Search Results - "Tsinman, Oksana"
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1
Ranking Itraconazole Formulations Based on the Flux through Artificial Lipophilic Membrane
Published in Pharmaceutical research (01-08-2018)“…Purpose The goal of the study was to evaluate a miniaturized dissolution-permeation apparatus (μFLUX™ apparatus) for its ability to benchmark several…”
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2
Prediction of Bioequivalence and Food Effect Using Flux- and Solubility-Based Methods
Published in Molecular pharmaceutics (07-10-2019)“…In this work, two different approaches have been developed to predict the food effect and the bioequivalence of marketed itraconazole (ITRA) formulations…”
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3
P-glycoprotein deficient mouse in situ blood–brain barrier permeability and its prediction using an in combo PAMPA model
Published in European journal of pharmaceutical sciences (10-09-2009)“…The purpose of the study was to assess the permeability of mouse blood–brain barrier (BBB) to a diverse set of compounds in the absence of P-glycoprotein (Pgp)…”
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4
The Permeation of Amphoteric Drugs through Artificial Membranes − An in Combo Absorption Model Based on Paracellular and Transmembrane Permeability
Published in Journal of medicinal chemistry (14-01-2010)“…The permeability characteristics of 33 amphoteric drugs (about 64% zwitterions at physiological pH) were studied using the parallel artificial membrane…”
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5
Miniaturized Rotating Disk Intrinsic Dissolution Rate Measurement: Effects of Buffer Capacity in Comparisons to Traditional Wood’s Apparatus
Published in Pharmaceutical research (01-11-2008)“…Purpose The objective was to investigate the feasibility of using a miniaturized disk intrinsic dissolution rate (IDR) apparatus to determine the…”
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6
Food effect risk assessment in preformulation stage using material sparing µFLUX methodology
Published in ADMET & DMPK (07-10-2022)“…The intake of food and meal type can strongly impact the bioavailability of orally administered drugs and can consequently impact drug efficacy and safety…”
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7
Acid-Base Cosolvent Method for Determining Aqueous Permeability of Amiodarone, Itraconazole, Tamoxifen, Terfenadine and Other Very Insoluble Molecules
Published in Chemical & pharmaceutical bulletin (01-05-2004)“…A high-throughput, UV-detection PAMPA (parallel artificial membrane permeability assay) cosolvent procedure is described, based on the use of 20% v/v…”
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8
Using pH Gradient Dissolution with In-Situ Flux Measurement to Evaluate Bioavailability and DDI for Formulated Poorly Soluble Drug Products
Published in AAPS PharmSciTech (01-10-2018)“…ABSTRACT This study described a pH-gradient dissolution method combined with flux measurements as an in vitro tool for assessing the risk of bioavailability…”
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9
Physicochemical Selectivity of the BBB Microenvironment Governing Passive Diffusion--Matching with a Porcine Brain Lipid Extract Artificial Membrane Permeability Model
Published in Pharmaceutical research (01-02-2011)“…Purpose To mimic the physicochemical selectivity of the blood-brain barrier (BBB) and to predict its passive permeability using a PAMPA model based on porcine…”
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10
The effect of formulation additives on in vitro dissolution-absorption profile and in vivo bioavailability of telmisartan from brand and generic formulations
Published in European journal of pharmaceutical sciences (01-03-2018)“…In this study, brand and four generic formulations of telmisartan, an antihypertensive drug, were used in in vitro simultaneous dissolution-absorption,…”
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11
Powder Dissolution Method for Estimating Rotating Disk Intrinsic Dissolution Rates of Low Solubility Drugs
Published in Pharmaceutical research (01-09-2009)“…Purpose The objective was to investigate the applicability and limitations of a novel approach for measuring intrinsic dissolution rates (IDR) of very small…”
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12
Skin–PAMPA: A new method for fast prediction of skin penetration
Published in European journal of pharmaceutical sciences (11-04-2012)“…The goal of this study was to develop a quick, reliable, and cost-effective permeability model for predicting transdermal penetration of compounds. The…”
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13
Dissolution Rate and Apparent Solubility of Poorly Soluble Drugs in Biorelevant Dissolution Media
Published in Molecular pharmaceutics (04-10-2010)“…A series of poorly soluble BCS class II compounds with “grease ball” characteristics were assessed for solubility and dissolution rate in biorelevant…”
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14
Spectrophotometric pKa determination of ionizable pharmaceuticals: Resolution of molecules with weak pH-dependent spectral shift
Published in Journal of pharmaceutical and biomedical analysis (10-10-2015)“…•A UV method for measuring pKa of drugs with weak spectral shift is developed.•The pKa values determined are in good agreement with literature data…”
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15
Investigation and Mathematical Description of the Real Driving Force of Passive Transport of Drug Molecules from Supersaturated Solutions
Published in Molecular pharmaceutics (07-11-2016)“…The aim of this study was to investigate the impact of formulation excipients and solubilizing additives on dissolution, supersaturation, and membrane…”
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16
PAMPA : A drug absorption in vitro model 13. chemical selectivity due to membrane hydrogen bonding: In combo comparisons of HDM-, DOPC-, and DS-PAMPA models
Published in European journal of pharmaceutical sciences (01-05-2006)“…This study compares the intrinsic permeability coefficients of 40 drug molecules, obtained by three popular variants of the PAMPA assay, based on: (a)…”
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17
Flux-Based Formulation Development—A Proof of Concept Study
Published in The AAPS journal (05-01-2022)“…The work aimed to develop the Absorption Driven Drug Formulation (ADDF) concept, which is a new approach in formulation development to ensure that the drug…”
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18
Solubility-excipient classification gradient maps
Published in Pharmaceutical research (01-03-2007)“…This study assessed the effect of excipients (sodium taurocholate, 2-hydroxypropyl-f-cyclodextrin, potassium chloride, propylene glycol,…”
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19
Effect of Formulation Additives on Drug Transport through Size-Exclusion Membranes
Published in Molecular pharmaceutics (06-08-2018)“…The aim of this research was to investigate the driving force of membrane transport through size-exclusion membranes and to provide a concentration-based…”
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20
PAMPA—a drug absorption in vitro model: 11. Matching the in vivo unstirred water layer thickness by individual-well stirring in microtitre plates
Published in European journal of pharmaceutical sciences (01-08-2004)“…Many plate-based in vitro assays of membrane permeability (e.g., Caco-2, MDCK, PAMPA) of sparingly soluble candidate molecules report permeability of water,…”
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