In vitro biological activity of resveratrol using a novel inhalable resveratrol spray-dried formulation.

Abstract:

:The aim of the study was to prepare inhalable resveratrol by spray drying for the treatment of chronic obstructive pulmonary disease (COPD). Resveratrol, with a spherical morphology and particle diameter less than 5 μm, was successfully manufactured. Fine particle fraction (FPF) and mass median aerodynamic diameter (MMAD) of spray-dried resveratrol was 39.9 ± 1.1% and 3.7 ± 0.1 μm, respectively, when assessed with an Andersen cascade impactor (ACI) at 60 l/min. The cytotoxicity results of resveratrol on Calu-3 revealed that the cells could tolerate high concentration of resveratrol (up to 160 μM). In addition, in transport experiments using Snapwells, it was observed that more than 80% of the deposited dry powder was transported across the Calu-3 cells to the basal chamber within four hours. The expression of interleukin-8 (IL-8) from Calu-3 induced with tumor necrosis factor alpha (TNF-α), transforming growth factor beta (TGF-β1) and lipopolysaccharide (LPS) were significantly reduced after treatment with spray-dried resveratrol. The antioxidant assay (radical scavenging activity and nitric oxide production) showed spray-dried resveratrol to possess an equivalent antioxidant property as compared to vitamin C. Results presented in this investigation suggested that resveratrol could potentially be developed as a dry powder for inhalation for the treatment of inflammatory lung diseases like COPD.

journal_name

Int J Pharm

authors

Trotta V,Lee WH,Loo CY,Haghi M,Young PM,Scalia S,Traini D

doi

10.1016/j.ijpharm.2015.06.033

subject

Has Abstract

pub_date

2015-08-01 00:00:00

pages

190-7

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(15)00553-0

journal_volume

491

pub_type

杂志文章
  • Amphotericin B-incorporated polymeric micelles composed of poly(d,l-lactide-co-glycolide)/dextran graft copolymer.

    abstract::In this study, we prepared amphotericin B (AmpB)-encapsulated polymeric micelle of poly(d,l-lactide-co-glycolide) (PLGA) grafted-dextran (DexLG) copolymer and characterized its physicochemical properties in vitro. The average particle size of AmpB-encpasulated DexLG polymeric micelles was around 30-150nm while particl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.12.011

    authors: Choi KC,Bang JY,Kim PI,Kim C,Song CE

    更新日期:2008-05-01 00:00:00

  • Near-infrared spectroscopy (NIRS) and chemometric analysis of Malaysian and UK paracetamol tablets: a spectral database study.

    abstract::The influx of medicines from different sources into healthcare systems of developing countries presents a challenge to monitor their origin and quality. The absence of a repository of reference samples or spectra prevents the analysis of tablets by direct comparison. A set of paracetamol tablets purchased in Malaysian...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.05.057

    authors: Said MM,Gibbons S,Moffat AC,Zloh M

    更新日期:2011-08-30 00:00:00

  • Synbiotic loaded chitosan-Ca-alginate microparticles reduces inflammation in the TNBS model of rat colitis.

    abstract::New therapeutic strategies against inflammatory bowel disease (IBD) consider the usage of probiotics, prebiotics and synbiotics as beneficial for the intestinal microbial balance. Limitations of such an approach are addressed into difference in survival, persistence, colonization and variable effects among different p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.049

    authors: Ivanovska TP,Mladenovska K,Zhivikj Z,Pavlova MJ,Gjurovski I,Ristoski T,Petrushevska-Tozi L

    更新日期:2017-07-15 00:00:00

  • Nanogel particulates located within diffusion cell receptor phases following topical application demonstrates uptake into and migration across skin.

    abstract::Despite growing evidence in support of nanogels as carriers in topical drug delivery, no empirical evidence has been forthcoming regarding a mechanism. Poly(N-isopropylacrylamide-copolymerized-acrylic acid) referred to as poly(NIPAM-co-AAc) and poly(N-isopropylacrylamide) known as (polyNIPAM) nanogels were synthesized...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.08.011

    authors: Samah NA,Williams N,Heard CM

    更新日期:2010-11-30 00:00:00

  • Monitoring of the freezing stage in a freeze-drying process using IR thermography.

    abstract::This paper presents a new Process Analytical Technology based on the use of an infrared camera and a mathematical model to estimate the ice crystal size distribution obtained at the end of the freezing stage of a vial freeze-drying process. Both empirical laws and first-principle based equations, already presented in ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.06.005

    authors: Colucci D,Maniaci R,Fissore D

    更新日期:2019-07-20 00:00:00

  • Chitosan oligosaccharide enhances binding of nanostructured lipid carriers to ocular mucins: Effect on ocular disposition.

    abstract::The objective of the study was to assess the effect of enhanced mucoadhesion of a cationic mucoadhesive nanostructured lipid carrier (NLC) on its ocular disposition after topical administration. The NLC was made mucoadhesive by surface coating with chitosan oligosaccharide (COS), a low molecular weight derivate of chi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119095

    authors: Pai RV,Vavia PR

    更新日期:2020-03-15 00:00:00

  • Paclitaxel-loaded microparticles and implants for the treatment of brain cancer: preparation and physicochemical characterization.

    abstract::The aim of this study was to prepare different types of paclitaxel-loaded, PLGA-based microparticles and lipidic implants, which can directly be injected into the brain tissue. Releasing the drug in a time-controlled manner over several weeks, these systems are intended to optimize the treatment of brain tumors. The l...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.07.028

    authors: Elkharraz K,Faisant N,Guse C,Siepmann F,Arica-Yegin B,Oger JM,Gust R,Goepferich A,Benoit JP,Siepmann J

    更新日期:2006-05-18 00:00:00

  • Role of individual test samples in optimal solutions in pharmaceuticals predicted using a nonlinear response surface method.

    abstract::Establishing a method to evaluate the reliability of an optimal solution is an exciting challenge for the nonlinear response surface method. We reported previously that the bootstrap (BS) resampling technique and Kohonen's self-organizing map are promising tools for meeting this challenge. To understand the usefulness...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.06.013

    authors: Onuki Y,Kikuchi S,Yasuda A,Takayama K

    更新日期:2010-08-30 00:00:00

  • A thermo-responsive and self-healing liposome-in-hydrogel system as an antitubercular drug carrier for localized bone tuberculosis therapy.

    abstract::Isoniazid (INH) is a first-line therapy for bone tuberculosis (TB), but its clinic benefits are limited by severe side-effects after long-time administration. While nano-drug delivery systems present as promising strategies for INH delivery, the therapeutic efficacies are usually suboptimal due to ineffective drug acc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.083

    authors: Liu P,Guo B,Wang S,Ding J,Zhou W

    更新日期:2019-03-10 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

  • Quality attributes and evaluation of pharmaceutical glass containers for parenterals.

    abstract::Pharmaceutical containers for parenterals have been predominantly manufactured using glass as a packaging material of choice, especially Type-I glass, since it has been regarded as a chemically inert and an effective container closure system (CCS). Nevertheless, there have been reports and recalls related to glass qua...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118510

    authors: Srinivasan C,Ma Y,Liu Y,Wang Y,Hengst L,Liu X,Toth R,Rodriguez J,Mohammad A,Bandaranayake BMB,Simon D,Beekman C,Korang-Yeboah M,Sivan S,Lee SL,Cruz CN

    更新日期:2019-09-10 00:00:00

  • Lipoprotein imitating nanoparticles: Lecithin coating binds ApoE and mediates non-lysosomal uptake leading to transcytosis over the blood-brain barrier.

    abstract::Lipoproteins are naturally occurring nano sized transport vehicles in the human body. Therefore, lipoproteins could be applied as a drug carrier system. Additionally, several reports of apolipoprotein mediated blood-brain barrier (BBB) crossing suggest lipoprotein mimicking nanoparticles (NPs) as possible drug deliver...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119821

    authors: Wünsch A,Mulac D,Langer K

    更新日期:2020-08-28 00:00:00

  • Influence of membrane structure on the preparation of colloidal lipid dispersions by premix membrane emulsification.

    abstract::Since premix membrane emulsification was developed as alternative technique for the preparation of emulsions and solid lipid particles as carrier systems for lipophilic drugs, many types of membranes have been used in this preparation process. The purpose of this study was to evaluate the influence of different types ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.02.013

    authors: Joseph S,Bunjes H

    更新日期:2013-03-25 00:00:00

  • Retention and distribution of two 99mTc-DTPA labelled vaginal dosage forms.

    abstract:UNLABELLED:To objectively evaluate the performance of new vaginal dosage forms, it is important to determine their time of residence and their distribution. This paper describes the in vivo characteristics of a reference and test product in this situation. METHOD:A randomised cross-over study was performed in the same...

    journal_title:International journal of pharmaceutics

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/j.ijpharm.2003.11.006

    authors: Chatterton BE,Penglis S,Kovacs JC,Presnell B,Hunt B

    更新日期:2004-03-01 00:00:00

  • 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. T...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119244

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

    更新日期:2020-04-30 00:00:00

  • New prospective in treatment of Parkinson's disease: studies on permeation of ropinirole through buccal mucosa.

    abstract::The aptitude of ropinirole to permeate the buccal tissue was tested using porcine mucosa mounted on Franz-type diffusion cells as ex vivo model. Drug permeation was also evaluated in presence of various penetration enhancers and in iontophoretic conditions. Ropinirole, widely used in treatment of motor fluctuations of...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.03.022

    authors: De Caro V,Giandalia G,Siragusa MG,Sutera FM,Giannola LI

    更新日期:2012-06-15 00:00:00

  • Critical attributes of formulation and of elaboration process of PLGA-protein microparticles.

    abstract::Low drug loading, burst effect during release and drug inactivation account for the main drawbacks of protein microencapsulation in poly(d,l-lactic-co-glycolic) acid (PLGA) matrix by the water-in oil-in water (W/O/W) solvent evaporation method. Thus, the current study was set to invest the critical attributes of formu...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.01.008

    authors: Martín-Sabroso C,Fraguas-Sánchez AI,Aparicio-Blanco J,Cano-Abad MF,Torres-Suárez AI

    更新日期:2015-03-01 00:00:00

  • Dehydration of trehalose dihydrate at low relative humidity and ambient temperature.

    abstract::The physico-chemical behaviour of trehalose dihydrate during storage at low relative humidity and ambient temperature was investigated, using a combination of techniques commonly employed in pharmaceutical research. Weight loss, water content determinations, differential scanning calorimetry and X-ray powder diffracti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.01.026

    authors: Jones MD,Hooton JC,Dawson ML,Ferrie AR,Price R

    更新日期:2006-04-26 00:00:00

  • Electrically controlled release of salicylic acid from poly(p-phenylene vinylene)/polyacrylamide hydrogels.

    abstract::The apparent diffusion coefficients, Dapp, and the release mechanisms of salicylic acid from salicylic acid-loaded polyacrylamide hydrogels, SA-loaded PAAM, and salicylic acid-doped poly(phenylene vinylene)/polyacrylamide hydrogels, SA-doped PPV/PAAM, were investigated. In the absence of an electric field, the diffusi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.12.032

    authors: Niamlang S,Sirivat A

    更新日期:2009-04-17 00:00:00

  • In vitro and in vivo evaluation of Pluronic F127-based ocular delivery system for timolol maleate.

    abstract::The purpose of this study was to develop Pluronic F127 (PF127) based formulations of timolol maleate (TM) aimed at enhancing its ocular bioavailability. The effect of isotonicity agents and PF127 concentrations on the rheological properties of the prepared formulations was examined. In an attempt to reduce the concent...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00234-x

    authors: El-Kamel AH

    更新日期:2002-07-08 00:00:00

  • Formulation strategies for the stabilization of tetanus toxoid in poly(lactide-co-glycolide) microspheres.

    abstract::The development of a single-dose tetanus vaccine based on Poly(Lactic acid) (PLA) or Poly(Lactide-co-Glycolide) (PLGA) microspheres has been complicated due to the instability of tetanus toxoid (TT) inside these systems. Herein we report an attempt to re-design PLGA microspheres by co-encapsulating TT in the dry solid...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00178-7

    authors: Sánchez A,Villamayor B,Guo Y,McIver J,Alonso MJ

    更新日期:1999-08-20 00:00:00

  • Low density porous carrier drug adsorption and release study by response surface methodology using different solvents.

    abstract::Low density porous carriers are widely used in the pharmaceutical applications. Response surface methodology, using 3(2) factorial design was used to study drug adsorption on and its release patterns from microporous polypropylene (Accurel MP 1000) in the absence of additives. Ibuprofen, as model drug, was adsorbed on...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.09.013

    authors: Sher P,Ingavle G,Ponrathnam S,Pawar AP

    更新日期:2007-02-22 00:00:00

  • A systematic study of captopril-loaded polyester fiber mats prepared by electrospinning.

    abstract::In this study, drug-loaded nanofibers were prepared by electrospinning captopril (CPL) with aliphatic biodegradable polyesters. Poly(L-lactic acid) (PLLA), poly(lactic-co-glycolic acid) (PLGA), and poly(lactic-co-ε-caprolactone) (PLCL) were used as filament-forming matrix polymers, and the concentration of CPL in each...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.09.055

    authors: Zhang H,Lou S,Williams GR,Branford-White C,Nie H,Quan J,Zhu LM

    更新日期:2012-12-15 00:00:00

  • Aiming for a moving target: challenges with impactor measurements of MDI aerosols.

    abstract::Experiments were conducted to illustrate some of the challenges associated with measuring dynamic MDI aerosols. Experimental HFA-134a solution MDIs containing 8 or 20% ethanol were measured using the Andersen cascade impactor using three different inlets. It was demonstrated that the size distribution of MDI aerosols ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.11.047

    authors: Stein SW

    更新日期:2008-05-01 00:00:00

  • Quaternization enhances the transgene expression efficacy of aminoglycoside-derived polymers.

    abstract::The objective of the present study was to synthesize and investigate the transgene expression efficacy of quaternized derivatives of aminoglycoside polymers in different cancer cell lines. A series of glycidyltrimethylammonium chloride (GTMAC) derivatives of aminoglycoside polymers (GTMAC-AM polymers), containing vary...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.026

    authors: Miryala B,Feng Y,Omer A,Potta T,Rege K

    更新日期:2015-07-15 00:00:00

  • Enhanced oral delivery of alendronate by sucrose fatty acids esters in rats and their absorption-enhancing mechanisms.

    abstract::Oral delivery is the most fascinating route for interminable drug remedy. However, the intestinal absorption of alendronate (ALN), a bisphosphonate drug after oral administration is very poor. Absorption enhancers, which help to achieve the efficiency-safety balance, are considered one of the most promising agents for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.10.046

    authors: Alama T,Katayama H,Hirai S,Ono S,Kajiyama A,Kusamori K,Katsumi H,Sakane T,Yamamoto A

    更新日期:2016-12-30 00:00:00

  • Classification of microcrystalline celluloses via structures of individual particles measured by synchrotron radiation X-ray micro-computed tomography.

    abstract::Microcrystalline cellulose (MCC) is one of the most important excipients due to its outstanding binding and tableting properties. Owing to the absence of high resolution characterization techniques at the single particle scale, 3D (three dimension) microstructure of MCC and its effects on formulation performance remai...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.019

    authors: Fang L,Yin X,Wu L,He Y,He Y,Qin W,Meng F,York P,Xu X,Zhang J

    更新日期:2017-10-15 00:00:00

  • Slow-release of famotidine from tablets consisting of chitosan/sulfobutyl ether β-cyclodextrin composites.

    abstract::An intermolecular complex formed from a 1:1 weight ratio of chitosan (CS, molecular weight 30 kDa) and sulfobutyl ether β-cyclodextrin (SBE-β-CyD, degree of substitution 7) was less soluble than either of the original components. The release of famotidine from tablets composed of a simple mixture of CS and SBE-β-CyD i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.022

    authors: Anraku M,Hiraga A,Iohara D,Pipkin JD,Uekama K,Hirayama F

    更新日期:2015-06-20 00:00:00

  • Montmorillonite nanodevices for the colon metronidazole delivery.

    abstract::The adsorption profiles of the antibiotic metronidazole (MNE) into the K10-montmorillonite (MMT-K10) clay and the subsequent release have been investigated as a function of pH and MNE/MMT-K10 ratio, in order to evaluate the potential of the MNE/MMT-K10 hybrids as controlled drug delivery system. The adsorption mechani...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.09.017

    authors: Calabrese I,Cavallaro G,Scialabba C,Licciardi M,Merli M,Sciascia L,Turco Liveri ML

    更新日期:2013-11-30 00:00:00

  • Alginate nanoparticles protect ferrous from oxidation: Potential iron delivery system.

    abstract::A novel, efficient delivery system for iron (Fe2+) was developed using the alginate biopolymer. Iron loaded alginate nanoparticles were synthesized by a controlled ionic gelation method and was characterized with respect to particle size, zeta potential, morphology and encapsulation efficiency. Successful loading was ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.09.053

    authors: Katuwavila NP,Perera AD,Dahanayake D,Karunaratne V,Amaratunga GA,Karunaratne DN

    更新日期:2016-11-20 00:00:00