-
1
-
-
0003781923
-
-
Oxford University Press, New York
-
R.L. Juliano (Ed.), Drug Delivery System, Oxford University Press, New York, 1980.
-
(1980)
Drug Delivery System
-
-
Juliano, R.L.1
-
7
-
-
0019779742
-
Pharmaceutical applications of cyclodextrin complexations
-
K. Uekama, Pharmaceutical applications of cyclodextrin complexations, Yakugaku Zasshi 101 (1981) 857-873.
-
(1981)
Yakugaku Zasshi
, vol.101
, pp. 857-873
-
-
Uekama, K.1
-
8
-
-
0343033288
-
Molecular encapsulation of drugs by cyclodextrins and congeners
-
S.D. Bruck (Ed.), CRC Press, Boca Raton, FL, Ch. 5
-
J. Pitha, L. Szente, J. Szejtli, Molecular encapsulation of drugs by cyclodextrins and congeners, in: S.D. Bruck (Ed.), Controlled Drug Delivery, Vol. I, CRC Press, Boca Raton, FL, 1983, Ch. 5.
-
(1983)
Controlled Drug Delivery
, vol.1
-
-
Pitha, J.1
Szente, L.2
Szejtli, J.3
-
11
-
-
0025810218
-
Development of aqueous parenteral formulations for carbamazepine through the use of modified cyclodextrins
-
M.E. Brewster, W.R. Anderson, K.S. Estes, N. Bodor, Development of aqueous parenteral formulations for carbamazepine through the use of modified cyclodextrins, J. Pharm. Sci. 80 (1991) 380-383.
-
(1991)
J. Pharm. Sci.
, vol.80
, pp. 380-383
-
-
Brewster, M.E.1
Anderson, W.R.2
Estes, K.S.3
Bodor, N.4
-
12
-
-
0002596801
-
Pharmaceutical use of cyclodextrins in various drug formulations
-
J. Szejtli, T. Osa (Eds.), Pergamon, Oxford
-
K. Uekama, T. Irie, Pharmaceutical use of cyclodextrins in various drug formulations, in: J. Szejtli, T. Osa (Eds.), Cyclodextrins. Comprehensive Supramolecular Chemistry, Vol. 3, Pergamon, Oxford, 1996.
-
(1996)
Cyclodextrins. Comprehensive Supramolecular Chemistry
, vol.3
-
-
Uekama, K.1
Irie, T.2
-
14
-
-
0000117775
-
Application of cyclodextrins. Drug absorption enhancement: Concepts, possibilities, limitations and trends
-
A.G. Boer (Ed.), Harwood Academic, Swizerland
-
K. Uekama, F. Hirayama, T. Irie, Application of cyclodextrins. Drug absorption enhancement: concepts, possibilities, limitations and trends, in: A.G. Boer (Ed.), Drug Targeting Delivery, Vol. 3, Harwood Academic, Swizerland, 1994, pp. 411-456.
-
(1994)
Drug Targeting Delivery
, vol.3
, pp. 411-456
-
-
Uekama, K.1
Hirayama, F.2
Irie, T.3
-
16
-
-
8244248457
-
Cyclodextrins: Their future in drug formulation and delivery
-
V.J. Stella, R.A. Rajewski, Cyclodextrins: their future in drug formulation and delivery, Pharm. Res. 14 (1997) 556-567.
-
(1997)
Pharm. Res.
, vol.14
, pp. 556-567
-
-
Stella, V.J.1
Rajewski, R.A.2
-
17
-
-
0031042310
-
Cyclodextrins-enabling excipients: Their present and future use in pharmaceuticals
-
D.O. Thompson, Cyclodextrins-enabling excipients: their present and future use in pharmaceuticals, CRC Crit. Rev. Ther. Drug Carrier Syst. 14 (1997) 1-104.
-
(1997)
CRC Crit. Rev. Ther. Drug Carrier Syst.
, vol.14
, pp. 1-104
-
-
Thompson, D.O.1
-
18
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
-
T. Loftsson, M.E. Brewster, 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
-
19
-
-
0029852699
-
Pharmaceutical applications of cyclodextrins. 2. In vivo drug delivery
-
R.A. Rajewski, V.J. Stella, Pharmaceutical applications of cyclodextrins. 2. In vivo drug delivery, J. Pharm. Sci. 85 (1996) 1142-1169.
-
(1996)
J. Pharm. Sci.
, vol.85
, pp. 1142-1169
-
-
Rajewski, R.A.1
Stella, V.J.2
-
20
-
-
0031054513
-
Pharmaceutical applications of cyclodextrins. III. Toxicological issues and safety evaluation
-
T. Irie, K. Uekama, Pharmaceutical applications of cyclodextrins. III. Toxicological issues and safety evaluation, J. Pharm. Sci. 86 (1997) 147-162.
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 147-162
-
-
Irie, T.1
Uekama, K.2
-
21
-
-
0032119526
-
Cyclodextrin drug carrier systems
-
K. Uekama, F. Hirayama, T. Irie, Cyclodextrin drug carrier systems, Chem. Rev. 98 (1998) 2045-2076.
-
(1998)
Chem. Rev.
, vol.98
, pp. 2045-2076
-
-
Uekama, K.1
Hirayama, F.2
Irie, T.3
-
22
-
-
0021810514
-
Amorphous water-soluble derivatives of cyclodextrins, nontoxic dissolution enhancing excipients
-
J. Pitha, J. Pitha, Amorphous water-soluble derivatives of cyclodextrins, nontoxic dissolution enhancing excipients, J. Pharm. Sci. 74 (1985) 987-990.
-
(1985)
J. Pharm. Sci.
, vol.74
, pp. 987-990
-
-
Pitha, J.1
Pitha, J.2
-
23
-
-
0021816582
-
Solubilization of drugs by modified β-cyclodextrins
-
B.W. Müller, U. Brauns, Solubilization of drugs by modified β-cyclodextrins, Int. J. Pharm. 26 (1985) 77-88.
-
(1985)
Int. J. Pharm.
, vol.26
, pp. 77-88
-
-
Müller, B.W.1
Brauns, U.2
-
24
-
-
0023676038
-
Pharmaceutical evaluation of hydroxyalkylethers of β-cyclodextrins
-
A. Yoshida, H. Arima, K. Uekama, J. Pitha, Pharmaceutical evaluation of hydroxyalkylethers of β-cyclodextrins, Int. J. Pharm. 46 (1988) 217-222.
-
(1988)
Int. J. Pharm.
, vol.46
, pp. 217-222
-
-
Yoshida, A.1
Arima, H.2
Uekama, K.3
Pitha, J.4
-
25
-
-
0024444076
-
The potential use of cyclodextrins in parenteral formulations
-
M.E. Brewster, J.W. Simpkins, M.S. Hora, W. Stern, N. Bodor, The potential use of cyclodextrins in parenteral formulations, J. Parent. Sci. Technol. 43 (1989) 231-240.
-
(1989)
J. Parent. Sci. Technol.
, vol.43
, pp. 231-240
-
-
Brewster, M.E.1
Simpkins, J.W.2
Hora, M.S.3
Stern, W.4
Bodor, N.5
-
26
-
-
0002558849
-
Isolation and characterization of branched cyclodextrins
-
K. Koizumi, T. Utamura, M. Sato, Y. Yagi, Isolation and characterization of branched cyclodextrins, Carbohydr. Res. 153 (1986) 55-67.
-
(1986)
Carbohydr. Res.
, vol.153
, pp. 55-67
-
-
Koizumi, K.1
Utamura, T.2
Sato, M.3
Yagi, Y.4
-
27
-
-
0024499690
-
Some physicochemical properties of branched β-cyclodextrins and their inclusion characteristics
-
M. Yamamoto, A. Yoshida, F. Hirayama, K. Uekama, Some physicochemical properties of branched β-cyclodextrins and their inclusion characteristics, Int. J. Pharm. 49 (1989) 163-171.
-
(1989)
Int. J. Pharm.
, vol.49
, pp. 163-171
-
-
Yamamoto, M.1
Yoshida, A.2
Hirayama, F.3
Uekama, K.4
-
28
-
-
0024977229
-
O-Carboxymethyl-O-ethyl-cyclomaltoheptaose as a delayed-release-type drug carrier. Improvement of the oral bioavailability of diltiazem
-
K. Uekama, Y. Horiuchi, T. Irie, F. Hirayama, O-Carboxymethyl-O-ethyl-cyclomaltoheptaose as a delayed-release-type drug carrier. Improvement of the oral bioavailability of diltiazem, Carbohydr. Res. 192 (1989) 323-330.
-
(1989)
Carbohydr. Res.
, vol.192
, pp. 323-330
-
-
Uekama, K.1
Horiuchi, Y.2
Irie, T.3
Hirayama, F.4
-
29
-
-
0025938358
-
Improvement, of stability and bioavailability of 1-hexylcarbamoyl-5-fluorouracil (HCFU) by O-carboxymethyl-O-ethyl-β-cyclodextrin
-
Y. Horiuchi, F. Hirayama, K. Uekama, Improvement, of stability and bioavailability of 1-hexylcarbamoyl-5-fluorouracil (HCFU) by O-carboxymethyl-O-ethyl-β-cyclodextrin, Yakugaku Zasshi 111 (1991) 592-599.
-
(1991)
Yakugaku Zasshi
, vol.111
, pp. 592-599
-
-
Horiuchi, Y.1
Hirayama, F.2
Uekama, K.3
-
30
-
-
0025968081
-
Release control of theophylline by β-cyclodextrin derivatives: Hybridizing effect of hydrophilic, hydrophobic and ionizable β-cyclodextrin complexes
-
Y. Horiuchi, K. Abe, F. Hirayama, K. Uekama, Release control of theophylline by β-cyclodextrin derivatives: hybridizing effect of hydrophilic, hydrophobic and ionizable β-cyclodextrin complexes, J. Control. Release 15 (1991) 177-183.
-
(1991)
J. Control. Release
, vol.15
, pp. 177-183
-
-
Horiuchi, Y.1
Abe, K.2
Hirayama, F.3
Uekama, K.4
-
32
-
-
0027279678
-
Development and pharmaceutical evaluation of hydrophobic derivatives as modified-release drug carrier
-
F. Hirayama, Development and pharmaceutical evaluation of hydrophobic derivatives as modified-release drug carrier, Yakugaku Zasshi 113 (1993) 425-437.
-
(1993)
Yakugaku Zasshi
, vol.113
, pp. 425-437
-
-
Hirayama, F.1
-
33
-
-
0023543437
-
Ethylated β-cyclodextrins as hydrophobic drug carriers: Sustained release of diltiazem in the rat
-
K. Uekama, N. Hirashima, H. Horiuchi, F. Hirayama, T. Ijitsu, M. Ueno, Ethylated β-cyclodextrins as hydrophobic drug carriers: sustained release of diltiazem in the rat, J. Pharm. Sci. 76 (1987) 660-661.
-
(1987)
J. Pharm. Sci.
, vol.76
, pp. 660-661
-
-
Uekama, K.1
Hirashima, N.2
Horiuchi, H.3
Hirayama, F.4
Ijitsu, T.5
Ueno, M.6
-
34
-
-
0027393910
-
Preparation of heptakis(2,6-di-O-ethyl)-β-cyclodextrin and its nuclear magnetic resonance spectroscopic characterization
-
F. Hirayama, M. Kurihara, Y. Horiuchi, T. Utsuki, K. Uekama, M. Yamasaki, Preparation of heptakis(2,6-di-O-ethyl)-β-cyclodextrin and its nuclear magnetic resonance spectroscopic characterization, Pharm. Res. 10 (1993) 208-213.
-
(1993)
Pharm. Res.
, vol.10
, pp. 208-213
-
-
Hirayama, F.1
Kurihara, M.2
Horiuchi, Y.3
Utsuki, T.4
Uekama, K.5
Yamasaki, M.6
-
35
-
-
0024955999
-
Sustained release of buserelin acetate, a luteinizing hormone-releasing hormone agonist, from the injectable oily preparation utilizing ethylated β-cyclodextrin
-
K. Uekama, H. Arima, T. Irie, K. Matsubara, K. Kuriki, Sustained release of buserelin acetate, a luteinizing hormone-releasing hormone agonist, from the injectable oily preparation utilizing ethylated β-cyclodextrin, J. Pharm. Pharmacol. 41 (1989) 874-876.
-
(1989)
J. Pharm. Pharmacol.
, vol.41
, pp. 874-876
-
-
Uekama, K.1
Arima, H.2
Irie, T.3
Matsubara, K.4
Kuriki, K.5
-
36
-
-
0028855247
-
Characterization of peracylated β-cyclodextrins with different chain lengths as a novel sustained release carrier for water-soluble drugs
-
F. Hirayama, M. Yamanaka, T. Horikawa, K. Uekama, Characterization of peracylated β-cyclodextrins with different chain lengths as a novel sustained release carrier for water-soluble drugs, Chem. Pharm. Bull. 43 (1995) 130-136.
-
(1995)
Chem. Pharm. Bull.
, vol.43
, pp. 130-136
-
-
Hirayama, F.1
Yamanaka, M.2
Horikawa, T.3
Uekama, K.4
-
37
-
-
0028087996
-
Controlled-release of the LHRH agonist buserelin acetate from injectable suspensions containing triacetylated cyclodextrins in an oil vehicle
-
K. Matsubara, T. Irie, K. Uekama, Controlled-release of the LHRH agonist buserelin acetate from injectable suspensions containing triacetylated cyclodextrins in an oil vehicle, J. Control. Release 31 (1994) 173-180.
-
(1994)
J. Control. Release
, vol.31
, pp. 173-180
-
-
Matsubara, K.1
Irie, T.2
Uekama, K.3
-
38
-
-
0001795431
-
Improvement of drug properties by cyclodextrins
-
C.G. Wermuth (Ed.), Academic Press, London, Ch. 37
-
K. Uekama, F. Hirayama, Improvement of drug properties by cyclodextrins, in: C.G. Wermuth (Ed.), The Practice of Medicinal Chemistry, Academic Press, London, 1996, Ch. 37, pp. 793-825.
-
(1996)
The Practice of Medicinal Chemistry
, pp. 793-825
-
-
Uekama, K.1
Hirayama, F.2
-
39
-
-
0019846019
-
Kinetic difference between hydrolyses of γ-cyclodextrin by human salivary and pancreatic α-amylases
-
J.J. Marshall, I. Miwa, Kinetic difference between hydrolyses of γ-cyclodextrin by human salivary and pancreatic α-amylases, Biochim. Biophys. Acta 661 (1981) 142-147.
-
(1981)
Biochim. Biophys. Acta
, vol.661
, pp. 142-147
-
-
Marshall, J.J.1
Miwa, I.2
-
40
-
-
0027085845
-
Acid-catalyzed hydrolysis of maltosyl-β-cyclodextrin
-
F. Hirayama, M. Yamamoto, K. Uekama, Acid-catalyzed hydrolysis of maltosyl-β-cyclodextrin, J. Pharm. Sci. 81 (1992) 913-916.
-
(1992)
J. Pharm. Sci.
, vol.81
, pp. 913-916
-
-
Hirayama, F.1
Yamamoto, M.2
Uekama, K.3
-
41
-
-
0001357555
-
Biopharmaceutical evaluation of maltosyl-β-cyclodextrin as a parenteral drug carrier
-
M. Yamamoto, H. Aritomi, T. Irie, F. Hirayama, K. Uekama, Biopharmaceutical evaluation of maltosyl-β-cyclodextrin as a parenteral drug carrier, S.T.P. Pharma Sci. 1 (1991) 397-402.
-
(1991)
S.T.P. Pharma Sci.
, vol.1
, pp. 397-402
-
-
Yamamoto, M.1
Aritomi, H.2
Irie, T.3
Hirayama, F.4
Uekama, K.5
-
42
-
-
0030610609
-
A-amino-[(4-biphenylyl)-acetyl]-α-, β-, and γ-cyclodextrins: Potential prodrugs for colon-specific delivery
-
A-amino-[(4-biphenylyl)-acetyl]-α-, β-, and γ-cyclodextrins: potential prodrugs for colon-specific delivery, J. Med. Chem. 40 (1997) 2755-2761.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2755-2761
-
-
Uekama, K.1
Minami, K.2
Hirayama, F.3
-
43
-
-
0022639287
-
Enhancement of bioavailability of cinnarizine from its β-cyclodextrin complex on oral administration with D,L-phenylalanine as a competing agent
-
T. Tokumura, M. Nambu, Y. Tsushima, K. Tatsuishi, M. Kayano, Y. Machida, T. Nagai, Enhancement of bioavailability of cinnarizine from its β-cyclodextrin complex on oral administration with D,L-phenylalanine as a competing agent, J. Pharm. Sci. 75 (1986) 391-394.
-
(1986)
J. Pharm. Sci.
, vol.75
, pp. 391-394
-
-
Tokumura, T.1
Nambu, M.2
Tsushima, Y.3
Tatsuishi, K.4
Kayano, M.5
Machida, Y.6
Nagai, T.7
-
44
-
-
0024595698
-
Effect of the interaction of drug-β-cyclodextrin complex with bile salts on the drug absorption from rat small intestinal lumen
-
K. Nakanishi, M. Masada, T. Nadai, K. Miyajima, Effect of the interaction of drug-β-cyclodextrin complex with bile salts on the drug absorption from rat small intestinal lumen, Chem. Pharm. Bull. 37 (1989) 211-214.
-
(1989)
Chem. Pharm. Bull.
, vol.37
, pp. 211-214
-
-
Nakanishi, K.1
Masada, M.2
Nadai, T.3
Miyajima, K.4
-
45
-
-
0030580115
-
Preparation and evaluation of ketoconazole-β-cyclodextrin multicomponent complexes
-
M.T. Esclusa-Diaz, M. Gayo-Otero, M.B. Perez-Marcos, J.L. Vila-Jato, J.J. Torres Labandeira, Preparation and evaluation of ketoconazole-β-cyclodextrin multicomponent complexes, Int. J. Pharm. 142 (1996) 183-187.
-
(1996)
Int. J. Pharm.
, vol.142
, pp. 183-187
-
-
Esclusa-Diaz, M.T.1
Gayo-Otero, M.2
Perez-Marcos, M.B.3
Vila-Jato, J.L.4
Torres Labandeira, J.J.5
-
46
-
-
0032550318
-
An econazole β-cyclodextrin inclusion complex: An unusual dissolution rate, supersaturation, and biological efficacy example
-
M. Pedersen, S. Bjerregaard, J. Jacobson, A.R. Larsen, A.M. Sorensen, An econazole β-cyclodextrin inclusion complex: an unusual dissolution rate, supersaturation, and biological efficacy example, Int. J. Pharm. 165 (1998) 57-68.
-
(1998)
Int. J. Pharm.
, vol.165
, pp. 57-68
-
-
Pedersen, M.1
Bjerregaard, S.2
Jacobson, J.3
Larsen, A.R.4
Sorensen, A.M.5
-
47
-
-
0344537810
-
Formulation studies of a new oral cephalosporin, cefotiam hexetil hydrochloride [SCE-2174 (2HCl)]
-
S. Hirai, H. Koyama, T. Makino, N. Kitamori, H. Toguchi, Formulation studies of a new oral cephalosporin, cefotiam hexetil hydrochloride [SCE-2174 (2HCl)], Yakuzaigaku 48 (1988) 189-196.
-
(1988)
Yakuzaigaku
, vol.48
, pp. 189-196
-
-
Hirai, S.1
Koyama, H.2
Makino, T.3
Kitamori, N.4
Toguchi, H.5
-
48
-
-
0021063653
-
Improvement of the oral bioavailability of digitalis glycosides by cyclodextrin complexation
-
K. Uekama, T. Fujinaga, F. Hirayama, M. Otagiri, M. Yamasaki, H. Seo, T. Hashimoto, M. Tsuruoka, Improvement of the oral bioavailability of digitalis glycosides by cyclodextrin complexation, J. Pharm. Sci. 72 (1983) 1338-1341.
-
(1983)
J. Pharm. Sci.
, vol.72
, pp. 1338-1341
-
-
Uekama, K.1
Fujinaga, T.2
Hirayama, F.3
Otagiri, M.4
Yamasaki, M.5
Seo, H.6
Hashimoto, T.7
Tsuruoka, M.8
-
49
-
-
85047693676
-
Oral pharmacokinetics of carbamazepine in dogs from commercial tablets and a cyclodextrin complex
-
C.J. Betlach, M.A. Gonzalez, B.C. Mckiernan, C. Neff-Davis, N. Bodor, Oral pharmacokinetics of carbamazepine in dogs from commercial tablets and a cyclodextrin complex, J. Pharm. Sci. 82 (1993) 1058-1060.
-
(1993)
J. Pharm. Sci.
, vol.82
, pp. 1058-1060
-
-
Betlach, C.J.1
Gonzalez, M.A.2
Mckiernan, B.C.3
Neff-Davis, C.4
Bodor, N.5
-
51
-
-
0028920379
-
β-Cyclodextrin derivatives, SBE-β-CD and HB-β-CD, increase the oral bioavailability of cinnarizine in beagle dogs
-
T. Järvinen, K. Järvinen, N. Schwarting, V.J. Stella, β-Cyclodextrin derivatives, SBE-β-CD and HB-β-CD, increase the oral bioavailability of cinnarizine in beagle dogs, J. Pharm. Sci. 84 (1995) 295-299.
-
(1995)
J. Pharm. Sci.
, vol.84
, pp. 295-299
-
-
Järvinen, T.1
Järvinen, K.2
Schwarting, N.3
Stella, V.J.4
-
52
-
-
0031024463
-
Crystallization and polymorphic transition behavior of chloramphenicol palmitate in 2-hydroxypropyl-β-cyclodextrin matrix
-
F. Hirayama, M. Usami, K. Kimura, K. Uekama, Crystallization and polymorphic transition behavior of chloramphenicol palmitate in 2-hydroxypropyl-β-cyclodextrin matrix, Eur. J. Pharm. Sci. 5 (1997) 23-30.
-
(1997)
Eur. J. Pharm. Sci.
, vol.5
, pp. 23-30
-
-
Hirayama, F.1
Usami, M.2
Kimura, K.3
Uekama, K.4
-
53
-
-
0030956201
-
Amorphous spironolactone-hydroxypropylated cyclodextrins with superior dissolution and oral bioavailability
-
O.A. Soliman, K. Kimura, F. Hirayama, K. Uekama, H.M. El-Sabbagh, A.H. Abd ElGawad, F.M. Hashim, Amorphous spironolactone-hydroxypropylated cyclodextrins with superior dissolution and oral bioavailability, Int. J. Pharm. 149 (1997) 73-83.
-
(1997)
Int. J. Pharm.
, vol.149
, pp. 73-83
-
-
Soliman, O.A.1
Kimura, K.2
Hirayama, F.3
Uekama, K.4
El-Sabbagh, H.M.5
Abd Elgawad, A.H.6
Hashim, F.M.7
-
54
-
-
0028116075
-
Effect of 2-hydroxypropyl-β-cyclodextrin on crystallization and polymorphic transition of nifedipine in solid state
-
F. Hirayama, Z. Wang, K. Uekama, Effect of 2-hydroxypropyl-β-cyclodextrin on crystallization and polymorphic transition of nifedipine in solid state, Pharm. Res. 11 (1994) 1766-1770.
-
(1994)
Pharm. Res.
, vol.11
, pp. 1766-1770
-
-
Hirayama, F.1
Wang, Z.2
Uekama, K.3
-
55
-
-
0022599556
-
Hydrophilic cyclodextrin derivatives enable effective oral administration of steroidal hormones
-
J. Pitha, S.M. Harman, M.E. Michel, Hydrophilic cyclodextrin derivatives enable effective oral administration of steroidal hormones, J. Pharm. Sci. 75 (1986) 165-167.
-
(1986)
J. Pharm. Sci.
, vol.75
, pp. 165-167
-
-
Pitha, J.1
Harman, S.M.2
Michel, M.E.3
-
56
-
-
0023612459
-
γ-Cyclodextrin: Testosterone complex suitable for sublingual administration
-
J. Pitha, E.J. Anaissie, K. Uekama, γ-Cyclodextrin: testosterone complex suitable for sublingual administration, J. Pharm. Sci. 76 (1987) 788-790.
-
(1987)
J. Pharm. Sci.
, vol.76
, pp. 788-790
-
-
Pitha, J.1
Anaissie, E.J.2
Uekama, K.3
-
57
-
-
0024401340
-
Testosterone in a cyclodextrin containing formulation: Behavioral and physiological effects of episode-like pulses in rats
-
G.T. Tayler, J. Weiss, J. Pitha, Testosterone in a cyclodextrin containing formulation: behavioral and physiological effects of episode-like pulses in rats, Pharm. Res. 6 (1989) 641-646.
-
(1989)
Pharm. Res.
, vol.6
, pp. 641-646
-
-
Tayler, G.T.1
Weiss, J.2
Pitha, J.3
-
58
-
-
0025798996
-
Sublingual administration of testosterone-hydroxypropyl-β-cyclodextrin inclusion complex simulates episodic androgen release in hypogonadal men
-
C.A. Stuenkel, R.E. Dudley, S.S. Yen, Sublingual administration of testosterone-hydroxypropyl-β-cyclodextrin inclusion complex simulates episodic androgen release in hypogonadal men, J. Clin. Endocrinol. Metab. 72 (1991) 1054-1059.
-
(1991)
J. Clin. Endocrinol. Metab.
, vol.72
, pp. 1054-1059
-
-
Stuenkel, C.A.1
Dudley, R.E.2
Yen, S.S.3
-
59
-
-
0028788046
-
Pharmacokinetics, bioefficacy, and safety of sublingual testosterone cyclodextrin in hypogonadal men: Comparison to testosterone enanthate
-
B. Salehian, C. Wang, G. Alexander, T. Davidson, V. McDonald, N. Berman, R.E. Dudley, F. Ziel, R.S. Swerdloff, Pharmacokinetics, bioefficacy, and safety of sublingual testosterone cyclodextrin in hypogonadal men: comparison to testosterone enanthate, J. Clin. Endocrinol. Metab. 80 (1995) 2567-3575.
-
(1995)
J. Clin. Endocrinol. Metab.
, vol.80
, pp. 2567-3575
-
-
Salehian, B.1
Wang, C.2
Alexander, G.3
Davidson, T.4
McDonald, V.5
Berman, N.6
Dudley, R.E.7
Ziel, F.8
Swerdloff, R.S.9
-
60
-
-
0030022065
-
Design and in vivo testing of 17β-estradiol- Hydroxypropyl-β-cyclodextrin sublingual tablets
-
H. Fridriksdottir, T. Loftsson, J.A. Gudmundsson, G.J. Bjarnason, M. Kjeld, T. Thorsteinsson, Design and in vivo testing of 17β-estradiol- hydroxypropyl-β-cyclodextrin sublingual tablets, Pharmazie 51 (1996) 39-42.
-
(1996)
Pharmazie
, vol.51
, pp. 39-42
-
-
Fridriksdottir, H.1
Loftsson, T.2
Gudmundsson, J.A.3
Bjarnason, G.J.4
Kjeld, M.5
Thorsteinsson, T.6
-
61
-
-
0024432730
-
Enhanced bioavailability of digoxin by γ-cyclodextrin complexation: Evaluation for sublingual and oral administrations in human
-
H. Seo, K. Uekama, Enhanced bioavailability of digoxin by γ-cyclodextrin complexation: evaluation for sublingual and oral administrations in human, Yakugaku Zasshi 109 (1989) 778-782.
-
(1989)
Yakugaku Zasshi
, vol.109
, pp. 778-782
-
-
Seo, H.1
Uekama, K.2
-
62
-
-
0029616701
-
Evaluation of gastrointestinal behavior in the rat of amphiphilic β-cyclodextrin nanocapsules, loaded with indomethacin
-
M. Skiba, C. Morvan, D. Duchêne, F. Puisieux, D. Wouessidjewe, Evaluation of gastrointestinal behavior in the rat of amphiphilic β-cyclodextrin nanocapsules, loaded with indomethacin, Int. J. Pharm. 126 (1995) 275-279.
-
(1995)
Int. J. Pharm.
, vol.126
, pp. 275-279
-
-
Skiba, M.1
Morvan, C.2
Duchêne, D.3
Puisieux, F.4
Wouessidjewe, D.5
-
63
-
-
0027269952
-
In vitro and in vivo evaluation of delayed-release behavior of diltiazem from its O-carboxymethyl-O-ethyl-β-cyclodextrin complex
-
K. Uekama, T. Horikawa, Y. Horiuchi, F. Hirayama, In vitro and in vivo evaluation of delayed-release behavior of diltiazem from its O-carboxymethyl-O-ethyl-β-cyclodextrin complex, J. Control. Release 25 (1993) 99-106.
-
(1993)
J. Control. Release
, vol.25
, pp. 99-106
-
-
Uekama, K.1
Horikawa, T.2
Horiuchi, Y.3
Hirayama, F.4
-
64
-
-
0028945752
-
In-vivo and in-vitro correlation for delayed-release behavior of a molsidomine/ O-carboxymethyl-O-ethyl-β-cyclodextrin complex in gastric acidity-controlled dogs
-
T. Horikawa, F. Hirayama, K. Uekama, In-vivo and in-vitro correlation for delayed-release behavior of a molsidomine/ O-carboxymethyl-O-ethyl-β-cyclodextrin complex in gastric acidity-controlled dogs, J. Pharm. Pharmacol. 47 (1995) 124-127.
-
(1995)
J. Pharm. Pharmacol.
, vol.47
, pp. 124-127
-
-
Horikawa, T.1
Hirayama, F.2
Uekama, K.3
-
65
-
-
0025305421
-
Slow-release characteristics of diltiazem from ethylated β-cyclodextrin complexes
-
Y. Horiuchi, F. Hirayama, K. Uekama, Slow-release characteristics of diltiazem from ethylated β-cyclodextrin complexes, J. Pharm. Sci. 79 (1990) 128-132.
-
(1990)
J. Pharm. Sci.
, vol.79
, pp. 128-132
-
-
Horiuchi, Y.1
Hirayama, F.2
Uekama, K.3
-
66
-
-
0023759862
-
Utilization of diethyl-β-cyclodextrin as a sustained-release carrier for isosorbide dinitrate
-
F. Hirayama, N. Hirashima, K. Abe, K. Uekama, T. Ijitsu, M. Ueno, Utilization of diethyl-β-cyclodextrin as a sustained-release carrier for isosorbide dinitrate, J. Pharm. Sci. 77 (1989) 233-236.
-
(1989)
J. Pharm. Sci.
, vol.77
, pp. 233-236
-
-
Hirayama, F.1
Hirashima, N.2
Abe, K.3
Uekama, K.4
Ijitsu, T.5
Ueno, M.6
-
67
-
-
0031013890
-
Sustained-release of flufenamic acid from a drug-triacetyl-β-cyclodextrin complex
-
K. Nakanishi, T. Masukawa, T. Nadai, K. Yoshii, S. Okada, K. Miyajima, Sustained-release of flufenamic acid from a drug-triacetyl-β-cyclodextrin complex, Biol. Pharm. Bull. 20 (1997) 66-70.
-
(1997)
Biol. Pharm. Bull.
, vol.20
, pp. 66-70
-
-
Nakanishi, K.1
Masukawa, T.2
Nadai, T.3
Yoshii, K.4
Okada, S.5
Miyajima, K.6
-
68
-
-
25444508474
-
Release-control of a water-soluble drug by film-forming trivaleryl-β-cyclodextrin
-
in press
-
M. Yamada, F. Hirayama, K. Uekama, Release-control of a water-soluble drug by film-forming trivaleryl-β-cyclodextrin, Drug Delivery System, 14, in press.
-
Drug Delivery System
, pp. 14
-
-
Yamada, M.1
Hirayama, F.2
Uekama, K.3
-
69
-
-
0028131276
-
Peracylated β-cyclodextrins as novel sustained-release carriers for a water-soluble drug, molsidomine
-
K. Uekama, T. Horikawa, M. Yamanaka, F. Hirayama, Peracylated β-cyclodextrins as novel sustained-release carriers for a water-soluble drug, molsidomine, J. Pharm. Pharmacol. 46 (1994) 714-717.
-
(1994)
J. Pharm. Pharmacol.
, vol.46
, pp. 714-717
-
-
Uekama, K.1
Horikawa, T.2
Yamanaka, M.3
Hirayama, F.4
-
70
-
-
84988148682
-
Enhanced bioavailability and reduced metabolism of salbutamol by perbutanoyl-β-cyclodextrin after oral administration in dogs
-
F. Hirayama, T. Horikawa, M. Yamanaka, K. Uekama, Enhanced bioavailability and reduced metabolism of salbutamol by perbutanoyl-β-cyclodextrin after oral administration in dogs, Pharm. Sci. 1 (1995) 517-520.
-
(1995)
Pharm. Sci.
, vol.1
, pp. 517-520
-
-
Hirayama, F.1
Horikawa, T.2
Yamanaka, M.3
Uekama, K.4
-
71
-
-
0030318104
-
Controlled release of diltiazem by a combination of short- And long-chain peracylated-β-cyclodextrins in dogs
-
O.A. Soliman, K. Kimura, F. Hirayama, K. Uekama, H.M. El-Sabbagh, A.H. Abd ElGawad, F.M. Hashim, Controlled release of diltiazem by a combination of short- and long-chain peracylated-β-cyclodextrins in dogs, Pharm. Sci. 2 (1996) 533-536.
-
(1996)
Pharm. Sci.
, vol.2
, pp. 533-536
-
-
Soliman, O.A.1
Kimura, K.2
Hirayama, F.3
Uekama, K.4
El-Sabbagh, H.M.5
Abd Elgawad, A.H.6
Hashim, F.M.7
-
72
-
-
0026505701
-
Inhibitory effect of 2-hydroxypropyl-β-cyclodextrin on crystal-growth of nifedipine during storage: Superior dissolution and oral bioavailability compared with polyvinylpyrrolidone K-30
-
K. Uekama, K. Ikegami, Z. Wang, Y. Horiuchi, F. Hirayama, Inhibitory effect of 2-hydroxypropyl-β-cyclodextrin on crystal-growth of nifedipine during storage: superior dissolution and oral bioavailability compared with polyvinylpyrrolidone K-30, J. Pharm. Pharmacol. 44 (1992) 73-78.
-
(1992)
J. Pharm. Pharmacol.
, vol.44
, pp. 73-78
-
-
Uekama, K.1
Ikegami, K.2
Wang, Z.3
Horiuchi, Y.4
Hirayama, F.5
-
73
-
-
0027380386
-
Release characteristics of nifedipine from 2-hydroxypropyl-β-cyclodextrin complex during storage and its modification of hybridizing polyvinylpyrrolidone K-30
-
Z. Wang, K. Ikegami, F. Hirayama, K. Uekama, Release characteristics of nifedipine from 2-hydroxypropyl-β-cyclodextrin complex during storage and its modification of hybridizing polyvinylpyrrolidone K-30, Chem. Pharm. Bull. 41 (1993) 1822-1826.
-
(1993)
Chem. Pharm. Bull.
, vol.41
, pp. 1822-1826
-
-
Wang, Z.1
Ikegami, K.2
Hirayama, F.3
Uekama, K.4
-
74
-
-
0027441148
-
Design and in-vitro evaluation of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-β-cyclodextrin and hydroxypropyl cellulose
-
Z. Wang, F. Hirayama, K. Uekama, Design and in-vitro evaluation of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-β-cyclodextrin and hydroxypropyl cellulose, J. Pharm. Pharmacol. 45 (1993) 942-946.
-
(1993)
J. Pharm. Pharmacol.
, vol.45
, pp. 942-946
-
-
Wang, Z.1
Hirayama, F.2
Uekama, K.3
-
75
-
-
0028237692
-
In-vivo and in-vitro evaluations of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-β-cyclodextrin and hydroxypropyl celluloses in dogs
-
Z. Wang, F. Hirayama, K. Uekama, In-vivo and in-vitro evaluations of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-β-cyclodextrin and hydroxypropyl celluloses in dogs, J. Pharm. Pharmacol. 46 (1994) 505-507.
-
(1994)
J. Pharm. Pharmacol.
, vol.46
, pp. 505-507
-
-
Wang, Z.1
Hirayama, F.2
Uekama, K.3
-
76
-
-
0025219744
-
Design and in vitro evaluation of slow-release dosage form of piretanide: Utility of β-cyclodextrin/cellulose derivative combination as a modified-release drug carrier
-
K. Uekama, K. Matsubara, K. Abe, Y. Horiuchi, F. Hirayama, N. Suzuki, Design and in vitro evaluation of slow-release dosage form of piretanide: utility of β-cyclodextrin/cellulose derivative combination as a modified-release drug carrier, J. Pharm. Sci. 79 (1990) 244-248.
-
(1990)
J. Pharm. Sci.
, vol.79
, pp. 244-248
-
-
Uekama, K.1
Matsubara, K.2
Abe, K.3
Horiuchi, Y.4
Hirayama, F.5
Suzuki, N.6
-
77
-
-
0022408524
-
Osmotic flow through controlled porosity films: An approach to delivery of water-soluble compounds
-
G.M. Zentner, G.S. Rork, K.J. Himmelstein, Osmotic flow through controlled porosity films: an approach to delivery of water-soluble compounds, J. Control. Release 2 (1989) 217-229.
-
(1989)
J. Control. Release
, vol.2
, pp. 217-229
-
-
Zentner, G.M.1
Rork, G.S.2
Himmelstein, K.J.3
-
79
-
-
0030053698
-
The interaction of charged and uncharged drugs with neutral (HB-β-CD) and anionically charged (SBE-β-CD) β-cyclodextrins
-
K. Okimoto, R.A. Rajewski, K. Uekama, J.A. Jana, V.J. Stella, The interaction of charged and uncharged drugs with neutral (HB-β-CD) and anionically charged (SBE-β-CD) β-cyclodextrins, Pharm. Res. 13 (1996) 256-264.
-
(1996)
Pharm. Res.
, vol.13
, pp. 256-264
-
-
Okimoto, K.1
Rajewski, R.A.2
Uekama, K.3
Jana, J.A.4
Stella, V.J.5
-
80
-
-
0344537806
-
7m-β-cyclodextrin
-
Santiago de Compostela
-
7m-β-cyclodextrin, in: Abstracts of the 9th International Symposium on Cyclodextrins, Santiago de Compostela, 1998, pp. 3-15.
-
(1998)
Abstracts of the 9th International Symposium on Cyclodextrins
, pp. 3-15
-
-
Okimoto, K.1
Miyake, M.2
Ohnishi, N.3
Irie, T.4
Uekama, K.5
Rajewski, R.A.6
Stella, V.J.7
-
81
-
-
0023632674
-
Redox drug delivery systems for targeting drugs to the brain
-
N. Bodor, Redox drug delivery systems for targeting drugs to the brain, Ann. NY Acad. Sci. 507 (1987) 289-306.
-
(1987)
Ann. NY Acad. Sci.
, vol.507
, pp. 289-306
-
-
Bodor, N.1
-
84
-
-
0030009471
-
In-vitro evaluation of biphenylylacetic acid-β-cyclodextrin conjugates as colon-targeting prodrugs: Drug release behavior in rat biological media
-
F. Hirayama, K. Minami, K. Uekama, In-vitro evaluation of biphenylylacetic acid-β-cyclodextrin conjugates as colon-targeting prodrugs: drug release behavior in rat biological media, J. Pharm. Pharmacol. 48 (1996) 27-31.
-
(1996)
J. Pharm. Pharmacol.
, vol.48
, pp. 27-31
-
-
Hirayama, F.1
Minami, K.2
Uekama, K.3
-
85
-
-
0031807470
-
Colon-specific drug delivery based on a cyclodextrin prodrug: Release behavior of biphenylylacetic acid from its cyclodextrin conjugates in rat intestinal tracts after oral administration
-
K. Minami, F. Hirayama, K. Uekama, Colon-specific drug delivery based on a cyclodextrin prodrug: release behavior of biphenylylacetic acid from its cyclodextrin conjugates in rat intestinal tracts after oral administration, J. Pharm. Sci. 87 (1998) 715-720.
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 715-720
-
-
Minami, K.1
Hirayama, F.2
Uekama, K.3
-
86
-
-
0029871091
-
The blood-brain barrier: Principles for targeting peptides and drugs to the central nervous system
-
D.J. Begley, The blood-brain barrier: principles for targeting peptides and drugs to the central nervous system, J. Pharm. Pharmacol. 48 (1996) 136-146.
-
(1996)
J. Pharm. Pharmacol.
, vol.48
, pp. 136-146
-
-
Begley, D.J.1
-
87
-
-
0006645882
-
Prodrugs versus soft drugs
-
H. Bundgaard (Ed.), Elsevier, Amsterdam, Ch. 11
-
N. Bodor, Prodrugs versus soft drugs, in: H. Bundgaard (Ed.), Design of Prodrugs. Elsevier, Amsterdam, 1985, Ch. 11, pp. 333-354.
-
(1985)
Design of Prodrugs
, pp. 333-354
-
-
Bodor, N.1
-
88
-
-
0024269519
-
Improved delivery through biological membranes. XXXI: Solubilization and stabilization of an estradiol chemical delivery system by modified β-cyclodextrins
-
M.E. Brewster, K. Estes, T. Loftsson, R. Perchalski, H. Derendorf, G. Mullersman, N. Bodor, Improved delivery through biological membranes. XXXI: solubilization and stabilization of an estradiol chemical delivery system by modified β-cyclodextrins, J. Pharm. Sci. 77 (1988) 981-985.
-
(1988)
J. Pharm. Sci.
, vol.77
, pp. 981-985
-
-
Brewster, M.E.1
Estes, K.2
Loftsson, T.3
Perchalski, R.4
Derendorf, H.5
Mullersman, G.6
Bodor, N.7
-
89
-
-
0023886573
-
Brain-enhanced delivery of testosterone using a chemical delivery system complexed with 2-hydoxypropyl-β-cyclodextrin
-
W.R. Anderson, J.W. Simpkins, M.E. Brewster, N. Bodor, Brain-enhanced delivery of testosterone using a chemical delivery system complexed with 2-hydoxypropyl-β-cyclodextrin, Drug Design Deliv. 2 (1988) 287-298.
-
(1988)
Drug Design Deliv.
, vol.2
, pp. 287-298
-
-
Anderson, W.R.1
Simpkins, J.W.2
Brewster, M.E.3
Bodor, N.4
-
90
-
-
0025824035
-
Solubilization and stabilization of a benzylpenicillin chemical delivery system by 2-hydroxypropyl-β-cyclodextrin
-
E. Pop, T. Loftsson, N. Bodor, Solubilization and stabilization of a benzylpenicillin chemical delivery system by 2-hydroxypropyl-β-cyclodextrin, Pharm. Res. 8 (1991) 1044-1049.
-
(1991)
Pharm. Res.
, vol.8
, pp. 1044-1049
-
-
Pop, E.1
Loftsson, T.2
Bodor, N.3
-
91
-
-
0030947274
-
Effect of a chemical delivery system for dexamethasone (Dex-CDS) on peritumoral edema in an experimental brain tumor model
-
T. Siegal, F. Soti, A. Biegon, E. Pop, M.E. Brewster, Effect of a chemical delivery system for dexamethasone (Dex-CDS) on peritumoral edema in an experimental brain tumor model, Pharm. Res. 14 (1997) 672-675.
-
(1997)
Pharm. Res.
, vol.14
, pp. 672-675
-
-
Siegal, T.1
Soti, F.2
Biegon, A.3
Pop, E.4
Brewster, M.E.5
-
92
-
-
0027471803
-
Synthesis of a new carrier: N(Leu-enkephalin)yl-6-amino-6-deoxy-cyclomaltoheptaose
-
F. Djedaini-Pilard, J. Désalos, B. Perly, Synthesis of a new carrier: N(Leu-enkephalin)yl-6-amino-6-deoxy-cyclomaltoheptaose, Tetrahedron Lett. 34 (1993) 2457-2460.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 2457-2460
-
-
Djedaini-Pilard, F.1
Désalos, J.2
Perly, B.3
-
93
-
-
0027191259
-
A new approach to enhance bioavailability of biologically active peptides: Conjugation of a 5 opioid agonist to β-cyclodextrin
-
M.K. Hristova-Kazmierski, P. Horan, P. Davis, H.I. Yamamura, T. Kramer, R. Horvath, W.M. Kazmierski, F. Porreca, V. Hruby, A new approach to enhance bioavailability of biologically active peptides: conjugation of a 5 opioid agonist to β-cyclodextrin, Bioorg. Med. Chem. Lett. 3 (1993) 831-834.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 831-834
-
-
Hristova-Kazmierski, M.K.1
Horan, P.2
Davis, P.3
Yamamura, H.I.4
Kramer, T.5
Horvath, R.6
Kazmierski, W.M.7
Porreca, F.8
Hruby, V.9
-
95
-
-
0027692111
-
Synthesis of bulky β-lactams for inhibition of cell surface β-lactamase activity
-
D.N. Karunaratne, S. Farmer, R.E.W. Hancock, Synthesis of bulky β-lactams for inhibition of cell surface β-lactamase activity, Bioconjugate Chem. 4 (1993) 434-439.
-
(1993)
Bioconjugate Chem.
, vol.4
, pp. 434-439
-
-
Karunaratne, D.N.1
Farmer, S.2
Hancock, R.E.W.3
-
96
-
-
0030888946
-
Impermeant antitumor sulfonylurea conjugates that inhibit plasma membrane NADH oxidase and growth of HeLa cells in culture: Identification of binding proteins from sera of cancer patients
-
C. Kim, W.C. MacKellar, N. Cho, S.R. Byrn, D.J. Morre, Impermeant antitumor sulfonylurea conjugates that inhibit plasma membrane NADH oxidase and growth of HeLa cells in culture: identification of binding proteins from sera of cancer patients, Biochim. Biophys. Acta 1324 (1997) 171-181.
-
(1997)
Biochim. Biophys. Acta
, vol.1324
, pp. 171-181
-
-
Kim, C.1
MacKellar, W.C.2
Cho, N.3
Byrn, S.R.4
Morre, D.J.5
-
97
-
-
0003880161
-
-
Garland Publishing, New York
-
B. Alberts, D. Bray, J. Lewis, M. Raff, K. Roberts, J.D. Watson (Ed.), Molecular Biology of the Cell, third ed., Garland Publishing, New York, 1994.
-
(1994)
Molecular Biology of the Cell, Third Ed.
-
-
Alberts, B.1
Bray, D.2
Lewis, J.3
Raff, M.4
Roberts, K.5
Watson, J.D.6
-
98
-
-
84963436258
-
New β-cyclodextrin derivatives possessing biologically active saccharide antennae
-
H. Parrot-Lopez, E. Leray, A.W. Coleman, New β-cyclodextrin derivatives possessing biologically active saccharide antennae, Supramol. Chem. 3 (1993) 37-42.
-
(1993)
Supramol. Chem.
, vol.3
, pp. 37-42
-
-
Parrot-Lopez, H.1
Leray, E.2
Coleman, A.W.3
-
99
-
-
0028215921
-
Synthesis of new oligosaccharidyl-thio-β-cyclodextrins (CDS): A novel family of potent drug-targeting vectors
-
L. Robertis, C. Lancelon-Pin, H. Driguez, F. Attioui, R. Bonaly, A. Marsura, Synthesis of new oligosaccharidyl-thio-β-cyclodextrins (CDS): a novel family of potent drug-targeting vectors, Bioorg. Med. Chem. Lett. 4 (1994) 1127-1130.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 1127-1130
-
-
Robertis, L.1
Lancelon-Pin, C.2
Driguez, H.3
Attioui, F.4
Bonaly, R.5
Marsura, A.6
-
100
-
-
0029065414
-
Chemical-enzymatic synthesis and bioactivity of mono-6-[gal-β-1,4-glcNAc-β-(1,6′)-hexyl]amido-6-deoxy- cycloheptaamylose
-
E. Leray, H. Parrot-Lopez, C. Auge, A.W. Coleman, C. Finance, R. Bonaly, Chemical-enzymatic synthesis and bioactivity of mono-6-[gal-β-1,4-glcNAc-β-(1,6′)-hexyl]amido-6-deoxy- cycloheptaamylose. J. Chem. Soc. Chem. Commun. (1995) 1019-1020.
-
(1995)
J. Chem. Soc. Chem. Commun.
, pp. 1019-1020
-
-
Leray, E.1
Parrot-Lopez, H.2
Auge, C.3
Coleman, A.W.4
Finance, C.5
Bonaly, R.6
-
101
-
-
0031014613
-
The specificity of association between concanavalin a and oligosaccharide-branched cyclodextrins with an optical biosensor
-
H. Imata, K. Kubota, K. Hattori, M. Aoyagi, C. Jindoh, The specificity of association between concanavalin A and oligosaccharide-branched cyclodextrins with an optical biosensor, Bioorg. Med. Chem. Lett. 7 (1997) 109-112.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 109-112
-
-
Imata, H.1
Kubota, K.2
Hattori, K.3
Aoyagi, M.4
Jindoh, C.5
-
102
-
-
0028673204
-
Recognition ability and cytotoxicity of some oligosaccharidyl substituted β-cyclodextrins
-
F. Attioui, A. Al-Omar, E. Leray, H. Parrot-Lopez, C. Finance, R. Bonaly, Recognition ability and cytotoxicity of some oligosaccharidyl substituted β-cyclodextrins, Biol. Cell 82 (1994) 161-167.
-
(1994)
Biol. Cell
, vol.82
, pp. 161-167
-
-
Attioui, F.1
Al-Omar, A.2
Leray, E.3
Parrot-Lopez, H.4
Finance, C.5
Bonaly, R.6
-
103
-
-
0029335250
-
Synthesis, hybridization properties, nuclease stability, and cellular uptake of the oligonucleotide-amino-β-cyclodextrins and adamantane conjugates
-
I. Habus, Q. Zhao, S. Agrawal, Synthesis, hybridization properties, nuclease stability, and cellular uptake of the oligonucleotide-amino-β-cyclodextrins and adamantane conjugates, Bioconjugate Chem. 6 (1995) 327-331.
-
(1995)
Bioconjugate Chem.
, vol.6
, pp. 327-331
-
-
Habus, I.1
Zhao, Q.2
Agrawal, S.3
-
104
-
-
0028060595
-
Synthesis of doxorubicin-cyclodextrin conjugates
-
H. Tanaka, K. Kominato, R. Yamamoto, T. Yoshioka, H. Nishida, H. Tone, R. Okamoto, Synthesis of doxorubicin-cyclodextrin conjugates, J. Antibiot. 47 (1994) 1025-1029.
-
(1994)
J. Antibiot.
, vol.47
, pp. 1025-1029
-
-
Tanaka, H.1
Kominato, K.2
Yamamoto, R.3
Yoshioka, T.4
Nishida, H.5
Tone, H.6
Okamoto, R.7
-
105
-
-
84882524409
-
Pharmacological investigations of new peptide-cyclodextrins
-
Santiago de Compostela
-
C. Péan, A. Wijkhuisen, F. Djedaini-Pilard, C. Créminon, J. Grassi, B. Perly, Pharmacological investigations of new peptide-cyclodextrins, in: Abstracts of the 9th International Symposium on Cyclodextrins, Santiago de Compostela, 1998, p. 3-P-43.
-
(1998)
Abstracts of the 9th International Symposium on Cyclodextrins
, pp. 3-P43
-
-
Péan, C.1
Wijkhuisen, A.2
Djedaini-Pilard, F.3
Créminon, C.4
Grassi, J.5
Perly, B.6
-
106
-
-
84882524409
-
In vitro and in vivo investigation of the specific binding of substance P-γ-cyclodextrin adduct (SB-γ-CD) to rat brain NK1 receptors
-
Santiago de Compostela
-
C. Péan, J. Fische, A. Wijkhuisen, F. Djedaini-Pilard, C. Créminon, B. Perly, M. Conrath, In vitro and in vivo investigation of the specific binding of substance P-γ-cyclodextrin adduct (SB-γ-CD) to rat brain NK1 receptors, in: Abstracts of the 9th International Symposium on Cyclodextrins, Santiago de Compostela, 1998, p. 3-P-56.
-
(1998)
Abstracts of the 9th International Symposium on Cyclodextrins
, pp. 3-P56
-
-
Péan, C.1
Fische, J.2
Wijkhuisen, A.3
Djedaini-Pilard, F.4
Créminon, C.5
Perly, B.6
Conrath, M.7
-
107
-
-
0032558114
-
Cyclodextrin as carrier of peptide hormones: Conformational and biological properties of β-cyclodextrin/gastrin constructs
-
N. Schaschke, S. Fiori, E. Weyher, C. Escrieut, D. Fourmy, G. Muller, L. Moroder, Cyclodextrin as carrier of peptide hormones: conformational and biological properties of β-cyclodextrin/gastrin constructs, J. Am. Chem. Soc. 120 (1998) 7030-7038.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 7030-7038
-
-
Schaschke, N.1
Fiori, S.2
Weyher, E.3
Escrieut, C.4
Fourmy, D.5
Muller, G.6
Moroder, L.7
|