Velocity distribution and shear rate variability resulting from changes in the impeller location in the USP dissolution testing apparatus II.

Abstract:

PURPOSE:The United States Pharmacopoeia (USP) imposes strict requirements on the geometry and operating conditions of the USP Dissolution Testing Apparatus II. A previously validated Computational Fluid Dynamics (CFD) approach was used here to study the hydrodynamics of USP Apparatus II when the impeller was placed at four different locations, all within the limits specified by USP. METHOD:CFD was used to predict the velocity profiles, energy dissipation rates, and strain rates when the impeller was placed in the reference location (centrally mounted, 25 mm off the vessel bottom), 2 mm off-center, 2 mm higher, and 2 mm lower than the reference location. RESULTS:Small changes in impeller location, especially if associated with loss of symmetry, produced extensive changes in velocity profiles and shear rates. Centrally located impellers, irrespective of their off-bottom clearance, produced non-uniform but nearly symmetric strain rates. The off-center impeller produced a more uniform but slightly asymmetric strain rate distribution. CONCLUSIONS:The system hydrodynamics depends strongly on small differences in equipment configurations and operating conditions, which are likely to affect significantly the flow field and shear rate experienced by the oral dosage form being tested, and hence the solid-liquid mass transfer and dissolution rate.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Bai G,Armenante PM

doi

10.1007/s11095-007-9477-z

subject

Has Abstract

pub_date

2008-02-01 00:00:00

pages

320-36

issue

2

eissn

0724-8741

issn

1573-904X

journal_volume

25

pub_type

杂志文章
  • Effect of Permeation Enhancers on the Buccal Permeability of Nicotine: Ex vivo Transport Studies Complemented by MALDI MS Imaging.

    abstract:PURPOSE:The purpose of this study was to assess the effect of several chemical permeation enhancers on the buccal permeability of nicotine and to image the spatial distribution of nicotine in buccal mucosa with and without buccal permeation enhancers. METHODS:The impact of sodium taurodeoxycholate (STDC), sodium dodec...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2332-y

    authors: Marxen E,Jin L,Jacobsen J,Janfelt C,Hyrup B,Nicolazzo JA

    更新日期:2018-02-21 00:00:00

  • The Impact of Inadequate Temperature Storage Conditions on Aggregate and Particle Formation in Drugs Containing Tumor Necrosis Factor-Alpha Inhibitors.

    abstract:PURPOSE:To measure aggregate and particle formation in tumor necrosis factor-alpha (TNF-α) inhibitors etanercept, adalimumab and certolizumab pegol product samples after exposure to freezing temperature conditions similar to storage conditions previously observed in patients' homes. METHODS:TNF-α inhibitors in their o...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2341-x

    authors: Vlieland ND,Nejadnik MR,Gardarsdottir H,Romeijn S,Sediq AS,Bouvy ML,Egberts ACG,van den Bemt BJF,Jiskoot W

    更新日期:2018-02-05 00:00:00

  • Controlled Endolysosomal Release of Agents by pH-responsive Polymer Blend Particles.

    abstract:PURPOSE:A key step of delivering extracellular agents to its intracellular target is to escape from endosomal/lysosomal compartments, while minimizing the release of digestive enzymes that may compromise cellular functions. In this study, we examined the intracellular distribution of both fluorecent cargoes and enzymes...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-015-1619-0

    authors: Zhan X,Tran KK,Wang L,Shen H

    更新日期:2015-07-01 00:00:00

  • Vaccine delivery to the oral cavity using coated microneedles induces systemic and mucosal immunity.

    abstract:PURPOSE:The objective of this study is to evaluate the feasibility of using coated microneedles to deliver vaccines into the oral cavity to induce systemic and mucosal immune responses. METHOD:Microneedles were coated with sulforhodamine, ovalbumin and two HIV antigens. Coated microneedles were inserted into the inner...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1335-1

    authors: Ma Y,Tao W,Krebs SJ,Sutton WF,Haigwood NL,Gill HS

    更新日期:2014-09-01 00:00:00

  • Pharmacokinetics of once-a-month injectable microspheres of leuprolide acetate.

    abstract::The pharmacokinetic parameters of leuprolide acetate, a potent analogue of LH-RH, were determined in rats and dogs after i.v. and s.c. dosing with leuprolide solution. The effective human dose of once-a-month injectable microspheres of leuprolide was estimated to be about 3.2 to 8.1 mg analogue/month using these param...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015818504906

    authors: Okada H,Inoue Y,Heya T,Ueno H,Ogawa Y,Toguchi H

    更新日期:1991-06-01 00:00:00

  • Analysis of a nanocrystalline polymer dispersion of ebselen using solid-state NMR, Raman microscopy, and powder X-ray diffraction.

    abstract:PURPOSE:Nanocrystalline drug-polymer dispersions are of significant interest in pharmaceutical delivery. The purpose of this work is to demonstrate the applicability of methods based on two-dimensional (2D) and multinuclear solid-state NMR (SSNMR) to a novel nanocrystalline pharmaceutical dispersion of ebselen with pol...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0713-9

    authors: Vogt FG,Williams GR

    更新日期:2012-07-01 00:00:00

  • Affinity capillary electrophoresis in pharmaceutics.

    abstract::The technique of Affinity capillary electrophoresis (ACE) is a useful tool to characterize complexation and partition equilibria. A wide range of applications in pharmaceutics has been presented: the determination of pKA values, of association constants between drugs and cyclodextrins or amphiphilic compounds as well ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:

    authors: Neubert RH,Schwarz MA,Mrestani Y,Plätzer M,Raith K

    更新日期:1999-11-01 00:00:00

  • Relative reactivity of dihydropyridine derivatives to electrogenerated superoxide ion in DMSO solutions: a voltammetric approach.

    abstract:PURPOSE:To evaluate the reaction of a large series of pharmacologically significant 1,4-dihydropyridine (1,4-DHP) compounds with superoxide (O2.-) in dimethylsulfoxide using differential pulse voltammetry and controlled potential electrolysis. METHODS:Differential pulse voltammetry was used to track the consumption of...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1022291624933

    authors: Oriz ME,Núñez-Vergara LJ,Squella JA

    更新日期:2003-02-01 00:00:00

  • High Content Solid Dispersions for Dose Window Extension: A Basis for Design Flexibility in Fused Deposition Modelling.

    abstract:PURPOSE:This study uses high drug content solid dispersions for dose window extension beyond current demonstrations using fused deposition modelling (FDM) to; i) accommodate pharmaceutically relevant doses of drugs of varying potencies at acceptable dosage form sizes and ii) enable enhanced dose flexibility via modular...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-019-2720-6

    authors: Govender R,Abrahmsén-Alami S,Folestad S,Larsson A

    更新日期:2019-12-17 00:00:00

  • Competitive inhibition of glycylsarcosine transport by enalapril in rabbit renal brush border membrane vesicles: interaction of ACE inhibitors with high-affinity H+/peptide symporter.

    abstract:PURPOSE:To examine the inhibitory potential of enalapril [and other angiotensin converting enzyme (ACE) inhibitors] on glycylsarcosine (GlySar) transport by the high-affinity renal peptide transporter. METHODS:Studies were performed in rabbit renal brush border membrane vesicles in which the uptake of radiolabeled Gly...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018847818766

    authors: Lin CJ,Akarawut W,Smith DE

    更新日期:1999-05-01 00:00:00

  • Enhancement of the physical stability of amorphous indomethacin by mixing it with octaacetylmaltose. inter and intra molecular studies.

    abstract:PURPOSE:To demonstrate a very effective and easy way of stabilization of amorphous indomethacin (IMC) by preparing binary mixtures with octaacetylmaltose (acMAL). In order to understand the origin of increased stability of amorphous system inter- and intramolecular interactions between IMC and acMAL were studied. METH...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1385-4

    authors: Kaminska E,Adrjanowicz K,Zakowiecki D,Milanowski B,Tarnacka M,Hawelek L,Dulski M,Pilch J,Smolka W,Kaczmarczyk-Sedlak I,Kaminski K

    更新日期:2014-10-01 00:00:00

  • Irinotecan Alters the Disposition of Morphine Via Inhibition of Organic Cation Transporter 1 (OCT1) and 2 (OCT2).

    abstract:PURPOSE:The organic cation transporters (OCTs) and multidrug and toxin extrusions (MATEs) together are regarded as an organic cation transport system critical to the disposition and response of many organic cationic drugs. Patient response to the analgesic morphine, a characterized substrate for human OCT1, is highly v...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-018-2526-y

    authors: Zhu P,Ye Z,Guo D,Xiong Z,Huang S,Guo J,Zhang W,Polli JE,Zhou H,Li Q,Shu Y

    更新日期:2018-10-25 00:00:00

  • Drug release kinetics and transport mechanisms from semi-interpenetrating networks of gelatin and poly(ethylene glycol) diacrylate.

    abstract:PURPOSE:To elucidate the key parameters affecting solute transport from semi-interpenetrating networks (sIPNs) comprised of poly(ethylene glycol) diacrylate (PEGdA) and gelatin that are partially crosslinked, water-swellable and biodegradable. Effects of material compositions, solute size, solubility, and loading densi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-009-9923-1

    authors: Fu Y,Kao WJ

    更新日期:2009-09-01 00:00:00

  • Evaluation of Intranasal Vaccine Delivery Using Anatomical Replicas of Infant Nasal Airways.

    abstract:PURPOSE:Nasal delivery is a favorable route for vaccination against most respiratory infections, as antigen deposited in the nasal turbinate and Waldeyer's ring areas induce mucosal and systemic immune responses. However, little is known about the nasal distribution of the vaccines, specifically for infants. METHODS:A...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02976-9

    authors: Wilkins JV Jr,Golshahi L,Rahman N,Li L

    更新日期:2021-01-15 00:00:00

  • Delivery of HSP90 Inhibitor Using Water Soluble Polymeric Conjugates with High Drug Payload.

    abstract:PURPOSE:HSP90 (Heat shock protein 90kD) has been validated as a therapeutic target in Castrate Resistant Prostate Cancer. Unfortunately, HSP90 inhibitors suffer from dose-limiting toxicities that hinder their clinical applications. Previously developed polymeric delivery systems for HSP90 inhibitors had either low drug...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2249-5

    authors: Suárez Del Pino JA,Kolhatkar R

    更新日期:2017-12-01 00:00:00

  • Regulation of miR-19 to breast cancer chemoresistance through targeting PTEN.

    abstract:PURPOSE:To explore whether miR-19 is involved in the regulation of multidrug resistance (MDR), one of the main causes of breast cancer mortality, and modulates sensitivity of tumor cells to chemotherapeutic agents. METHODS:We analyzed miRNA expression levels in three MDR cell lines in comparison with their parent cell...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-011-0570-y

    authors: Liang Z,Li Y,Huang K,Wagar N,Shim H

    更新日期:2011-12-01 00:00:00

  • Synthesis and in vitro evaluation of a novel chitosan-glutathione conjugate.

    abstract:PURPOSE:It was the aim of this study to synthesize and characterize a novel chitosan-glutathione (GSH) conjugate providing improved mucoadhesive and permeation-enhancing properties. METHODS:Mediated by carbodiimide and N-hydroxysuccinimide, glutathione was covalently attached to chitosan via the formation of an amide ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-005-6248-6

    authors: Kafedjiiski K,Föger F,Werle M,Bernkop-Schnürch A

    更新日期:2005-09-01 00:00:00

  • On the Nature of Physiologically-Based Pharmacokinetic Models -A Priori or A Posteriori? Mechanistic or Empirical?

    abstract::Physiologically-based pharmacokinetic (PBPK) models explicitly incorporate tissue-specific blood flows, partition coefficients, and metabolic processes. Since PBPK models are derived using physiologic parameters and interactions of the compound with tissue components, these models are considered to be "bottom up" as o...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-016-2089-8

    authors: Korzekwa K,Nagar S

    更新日期:2017-03-01 00:00:00

  • The relationship between the glass transition temperature and the water content of amorphous pharmaceutical solids.

    abstract::The glass transition temperature of an amorphous pharmaceutical solid is a critical physical property which can dramatically influence its chemical stability, physical stability, and viscoelastic properties. Water frequently acts as a potent plasticizer for such materials, and since many amorphous solids spontaneously...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018941810744

    authors: Hancock BC,Zografi G

    更新日期:1994-04-01 00:00:00

  • Influence of Production Process and Scale on Quality of Polypeptide Drugs: a Case Study on GLP-1 Analogs.

    abstract:PURPOSE:Manufacturing processes for polypeptide/protein drugs are designed to ensure robust quality, efficacy and safety. Process differences introduced by follow-on manufacturers may result in changes in quality and clinical outcomes. This study investigated the impact of production methods on the stability and impuri...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02817-9

    authors: Staby A,Steensgaard DB,Haselmann KF,Marino JS,Bartholdy C,Videbæk N,Schelde O,Bosch-Traberg H,Spang LT,Asgreen DJ

    更新日期:2020-06-08 00:00:00

  • Targeting of liposomes via PSGL1 for enhanced tumor accumulation.

    abstract:PURPOSE:To improve the delivery of liposomes to tumors using P-selectin glycoprotein ligand 1 (PSGL1) mediated binding to selectin molecules, which are upregulated on tumorassociated endothelium. METHODS:PSGL1 was orientated and presented on the surface of liposomes to achieve optimal selectin binding using a novel st...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0875-5

    authors: Carlisle R,Seymour LW,Coussios CC

    更新日期:2013-02-01 00:00:00

  • Variations of in vitro nitroglycerine permeation through human epidermis.

    abstract::The fluxes of nitroglycerine (NG) through human abdominal epidermis from different individuals were measured in vitro at 32°C. The mean NG flux for the entire group was 16.9 µg/cm(2) × hr, with a standard deviation of 47.7%. There are no significant differences in the means and the variances of NG fluxes between males...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/A:1016381017357

    authors: Langguth P,Spahn H,Mutschler E

    更新日期:1986-02-01 00:00:00

  • In vitro human epidermal and polyethylene membrane penetration and retention of the sunscreen benzophenone-3 from a range of solvents.

    abstract:PURPOSE:To study epidermal and polyethylene membrane penetration and retention of the sunscreen benzophenone-3 (BP) from a range of single solvent vehicles and evaluate solvent effects on permeability parameters. METHODS:The solubility of BP was measured in a number of solvents. Penetration of BP across human epidermi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1011958006973

    authors: Jiang R,Benson HA,Cross SE,Roberts MS

    更新日期:1998-12-01 00:00:00

  • The influence of regional deposition on the pharmacokinetics of pulmonary-delivered human growth hormone in rabbits.

    abstract::The pulmonary deposition and pharmacokinetics of human growth hormone (hGH), administered by aerosol and instillate, in formulations containing 99mTc-DTPA (for gamma scintigraphic imaging) have been studied in five male New Zealand White rabbits. Gamma scintigraphy indicated that the peripheral:central deposition tend...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016292232513

    authors: Colthorpe P,Farr SJ,Smith IJ,Wyatt D,Taylor G

    更新日期:1995-03-01 00:00:00

  • Liposomal induction of a heat-stable macrophage priming factor to induce nitric oxide in response to LPS.

    abstract:PURPOSE:The effects of liposomes on nitric oxide (NO) production from mouse peritoneal macrophages following intraperitoneal injection of liposomes were investigated. METHODS:Mouse peritoneal macrophages were collected following intraperitoneal injection of liposomes and cultured with and without lipopolysaccharide (L...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016034303012

    authors: Aramaki Y,Arima H,Hara T,Tsuchiya S

    更新日期:1996-09-01 00:00:00

  • Pharmacokinetics and pharmacodynamics of 7-nitroindazole, a selective nitric oxide synthase inhibitor, in the rat hippocampus.

    abstract:PURPOSE:This study was conducted to assess the pharmacokinetics and pharmacodynamics of 7-nitroindazole (7-NI), a selective inhibitor of neuronal nitric oxide synthase (NOS). METHODS:Male Sprague-Dawley rats were equipped with peritoneal/ venous cannulae and a microdialysis probe in the hippocampal cortex. Rats receiv...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1013042817281

    authors: Bush MA,Pollack GM

    更新日期:2001-11-01 00:00:00

  • Aerodynamic factors responsible for the deaggregation of carrier-free drug powders to form micrometer and submicrometer aerosols.

    abstract:PURPOSE:To employ in vitro experiments combined with computational fluid dynamics (CFD) analysis to determine which aerodynamic factors were most responsible for deaggregating carrier-free powders to form micrometer and submicrometer aerosols from a capsule-based platform. METHODS:Eight airflow passages were evaluated...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-1001-z

    authors: Longest PW,Son YJ,Holbrook L,Hindle M

    更新日期:2013-06-01 00:00:00

  • Comparison of the hanson microette and the Van Kel apparatus for in vitro release testing of topical semisolid formulations.

    abstract:PURPOSE:The major goal of this study was to compare the relative utility of the Hanson Microette and the Van Kel apparatus, two fully automated devices, as in vitro release tests (IVRT) for semisolids. We attempted to develop methodology that can be used to discriminate formulation changes, and to evaluate the precisio...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012256923340

    authors: Rapedius M,Blanchard J

    更新日期:2001-10-01 00:00:00

  • A novel peptide nanomedicine against acute lung injury: GLP-1 in phospholipid micelles.

    abstract:PURPOSE:Treatment of acute lung injury (ALI) observed in Gram-negative sepsis represents an unmet medical need due to a high mortality rate and lack of effective treatment. Accordingly, we developed and characterized a novel nanomedicine against ALI. We showed that when human glucagon-like peptide 1(7-36) (GLP-1) self-...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-010-0322-4

    authors: Lim SB,Rubinstein I,Sadikot RT,Artwohl JE,Önyüksel H

    更新日期:2011-03-01 00:00:00

  • Pharmacokinetics of a hematoregulatory peptide (SK&F107647) in healthy male volunteers and in patients with colorectal or pancreatic adenocarcinoma not amenable to standard therapy.

    abstract:PURPOSE:To describe the pharmacokinetics of SK&F 107647, a synthetic hematoregulatory peptide, in healthy volunteers and in patients with adenocarcinoma. METHODS:SK&F 107647 pharmacokinetics were evaluated in 2 dose-escalation studies. Volunteers received SK&F 107647 as single 15-minute iv infusion doses of 1, 10, 100...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1007512617139

    authors: Zia-Amirhosseini P,Harris RZ,Cowley HC,Valle JW,Citerone DR,Boppana VK,Scarffe H,Watson P,Davis CB

    更新日期:2000-04-01 00:00:00