-
1
-
-
0016758570
-
Sevoflurane: A new inhalational anesthetic agent
-
Wallin, R.F.; Regan, B.M.; Napoli, M.D.; Stern, I.J. Sevoflurane: A new inhalational anesthetic agent. Anesth. Analg. 1975, 54, 758-766.
-
(1975)
Anesth. Analg.
, vol.54
, pp. 758-766
-
-
Wallin, R.F.1
Regan, B.M.2
Napoli, M.D.3
Stern, I.J.4
-
2
-
-
0002104577
-
Inhalation anesthesia, Chapter 15
-
4th ed.; Barash, P.G., Cullen, B.F., Stoelting, R.K. Lippincott Williams& Wilkins: Philadelphia, PA, USA
-
Ebert, T.J.; Schmid, P.G., III. Inhalation Anesthesia, Chapter 15. In Clinical Anesthesia, 4th ed.; Barash, P.G., Cullen, B.F., Stoelting, R.K., Eds.; Lippincott Williams& Wilkins: Philadelphia, PA, USA, 2001; pp. 377-387.
-
(2001)
Clinical Anesthesia
, pp. 377-387
-
-
Ebert, T.J.1
Schmid, P.G.2
-
3
-
-
0028988860
-
Nephrotoxicity of sevoflurane compound A [fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether] in rats: Evidence for glutathione and cysteine conjugate formation and the role of renal cysteine conjugate beta-lyase
-
Jin, L.; Baillie, T.A.; Davis, M.R.; Kharasch, E.D. Nephrotoxicity of sevoflurane compound A [fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether] in rats: Evidence for glutathione and cysteine conjugate formation and the role of renal cysteine conjugate beta-lyase. Biochem. Biophys. Res. Commun. 1995, 210, 498-506.
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.210
, pp. 498-506
-
-
Jin, L.1
Baillie, T.A.2
Davis, M.R.3
Kharasch, E.D.4
-
4
-
-
0030950971
-
Studies of the mechanism of nephrotoxicity of compound A in rats
-
Martin, J.L.; Kandel, L.; Laster, M.J.; Kerschmann, R.L.; Eger, E.I., II. Studies of the mechanism of nephrotoxicity of compound A in rats. J. Anaesth. 1997, 11, 32-37.
-
(1997)
J. Anaesth.
, vol.11
, pp. 32-37
-
-
Martin, J.L.1
Kandel, L.2
Laster, M.J.3
Kerschmann, R.L.4
Eger, E.I.5
-
5
-
-
0032868056
-
New injectable melphan formulations utilizing (SBE)7m-b-CD or HP-b-CD
-
Ma, D.Q.; Rajewski, R.A.; Stella, V.J. New injectable melphan formulations utilizing (SBE)7m-b-CD or HP-b-CD. Int. J. Pharm. 1999, 189, 227-234.
-
(1999)
Int. J. Pharm.
, vol.189
, pp. 227-234
-
-
Ma, D.Q.1
Rajewski, R.A.2
Stella, V.J.3
-
6
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
-
Loftsson, T.; Brewster, M.E. Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. J. Pharm. Sci. 1996, 85, 1017-1025.
-
(1996)
J. Pharm. Sci.
, vol.85
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
7
-
-
83555176134
-
Sulfobutyl ether(7) beta-cyclodextrin (SBE(7) beta-CD) carbamazepine complex: Preparation, characterization, molecular modeling, and evaluation of in vivo anti-epileptic activity
-
Jain, A.S.; Date, A.A.; Pissurlenkar, R.R.; Coutinho, E.C.; Nagarsenker, M.S. Sulfobutyl ether(7) beta-cyclodextrin (SBE(7) beta-CD) carbamazepine complex: Preparation, characterization, molecular modeling, and evaluation of in vivo anti-epileptic activity. AAPS PharmSciTech 2011, 12, 1163-1175.
-
(2011)
AAPS PharmSciTech
, vol.12
, pp. 1163-1175
-
-
Jain, A.S.1
Date, A.A.2
Pissurlenkar, R.R.3
Coutinho, E.C.4
Nagarsenker, M.S.5
-
8
-
-
0036827704
-
Protective effect of sulfobutyl ether beta-cyclodextrin on DY-9760e-induced hemolysis in vitro
-
Nagase, Y.; Hirata, M.; Arima, H.; Tajiri, S.; Nishimoto, Y.; Hirayama, F.; Irie, T.; Uekama, K. Protective effect of sulfobutyl ether beta-cyclodextrin on DY-9760e-induced hemolysis in vitro. J. Pharm. Sci. 2002, 91, 2382-2389.
-
(2002)
J. Pharm. Sci.
, vol.91
, pp. 2382-2389
-
-
Nagase, Y.1
Hirata, M.2
Arima, H.3
Tajiri, S.4
Nishimoto, Y.5
Hirayama, F.6
Irie, T.7
Uekama, K.8
-
9
-
-
0031036821
-
Intestinal safety of water-soluble beta-cyclodextrins in paediatric oral solutions of spironolactone: Effects on human intestinal epithelial Caco-2 cells
-
Tötterman, A.M.; Schipper, N.G.; Thompson, D.O.; Mannermaa, J.P. Intestinal safety of water-soluble beta-cyclodextrins in paediatric oral solutions of spironolactone: Effects on human intestinal epithelial Caco-2 cells. J. Pharm. Pharmacol. 1997, 49, 43-48.
-
(1997)
J. Pharm. Pharmacol.
, vol.49
, pp. 43-48
-
-
Tötterman, A.M.1
Schipper, N.G.2
Thompson, D.O.3
Mannermaa, J.P.4
-
10
-
-
0031054513
-
Pharmaceutical applications of cyclodextrins. III. Toxicological issues and safety evaluation
-
Irie, T.; Uekama, K. Pharmaceutical applications of cyclodextrins. III. Toxicological issues and safety evaluation. J. Pharm. Sci. 1997, 86, 147-162.
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 147-162
-
-
Irie, T.1
Uekama, K.2
-
11
-
-
77953545760
-
Evaluation of the cytotoxicity of beta-cyclodextrin derivatives: Evidence for the role of cholesterol extraction
-
Kiss, T.; Fenyvesi, F.; Bácskay, I.; Váradi, J.; Fenyvesi, E.; Iványi, R.; Szente, L.; Tósaki, A.; Vecsernyés, M. Evaluation of the cytotoxicity of beta-cyclodextrin derivatives: Evidence for the role of cholesterol extraction. Eur. J. Pharm. Sci. 2010, 40, 376-380.
-
(2010)
Eur. J. Pharm. Sci.
, vol.40
, pp. 376-380
-
-
Kiss, T.1
Fenyvesi, F.2
Bácskay, I.3
Váradi, J.4
Fenyvesi, E.5
Iványi, R.6
Szente, L.7
Tósaki, A.8
Vecsernyés, M.9
-
12
-
-
4844220197
-
In vitro and in vivo evaluation of a sulfobutyl ether beta-cyclodextrin enabled etomidate formulation
-
McIntosh, M.P.; Schwarting, N.; Rajewski, R.A. In vitro and in vivo evaluation of a sulfobutyl ether beta-cyclodextrin enabled etomidate formulation. J. Pharm. Sci. 2004, 93, 2585-2594.
-
(2004)
J. Pharm. Sci.
, vol.93
, pp. 2585-2594
-
-
McIntosh, M.P.1
Schwarting, N.2
Rajewski, R.A.3
-
13
-
-
4444281364
-
Toward the development of an injectable dosage form of propofol: Preparation and evaluation of propofol-sulfobutyl ether 7-beta-cyclodextrin complex
-
Babu, M.K.; Godiwala, T.N. Toward the development of an injectable dosage form of propofol: Preparation and evaluation of propofol-sulfobutyl ether 7-beta-cyclodextrin complex. Pharm. Dev. Technol. 2004, 9, 265-275.
-
(2004)
Pharm. Dev. Technol.
, vol.9
, pp. 265-275
-
-
Babu, M.K.1
Godiwala, T.N.2
-
14
-
-
34247188523
-
Evaluation of mean arterial blood pressure, heart rate, and sympathetic nerve activity in rabbits after administration of two formulations of etomidate
-
McIntosh, M.P.; Narita, H.; Kameyama, Y.; Rajewski, R.A.; Goto, H. Evaluation of mean arterial blood pressure, heart rate, and sympathetic nerve activity in rabbits after administration of two formulations of etomidate. Vet. Anaesth. Analg. 2007, 34, 149-156.
-
(2007)
Vet. Anaesth. Analg.
, vol.34
, pp. 149-156
-
-
McIntosh, M.P.1
Narita, H.2
Kameyama, Y.3
Rajewski, R.A.4
Goto, H.5
-
15
-
-
84937854458
-
Alphaxalone reformulated: A water-soluble intravenous anesthetic preparation in sulfobutyl-ether-beta-cyclodextrin
-
Goodchild, C.S.; Serrao, J.M.; Kolosov, A.; Boyd, B.J. Alphaxalone Reformulated: A Water-Soluble Intravenous Anesthetic Preparation in Sulfobutyl-Ether-beta-Cyclodextrin. Anesth. Analg. 2014, doi:10.1213/ANE.0000000000000559.
-
(2014)
Anesth. Analg.
-
-
Goodchild, C.S.1
Serrao, J.M.2
Kolosov, A.3
Boyd, B.J.4
-
16
-
-
63649163814
-
Preparation and solid-state characterization of inclusion complexes formed between miconazole and methyl-beta-cyclodextrin
-
Ribeiro, A.; Figueiras, A.; Santos, D.; Veiga, F. Preparation and solid-state characterization of inclusion complexes formed between miconazole and methyl-beta-cyclodextrin. AAPS PharmSciTech 2008, 9, 1102-1109.
-
(2008)
AAPS PharmSciTech
, vol.9
, pp. 1102-1109
-
-
Ribeiro, A.1
Figueiras, A.2
Santos, D.3
Veiga, F.4
-
17
-
-
1642399085
-
Physicochemical characterization and dissolution properties of meloxicam-cyclodextrin binary systems
-
Naidu, N.B.; Chowdary, K.P.; Murthy, K.V.; Satyanarayana, V.; Hayman, A.R.; Becket, G. Physicochemical characterization and dissolution properties of meloxicam-cyclodextrin binary systems. J. Pharm. Biomed. Anal. 2004, 35, 75-86.
-
(2004)
J. Pharm. Biomed. Anal.
, vol.35
, pp. 75-86
-
-
Naidu, N.B.1
Chowdary, K.P.2
Murthy, K.V.3
Satyanarayana, V.4
Hayman, A.R.5
Becket, G.6
-
18
-
-
1942439735
-
Photostability studies on nicardipine-cyclodextrin complexes by capillary electrophoresis
-
Pomponio, R.; Gotti, R.; Fiori, J.; Cavrini, V.; Mura, P.; Cirri, M.; Maestrelli, F. Photostability studies on nicardipine-cyclodextrin complexes by capillary electrophoresis. J. Pharm. Biomed. Anal. 2004, 35, 267-275.
-
(2004)
J. Pharm. Biomed. Anal.
, vol.35
, pp. 267-275
-
-
Pomponio, R.1
Gotti, R.2
Fiori, J.3
Cavrini, V.4
Mura, P.5
Cirri, M.6
Maestrelli, F.7
-
19
-
-
79955639503
-
Effect of cyclodextrin derivation and amorphous state of complex on accelerated degradation of ziprasidone
-
Hong, J.; Shah, J.C.; Mcgonagle, M.D. Effect of cyclodextrin derivation and amorphous state of complex on accelerated degradation of ziprasidone. J. Pharm. Sci. 2011, 100, 2703-2716.
-
(2011)
J. Pharm. Sci.
, vol.100
, pp. 2703-2716
-
-
Hong, J.1
Shah, J.C.2
Mcgonagle, M.D.3
-
20
-
-
0000308862
-
Neues Verfahren zur maßanalytischen Bestimmung des Wassergehaltes von Flüssigkeiten und festen Körpern
-
Fischer, K. Neues Verfahren zur maßanalytischen Bestimmung des Wassergehaltes von Flüssigkeiten und festen Körpern. Angew. Chem. 1935, 48, 394-396.
-
(1935)
Angew. Chem.
, vol.48
, pp. 394-396
-
-
Fischer, K.1
-
21
-
-
84878273938
-
Changes in sevoflurane plasma concentration with delivery through the oxygenator during on-pump cardiac surgery
-
Nitzschke, R.; Wilgusch, J.; Kersten, J.F.; Trepte, C.J.; Haas, S.A.; Reuter, D.A.; Goetz, A.E.; Goepfert, M.S. Changes in sevoflurane plasma concentration with delivery through the oxygenator during on-pump cardiac surgery. Br. J. Anaesth. 2013, 110, 957-965.
-
(2013)
Br. J. Anaesth.
, vol.110
, pp. 957-965
-
-
Nitzschke, R.1
Wilgusch, J.2
Kersten, J.F.3
Trepte, C.J.4
Haas, S.A.5
Reuter, D.A.6
Goetz, A.E.7
Goepfert, M.S.8
-
22
-
-
79955093145
-
Determination of site of absorption of propranolol in rat gut using in situ single-pass intestinal perfusion
-
Nagare, N.; Damre, A.; Singh, K.S.; Mallurwar, S.R.; Iyer, S.; Naik, A.; Chintamaneni, M. Determination of site of absorption of propranolol in rat gut using in situ single-pass intestinal perfusion. Indian J. Pharm. Sci. 2010, 72, 625-629.
-
(2010)
Indian J. Pharm. Sci.
, vol.72
, pp. 625-629
-
-
Nagare, N.1
Damre, A.2
Singh, K.S.3
Mallurwar, S.R.4
Iyer, S.5
Naik, A.6
Chintamaneni, M.7
-
23
-
-
84875480531
-
A validated RP-HPLC method for simultaneous determination of propranolol and valsartan in bulk drug and gel formulation
-
Imam, S.S.; Ahad, A.; Agil, M.; Sultana, Y.; Ali, A. A validated RP-HPLC method for simultaneous determination of propranolol and valsartan in bulk drug and gel formulation. J. Pharm. Bioallied Sci. 2013, 5, 61-65.
-
(2013)
J. Pharm. Bioallied Sci.
, vol.5
, pp. 61-65
-
-
Imam, S.S.1
Ahad, A.2
Agil, M.3
Sultana, Y.4
Ali, A.5
-
24
-
-
0027585041
-
Effect of propranolol hydrochloride on blood cell lipids in relation to partition coefficient and biological activity
-
Dutta, H.; Sengupta, M.; Pal, D.K.; De, A.U.; Sengupta, C. Effect of propranolol hydrochloride on blood cell lipids in relation to partition coefficient and biological activity. Indian J. Biochem. Biophys. 1993, 30, 128-132.
-
(1993)
Indian J. Biochem. Biophys.
, vol.30
, pp. 128-132
-
-
Dutta, H.1
Sengupta, M.2
Pal, D.K.3
De, A.U.4
Sengupta, C.5
-
25
-
-
0032844221
-
The influence of plasma binding on absorption/exsorption in the Caco-2 model of human intestinal absorption
-
Walgren, R.A.; Walle, T. The influence of plasma binding on absorption/exsorption in the Caco-2 model of human intestinal absorption. J. Pharm. Pharmacol. 1999, 51, 1037-1040.
-
(1999)
J. Pharm. Pharmacol.
, vol.51
, pp. 1037-1040
-
-
Walgren, R.A.1
Walle, T.2
-
26
-
-
84908130788
-
Transport of hop aroma compounds across Caco-2 monolayers
-
Heinlein, A.; Metzger, M.; Walles, H.; Buettner, A. Transport of hop aroma compounds across Caco-2 monolayers. Food Funct. 2014, 5, 2719-2730.
-
(2014)
Food Funct
, vol.5
, pp. 2719-2730
-
-
Heinlein, A.1
Metzger, M.2
Walles, H.3
Buettner, A.4
-
27
-
-
77949814630
-
The evolving role of the Caco-2 cell model to estimate intestinal absorption potential and elucidate transport mechanisms
-
2nd ed.; Smith, C.G., O'Donnell, J.T., Eds.; Informa Healthcare USA, Inc.: New York, NY, USA
-
Hidalgo, I.; Li, J. The evolving role of the Caco-2 cell model to estimate intestinal absorption potential and elucidate transport mechanisms. In The Process of New Drug Discovery and Development, 2nd ed.; Smith, C.G., O'Donnell, J.T., Eds.; Informa Healthcare USA, Inc.: New York, NY, USA, 2006; pp. 161-186.
-
(2006)
The Process of New Drug Discovery and Development
, pp. 161-186
-
-
Hidalgo, I.1
Li, J.2
-
28
-
-
0032826794
-
Use of a Caco-2 cell culture model for the characterization of intestinal absorption of antibiotics
-
Biganzoli, E.; Cavenaghi, L.A.; Rossi, R.; Brunati, M.C.; Nolli, M.L. Use of a Caco-2 cell culture model for the characterization of intestinal absorption of antibiotics. Il Farmaco 1999, 54, 594-599.
-
(1999)
Il Farmaco
, vol.54
, pp. 594-599
-
-
Biganzoli, E.1
Cavenaghi, L.A.2
Rossi, R.3
Brunati, M.C.4
Nolli, M.L.5
-
29
-
-
0025892002
-
The effects of cyclodextrins on the disposition of intravenously injected drugs in the rat
-
Frijlink, H.W.; Franssen, E.J.; Eissens, A.C.; Oosting, R.; Lerk, C.F.; Meijer, D.K. The effects of cyclodextrins on the disposition of intravenously injected drugs in the rat. Pharm. Res. 1991, 8, 380-384.
-
(1991)
Pharm. Res.
, vol.8
, pp. 380-384
-
-
Frijlink, H.W.1
Franssen, E.J.2
Eissens, A.C.3
Oosting, R.4
Lerk, C.F.5
Meijer, D.K.6
-
30
-
-
22944491152
-
Sulfobutyl ether-beta-cyclodextrins: Promising supramolecular carriers for aqueous organometallic catalysis
-
Blach, P.; Landy, D.; Fourmentin, S.; Surpateanu, G.; Bricout, H.; Ponchel, A.; Hapiot, F.; Monflier, E. Sulfobutyl ether-beta-cyclodextrins: Promising supramolecular carriers for aqueous organometallic catalysis. Adv. Synth. Catal. 2005, 347, 1301-1307.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1301-1307
-
-
Blach, P.1
Landy, D.2
Fourmentin, S.3
Surpateanu, G.4
Bricout, H.5
Ponchel, A.6
Hapiot, F.7
Monflier, E.8
-
31
-
-
78249286843
-
Phase solubility,1 H NMR and molecular modelling studies of bupivacaine hydrochloride complexation with different cyclodextrin derivates
-
Jug, M.; Mennini, N.; Melani, F.; Maestrelli, F.; Mura, P. Phase solubility,1 H NMR and molecular modelling studies of bupivacaine hydrochloride complexation with different cyclodextrin derivates. Chem. Phys. Lett. 2010, 500, 347-354.
-
(2010)
Chem. Phys. Lett.
, vol.500
, pp. 347-354
-
-
Jug, M.1
Mennini, N.2
Melani, F.3
Maestrelli, F.4
Mura, P.5
-
32
-
-
84870380973
-
Cyclodextrin dimer complexes of dopamine and levodopa derivatives to assess drug delivery to the central nervous system: ADME and molecular docking studies
-
Shityakov, S.; Broscheit, J.; Förster, C. alpha-Cyclodextrin dimer complexes of dopamine and levodopa derivatives to assess drug delivery to the central nervous system: ADME and molecular docking studies. Int. J. Nanomed. 2012, 7, 3211-3219.
-
(2012)
Int. J. Nanomed.
, vol.7
, pp. 3211-3219
-
-
Shityakov, S.1
Broscheit, J.2
Förster, C.3
-
33
-
-
84987741037
-
In silico predictive model to determine vector-mediated transport properties for the blood-brain barrier choline transporter
-
Shityakov, S.; Forster, C. In silico predictive model to determine vector-mediated transport properties for the blood-brain barrier choline transporter. Adv. Appl. Bioinform. Chem. 2014, 7, 23-36.
-
(2014)
Adv. Appl. Bioinform. Chem.
, vol.7
, pp. 23-36
-
-
Shityakov, S.1
Forster, C.2
-
34
-
-
84861495307
-
Molecular docking using the molecular lipophilicity potential as hydrophobic descriptor: Impact on GOLD docking performance
-
Nurisso, A.J.; Bravo, J.; Carrupt, P.A.; Daina, A. Molecular docking using the molecular lipophilicity potential as hydrophobic descriptor: Impact on GOLD docking performance. J. Chem. Inf. Model. 2012, 52, 1319-1327.
-
(2012)
J. Chem. Inf. Model.
, vol.52
, pp. 1319-1327
-
-
Nurisso, A.J.1
Bravo, J.2
Carrupt, P.A.3
Daina, A.4
-
35
-
-
49149147973
-
Iterative Partial Equalization of Orbital Electronegativity-A Rapid Access to Atomic Charges
-
Gasteiger, J.; Marsili, M. Iterative Partial Equalization of Orbital Electronegativity-A Rapid Access to Atomic Charges. Tetrahedron 1980, 36, 3219-3228.
-
(1980)
Tetrahedron
, vol.36
, pp. 3219-3228
-
-
Gasteiger, J.1
Marsili, M.2
-
36
-
-
0029705324
-
Automated docking of flexible ligands: Applications of AutoDock
-
Goodsell, D.S.; Morris, G.M.; Olson, A.J. Automated docking of flexible ligands: Applications of AutoDock. J. Mol. Recognit. 1996, 9, 1-5.
-
(1996)
J. Mol. Recognit.
, vol.9
, pp. 1-5
-
-
Goodsell, D.S.1
Morris, G.M.2
Olson, A.J.3
-
37
-
-
77953325845
-
Ligand docking and binding site analysis with PyMOL and Autodock/Vina
-
Seeliger, D.; de Groot, B.L. Ligand docking and binding site analysis with PyMOL and Autodock/Vina. J. Comput. Aided Mol. Des. 2010, 24, 417-422.
-
(2010)
J. Comput. Aided Mol. Des.
, vol.24
, pp. 417-422
-
-
Seeliger, D.1
De Groot, B.L.2
-
38
-
-
84911926579
-
Ionization states, cellular toxicity and molecular modeling studies of midazolam complexed with trimethyl-beta-cyclodextrin
-
Shityakov, S.; Sohajda, T.; Puskás, I.; Roewer, N.; Förster, C.; Broscheit, J.A. Ionization states, cellular toxicity and molecular modeling studies of midazolam complexed with trimethyl-beta-cyclodextrin. Molecules 2014, 19, 16861-16876.
-
(2014)
Molecules
, vol.19
, pp. 16861-16876
-
-
Shityakov, S.1
Sohajda, T.2
Puskás, I.3
Roewer, N.4
Förster, C.5
Broscheit, J.A.6
-
39
-
-
0028411658
-
Molecular lipophilicity potential, a tool in 3D QSAR: Method and applications
-
Gaillard, P.; Carrupt, P.A.; Testa, B.; Boudon, A. Molecular lipophilicity potential, a tool in 3D QSAR: Method and applications. J. Comput. Aided Mol. Des. 1994, 8, 83-96.
-
(1994)
J. Comput. Aided Mol. Des.
, vol.8
, pp. 83-96
-
-
Gaillard, P.1
Carrupt, P.A.2
Testa, B.3
Boudon, A.4
-
40
-
-
84904396014
-
MLP Tools: A PyMOL plugin for using the molecular lipophilicity potential in computer-aided drug design
-
Oberhauser, N.; Nurisso, A.; Carrupt, P.A. MLP Tools: A PyMOL plugin for using the molecular lipophilicity potential in computer-aided drug design. J. Comput. Aided. Mol. Des. 2014, 28, 587-596.
-
(2014)
J. Comput. Aided. Mol. Des.
, vol.28
, pp. 587-596
-
-
Oberhauser, N.1
Nurisso, A.2
Carrupt, P.A.3
|