Assay for hydralazine as its stable p-nitrobenzaldehyde hydrazone.

Abstract:

:A new method of analysis for the antihypertensive drug, hydralazine, is introduced. The assay involves the addition of p-nitrobenzaldehyde to blood samples containing hydralazine, to form a stable Schiff's base, hydralazine p-nitrobenzaldehyde hydrazone. The derivative is extracted from the blood into hexane and the samples are dried under a nitrogen stream. The extracts are then dissolved in mobile phase and analyzed using high-performance liquid chromatography. The extracted samples can be stored for at least 7 days at room temperature or at -20 degrees C. The sensitivity of the assay is better than 300 pg/ml using 3-ml blood samples, and the range can extend to 640 ng/ml. The stability of the extracted samples plus the sensitivity and simplicity of the assay are the main advantages of the method over other selective methods for hydralazine.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Semple HA,Tam YK,Tin S,Coutts RT

doi

10.1023/a:1015915812987

subject

Has Abstract

pub_date

1988-06-01 00:00:00

pages

383-6

issue

6

eissn

0724-8741

issn

1573-904X

journal_volume

5

pub_type

杂志文章
  • 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

  • Molecular Targets of the Hydrophobic Block of Pluronics in Cells: a Photo Affinity Labelling Approach.

    abstract:PURPOSE:Pluronics are known as inhibitors of multidrug resistance thus making tumor cells sensitive to therapeutic doses of drugs. The purpose of our study consists in revealing molecular targets of the hydrophobic poly(propylene oxide) block of pluronics in living cells and the dependence of the polymers chemosensitiz...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-018-2484-4

    authors: Zhirnov A,Nam E,Badun G,Romanyuk A,Ezhov A,Melik-Nubarov N,Grozdova I

    更新日期:2018-09-06 00:00:00

  • Physiologically based pharmacokinetic model for composite nanodevices: effect of charge and size on in vivo disposition.

    abstract:PURPOSE:To characterize temporal exposure and elimination of 5 gold/dendrimer composite nanodevices (CNDs) (5 nm positive, negative, and neutral, 11 nm negative, 22 nm positive) in mice using a physiologically based mathematical model. METHODS:400 ug of CNDs is injected intravenously to mice bearing melanoma cell line...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0784-7

    authors: Mager DE,Mody V,Xu C,Forrest A,Lesniak WG,Nigavekar SS,Kariapper MT,Minc L,Khan MK,Balogh LP

    更新日期:2012-09-01 00:00:00

  • In Vivo performance of ophthalmic preparations of betamethasone and phenylephrine hydrochloride in the rabbit eye: Effect of polyvinyl alcohol.

    abstract::The effect of different concentrations of polyvinyl alcohol 14000 and 72000 (PVA 14 and 72) on the activity of betamethasone and phenylephrine hydrochloride in the rabbit eye was investigated. The polymer of higher molecular weight exerts a more pronounced effect at relatively lower viscosities. Effects on the intraoc...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/A:1016398915965

    authors: Kassem MA,Attia MA,Habib FS,Mohamed AR

    更新日期:1986-08-01 00:00:00

  • Characterizing the expression of CYP3A4 and efflux transporters (P-gp, MRP1, and MRP2) in CYP3A4-transfected Caco-2 cells after induction with sodium butyrate and the phorbol ester 12-O-tetradecanoylphorbol-13-acetate.

    abstract:PURPOSE:To examine the changes in expression levels of CYP3A4 and efflux transporters in CYP3A4-transfected Caco-2 (colon carcinoma) cells in the presence of the inducers sodium butyrate (NaB) and 12-O-tetradecanoylphorbol-13-acetate (TPA). To characterize the transport of [3H]-digoxin and the metabolism of midazolam i...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1010914624111

    authors: Cummins CL,Mangravite LM,Benet LZ

    更新日期:2001-08-01 00:00:00

  • Solid lipid nanoparticles as delivery systems for bromocriptine.

    abstract:PURPOSE:The present investigation describes a formulative study for the development of innovative drug delivery systems for bromocriptine. METHODS:Solid lipid nanoparticles (SLN) based on different lipidic components have been produced and characterized. Morphology and dimensional distribution have been investigated b...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9514-y

    authors: Esposito E,Fantin M,Marti M,Drechsler M,Paccamiccio L,Mariani P,Sivieri E,Lain F,Menegatti E,Morari M,Cortesi R

    更新日期:2008-07-01 00:00:00

  • Functional identification of a novel transport system for endogenous and synthetic opioid peptides in the rabbit conjunctival epithelial cell line CJVE.

    abstract:PURPOSE:To investigate whether conjunctival epithelial cells express transport processes for opioid peptides. METHODS:We monitored the uptake of [(3)H]deltorphin II and [(3)H]DADLE, two hydrolysis-resistant synthetic opioid peptides, in the rabbit conjunctival epithelial cell line CJVE and elucidated the characteristi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-008-9709-x

    authors: Ananth S,Karunakaran S,Martin PM,Nagineni CN,Hooks JJ,Smith SB,Prasad PD,Ganapathy V

    更新日期:2009-05-01 00:00:00

  • Pharmaceutical equivalence by design for generic drugs: modified-release products.

    abstract::The Office of Generic Drugs has ensured the high quality of generic products based upon two requirements: pharmaceutical equivalence and bioequivalence to the reference listed drug (RLD). This paradigm has been used with success toward ensuring quality generic drug products that provide the same therapeutic benefit as...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-011-0397-6

    authors: Raw AS,Lionberger R,Yu LX

    更新日期:2011-07-01 00:00:00

  • Adhesion of powders for inhalation: an evaluation of drug detachment from surfaces following deposition from aerosol streams.

    abstract:PURPOSE:To evaluate micronized powder retention and detachment from inhaler surfaces following reproducible deposition by impaction, coupled with centrifugal particle detachment (CPD). METHODS:Micronized albuterol sulfate (AS) and beclomethasone dipropionate (BDP) were aerosolized as dry powders and deposited by casca...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1014451203619

    authors: Clarke MJ,Peart J,Cagnani S,Byron PR

    更新日期:2002-03-01 00:00:00

  • Machine Learning Platform to Discover Novel Growth Inhibitors of Neisseria gonorrhoeae.

    abstract:PURPOSE:To advance fundamental biological and translational research with the bacterium Neisseria gonorrhoeae through the prediction of novel small molecule growth inhibitors via naïve Bayesian modeling methodology. METHODS:Inspection and curation of data from the publicly available ChEMBL web site for small molecule ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02876-y

    authors: Pereira JC,Daher SS,Zorn KM,Sherwood M,Russo R,Perryman AL,Wang X,Freundlich MJ,Ekins S,Freundlich JS

    更新日期:2020-07-13 00:00:00

  • Rapid-Acting and Human Insulins: Hexamer Dissociation Kinetics upon Dilution of the Pharmaceutical Formulation.

    abstract:PURPOSE:Comparison of the dissociation kinetics of rapid-acting insulins lispro, aspart, glulisine and human insulin under physiologically relevant conditions. METHODS:Dissociation kinetics after dilution were monitored directly in terms of the average molecular mass using combined static and dynamic light scattering....

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2233-0

    authors: Gast K,Schüler A,Wolff M,Thalhammer A,Berchtold H,Nagel N,Lenherr G,Hauck G,Seckler R

    更新日期:2017-11-01 00:00:00

  • Influence of surface properties at biodegradable microsphere surfaces: effects on plasma protein adsorption and phagocytosis.

    abstract:OBJECTIVE:The objective of this work was to determine plasma protein adsorption and macrophage phagocytosis of biodegradable polyanhydride, polylactic acid and polylactic-co-glycolic acid microspheres prepared by both spray-drying and solvent evaporation techniques. METHODS:Microspheres were characterized by scanning ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1011935222652

    authors: Lacasse FX,Filion MC,Phillips NC,Escher E,McMullen JN,Hildgen P

    更新日期:1998-02-01 00:00:00

  • Polymer chemistry influences monocytic uptake of polyanhydride nanospheres.

    abstract:PURPOSE:To demonstrate that polyanhydride copolymer chemistry affects the uptake and intracellular compartmentalization of nanospheres by THP-1 human monocytic cells. METHODS:Polyanhydride nanospheres were prepared by an anti-solvent nanoprecipitation technique. Morphology and particle diameter were confirmed via scan...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-008-9760-7

    authors: Ulery BD,Phanse Y,Sinha A,Wannemuehler MJ,Narasimhan B,Bellaire BH

    更新日期:2009-03-01 00:00:00

  • Enhanced Follicular Delivery of Finasteride to Human Scalp Skin Using Heat and Chemical Penetration Enhancers.

    abstract:PURPOSE:The aim of this work was to evaluate whether improved topical delivery of finasteride, focussed to the hair follicles of human scalp skin could be achieved with application of short durations of heat and use of specific chemical penetration enhancers. METHODS:Franz cell experiments with human scalp skin were p...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02822-y

    authors: Farah HA,Brown MB,McAuley WJ

    更新日期:2020-05-31 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

  • 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

  • Enhanced oral delivery of curcumin from N-trimethyl chitosan surface-modified solid lipid nanoparticles: pharmacokinetic and brain distribution evaluations.

    abstract:PURPOSE:Solid lipid nanoparticles (SLNs) have been proposed as a colloidal carrier system that could enhance the oral bioavailability of curcumin. However, a burst release of the loaded drug, which occurs in acidic environments, has been a main obstacle to the oral delivery of curcumin by using SLNs as a carrier system...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1469-1

    authors: Ramalingam P,Ko YT

    更新日期:2015-02-01 00:00:00

  • Influence of bloodflow on the absorption of theophylline from the jejunum of the rat.

    abstract::The influence of the jejunal bloodflow on the absorption of theophylline was investigated. The bloodflow through a segment under investigation was varied by changing the systemic blood pressure by means of a donor blood infusion into the jugular vein or by an infusion of isoprenaline or levarterenol into a femoral vei...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/A:1016374508542

    authors: Schurgers N,de Blaey CJ

    更新日期:1984-01-01 00:00:00

  • PCBP2 siRNA reverses the alcohol-induced pro-fibrogenic effects in hepatic stellate cells.

    abstract:PURPOSE:Type I collagen accumulates during liver fibrosis primarily because α-complex protein-2 (αCP(2)), encoded by the poly(rC) binding protein 2 (PCBP2) gene, binds to the 3' end of the collagen mRNA and increases its half-life. This study aimed to reverse the pro-fibrogenic effect of alcohol on hepatic stellate cel...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-011-0475-9

    authors: Shukla RS,Qin B,Wan YJ,Cheng K

    更新日期:2011-12-01 00:00:00

  • Assessment of physical stability of an antibody drug conjugate by higher order structure analysis: impact of thiol- maleimide chemistry.

    abstract:PURPOSE:To provide a systematic biophysical approach towards a better understanding of impact of conjugation chemistry on higher order structure and physical stability of an antibody drug conjugate (ADC). METHODS:ADC was prepared using thiol-maleimide chemistry. Physical stabilities of ADC and its parent IgG1 mAb were...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-1274-2

    authors: Guo J,Kumar S,Prashad A,Starkey J,Singh SK

    更新日期:2014-07-01 00:00:00

  • Nebulization of liposomes. I. Effects of lipid composition.

    abstract::A series of multilamellar liposome dispersions was prepared from lipids of soy phosphatidylcholine or hydrogenated soy phosphatidylcholine containing from 0 to 30 mol% of either cholesterol, stearylamine, or dipalmitoyl phosphatidylglycerol. The liposome dispersions were aerosolized with a Collison nebulizer for 80 mi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015924124180

    authors: Niven RW,Schreier H

    更新日期:1990-11-01 00:00:00

  • The effect of formulation on the antimicrobial activity of cetylpyridinium chloride in candy based lozenges.

    abstract:PURPOSE:The purpose of this investigation was to determine the influence on the antimicrobial activity of cetylpyridinium chloride of the various components of the formulation of each of six candy based lozenges. METHODS:In vivo activity was investigated using six volunteers by determining the reduction in colony form...

    journal_title:Pharmaceutical research

    pub_type: 临床试验,杂志文章

    doi:10.1023/a:1016002322692

    authors: Richards RM,Xing JZ,Weir LF

    更新日期:1996-04-01 00:00:00

  • Comparison of CYP2D6 content and metoprolol oxidation between microsomes isolated from human livers and small intestines.

    abstract:PURPOSE:To assess the role of intestinal CYP2D6 in oral first-pass drug clearance by comparing the enzyme content and catalytic activity of a prototype CYP2D6 substrate, metoprolol, between microsomes prepared from human intestinal mucosa and from human livers. METHODS:Microsomes were prepared from a panel of 31 human...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018989211864

    authors: Madani S,Paine MF,Lewis L,Thummel KE,Shen DD

    更新日期:1999-08-01 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

  • Nonlinear disposition of intravenous 2',3'-dideoxyinosine in rats.

    abstract::The pharmacokinetics of 2',3'-dideoxyinosine (ddI) were examined in rats given intravenous doses of 8, 40, or 200 mg/kg. The concentrations of ddI in whole blood and plasma were identical. The concentration decline was multiexponential, with mean half-lives of 2 and 20 min for the first and second phases, respectively...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015866714224

    authors: Wientjes MG,Mukherji E,Au JL

    更新日期:1992-08-01 00:00:00

  • Structure in dehydrated trehalose dihydrate--evaluation of the concept of partial crystallinity.

    abstract:PURPOSE:(i) To use trehalose as a model compound to evaluate the concept of crystallinity in pharmaceuticals. (ii) To understand the structural nature of dehydrated trehalose dihydrate. MATERIALS AND METHODS:Trehalose dihydrate was dehydrated isothermally at several temperatures below 100 degrees C and the anhydrous p...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-9058-6

    authors: Rani M,Govindarajan R,Surana R,Suryanarayanan R

    更新日期:2006-10-01 00:00:00

  • Analysis of the compression mechanics of pharmaceutical agglomerates of different porosity and composition using the Adams and Kawakita equations.

    abstract:PURPOSE:To analyze the mechanics of some pharmaceutical agglomerates during uniaxial confined compression by using compression parameters derived from the Heckel, Kawakita and Adams equations, and to study the influence of these compression parameters on the tablet-forming ability of agglomerates. METHODS:Force and di...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1007575120817

    authors: Nicklasson F,Alderborn G

    更新日期:2000-08-01 00:00:00

  • Bilateral Effects of Excipients on Protein Stability: Preferential Interaction Type of Excipient and Surface Aromatic Hydrophobicity of Protein.

    abstract:PURPOSE:Understanding the mechanism of protein-excipient interaction and illuminating the influencing factors on protein stability are key steps in the rational design of protein formulations. The objective of this study was to assess effects of preferential interaction type of excipient and surface aromatic hydrophobi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2152-0

    authors: Wen L,Zheng X,Wang X,Lan H,Yin Z

    更新日期:2017-07-01 00:00:00

  • Dose-dependent pharmacokinetics of carbamazepine in rats: determination of the formation clearance of carbamazepine-10,11-epoxide.

    abstract::The dose dependency of carbamazepine pharmacokinetics was characterized in rats, a common test animal for antiepileptic drug efficacy. With a randomized Latin square schedule, 5, 10, and 20 mg/kg doses of carbamazepine were injected intravenously into six Sprague-Dawley rats followed by the administration of a 5 or 10...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015872901523

    authors: Remmel RP,Sinz MW,Cloyd JC

    更新日期:1990-05-01 00:00:00

  • Surface functionalization of mesoporous silica nanoparticles controls loading and release behavior of mitoxantrone.

    abstract:PURPOSE:To investigate the effect of surface functionalization of mesoporous silica nanoparticles (MSN) on crystallization, loading, release and activity of mitoxantrone (MTX). METHODS:Thiol-, amine-, and mixed thiol/amine-functionalized MSN were synthesized and characterized by electron microscopy, thermogravimetry, ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0766-9

    authors: Wani A,Muthuswamy E,Savithra GH,Mao G,Brock S,Oupický D

    更新日期:2012-09-01 00:00:00