-
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
-
1:CAS:528:DC%2BD3MXislGhtLc%3D 11313170 10.1016/S0959-8049(00)00416-0
-
Cocquyt V, Van Belle S, Reinhardt RR, Decramer ML, O'Brien M, Schellens JH, et al. 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. 2001;37:835-42.
-
(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
-
1:CAS:528:DyaK1MXhtV2gtrY%3D 9917226 10.1056/NEJM199901213400304
-
Navari RM, Reinhardt RR, Gralla RJ, Kris MG, Hesketh PJ, Khojasteh A, et al. Reduction of cisplatin-induced emesis by a selective neurokinin-1-receptor antagonist. L-754, 030 Antiemetic Trials Group. N Engl J Med. 1999;340:190-5.
-
(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
-
-
17144408417
-
The oral NK1 antagonist aprepitant for prevention of nausea and vomiting in patients receiving highly emetogenic chemotherapy: A review
-
10.2165/00024669-200504010-00003
-
De Wit R, Hesketh PJ, Warr D, Petty K, Carides AD, Evans JK, et al. The oral NK1 antagonist aprepitant for prevention of nausea and vomiting in patients receiving highly emetogenic chemotherapy: a review. Am J Cancer. 2005;4:35-48.
-
(2005)
Am J Cancer
, vol.4
, pp. 35-48
-
-
De Wit, R.1
Hesketh, P.J.2
Warr, D.3
Petty, K.4
Carides, A.D.5
Evans, J.K.6
-
4
-
-
32144442187
-
Lack of efficacy of the substance P(Neurokinin 1 Receptor) antagonist aprepitant in the treatment of major depressive disorder
-
1:CAS:528:DC%2BD28Xhtlaqu74%3D 16248986 10.1016/j.biopsych.2005.07.013
-
Keller M, Montgomery S, Ball W, Morrison M, Snavely D, Liu GH, et al. Lack of efficacy of the substance P(Neurokinin 1 Receptor) antagonist aprepitant in the treatment of major depressive disorder. Biol Psychiatry. 2006;59:216-23.
-
(2006)
Biol Psychiatry
, vol.59
, pp. 216-223
-
-
Keller, M.1
Montgomery, S.2
Ball, W.3
Morrison, M.4
Snavely, D.5
Liu, G.H.6
-
5
-
-
44049083952
-
Nanomedicines in the treatment of emesis during chemotherapy: Focus on aprepitant
-
1:CAS:528:DC%2BD2sXmsF2ls74%3D 2673828 17722507 10.2147/nano.2007.2.1.13
-
Olver I, Shelukar S, Thompson KC. Nanomedicines in the treatment of emesis during chemotherapy: focus on aprepitant. Int J Nanomedicine. 2007;2:13-8.
-
(2007)
Int J Nanomedicine
, vol.2
, pp. 13-18
-
-
Olver, I.1
Shelukar, S.2
Thompson, K.C.3
-
6
-
-
77955656443
-
Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans
-
1:CAS:528:DC%2BC3cXhtVektL%2FP 20576487 10.1016/j.ejpb.2010.05.009
-
Shono Y, Jantratid E, Kesisoglou F, Reppas C, Dressman JB. Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans. Eur J Pharm Biopharm. 2010;76:95-104.
-
(2010)
Eur J Pharm Biopharm
, vol.76
, pp. 95-104
-
-
Shono, Y.1
Jantratid, E.2
Kesisoglou, F.3
Reppas, C.4
Dressman, J.B.5
-
7
-
-
2342616739
-
Incidence of chemotherapy-induced nausea and emesis after modern antiemetics
-
15139073 10.1002/cncr.20230
-
Grunberg SM, Deuson RR, Mavros P, Geling O, Hansen M, Cruciani G, et al. Incidence of chemotherapy-induced nausea and emesis after modern antiemetics. Cancer. 2004;100:2261-8.
-
(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
-
-
0035937599
-
Nanosuspensions as particulate drug formulations in therapy: Rationale for development and what we can expect for the future
-
11251242 10.1016/S0169-409X(00)00118-6
-
Müller RH, Jacobs C, Kayser O. Nanosuspensions as particulate drug formulations in therapy: rationale for development and what we can expect for the future. Adv Drug Deliv Rev. 2001;47:3-19.
-
(2001)
Adv Drug Deliv Rev
, vol.47
, pp. 3-19
-
-
Müller, R.H.1
Jacobs, C.2
Kayser, O.3
-
9
-
-
9644254099
-
Solid dispersions of nimodipine and polyethylene glycol 2000: Dissolution properties and physico-chemical characterisation Original Research Article
-
1:CAS:528:DC%2BD2cXhtValsrjL 15567307 10.1016/j.ejpb.2004.08.005
-
Urbanetz NA, Lippold BC. Solid dispersions of nimodipine and polyethylene glycol 2000: dissolution properties and physico-chemical characterisation Original Research Article. Eur J Pharm Biopharm. 2005;59:107-18.
-
(2005)
Eur J Pharm Biopharm
, vol.59
, pp. 107-118
-
-
Urbanetz, N.A.1
Lippold, B.C.2
-
11
-
-
13544258798
-
Preformulation study of the inclusion complex warfarin-β- cyclodextrin
-
1:CAS:528:DC%2BD2MXhtFejtLY%3D 15707726 10.1016/j.ijpharm.2004.11.013
-
Zingone G, Rubessa F. Preformulation study of the inclusion complex warfarin-β-cyclodextrin. Int J Pharm. 2005;291:3-10.
-
(2005)
Int J Pharm
, vol.291
, pp. 3-10
-
-
Zingone, G.1
Rubessa, F.2
-
12
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
-
1:CAS:528:DyaK28XlsFSrsr4%3D 8897265 10.1021/js950534b
-
Loftsson T, Brewster ME. Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. J Pharm Sci. 1996;85:1017-25.
-
(1996)
J Pharm Sci
, vol.85
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
13
-
-
0032215146
-
Characterization of an inclusion complex of cholesterol and hydroxypropyl-β-cyclodextrin
-
10.1016/S0939-6411(98)00033-2
-
Robert O, Williams III, Mahaguna V, Sriwongjanya M. Characterization of an inclusion complex of cholesterol and hydroxypropyl-β-cyclodextrin. Eur J Pharm Biopharm. 1998;46:355-60.
-
(1998)
Eur J Pharm Biopharm
, vol.46
, pp. 355-360
-
-
Robert, O.1
Williams, I.I.I.2
Mahaguna, V.3
Sriwongjanya, M.4
-
14
-
-
0037333948
-
Phase solubility studies of pure (-)-α-bisabolol andcamomile essential oil with β-cyclodextrin
-
1:CAS:528:DC%2BD3sXhvFaisrs%3D 12637105 10.1016/S0939-6411(02)00166-2
-
Waleczek KJ, Cabral Marques HM, Hempel B, Schmidt PC. Phase solubility studies of pure (-)-α-bisabolol andcamomile essential oil with β-cyclodextrin. Eur J Pharm Biopharm. 2003;55:247-51.
-
(2003)
Eur J Pharm Biopharm
, vol.55
, pp. 247-251
-
-
Waleczek, K.J.1
Cabral Marques, H.M.2
Hempel, B.3
Schmidt, P.C.4
-
15
-
-
30344458488
-
Preparation and characterization of inclusion complexes of prazosin hydrochloride with β-cyclodextrin and hydroxypropyl-β-cyclodextrin
-
1:CAS:528:DC%2BD28XksFCjuw%3D%3D 16095859 10.1016/j.jpba.2005.06.022
-
Liu LX, Zhu SY. Preparation and characterization of inclusion complexes of prazosin hydrochloride with β-cyclodextrin and hydroxypropyl-β- cyclodextrin. J Pharm Biomed Anal. 2006;40:122-7.
-
(2006)
J Pharm Biomed Anal
, vol.40
, pp. 122-127
-
-
Liu, L.X.1
Zhu, S.Y.2
-
16
-
-
0000817098
-
Phase solubility techniques
-
1:CAS:528:DyaF2MXktlGitrg%3D
-
Higuchi T, Connors KA. Phase solubility techniques. Adv Anal Chem Instrum. 1965;4:117-212.
-
(1965)
Adv Anal Chem Instrum
, vol.4
, pp. 117-212
-
-
Higuchi, T.1
Connors, K.A.2
-
17
-
-
84885598581
-
Inclusion complex of aprepitant with cyclodextrin: Evaluation of physico-chemical and pharmacokinetic properties
-
1:CAS:528:DC%2BC3sXhsFCrt7vK 23240730 10.3109/03639045.2012.737331
-
Ridhurkar DN, Ansari KA, Kumar D, Kaul NS, Krishnamurthy T, Dhawan S, et al. Inclusion complex of aprepitant with cyclodextrin: evaluation of physico-chemical and pharmacokinetic properties. Drug Dev Ind Pharm. 2013;39(11):1783-92.
-
(2013)
Drug Dev Ind Pharm
, vol.39
, Issue.11
, pp. 1783-1792
-
-
Ridhurkar, D.N.1
Ansari, K.A.2
Kumar, D.3
Kaul, N.S.4
Krishnamurthy, T.5
Dhawan, S.6
Pillai, R.7
-
19
-
-
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
-
1:CAS:528:DC%2BD2cXosFSrsbg%3D 15488686 10.1016/j.ijpharm.2004.08.001
-
Wu YH, Loper A, Landis E, Hettrick L, Novak L, Lynn K, et al. 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. 2004;285:135-46.
-
(2004)
Int J Pharm
, vol.285
, pp. 135-146
-
-
Wu, Y.H.1
Loper, A.2
Landis, E.3
Hettrick, L.4
Novak, L.5
Lynn, K.6
-
20
-
-
0036172264
-
Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds
-
1:CAS:528:DC%2BD38Xms1Glsg%3D%3D 11803134 10.1016/S0928-0987(01)00208-1
-
Fernandes CM, Teresa Vieira M, Veiga FJ. Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds. Eur J Pharm Sci. 2002;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
-
21
-
-
33847645406
-
A study on the supramolecular structure of inclusion complex of β-cyclodextrin with prazosin hydrochloride
-
1:CAS:528:DC%2BD2sXislWhu74%3D 10.1016/j.carbpol.2006.11.007
-
Liu LX, Zhu SY. A study on the supramolecular structure of inclusion complex of β-cyclodextrin with prazosin hydrochloride. Carbohydr Polym. 2007;68:472-6.
-
(2007)
Carbohydr Polym
, vol.68
, pp. 472-476
-
-
Liu, L.X.1
Zhu, S.Y.2
-
22
-
-
0001470568
-
Drugs in cyclodextrins, in liposomes: A novel approach to the chemical stability of drugs sensitive to hydrolysis
-
1:CAS:528:DyaK1cXitVeqtL0%3D 10.1016/S0378-5173(97)00421-3
-
Loukas YL, Vraka V, Gregoriadis G. Drugs in cyclodextrins, in liposomes: a novel approach to the chemical stability of drugs sensitive to hydrolysis. Int J Pharm. 1998;162:137-42.
-
(1998)
Int J Pharm
, vol.162
, pp. 137-142
-
-
Loukas, Y.L.1
Vraka, V.2
Gregoriadis, G.3
|