Electromigration of ions across the skin: determination and prediction of transport numbers.

Abstract:

:In iontophoresis, an electric field across the skin induces electromigration of exogenously applied and endogenously present ions. The approach can be used to improve dramatically drug delivery by elimination of competing co-ions in the externally applied formulation, as this maximizes the fraction of current carried by (i.e., the transport number of) the drug. In this study, the dependence of the transport number on the nature of the ions present at the anode and cathode was examined using 12 different combinations of ions (4 cations x 3 anions). Cationic transport numbers (t(C+) (o)) were a function of their inherent mobilities and depended upon those of the single anion at the cathode; however, t(C+) (o) was independent of the counter-ion concentration. The extensive data obtained agreed well, furthermore, with a theoretical framework previously developed for this so-called "single-ion" situation. In addition, there was a strong correlation between ionic transport numbers in the skin and those in aqueous solution, which are easily estimated from measurements of ionic mobility. It follows that it should be possible, from the framework developed here, to establish a predictive tool, combining theory with simple experiments, for the optimization of iontophoretic drug delivery.

journal_name

J Pharm Sci

authors

Mudry B,Guy RH,Delgado-Charro MB

doi

10.1002/jps.20561

subject

Has Abstract

pub_date

2006-03-01 00:00:00

pages

561-9

issue

3

eissn

0022-3549

issn

1520-6017

pii

S0022-3549(16)31976-1

journal_volume

95

pub_type

杂志文章
  • Chemistry and pharmacology of homologs of 6-acetyl-and 3,6-diacetylmorphine.

    abstract::3,6-Diformyl- and 3,6-dipropanoylmorphine and 6-formyl- and 6-propanoylmorphine were prepared to obtain longer acting, heroin-like compounds. The 6-acylated compounds were more potent than heroin subcutaneously and were orally effective, and their duration of action was at least two to three times greater than that of...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600660242

    authors: May EL,Jacobson AE

    更新日期:1977-02-01 00:00:00

  • Biophysical and structural characterisation of nucleic acid complexes with modified cyclodextrins using circular dichroism.

    abstract::Modified cyclodextrins (CDs) have shown great promise as non-viral gene and siRNA delivery vectors in a range of in vitro and in vivo studies. In the current study, structural and biophysical characterisation of selected CDs was carried out to enhance our understanding of their interaction with nucleic acids. The meth...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.23922

    authors: O'Mahony AM,Cronin MF,McMahon A,Evans JC,Daly K,Darcy R,O'Driscoll CM

    更新日期:2014-05-01 00:00:00

  • Prediction of the association state of insulin using spectral parameters.

    abstract::Human insulin exists in different association states, from monomer to hexamer, depending on the conditions. In the presence of zinc the "normal" state is a hexamer. The structural properties of 20 variants of human insulin were studied by near-UV circular dichroism, fluorescence spectroscopy, and small-angle X-ray sca...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.10355

    authors: Uversky VN,Garriques LN,Millett IS,Frokjaer S,Brange J,Doniach S,Fink AL

    更新日期:2003-04-01 00:00:00

  • Noninvasive identification of materials inside USP vials with Raman spectroscopy and a Raman spectral library.

    abstract::A commercial dispersive Raman spectrometer operating at 785 nm with a CCD detector was used to acquire spectra of USP reference materials inside amber USP vials. The laser and collection beams were directed through the bottom of the vials, resulting in a 60% loss of signal. The Raman shift was calibrated with a 4-acet...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1021/js970330q

    authors: McCreery RL,Horn AJ,Spencer J,Jefferson E

    更新日期:1998-01-01 00:00:00

  • Analysis and prediction of partition coefficients of meta- and para-disubstituted benzenes in terms of substituent effects.

    abstract::The hydrophobic substituent parameter for a system of meta- and para-disubstituted benzenes, XC6H4Y, defined as pi X/PhY = log PXC6H4Y - log PC6H5Y, where P is the octanol-water partition coefficient and X and Y are variable and fixed substituents, respectively, varies from one system to another, according to the vari...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600720319

    authors: Fujita T

    更新日期:1983-03-01 00:00:00

  • Reaction of a peptide with polyvinylpyrrolidone in the solid state.

    abstract::During stability studies at high temperature (70 degrees C) and low relative humidity ( approximately 0%), the recovery of an asparagine containing hexapeptide (VYPNGA) and its known deamidation products from solid polyvinylpyrrolidone (PVP) matrices was incomplete. To determine the causes of this mass loss, formulati...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.10316

    authors: D'Souza AJ,Schowen RL,Borchardt RT,Salsbury JS,Munson EJ,Topp EM

    更新日期:2003-03-01 00:00:00

  • Effects of film coatings on tablet hardness.

    abstract::The effects of five conventional film-coating materials on tablet hardness were studied. Placebos showed apparently linear increases in hardness as coatings were applied. Completely coated samples exhibited hardness increases from 50 to 140%, with a corresponding 3% increase in tablet weight. Equations were derived re...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600650908

    authors: Stern PW

    更新日期:1976-09-01 00:00:00

  • Ultracentrifugal study of effect of sodium chloride on micelle size of fusidate sodium.

    abstract::Apparent micellar molecular weights were determined with the antibiotic fusidate sodium by ultracentrifugation in varying counterion concentrations (Na+). The effects of buffer salts, pH, sodium chloride concentration, and drug concentration were studied. The results strongly support the concept of the formation of pr...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600640536

    authors: Richard AJ

    更新日期:1975-05-01 00:00:00

  • Antiradiation compounds XV: condensations of carbon disulfide with amino, chloro, cyanomethyl, and sulfonamido heterocycles.

    abstract::Condensations of carbon disulfide were carried out with amino, chloro, and diamino heterocycles to give condensed ring thiazoline-2-thiones and imidazoline-2-thiones, with cyanomethyl heterocycles to give dithio acid derivatives, and with heterocyclic sulfonamides to give sulfonyldithiocarbamates. Of several examples ...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600640823

    authors: Foye WO,Kauffman JM,Lanzillo JJ,LaSala EF

    更新日期:1975-08-01 00:00:00

  • Hybrid films from blends of chitosan and egg phosphatidylcholine for localized delivery of paclitaxel.

    abstract::Chitosan and egg phosphatidylcholine (ePC) were used as a unique combination to prepare composite films for localized drug delivery. In comparison to other phospholipids analyzed, ePC was found to produce chitosan-based films with minimal swelling and a high degree of stability. The properties of the chitosan-ePC film...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.20379

    authors: Grant J,Blicker M,Piquette-Miller M,Allen C

    更新日期:2005-07-01 00:00:00

  • The biowaiver procedure: its application to antituberculosis products in the WHO prequalification programme.

    abstract::In 2005, the World Health Organization (WHO) proposed that provided an active pharmaceutical ingredient could meet certain criteria, bioequivalence could be evaluated with a set of laboratory tests, obviating the need for expensive and time-consuming pharmacokinetic studies in humans. The aim of this work was to deter...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.22349

    authors: Strauch S,Jantratid E,Stahl M,Rägo L,Dressman JB

    更新日期:2011-03-01 00:00:00

  • Discontinuous oral absorption of cimetropium bromide, a new antispasmodic drug.

    abstract::The pharmacokinetic profiles of cimetropium bromide, after either intravenous injection of 10 mg or oral ingestion of 200 mg, were determined in eight healthy volunteers. After intravenous administration, the plasma levels and urinary excretion indicated that the drug is distributed and eliminated at a rapid rate (ter...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600750713

    authors: Imbimbo BP,Daniotti S,Vidi A,Foschi D,Saporiti F,Ferrante L

    更新日期:1986-07-01 00:00:00

  • Pharmacokinetics of nitroglycerin in rats.

    abstract::The plasma nitroglycerin levels obtained after intracardial (0.7 mg/kg), oral (7 mg/kg), and topical (7--14 mg/kg) doses of nitroglycerin in rats are reported. Nitroglycerin followed essentially one-compartment kinetics after intracardial administration, showing a mean half-life of about 4 min and a mean apparent volu...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600670446

    authors: Yap PS,Fung HL

    更新日期:1978-04-01 00:00:00

  • Use of fluorometry in assessing the efficacy of a cation-sensitive gel as an ophthalmic vehicle: comparison with scintigraphy.

    abstract::Gelrite, a heteropolysaccharide that forms a gel in the presence of cations, was tested in humans for its efficacy as an ophthalmic vehicle by a nonivasive fluorometric technique. Fluorescein was used as the tracer, and its concentration in the anterior chamber was used as the principal measure of bioavailability. The...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600810704

    authors: Maurice DM,Srinivas SP

    更新日期:1992-07-01 00:00:00

  • Intravenous dosing conditions may affect systemic clearance for highly lipophilic drugs: implications for lymphatic transport and absolute bioavailability studies.

    abstract::The clearance (Cl) and volume of distribution (V(ss)) of a lipophilic, lymphatically transported drug, halofantrine (Hf) have been evaluated after intravenous delivery to the systemic circulation in ex vivo lymph and plasma, and compared with the data obtained after administration of a lipid-based emulsion and a lipid...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.23211

    authors: Caliph SM,Trevaskis NL,Charman WN,Porter CJ

    更新日期:2012-09-01 00:00:00

  • Determination of phenylpropanolamine salts in dosage forms through fluroescent derivative formation.

    abstract::Phenylpropanolamine was determined by measuring its fluorescent fluorescamine derivative. The method is rapid, sensitive, and easily automated. Statistics are presented for an effervescent cold product, and recovery data are presented for other commercially available products. ...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600671137

    authors: Shankle LL

    更新日期:1978-11-01 00:00:00

  • Transdermal delivery of nonsteroidal anti-inflammatory drugs mediated by polyamidoamine (PAMAM) dendrimers.

    abstract::Nonsteroidal anti-inflammatory drugs (NSAIDs) are among the most frequently used drugs in the world, primarily for symptoms associated with osteoarthritis and other chronic musculoskeletal conditions. However, adverse effects caused by oral administration, such as local or systemic disturbance in the gastrointestinal ...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.20745

    authors: Cheng Y,Man N,Xu T,Fu R,Wang X,Wang X,Wen L

    更新日期:2007-03-01 00:00:00

  • Optimal Dosing Regimen of Phenytoin for Korean Epilepsy Patients: From Premature Babies to the Elderly.

    abstract::Phenytoin has been decreasingly used because of the high interindividual variability in drug concentration and the narrow therapeutic window. Despite such drawbacks, phenytoin is still essential as a second-line therapy for status epilepticus when patients are resistant to benzodiazepines. This study aimed to develop ...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1016/j.xphs.2019.03.022

    authors: Guk J,Lee SG,Chae D,Kim JH,Park K

    更新日期:2019-08-01 00:00:00

  • The pharmacology of radiolabeled cationic antimicrobial peptides.

    abstract::Cationic antimicrobial peptides are good candidates for new diagnostics and antimicrobial agents. They can rapidly kill a broad range of microbes and have additional activities that have impact on the quality and effectiveness of innate responses and inflammation. Furthermore, the challenge of bacterial resistance to ...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章,评审

    doi:10.1002/jps.21034

    authors: Brouwer CP,Wulferink M,Welling MM

    更新日期:2008-05-01 00:00:00

  • Mechanistic study of the effect of roller compaction and lubricant on tablet mechanical strength.

    abstract::Heckel analysis, tablet tensile strength, and indentation hardness were determined for a series of sieved and roller compacted microcrystalline cellulose mixtures under both unlubricated and lubricated conditions with magnesium stearate. These results have been used to evaluate the loss of reworkability following roll...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.20938

    authors: He X,Secreast PJ,Amidon GE

    更新日期:2007-05-01 00:00:00

  • Application of salivary concentration data to pharmacokinetic studies with antipyrine.

    abstract::The concentrations of antipyrine in plasma and saliva were equivalent in normal volunteers and in patients with acute viral hepatitis following oral doses of antipyrine. Estimates of clearance, volume of distribution, and half-life made from either plasma or saliva samples were not statistically different in these sub...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600660140

    authors: Meffin PJ,Williams RL,Blaschke TF,Rowland M

    更新日期:1977-01-01 00:00:00

  • TLC differentiation of butyrophenone and diphenylbutylpiperidine compounds from phenothiazine derivatives.

    abstract::A procedure is described for TLC detection and differentiation of the butyrophenone-diphenylbutylpiperidine group and phenothiazine derivatives at the microgram level. A two-dimensional TLC method to separate butyrophenone and diphenylbutylpiperidine compounds is reported. A variety of possible detection reagents were...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600680834

    authors: Pluym A

    更新日期:1979-08-01 00:00:00

  • Prediction of Losartan-Active Carboxylic Acid Metabolite Exposure Following Losartan Administration Using Static and Physiologically Based Pharmacokinetic Models.

    abstract::The aim of this study was to evaluate a strategy based on static and dynamic physiologically based pharmacokinetic (PBPK) modeling for the prediction of metabolite and parent drug area under the time-concentration curve ratio (AUCm/AUCp) and their PK profiles in humans using in vitro data when active transport process...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1016/j.xphs.2017.03.032

    authors: Nguyen HQ,Lin J,Kimoto E,Callegari E,Tse S,Obach RS

    更新日期:2017-09-01 00:00:00

  • Simultaneous determination of unlabeled and carbon-13-labeled etoricoxib, a new cyclooxygenase-2 inhibitor, in human plasma using HPLC-MS/MS.

    abstract::A method for the simultaneous determination of etoricoxib and its carbon-13 analog ((13)C(6)-etoricoxib) from human plasma has been developed and used to support bioavailability studies. Plasma samples (0.5 mL) were extracted by using a 3M Empore 96-well plate (C(8)) and the resulting extracts were analyzed by using a...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.10038

    authors: Rose MJ,Agrawal N,Woolf EJ,Matuszewski BK

    更新日期:2002-02-01 00:00:00

  • Optical crystallographic characteristics of some USP drugs.

    abstract::Optical crystallographic data were determined on a variety of newer USP drugs for which data had not been previously obtained. The ingredients in an unknown sample can be identified by polarized light microscopy by mounting small amounts of the material in successive specific refractive index liquids and determining r...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600821218

    authors: Jordan DD

    更新日期:1993-12-01 00:00:00

  • Determination of drug plasma protein binding by solid phase microextraction.

    abstract::The plasma protein binding of drugs has been shown to have significant effects on the quantitative relationship between clinical pharmacokinetics and pharmacodynamics. In many clinical situations, measurement of the total drug concentration does not provide the needed information concerning the unbound fraction of dru...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.20558

    authors: Musteata FM,Pawliszyn J,Qian MG,Wu JT,Miwa GT

    更新日期:2006-08-01 00:00:00

  • The complex inter-relationships between protein flexibility and stability.

    abstract::The ability to successfully formulate and manufacture therapeutic protein dosage forms requires a thorough understanding of their physico-chemical properties. Proteins are inherently dynamic molecules of marginal stability. These properties present unique challenges to the pharmaceutical scientist attempting to develo...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章,评审

    doi:10.1002/jps.21269

    authors: Kamerzell TJ,Middaugh CR

    更新日期:2008-09-01 00:00:00

  • Kinetics and mechanism of oxidation of promazine and promethazine by ferric perchlorate.

    abstract::The equilibrium constants, kinetics, and mechanism of promazine and promethazine oxidation by ferric perchlorate were investigated at different temperatures and acidities using a stopped-flow spectrophotometric technique. The overall reaction can be represented as follows: (formula: see text) where P+ represents the r...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.2600670212

    authors: Gasco MR,Carlotti ME

    更新日期:1978-02-01 00:00:00

  • Enhancing effects of lipophilic vehicles on skin penetration of methyl nicotinate in vivo.

    abstract::Vehicle effects may be caused by thermodynamic effects and by specific (penetration enhancing) effects. To investigate the effects of various lipophilic vehicles on drug penetration, an in vivo permeability study was conducted with methyl nicotinate as the model drug. The drug was dissolved in the respective vehicles ...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 临床试验,杂志文章

    doi:10.1002/jps.2600840214

    authors: Leopold CS,Lippold BC

    更新日期:1995-02-01 00:00:00

  • In situ monitoring of polymorph transformation of clopidogrel hydrogen sulfate using measurement of ultrasonic velocity.

    abstract::Transformation of polymorph I of clopidogrel hydrogen sulfate (CHS) to polymorph II of CHS during the crystallization was monitored by using in situ measurement of ultrasonic velocity. Drowning-out crystallization using methanol as a solvent and isopropyl alcohol as nonsolvent was carried out. The polymorphs were iden...

    journal_title:Journal of pharmaceutical sciences

    pub_type: 杂志文章

    doi:10.1002/jps.21313

    authors: Kim HJ,Kim KJ

    更新日期:2008-10-01 00:00:00