Detalles de la búsqueda
1.
Physical-Chemical Characterization of Octreotide Encapsulated in Commercial Glucose-Star PLGA Microspheres.
Mol Pharm
; 17(11): 4141-4151, 2020 11 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-32876463
2.
Striking the Optimal Solubility-Permeability Balance in Oral Formulation Development for Lipophilic Drugs: Maximizing Carbamazepine Blood Levels.
Mol Pharm
; 14(1): 319-327, 2017 01 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-27981848
3.
Toward Successful Cyclodextrin Based Solubility-Enabling Formulations for Oral Delivery of Lipophilic Drugs: Solubility-Permeability Trade-Off, Biorelevant Dissolution, and the Unstirred Water Layer.
Mol Pharm
; 14(6): 2138-2146, 2017 06 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28505451
4.
Quantification of carbamazepine and its 10,11-epoxide metabolite in rat plasma by UPLC-UV and application to pharmacokinetic study.
Biomed Chromatogr
; 28(7): 934-8, 2014 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-24327551
5.
In vitro performance of composition-equivalent PLGA microspheres encapsulating exenatide acetate by solvent evaporation.
Int J Pharm
; 643: 123213, 2023 Aug 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-37423376
6.
The solubility-permeability interplay when using cosolvents for solubilization: revising the way we use solubility-enabling formulations.
Mol Pharm
; 9(3): 581-90, 2012 Mar 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-22280478
7.
A win-win solution in oral delivery of lipophilic drugs: supersaturation via amorphous solid dispersions increases apparent solubility without sacrifice of intestinal membrane permeability.
Mol Pharm
; 9(7): 2009-16, 2012 Jul 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-22632106
8.
Minimizing the initial burst of octreotide acetate from glucose star PLGA microspheres prepared by the solvent evaporation method.
Int J Pharm
; 624: 121842, 2022 Aug 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-35609832
9.
Efficient aqueous remote loading of peptides in poly(lactic-co-glycolic acid).
Nat Commun
; 13(1): 3282, 2022 06 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35676271
10.
Development and characterization of composition-equivalent formulations to the Sandostatin LAR® by the solvent evaporation method.
Drug Deliv Transl Res
; 12(3): 695-707, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34215997
11.
The solubility-permeability interplay: mechanistic modeling and predictive application of the impact of micellar solubilization on intestinal permeation.
Mol Pharm
; 8(5): 1848-56, 2011 Oct 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-21800883
12.
Adequate formulation approach for oral chemotherapy: Etoposide solubility, permeability, and overall bioavailability from cosolvent- vs. vitamin E TPGS-based delivery systems.
Int J Pharm
; 597: 120295, 2021 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-33497706
13.
Characterization of attributes and in vitro performance of exenatide-loaded PLGA long-acting release microspheres.
Eur J Pharm Biopharm
; 158: 401-409, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33122118
14.
The solubility, permeability and the dose as key factors in formulation development for oral lipophilic drugs: Maximizing the bioavailability of carbamazepine with a cosolvent-based formulation.
Int J Pharm
; 582: 119307, 2020 May 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-32276090
15.
Segmental-Dependent Intestinal Drug Permeability: Development and Model Validation of In Silico Predictions Guided by In Vivo Permeability Values.
J Pharm Sci
; 108(1): 316-325, 2019 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-30055228
16.
Advantageous Solubility-Permeability Interplay When Using Amorphous Solid Dispersion (ASD) Formulation for the BCS Class IV P-gp Substrate Rifaximin: Simultaneous Increase of Both the Solubility and the Permeability.
AAPS J
; 19(3): 806-813, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28204967
17.
Concomitant solubility-permeability increase: Vitamin E TPGS vs. amorphous solid dispersion as oral delivery systems for etoposide.
Eur J Pharm Biopharm
; 121: 97-103, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28958946
18.
The solubility-permeability interplay and oral drug formulation design: Two heads are better than one.
Adv Drug Deliv Rev
; 101: 99-107, 2016 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27129443
19.
Hydrotropic Solubilization of Lipophilic Drugs for Oral Delivery: The Effects of Urea and Nicotinamide on Carbamazepine Solubility-Permeability Interplay.
Front Pharmacol
; 7: 379, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27826241
20.
Segmental-dependent permeability throughout the small intestine following oral drug administration: Single-pass vs. Doluisio approach to in-situ rat perfusion.
Int J Pharm
; 515(1-2): 201-208, 2016 Dec 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-27667756