Rationally designed hyaluronic acid-based nano-complexes for pentamidine delivery.

Abstract:

:Nanoparticles of polymeric complexes made of hyaluronic acid and polyarginine were investigated for the encapsulation of the cationic hydrophilic drug pentamidine isethionate. The interaction between the anionic hyaluronic acid and the cationic pentamidine resulting in the formation of polyelectrolyte complexes was firstly studied. Then, nanoparticles made of hyaluronic acid and polyarginine loaded with pentamidine were developed. These drug delivery systems consist of a monodisperse population of negatively charged pentamidine-loaded nanoparticles with a high drug encapsulation rate (80%). Such high encapsulation efficiency coming from ion exchange was confirmed by measurements of the counterion isethionate released from pentamidine during nanoparticles formation. Besides, freeze-dried pentamidine-loaded nanoparticles kept their integrity after their reconstitution in water. In vitro studies on human lung (A549) and breast (MDA-MB-231) cancer cell lines showed that pentamidine-loaded nanoparticles were more cytotoxic in comparison to the free drug, suggesting an enhanced internalization of encapsulated drug by cancer cells.

journal_name

Int J Pharm

authors

Carton F,Chevalier Y,Nicoletti L,Tarnowska M,Stella B,Arpicco S,Malatesta M,Jordheim LP,Briançon S,Lollo G

doi

10.1016/j.ijpharm.2019.118526

subject

Has Abstract

pub_date

2019-09-10 00:00:00

pages

118526

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(19)30570-8

journal_volume

568

pub_type

杂志文章
  • Just how prevalent are peptide therapeutic products? A critical review.

    abstract::How prevalent are peptide therapeutic products? How innovative are the formulations used to deliver peptides? This review provides a critical analysis of therapeutic peptide products and the formulations approved by the United States Food and Drug administration (FDA), the European Medicines Agency (EMA), and the Japa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.119491

    authors: Zhang Y,Zhang H,Ghosh D,Williams RO 3rd

    更新日期:2020-09-25 00:00:00

  • Application of spherical silicate to prepare solid dispersion dosage forms with aqueous polymers.

    abstract::The objective of this study is to prepare and characterize solid dispersions of nifedipine (NP) using porous spherical silicate micro beads (MB) that were approximately 100 μm in diameter with vinylpyrrolidone/vinyl acetate copolymer (PVP/VA) and a Wurster-type fluidized bed granulator. Compared with previously report...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.07.037

    authors: Nagane K,Kimura S,Ukai K,Takahashi C,Ogawa N,Yamamoto H

    更新日期:2015-09-30 00:00:00

  • Effects of conditions for preparing nanoparticles composed of aminoethylcarbamoyl-beta-cyclodextrin and ethylene glycol diglycidyl ether on trap efficiency of a guest molecule.

    abstract::Nanoparticles comprising copolymers of aminoethylcarbamoyl-beta-cyclodextrin (AEC-beta-CD) and ethylene glycol diglycidyl ether (EGDGE) are prepared by an interfacial polyaddition reaction in a miniemulsion system. Polymers are formed in a W/O emulsion containing 0.25-10.0% (w/w) water and 5.0% (w/w) surfactant (MO-3S...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.12.015

    authors: Eguchi M,Du YZ,Ogawa Y,Okada T,Yumoto N,Kodaka M

    更新日期:2006-03-27 00:00:00

  • Recent advances in local drug delivery to the inner ear.

    abstract::Inner ear diseases are not adequately treated by systemic drug administration mainly because of the blood-perilymph barrier that reduces exchanges between plasma and inner ear fluids. Local drug delivery methods including intratympanic and intracochlear administrations are currently developed to treat inner ear disord...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2015.08.015

    authors: El Kechai N,Agnely F,Mamelle E,Nguyen Y,Ferrary E,Bochot A

    更新日期:2015-10-15 00:00:00

  • Nano-encapsulation of a novel anti-Ran-GTPase peptide for blockade of regulator of chromosome condensation 1 (RCC1) function in MDA-MB-231 breast cancer cells.

    abstract::Ran is a small ras-related GTPase and is highly expressed in aggressive breast carcinoma. Overexpression induces malignant transformation and drives metastatic growth. We have designed a novel series of anti-Ran-GTPase peptides, which prevents Ran hydrolysis and activation, and although they display effectiveness in s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.006

    authors: Haggag YA,Matchett KB,Dakir el-H,Buchanan P,Osman MA,Elgizawy SA,El-Tanani M,Faheem AM,McCarron PA

    更新日期:2017-04-15 00:00:00

  • Effect of medium-chain triglycerides on the release behavior of Endostar encapsulated PLGA microspheres.

    abstract::The incomplete release of Endostar from PLGA microspheres was observed in our previous study. In the present study, we focused on the effect of medium-chain triglycerides (MCT) on the in vitro/in vivo release behavior of Endostar encapsulated PLGA microspheres, which were prepared by a water-in-oil-in-water (W/O/W) do...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.07.018

    authors: Meng B,Li L,Hua S,Wang Q,Liu C,Xu X,Yin X

    更新日期:2010-09-15 00:00:00

  • PLGA microparticles with zero-order release of the labile anti-Parkinson drug apomorphine.

    abstract::The treatment of patients suffering from advanced Parkinson's disease is highly challenging, because the efficacy of the "gold standard" levodopa declines with time. Co-administration of the dopamine receptor agonist apomorphine is beneficial, but difficult due to the poor oral bioavailability and short half-life of t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.01.008

    authors: Regnier-Delplace C,Thillaye du Boullay O,Siepmann F,Martin-Vaca B,Degrave N,Demonchaux P,Jentzer O,Bourissou D,Siepmann J

    更新日期:2013-02-25 00:00:00

  • NMR imaging of chitosan and carboxymethyl starch tablets: swelling and hydration of the polyelectrolyte complex.

    abstract::The hydration and swelling properties of the tablets made of chitosan, carboxymethyl starch, and a polyelectrolyte complex of these two polysaccharides have been studied by NMR imaging. We studied the effect of pH and ionic strength on the swelling of the tablets and on the diffusion of fluid into the tablets in water...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.08.008

    authors: Wang YJ,Assaad E,Ispas-Szabo P,Mateescu MA,Zhu XX

    更新日期:2011-10-31 00:00:00

  • Application of artificial neural networks (ANNs) and genetic programming (GP) for prediction of drug release from solid lipid matrices.

    abstract::The aim of the present study was to develop a semi-empirical mathematical model, which is able to predict the release profiles of solid lipid extrudates of different dimensions. The development of the model was based on the application of ANNs and GP. ANNs' abilities to deal with multidimensional data were exploited. ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.05.021

    authors: Güres S,Mendyk A,Jachowicz R,Dorożyński P,Kleinebudde P

    更新日期:2012-10-15 00:00:00

  • The effect of processing variables on the physical characteristics of non-ionic surfactant vesicles (niosomes) formed from a hexadecyl diglycerol ether.

    abstract::Niosomes are vesicles formed by self-assembly of non-ionic surfactants. In this investigation, the effects of processing variables, particularly temperature and sonication, on the physical characteristics and phase transitional behaviour of two niosomal systems based on a hexadecyl diglycerol ether (C(16)G(2)) have be...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00362-8

    authors: Arunothayanun P,Bernard MS,Craig DQ,Uchegbu IF,Florence AT

    更新日期:2000-05-15 00:00:00

  • Preliminary evaluation of a novel oral delivery system for rhPTH1-34: in vitro and in vivo.

    abstract::rhPTH1-34 is clinically used for osteoporosis treatment. However, this peptide drug has no oral bioavailability because of proteolysis and low membrane permeability in gastrointestinal gut. This study explored the possibility of absorption enhancement for rhPTH1-34 through the oral delivery of the microemulsion. The m...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.08.029

    authors: Guo L,Ma E,Zhao H,Long Y,Zheng C,Duan M

    更新日期:2011-11-25 00:00:00

  • Glutathione-responsive self-delivery nanoparticles assembled by curcumin dimer for enhanced intracellular drug delivery.

    abstract::Poor water solubility, short half-life, and low drug efficacy posed a challenge for clinical application of curcumin (CUR). In this work, a kind of CUR prodrug was synthesized by coupling two CUR molecules with a mono-thioether linker for glutathione (GSH)-responsive drug delivery. The synthesized CUR prodrug (CUR-S-C...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.07.061

    authors: Zhang H,Zhang Y,Chen Y,Zhang Y,Wang Y,Zhang Y,Song L,Jiang B,Su G,Li Y,Hou Z

    更新日期:2018-10-05 00:00:00

  • Enhanced anti-glioblastoma efficacy by PTX-loaded PEGylated poly(ɛ-caprolactone) nanoparticles: In vitro and in vivo evaluation.

    abstract::The aim of this work was to investigate the anti-tumor effect of paclitaxel (PTX)-loaded methoxy poly(ethylene glycol)-poly(ɛ-caprolactone) nanoparticles (MPEG-NP/PTX) against glioblastoma multiforme (GBM). MPEG-NP/PTX was prepared by the emulsion and evaporation technique with particle size of 72.5±2.2nm and did not ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.005

    authors: Xin H,Chen L,Gu J,Ren X,Wei Z,Luo J,Chen Y,Jiang X,Sha X,Fang X

    更新日期:2010-12-15 00:00:00

  • Crystal structures, dissolution and pharmacokinetic study on a novel phosphodiesterase-4 inhibitor chlorbipram cocrystals.

    abstract::Cocrystallization of chlorbipram (ChBP), a novel phosphodiesterase-4 (PDE) inhibitor with water insoluble property developed in our lab, was performed to improve the physicochemical properties and bioavailability in the present study. Three new cocrystals with fumaric aicd (FA), gentisic acid (GA) and salicylic acid (...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118984

    authors: Zhou J,Li L,Zhang H,Xu J,Huang D,Gong N,Han W,Yang X,Zhou Z

    更新日期:2020-02-25 00:00:00

  • Freeze-dried cake structural and physical heterogeneity in relation to freeze-drying cycle parameters.

    abstract::Freeze-drying is the preferred method to manufacture proteins in their solid state thus the understanding of the relationship between cycle parameters and cake properties remains of great interest. The present study aims to investigate the influence of the freezing conditions in the material properties at different la...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119891

    authors: Badal Tejedor M,Fransson J,Millqvist-Fureby A

    更新日期:2020-11-30 00:00:00

  • Dissolution performance of binary amorphous drug combinations--Impact of a second drug on the maximum achievable supersaturation.

    abstract::An increased number of amorphous formulations of poorly water soluble drugs are being introduced into the market due to their higher transient solubility and thus faster absorption and higher bioavailability. While most amorphous drug products contain a single drug substance, there is a growing trend towards co-formul...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.026

    authors: Trasi NS,Taylor LS

    更新日期:2015-12-30 00:00:00

  • Application of acid-treated yeast cell wall (AYC) as a pharmaceutical additive. III. AYC aqueous coating onto granules and film formation mechanism of AYC.

    abstract::From the viewpoint of effective utilization of natural resources and development of new pharmaceutical materials, acid-treated yeast cell wall (AYC) was prepared via a novel approach involving acidification of brewers' yeast cell wall. AYC aqueous dispersion containing 5% (w/v) AYC and 0.5% (w/v) glycerol was prepared...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00008-x

    authors: Yuasa H,Kaneshige J,Ozeki T,Kasai T,Eguchi T,Ishiwaki N

    更新日期:2002-04-26 00:00:00

  • Synergistic interactions between doxycycline and terpenic components of essential oils encapsulated within lipid nanocapsules against gram negative bacteria.

    abstract::The combination of essential oils (EOs) with antibiotics provides a promising strategy towards combating resistant bacteria. We have selected a mixture of 3 major components extracted from EOs: carvacrol (oregano oil), eugenol (clove oil) and cinnamaldehyde (cinnamon oil). These compounds were successfully encapsulate...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.11.042

    authors: Valcourt C,Saulnier P,Umerska A,Zanelli MP,Montagu A,Rossines E,Joly-Guillou ML

    更新日期:2016-02-10 00:00:00

  • Examination of oxidized cellulose as a macromolecular prodrug carrier: preparation and characterization of an oxidized cellulose-phenylpropanolamine conjugate.

    abstract::The purpose of this study was to investigate the use of 6-carboxycellulose (OC), a biocompatible and bioresorbable polymer, as a prodrug carrier for amine drugs. Phenylpropanolamine hydrochloride (PPA.HCl) was used as a model drug. OC and PPA were reacted in dimethylformamide (DMF) in the presence of 1,3-dicyclohexylc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00725-6

    authors: Zhu L,Kumar V,Banker GS

    更新日期:2001-07-31 00:00:00

  • Gastro intestinal tracking and gastric emptying of solid dosage forms in rats using X-ray imaging.

    abstract::The aim of this research was to study the gastrointestinal transit and gastric emptying of non-disintegrating solid dosage forms in rats using X-ray imaging. Commercial gelatin minicapsules were filled with barium sulfate and enterically coated using Eudragit S100. The capsules were administered orally to rats followe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.01.001

    authors: Saphier S,Rosner A,Brandeis R,Karton Y

    更新日期:2010-03-30 00:00:00

  • Emerging trends in the stabilization of amorphous drugs.

    abstract::The number of active pharmaceutical substances having high therapeutic potential but low water solubility is constantly increasing, making it difficult to formulate these compounds as oral dosage forms. The solubility and dissolution rate, and thus potentially the bioavailability, of these poorly water-soluble drugs c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2012.04.066

    authors: Laitinen R,Löbmann K,Strachan CJ,Grohganz H,Rades T

    更新日期:2013-08-30 00:00:00

  • Vesicle formation from hexasubstituted cyclophosphazenic derivatives.

    abstract::Hexakis[butoxytris(ethoxy)]cyclophosphazene (3a), hexakis[dodecyloxytetrakis (ethoxy)]cyclophosphazene (3b) and hexakis[hexadecyloxyeicosanekis(ethoxy)]cyclophosphazene+ ++ (3c) were synthesised and their ability to form niosomes was studied. All synthesised compounds in the presence of cholesterol were shown to form ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00024-1

    authors: Baroli B,Delogu G,Fadda AM,Podda G,Sinico C

    更新日期:1999-06-25 00:00:00

  • Newly developed surface modification punches treated with alloying techniques reduce sticking during the manufacture of ibuprofen tablets.

    abstract::Sticking is a serious problem during the manufacturing process of tablets. In order to prevent this, we used alloying techniques to prepare metal hardening (MH) and electron beam processing infinite product (EIP) punches with rougher asperity of surfaces than a hard chrome plated (HCr) punch. This study evaluated the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.12.006

    authors: Uchimoto T,Iwao Y,Yamamoto T,Sawaguchi K,Moriuchi T,Noguchi S,Itai S

    更新日期:2013-01-30 00:00:00

  • Pharmacokinetics of Huperzine A after transdermal and oral administration in beagle dogs.

    abstract::Comparison of single and multiple dose pharmacokinetics between patches and conventional tablets of Huperzine A (Hup-A) was performed in beagle dogs to evaluate the patches' controlled drug release characteristics in vivo, a newly developed transdermal system for treatment of Alzheimer disease. Results showed that tra...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.01.007

    authors: Ye JC,Zeng S,Zheng GL,Chen GS

    更新日期:2008-05-22 00:00:00

  • Targeted killing of cancer cells in vivo and in vitro with IGF-IR antibody-directed carbon nanohorns based drug delivery.

    abstract::Oxidized single-wall carbon nanohorns (oxSWNHs) have shown great potential in drug delivery. The purpose of this study was to design an effective targeted drug delivery system (DDS) based on oxSWNHs, which could carry high dose of drug to tumor sites and improve the therapeutic efficacy with less adverse effects. OxSW...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.12.015

    authors: Li N,Zhao Q,Shu C,Ma X,Li R,Shen H,Zhong W

    更新日期:2015-01-30 00:00:00

  • Enhancement of the stability of BCNU using self-emulsifying drug delivery systems (SEDDS) and in vitro antitumor activity of self-emulsified BCNU-loaded PLGA wafer.

    abstract::The main purpose of this study was to develop self-emulsifying drug delivery systems (SEDDS) for the improvement of the stability of 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) after released from poly (D,L-lactide-co-glycolide) (PLGA) wafer and to evaluate its in vitro antitumor activity against 9L gliosarcoma cells....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.03.034

    authors: Chae GS,Lee JS,Kim SH,Seo KS,Kim MS,Lee HB,Khang G

    更新日期:2005-09-14 00:00:00

  • Entrapment and release of saquinavir using novel cationic solid lipid nanoparticles.

    abstract::Cationic solid lipid nanoparticles (CSLNs) with entrapped saquinavir (SQV) were fabricated by microemulsion method. Here, CSLNs were stabilized by polysorbate 80, and the lipid phase contained cationic stearylamine (SA) and dioctadecyldimethyl ammonium bromide (DODAB) and nonionic Compritol 888 ATO (CA) and cacao butt...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.08.050

    authors: Kuo YC,Chen HH

    更新日期:2009-01-05 00:00:00

  • Co-delivery of zinc and 5-aminosalicylic acid from alginate/N-succinyl-chitosan blend microspheres for synergistic therapy of colitis.

    abstract::The present study developed novel zinc ion cross-linked alginate/N-succinyl-chitosan (NSC) blend microspheres (MS) for co-delivery of zinc and 5-aminosalicylic acid (5-ASA) for synergistic therapy of colitis. Physicochemical characterization of blend MS was assessed using scanning electron microscopy (SEM), Fourier tr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.11.036

    authors: Duan H,Lü S,Qin H,Gao C,Bai X,Wei Y,Wu X,Liu M,Zhang X,Liu Z

    更新日期:2017-01-10 00:00:00

  • Characterization of strain rate sensitivity in pharmaceutical materials using indentation creep analysis.

    abstract::Understanding how a material's response to stress changes as the stress is applied at different rates is important in predicting performance of pharmaceutical powders during tablet compression. Widely used methods for determining strain rate sensitivity (SRS) are empirically based and can often provide inconsistent or...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.09.006

    authors: Katz JM,Buckner IS

    更新日期:2013-02-14 00:00:00

  • Evaluation of soluble fentanyl microneedles for loco-regional anti-nociceptive activity.

    abstract::The use of opioids for treating acute and chronic pain condition is a common clinical practice. When delivered systemically, the analgesic activity is mediated through the central pathway, which although effective, leads to various adverse effects such as dependence, abuse and respiratory depression. Fentanyl is an op...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.04.066

    authors: Maurya A,Rangappa S,Bae J,Dhawan T,Ajjarapu SS,Murthy SN

    更新日期:2019-06-10 00:00:00