Poly(ε-caprolactone)/triclosan loaded polylactic acid nanoparticles composite: A long-term antibacterial bionanocomposite with sustained release.

Abstract:

:In this study, the antibacterial bionanocomposites of poly(ε-caprolactone) (PCL) with different concentrations of triclosan (TC) loaded polylactic acid (PLA) nanoparticles (30wt% triclosan) (LATC30) were fabricated via a melt mixing process in order to lower the burst release of PCL and to extend the antibacterial activity during its performance. Due to the PLA's higher glass transition temperature (Tg) and less flexibility compared with PCL; the PLA nanoparticles efficiently trapped the TC particles, reduced the burst release of TC from the bionanocomposites; and extended the antibacterial property of the samples up to two years. The melt mixing temperature was adjusted to a temperature lower than the melting point of LATC30 nanoparticles; therefore, these nanoparticles were dispersed in the PCL matrix without any chemical reaction and/or drug extraction. The sustained release behavior of TC from PCL remained unchanged since no significant changes occurred in the samples' crystallinity compared with that in the neat PCL. The elastic moduli of samples were enhanced once LATC30 is included. This is necessary since the elastic modulus is decreased with water absorption. The rheological behaviors of samples showed appropriate properties for melt electro-spinning. A stable process was established as the relaxation time of the bionanocomposites was increased. The hydrophilic properties of samples were increased with increasing LATC30. The proliferation rate of the fibroblast (L929) cells was enhanced as the content of nanoparticles was increased. A system similar to this could be implemented to prepare long-term antibacterial and drug delivery systems based on PCL and various low molecular weight drugs. The prepared bionanocomposites are considered as candidates for the soft connective tissue engineering and long-term drug delivery.

journal_name

Int J Pharm

authors

Kaffashi B,Davoodi S,Oliaei E

doi

10.1016/j.ijpharm.2016.05.009

subject

Has Abstract

pub_date

2016-07-11 00:00:00

pages

10-21

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(16)30376-3

journal_volume

508

pub_type

杂志文章
  • Improved photodynamic activity of porphyrin loaded into nanoparticles: an in vivo evaluation using chick embryos.

    abstract::Hydrophobic porphyrins are potentially interesting molecules for the photodynamic therapy (PDT) of solid cancers or ocular vascularization diseases. Their pharmaceutical development is, however, hampered by their lipophilicity, which renders formulation difficult especially when intravenous administration is needed. E...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.07.029

    authors: Vargas A,Pegaz B,Debefve E,Konan-Kouakou Y,Lange N,Ballini JP,van den Bergh H,Gurny R,Delie F

    更新日期:2004-11-22 00:00:00

  • Robustness testing, using experimental design, of a flow-through dissolution method for a product where the actives have markedly differing solubility properties.

    abstract::The use of experimental design for the robustness testing of a flow-through dissolution method (Ph Eur/USP Apparatus 4) for atovaquone, one of the drug substances in a dual-active anti-malarial tablet formulation, Malarone tablets, is described. This procedure was developed to overcome the suppression of the atovaquon...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00509-3

    authors: Bloomfield MS,Butler WC

    更新日期:2000-09-25 00:00:00

  • Pharmacokinetics of Huperzine A after transdermal and oral administration in beagle dogs.

    abstract::Comparison of single and multiple dose pharmacokinetics between patches and conventional tablets of Huperzine A (Hup-A) was performed in beagle dogs to evaluate the patches' controlled drug release characteristics in vivo, a newly developed transdermal system for treatment of Alzheimer disease. Results showed that tra...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.01.007

    authors: Ye JC,Zeng S,Zheng GL,Chen GS

    更新日期:2008-05-22 00:00:00

  • Flavonoid nanocrystals produced by ARTcrystal®-technology.

    abstract::ARTcrystal(®)-technology is a novel technique for a more efficient production of nanocrystals. It consists of a high speed stirring (HSS) step as pre-milling and subsequent high pressure homogenization (HPH) at reduced pressure and cycle numbers. In this study, three antioxidants, rutin, hesperidin and apigenin, were ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.11.008

    authors: Scholz P,Keck CM

    更新日期:2015-03-30 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

  • Folic acid transport via high affinity carrier-mediated system in human retinoblastoma cells.

    abstract::The primary objective of this study was to investigate the expression of a specialized carrier-mediated system for folic acid and to delineate its uptake mechanism and intracellular trafficking in a human derived retinoblastoma cell line (Y-79). Uptake of [3H]Folic acid was determined at various concentrations, pH, te...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.12.008

    authors: Kansara V,Paturi D,Luo S,Gaudana R,Mitra AK

    更新日期:2008-05-01 00:00:00

  • Combined effects of iontophoretic and chemical enhancement on drug delivery. II. Transport across human and murine skin.

    abstract::This paper reports measurements of the release characteristics of the model drug salbutamol from a liquid crystalline vehicle across both human and hairless murine skin in vitro. The use of oleic acid and iontophoresis as penetration enhancement techniques, used separately and simultaneously, was also investigated. Ov...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.04.004

    authors: Nolan LM,Corish J,Corrigan OI,Fitzpatrick D

    更新日期:2007-08-16 00:00:00

  • Understanding Flow Properties of Mannitol Powder at a Range of Temperature and Humidity.

    abstract::Inadequate flowability of powders in industries during handling can cause many problems. For example, lack of flow from hoppers, poor tablet weight consistency, and low production rate in tableting. Many factors are known to commonly affect flow properties of powders, such as temperature, humidity and conditioning dur...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2021.120244

    authors: Salehi H,Karde V,Hajmohammadi H,Dissanayake S,Larsson SH,Y Y Heng J,Bradley M

    更新日期:2021-01-20 00:00:00

  • Ligand anchored dendrimers based nanoconstructs for effective targeting to cancer cells.

    abstract::Dendrimers are considered versatile carriers especially for the treatment of diseases like cancer, AIDS, malaria etc. Cancer is a worldwide threat particularly in developing countries. A breakthrough research in this regard is a prime requirement. In the present study, folic acid was conjugated to fifth generation pol...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.04.002

    authors: Gupta U,Dwivedi SK,Bid HK,Konwar R,Jain NK

    更新日期:2010-06-30 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

  • Preparation and characterization of lipid nanoparticle/pDNA complexes for STAT3 downregulation and overcoming chemotherapy resistance in lung cancer cells.

    abstract::Developments in the field of molecular oncology have revealed that resistance to chemotherapeutics is acqured through several mechanisms including overexpression of common oncogenic proteins. Signal Transducer and Activator of Transcription 3 (STAT3) is one of these oncogenes that is overexpressed in many cancer types...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.034

    authors: Kotmakçı M,Çetintaş VB,Kantarcı AG

    更新日期:2017-06-15 00:00:00

  • Degradation kinetics of 4-dedimethylamino sancycline, a new anti-tumor agent, in aqueous solutions.

    abstract::The kinetics of degradation of the new anti-tumor drug, 4-dedimethylamino sancycline (col-3) in aqueous solution at 25oC were investigated by high-pressure liquid chromatography (HPLC) over the pH-range of 2-10. The influences of pH, buffer concentration, light, temperature, and some additives on the degradation rate ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(98)00417-7

    authors: Pinsuwan S,Alvarez-Núñez FA,Tabibi ES,Yalkowsky SH

    更新日期:1999-04-20 00:00:00

  • A new expanded solubility parameter approach.

    abstract::The partial or Hansen solubility parameters (HSP) are important properties of the various substances and very useful tools for the selection of their solvents or the prediction of their behaviour in numerous applications. Their design and evaluation relies on the basic rule of "similarity matching" for solubility. The...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.01.001

    authors: Stefanis E,Panayiotou C

    更新日期:2012-04-15 00:00:00

  • Evaluation of the effect of rifampicin on the biophysical properties of the membranes: significance for therapeutic and side effects.

    abstract::This work aims to study the biophysical interactions of rifampicin (RIF) with three-dimensional macrophage membrane models, under environments with physiological and pathological relevance. The interaction of RIF with liposomes formed by 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in different pH values (i.e., ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.03.005

    authors: Pinheiro M,Pisco S,Silva AS,Nunes C,Reis S

    更新日期:2014-05-15 00:00:00

  • A novel approach to oral iron delivery using ferrous sulphate loaded solid lipid nanoparticles.

    abstract::Iron (Fe) loaded solid lipid nanoparticles (SLN's) were formulated using stearic acid and iron absorption was evaluated in vitro using the cell line Caco-2 with intracellular ferritin formation as a marker of iron absorption. Iron loading was optimised at 1% Fe (w/w) lipid since an inverse relation was observed betwee...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.08.070

    authors: Zariwala MG,Elsaid N,Jackson TL,Corral López F,Farnaud S,Somavarapu S,Renshaw D

    更新日期:2013-11-18 00:00:00

  • Surface dissolution UV imaging for characterization of superdisintegrants and their impact on drug dissolution.

    abstract::Superdisintegrants are a key excipient used in immediate release formulations to promote fast tablet disintegration, therefore understanding the impact of superdisintegrant variability on product performance is important. The current study examined the impact of superdisintegrant critical material attributes (viscosit...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119080

    authors: Zarmpi P,Flanagan T,Meehan E,Mann J,Fotaki N

    更新日期:2020-03-15 00:00:00

  • Tramadol sensing in non-invasive biological fluids using a voltammetric electronic tongue and an electrochemical sensor based on biomimetic recognition.

    abstract::Tramadol (TRA) is a weak opioid analgesic, prescribed to relieve mild to moderately severe pain. However, side effects of TRA overdoses, including vomiting, depression, tachycardia, convulsions, morbidity and mortality are often reported. In this study, an electrochemical sensor based on molecularly imprinted conducti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120114

    authors: Diouf A,Aghoutane Y,Burhan H,Sen F,Bouchikhi B,El Bari N

    更新日期:2021-01-25 00:00:00

  • Acid-base interactions in amorphous solid dispersions of lumefantrine prepared by spray-drying and hot-melt extrusion using X-ray photoelectron spectroscopy.

    abstract::This study investigates drug-excipient interactions in amorphous solid dispersions (ASDs) of the model basic compound lumefantrine (LMN), with five acidic polymers. X-ray photoelectron spectroscopy (XPS) was used to measure the extent of the protonation of the tertiary amine in LMN by the five acidic polymers. The ext...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.06.126

    authors: Song Y,Zemlyanov D,Chen X,Su Z,Nie H,Lubach JW,Smith D,Byrn S,Pinal R

    更新日期:2016-12-05 00:00:00

  • Stability of luciferase plasmid entrapped in cationic bilayer vesicles.

    abstract::Characteristics and physical stability of luciferase plasmid (pLuc) entrapped in cationic bilayer vesicles prepared from various molar ratios of amphiphiles (DPPC, Tween61 or Span60), cholesterol (Chol) and cationic charge lipid (DDAB) were investigated. The cationic liposomes were composed of DPPC/Chol/DDAB in the mo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.01.001

    authors: Manosroi A,Thathang K,Werner RG,Schubert R,Manosroi J

    更新日期:2008-05-22 00:00:00

  • Quaternary polymethacrylate-magnesium aluminum silicate films: molecular interactions, mechanical properties and tackiness.

    abstract::The aim of this study was to investigate the impact of the addition of magnesium aluminum silicate (MAS), a natural clay, on the properties of polymeric films based on quaternary polymethacrylates (QPMs). Two commercially available aqueous QPM dispersions were studied: Eudragit(®) RS 30D and Eudragit(®) RL 30D (the dr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.10.016

    authors: Rongthong T,Sungthongjeen S,Siepmann J,Pongjanyakul T

    更新日期:2013-12-15 00:00:00

  • Prolongation of residence time of liposome by surface-modification with mixture of hydrophilic polymers.

    abstract::The objective of this study is to evaluate the biodistribution characteristics of liposomes surface-modified with the mixture of polyethylene glycol (PEG) and polyvinyl alcohol (PVA) as a drug carrier for passive targeting of drugs. The liposomes (egg phosphatidylcholine:cholesterol=55:40, molar ratio) modified with b...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.04.004

    authors: Shehata T,Ogawara K,Higaki K,Kimura T

    更新日期:2008-07-09 00:00:00

  • Rhamnolipids as emulsifying agents for essential oil formulations: antimicrobial effect against Candida albicans and methicillin-resistant Staphylococcus aureus.

    abstract::This work examines the influence of essential oil composition on emulsification with rhamnolipids and their use as therapeutic antimicrobial agents against two opportunistic pathogens, methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans. Rhamnolipids, produced by Pseudomonas aeruginosa, with waste ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.09.039

    authors: Haba E,Bouhdid S,Torrego-Solana N,Marqués AM,Espuny MJ,García-Celma MJ,Manresa A

    更新日期:2014-12-10 00:00:00

  • Determination of bisphenol A in water and the medical devices used in hemodialysis treatment.

    abstract::Bisphenol A (BPA) is an endocrine disruptor found in food containers and plastic beverages and also in medical devices such as dialyzers. The aim of this study is while taking into account the BPA originating in medical devices and the water used in dialysate production, to provide the first published investigation of...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.03.003

    authors: Bacle A,Thevenot S,Grignon C,Belmouaz M,Bauwens M,Teychene B,Venisse N,Migeot V,Dupuis A

    更新日期:2016-05-30 00:00:00

  • Liposome surface charge influence on skin penetration behaviour.

    abstract::Vesicular systems have shown their ability to increase dermal and transdermal drug delivery. Their mechanism of drug transport into and through the skin has been investigated but remains a much debated question. Several researchers have outlined that drug penetration can be influenced by modifying the surface charge o...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.03.049

    authors: Gillet A,Compère P,Lecomte F,Hubert P,Ducat E,Evrard B,Piel G

    更新日期:2011-06-15 00:00:00

  • Advanced topical formulations (ATF).

    abstract::Topical formulations aim to target the skin for a variety of cosmetic, protective or therapeutic needs. Despite the use of creams and ointments over the millennia, the bioavailability of actives from topical preparations remains quite low, often not exceeding 1-2% of the applied dose. In this review we examine the rea...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.05.065

    authors: Hadgraft J,Lane ME

    更新日期:2016-11-30 00:00:00

  • Advances and challenges in nanocarriers and nanomedicines for veterinary application.

    abstract::To ensure success in the development and manufacturing of nanomedicines requires forces of an interdisciplinary team that combines medicine, engineering, chemistry, biology, material and pharmaceutical areas. Numerous researches in nanotechnology applied to human health are available in the literature. Althought, the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.119214

    authors: Carvalho SG,Araujo VHS,Dos Santos AM,Duarte JL,Silvestre ALP,Fonseca-Santos B,Villanova JCO,Gremião MPD,Chorilli M

    更新日期:2020-04-30 00:00:00

  • The solubility, permeability and the dose as key factors in formulation development for oral lipophilic drugs: Maximizing the bioavailability of carbamazepine with a cosolvent-based formulation.

    abstract::The purpose of this research was to investigate drug dose, solubility, permeability, and their interplay, as key factors in oral formulation development for lipophilic drugs. A PEG400-based formulation was studied for five doses of the lipophilic drug carbamazepine, accounting for biorelevant dissolution of the dose i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119307

    authors: Fine-Shamir N,Beig A,Miller JM,Dahan A

    更新日期:2020-05-30 00:00:00

  • Enhanced oral bioavailability of docetaxel in rats by four consecutive days of pre-treatment with curcumin.

    abstract::As with many other anti-cancer agents, docetaxel is a substrate for ATP-binding cassette transporters such as P-glycoprotein and its metabolism is mainly catalysed by CYP3A. In order to improve the oral bioavailability of docetaxel, a component of turmeric, curcumin, which can down-regulate the intestinal P-glycoprote...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.08.015

    authors: Yan YD,Kim DH,Sung JH,Yong CS,Choi HG

    更新日期:2010-10-31 00:00:00

  • Lipase degradation of Dynasan 114 and 116 solid lipid nanoparticles (SLN)--effect of surfactants, storage time and crystallinity.

    abstract::In vivo drug release from solid lipid nanoparticles (SLN) takes place by diffusion and degradation of the lipid matrix. SLN with different degree of crystallinity were prepared to study the effect of crystallinity on the degradation velocity. These SLN were produced by using glycerides with different length of fatty a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00035-2

    authors: Olbrich C,Kayser O,Müller RH

    更新日期:2002-04-26 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