Inhalation treatment of idiopathic pulmonary fibrosis with curcumin large porous microparticles.

Abstract:

:Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with high mortality and poor prognosis. Curcumin shows anti-inflammatory effect by suppressing pro-inflammatory cytokines and inhibiting NF-κB mediated inflammation. Here, we developed inhalable curcumin-loaded poly(lactic-co-glycolic)acid (PLGA) large porous microparticles (LPMPs) for the treatment of IPF. Curcumin LPMPs were rough and loose particles with many pores on the surfaces and channels in the inner spaces. The mean geometric diameter of them was larger than 10 µm while the aerodynamic diameter was only 3.12 µm due to their porous structures. They showed a fine particle fraction (FPF) <4.46 μm of 13.41%, 71% cumulative release after 9 h, and more importantly, they avoided uptake by alveolar macrophages. Therefore, most of released curcumin had opportunities to enter lung tissues. Rat pulmonary fibrosis models were established via once intratracheal administration of bleomycin. Curcumin powders and curcumin LPMPs were administered on Days 2, 7, 14, and 21. Curcumin LPMPs remarkably attenuated lung injuries, decreased hydroxyproline contents, reduced the synthesis of collagen I, and inhibited the expressions of TNF-α, TGF-β1, NF-κB p65 and MMP9. Moreover, curcumin LPMPs showed higher antifibrotic activity than curcumin powders. Curcumin LPMPs are a promising inhalable medication for the treatment of IPF.

journal_name

Int J Pharm

authors

Hu Y,Li M,Zhang M,Jin Y

doi

10.1016/j.ijpharm.2018.09.031

subject

Has Abstract

pub_date

2018-11-15 00:00:00

pages

212-222

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(18)30682-3

journal_volume

551

pub_type

杂志文章
  • Evaluation of skin permeation and anti-inflammatory and analgesic effects of new naproxen microemulsion formulations.

    abstract::The aim of this study was to evaluate the potential application of microemulsions as a transdermal drug delivery for naproxen (Np). The pseudo-ternary phase diagrams were developed for microemulsions composed of isopropyl myristate, Span 80, Labrafil M, Labrasol, and Cremophor EL, ethanol and isopropyl alcohol and 0.5...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.06.026

    authors: Ustündağ Okur N,Apaydın S,Karabay Yavaşoğlu NÜ,Yavaşoğlu A,Karasulu HY

    更新日期:2011-09-15 00:00:00

  • Design, synthesis and evaluation of N-acetyl glucosamine (NAG)-PEG-doxorubicin targeted conjugates for anticancer delivery.

    abstract::Efficacy of anticancer drug is limited by the severe adverse effects induced by drug; therefore the crux is in designing delivery systems targeted only to cancer cells. Toward this objectives, we propose, synthesis of poly(ethylene glycol) (PEG)-doxorubicin (DOX) prodrug conjugates consisting N-acetyl glucosamine (NAG...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.05.078

    authors: Pawar SK,Badhwar AJ,Kharas F,Khandare JJ,Vavia PR

    更新日期:2012-10-15 00:00:00

  • Ondansetron buccal administration for paediatric use: A comparison between films and wafers.

    abstract::The objective of this study was the development of different solid formulations, such as wafers and films, for buccal administration of ondansetron, a selective and potent antagonist of 5-hydroxytryptamine 3 receptors used in children for the treatment of nausea and vomiting. Wafers and films have been prepared drying...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119228

    authors: Giordani B,Abruzzo A,Prata C,Nicoletta FP,Dalena F,Cerchiara T,Luppi B,Bigucci F

    更新日期:2020-04-30 00:00:00

  • Simultaneous determination of amiloride and furosemide in pharmaceutical formulations by first digital derivative spectrophotometry.

    abstract::This work presents a simple and fast method for the simultaneous determination of amiloride and furosemide by digital derivative spectrophotometry. HCl 1 x 10(-2) mol/l dissolved in ethanol was used as solvent and to extract drugs from formulations. Subsequently the samples were evaluated directly by first digital der...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00482-9

    authors: Inés Toral M,Pope S,Quintanilla S,Richter P

    更新日期:2002-12-05 00:00:00

  • Modeling and simulation of compact strength due to particle bonding using a hybrid discrete-continuum approach.

    abstract::The compaction of powder beds into solid bodies occurs by virtue of the formation of inter-particle bonds. The mechanical strength of the compact depends on the type of bonding interaction, as well as, the inter-particle contact area created in the compression process. A hybrid quasi-continuum computational approach h...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.06.006

    authors: Koynov A,Akseli I,Cuitiño AM

    更新日期:2011-10-14 00:00:00

  • Needle-free intravaginal DNA vaccination using a stearoyl oligopeptide carrier promotes local gene expression and immune responses.

    abstract::The vaginal mucosa is the most common site of infection for viruses that are transmitted through heterosexual intercourse, including human immunodeficiency virus and papillomavirus. Thus, in order to prevent or respond to these infections, strong vaginal immunity is required as the first line of defense. We previously...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.02.018

    authors: Kanazawa T,Tamura T,Yamazaki M,Takashima Y,Okada H

    更新日期:2013-04-15 00:00:00

  • Pharmacokinetics and absolute bioavailability of oral cefuroxime axetil in the rat.

    abstract::The objectives of this study were to determine the oral bioavailability of cefuroxime (C) and to evaluate the pharmacokinetic model that best describes the plasma concentration behaviour following single intravenous (IV), intraperitoneal (IP) and oral single doses. The same dose of C was administered by IV, IP and ora...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00420-8

    authors: Ruiz-Carretero P,Nacher A,Merino-Sanjuan M,Casabo VG

    更新日期:2000-07-20 00:00:00

  • Terahertz pulsed imaging as an advanced characterisation tool for film coatings--a review.

    abstract::Solid dosage forms are the pharmaceutical drug delivery systems of choice for oral drug delivery. These solid dosage forms are often coated to modify the physico-chemical properties of the active pharmaceutical ingredients (APIs), in particular to alter release kinetics. Since the product performance of coated dosage ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2013.03.053

    authors: Haaser M,Gordon KC,Strachan CJ,Rades T

    更新日期:2013-12-05 00:00:00

  • Characterization and biological properties of NanoCUR formulation and its effect on major human cytochrome P450 enzymes.

    abstract::Curcumin (CUR) has been formulated into a host of nano-sized formulations in a bid to improve its in vivo solubility, stability and bioavailability. The aim of this study was to investigate whether the encapsulation of CUR in nanocarriers would impede its biological interactivity, specifically its potential anti-cance...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.08.066

    authors: Shamsi S,Chen Y,Lim LY

    更新日期:2015-11-10 00:00:00

  • In vitro and in vivo evaluation of potassium chloride sustained release formulation prepared with saturated polyglycolyed glycerides matrices.

    abstract::The aim of the present work was to evaluate the effect of sustained release of potassium chloride semi-solid matrices prepared with different kinds and added amounts of Gelucires by the in vitro dissolution test and in vivo oral absorption study, and compared with a commercial product (slow-K). The results indicating ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00264-8

    authors: Wu PC,Tsai MJ,Huang YB,Chang JS,Tsai YH

    更新日期:2002-08-28 00:00:00

  • Rhamnolipids as emulsifying agents for essential oil formulations: antimicrobial effect against Candida albicans and methicillin-resistant Staphylococcus aureus.

    abstract::This work examines the influence of essential oil composition on emulsification with rhamnolipids and their use as therapeutic antimicrobial agents against two opportunistic pathogens, methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans. Rhamnolipids, produced by Pseudomonas aeruginosa, with waste ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.09.039

    authors: Haba E,Bouhdid S,Torrego-Solana N,Marqués AM,Espuny MJ,García-Celma MJ,Manresa A

    更新日期:2014-12-10 00:00:00

  • Improvement of antischistosomal activity of praziquantel by incorporation into phosphatidylcholine-containing liposomes.

    abstract::Praziquantel (PZQ) is effective against all known species of Schistosomes that infect humans. The failure of mass treatment of schistosomiasis has been attributed to the fact that therapy is not sufficiently long-lasting. This effect may be due to the low bioavailability of PZQ that has a low hydrosolubility and fast ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.02.009

    authors: Mourão SC,Costa PI,Salgado HR,Gremião MP

    更新日期:2005-05-13 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

  • Synthesis and evaluation of styrene-maleic acid copolymer conjugated amphotericin B.

    abstract::Amphotericin B (AmB), which plays a central role in the treatment of systemic fungal infections, is difficult to formulate because it's sparingly soluble in water and organic solvents. We previously prepared AmB-loaded micelles using styrene-maleic acid copolymer (SMA). Although solubilization was achieved by this for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118719

    authors: Banshoya K,Kaneo Y,Tanaka T,Yamamoto S,Maeda H

    更新日期:2019-12-15 00:00:00

  • Design of a fluid energy single vessel powder processor for pharmaceutical use.

    abstract::This study introduces a motionless novel single vessel powder processor designed to carry out all of the unit operations in the preparation of powders for tableting. The processor used controllable fluid dynamics to provide the energy for each unit operation. The vessel design was evaluated using a computational fluid...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00033-2

    authors: Kay GR,Staniforth JN,Tobyn MJ,Horrill MD,Newnes LB,MacGregor SA,Li M,Atherton G,Lamming RC,Hajee DW

    更新日期:1999-04-30 00:00:00

  • Strategies for bringing drug delivery tools into discovery.

    abstract::The past decade has yielded a significant body of literature discussing approaches for development and discovery collaboration in the pharmaceutical industry. As a result, collaborations between discovery groups and development scientists have increased considerably. The productivity of pharma companies to deliver new...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2011.03.024

    authors: Kwong E,Higgins J,Templeton AC

    更新日期:2011-06-30 00:00:00

  • Polymer particle erosion controlling drug release. I. Factors influencing drug release and characterization of the release mechanism.

    abstract::The present study deals with controlled drug delivery from hydrocolloid tablets by polymer particle erosion. The influence of excipients and formulation factors on the dissolution behaviour of the methyl hydroxyethyl cellulose (MHEC)-tablets is investigated. Linear drug release with low susceptibility to hydrodynamic ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00596-8

    authors: Zuleger S,Lippold BC

    更新日期:2001-04-17 00:00:00

  • Systematic evaluation of design features enables efficient selection of Π electron-stabilized polymeric micelles.

    abstract::Polymeric micelles (PM) based on poly(ethylene glycol)-b-poly(N-2-benzoyloxypropyl methacrylamide) (mPEG-b-p(HPMA-Bz)) loaded with paclitaxel (PTX-PM) have shown promising results in overcoming the suboptimal efficacy/toxicity profile of paclitaxel. To get insight into the stability of PTX-PM formulations upon storage...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119409

    authors: Sheybanifard M,Beztsinna N,Bagheri M,Buhl EM,Bresseleers J,Varela-Moreira A,Shi Y,van Nostrum CF,van der Pluijm G,Storm G,Hennink WE,Lammers T,Metselaar JM

    更新日期:2020-06-30 00:00:00

  • Starch-free grewia gum matrices: Compaction, swelling, erosion and drug release behaviour.

    abstract::Polysaccharides are suitable for application as hydrophilic matrices because of their ability to hydrate and swell upon contact with fluids, forming a gel layer which controls drug release. When extracted from plants, polysaccharides often contain significant quantities of starch that impacts upon their functional pro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.071

    authors: Nep EI,Asare-Addo K,Ghori MU,Conway BR,Smith AM

    更新日期:2015-12-30 00:00:00

  • Development of a nanoamorphous exosomal delivery system as an effective biological platform for improved encapsulation of hydrophobic drugs.

    abstract::Despite their great potential, the nano-sized extracellular vesicles are yet to become effective delivery systems for poorly water-soluble drugs. Here, we present a novel platform of exosomes as a drug delivery system by engineering of a poorly water-soluble drug into a poloxamer-based molecular nanostructured dispers...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.06.028

    authors: Tran PHL,Wang T,Yin W,Tran TTD,Barua HT,Zhang Y,Midge SB,Nguyen TNG,Lee BJ,Duan W

    更新日期:2019-07-20 00:00:00

  • New silica nanostructure for the improved delivery of topical antibiotics used in the treatment of staphylococcal cutaneous infections.

    abstract::In this paper, we report the synthesis, characterization (FT-IR, XRD, BET, HR-TEM) and bioevaluation of a novel γ-aminobutiric acid/silica (noted GABA-SiO₂ or γ-SiO₂) hybrid nanostructure, for the improved release of topical antibiotics, used in the treatment of Staphylococcus aureus infections. GABA-SiO₂ showed IR ba...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.07.016

    authors: Grumezescu AM,Ghitulica CD,Voicu G,Huang KS,Yang CH,Ficai A,Vasile BS,Grumezescu V,Bleotu C,Chifiriuc MC

    更新日期:2014-03-25 00:00:00

  • Investigating the role of cholesterol in the formation of non-ionic surfactant based bilayer vesicles: thermal analysis and molecular dynamics.

    abstract::The aim of this research was to investigate the molecular interactions occurring in the formulation of non-ionic surfactant based vesicles composed monopalmitoyl glycerol (MPG), cholesterol (Chol) and dicetyl phosphate (DCP). In the formulation of these vesicles, the thermodynamic attributes and surfactant interaction...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.11.063

    authors: Wilkhu JS,Ouyang D,Kirchmeier MJ,Anderson DE,Perrie Y

    更新日期:2014-01-30 00:00:00

  • Transdermal permeation enhancement of N-trimethyl chitosan for testosterone.

    abstract::The aim of this study was to evaluate the transdermal permeation enhancement of N-trimethyl chitosan (TMC) with different degrees of quaternization (DQ). TMCs with DQ of 40 and 60% (TMC40 and TMC60) were synthesized and characterized by (1)H NMR. Testosterone (TS) used as an effective drug, four different gels were pr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.12.050

    authors: He W,Guo X,Zhang M

    更新日期:2008-05-22 00:00:00

  • 3D printing of tablets using inkjet with UV photoinitiation.

    abstract::Additive manufacturing (AM) offers significant potential benefits in the field of drug delivery and pharmaceutical/medical device manufacture. Of AM processes, 3D inkjet printing enables precise deposition of a formulation, whilst offering the potential for significant scale up or scale out as a manufacturing platform...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.085

    authors: Clark EA,Alexander MR,Irvine DJ,Roberts CJ,Wallace MJ,Sharpe S,Yoo J,Hague RJM,Tuck CJ,Wildman RD

    更新日期:2017-08-30 00:00:00

  • Calcium phosphate nanoparticles as novel non-viral vectors for targeted gene delivery.

    abstract::Calcium phosphate nanoparticles present a unique class of non-viral vectors, which can serve as efficient and alternative DNA carriers for targeted delivery of genes. In this study we report the design and synthesis of ultra-low size, highly monodispersed DNA doped calcium phosphate nanoparticles of size around 80 nm ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00452-0

    authors: Roy I,Mitra S,Maitra A,Mozumdar S

    更新日期:2003-01-02 00:00:00

  • Characterisation of a novel solid lipid nanoparticle carrier system based on binary mixtures of liquid and solid lipids.

    abstract::A drug carrier of colloidal lipid particles with improved payloads and enhanced storage stability was investigated. Based on the experiences with hard fats nanoparticles, a new type of solid lipid nanoparticles (SLN) has been developed by incorporating triglyceride containing oils in the solid core of said particle. T...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00378-1

    authors: Jenning V,Thünemann AF,Gohla SH

    更新日期:2000-04-20 00:00:00

  • Kinetic stability studies of HBV vaccine in a microneedle patch.

    abstract::This study systematically demonstrated the antigenicity kinetics of HBV vaccine microneedles (MNs) during the fabrication, application and storage. To improve the stability of HBsAg in a microneedle patch, several selected saccharides were added to the MN formulations as stabilizers. According to the experimental data...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118489

    authors: Zhu DD,Zhang XP,Yu HL,Liu RX,Shen CB,Zhang WF,Cui Y,Guo XD

    更新日期:2019-08-15 00:00:00

  • Innovative pMDI formulations of spray-dried nanoparticles for efficient pulmonary drug delivery.

    abstract::For drug delivery to the lungs, the aerodynamic size of drug particles plays a predominant role in determining the sites of deposition in the airway, and the particles with the size less than 2μm are highly expected as they will be preferably delivered to the ideal site of alveolar regions. In this paper, a novel plat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.07.040

    authors: Li HY,Xu EY

    更新日期:2017-09-15 00:00:00

  • Nanostructure of liquid crystalline matrix determines in vitro sustained release and in vivo oral absorption kinetics for hydrophilic model drugs.

    abstract::Nanostructured lipid-based liquid crystalline systems have been proposed as sustained oral drug delivery systems, but the interplay between their intrinsic release rates, susceptibility to digestive processes, and the manner in which these effects impact on their application in vivo, are not well understood. In this s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.08.022

    authors: Lee KW,Nguyen TH,Hanley T,Boyd BJ

    更新日期:2009-01-05 00:00:00

  • Enhanced solubility and antibacterial activity of lipophilic fluoro-substituted N-benzoyl-2-aminobenzothiazoles by complexation with β-cyclodextrins.

    abstract::Some lipophilic fluoro-substituted N-benzoyl-2-aminobenzothiazole antibacterial agents have been evaluated for their activity in the presence of cyclodextrins (CDs) containing aqueous solutions where CDs are adopted as solubilizing excipients for improving the poor water solubility of these compounds. For such purpose...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.11.024

    authors: Trapani A,De Laurentis N,Armenise D,Carrieri A,Defrenza I,Rosato A,Mandracchia D,Tripodo G,Salomone A,Capriati V,Franchini C,Corbo F

    更新日期:2016-01-30 00:00:00