-
1
-
-
0034888569
-
In vitro-in vivo correlation (IVIVC) models for metformin after administration of modified-release (MR) oral dosage forms to healthy human volunteers
-
Balan G, Timmins P, Greene DS, et al. (2001). In vitro-in vivo correlation (IVIVC) models for metformin after administration of modified-release (MR) oral dosage forms to healthy human volunteers. J Pharm Sci 90:1176-85.
-
(2001)
J Pharm Sci
, vol.90
, pp. 1176-1185
-
-
Balan, G.1
Timmins, P.2
Greene, D.S.3
-
2
-
-
0038061542
-
Direct, differential-equation-based in-vitro-in-vivo correlation (IVIVC) method
-
Buchwald P. (2003). Direct, differential-equation-based in-vitro-in-vivo correlation (IVIVC) method. J Pharm Pharmacol 55:495-504.
-
(2003)
J Pharm Pharmacol
, vol.55
, pp. 495-504
-
-
Buchwald, P.1
-
3
-
-
52449096784
-
Assuring quality and performance of sustained and controlled release parenterals: Workshop report
-
Burgess DJ, Hussain AS, Ingallinera TS, et al. (2002). Assuring quality and performance of sustained and controlled release parenterals: workshop report. AAPS PharmSci 4:E7-8.
-
(2002)
AAPS PharmSci
, vol.4
, pp. E7-E8
-
-
Burgess, D.J.1
Hussain, A.S.2
Ingallinera, T.S.3
-
4
-
-
0026648961
-
Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom. Further evidence for an exendin receptor on dispersed acini from guinea pig pancreas
-
Eng J, Kleinman WA, Singh L, et al. (1992). Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom. Further evidence for an exendin receptor on dispersed acini from guinea pig pancreas. J Biol Chem 267:7402-5.
-
(1992)
J Biol Chem
, vol.267
, pp. 7402-7405
-
-
Eng, J.1
Kleinman, W.A.2
Singh, L.3
-
5
-
-
0027184119
-
Exendin-4 is a high potency agonist and truncated exendin-(9-39)-amide an antagonist at the glucagon-like peptide 1 - (7-36)-amide receptor of insulin-secreting beta-cells
-
Goke R, Fehmann HC, Linn T, et al. (1993). Exendin-4 is a high potency agonist and truncated exendin-(9-39)-amide an antagonist at the glucagon-like peptide 1 - (7-36)-amide receptor of insulin-secreting beta-cells. J Biol Chem 268:19650-5.
-
(1993)
J Biol Chem
, vol.268
, pp. 19650-19655
-
-
Goke, R.1
Fehmann, H.C.2
Linn, T.3
-
6
-
-
33947387173
-
A PK-PD model for predicting the impact of age, CYP2C9, and VKORC1 genotype on individualization of warfarin therapy
-
Hamberg AK, Dahl ML, Barban M, et al. (2007). A PK-PD model for predicting the impact of age, CYP2C9, and VKORC1 genotype on individualization of warfarin therapy. Clin Pharmacol Ther 81:529-38.
-
(2007)
Clin Pharmacol Ther
, vol.81
, pp. 529-538
-
-
Hamberg, A.K.1
Dahl, M.L.2
Barban, M.3
-
7
-
-
0037148655
-
Prediction of plasma concentration-time curve of orally administered theophylline based on a scintigraphic monitoring of gastrointestinal transit in human volunteers
-
Haruta S, Kawai K, Nishii R, et al. (2002). Prediction of plasma concentration-time curve of orally administered theophylline based on a scintigraphic monitoring of gastrointestinal transit in human volunteers. Int J Pharm 233:179-90.
-
(2002)
Int J Pharm
, vol.233
, pp. 179-190
-
-
Haruta, S.1
Kawai, K.2
Nishii, R.3
-
8
-
-
67349187909
-
Application of biorelevant dissolution tests to the prediction of in vivo performance of diclofenac sodium from an oral modified-release pellet dosage form
-
Jantratid E, De Maio V, Ronda E, et al. (2009). Application of biorelevant dissolution tests to the prediction of in vivo performance of diclofenac sodium from an oral modified-release pellet dosage form. Eur J Pharm Sci 37:434-41.
-
(2009)
Eur J Pharm Sci
, vol.37
, pp. 434-441
-
-
Jantratid, E.1
De Maio, V.2
Ronda, E.3
-
9
-
-
0037335355
-
Preparation and in vitro/in vivo evaluation of insulin-loaded poly (acryloyl-hydroxyethyl starch) - PLGA composite microspheres
-
Jiang G, Qiu W, DeLuca PP. (2003). Preparation and in vitro/in vivo evaluation of insulin-loaded poly (acryloyl-hydroxyethyl starch) - PLGA composite microspheres. Pharm Res 20:452-9.
-
(2003)
Pharm Res
, vol.20
, pp. 452-459
-
-
Jiang, G.1
Qiu, W.2
DeLuca, P.P.3
-
10
-
-
0037133127
-
Assessment of protein release kinetics, stability and protein polymer interaction of lysozyme encapsulated poly (D, L-lactide-co-glycolide) microspheres
-
Jiang G, Woo BH, Kang FR, et al. (2002). Assessment of protein release kinetics, stability and protein polymer interaction of lysozyme encapsulated poly (D, L-lactide-co-glycolide) microspheres. J Control Release 79:137-45.
-
(2002)
J Control Release
, vol.79
, pp. 137-145
-
-
Jiang, G.1
Woo, B.H.2
Kang, F.R.3
-
11
-
-
41549102580
-
Selection of drug candidates for gastroretentive dosage forms: Pharmacokinetics following continuous intragastric mode of administration in a rat model
-
Kagan L, Hoffman A. (2008). Selection of drug candidates for gastroretentive dosage forms: pharmacokinetics following continuous intragastric mode of administration in a rat model. Eur J Pharm Biopharm 69:238-46.
-
(2008)
Eur J Pharm Biopharm
, vol.69
, pp. 238-246
-
-
Kagan, L.1
Hoffman, A.2
-
12
-
-
70350244684
-
Pharmacokinetics and efficacy of a biweekly dosage formulation of exenatide in Zucker diabetic fatty (ZDF) rats
-
Kwak HH, Shim WS, Hwang S, et al. (2009). Pharmacokinetics and efficacy of a biweekly dosage formulation of exenatide in Zucker diabetic fatty (ZDF) rats. Pharm Res 26:2504-12.
-
(2009)
Pharm Res
, vol.26
, pp. 2504-2512
-
-
Kwak, H.H.1
Shim, W.S.2
Hwang, S.3
-
13
-
-
79960592269
-
Use of conventional surfactant media as surrogates for FaSSIF in simulating in vivo dissolution of BCS class II drugs
-
Lehto P, Kortejarvi H, Liimatainen A, et al. (2011). Use of conventional surfactant media as surrogates for FaSSIF in simulating in vivo dissolution of BCS class II drugs. Eur J Pharm Biopharm 78:531-8.
-
(2011)
Eur J Pharm Biopharm
, vol.78
, pp. 531-538
-
-
Lehto, P.1
Kortejarvi, H.2
Liimatainen, A.3
-
14
-
-
84855448977
-
A mechanism-based pharmacokinetic/pharmacodynamic model for CYP3A1/2 induction by dexamethasone in rats
-
Li L, Li ZQ, Deng CH, et al. (2012a). A mechanism-based pharmacokinetic/pharmacodynamic model for CYP3A1/2 induction by dexamethasone in rats. Acta Pharmacol Sin 33:127-36.
-
(2012)
Acta Pharmacol Sin
, vol.33
, pp. 127-136
-
-
Li, L.1
Li, Z.Q.2
Deng, C.H.3
-
15
-
-
84865359777
-
Application of model-based methods to characterize exenatide-loaded double-walled microspheres: In vivo release, pharmacokinetic/pharmacodynamic model, and in vitro and in vivo correlation
-
Li XG, Li L, Wang XP, et al. (2012b). Application of model-based methods to characterize exenatide-loaded double-walled microspheres: In vivo release, pharmacokinetic/pharmacodynamic model, and in vitro and in vivo correlation. J Pharm Sci 101:3946-61.
-
(2012)
J Pharm Sci
, vol.101
, pp. 3946-3961
-
-
Li, X.G.1
Li, L.2
Wang, X.P.3
-
16
-
-
84865360479
-
Pharmacokinetic/pharmacodynamic studies on exenatide in diabetic rats
-
Li XG, Li L, Zhou X, et al. (2012c). Pharmacokinetic/pharmacodynamic studies on exenatide in diabetic rats. Acta Pharm Sin 33:1379-86.
-
(2012)
Acta Pharm Sin
, vol.33
, pp. 1379-1386
-
-
Li, X.G.1
Li, L.2
Zhou, X.3
-
17
-
-
0034657131
-
Pharmacokinetics of prolonged-release CPT-11-loaded microspheres in rats
-
Machida Y, Onishi H, Kurita A, et al. (2000). Pharmacokinetics of prolonged-release CPT-11-loaded microspheres in rats. J Control Release 66:159-75.
-
(2000)
J Control Release
, vol.66
, pp. 159-175
-
-
Machida, Y.1
Onishi, H.2
Kurita, A.3
-
18
-
-
0034752734
-
Pharmacokinetic actions of exendin-4 in the rat: Comparison with glucagon-like peptide-1
-
Parkes DG, Jodka C, Smith P, et al. (2001). Pharmacokinetic actions of exendin-4 in the rat: comparison with glucagon-like peptide-1. Drug Develop Res 53:260-7.
-
(2001)
Drug Develop Res
, vol.53
, pp. 260-267
-
-
Parkes, D.G.1
Jodka, C.2
Smith, P.3
-
19
-
-
0347360186
-
Pharmacology of exenatide (synthetic exendin-4): A potential therapeutic for improved glycemic control of type 2 diabetes
-
Parkes DG, Nielsen LL, Young AA. (2004). Pharmacology of exenatide (synthetic exendin-4): a potential therapeutic for improved glycemic control of type 2 diabetes. Regul Pept 117:77-88.
-
(2004)
Regul Pept
, vol.117
, pp. 77-88
-
-
Parkes, D.G.1
Nielsen, L.L.2
Young, A.A.3
-
20
-
-
0033761823
-
A new rat model of type 2 diabetes: The fat-fed, streptozotocin-treated rat
-
Reed MJ, Meszaros K, Entes LJ, et al. (2000). A new rat model of type 2 diabetes: the fat-fed, streptozotocin-treated rat. Metabolism 49:1390-4.
-
(2000)
Metabolism
, vol.49
, pp. 1390-1394
-
-
Reed, M.J.1
Meszaros, K.2
Entes, L.J.3
-
21
-
-
0030699113
-
A new strategy to determine the actual protein content of poly (lactide-co-glycolide) microspheres
-
Sah H. (1997). A new strategy to determine the actual protein content of poly (lactide-co-glycolide) microspheres. J Pharm Sci 86:1315-18.
-
(1997)
J Pharm Sci
, vol.86
, pp. 1315-1318
-
-
Sah, H.1
-
22
-
-
34748854885
-
Implementation of a transit compartment model for describing drug absorption in pharmacokinetic studies
-
Savic RM, Jonker DM, Kerbusch T, et al. (2007). Implementation of a transit compartment model for describing drug absorption in pharmacokinetic studies. J Pharmacokinet Pharmacodyn 34:711-26.
-
(2007)
J Pharmacokinet Pharmacodyn
, vol.34
, pp. 711-726
-
-
Savic, R.M.1
Jonker, D.M.2
Kerbusch, T.3
-
23
-
-
0030580130
-
Preparation and evaluation of insulin-loaded poly (DL-lactide) microspheres using an experimental design
-
Soriano I, Evora C, Llabres M. (1996). Preparation and evaluation of insulin-loaded poly (DL-lactide) microspheres using an experimental design. Int J Pharm 142:135-42.
-
(1996)
Int J Pharm
, vol.142
, pp. 135-142
-
-
Soriano, I.1
Evora, C.2
Llabres, M.3
-
24
-
-
0024745613
-
In vitro and in vivo degradation of poly (D, L lactide/glycolide) type microspheres made by solvent evaporation method
-
Spenlehauer G, Vert M, Benoit JP, et al. (1989). In vitro and in vivo degradation of poly (D, L lactide/glycolide) type microspheres made by solvent evaporation method. Biomaterials 10:557-63.
-
(1989)
Biomaterials
, vol.10
, pp. 557-563
-
-
Spenlehauer, G.1
Vert, M.2
Benoit, J.P.3
-
25
-
-
47349102221
-
Synchronic release of two hormonal contraceptives for about one month from the PLGA microspheres: In vitro and in vivo studies
-
Sun Y, Wang J, Zhang X, et al. (2008). Synchronic release of two hormonal contraceptives for about one month from the PLGA microspheres: in vitro and in vivo studies. J Control Release 129:192-9.
-
(2008)
J Control Release
, vol.129
, pp. 192-199
-
-
Sun, Y.1
Wang, J.2
Zhang, X.3
-
26
-
-
0031835741
-
Transit compartments versus gamma distribution function to model signal transduction processes in pharmacodynamics
-
Sun YN, Jusko WJ. (1998). Transit compartments versus gamma distribution function to model signal transduction processes in pharmacodynamics. J Pharm Sci 87:732-7.
-
(1998)
J Pharm Sci
, vol.87
, pp. 732-737
-
-
Sun, Y.N.1
Jusko, W.J.2
-
27
-
-
0033151448
-
Factors affecting the degradation rate of poly (lactide-co-glycolide) microspheres in vivo and in vitro
-
Tracy MA, Ward KL, Firouzabadian L, et al. (1999). Factors affecting the degradation rate of poly (lactide-co-glycolide) microspheres in vivo and in vitro. Biomaterials 20:1057-62.
-
(1999)
Biomaterials
, vol.20
, pp. 1057-1062
-
-
Tracy, M.A.1
Ward, K.L.2
Firouzabadian, L.3
-
28
-
-
77955418929
-
Issues in long-term protein delivery using biodegradable microparticles
-
Ye ML, Kim S, Park K. (2010). Issues in long-term protein delivery using biodegradable microparticles. J Control Release 146:241-60.
-
(2010)
J Control Release
, vol.146
, pp. 241-260
-
-
Ye, M.L.1
Kim, S.2
Park, K.3
-
29
-
-
0032908654
-
Glucose-lowering and insulin-sensitizing actions of exendin-4 Studies in obese diabetic (ob/ob, db/db) mice, diabetic fatty Zucker rats, and diabetic rhesus monkeys (Macaca mulatta)
-
Young AA, Gedulin BR, Bhavsar S, et al. (1999). Glucose-lowering and insulin-sensitizing actions of exendin-4 Studies in obese diabetic (ob/ob, db/db) mice, diabetic fatty Zucker rats, and diabetic rhesus monkeys (Macaca mulatta). Diabetes 48:1026-34.
-
(1999)
Diabetes
, vol.48
, pp. 1026-1034
-
-
Young, A.A.1
Gedulin, B.R.2
Bhavsar, S.3
-
30
-
-
0030580951
-
Transport approaches to the biopharmaceutical design of oral drug delivery systems: Prediction of intestinal absorption
-
Yu LX, Lipka E, Crison JR, et al. (1996). Transport approaches to the biopharmaceutical design of oral drug delivery systems: prediction of intestinal absorption. Adv Drug Deliv Rev 19:359-76.
-
(1996)
Adv Drug Deliv Rev
, vol.19
, pp. 359-376
-
-
Yu, L.X.1
Lipka, E.2
Crison, J.R.3
-
31
-
-
41249098853
-
Evaluation of in vivo-in vitro release of dexamethasone from PLGA microspheres
-
Zolnik BS, Burgess DJ. (2008). Evaluation of in vivo-in vitro release of dexamethasone from PLGA microspheres. J Control Release 127:137-45.
-
(2008)
J Control Release
, vol.127
, pp. 137-145
-
-
Zolnik, B.S.1
Burgess, D.J.2
|