Interaction of biodegradable nanoparticles with intestinal cells: the effect of surface hydrophilicity.

Abstract:

:The aim of the present work was to study the influence of surface hydrophilicity of biodegradable polymeric nanoparticles on cellular uptake by Caco-2 cells. Poly(D,L-lactide-co-glycolide acid) particles loaded with a fluorescent dye, 3,3'-dioctadecyloxacarbo-cyanine perchlorate (DiO), were prepared by the emulsion-evaporation process. Three batches of particles with narrow size distribution (100, 300 and 1000 nm) were produced using selective centrifugation. One set of particles was coated by adsorption of chitosan to increase the hydrophilicity of the particles. The interaction of particles with Caco-2 cells was determined by fluorescence spectroscopy and the number of particles associated with one single cell was then calculated. Interaction with cells was clearly dependant on particle size and surface hydrophilicity. Particles in the range of 100 nm presented higher interaction when compared to larger particles. Approximately 6000 uncoated particles and more than 30,000 chitosan-coated particles were quantified per cell. Confocal microscopy confirmed the spectroscopic measurements and revealed the location of the particles in the cell monolayer. Only small particles were observed intracellularly, whereas particles larger than 300 nm were associated with the apical membranes. The location of particles <300 nm appeared to be intracellular and some particles colocalized with the nucleus.

journal_name

Int J Pharm

authors

Gaumet M,Gurny R,Delie F

doi

10.1016/j.ijpharm.2009.10.008

subject

Has Abstract

pub_date

2010-05-05 00:00:00

pages

45-52

issue

1

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(09)00717-0

journal_volume

390

pub_type

杂志文章
  • Polymer nanoassemblies with hydrophobic pendant groups in the core induce false positive siRNA transfection in luciferase reporter assays.

    abstract::Poly(ethylene glycol)-conjugated polyethylenimine (PEG-PEI) is a widely studied cationic polymer used to develop non-viral vectors for siRNA therapy of genetic disorders including cancer. Cell lines stably expressing luciferase reporter protein typically evaluate the transfection efficacy of siRNA/PEG-PEI complexes, h...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.056

    authors: Rheiner S,Reichel D,Rychahou P,Izumi T,Yang HS,Bae Y

    更新日期:2017-08-07 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

  • 3D printed orodispersible films with Aripiprazole.

    abstract::Three dimensional printing technology is gaining in importance because of its increasing availability and wide applications. One of the three dimensional printing techniques is Fused Deposition Modelling (FDM) which works on the basis of hot melt extrusion-well known in the pharmaceutical technology. Combination of fu...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.052

    authors: Jamróz W,Kurek M,Łyszczarz E,Szafraniec J,Knapik-Kowalczuk J,Syrek K,Paluch M,Jachowicz R

    更新日期:2017-11-30 00:00:00

  • Biological activity of heterologous murine interleukin-10 and preliminary studies on the use of a dextrin nanogel as a delivery system.

    abstract::Interleukin-10 (IL-10) is an anti-inflammatory cytokine, which active form is a non-covalent homodimer with two intramolecular disulphide bonds essential for its biological activity. A mutated form of murine IL-10 was successfully expressed in E. coli, recovered and purified from inclusion bodies. Its ability to reduc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.08.040

    authors: Carvalho V,Castanheira P,Faria TQ,Gonçalves C,Madureira P,Faro C,Domingues L,Brito RM,Vilanova M,Gama M

    更新日期:2010-11-15 00:00:00

  • Differences in physical chemistry and dissolution rate of solid particle aerosols from solution pressurised inhalers.

    abstract::Solution composition alters the dynamics of beclomethasone diproprionate (BDP) particle formation from droplets emitted by pressurised metered dose inhalers (pMDIs). The hypothesis that differences in inhaler solutions result in different solid particle physical chemistry was tested using a suite of complementary calo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.01.033

    authors: Buttini F,Miozzi M,Balducci AG,Royall PG,Brambilla G,Colombo P,Bettini R,Forbes B

    更新日期:2014-04-25 00:00:00

  • Preparation of dual crosslinked alginate-chitosan blend gel beads and in vitro controlled release in oral site-specific drug delivery system.

    abstract::Alginate-chitosan (ALG-CS) blend gel beads were prepared based on Ca2+ or dual crosslinking with various proportions of alginate and chitosan. The homogeneous solution of alginate and chitosan was dripped into the solution of calcium chloride; the resultant Ca2+ single crosslinked beads were dipped in the solution of ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.12.019

    authors: Xu Y,Zhan C,Fan L,Wang L,Zheng H

    更新日期:2007-05-24 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

  • Contribution of TRPV1 and multidrug resistance proteins in the permeation of capsaicin across different intestinal regions.

    abstract:OBJECTIVE:The aim of the study was to observe the characteristic of permeation of capsaicin across jejunum, ileum and colon in the rat, and to investigate the role of transient receptor potential cation channel (TRPV1). The interaction of capsaicin with P-glycoprotein (P-gp), multidrug resistance-associated protein 2 (...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.02.007

    authors: Duan L,Yan Y,Sun Y,Zhao B,Hu W,Li G

    更新日期:2013-03-10 00:00:00

  • Response surface methodology as a predictive tool for determining the effects of preparation conditions on the physicochemical properties of poly(isobutylcyanoacrylate) nanoparticles.

    abstract::Preparation conditions of nanoparticles greatly influence their physicochemical characteristics. A factorial design was used to evaluate the influence of these conditions on the particle diameter, zeta potential, polydispersity, percentage recovery, and molecular weight of poly(isobutylcyanoacrylate) nanoparticles. Th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00311-7

    authors: McCarron PA,Woolfson AD,Keating SM

    更新日期:1999-12-20 00:00:00

  • Buccal absorption of ergotamine tartrate using the bioadhesive tablet system in guinea-pigs.

    abstract::The buccal administration of ergotamine tartrate (ET) combined with polyvinyl alcohol (PVA) gel brought about higher plasma concentration of ET compared with that of oral administration of capsules in guinea-pigs. T(max) of ET in plasma of buccal administration was significantly smaller than that of oral administratio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00070-4

    authors: Tsutsumi K,Obata Y,Nagai T,Loftsson T,Takayama K

    更新日期:2002-05-15 00:00:00

  • Comparison of in vitro cell models in predicting in vivo brain entry of drugs.

    abstract::Although several in vitro models have been reported to predict the ability of drug candidates to cross the blood-brain barrier, their real in vivo relevance has rarely been evaluated. The present study demonstrates the in vivo relevance of simple unidirectional permeability coefficient (P(app)) determined in three in ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.09.016

    authors: Hakkarainen JJ,Jalkanen AJ,Kääriäinen TM,Keski-Rahkonen P,Venäläinen T,Hokkanen J,Mönkkönen J,Suhonen M,Forsberg MM

    更新日期:2010-12-15 00:00:00

  • A novel formulation of solubilised amphotericin B designed for ophthalmic use.

    abstract::Amphotericin B (AmB) is a wide spectrum antifungal with low incidence of clinical resistance. However, there are no licensed topical formulations with AmB in most developed countries. Extemporaneous preparations of AmB are frequently prepared from available marketed parenteral formulations. Herein, a solution of AmB w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.07.065

    authors: Serrano DR,Ruiz-Saldaña HK,Molero G,Ballesteros MP,Torrado JJ

    更新日期:2012-11-01 00:00:00

  • Liposome encapsulation of curcumin: physico-chemical characterizations and effects on MCF7 cancer cell proliferation.

    abstract::The role of curcumin (diferuloylmethane), for cancer treatment has been an area of growing interest. However, due to its low absorption, the poor bioavailability of curcumin limits its clinical use. In this study, we reported an approach of encapsulation a curcumin by nanoliposome to achieve an improved bioavailabilit...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.12.007

    authors: Hasan M,Belhaj N,Benachour H,Barberi-Heyob M,Kahn CJ,Jabbari E,Linder M,Arab-Tehrany E

    更新日期:2014-01-30 00:00:00

  • The influence of high shear mixing on ternary dry powder inhaler formulations.

    abstract::The blending process is a key step in the production of dry powder inhaler formulations, but only little is known about the influence of process parameters. This is especially true for high shear blending of ternary formulations. For this reason, this study aims to investigate the influence of high shear mixing proces...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.10.033

    authors: Hertel M,Schwarz E,Kobler M,Hauptstein S,Steckel H,Scherließ R

    更新日期:2017-12-20 00:00:00

  • Roll compaction process modeling: transfer between equipment and impact of process parameters.

    abstract::In this study, the roll compaction of an intermediate drug load formulation was performed using horizontally and vertically force fed roll compactors. The horizontally fed roll compactor was equipped with an instrumented roll technology allowing the direct measurement of normal stress at the roll surface, while the ve...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.02.042

    authors: Souihi N,Reynolds G,Tajarobi P,Wikström H,Haeffler G,Josefson M,Trygg J

    更新日期:2015-04-30 00:00:00

  • Prediction of aqueous solubility of drug-like molecules using a novel algorithm for automatic adjustment of relative importance of descriptors implemented in counter-propagation artificial neural networks.

    abstract::In this work, we present a novel approach for the development of models for prediction of aqueous solubility, based on the implementation of an algorithm for the automatic adjustment of descriptor's relative importance (AARI) in counter-propagation artificial neural networks (CPANN). Using this approach, the interpret...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.08.022

    authors: Erić S,Kalinić M,Popović A,Zloh M,Kuzmanovski I

    更新日期:2012-11-01 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

  • Phospholipid components of the synthetic pulmonary surfactant CHF5633 probed by fluorescence spectroscopy.

    abstract::CHF5633 (Chiesi Farmaceutici, Italy) is a synthetic pulmonary surfactant currently under clinical development for the treatment of Respiratory Distress Syndrome in premature infants. The product is composed of phospholipids in liposomal organization, together with two peptide analogues of human surfactant proteins B a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.10.045

    authors: Faggiano S,Ronda L,Raboni S,Sartor F,Cavatorta V,Sgarbi E,Caivano G,Pertile M,Mozzarelli A

    更新日期:2018-12-20 00:00:00

  • In vitro and in vivo evaluation of a melamine dendrimer as a vehicle for drug delivery.

    abstract::Cell-based and acute and subchronic in vivo toxicity profiles of a dendrimer based on melamine reveal that this class of molecules warrants additional study as vehicles for drug delivery. In cell culture, a substantial decrease in viability was observed at 0.1 mg/mL. For the acute studies, mice were administered 2.5, ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2004.04.023

    authors: Neerman MF,Zhang W,Parrish AR,Simanek EE

    更新日期:2004-08-20 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

  • pH-responsive PepFect cell-penetrating peptides.

    abstract::A series of cell-penetrating PepFect peptide analogues was developed by substitutions of the galanin-derived N-terminal sequence. Histidine modifications were incorporated in order to make the peptides pH-responsive. The peptides were all able to form non-covalent complexes with an oligonucleotide cargo by co-incubati...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.01.055

    authors: Regberg J,Vasconcelos L,Madani F,Langel Ü,Hällbrink M

    更新日期:2016-03-30 00:00:00

  • Preparation and optimization of a drug delivery system based on berberine chloride-immobilized MgAl hydrotalcite.

    abstract::Hydrotalcite (HT), also known as a layered double hydroxide (LDH) compound, has been widely used in past years in the formulation of drugs due to its specific properties including good biocompatibility, null toxicity, high chemical stability and pH-dependent solubility which aid in drug controlled release. In this wor...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.04.048

    authors: Djebbi MA,Bouaziz Z,Elabed A,Sadiki M,Elabed S,Namour P,Jaffrezic-Renault N,Amara AB

    更新日期:2016-06-15 00:00:00

  • Predicting the gastrointestinal behaviour of modified-release products: utility of a novel dynamic dissolution test apparatus involving the use of bicarbonate buffers.

    abstract::The establishment of physiologically relevant in vitro-in vivo correlations (IV-IVCs) is key for any biorelevant dissolution test. Historically, bicarbonate buffers have produced better correlations than compendial phosphate buffered media, though such tests are usually performed at a constant pH experiment, overlooki...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.09.003

    authors: Merchant HA,Goyanes A,Parashar N,Basit AW

    更新日期:2014-11-20 00:00:00

  • Vesicles as antibiotic carrier: State of art.

    abstract::Antimicrobial resistance (AMR) has become a global health problem. Bacteria are able to adapt to different environments, with the presence or absence of a host, forming colonies and biofilms. In fact, biofilm formation confers chemical protection to the microbial cells, thus making most of the conventional antibiotics...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.119478

    authors: Marchianò V,Matos M,Serrano-Pertierra E,Gutiérrez G,Blanco-López MC

    更新日期:2020-07-30 00:00:00

  • Core-shell structured Fe3O4@TiO2-doxorubicin nanoparticles for targeted chemo-sonodynamic therapy of cancer.

    abstract::To facilitate targeting drug delivery and combined therapy, we develop titanium dioxide-encapsulated Fe3O4 nanoparticles (Fe3O4@TiO2 NPs). Titanium dioxide (TiO2), which is employed as a sonosensitizer for sonodynamic therapy (SDT), can also be used for the loading of doxorubicin (DOX). The fabricated Fe3O4@TiO2 NPs e...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.03.070

    authors: Shen S,Wu L,Liu J,Xie M,Shen H,Qi X,Yan Y,Ge Y,Jin Y

    更新日期:2015-01-01 00:00:00

  • Type of pH sensitive linker reveals different time-dependent intracellular localization, in vitro and in vivo efficiency in alpha-fetoprotein receptor targeted doxorubicin conjugate.

    abstract::Despite the presence of a variety of modern anticancer drugs at the market, doxorubicin (Dox) is still widely used in antineoplastic therapy, although its administration causes severe side effects. To enhance specific activity of such molecules, various approaches have been exploited: targeted moieties like monoclonal...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.073

    authors: Mollaev M,Gorokhovets N,Nikolskaya E,Faustova M,Zabolotsky A,Zhunina O,Sokol M,Zamulaeva I,Severin E,Yabbarov N

    更新日期:2019-03-25 00:00:00

  • Preparation of spray dried submicron particles: Part B - Particle recovery by electrostatic precipitation.

    abstract::The low bioavailability of poorly water-soluble drugs is currently one of the major focuses of pharmaceutical research. One strategy currently being investigated to overcome this limitation is to decrease the particle size of the active pharmaceutical ingredients (API). An innovative process for this is spray drying w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.06.069

    authors: Dobrowolski A,Strob R,Nietfeld J,Pieloth D,Wiggers H,Thommes M

    更新日期:2018-09-05 00:00:00

  • Percutaneous absorption of non-steroidal anti-inflammatory drugs from in situ gelling xyloglucan formulations in rats.

    abstract::The potential of gels formed in situ by dilute aqueous solutions of a xyloglucan polysaccharide derived from tamarind seed as sustained release vehicles for percutaneous administration of non-steroidal anti-inflammatory drugs has been assessed by in vitro and in vivo studies. Chilled aqueous solutions of xyloglucan th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00394-0

    authors: Takahashi A,Suzuki S,Kawasaki N,Kubo W,Miyazaki S,Loebenberg R,Bachynsky J,Attwood D

    更新日期:2002-10-10 00:00:00

  • A novel antimicrobial peptide-derived vehicle for oligodeoxynucleotide delivery to inhibit TNF-α expression.

    abstract::Indolicidin (IL), an antimicrobial peptide, was investigated as a vehicle to promote oligodeoxynucleotides (ODNs) delivery. To increase charge density, IL was dimerized by adding a cysteine to its C or N terminus, which was denoted as ILC or CIL, respectively. In contrast to IL, cytotoxicity of ILC and CIL was signifi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.082

    authors: Hu WW,Huang SC,Jin SC

    更新日期:2019-03-10 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