Endothelial progenitor cell secretome delivered by novel polymeric nanoparticles in ischemic hindlimb.

Abstract:

:Endothelial progenitor cells (EPCs) contribute to ischemic tissue repair by paracrine secretion up-regulated by hypoxia. In this study we use novel nanoparticles (NPs) as carriers for a controlled release of EPC secretome (CM) to improve their angiogenic properties. The in vivo effect in ischemic hindlimb rat model was evaluated, comparing hypoxic EPC-CM-NPs with hypoxic EPC-CM alone. A proteomic characterization of hypoxic CM and the in vitro effect on endothelial cells (HUVECs) were also performed. Up to 647 protein, 17 of which with angiogenic properties, were upregulated by hypoxia. Moreover, hypoxic EPC-CM significantly promoted capillary-like structures on Matrigel. A significant increase of blood perfusion in ischemic limbs at 2 weeks with EPC-CM-loaded NPs as compared to both EPC-CM and control and a significant increase of capillary formation were observed. The use of EPC-CM-NPs significantly improved neoangiogenesis in vivo, underlining the advantages of controlled release in regenerative medicine.

journal_name

Int J Pharm

authors

Felice F,Piras AM,Rocchiccioli S,Barsotti MC,Santoni T,Pucci A,Burchielli S,Chiellini F,Ucciferri N,Solaro R,Altomare A,Cecchettini A,Di Stefano R

doi

10.1016/j.ijpharm.2018.03.015

subject

Has Abstract

pub_date

2018-05-05 00:00:00

pages

82-89

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(18)30161-3

journal_volume

542

pub_type

杂志文章
  • 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

  • Thiolated chitosan: development and in vitro evaluation of an oral delivery system for acyclovir.

    abstract::The aim of the study was to develop a novel oral delivery system for the efflux pump substrate acyclovir (ACY) utilizing thiolated chitosan as excipient which is capable of inhibiting P-glycoprotein (P-gp). Three chitosan-4-thiobutylamidine (Chito-TBA) conjugates with increasing molecular mass (Chito-9.4kDa-TBA, Chito...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.07.004

    authors: Palmberger TF,Hombach J,Bernkop-Schnürch A

    更新日期:2008-02-04 00:00:00

  • Efficacy of edelfosine lipid nanoparticles in breast cancer cells.

    abstract::Breast cancer is a heterogeneous group of neoplasms predominantly originating in the terminal duct lobular units. It represents the leading cause of cancer death in women and the survival frequencies for patients at advanced stages of the disease remain low. New treatment options need to be researched to improve these...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.04.068

    authors: Aznar MÁ,Lasa-Saracíbar B,Estella-Hermoso de Mendoza A,Blanco-Prieto MJ

    更新日期:2013-10-01 00:00:00

  • Spray-dried chitinosans. Part II: in vitro drug release from tablets made from spray-dried chitinosans.

    abstract:PURPOSE:Application of spray-dried chitinosans as excipients for use in drug delivery systems was explored. METHODS:Spray- and tray-dried chitinosans previously N-deacetylated and depolymerized were used. Directly compressed tablets (200mg) containing tetracycline, chitinosan, and magnesium stearate were prepared. The...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00605-1

    authors: Rege PR,Garmise RJ,Block LH

    更新日期:2003-02-18 00:00:00

  • Hydrodynamic size characterization of a self-emulsifying lipid pharmaceutical excipient by Taylor dispersion analysis with fluorescent detection.

    abstract::In this work, the sizing of microemulsion droplets of a lipid-based pharmaceutical excipient (Labrasol® ALF) is performed by Taylor dispersion analysis (TDA) using fluorescent detection. An hydrophobic fluorescent marker is used to tag the microemulsion droplet and to increase the sensitivity of detection (compared to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.09.016

    authors: Chamieh J,Jannin V,Demarne F,Cottet H

    更新日期:2016-11-20 00:00:00

  • Role of the elasticity of pharmaceutical materials on the interfacial mechanical strength of bilayer tablets.

    abstract::The effect of the elasticity of various pharmaceutical materials on the interfacial adhesion in bilayer tablets was investigated. The elastic properties of five pharmaceutical products were characterized by their total elastic recovery. To test the interfacial strength of the bilayer tablets a new flexural test was pr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.09.009

    authors: Busignies V,Mazel V,Diarra H,Tchoreloff P

    更新日期:2013-11-30 00:00:00

  • Novel combination of non-invasive morphological and solid-state characterisation of drug-loaded core-shell electrospun fibres.

    abstract::In recent years, core-shell nanofibrous drug delivery systems have received increasing attention due to their ability to incorporate two or more active pharmaceutical ingredients (APIs) individually into the desired layer (either core or sheath) and thereby finely tune the release profiles of even incompatible drugs i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119706

    authors: Kazsoki A,Farkas A,Balogh-Weiser D,Mancuso E,Sharma PK,Lamprou DA,Zelkó R

    更新日期:2020-09-25 00:00:00

  • Preparation, characterization and in vitro release study of a glutathione-dependent polymeric prodrug Cis-3-(9H-purin-6-ylthio)-acrylic acid-graft-carboxymethyl chitosan.

    abstract::In this work, an amphiphilic polymeric prodrug Cis-3-(9H-purin-6-ylthio)-acrylic acid-graft-carboxymethyl chitosan (PTA-g-CMCS) was designed and synthesized. In aqueous solution, this grafted polymer can self-assemble into spherical micelles with a size ranging from 104 to 285 nm and zeta potential ranging from -12.3 ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.043

    authors: Gong XY,Yin YH,Huang ZJ,Lu B,Xu PH,Zheng H,Xiong FL,Xu HX,Xiong X,Gu XB

    更新日期:2012-10-15 00:00:00

  • A novel flunarizine hydrochloride-loaded organogel for intraocular drug delivery in situ: Design, physicochemical characteristics and inspection.

    abstract::We developed a safe and efficacious drug delivery system for treatment of brain diseases. A novel in-situ gel system was prepared using soybean oil, stearic acid and N-methyl-2-pyrrolidinone (NMP) (10:1:3, v/w/v). This system had low viscosity as a sol in vitro and turned into a solid or semi-solid gel in situ after a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119027

    authors: Dai M,Bai L,Zhang H,Ma Q,Luo R,Lei F,Fei Q,He N

    更新日期:2020-02-25 00:00:00

  • Cyclodextrin-containing poly(ethyleneoxide) tablets for the delivery of poorly soluble drugs: potential as buccal delivery system.

    abstract::The aim of this work was to develop a tablet for the buccal delivery of the poorly soluble drug carvedilol (CAR), based on poly(ethyleneoxide) (PEO) as bioadhesive sustained-release platform and hydroxypropyl-beta-cyclodextrin (HPbetaCD) as modulator of drug release. As first, PEO tablets loaded with CAR/HPbetaCD bina...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.03.031

    authors: Cappello B,De Rosa G,Giannini L,La Rotonda MI,Mensitieri G,Miro A,Quaglia F,Russo R

    更新日期:2006-08-17 00:00:00

  • Temperature-sensitive copolymer-coated fluorescent mesoporous silica nanoparticles as a reactive oxygen species activated drug delivery system.

    abstract::In this study, a temperature and ROS-responsive drug delivery system ROSP@MSN based on mesoporous silica nanoparticles has been designed and synthesized by taking advantage of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acrylate modified polymers (ROSP) as "nano-valve", which can respond selectively to cance...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.11.025

    authors: Yu F,Wu H,Tang Y,Xu Y,Qian X,Zhu W

    更新日期:2018-01-30 00:00:00

  • Protease-functionalized mucus penetrating microparticles: In-vivo evidence for their potential.

    abstract::The focus of the current study was to explore whether immobilization of proteases to microparticles could result in their enhanced penetration into mucus. The proteases papain (PAP) and bromelain (BROM) were covalently attached to a polyacrylate (PAA; Carbopol 971P) via amide bond formation based on carbodiimide react...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.08.114

    authors: Mahmood A,Laffleur F,Leonaviciute G,Bernkop-Schnürch A

    更新日期:2017-10-30 00:00:00

  • Dermal delivery of Fe-chlorophyllin via ultradeformable nanovesicles for photodynamic therapy in melanoma animal model.

    abstract::Melanoma is resistant to chemotherapeutics with poor prognosis and high potential of metastasis. Photodynamic therapy (PDT) represents a localized therapeutic modality, as cytotoxicity occurs when light activates photosensitizer (PS) at the tumour site. The aim of this study is dermal delivery of a high molecular weig...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.06.057

    authors: Rady M,Gomaa I,Afifi N,Abdel-Kader M

    更新日期:2018-09-05 00:00:00

  • Drug/lactose co-micronization by jet milling to improve aerosolization properties of a powder for inhalation.

    abstract::The aim of this work was to formulate a powder for inhalation with fusafungine, a drug substance initially highly cohesive. The classical approach based on micronization by jet milling to prepare respirable drug particles and then blending with a carrier was first applied. A fractional factorial experimental design wa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.05.009

    authors: Giry K,Péan JM,Giraud L,Marsas S,Rolland H,Wüthrich P

    更新日期:2006-09-14 00:00:00

  • Interaction of cationic partial dendrimers with charged and neutral liposomes.

    abstract::Amphipathic partial dendrimers having three lipidic (C(14)) chains coupled to dendritic lysine head groups with eight, 16 or 32 free terminal amino groups have been synthesised by solid-phase peptide synthesis. Liposomes were prepared with positive, negative and neutral charge using the dehydration-rehydration method ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00635-9

    authors: Purohit G,Sakthivel T,Florence AT

    更新日期:2001-02-19 00:00:00

  • Preparation, formula optimization and antitumor actions of mannitol coupling camptothecin nanoparticles.

    abstract::The purpose of this work is to prepare a formulation using mannitol coupling Camptothecin (CPT) nanoparticles (CPT-NPs) to circumvent the difficult solubilization practice based on central composite experimental statistical design. CPT-NPs were prepared with a high-pressure homogenization technique method. The indepen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.02.019

    authors: Wang Z,Li Q,Zhao X,Sun B,Zhu Q,Gao W,Hua C

    更新日期:2014-04-25 00:00:00

  • Incorporation of a model protein into chitosan-bile salt microparticles.

    abstract::In order to develop a mucosal delivery system based on biocompatible polymers, a new methodology for production of protein-loaded microparticles is developed. Chitosan anionic precipitation/coacervation is accomplished by the addition of sodium deoxycholate (DCA). These microparticles were prepared under mild conditio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.01.006

    authors: Lameiro MH,Lopes A,Martins LO,Alves PM,Melo E

    更新日期:2006-04-07 00:00:00

  • Investigation of L-leucine in reducing the moisture-induced deterioration of spray-dried salbutamol sulfate power for inhalation.

    abstract::The aim of this study was to investigate the ability of L-leucine (LL) in preventing moisture-induced deterioration in the in vitro aerosolization performance of spray-dried (SD) salbutamol sulfate (SS). Increasing mass fraction of LL (5-80%) were co-spray dried with SS, and the physicochemical properties of the powde...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.07.033

    authors: Li L,Leung SSY,Gengenbach T,Yu J,Gao GF,Tang P,Zhou QT,Chan HK

    更新日期:2017-09-15 00:00:00

  • Stabilization of insulin against agitation-induced aggregation by the GMO cubic phase gel.

    abstract::The main objective of the study was to evaluate if the liquid crystalline cubic phase gel of glyceryl monooleate (GMO) protects insulin from agitation induced aggregation. The aggregation of Humulin(R), Regular Iletin I(R) and Regular Iletin II(R), in cubic phase GMO gels at 30 U/g of gel was compared with that in PBS...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00288-4

    authors: Sadhale Y,Shah JC

    更新日期:1999-11-25 00:00:00

  • Development of controlled release inhalable polymeric microspheres for treatment of pulmonary hypertension.

    abstract::Pulmonary hypertension (PAH) is a condition of the lungs characterised by an elevated arterial pressure and increased vascular resistance. Existing medications have to be administered frequently, resulting in non compliance by patients. Little work has been reported to date where microspheres have been developed to co...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.04.011

    authors: Saigal A,Ng WK,Tan RB,Chan SY

    更新日期:2013-06-25 00:00:00

  • In-line monitoring of partial and overall solid concentration during solvent-mediated phase transition using Raman spectroscopy.

    abstract::A calibration strategy for the continuous monitoring of solvent-mediated phase transition was developed using in situ Raman spectroscopy. Citric acid which exhibits enantiotropy during its anhydrous/monohydrate phase transition was selected as a model organic product. Using 25 samples in suspension, specific calibrati...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.009

    authors: Caillet A,Puel F,Fevotte G

    更新日期:2006-01-13 00:00:00

  • Controlled release from hydrogel-based solid matrices. A model accounting for water up-take, swelling and erosion.

    abstract::Design and realization of drug delivery systems based on polymer matrices could be greatly improved by modeling the phenomena which take place after the systems administration. Availability of a reliable mathematical model, able to predict the release kinetic from drug delivery systems, could actually replace the reso...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.01.023

    authors: Lamberti G,Galdi I,Barba AA

    更新日期:2011-04-04 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

  • In vitro and in vivo characterization of nanoparticles made of MeO-PEG amine/PLA block copolymer and PLA.

    abstract::The preparative method of a block copolymer of poly(dl-lactic acid) (PLA) and methoxypolyethylene glycol amine (MeO-PEG(N)), named PLA-(MeO-PEG), was refined. The degree of introduction of MeO-PEG(N) into PLA increased up to 55% (mol/mol) using a dichloromethane/methanol mixture (1:1, v/v) as a solvent at the reductiv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.02.057

    authors: Sasatsu M,Onishi H,Machida Y

    更新日期:2006-07-24 00:00:00

  • Effect of divalent anions on photodegradation kinetics and pathways of riboflavin in aqueous solution.

    abstract::The present investigation is based on a study of the effect of buffer and non-buffer divalent anions (phosphate, sulphate, tartrate, succinate, malonate) on the kinetics, product distribution and photodegradation pathways of riboflavin (RF) at pH 6.0-8.0. RF solutions (5x10(-5)M) were photodegraded in the presence of ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.01.042

    authors: Ahmad I,Ahmed S,Sheraz MA,Vaid FH,Ansari IA

    更新日期:2010-05-10 00:00:00

  • Effects of carriers on transgene expression from plasmids containing a DNA sequence with high histone affinity.

    abstract::The intranuclear disposition of plasmid DNA is highly important for transgene expression. The effects of a left-handedly curved sequence with high histone affinity on transgene expression were examined in COS-7 cells with two kinds of carriers (Lipofectamine Plus and TransIT-LT1). Three plasmids containing the curved ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.04.032

    authors: Kamiya H,Fukunaga S,Ohyama T,Harashima H

    更新日期:2009-07-06 00:00:00

  • Engineered DNA nanodrugs alleviate inflammation in inflammatory arthritis.

    abstract::Rheumatoid arthritis (RA) is an autoimmune disease featured with chronic joint inflammation. Suppression of inflammation is critical to RA treatment and joint protection. In this study, DNA nanodrugs are prepared via the conjugation of NF-κB decoy oligodeoxynucleotides (dODNs) and VCAM-1 targeted peptides (P) onto sel...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119047

    authors: Wang Z,Chu X,Li N,Fu L,Gu H,Zhang N

    更新日期:2020-03-15 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

  • Nanohybrid biodegradable scaffolds for TGF-β3 release for the chondrogenic differentiation of human mesenchymal stem cells.

    abstract::An ideal scaffold for bone tissue engineering should have chondroinductive, biodegradable, and biocompatible properties, as well as the ability to absorb and slowly release the biological molecules. In order to develop such a system to support bone tissue regeneration, in the present study, we developed a three-dimens...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119248

    authors: Qasim M,Le NXT,Nguyen TPT,Chae DS,Park SJ,Lee NY

    更新日期:2020-05-15 00:00:00

  • Development of self-emulsifying drug delivery systems (SEDDS) for ciprofloxacin with improved mucus permeating properties.

    abstract::The aim of this study was to develop a self-emulsifying drug delivery system (SEDDS) containing the fluoroquinolone antibiotic ciprofloxacin (CIP) exhibiting highly mucus permeating properties and antimicrobial activity in in vitro models. Various SEDDS formulations were developed and evaluated regarding droplet size,...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.06.005

    authors: Zaichik S,Steinbring C,Menzel C,Knabl L,Orth-Höller D,Ellemunter H,Niedermayr K,Bernkop-Schnürch A

    更新日期:2018-08-25 00:00:00