R, et al. SAXS investigation of a cubic to a sponge (L3) phase transition in self-assembled lipid nanocarriers. Phys Chem Chem Phys. 2011;13(8):3073-3081.
-
(2011)
Phys Chem Chem Phys
, vol.13
, Issue.8
, pp. 3073-3081
-
-
Angelov, B.1
Angelova, A.2
Mutafchieva, R.3
-
45
-
-
79951665122
-
Self-assembled multicompartment liquid crystalline lipid carriers for protein, peptide, and nucleic acid drug delivery
-
Angelova A, Angelov B, Mutafchieva R, Lesieur S, Couvreur P. Self-assembled multicompartment liquid crystalline lipid carriers for protein, peptide, and nucleic acid drug delivery. Acc Chem Res. 2011;44(2):147-156.
-
(2011)
Acc Chem Res
, vol.44
, Issue.2
, pp. 147-156
-
-
Angelova, A.1
Angelov, B.2
Mutafchieva, R.3
Lesieur, S.4
Couvreur, P.5
-
46
-
-
0025779774
-
In vitro and in vivo inhibition of pulmonary cytochrome P450 activities by piperine, a major ingredient of piper species
-
Reen RK, Singh J. In vitro and in vivo inhibition of pulmonary cytochrome P450 activities by piperine, a major ingredient of piper species. Indian J Exp Biol. 1991;29(6):568-573.
-
(1991)
Indian J Exp Biol
, vol.29
, Issue.6
, pp. 568-573
-
-
Reen, R.K.1
Singh, J.2
-
47
-
-
60349094657
-
Bioconversion of red ginseng saponins in the gastro-intestinal tract in vitro model studied by high-performance liquid chromatography-high resolution Fourier transform ion cyclotron resonance mass spectrometry
-
Kong HW, Wang M, Venema K, et al. Bioconversion of red ginseng saponins in the gastro-intestinal tract in vitro model studied by high-performance liquid chromatography-high resolution Fourier transform ion cyclotron resonance mass spectrometry. J Chromatogr A. 2009; 1216(11):2195-2203.
-
(2009)
J Chromatogr A
, vol.1216
, Issue.11
, pp. 2195-2203
-
-
Kong, H.W.1
Wang, M.2
Venema, K.3
-
48
-
-
59849098283
-
Studies on absorption, distribution and metabolism of ginseng in humans after oral administration
-
Lee J, Lee E, Kim D, Lee J, Yoo J, Koh B. Studies on absorption, distribution and metabolism of ginseng in humans after oral administration. J Ethnopharmacol. 2009;122(1):143-148.
-
(2009)
J Ethnopharmacol
, vol.122
, Issue.1
, pp. 143-148
-
-
Lee, J.1
Lee, E.2
Kim, D.3
Lee, J.4
Yoo, J.5
Koh, B.6
-
49
-
-
78751581865
-
Analysis of human and animal fecal microbiota for microbial source tracking
-
Lee JE, Lee S, Sung J, Ko G. Analysis of human and animal fecal microbiota for microbial source tracking. ISME J. 2011;5(2):362-365.
-
(2011)
ISME J
, vol.5
, Issue.2
, pp. 362-365
-
-
Lee, J.E.1
Lee, S.2
Sung, J.3
Ko, G.4
-
50
-
-
0024506814
-
C-ring cleavage of flavonoids by human intestinal bacteria
-
Winter J, Moore LH, Dowell VR Jr, Bokkenheuser VD. C-ring cleavage of flavonoids by human intestinal bacteria. Appl Environ Microbiol. 1989;55(5):1203-1208.
-
(1989)
Appl Environ Microbiol
, vol.55
, Issue.5
, pp. 1203-1208
-
-
Winter, J.1
Moore, L.H.2
Dowell Jr., V.R.3
Bokkenheuser, V.D.4
-
51
-
-
0030476584
-
Purification and characterization of alpha-l-rhamnosidase from Bacteroides JY-6, a human intestinal bacterium
-
Jang IS, Kim DH. Purification and characterization of alpha-l-rhamnosidase from Bacteroides JY-6, a human intestinal bacterium. Biol Pharm Bull. 1996;19(12):1546-1549.
-
(1996)
Biol Pharm Bull
, vol.19
, Issue.12
, pp. 1546-1549
-
-
Jang, I.S.1
Kim, D.H.2
-
52
-
-
0032814501
-
Metabolism of quercetin by human intestinal bacteria and its relation to some biological activities
-
Kim DH, Kim SY, Park SY, Han MJ. Metabolism of quercetin by human intestinal bacteria and its relation to some biological activities. Biol Pharm Bull. 1999;22(7):749-751.
-
(1999)
Biol Pharm Bull
, vol.22
, Issue.7
, pp. 749-751
-
-
Kim, D.H.1
Kim, S.Y.2
Park, S.Y.3
Han, M.J.4
-
53
-
-
0042526129
-
Degradation of ginsenosides in humans after oral administration
-
Tawab MA, Bahr U, Karas M, Wurglics M, Schubert-Zsilavecz M. Degradation of ginsenosides in humans after oral administration. Drug Metab Dispos. 2003;31(8):1065-1071.
-
(2003)
Drug Metab Dispos
, vol.31
, Issue.8
, pp. 1065-1071
-
-
Tawab, M.A.1
Bahr, U.2
Karas, M.3
Wurglics, M.4
Schubert-Zsilavecz, M.5
-
54
-
-
3142621044
-
Proof of the mysterious efficacy of ginseng: Basic and clinical trials: Metabolic activation of ginsenoside: Deglycosylation by intestinal bacteria and esterification with fatty acid
-
Hasegawa H. Proof of the mysterious efficacy of ginseng: basic and clinical trials: metabolic activation of ginsenoside: deglycosylation by intestinal bacteria and esterification with fatty acid. J Pharmacol Sci. 2004;95(2):153-157.
-
(2004)
J Pharmacol Sci
, vol.95
, Issue.2
, pp. 153-157
-
-
Hasegawa, H.1
|