-
1
-
-
0035053631
-
Comparison of L-758 298, a prodrug for the selective neurokinin-1 antagonist L-754,030, with ondansetron for the prevention of cisplatin-induced emesis
-
Cocquyt V, Van Belle S, Reinhardt RR, Decramer ML, OBrien M, Schellens JH et al (2001). Comparison of L-758,298, a prodrug for the selective neurokinin-1 antagonist, L-754,030, with ondansetron for the prevention of cisplatin-induced emesis. Eur J Cancer, 37:835-842
-
(2001)
Eur J Cancer
, vol.37
, pp. 835-842
-
-
Cocquyt, V.1
Van Belle, S.2
Reinhardt, R.R.3
Decramer, M.L.4
O'Brien, M.5
Schellens, J.H.6
-
2
-
-
0033590464
-
Reduction of cisplatin-induced emesis by a selective neurokinin-1- receptor antagonist. L-754,030 Antiemetic Trials Group
-
Navari RM, Reinhardt RR, Gralla RJ, Kris MG, Hesketh PJ, Khojasteh A et al. (1999). Reduction of cisplatin-induced emesis by a selective neurokinin-1-receptor antagonist. L-754,030 Antiemetic Trials Group. N Engl J Med, 340:190-195
-
(1999)
N Engl J Med
, vol.340
, pp. 190-195
-
-
Navari, R.M.1
Reinhardt, R.R.2
Gralla, R.J.3
Kris, M.G.4
Hesketh, P.J.5
Khojasteh, A.6
-
3
-
-
0035868769
-
Prevention of cisplatin-induced emesis by the oral neurokinin-1 antagonist, MK-869, in combination with granisetron and dexamethasone or with dexamethasone alone
-
Campos D, Pereira JR, Reinhardt RR, Carracedo C, Poli S, Vogel C et al (2001). Prevention of cisplatin-induced emesis by the oral neurokinin-1 antagonist, MK-869, in combination with granisetron and dexamethasone or with dexamethasone alone. J Clin Oncol, 19:1759-1767
-
(2001)
J Clin Oncol
, vol.19
, pp. 1759-1767
-
-
Campos, D.1
Pereira, J.R.2
Reinhardt, R.R.3
Carracedo, C.4
Poli, S.5
Vogel, C.6
-
4
-
-
0036604223
-
Prevention of cisplatin-induced acute and delayed emesis by the selective neurokinin-1 antagonists, L-758,298 and MK-869
-
Van Belle S, Lichinitser MR, Navari RM, Garin AM, Decramer ML, Riviere A et al. (2002). Prevention of cisplatin-induced acute and delayed emesis by the selective neurokinin-1 antagonists, L-758,298 and MK-869. Cancer, 94:3032-3041
-
(2002)
Cancer
, vol.94
, pp. 3032-3041
-
-
Van Belle, S.1
Lichinitser, M.R.2
Navari, R.M.3
Garin, A.M.4
Decramer, M.L.5
Riviere, A.6
-
5
-
-
11144335472
-
Prevention of chemotherapy and radiotherapy-induced emesis: Results of the Perugia Consensus Conference
-
Antiemetic Subcommittee of the Multinational Association of supportive care in Cancer (MASCC
-
Antiemetic Subcommittee of the Multinational Association of supportive care in Cancer (MASCC). (1998). Prevention of chemotherapy and radiotherapy-induced emesis: Results of the Perugia Consensus Conference. Ann Oncol, 9:1022-1029
-
(1998)
Ann Oncol
, vol.9
, pp. 1022-1029
-
-
-
6
-
-
0030187153
-
Comparative studies of various antiemetic regimens
-
Roila F, Tonato M, Ballatori E, Del Favero A. (1996). Comparative studies of various antiemetic regimens. Support Care Cancer, 4:270-280
-
(1996)
Support Care Cancer
, vol.4
, pp. 270-280
-
-
Roila, F.1
Tonato, M.2
Ballatori, E.3
Del Favero, A.4
-
7
-
-
2342616739
-
Incidence of chemotherapy-induced nausea and emesis after modern antiemetics
-
Grunberg SM, Deuson RR, Mavros P, Geling O, Hansen M, Cruciani G et al. (2004). Incidence of chemotherapy-induced nausea and emesis after modern antiemetics. Cancer, 100:2261-2268
-
(2004)
Cancer
, vol.100
, pp. 2261-2268
-
-
Grunberg, S.M.1
Deuson, R.R.2
Mavros, P.3
Geling, O.4
Hansen, M.5
Cruciani, G.6
-
8
-
-
20844446627
-
The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: A Beagle dog model predicts improved bioavailability and diminished food effect on absorption in human
-
Wu Y, Loper A, Landis E, Hettrick L, Novak L, Lynn K et al. (2004). The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: A Beagle dog model predicts improved bioavailability and diminished food effect on absorption in human. Int J Pharm, 285:135-146
-
(2004)
Int J Pharm
, vol.285
, pp. 135-146
-
-
Wu, Y.1
Loper, A.2
Landis, E.3
Hettrick, L.4
Novak, L.5
Lynn, K.6
-
10
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system new scientific approaches to international regulatory standards
-
Löbenberg R, Amidon GL. (2000). Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur J Pharm Biopharm, 50:3-12
-
(2000)
Eur J Pharm Biopharm
, vol.50
, pp. 3-12
-
-
Löbenberg, R.1
Amidon, G.L.2
-
11
-
-
77955656443
-
Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans
-
Yasushi S, Ekarat J, Filippos K, Christos R, Jennifer BD. (2010). Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans. Eur J Pharm Biopharm, 76:95-104
-
(2010)
Eur J Pharm Biopharm
, vol.76
, pp. 95-104
-
-
Yasushi, S.1
Ekarat, J.2
Filippos, K.3
Christos, R.4
Jennifer, B.D.5
-
12
-
-
78349309563
-
Optimization of formulation and process variable of nanosuspension: An industrial perspective
-
Dhananjay SS, Seshasai MM, Gowthamrajanb K, Giriraj KT, Rajesh V, Parchuri SR. (2010). Optimization of formulation and process variable of nanosuspension: An industrial perspective. Int J Pharm, 402:213-220
-
(2010)
Int J Pharm
, vol.402
, pp. 213-220
-
-
Dhananjay, S.S.1
Seshasai, M.M.2
Gowthamrajanb, K.3
Giriraj, K.T.4
Rajesh, V.5
Parchuri, S.R.6
-
13
-
-
0035937599
-
Nanosuspensions as particulate drug formulations in therapy rationale for development and what we can expect for the future
-
Müller RH, Jacobs C, Kayser O. (2001). Nanosuspensions as particulate drug formulations in therapy. Rationale for development and what we can expect for the future. Adv Drug Deliv Rev, 47:3-19
-
(2001)
Adv Drug Deliv Rev
, vol.47
, pp. 3-19
-
-
Müller, R.H.1
Jacobs, C.2
Kayser, O.3
-
14
-
-
54349125120
-
Production and in vitro characterization of solid dosage form incorporating drug nanoparticles
-
Basa S, Muniyappan T, Karatgi P, Prabhu R, Pillai R. (2008). Production and in vitro characterization of solid dosage form incorporating drug nanoparticles. Drug Dev Ind Pharm, 34:1209-1218
-
(2008)
Drug Dev Ind Pharm
, vol.34
, pp. 1209-1218
-
-
Basa, S.1
Muniyappan, T.2
Karatgi, P.3
Prabhu, R.4
Pillai, R.5
-
15
-
-
85047692219
-
Novel formulation strategies for improving oral bioavailability of drugs with poor membrane permeation or presystemic metabolism
-
Aungst BJ. (1993). Novel formulation strategies for improving oral bioavailability of drugs with poor membrane permeation or presystemic metabolism. J Pharm Sci, 82:979-987
-
(1993)
J Pharm Sci
, vol.82
, pp. 979-987
-
-
Aungst, B.J.1
-
16
-
-
0342617694
-
Lipid-based vehicles for the oral delivery of poorly water soluble drugs
-
Humberstone AJ, Charman WN. (1997). Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv Drug Deliv Rev, 25:103-128
-
(1997)
Adv Drug Deliv Rev
, vol.25
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
17
-
-
0029562489
-
Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects
-
Constantinides PP. (1995). Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects. Pharm Res, 12:1561-1572
-
(1995)
Pharm Res
, vol.12
, pp. 1561-1572
-
-
Constantinides, P.P.1
-
18
-
-
0033805858
-
Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and selfmicroemulsifying drug delivery systems
-
Pouton CW. (2000). Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and selfmicroemulsifying drug delivery systems. Eur J Pharm Sci, 11 Suppl2:S93-S98
-
(2000)
Eur J Pharm Sci
, vol.11
, Issue.SUPPL. 12
-
-
Pouton, C.W.1
-
19
-
-
10444279209
-
Cyclodextrin-based pharmaceutics: Past, present and future
-
Davis ME, Brewster ME. (2004). Cyclodextrin-based pharmaceutics: Past, present and future. Nat Rev Drug Discov, 3:1023-1035
-
(2004)
Nat Rev Drug Discov
, vol.3
, pp. 1023-1035
-
-
Davis, M.E.1
Brewster, M.E.2
-
20
-
-
70349992906
-
Design and development of IT-101, a cyclodextrin-containing polymer conjugate of camptothecin
-
Davis ME. (2009). Design and development of IT-101, a cyclodextrin-containing polymer conjugate of camptothecin. Adv Drug Deliv Rev, 61:1189-1192
-
(2009)
Adv Drug Deliv Rev
, vol.61
, pp. 1189-1192
-
-
Davis, M.E.1
-
21
-
-
79953252044
-
Drug product development and pharmacological evaluation of a sparingly soluble novel camptothecin analog for peroral administration
-
Vijaykumar N, Pradeep K, Srinivasarao P, Raviraj P. (2010). Drug product development and pharmacological evaluation of a sparingly soluble novel camptothecin analog for peroral administration. Drug Delivery, 18:294-303
-
(2010)
Drug Delivery
, vol.18
, pp. 294-303
-
-
Vijaykumar, N.1
Pradeep, K.2
Srinivasarao, P.3
Raviraj, P.4
-
22
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins 1 drug solubilization and stabilization
-
Loftsson T, Brewster ME. (1996). Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. J Pharm Sci, 85:1017-1025
-
(1996)
J Pharm Sci
, vol.85
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
24
-
-
37849188962
-
Complexes of starch with inorganic guests
-
Horton D, ed. San Diego Academic Press
-
Tomasik P, Schilling CH. (1998). Complexes of starch with inorganic guests. In: Horton D, ed. Advances in Carbohydrate Chemistry and Biochemistry. Vol. 53. San Diego: Academic Press, 263-243
-
(1998)
Advances in Carbohydrate Chemistry and Biochemistry
, vol.53
, pp. 263-243
-
-
Tomasik, P.1
Schilling, C.H.2
-
26
-
-
24344508654
-
Evaluation of cyclodextrin solubilization of drugs
-
Loftsson T, Hreinsdósttir D, Másson M. (2005). Evaluation of cyclodextrin solubilization of drugs. Int J Pharm, 302:18-28
-
(2005)
Int J Pharm
, vol.302
, pp. 18-28
-
-
Loftsson, T.1
Hreinsdósttir, D.2
Másson, M.3
-
27
-
-
0001146107
-
Solubility behavior of B-cyclodextrin in water/cosolvent mixtures
-
Chatjigakis AK, Donze C, Coleman AW. (1992). Solubility behavior of B-cyclodextrin in water/cosolvent mixtures. Anal Chem, 64:1632-1634
-
(1992)
Anal Chem
, vol.64
, pp. 1632-1634
-
-
Chatjigakis, A.K.1
Donze, C.2
Coleman, A.W.3
-
29
-
-
44749087279
-
Dissolution media simulating conditions in the proximal human gastrointestinal tract: An update
-
Ekarat J, Niels J, Christos R, Jennifer BD. (2008). Dissolution Media Simulating Conditions in the Proximal Human Gastrointestinal Tract: An Update. Pharm Res, 25:1663-1676
-
(2008)
Pharm Res
, vol.25
, pp. 1663-1676
-
-
Ekarat, J.1
Niels, J.2
Christos, R.3
Jennifer, B.D.4
-
30
-
-
0037409270
-
Study of solubility of isoproturon by its complexation with beta-cyclodextrin
-
Manolikar MK, Sawant MR. (2003). Study of solubility of isoproturon by its complexation with beta-cyclodextrin. Chemosphere, 51:811-816
-
(2003)
Chemosphere
, vol.51
, pp. 811-816
-
-
Manolikar, M.K.1
Sawant, M.R.2
-
31
-
-
0036172264
-
Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds
-
Fernandes CM, Teresa Vieira M, Veiga FJ. (2002). Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds. Eur J Pharm Sci, 15:79-88
-
(2002)
Eur J Pharm Sci
, vol.15
, pp. 79-88
-
-
Fernandes, C.M.1
Teresa Vieira, M.2
Veiga, F.J.3
-
32
-
-
0001470568
-
Drugs, in cyclodextrins in liposomes: A novel approach to the chemical stability of drugs sensitive to hydrolysis
-
Loukas YL, Vraka V, Gregoriadis G. (1998). Drugs, in cyclodextrins in liposomes: A novel approach to the chemical stability of drugs sensitive to hydrolysis. Int J Pharm, 162:137-142
-
(1998)
Int J Pharm
, vol.162
, pp. 137-142
-
-
Loukas, Y.L.1
Vraka, V.2
Gregoriadis, G.3
|