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 polymers during dressing fabrication. In addition, preparation of many of these dressings is laborious, and may impose damaging effects on fragile therapeutic molecules. The objective of this study is to address these problems by developing a tunable, biocompatible, and biodegradable CS-based dressing for wound treatment. The dressing is fabricated via electrostatic interactions between CS and carmellose (CM). Its swelling properties, erosion behavior, loading efficiency and drug release sustainability can be tuned by simply changing the CS/CM mass-to-mass ratio. Upon loaded with minocycline hydrochloride, the dressing effectively protects the wound in mice from infection and enhances wound closure. Regarding its high tunability and promising in vivo performance, our dressing warrants further development as a user-friendly dressing for use in wound care.

journal_name

Int J Pharm

authors

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

doi

10.1016/j.ijpharm.2019.05.045

subject

Has Abstract

pub_date

2019-07-20 00:00:00

pages

101-110

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(19)30404-1

journal_volume

566

pub_type

杂志文章
  • Powder, capsule and device: An imperative ménage à trois for respirable dry powders.

    abstract:OBJECTIVES:The development of inhaled products to treat or to prevent lung infection is a very active research field in drug delivery. The pulmonary route is extremely attractive but very challenging. This paper reports the study of excipient, capsule brand and device influence on the aerodynamic behavior of dry powder...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.08.012

    authors: Schoubben A,Blasi P,Giontella A,Giovagnoli S,Ricci M

    更新日期:2015-10-15 00:00:00

  • One-week in vivo sustained release of a peptide formulated into in situ forming implants.

    abstract::The LR12 peptide has been reported to reduce the size of infarct and improve both cardiac function and survival in myocardial infarction in murine models, after daily repeated intraperitoneal injections. In order to protect peptide from degrading and to prolong its release, in situ implants based on biocompatible biod...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.046

    authors: Parent M,Clarot I,Gibot S,Derive M,Maincent P,Leroy P,Boudier A

    更新日期:2017-04-15 00:00:00

  • The novel immunogenic chimeric peptide vaccine to elicit potent cellular and mucosal immune responses against HTLV-1.

    abstract::This study reports on the immunogenicity assessment of a novel chimeric peptide vaccine including Tax, gp21, gp46, and gag immunodominant epitopes of human T-cell lymphotropic virus type 1 (HTLV-1) to induce immunity against HTLV-1 after subcutaneous (SC) or intranasal administration in a mice model. Additionally, to ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.07.069

    authors: Kabiri M,Sankian M,Hosseinpour M,Tafaghodi M

    更新日期:2018-10-05 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

  • Investigation of the parameters used in fused deposition modeling of poly(lactic acid) to optimize 3D printing sessions.

    abstract::This study assesses the feasibility of printing implantable devices using 3D printing Fused deposition modeling (FDM) technology. The influence of the deposition temperature, the deposition rate and the layer thickness on the printing process and the physical properties of the devices were evaluated. The filaments wer...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.05.008

    authors: Carlier E,Marquette S,Peerboom C,Denis L,Benali S,Raquez JM,Amighi K,Goole J

    更新日期:2019-06-30 00:00:00

  • Advances of nanosystems containing cyclodextrins and their applications in pharmaceuticals.

    abstract::For many years, researchers have worked with supramolecular structures involving inclusion complexes with cyclodextrins. These studies have resulted in new commercially available drugs which have been of great benefit. More recently, studies using nanoparticles, including nanosystems containing cyclodextrins, have bec...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2019.01.041

    authors: Menezes PDP,Andrade TA,Frank LA,de Souza EPBSS,Trindade GDGG,Trindade IAS,Serafini MR,Guterres SS,Araújo AAS

    更新日期:2019-03-25 00:00:00

  • Evaluation of novel lipid based formulation of β-Artemether and Lumefantrine in murine malaria model.

    abstract::The present investigation aims at formulating lipid based drug delivery system of β-Artemether and Lumefantrine and comparative pharmacological evaluation with innovator formulation. Commercial modified oil and indigenous natural fatty acids comprised the oily phase in developing lipidic formulation of β-Artemether an...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.07.033

    authors: Patil S,Suryavanshi S,Pathak S,Sharma S,Patravale V

    更新日期:2013-10-15 00:00:00

  • Studies on the in vitro ion exchange kinetics and thermodynamics and in vivo pharmacokinetics of the carbinoxamine-resin complex.

    abstract::The short half-life and bitter taste of carbinoxamine maleate2 (CAM) lead to poor compliance by pediatric patients who are being treated for allergic rhinitis. To address these issues, carbinoxamine-resin complexes3 (CRCs) were prepared by ion exchange and then coated with Kollicoat SR 30D. The resultant microencapsul...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119779

    authors: Deng Y,Wang T,Li J,Sun W,He H,Gou J,Wang Y,Yin T,Zhang Y,Tang X

    更新日期:2020-10-15 00:00:00

  • 1H NMR quantification of spray dried and spray freeze-dried saccharide carriers in dry powder inhaler formulations.

    abstract::Quantitative analysis using proton NMR (1H qNMR) has been employed in various areas such as pharmaceutical analysis (e.g., dissolution study), vaccines, natural products analysis, metabolites, and macrolide antibiotics in agriculture industry. However, it is not routinely used in the quantification of saccharides in d...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.03.030

    authors: Babenko M,Peron JR,Kaialy W,Calabrese G,Alany RG,ElShaer A

    更新日期:2019-06-10 00:00:00

  • A new topical formulation for psoriasis: development of methotrexate-loaded nanostructured lipid carriers.

    abstract::The aim of the present work was to develop and assess the potential of nanostructured lipid carriers (NLCs) loaded with methotrexate as a new approach for topical therapy of psoriasis. Methotrexate-loaded NLCs were prepared via a modified hot homogenization combined with ultrasonication techniques using either polysor...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.10.067

    authors: Pinto MF,Moura CC,Nunes C,Segundo MA,Costa Lima SA,Reis S

    更新日期:2014-12-30 00:00:00

  • Influence of in vitro release methods on assessment of tobramycin ophthalmic ointments.

    abstract::The current investigation was carried out to identify appropriate parameters for measuring the in vitro release of tobramycin (TOB) ophthalmic ointments and to evaluate the feasibility of in vitro release testing methods to assess the product performance. Drug release was assessed using USP dissolution apparatus IV an...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119938

    authors: Patere S,Newman B,Wang Y,Choi S,Mekjaruskul C,Jay M,Lu X

    更新日期:2020-11-30 00:00:00

  • Transcellular brain drug delivery: A review on recent advancements.

    abstract::The blood-brain barrier (BBB) has a pivotal role in maintaining brain homeostasis. It robustly protects the brain parenchyma against the invasion of irrelevant substances, which may interrupt its critical function. From a pharmaceutical point of view, such a barrier may cause central nervous system (CNS) disorders ref...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.119582

    authors: Azarmi M,Maleki H,Nikkam N,Malekinejad H

    更新日期:2020-08-30 00:00:00

  • A single-layer film coating for colon-targeted oral delivery.

    abstract::Most pH-sensitive polymer coating studies for potential colonic delivery systems apply multiple layers to protect the active agent from degradation and early release in the stomach and small intestine. This study designed a single-coat pH-sensitive layer for colon-specific delivery with a potential biopolymer, namely,...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.01.066

    authors: Nguyen MNU,Tran PHL,Tran TTD

    更新日期:2019-03-25 00:00:00

  • Superparamagnetic chitosan nanocomplexes for colorectal tumor-targeted delivery of irinotecan.

    abstract::Conventional chemotherapy is effective for metastatic tumors widely present in colorectal cancer patients; however, chemotherapy may cause severe systemic toxicity due to a lack of specificity towards cancer cells. Effective delivery systems that can enhance targeted drug delivery to the desired tumor site and simulta...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119394

    authors: Wu D,Zhu L,Li Y,Wang H,Xu S,Zhang X,Wu R,Yang G

    更新日期:2020-06-30 00:00:00

  • Hydrodynamics-induced variability in the USP apparatus II dissolution test.

    abstract::The USP tablet dissolution test is an analytical tool used for the verification of drug release processes and formulation selection within the pharmaceutical industry. Given the strong impact of this test, it is surprising that operating conditions and testing devices have been selected empirically. In fact, the flow ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.08.003

    authors: Baxter JL,Kukura J,Muzzio FJ

    更新日期:2005-03-23 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

  • Permeation of several drugs through keratinized epithelial-free membrane of hamster cheek pouch.

    abstract::The hamster cheek pouch mucosa was selected as a substitute for the human buccal mucosa in an in vitro permeation study. Considering that a keratinized layer is not present in the human buccal mucosa, keratinized epithelial-free hamster cheek pouch (KEF-membrane) was prepared by chemical splitting. To confirm the usef...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(98)00329-9

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

    更新日期:1999-01-15 00:00:00

  • Transdermal permeation of selegiline from hydrogel-membrane drug delivery systems.

    abstract::In the present work, we attempted to design a transdermal system for delivering selegiline using a hydrogel-based drug reservoir and a rate-controlling membrane (Solupor polyethylene membranes). The appearances of these preparations were evaluated by scanning electron microscopy (SEM), and the in vitro skin permeation...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.06.025

    authors: Fang JY,Hung CF,Chi CH,Chen CC

    更新日期:2009-10-01 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

  • In-line monitoring of pellet coating thickness growth by means of visual imaging.

    abstract::Coating thickness is the most important attribute of coated pharmaceutical pellets as it directly affects release profiles and stability of the drug. Quality control of the coating process of pharmaceutical pellets is thus of utmost importance for assuring the desired end product characteristics. A visual imaging tech...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.04.066

    authors: Oman Kadunc N,Sibanc R,Dreu R,Likar B,Tomaževič D

    更新日期:2014-08-15 00:00:00

  • Influence of monocaprin on the permeability of a diacidic drug BTA-243 across Caco-2 cell monolayers and everted gut sacs.

    abstract::This study explores the potential of the monoglyceride monocaprin as an enhancer of the epithelial permeability of the beta(3)-adrenoceptor agonist BTA-243, as an approach to improving the bioavailability of this drug. The permeabilities of BTA-243 and mannitol (paracellular marker) in Caco-2 cell monolayer and everte...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00343-5

    authors: Brown JR,Collett JH,Attwood D,Ley RW,Sims EE

    更新日期:2002-10-01 00:00:00

  • Enhanced stability of rubbery amylose-rich maize starch films plasticized with a combination of sorbitol and glycerol.

    abstract::Well known aging problems with rubbery starch films are the migration of plasticizer and increased crystallinity leading to embrittlement. The effects of a combination of sorbitol and glycerol used as plasticizers on mechanical, moisture permeability and solid-state properties of rubbery amylose maize starch (Hylon VI...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00585-9

    authors: Krogars K,Heinämäki J,Karjalainen M,Niskanen A,Leskelä M,Yliruusi J

    更新日期:2003-01-30 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

  • Protein aggregation--pathways and influencing factors.

    abstract::Proteins generally will tend to aggregate under a variety of environmental conditions in comparison with small drug molecules. The extent of aggregation is dependent on many factors that can be broadly classified as intrinsic (primary, secondary, tertiary or quaternary structure) or extrinsic (environment in which pro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2010.02.025

    authors: Wang W,Nema S,Teagarden D

    更新日期:2010-05-10 00:00:00

  • The uses of resveratrol for neurological diseases treatment and insights for nanotechnology based-drug delivery systems.

    abstract::Neurological disorders have been growing in recent years and are highly prevalent globally. Resveratrol (RES) is a natural product from plant sources such as grape skins. This compound has shown biological activity in many diseases, in particular, those that act on the central nervous system. The mechanism of action a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.119832

    authors: Fonseca-Santos B,Chorilli M

    更新日期:2020-08-30 00:00:00

  • Vascular targeting of doxorubicin using cationic liposomes.

    abstract::Tumor vessel has been recognized as an important target for anticancer therapy. Cationic liposomes have been shown to selectively target tumor endothelial cells, thus can potentially be used as a carrier for chemotherapy agents. In this study, cationic liposomes containing 20 mol% cationic lipid dimethyl dioctadecyl a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.01.003

    authors: Wu J,Lee A,Lu Y,Lee RJ

    更新日期:2007-06-07 00:00:00

  • Hydrogel based approaches for cardiac tissue engineering.

    abstract::Heart failure still represents the leading cause of death worldwide. Novel strategies using stem cells and growth factors have been investigated for effective cardiac tissue regeneration and heart function recovery. However, some major challenges limit their translation to the clinic. Recently, biomaterials have emerg...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.10.061

    authors: Saludas L,Pascual-Gil S,Prósper F,Garbayo E,Blanco-Prieto M

    更新日期:2017-05-25 00:00:00

  • Decylglucoside-based microemulsions for cutaneous localization of lycopene and ascorbic acid.

    abstract::Cutaneous delivery of combinations of antioxidants offers the possibility of enhanced protection against UV-radiation. In this study, we investigated the potential of sugar-based microemulsions containing monoglycerides to promote simultaneous cutaneous delivery of lycopene and ascorbic acid, and increase tissue antio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.016

    authors: Pepe D,Phelps J,Lewis K,Dujack J,Scarlett K,Jahan S,Bonnier E,Milic-Pasetto T,Hass MA,Lopes LB

    更新日期:2012-09-15 00:00:00

  • Targeted antifungal delivery system: beta-glucosidase sensitive nystatin-star poly(ethylene glycol) conjugate.

    abstract::A new targeted intravenous conjugate of nystatin with pentaerythritol poly(ethylene glycol)ether has been prepared and characterised (NY(4)-sPEG, M=25 160). The conjugate contains a beta-d-glucopyranoside molecular switch sensitive to beta-glucosidases (E.C.3.2.1.21), which are specifically present in the enzyme outfi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.10.034

    authors: Bílková E,Imramovský A,Buchta V,Sedlák M

    更新日期:2010-02-15 00:00:00

  • Characterization of alginate/poly-L-lysine particles as antisense oligonucleotide carriers.

    abstract::The gel forming characteristics of alginate in the presence of calcium ions and further crosslinking with poly-L-lysine led to the formation of sponge-like nano- and microparticles. The particle size was varied by adjusting the final concentrations of and proportions between the components. The region for particle for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00030-3

    authors: González Ferreiro M,Tillman L,Hardee G,Bodmeier R

    更新日期:2002-06-04 00:00:00