Dry powdered aerosols of diatrizoic acid nanoparticle agglomerates as a lung contrast agent.

Abstract:

:Aerosolized contrast agents may improve the resolution of biomedical imaging modalities and enable more accurate diagnosis of lung diseases. Many iodinated compounds, such as diatrizoic acid, have been shown to be safe and useful for radiographic examination of the airways. Formulations of such compounds must be improved in order to allow imaging of the smallest airways. Here, diatrizoic acid nanoparticle agglomerates were created by assembling nanoparticles into inhalable microparticles that may augment deposition in the lung periphery. Nanoparticle agglomerates were fully characterized and safety was determined in vivo. After dry powder insufflation to rats, no acute alveolar tissue damage was observed 2h post-dose. Diatrizoic acid nanoparticle agglomerates possess the characteristics of an efficient and safe inhalable lung contrast agent.

journal_name

Int J Pharm

authors

El-Gendy N,Aillon KL,Berkland C

doi

10.1016/j.ijpharm.2010.03.009

subject

Has Abstract

pub_date

2010-05-31 00:00:00

pages

305-12

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(10)00183-3

journal_volume

391

pub_type

杂志文章
  • Silicon microfluidic flow focusing devices for the production of size-controlled PLGA based drug loaded microparticles.

    abstract::The increasing realisation of the impact of size and surface properties on the bio-distribution of drug loaded colloidal particles has driven the application of micro fabrication technologies for the precise engineering of drug loaded microparticles. This paper demonstrates an alternative approach for producing size c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.03.051

    authors: Keohane K,Brennan D,Galvin P,Griffin BT

    更新日期:2014-06-05 00:00:00

  • Development and characterisation of sustained release solid dispersion oral tablets containing the poorly water soluble drug disulfiram.

    abstract::Administration of drugs via the oral route is the most common and preferred route due to its ease of administration, cost-effectiveness and flexibility in design. However, if the drug being administered has limited aqueous solubility it can result in poor bioavailability. Furthermore, the low pH of the stomach as well...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.11.029

    authors: Shergill M,Patel M,Khan S,Bashir A,McConville C

    更新日期:2016-01-30 00:00:00

  • Effect of sulfobutyl ether-β-cyclodextrin on bioavailability of insulin glargine and blood glucose level after subcutaneous injection to rats.

    abstract::Insulin glargine is the first long-acting basal insulin analogue used for subcutaneous administration once daily in patients with type 1 or type 2 diabetes mellitus. To obtain the further bioavailability and the sustained glucose lowering effect of insulin glargine, in the present study, we investigated the effect of ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.07.018

    authors: Uehata K,Anno T,Hayashida K,Motoyama K,Hirayama F,Ono N,Pipkin JD,Uekama K,Arima H

    更新日期:2011-10-31 00:00:00

  • Effect of side-chain structures on gene transfer efficiency of biodegradable cationic polyphosphoesters.

    abstract::Cationic polyphosphoesters (PPEs) with different side-chain charge groups were designed and synthesized as biodegradable gene carriers. Poly(N-methyl-2-aminoethyl propylene phosphate) (PPE-MEA), with a secondary amino group (-CH(2)CH(2)NHCH3) side chain released DNA in several hours at N/P (amino group of polymer to p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.07.006

    authors: Wang J,Huang SW,Zhang PC,Mao HQ,Leong KW

    更新日期:2003-10-20 00:00:00

  • Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes.

    abstract::The purpose of the present study was to evaluate the enhancement of tolbutamide (TBM) oral bioavailability and hypoglycaemic activity through complexation with beta-cyclodextrin (beta-CD) and hydroxypropyl-beta-cyclodextrin (HP-beta-CD). TBM and its freeze-dried inclusion complexes were administered to rabbits (New ze...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00445-2

    authors: Veiga F,Fernandes C,Teixeira F

    更新日期:2000-07-20 00:00:00

  • Heat shock protein derivatives for delivery of antigens to antigen presenting cells.

    abstract::Delivery of antigens to antigen presenting cells (APCs) is a key issue for developing effective cancer vaccines. Controlling the tissue distribution of antigens can increase antigen-specific immune responses, including the induction of cytotoxic T lymphocytes (CTL). Heat shock protein 70 (Hsp70) forms complexes with a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2007.09.030

    authors: Nishikawa M,Takemoto S,Takakura Y

    更新日期:2008-04-16 00:00:00

  • Serum-stable, long-circulating paclitaxel-loaded colloidal carriers decorated with a new amphiphilic PEG derivative.

    abstract::The paper describes sterically stabilized lipid nanocapsules (LNC) and multilamellar liposomes (MLV) coated using a new amphiphilic conjugate of PEG(2000) with a 2-alkyl-lipoamino acid (LAA). A complement activation assay (CH50) and uptake experiments by THP-1 macrophage cells were used to assess in vitro the effectiv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.01.038

    authors: Basile L,Passirani C,Huynh NT,Béjaud J,Benoit JP,Puglisi G,Pignatello R

    更新日期:2012-04-15 00:00:00

  • Direct quantification of unencapsulated doxorubicin in liposomal doxorubicin formulations using capillary electrophoresis.

    abstract::To understand the quality, efficacy, and safety of liposomal drugs, it is necessary to develop a robust and accurate method for the separation and the quantification of unencapsulated and liposome-associated drugs (or liposomal encapsulated drugs). Conventional methods involve separation of unencapsulated and liposome...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.07.019

    authors: Ansar SM,Jiang W,Mudalige T

    更新日期:2018-10-05 00:00:00

  • A system for the production and delivery of monodisperse salbutamol aerosols to the lungs.

    abstract::An aerosol system is described for the generation and delivery of measured doses of monodisperse therapeutic drug particles to the human lungs. The system comprises a spinning top aerosol generator (STAG), aerosol chamber and inhalation control unit. Monodisperse aerosols allow drug particle size effects to be studied...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00032-2

    authors: Biddiscombe MF,Usmani OS,Barnes PJ

    更新日期:2003-03-26 00:00:00

  • An intravenous application of magnetic nanoparticles for osteomyelitis treatment: An efficient alternative.

    abstract::The infection of bone and bone marrow is called osteomyelitis. Treatment is difficult since antibiotics can not reach with enough concentration to the infected area. For the first time in this study, we have developed gentamicin-loaded magnetic gelatin nanoparticles (GMGNPs) for nanocarrier-mediated and magnetically t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119999

    authors: Ak G,Bozkaya ÜF,Yılmaz H,Sarı Turgut Ö,Bilgin İ,Tomruk C,Uyanıkgil Y,Hamarat Şanlıer Ş

    更新日期:2021-01-05 00:00:00

  • In vivo efficacy of paclitaxel-loaded injectable in situ-forming gel against subcutaneous tumor growth.

    abstract::Injectable in situ-forming gels have received considerable attention as localized drug delivery systems. Here, we examined a poly(ethylene glycol)-b-polycaprolactone (MPEG-PCL) diblock copolymer gel as an injectable drug depot for paclitaxel (Ptx). The copolymer solution remained liquid at room temperature and rapidly...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.03.033

    authors: Lee JY,Kim KS,Kang YM,Kim ES,Hwang SJ,Lee HB,Min BH,Kim JH,Kim MS

    更新日期:2010-06-15 00:00:00

  • Properties of solid dispersions of piroxicam in polyvinylpyrrolidone.

    abstract::Solid dispersions of piroxicam were prepared with polyvinylpyrrolidone (PVP) K-17 PF and PVP K-90 by solvent method. The physical state and drug:PVP interaction of solid dispersions and physical mixtures were characterized by X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy and differential scanning c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00070-8

    authors: Tantishaiyakul V,Kaewnopparat N,Ingkatawornwong S

    更新日期:1999-04-30 00:00:00

  • Characterization of inhalation aerosols: a critical evaluation of cascade impactor analysis and laser diffraction technique.

    abstract::Cascade impactor analysis is the standard technique for in vitro characterization of aerosol clouds generated by medical aerosol generators. One important reason for using this inertial separation principle is that drug fractions are classified into aerodynamic size ranges that are relevant to the deposition in the re...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00526-4

    authors: de Boer AH,Gjaltema D,Hagedoorn P,Frijlink HW

    更新日期:2002-12-05 00:00:00

  • Drug-in-cyclodextrin-in-liposomes: A novel drug delivery system for flurbiprofen.

    abstract::A novel delivery system based on drug-cyclodextrin (CD) complexation and liposomes has been developed to improve therapeutic effect. Three different means, i.e., co-evaporation (COE), co-ground (GR) and co-lyophilization (COL) and three different CDs (β-CD, HP-β-CD and SBE-β-CD) were contrasted to investigate the char...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.07.011

    authors: Zhang L,Zhang Q,Wang X,Zhang W,Lin C,Chen F,Yang X,Pan W

    更新日期:2015-08-15 00:00:00

  • Encapsulation of an antivasospastic drug, fasudil, into liposomes, and in vitro stability of the fasudil-loaded liposomes.

    abstract::The objectives of this work were to develop a liposomal fasudil, an antivasospastic drug, as a possible means to deliver the encapsulated drug to the brain, and to characterize the stability of the liposomal formulation in vitro. Transmembrane electrochemical gradients of H+ or ammonium sulfate were created, and their...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00896-1

    authors: Ishida T,Takanashi Y,Doi H,Yamamoto I,Kiwada H

    更新日期:2002-01-31 00:00:00

  • Wheat germ agglutinin-grafted lipid nanoparticles: preparation and in vitro evaluation of the association with Caco-2 monolayers.

    abstract::A bioadhesive drug delivery system, wheat germ agglutinin (WGA)-grafted lipid nanoparticles, was developed for the oral delivery of bufalin (a hydrophobic active component extracted from the traditional Chinese medicine Chan'su). The lipid nanoparticles associated with poly(vinyl alcohol) (PVA) were prepared by high-p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.06.030

    authors: Liu Y,Wang P,Sun C,Feng N,Zhou W,Yang Y,Tan R,Chen Z,Wu S,Zhao J

    更新日期:2010-09-15 00:00:00

  • Kinetics of solvent extraction/evaporation process for PLGA microparticle fabrication.

    abstract::Organic solvent extraction/evaporation from an o/w-dispersion has been widely used for the fabrication of PLGA microparticles. The purpose of this work was to elucidate the kinetics of the solvent extraction/evaporation process. A mathematical diffusion model was developed and applied to predict the duration of the so...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.08.015

    authors: Katou H,Wandrey AJ,Gander B

    更新日期:2008-11-19 00:00:00

  • Interlaboratory testing of Insent e-tongues.

    abstract::The first interlaboratory testing of electronic taste sensing systems was performed within five participating centers, each working with the Insent (Insent Inc., Atsugi-Shi, Japan) e-tongue. Preparation of the samples for the comprised four experiments, shipping of the samples and evaluation of the results was perform...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.02.036

    authors: Pein M,Gondongwe XD,Habara M,Winzenburg G

    更新日期:2014-08-05 00:00:00

  • Secondary structure alterations in insulin and growth hormone water-in-oil emulsions.

    abstract::Water-in-oil (w/o) emulsions have shown a promising release profile of small drug molecules and proteins. However, the major concerns are the structural stability, the retention of the activity and to avoid unwanted immunological reactions caused by the changes in protein structure. In the present study, the secondary...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00668-3

    authors: Jørgensen L,Vermehren C,Bjerregaard S,Froekjaer S

    更新日期:2003-03-18 00:00:00

  • Terahertz pulsed spectroscopy and imaging for pharmaceutical applications: a review.

    abstract::The terahertz region of the electromagnetic spectrum spans the frequency range between the infrared and the microwave. Traditionally the exploitation of this spectral region has been difficult owing to the lack of suitable source and detector. Over the last ten years or so, terahertz technology has advanced considerab...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2011.01.012

    authors: Shen YC

    更新日期:2011-09-30 00:00:00

  • Chemical enhancer solubility in human stratum corneum lipids and enhancer mechanism of action on stratum corneum lipid domain.

    abstract::Previously, chemical enhancer-induced permeation enhancement on human stratum corneum (SC) lipoidal pathway at enhancer thermodynamic activities approaching unity in the absence of cosolvents (defined as Emax) was determined and hypothesized to be related to the enhancer solubilities in the SC lipid domain. The object...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.09.014

    authors: Ibrahim SA,Li SK

    更新日期:2010-01-04 00:00:00

  • Electrospun protein nanofibers in healthcare: A review.

    abstract::Electrospun nanofibers are being utilized for a wide range of healthcare applications. A plethora of natural and synthetic polymers are exploited for their ability to be electrospun and replace the complex habitat provided by the extracellular matrix for the cells. The fabrication of nanofibers can be tuned to act as ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.03.013

    authors: Babitha S,Rachita L,Karthikeyan K,Shoba E,Janani I,Poornima B,Purna Sai K

    更新日期:2017-05-15 00:00:00

  • Distribution of salicylic acid in human stratum corneum following topical application in vivo: a comparison of six different formulations.

    abstract::Distribution of salicylic acid in human stratum corneum from treatment of six different formulations was assessed by quantitation of drug content in sequentially tape-stripped stratum corneum after a single 2-h dose was applied unoccluded to skin on the ventral forearm of four female subjects. The profile and total am...

    journal_title:International journal of pharmaceutics

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/s0378-5173(99)00217-3

    authors: Tsai J,Chuang S,Hsu M,Sheu H

    更新日期:1999-10-25 00:00:00

  • Mucoadhesive microspheres prepared by interpolymer complexation and solvent diffusion method.

    abstract::Mucoadhesive microspheres were prepared to increase gastric residence time using an interpolymer complexation of poly(acrylic acid) (PAA) with poly(vinyl pyrrolidone) (PVP) and a solvent diffusion method. The complexation between poly(acrylic acid) and poly(vinyl pyrrolidone) as a result of hydrogen bonding was confir...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.10.016

    authors: Chun MK,Cho CS,Choi HK

    更新日期:2005-01-20 00:00:00

  • Enhancing effect of surfactants on fexofenadine.HCl transport across the human nasal epithelial cell monolayer.

    abstract::The effect of various surfactants (sodium cholate, sodium taurocholate, Tween 80 and Poloxamer F68) on enhancing the transepithelial permeability of fexofenadine.HCl was evaluated in a human nasal epithelial cell monolayer model. The cytotoxicity of the surfactants on the human nasal epithelial cells was evaluated by ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.08.043

    authors: Lin H,Gebhardt M,Bian S,Kwon KA,Shim CK,Chung SJ,Kim DD

    更新日期:2007-02-07 00:00:00

  • Pharmaceutical development and preliminary clinical testing of an oral solid dispersion formulation of docetaxel (ModraDoc001).

    abstract::For use in chronic oral chemotherapeutic regimens, the potent anticancer drug docetaxel needs a solid oral dosage form. Because docetaxel has a very low permeability and a very low aqueous solubility (biopharmaceutical classification system class IV), a pharmacokinetic booster was combined with a newly developed solid...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,随机对照试验

    doi:10.1016/j.ijpharm.2011.08.041

    authors: Moes JJ,Koolen SL,Huitema AD,Schellens JH,Beijnen JH,Nuijen B

    更新日期:2011-11-28 00:00:00

  • Statistical optimisation of diclofenac sustained release pellets coated with polymethacrylic films.

    abstract::The objective of the present study was to evaluate three formulation parameters for the application of polymethacrylic films from aqueous dispersions in order to obtain multiparticulate sustained release of diclofenac sodium. Film coating of pellet cores was performed in a laboratory fluid bed apparatus. The chosen in...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00061-9

    authors: Kramar A,Turk S,Vrecer F

    更新日期:2003-04-30 00:00:00

  • Relating the tableting behavior of piroxicam polytypes to their crystal structures using energy-vector models.

    abstract::Piroxicam crystallises into two polytypes, α1 and α2, with crystal structures that contain identical molecular layers but differ in the way that these layers are stacked. In spite of having close structural similarity, the polytypes have significantly different powder tabletting behaviour: α2 forms only weak tablets a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.03.040

    authors: Upadhyay PP,Sun CC,Bond AD

    更新日期:2018-05-30 00:00:00

  • Mechanistic study on rapid fabrication of fibrous films via centrifugal melt spinning.

    abstract::Fibrous films have attracted considerable attention in the field of drug delivery and wound dressings owing to their porous structure and highly aligned fiber orientation. However, current fabrication methods such as electrospinning have certain limitations, including high voltage requirement and conductivity dependen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.02.005

    authors: Yang Y,Zheng N,Zhou Y,Shan W,Shen J

    更新日期:2019-04-05 00:00:00

  • Delivery of tissue plasminogen activator and streptokinase magnetic nanoparticles to target vascular diseases.

    abstract::Thrombolytic therapy for acute myocardial infarction standardly makes use of the medications streptokinase (SK) and tissue plasminogen activator (tPA). In this study, the potential of silica-coated magnetic nanoparticles (SiO2-MNPs) as nanocarriers clinical thrombolytic therapy was investigated. SiO2-MNPs for use in t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.09.008

    authors: Tadayon A,Jamshidi R,Esmaeili A

    更新日期:2015-11-10 00:00:00