Effect of moisture content on compression properties of two dextrose-based directly compressible diluents.

Abstract:

:Moisture sorption characteristics and the effect of moisture content on the compression properties of two dextrose-based directly compressible diluents, namely, Emdex (diluent A) and Sweetrex (diluent B) were studied. Both diluents sorbed moisture rapidly at relative humidities greater than 60%. For both the diluents, pressures required to compress tablets to the same relative density decreased with increasing moisture content. Yield pressures calculated from linear Heckel plots obtained from the compression data of both diluents reflected decreasing values with increasing moisture content. Three-way surface profile graphs of moisture content versus tablet parameters such as crushing force, relative density, and compression pressure give a unique overall picture of the compression properties of a diluent and offer the tablet formulator a useful tool for diluent comparison.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Shukla AJ,Price JC

doi

10.1023/a:1015889414533

subject

Has Abstract

pub_date

1991-03-01 00:00:00

pages

336-40

issue

3

eissn

0724-8741

issn

1573-904X

journal_volume

8

pub_type

杂志文章
  • Predicting effect of food on extent of drug absorption based on physicochemical properties.

    abstract:PURPOSE:To develop a statistical model for predicting effect of food on the extent of absorption (area under the curve of time-plasma concentration profile, AUC) of drugs based on physicochemical properties. MATERIALS AND METHODS:Logistic regression was applied to establish the relationship between the effect of food ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9236-1

    authors: Gu CH,Li H,Levons J,Lentz K,Gandhi RB,Raghavan K,Smith RL

    更新日期:2007-06-01 00:00:00

  • Correction to: Bioreducible Poly(Amino Ethers) Based mTOR siRNA Delivery for Lung Cancer.

    abstract::Under the heading "Methods-Synthesis of the Bioreducible Modified-PAE (mPAE)", on page 3, line 14-17, there is an error. The quantity unit of PAE and 2-iminothiolane hydrochloride needs to be corrected to mg instead of g. ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,已发布勘误

    doi:10.1007/s11095-018-2488-0

    authors: Gandhi NS,Godeshala S,Koomoa-Lange DT,Miryala B,Rege K,Chougule MB

    更新日期:2018-09-05 00:00:00

  • Enhanced delivery of 5-iodo-2'-deoxyuridine to the brain parenchyma.

    abstract::5'-Ester derivatives of 5-iodo-2'-deoxyuridine (IDU) with varying degrees of lipophilicity were examined to evaluate the effectiveness of lipophilic ester prodrugs for enhanced and sustained delivery of IDU to the brain parenchyma. Approximately 1.0% (1.0 +/- 0.19; n = 4) of the total radioactivity was found in the br...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015803922401

    authors: Ghosh MK,Mitra AK

    更新日期:1992-09-01 00:00:00

  • Pharmacokinetic Modeling of the Impact of P-glycoprotein on Ondansetron Disposition in the Central Nervous System.

    abstract:PURPOSE:Modulation of 5-HT3 receptor in the central nervous system (CNS) is a promising approach for treatment of neuropathic pain. The goal was to evaluate the role of P-glycoprotein (Pgp) in limiting exposure of different parts of the CNS to ondansetron (5-HT3 receptor antagonist) using wild-type and genetic knockout...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02929-2

    authors: Chiang M,Back HM,Lee JB,Oh S,Guo T,Girgis S,Park C,Haroutounian S,Kagan L

    更新日期:2020-09-28 00:00:00

  • In vitro/in vivo correlation for 14C-methylated lysozyme release from poly(ether-ester) microspheres.

    abstract:PURPOSE:The purpose of this study was to obtain an in vitro/in vivo correlation for the sustained release of a protein from poly(ethylene glycol) terephthalate (PEGT)/poly(butylene terephthalate) (PBT) microspheres. METHODS:Radiolabeled lysozyme was encapsulated in PEGT/PBT microspheres via a water-in-oil-in-water emu...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/B:PHAM.0000019303.12086.d1

    authors: van Dijkhuizen-Radersma R,Wright SJ,Taylor LM,John BA,de Groot K,Bezemer JM

    更新日期:2004-03-01 00:00:00

  • Glucuronidation metabolic kinetics of valproate in guinea pigs: nonlinear at clinical concentration levels.

    abstract:PURPOSE:Nonlinear conjugation metabolic rate of valproic acid (VPA) has been speculated previously from plasma elimination and liver concentration of VPA in guinea pigs. The purposes of the present study were to assess our speculation by direct measurement of VPA glucuronidation rate in vitro. METHODS:VPA at various c...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016028707130

    authors: Yu HY,Shen YZ

    更新日期:1996-08-01 00:00:00

  • High-performance liquid chromatographic (HPLC) assay using fluorescence detection for the simultaneous determination of gallopamil and norgallopamil in human plasma.

    abstract::Gallopamil is a calcium-channel antagonist with reported activity in experimental animals three to five times higher than that of verapamil. An automated high-performance liquid chromatographic (HPLC) method with fluorescence detection is described for the simultaneous determination of gallopamil and its metabolite no...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016401405119

    authors: McLean AM,Babcock-Atkinson E,Rein K,Ruggirello DA,Gonzalez MA,Noonan PK

    更新日期:1987-08-01 00:00:00

  • Quantitative Fourier transform-infrared/attenuated total reflectance (FT-IR/ATR) analysis of trimethoprim and sulfamethoxazole in a pharmaceutical formulation using partial least squares.

    abstract::An alternative procedure for the simultaneous determination of trimethoprim and sulfamethoxazole in an intravenous pharmaceutical formulation is presented. Infrared spectra of 14 calibration and 6 validation samples were collected using Fourier transform-infrared/attenuated total reflectance (FT-IR/ATR). Partial least...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015957632242

    authors: Hartauer KJ,Guillory JK

    更新日期:1989-07-01 00:00:00

  • Aggregation mechanism of an IgG2 and two IgG1 monoclonal antibodies at low pH: from oligomers to larger aggregates.

    abstract:PURPOSE:To identify the aggregation mechanism and the stability characteristics of three different monoclonal antibodies under acidic conditions. METHODS:The aggregation kinetics is analyzed by a combination of light scattering, size exclusion chromatography and fluorescence techniques and the aggregation data are cor...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0885-3

    authors: Arosio P,Rima S,Morbidelli M

    更新日期:2013-03-01 00:00:00

  • Tolerability and absorption enhancement of intranasally administered octreotide by sodium taurodihydrofusidate in healthy subjects.

    abstract::Nasal sprays containing different concentrations of the somatostatin analogue octreotide and sodium tauro-24,25-dihydrofusidate (STDHF) as an absorption promoter were evaluated in two consecutive pharmacokinetic studies in healthy volunteers to characterize their bioavailability and local tolerability. The concentrati...

    journal_title:Pharmaceutical research

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1023/a:1018927710280

    authors: Kissel T,Drewe J,Bantle S,Rummelt A,Beglinger C

    更新日期:1992-01-01 00:00:00

  • Dependence of the molecular mobility and protein stability of freeze-dried gamma-globulin formulations on the molecular weight of dextran.

    abstract:PURPOSE:The effect of the molecular weight of dextran on the molecular mobility and protein stability of freeze-dried serum gamma-globulin (BGG) formulations was studied. The stabilizing effect of higher molecular weight dextran is discussed in relation to the molecular mobility of the formulations. METHODS:The molecu...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012194220970

    authors: Yoshioka S,Aso Y,Kojima S

    更新日期:1997-06-01 00:00:00

  • Biomimetic metabolism of artelinic acid by chemical cytochrome P-450 model systems.

    abstract:PURPOSE:To study the reaction of artelinic acid with chemical model systems of cytochrome P-450 as a means of obtaining authentic samples of the putative metabolites necessary for identification of the mammalian metabolites of artelinic acid. METHODS:Artelinic acid was reacted with different organic complexes of iron(...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012185124972

    authors: Idowu OR,Lin AJ,Grace JM,Peggins JO

    更新日期:1997-10-01 00:00:00

  • A novel oligodeoxynucleotide inhibitor of thrombin. II. Pharmacokinetics in the cynomolgus monkey.

    abstract:PURPOSE:To determine the pharmacokinetics of GS-522, an oligodeoxynucleotide (GGTTGGTGTGGTTGG) inhibitor of thrombin, after constant infusion and bolus administration in the cynomolgus monkey. METHODS:Using a stability indicating HPLC method, the GS-522 plasma concentration versus time data were obtained after constan...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016295907266

    authors: Lee WA,Fishback JA,Shaw JP,Bock LC,Griffin LC,Cundy KC

    更新日期:1995-12-01 00:00:00

  • Accurate determination of skin flux from flow-through diffusion cell data.

    abstract:PURPOSE:The goal of this investigation was to demonstrate whether the intrinsic flux of a drug diffusing across a membrane mounted in a flow-through diffusion cell may be accurately and easily determined by accounting for the accumulation in the receiver chamber. METHODS:Mathematical modeling, applied to transdermal d...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016216611809

    authors: Harrison DJ,Knutson K

    更新日期:1995-12-01 00:00:00

  • Novel beads made of alpha-cyclodextrin and oil for topical delivery of a lipophilic drug.

    abstract:PURPOSE:To investigate the potential of a novel lipid carrier, comprising beads of alpha-cyclodextrin and soybean oil, for topical drug delivery. Adapalene was chosen as a model drug to explore the ability of the beads to encapsulate and release a highly lipophilic compound. MATERIALS AND METHODS:Adapalene-loaded bead...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9395-0

    authors: Trichard L,Delgado-Charro MB,Guy RH,Fattal E,Bochot A

    更新日期:2008-02-01 00:00:00

  • Aerosol dispersion of respirable particles in narrow size distributions produced by jet-milling and spray-drying techniques.

    abstract:PURPOSE:To examine the effect of particle size and morphology on aerosol dispersion using jet-milled and spray-dried mannitol particles in narrow size distributions within the respirable range. METHODS:Particle size and morphology were examined by laser diffraction and scanning electron microscopy, respectively. Aeros...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000033007.27278.60

    authors: Louey MD,Van Oort M,Hickey AJ

    更新日期:2004-07-01 00:00:00

  • In vivo fluorescence imaging of IgG1 aggregates after subcutaneous and intravenous injection in mice.

    abstract:PURPOSE:To monitor the biodistribution of IgG1 aggregates upon subcutaneous (SC) and intravenous (IV) administration in mice and measure their propensity to stimulate an early immune response. METHODS:A human mAb (IgG1) was fluorescently labeled, aggregated by agitation stress and injected in SKH1 mice through SC and ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-1154-9

    authors: Filipe V,Que I,Carpenter JF,Löwik C,Jiskoot W

    更新日期:2014-01-01 00:00:00

  • Development of a Two-Dimensional Model for Predicting Transdermal Permeation with the Follicular Pathway: Demonstration with a Caffeine Study.

    abstract:PURPOSE:The development of a new two-dimensional (2D) model to predict follicular permeation, with integration into a recently reported multi-scale model of transdermal permeation is presented. METHODS:The follicular pathway is modelled by diffusion in sebum. The mass transfer and partition properties of solutes in li...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2209-0

    authors: Kattou P,Lian G,Glavin S,Sorrell I,Chen T

    更新日期:2017-10-01 00:00:00

  • Intranasal delivery--modification of drug metabolism and brain disposition.

    abstract::Intranasal route continues to be one of the main focuses of drug delivery research. Although it is generally perceived that the nasal route could avoid the first-pass metabolism in liver and gastrointestinal tract, the role of metabolic conversions in systemic and brain-targeted deliveries of the parent compounds and ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-010-0127-5

    authors: Wong YC,Zuo Z

    更新日期:2010-07-01 00:00:00

  • Evaluation of an enzyme-containing capsular shaped pulsatile drug delivery system.

    abstract:PURPOSE:To develop an enzymatically-controlled pulsatile drug release system based on an impermeable capsule body, which contains the drug and is closed by an erodible pectin/pectinase-plug. METHODS:The plug was prepared by direct compression of pectin and pectinase in different ratios. In addition to the disintegrati...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018959327311

    authors: Krögel I,Bodmeier R

    更新日期:1999-09-01 00:00:00

  • Dissolving Microneedle Patches for Dermal Vaccination.

    abstract::The dermal route is an attractive route for vaccine delivery due to the easy skin accessibility and a dense network of immune cells in the skin. The development of microneedles is crucial to take advantage of the skin immunization and simultaneously to overcome problems related to vaccination by conventional needles (...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-017-2223-2

    authors: Leone M,Mönkäre J,Bouwstra JA,Kersten G

    更新日期:2017-11-01 00:00:00

  • Mechanisms of transport and structure-permeability relationship of sulfasalazine and its analogs in Caco-2 cell monolayers.

    abstract:PURPOSE:To investigate the mechanisms involved in transport of sulfasalazine in Caco-2 cells. METHODS:Permeability coefficients of sulfasalazine and its analogs across Caco-2 cell monolayers were measured as a function of direction of transport, energy and concentration dependence, and in the presence of inhibitors of...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1026450326712

    authors: Liang E,Proudfoot J,Yazdanian M

    更新日期:2000-10-01 00:00:00

  • Textural analysis and flow rheometry of novel, bioadhesive antimicrobial oral gels.

    abstract:PURPOSE:This study examined the rheological and textural characteristics (hardness, compressibilty, adhesiveness and cohesiveness) of bioadhesive oral gels containing the antimicrobial agent chlorhexidine. METHODS:Textural analysis was performed using a Stable Micro Systems texture analyser (model TA-XT 2) in texture ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012091231023

    authors: Jones DS,Woolfson AD,Brown AF

    更新日期:1997-04-01 00:00:00

  • Targeting, endocytosis, and lysosomal delivery of active enzymes to model human neurons by ICAM-1-targeted nanocarriers.

    abstract:PURPOSE:Delivery of therapeutics to neurons is paramount to treat neurological conditions, including many lysosomal storage disorders. However, key aspects of drug-carrier behavior in neurons are relatively unknown: the occurrence of non-canonical endocytic pathways (present in other cells); whether carriers that trave...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1531-z

    authors: Hsu J,Hoenicka J,Muro S

    更新日期:2015-04-01 00:00:00

  • Cutaneous metabolism of nitroglycerin in vitro. II. Effects of skin condition and penetration enhancement.

    abstract::The effects of skin storage, skin preparation, skin pretreatment with a penetration enhancer, and skin barrier removal by adhesive tape-stripping on the concurrent cutaneous transport and metabolism of nitroglycerin (GTN) have been studied in vitro using hairless mouse skin. Storing the skin for 10 days at 4 degrees C...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015822431178

    authors: Higo N,Hinz RS,Lau DT,Benet LZ,Guy RH

    更新日期:1992-03-01 00:00:00

  • A population pharmacokinetic model for montelukast disposition in adults and children.

    abstract:PURPOSE:The purpose was to develop a population pharmacokinetic model for montelukast after intravenous administration. Clinical trial simulations were conducted using the model developed to identify the lowest intravenous dose in 6- to 14-year-old children that would give montelukast systemic exposures that were compa...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,随机对照试验

    doi:10.1007/s11095-005-2493-y

    authors: Ramakrishnan R,Migoya E,Knorr B

    更新日期:2005-04-01 00:00:00

  • New respirable and fast dissolving itraconazole dry powder composition for the treatment of invasive pulmonary aspergillosis.

    abstract:PURPOSE:Novel itraconazole (ITZ)-based dry powders for inhalation (DPI) were optimized for aerodynamic and dissolution properties and contained excipients that are acceptable for inhalation. METHODS:The DPI were produced by spray drying solutions. The drug content, crystallinity state, and morphological evaluation of ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0779-4

    authors: Duret C,Wauthoz N,Sebti T,Vanderbist F,Amighi K

    更新日期:2012-10-01 00:00:00

  • Purification and identification of high molecular weight products formed during storage of neutral formulation of human insulin.

    abstract:PURPOSE:To identify High Molecular Weight Products (HMWP) formed in human insulin formulation during storage. METHODS:Commercial formulation of human insulin was stored at 37°C for 1 year and HMWP was isolated using preparative size exclusion chromatography (SEC) and reverse phase (RP) chromatography. The primary stru...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1600-3

    authors: Hjorth CF,Hubálek F,Andersson J,Poulsen C,Otzen D,Naver H

    更新日期:2015-06-01 00:00:00

  • Intra- and inter-subject variabilities of CGP 33101 after replicate single oral doses of two 200-mg tablets and 400-mg suspension.

    abstract:PURPOSE:The purpose of this study was to use a replicate designed trial to assess the overall, intra- and inter-subject variabilities in pharmacokinetic parameters of CGP 33101 after oral administration of tablets relative to that of powder suspended in water, and to determine the relative proportion of the intra-subje...

    journal_title:Pharmaceutical research

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1023/a:1016275402723

    authors: Cheung WK,Kianifard F,Wong A,Mathieu J,Cook T,John V,Redalieu E,Chan K

    更新日期:1995-12-01 00:00:00

  • Correlation among agonist dose, rate of import, and transcriptional activity of liganded progesterone receptor B isoform in living cells.

    abstract:PURPOSE:To determine the correlation among progesterone dose, rate of import of progesterone-occupied progesterone receptor (PR) complexes into the nucleus of cells, and transcriptional activity of progesterone-PR complexes. METHODS:Live cell imaging and time-lapse microscopy of green fluorescent protein-tagged PR wer...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1026127015761

    authors: Li H,Yan G,Kern SE,Lim CS

    更新日期:2003-10-01 00:00:00