The biopharmaceutical classification system of excipients.
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[1] J. Czarnocka,et al. Gastro-resistant characteristics of GRAS-grade enteric coatings for pharmaceutical and nutraceutical products. , 2015, International journal of pharmaceutics.
[2] N. Shaik,et al. Investigation of the micellar effect of pluronic P85 on P-glycoprotein inhibition: cell accumulation and equilibrium dialysis studies. , 2009, Journal of pharmaceutical sciences.
[3] J. Crison,et al. A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability , 1995, Pharmaceutical Research.
[4] A. Takeshita,et al. Acetyl tributyl citrate, the most widely used phthalate substitute plasticizer, induces cytochrome p450 3a through steroid and xenobiotic receptor. , 2011, Toxicological sciences : an official journal of the Society of Toxicology.
[5] Wenpeng Zhang,et al. The Effects of Pharmaceutical Excipients on Gastrointestinal Tract Metabolic Enzymes and Transporters—an Update , 2016, The AAPS Journal.
[6] K. Pang. Modeling of intestinal drug absorption: roles of transporters and metabolic enzymes (for the Gillette Review Series). , 2003, Drug metabolism and disposition: the biological fate of chemicals.
[7] A. Basit,et al. The effect of polyoxyethylene polymers on the transport of ranitidine in Caco-2 cell monolayers. , 2011, International journal of pharmaceutics.
[8] I. Legen,et al. The evaluation of some pharmaceutically acceptable excipients as permeation enhancers for amoxicillin. , 2006, International journal of pharmaceutics.
[9] A. Basit,et al. An investigation into moisture barrier film coating efficacy and its relevance to drug stability in solid dosage forms. , 2016, International journal of pharmaceutics.
[10] G. Eytan,et al. Modulation of P‐glycoprotein‐mediated multidrug resistance by acceleration of passive drug permeation across the plasma membrane , 2007, The FEBS journal.
[11] R. Schubert,et al. The application of P‐gp inhibiting phospholipids as novel oral bioavailability enhancers — An in vitro and in vivo comparison , 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[12] F. Guengerich,et al. Oxidation of nonionic detergents by cytochrome P450 enzymes. , 1998, Archives of biochemistry and biophysics.
[13] Bruno Sarmento,et al. Amorphous solid dispersions: Rational selection of a manufacturing process. , 2016, Advanced drug delivery reviews.
[14] Thorsteinn Loftsson,et al. Excipient pharmacokinetics and profiling. , 2015, International journal of pharmaceutics.
[15] J. Qiu,et al. Inhibitive effect of cremophor RH40 or tween 80-based self-microemulsiflying drug delivery system on cytochrome P450 3A enzymes in murine hepatocytes , 2010, Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban.
[16] Josh Hanna,et al. An accurate and precise representation of drug ingredients , 2016, J. Biomed. Semant..
[17] R. Schubert,et al. Inhibitory effect of phospholipids on P-glycoprotein: cellular studies in Caco-2, MDCKII mdr1 and MDCKII wildtype cells and P-gp ATPase activity measurements. , 2012, Biochimica et biophysica acta.
[18] A. Al-Mohizea. Influence of intestinal efflux pumps on the absorption and transport of furosemide. , 2010, Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society.
[19] Rongqin Huang,et al. Effects of polyoxyethylene (40) stearate on the activity of P-glycoprotein and cytochrome P450. , 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[20] Leslie Z Benet,et al. Intestinal drug transporters: an overview. , 2013, Advanced drug delivery reviews.
[21] J. Iqbal,et al. Thiomers: Inhibition of cytochrome P450 activity. , 2011, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[22] J. Qiu,et al. Effect of pluronic F68 block copolymer on P-glycoprotein transport and CYP3A4 metabolism. , 2008, International journal of pharmaceutics.
[23] Claus-Michael Lehr,et al. Vitamin E TPGS P-glycoprotein inhibition mechanism: influence on conformational flexibility, intracellular ATP levels, and role of time and site of access. , 2010, Molecular pharmaceutics.
[24] Kexin Liu,et al. P-gp Inhibition-Based Strategies for Modulating Pharmacokinetics of Anticancer Drugs: An Update. , 2016, Current drug metabolism.
[25] P. Colombo,et al. Pharmacokinetics evaluation of soft agglomerates for prompt delivery of enteric pantoprazole-loaded microparticles. , 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[26] Abdul W. Basit,et al. Concentration-Dependent Effects of Polyethylene Glycol 400 on Gastrointestinal Transit and Drug Absorption , 2003, Pharmaceutical Research.
[27] Jörg Huwyler,et al. In vitro investigation on the impact of the surface-active excipients Cremophor EL, Tween 80 and Solutol HS 15 on the metabolism of midazolam. , 2004, Biopharmaceutics & drug disposition.
[28] Tao Yi,et al. Interactions between human multidrug resistance related protein (MRP2; ABCC2) and excipients commonly used in self-emulsifying drug delivery systems (SEDDS). , 2013, International journal of pharmaceutics.
[29] Tom O. McDonald,et al. Mediation of in vitro cytochrome p450 activity by common pharmaceutical excipients. , 2013, Molecular pharmaceutics.
[30] Werner Weitschies,et al. Effects of non-ionic surfactants on cytochrome P450-mediated metabolism in vitro. , 2011, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[31] K. Wasan,et al. Lipid excipients Peceol and Gelucire 44/14 decrease P-glycoprotein mediated efflux of rhodamine 123 partially due to modifying P-glycoprotein protein expression within Caco-2 cells. , 2007, Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques.
[32] J. Polli,et al. Effects of Commonly Used Excipients on the Expression of CYP3A4 in Colon and Liver Cells , 2010, Pharmaceutical Research.
[33] Tao Yi,et al. Inhibition of human efflux transporter ABCC2 (MRP2) by self-emulsifying drug delivery system: influences of concentration and combination of excipients. , 2014, Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques.
[34] S. Ho,et al. Commonly Used Excipients Modulate UDP-Glucuronosyltransferase 2B7 Activity to Improve Nalbuphine Oral Bioavailability in Humans , 2014, Pharmaceutical Research.
[35] D. J. Price,et al. Enhanced oral delivery of celecoxib via the development of a supersaturable amorphous formulation utilising mesoporous silica and co-loaded HPMCAS. , 2016, International journal of pharmaceutics.
[36] S. Dadashzadeh,et al. Enhanced Permeability of Etoposide across Everted Sacs of Rat Small Intestine by Vitamin E-TPGS , 2013, Iranian journal of pharmaceutical research : IJPR.
[37] Xingguo Cheng,et al. Cytotoxicity assessment of lipid-based self-emulsifying drug delivery system with Caco-2 cell model: Cremophor EL as the surfactant. , 2016, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[38] A. Kabanov,et al. Effect of Pluronic P85 on ATPase Activity of Drug Efflux Transporters , 2004, Pharmaceutical Research.
[39] J. Qiu,et al. Excipients enhance intestinal absorption of ganciclovir by P-gp inhibition: assessed in vitro by everted gut sac and in situ by improved intestinal perfusion. , 2011, International journal of pharmaceutics.
[40] H. Petereit,et al. Film coatings for taste masking and moisture protection. , 2013, International journal of pharmaceutics.
[41] Minoru Ishikawa,et al. Interaction of Modified Cyclodextrins with Cytochrome P-450 , 2005, Bioscience, biotechnology, and biochemistry.
[42] K. Maeda,et al. Effects of Cremophor EL on the absorption of orally administered saquinavir and fexofenadine in healthy subjects. , 2015, Drug metabolism and pharmacokinetics.
[43] Yu-hui Wei,et al. Effects of Pluronic F68 and Labrasol on the intestinal absorption and pharmacokinetics of rifampicin in rats , 2011, Archives of pharmacal research.
[44] X. Mao,et al. Pharmaceutical excipients inhibit cytochrome P450 activity in cell free systems and after systemic administration. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[45] R. Kappl,et al. Mechanism of inhibition of P-glycoprotein mediated efflux by vitamin E TPGS: influence on ATPase activity and membrane fluidity. , 2007, Molecular pharmaceutics.
[46] T. Kiss,et al. Evaluation of cytotoxicity of surfactants used in self-micro emulsifying drug delivery systems and their effects on paracellular transport in Caco-2 cell monolayer. , 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[47] Christopher J H Porter,et al. Impact of cremophor-EL and polysorbate-80 on digoxin permeability across rat jejunum: delineation of thermodynamic and transporter related events using the reciprocal permeability approach. , 2007, Journal of pharmaceutical sciences.
[48] Christopher A Lipinski,et al. Rule of five in 2015 and beyond: Target and ligand structural limitations, ligand chemistry structure and drug discovery project decisions. , 2016, Advanced drug delivery reviews.
[49] Christopher J. H. Porter,et al. An in vitro examination of the impact of polyethylene glycol 400, pluronic P85, and vitamin E d-a-tocopheryl polyethylene glycol 1000 succinate on P-glycoprotein efflux and enterocyte-based metabolism in excised rat intestine , 2002, AAPS PharmSci.
[50] Vivek S. Dave,et al. Excipient variability and its impact on dosage form functionality. , 2015, Journal of pharmaceutical sciences.
[51] H. Lee,et al. Enhanced oral bioavailability of morin administered in mixed micelle formulation with PluronicF127 and Tween80 in rats. , 2015, Biological & pharmaceutical bulletin.
[52] K. Wasan,et al. Effects of monoglycerides on P-glycoprotein: modulation of the activity and expression in Caco-2 cell monolayers. , 2008, Molecular pharmaceutics.
[53] P. Patel,et al. Formulation and characterization of sustained release dosage form of moisture sensitive drug , 2015, International journal of pharmaceutical investigation.
[54] Stephen G. Aller. Structure of P-Glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding , 2010 .
[55] M. Vore,et al. Expression and Localization of Multidrug Resistant Protein mrp 2 in Rat Small Intestine 1 , 2000 .
[56] G. Szakács,et al. Sucrose esters increase drug penetration, but do not inhibit p-glycoprotein in caco-2 intestinal epithelial cells. , 2014, Journal of pharmaceutical sciences.
[57] R. Borchardt,et al. Absorption barriers in the rat intestinal mucosa. 3: Effects of polyethoxylated solubilizing agents on drug permeation and metabolism. , 2010, Journal of pharmaceutical sciences.
[58] L. Bromberg,et al. Effects of polyether-modified poly(acrylic acid) microgels on doxorubicin transport in human intestinal epithelial Caco-2 cell layers. , 2003, Journal of controlled release : official journal of the Controlled Release Society.
[59] Gerd Mikus,et al. Pharmacokinetic and pharmaceutic interaction between digoxin and Cremophor RH40 , 2003, Clinical pharmacology and therapeutics.
[60] D. Shen,et al. Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism. , 1997, The Journal of pharmacology and experimental therapeutics.
[61] P. Pohl,et al. Ionophoric activity of pluronic block copolymers. , 2004, Biochemistry.
[62] Leslie Z. Benet,et al. The Role of Transporters in the Pharmacokinetics of Orally Administered Drugs , 2009, Pharmaceutical Research.
[63] Jin-hua Zhao,et al. [Recent advance in the mechanism study of polymeric inhibitors of P-glycoprotein]. , 2010, Yao xue xue bao = Acta pharmaceutica Sinica.
[64] James E Polli,et al. Effects of nonionic surfactants on membrane transporters in Caco-2 cell monolayers. , 2002, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[65] S. Oswald,et al. Pharmaceutical excipients influence the function of human uptake transporting proteins. , 2012, Molecular pharmaceutics.
[66] F. Ahmad,et al. The emerging role of P-glycoprotein inhibitors in drug delivery: a patent review , 2011, Expert opinion on therapeutic patents.
[67] Yuichi Sugiyama,et al. Effect of excipients on breast cancer resistance protein substrate uptake activity. , 2007, Journal of controlled release : official journal of the Controlled Release Society.
[68] Georges Houin,et al. Impact of excipients on the absorption of P-glycoprotein substrates in vitro and in vivo. , 2004, International journal of pharmaceutics.
[69] J. Silverman,et al. Inhibition of P-glycoprotein by D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS). , 1999, Pharmaceutical research.
[70] Gérard Hopfgartner,et al. P‐Glycoprotein and Surfactants: Effect on Intestinal Talinolol Absorption , 2005, Clinical pharmacology and therapeutics.
[71] Werner Weitschies,et al. Commonly used nonionic surfactants interact differently with the human efflux transporters ABCB1 (p-glycoprotein) and ABCC2 (MRP2). , 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[72] M. Vore,et al. Expression and localization of multidrug resistant protein mrp2 in rat small intestine. , 2000, The Journal of pharmacology and experimental therapeutics.
[73] J. Silverman,et al. Inhibition of P-Glycoprotein by D-α-Tocopheryl Polyethylene Glycol 1000 Succinate (TPGS) , 1999, Pharmaceutical Research.
[74] Jun Qiu,et al. Nonionic surfactants are strong inhibitors of cytochrome P450 3A biotransformation activity in vitro and in vivo. , 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[75] Jean-Michel Kauffmann,et al. The effects of excipients on transporter mediated absorption. , 2010, International journal of pharmaceutics.
[76] J. Qiu,et al. Effect of pluronic P123 and F127 block copolymer on P-glycoprotein transport and CYP3A metabolism , 2011, Archives of pharmacal research.
[77] A. Florence,et al. Effects of Some Non‐ionic Surfactants on Transepithelial Permeability in Caco‐2 Cells , 2000, The Journal of pharmacy and pharmacology.
[78] Zhong Zuo,et al. Intestinal transport of bis(12)‐hupyridone in Caco‐2 cells and its improved permeability by the surfactant Brij‐35 , 2011, Biopharmaceutics & drug disposition.
[79] Hua Zhou,et al. A new mechanism for increasing the oral bioavailability of scutellarin with Cremophor EL: Activation of MRP3 with concurrent inhibition of MRP2 and BCRP. , 2016, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.