Design of surface ligands for blood compatible gold nanoparticles: Effect of charge and binding energy.

Abstract:

:Gold nanoparticle (AuNP) interaction with the blood compartment as a function of their charge and the binding energy of their surface ligand was explored. Citrate, polyallylamine and cysteamine stabilized AuNP along with dihydrolipoic acid and polyethylene glycol capped AuNP were synthesized and fully characterized. Their interactions with model proteins (human albumin and human fibrinogen) were studied. Complexes formed between AuNP and protein revealed several behaviors ranging from corona formation to aggregation. Protein fluorescence quenching as a function of temperature and AuNP concentration allowed the determination of the thermodynamic parameters describing these interactions. The hemolysis induced by AuNP was also probed: an increasing or a decreasing of hemolysis ratio induced by AuNP was observed as of function of protein corona formation. Taken together, our results drew up a composite sketch of an ideal surface ligand for blood compatible AuNP. This capping agent should be strongly bound to the gold core by one or more thiol groups and it must confer a negative charge to the particles.

journal_name

Int J Pharm

authors

Beurton J,Lavalle P,Pallotta A,Chaigneau T,Clarot I,Boudier A

doi

10.1016/j.ijpharm.2020.119244

subject

Has Abstract

pub_date

2020-04-30 00:00:00

pages

119244

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(20)30228-3

journal_volume

580

pub_type

杂志文章
  • Degradable, thermo-, pH- and redox-sensitive hydrogel microcapsules for burst and sustained release of drugs.

    abstract::Polymer microcapsules offer a possibility of storing increased amounts of drugs. Appropriate design and composition of the microcapsules allow tuning of the drug-release process. In this paper, we report on synthesis of hydrogel microcapsules sensitive to temperature and pH and degradable by glutathione and hydrogen p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118589

    authors: Mackiewicz M,Romanski J,Drabczyk K,Waleka E,Stojek Z,Karbarz M

    更新日期:2019-10-05 00:00:00

  • Preparation and characterization of "dextran-magnetic layered double hydroxide-fluorouracil" targeted liposomes.

    abstract::This work was aimed at assessing the preparation and characteristics of "dextran-magnetic layered double hydroxide-fluorouracil" liposomes (DMFL). DMFL was prepared by the optimized reverse evaporation method, which concerned the entrapment efficiency and slow-released effect. The factors affecting the entrapment effi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.04.010

    authors: Huang J,Gou G,Xue B,Yan Q,Sun Y,Dong LE

    更新日期:2013-06-25 00:00:00

  • The effects of esterified solvents on the diffusion of a model compound across human skin: an ATR-FTIR spectroscopic study.

    abstract::Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy has been used to investigate the effects of three fatty acid esters on skin permeation. Propylene glycol diperlargonate (DPPG), isopropyl myristate (IPM) and isostearyl isostearate (ISIS) were selected as pharmaceutically relevant solvents...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.02.022

    authors: McAuley WJ,Chavda-Sitaram S,Mader KT,Tetteh J,Lane ME,Hadgraft J

    更新日期:2013-04-15 00:00:00

  • Preparation and characterization of a synthetic curcumin analog inclusion complex and preliminary evaluation of in vitro antileishmanial activity.

    abstract::The aim of this work was to prepare and characterize inclusion complexes between a synthetic curcumin analog (dibenzalacetone, DBA) and beta-cyclodextrin (β-CD); and to evaluate their in vitro antileishmanial activity. DBA was synthetized and characterized by spectroscopic methods and the inclusion complexes were obta...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119764

    authors: Pinto LMA,Adeoye O,Thomasi SS,Francisco AP,Carvalheiro MC,Cabral-Marques H

    更新日期:2020-08-25 00:00:00

  • Surface activity of a non-micelle forming compound containing a surface-active impurity.

    abstract:PURPOSE:The purpose of this study is to characterize the surface activity of a water-soluble compound and its ability to form aggregates/micelles. METHODS:Aqueous solutions of the compound were prepared at various concentrations. Surface tension was determined using drop volume and Wilhelmy plate methods. Moreover, co...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.10.034

    authors: Al-Maaieh A,Aburub A

    更新日期:2007-04-04 00:00:00

  • Control, communication and monitoring of intravaginal drug delivery in dairy cows.

    abstract::We present the design of an electronically controlled drug delivery system. The intravaginally located device is a low-invasive platform that can measure and react inside the cow vagina while providing external control and monitoring ability. The electronics manufactured from off the shelf components occupies 16 mL of...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.05.023

    authors: Cross PS,Künnemeyer R,Bunt CR,Carnegie DA,Rathbone MJ

    更新日期:2004-09-10 00:00:00

  • Stabilization of gene delivery systems by freeze-drying.

    abstract::Freeze-drying of three different forms of gene delivery systems was performed using a controlled two-step drying process and 10% sucrose as lyoprotectant. Complexes of pCMVL plasmid with transferrin-conjugated polyethylenimine, adenovirus-enhanced transferrinfection consisting of pCMVL/transferrin-polylysine complexes...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(97)00244-5

    authors: Talsma H,Cherng J,Lehrmann H,Kursa M,Ogris M,Hennink WE,Cotten M,Wagner E

    更新日期:1997-11-28 00:00:00

  • Controlled-release triple anti-inflammatory therapy based on novel gastroretentive sponges: characterization and magnetic resonance imaging in healthy volunteers.

    abstract::The current work aimed to develop novel composite sponges of chitosan (CH)-chondroitin sulfate (CS) as a low-density gastroretentive delivery system for lornoxicam (LOR). This triple anti-inflammatory therapy-loaded matrices are expected to expand and float upon contact with gastric fluids for prolonged times. CH and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.06.013

    authors: Tadros MI,Fahmy RH

    更新日期:2014-09-10 00:00:00

  • Effects of different combinations of nanocrystallization technologies on avanafil nanoparticles: in vitro, in vivo and stability evaluation.

    abstract::The study investigated the effects of different combined top-down and bottom-up nanocrystallization technologies on particle size and solid state of avanafil nanoparticles. Combined antisolvent precipitation-ultrasonication (sonoprecipitation) technique was adopted to prepare 18 formulas according to 32.21 factorial d...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.12.012

    authors: Soliman KA,Ibrahim HK,Ghorab MM

    更新日期:2017-01-30 00:00:00

  • A comparative in vitro assessment of the drug release performance of pH-responsive polymers for ileo-colonic delivery.

    abstract::The aim of this study was to investigate the in vitro dissolution characteristics of pH-responsive polymers in a variety of simulated fluids. Prednisolone tablets were fabricated and coated with the following polymer systems: Eudragit S (organic solution), Eudragit S (aqueous dispersion), Eudragit FS (aqueous dispersi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.038

    authors: Ibekwe VC,Fadda HM,Parsons GE,Basit AW

    更新日期:2006-02-03 00:00:00

  • A biocompatible and easy-to-make polyelectrolyte dressing with tunable drug delivery properties for wound care.

    abstract::Chitosan (CS) is a biodegradable and biocompatible polysaccharide which displays immune-stimulatory effects and anti-bacterial properties to facilitate wound closure. Over the years, different CS-based dressings have been developed; however, most of them are not fully biodegradable due to the involvement of synthetic ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.05.045

    authors: Lai WF,Hu C,Deng G,Lui KH,Wang X,Tsoi TH,Wang S,Wong WT

    更新日期:2019-07-20 00:00:00

  • Physicochemical studies on Ciclopirox olamine complexes with divalent metal ions.

    abstract::Ciclopirox olamine (CPO) metal complexes have been prepared and characterized using elemental analysis, infra red (IR), melting point and differential scanning calorimetry (DSC). Spectroscopic titration using molar ratio method indicated the occurrence of 1:1 complexes for CPO with almost all the examined metals. Phys...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.11.009

    authors: Tarawneh RT,Hamdan II,Bani-Jaber A,Darwish RM

    更新日期:2005-01-31 00:00:00

  • Paediatric formulations--getting to the heart of the problem.

    abstract::Many medicines prescribed for children are unlicensed. Solid dosage forms present problems as children have difficulty swallowing whole tablets or capsules. When medicines are not licensed for children, it is unlikely that there will be a suitable, licensed liquid formulation and so extemporaneous liquid preparations ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.05.006

    authors: Standing JF,Tuleu C

    更新日期:2005-08-26 00:00:00

  • Synthesis and characterization of biocompatible poly(organophosphazenes) aiming for local delivery of protein drugs.

    abstract::Biocompatible and thermosensitive poly(organophosphazenes) with a lower critical solution temperature (LCST) below body temperature have been designed with the aim for the local delivery of peptide and protein drugs. These polymers could be synthesized by introducing short chain tri- or tetraethylene glycol as a hydro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.02.009

    authors: Seong JY,Jun YJ,Kim BM,Park YM,Sohn YS

    更新日期:2006-05-11 00:00:00

  • Formulation optimization and topical delivery of quercetin from solid lipid based nanosystems.

    abstract::The presence of large amounts of reactive oxygen species (ROS) leads to oxidative stress that can damage cell membranes, lead to DNA breakage and cause inactivation of free radical scavenger enzymes, eventually resulting in skin damage. Quercetin is a natural flavonoid that has been shown to have the highest anti-radi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.12.013

    authors: Bose S,Du Y,Takhistov P,Michniak-Kohn B

    更新日期:2013-01-30 00:00:00

  • Peptide ligand-mediated liposome distribution and targeting to EGFR expressing tumor in vivo.

    abstract::Epidermal growth factor receptor (EGFR) is an important anti-cancer therapy target that is applicable to many cancer types. We had previously reported the screening and discovery of a novel peptide ligand against EGFR named GE11. It was shown to bind to EGFR competitively with EGF and mediate gene delivery to cancer c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.07.012

    authors: Song S,Liu D,Peng J,Sun Y,Li Z,Gu JR,Xu Y

    更新日期:2008-11-03 00:00:00

  • Partially hydrolyzed polyvinyl alcohol for fusion-based pharmaceutical formulation processes: Evaluation of suitable plasticizers.

    abstract::The present study evaluates the effect of several pharmaceutical plasticizers on the thermo-physical and physicochemical properties of partially hydrolyzed poly(vinyl alcohol) (PVA) used in fusion-based pharmaceutical formulation processes. Specifically, the effect of mannitol (MAN), sorbitol (SOR), sucrose (SUC), anh...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119121

    authors: Katopodis K,Kapourani A,Vardaka E,Karagianni A,Chorianopoulou C,Kontogiannopoulos KN,Bikiaris DN,Kachrimanis K,Barmpalexis P

    更新日期:2020-03-30 00:00:00

  • Cyclodextrin containing biodegradable particles: from preparation to drug delivery applications.

    abstract::Cyclodextrins (CDs) offer a very broad spectrum of applications in diverse fields of drug delivery. They are a family of cyclic α-(1-4)-linked oligosaccharides of α-d-glucopyranose subunits forming a more hydrophobic central cavity and a hydrophilic outer shell. CDs bear cage like supramolecular structures, similar to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2013.12.004

    authors: Zafar N,Fessi H,Elaissari A

    更新日期:2014-01-30 00:00:00

  • The determination of a diffusional pathlength through the stratum corneum.

    abstract::The stratum corneum possesses a very heterogenous structure. As such a diffusing molecule can access a number of different pathways. It is probable that the excellent barrier properties of the stratum corneum result from a tortuous diffusional pathway around the dead cells. However, there are considerable problems in ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00161-1

    authors: Bunge AL,Guy RH,Hadgraft J

    更新日期:1999-10-15 00:00:00

  • Incorporation of benzoyl peroxide nanocrystals into adapalene-loaded solid lipid microparticles: Part II - Solid-in-Oil dispersion of nanoparticulate benzoyl peroxide.

    abstract::Benzoyl peroxide as a monotherapeutic and in combination with adapalene is a cornerstone of current acne therapy, but its unfavourable side effect profile reduces the therapeutic value of this compound. The incorporation into an adapalene-loaded microparticulate lipid matrix, which - via the principle of targeted eros...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118792

    authors: Brammann C,Müller-Goymann CC

    更新日期:2019-12-15 00:00:00

  • Novel self-floating tablet for enhanced oral bioavailability of metformin based on cellulose.

    abstract::Metformin has several problems such as low bioavailability, short half-life, and narrow absorption window, sustained and site-specific drug delivery system is required. Floating drug delivery systems are very useful to achieve these purposes. However, conventional floating systems have several limitations; lag time, a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120113

    authors: Wook Huh H,Na YG,Kang H,Kim M,Han M,Mai Anh Pham T,Lee H,Baek JS,Lee HK,Cho CW

    更新日期:2021-01-05 00:00:00

  • Effects of non-ionic surfactants as permeation enhancers towards piroxicam from the poloxamer gel through rat skins.

    abstract::The enhancing effects of non-ionic surfactants on the permeation of piroxicam from the poloxamer gels were evaluated using Franz diffusion cells fitted with excised rat skins. The effectiveness of penetration enhancers, the ratio of piroxicam flux in the presence or absence of enhancers, was defined as the enhancement...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00699-8

    authors: Shin SC,Cho CW,Oh IJ

    更新日期:2001-07-17 00:00:00

  • Marinosomes, marine lipid-based liposomes: physical characterization and potential application in cosmetics.

    abstract::Marinosomes are liposomes based on a natural marine lipid extract containing a high polyunsaturated fatty acid (PUFA) ratio. They were prepared and characterized in conditions that mimic that of topical application in terms of pH, temperature and calcium. Marinosomes were stable in storage conditions for 1 month. At l...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00217-x

    authors: Moussaoui N,Cansell M,Denizot A

    更新日期:2002-08-21 00:00:00

  • Evaluation of manufacturing process parameters causing multilayer tablets delamination.

    abstract::The aim of this study was to evaluate the influence of tableting process parameters, i.e. turret rotation speed, pre-compaction and main compaction pressures, and their interactions on layer adhesion of bilayer tablets. The elastic recovery after compaction was used as estimation for the elasticity of the material. Th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118607

    authors: Bellini M,Walther M,Bodmeier R

    更新日期:2019-10-30 00:00:00

  • Applications of NIR spectroscopy to monitoring and analyzing the solid state during industrial crystallization processes.

    abstract::Fiber-optic near infrared (NIR) spectroscopy was used to investigate several key features of the polymorphic transitions observed during the crystallization and the filtration of SaC, an Active Pharmaceutical Ingredient (API) produced by Sanofi-Synthelabo. Using few samples, the spectroscopic data were calibrated to p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.01.003

    authors: Févotte G,Calas J,Puel F,Hoff C

    更新日期:2004-04-01 00:00:00

  • Self-nanoemulsifying drug delivery system of persimmon leaf extract: Optimization and bioavailability studies.

    abstract::In current study, a self-nanoemulsifying drug delivery system (SNEDDS) of persimmon (Diospyros kaki) leaf extract (PLE) was developed and characterized to compare its in vitro dissolution and relative bioavailability with commercially available tablets (Naoxinqing tablets). Pseudo-ternary phase diagrams were construct...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.08.024

    authors: Li W,Yi S,Wang Z,Chen S,Xin S,Xie J,Zhao C

    更新日期:2011-11-25 00:00:00

  • Molecular expression and functional activity of sodium dependent multivitamin transporter in human prostate cancer cells.

    abstract::Nutrient transporters expressed on cell membrane have been targeted for enhancing bioavailability of poorly permeable drugs. Sodium dependent multivitamin transporter (SMVT) is once such carrier system, utilized for improving drug targeting to specific tissues. Therefore, the main objective of this study is to charact...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.011

    authors: Patel M,Vadlapatla RK,Shah S,Mitra AK

    更新日期:2012-10-15 00:00:00

  • Application of experimental design methodology in development and optimization of drug release method.

    abstract::The aim of our research was to apply experimental design methodology in the development and optimization of drug release methods. Diclofenac sodium (2-[(2,6-dichlorophenyl)amino]benzeneacetic acid monosodium salt) was selected as a model drug and Naklofen retard prolonged release tablets, containing 100 mg of diclofen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.07.041

    authors: Kincl M,Turk S,Vrecer F

    更新日期:2005-03-03 00:00:00

  • Investigation of 3D ordered macroporous carbon with different polymer coatings and their application as an oral vaccine carrier.

    abstract::3-D ordered macroporous carbon with different polymer coatings were developed as new oral vaccine immunological systems. Poly dimethyl diallyl ammonium (PDDA), polyethyleneimine (PEI) and chitosan (CTS), three different polymers with electropositive or adsorption-promoting properties, were chosen as the coating materi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.045

    authors: Zhao Q,Zhang Q,Yue Y,Huang J,Di D,Gao Y,Shao X,Wang S

    更新日期:2015-06-20 00:00:00

  • Preparation of an injectable depot system for long-term delivery of alendronate and evaluation of its anti-osteoporotic effect in an ovariectomized rat model.

    abstract::We prepared an injectable depot system for the long-term delivery of alendronate using a solid/water/oil/water multiple emulsion technique with poly(lactic-co-glycolic acid) as a carrier. The microparticles were spherical with smooth surfaces, ranging from 20 to 70 μm in size. The microspheres (ALD-HA-RG504H-MC70) wer...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.01.020

    authors: Bae J,Park JW

    更新日期:2015-03-01 00:00:00