In vitro and in silico characterization of fibrous scaffolds comprising alternate colistin sulfate-loaded and heat-treated polyvinyl alcohol nanofibrous sheets.

Abstract:

:A multilayer mat for dispensing colistin sulfate through a body surface was prepared by electrospinning. The fabricated system comprised various polyvinyl alcohol fibrous layers prepared with or without the active ingredient. One of the electrospun layers contained water-soluble colistin sulfate and the other was prepared from the same polymer type and composition without the active drug and was finally heat-treated. The heat treatment modified the supramolecular structure and conferred the polymer nanofibre with the rate-controlling function. The microstructure of different layers was tracked by positron annihilation lifetime spectroscopy, and detailed morphological analysis of the fibre mats was performed using a scanning electron microscope. The drug-release profiles of various layer arrangements were studied in relation to their antimicrobial activity. The finite element method was applied to overcome the challenge of diffusion-controlled drug release from multilayer polymer scaffolds. The finite element method was first verified using analytical solutions for a simple arrangement (one drug-loaded swellable fibre and one rate-controlling nonswellable fibre) under perfect sink conditions and in a well-stirred finite volume. The effect of alternate layer arrangements on the drug-release profiles was also investigated to plan for controlled topical drug release from fibrous scaffolds. This design is expected to aid in increasing local effectiveness, thus reducing the systemic loading and the consequent side effects of colistin.

journal_name

Int J Pharm

authors

Sebe I,Ostorházi E,Bodai Z,Eke Z,Szakács J,Kovács NK,Zelkó R

doi

10.1016/j.ijpharm.2017.03.044

subject

Has Abstract

pub_date

2017-05-15 00:00:00

pages

151-158

issue

1

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(17)30220-X

journal_volume

523

pub_type

杂志文章
  • 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

  • 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

  • Comparison of two hard keratinous substrates submitted to the action of a keratinase using an experimental design.

    abstract::The influence of temperature, pH, keratinase concentration, substrate concentration and incubation time on the soluble proteins released by a new keratinase from Doratomyces microsporus was studied with a second-order experimental design. Only 15 or 18 spectrophotometric analyses were required to determine the optimal...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00749-9

    authors: Vignardet C,Guillaume YC,Michel L,Friedrich J,Millet J

    更新日期:2001-08-14 00:00:00

  • Preparation and characterization of the ion-fixed mixed micelles with superior stability.

    abstract::The inherent instability of micelles remains a main challenge for antitumor drug delivery, the objective of this study is to prepare and characterize the ion-fixed mixed micelles with significantly improved stability. The mixed micelles and ion-fixed mixed micelles combining the carboxy-containing PLA (PLA-COO(-)) and...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.05.011

    authors: Li Y,Fu Y,Guo H,Zhang L,Huang L,Yang L

    更新日期:2015-07-15 00:00:00

  • Application of statistical experimental design to study the formulation variables influencing the coating process of lidocaine liposomes.

    abstract::In this paper, we have used statistical experimental design to investigate the effect of several factors in coating process of lidocaine hydrochloride (LID) liposomes by a biodegradable polymer (chitosan, CH). These variables were the concentration of CH coating solution, the dripping rate of this solution on the lipo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.01.024

    authors: González-Rodríguez ML,Barros LB,Palma J,González-Rodríguez PL,Rabasco AM

    更新日期:2007-06-07 00:00:00

  • Polymorphism and stability of ibuprofen/nicotinamide cocrystal: The effect of the crystalline synthesis method.

    abstract::The development over the past decade of design strategies for cocrystal preparation have led to numerous methods for the synthesis of cocrystal without take care of their influence on the precise structure and stability of cocrystalline states. On the other hand the mechanism of cocrystal formation remains widely uncl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119454

    authors: Guerain M,Guinet Y,Correia NT,Paccou L,Danède F,Hédoux A

    更新日期:2020-06-30 00:00:00

  • Non-viral gene delivery carrier and its three-dimensional transfection system.

    abstract::An increasing number of non-viral vectors are being developed for the use of gene delivery nowadays, among which cationic polymers and lipoplexes receive most attention. Most of these researches are focused on how to increase the transfection efficiency of non-viral vectors as well as the reduction of toxicity. In thi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2009.11.006

    authors: He CX,Tabata Y,Gao JQ

    更新日期:2010-02-15 00:00:00

  • Stability study of amorphous valdecoxib.

    abstract::Formulation of poorly water-soluble drugs in the most stable dosage form for oral delivery perhaps presents the greatest challenge to pharmaceutical industry. Physical transformation of drug substance into its more soluble but metastable amorphous form is one of the approaches for improving dissolution rate of such dr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.06.009

    authors: Ambike AA,Mahadik KR,Paradkar A

    更新日期:2004-09-10 00:00:00

  • Induction of immunogenic cell death of cancer cells through nanoparticle-mediated dual chemotherapy and photothermal therapy.

    abstract::The use of nanomedicines to induce immunogenic cell death is a new strategy that aims to increase tumor immunogenicity and thereby prime tumors for further immunotherapies. In this study, we developed a nanoparticle formulation for combinatory chemotherapy and photothermal therapy based only on materials previously us...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119787

    authors: Heshmati Aghda N,Abdulsahib SM,Severson C,Lara EJ,Torres Hurtado S,Yildiz T,Castillo JA,Tunnell JW,Betancourt T

    更新日期:2020-09-06 00:00:00

  • Double-layer weekly sustained release transdermal patch containing gestodene and ethinylestradiol.

    abstract::The combination therapy of gestodene (GEST) and ethinylestradiol (EE) has shown advanced contraception effect and lower side effect. The present study was designed to develop a weekly sustained release matrix type transdermal patch containing GEST and EE using blends of different polymeric combinations. The multiple-l...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.05.017

    authors: Gao Y,Liang J,Liu J,Xiao Y

    更新日期:2009-07-30 00:00:00

  • The use of MTDSC to assess the amorphous phase content of a micronized drug substance.

    abstract::Mechanical treatments such as grinding, milling or micronization applied to crystalline drug substances may induce changes such as the occurrence of crystal defects and/or amorphous regions. These changes are likely to affect the chemical and physical properties of the material as well as the corresponding drug produc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00273-2

    authors: Guinot S,Leveiller F

    更新日期:1999-12-01 00:00:00

  • Preparation and characterization of mucoadhesive polymer-coated nanoparticles.

    abstract::The transmucosal routes such as pulmonary, nasal and oral routes are most important and common routes for drug delivering to the body. However, peptide and protein drugs are degraded before they reach the blood stream and cannot cross the mucosal barriers. The mucoadhesive polymer-coated nanoparticles colloidal carrie...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.02.031

    authors: Cui F,Qian F,Yin C

    更新日期:2006-06-19 00:00:00

  • Simultaneous effects of tocopheryl polyethylene glycol succinate (TPGS) on local hair growth promotion and systemic absorption of topically applied minoxidil in a mouse model.

    abstract::In this study, topical minoxidil solutions supplemented with TPGS in cosolvent systems of various compositions consisting of water, alcohol, and polyethylene glycol 400 were designed to evaluate the efficacy of promoting hair growth after topical application and the safety in terms of the amount of minoxidil absorbed ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.09.005

    authors: Chen CH,Sheu MT,Wu AB,Lin KP,Ho HO

    更新日期:2005-12-08 00:00:00

  • Physicochemical characteristics of quinupramine in the EVA matrix.

    abstract::Ethylene-vinyl acetate (EVA) is widely used as a membrane or matrix for transdermal drug delivery systems. In an attempt to determine the state of a drug in the EVA matrix, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and thermal analysis of the quinupramine-EVA matrix were carried out and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.06.016

    authors: Cho CW,Choi JS,Shin SC

    更新日期:2006-08-31 00:00:00

  • Pharmacokinetics and absolute bioavailability of oral cefuroxime axetil in the rat.

    abstract::The objectives of this study were to determine the oral bioavailability of cefuroxime (C) and to evaluate the pharmacokinetic model that best describes the plasma concentration behaviour following single intravenous (IV), intraperitoneal (IP) and oral single doses. The same dose of C was administered by IV, IP and ora...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00420-8

    authors: Ruiz-Carretero P,Nacher A,Merino-Sanjuan M,Casabo VG

    更新日期:2000-07-20 00:00:00

  • A measurement system analysis with design of experiments: Investigation of the adhesion performance of a pressure sensitive adhesive with the probe tack test.

    abstract::The tack of a pressure sensitive adhesive (PSA) is not an inherent material property and strongly depends on the measurement conditions. Following the concept of a measurement system analysis (MSA), influencing factors of the probe tack test were investigated by a design of experiments (DoE) approach. A response surfa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.09.061

    authors: Michaelis M,Leopold CS

    更新日期:2015-12-30 00:00:00

  • Bovine serum albumin-meloxicam nanoaggregates laden contact lenses for ophthalmic drug delivery in treatment of postcataract endophthalmitis.

    abstract::Postcataract endophthalmitis treatment through eye drops is of low corneal bioavailability and short residence time. The dominant NSAIDs therapy also suffers from severe ocular irritancy and low patients compliance. This study dispersed bovine serum albumin (BSA) coated meloxicam (MX) nanocrystals encapsulating nanoag...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.08.043

    authors: Zhang W,Zu D,Chen J,Peng J,Liu Y,Zhang H,Li S,Pan W

    更新日期:2014-11-20 00:00:00

  • Silica nanoparticle coated liposomes: a new type of hybrid nanocapsule for proteins.

    abstract::A hybrid silica-liposome nanocapsule system containing insulin has been developed and the encapsulation, protection and release properties are evaluated. The formulation strategy is based on using insulin-loaded 1,2-dipalmitoyl-sn-glycero-3-phosphocholine and cholesterol liposomes as a template for the deposition of i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.03.061

    authors: Mohanraj VJ,Barnes TJ,Prestidge CA

    更新日期:2010-06-15 00:00:00

  • Understanding the structure and stability of paclitaxel nanocrystals.

    abstract::Previously, PTX/Pluronic F127 nanocrystals were prepared in our laboratory using the stabilization of nanocrystals (SNC) method. For PTX nanocrystals, dosages could be increased to yield improved antitumor activity over Taxol without incidence of acute toxicity. The objectives of this current study are to further unde...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.02.013

    authors: Deng J,Huang L,Liu F

    更新日期:2010-05-10 00:00:00

  • Formation of multicellular tumor spheroids induced by cyclic RGD-peptides and use for anticancer drug testing in vitro.

    abstract::Development of novel anticancer formulations is a priority challenge in biomedicine. However, in vitro models based on monolayer cultures (2D) which are currently used for cytotoxicity tests leave much to be desired. More and more attention is focusing on 3D in vitro systems which can better mimic solid tumors. The ai...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.04.005

    authors: Akasov R,Zaytseva-Zotova D,Burov S,Leko M,Dontenwill M,Chiper M,Vandamme T,Markvicheva E

    更新日期:2016-06-15 00:00:00

  • Next generation of buccadhesive excipient: Preactivated carboxymethyl cellulose.

    abstract:AIM:Assessment of preactivated carboxymethyl cellulose as potential excipient for buccal drug delivery. METHODS:Firstly, carboxymethyl cellulose (CMC) and cysteine (SH) were covalently coupled via amide bond formation to obtain thiolated carboxymethyl cellulose (CMC-SH). Further, preactivated carboxymethyl cellulose (...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.01.012

    authors: Laffleur F,Bacher L,Vanicek S,Menzel C,Muhammad I

    更新日期:2016-03-16 00:00:00

  • Transdermal delivery of naloxone: effect of water, propylene glycol, ethanol and their binary combinations on permeation through rat skin.

    abstract::The effect of the solvent systems water, ethanol (EtOH), propylene glycol (PG) and their binary combinations was studied on the ex vivo permeation profile of the opioid receptor antagonist, naloxone, through rat skin. Fourier transform-infrared (FT-IR) spectroscopic studies were done to investigate the effect of enhan...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00634-2

    authors: Panchagnula R,Salve PS,Thomas NS,Jain AK,Ramarao P

    更新日期:2001-05-21 00:00:00

  • Improvement of physicochemical properties of N-4472. Part II: characterization of N-4472 microemulsion and the enhanced oral absorption.

    abstract::The optimized formulation of N-4472, N-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)-4,6-difluorophenyl]-N'-[4-(N-benzylpiperidyl)] urea, which was a poorly water-soluble drug, was developed by utilizing the complexation between N-4472 and L-ascorbic acid (VC). It was found that the formulation with Gelucire((R)) 44/14, H...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00346-0

    authors: Itoh K,Matsui S,Tozuka Y,Oguchi T,Yamamoto K

    更新日期:2002-10-10 00:00:00

  • Prostaglandin E1 encapsulated into lipid nanoparticles improves its anti-inflammatory effect with low side-effect.

    abstract::Prostaglandin E(1) (PGE1) shows various pharmacological activities including anti-inflammation. However, the rapid metabolization and inactivation of the intravenously administered PGE1 during the first passage through the lungs result in significant non-compliance in clinical trials which greatly limits its applicati...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.12.019

    authors: Gao Y,Xu P,Chen L,Li Y

    更新日期:2010-03-15 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

  • Bioavailability of ibuprofen from matrix mini-tablets based on a mixture of starch and microcrystalline wax.

    abstract::The bioavailability of ibuprofen from matrix mini-tablets based on microcrystalline wax and a starch derivative was tested. An oral dose of 300 mg of ibuprofen was administered to healthy volunteers (n=8) in a randomized cross-over study design either as a commercial matrix formulation (Ibu-Slow 600) or as mini-tablet...

    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/s0378-5173(00)00549-4

    authors: De Brabander C,Vervaet C,Görtz JP,Remon JP,Berlo JA

    更新日期:2000-11-04 00:00:00

  • Relationships between surface free energy, surface texture parameters and controlled drug release in hydrophilic matrices.

    abstract::The study of controlled release and drug release devices has been dominated by considerations of the bulk or average properties of material or devices. Yet the outermost surface atoms play a central role in their performance. The objective of this article has been to characterize the surface of hydrophilic matrix tabl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.11.054

    authors: Saurí J,Suñé-Negre JM,Díaz-Marcos J,Vilana J,Millán D,Ticó JR,Miñarro M,Pérez-Lozano P,García-Montoya E

    更新日期:2015-01-15 00:00:00

  • Prediction of the human oral bioavailability by using in vitro and in silico drug related parameters in a physiologically based absorption model.

    abstract::Estimates of the human oral absolute bioavailability were made by using a physiological-based pharmacokinetic model of absorption and the drug solubility at the gastrointestinal pH range 1.5-7.5, the apparent permeability (P(app)) in Caco-2 cells and the intrinsic clearance (Cl(int)) in human hepatocytes suspensions a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.03.019

    authors: Paixão P,Gouveia LF,Morais JA

    更新日期:2012-06-15 00:00:00

  • A Design of Experiment (DoE) approach to optimise spray drying process conditions for the production of trehalose/leucine formulations with application in pulmonary delivery.

    abstract::The present study evaluates the effect of L-leucine concentration and operating parameters of a laboratory spray dryer on characteristics of trehalose dry powders, with the goal of optimizing production of these powders for inhaled drug delivery. Trehalose/L-leucine mixtures were spray dried from aqueous solution usin...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.03.004

    authors: Focaroli S,Mah PT,Hastedt JE,Gitlin I,Oscarson S,Fahy JV,Healy AM

    更新日期:2019-05-01 00:00:00

  • Xanthan and galactomannan (from M. scabrella) matrix tablets for oral controlled delivery of theophylline.

    abstract::Directly compressed theophylline tablets, containing commercial xanthan (X) (Keltrol) and a highly hydrophilic galactomannan (G) from the seeds of Mimosa scabrella (a brazilian leguminous tree called bracatinga) as release-controlling agents, were obtained. Gums were used at 4, 8, 12.5 and 25% (w/w), either alone or i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.02.007

    authors: Vendruscolo CW,Andreazza IF,Ganter JL,Ferrero C,Bresolin TM

    更新日期:2005-05-30 00:00:00