Chitosan-magnesium aluminum silicate composite dispersions: characterization of rheology, flocculate size and zeta potential.

Abstract:

:Composite dispersions of chitosan (CS), a positively charged polymer, and magnesium aluminum silicate (MAS), a negatively charged clay, were prepared and rheology, flocculate size and zeta potential of the CS-MAS dispersions were investigated. High and low molecular weights of CS (HCS and LCS, respectively) were used in this study. Moreover, the effects of heat treatment at 60 degrees C on the characteristics of the CS-MAS dispersions and the zeta potential of MAS upon addition of CS at different pHs were examined. Incorporation of MAS into CS dispersions caused an increase in viscosity and a shift of CS flow type from Newtonian to pseudoplastic flow with thixotropic properties. Heat treatment brought about a significant decrease in viscosity and hysteresis area of the composite dispersions. Microscopic studies showed that flocculation of MAS occurred after mixing with CS. The size and polydispersity index of the HCS-MAS flocculate were greater than those of the LCS-MAS flocculate. However, a narrower size distribution and the smaller size of the HCS-MAS flocculate were found after heating at 60 degrees C. Zeta potentials of the CS-MAS flocculates were positive and slightly increased with increasing MAS content. In the zeta potential studies, the negative charge of the MAS could be neutralized by the addition of CS. Increasing the pH and molecular weight of CS resulted in higher CS concentrations required to neutralize the charge of MAS. These findings suggest that the electrostatic interaction between CS and MAS caused a change in flow behavior and flocculation of the composite dispersions, depending on the molecular weight of CS. Heat treatment affected the rheological properties and the flocculate size of the composite dispersions. Moreover, pH of medium and molecular weight of CS influence the zeta potential of MAS.

journal_name

Int J Pharm

authors

Khunawattanakul W,Puttipipatkhachorn S,Rades T,Pongjanyakul T

doi

10.1016/j.ijpharm.2007.09.038

subject

Has Abstract

pub_date

2008-03-03 00:00:00

pages

227-35

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(07)00826-5

journal_volume

351

pub_type

杂志文章
  • Improved formulation of cationic solid lipid nanoparticles displays cellular uptake and biological activity of nucleic acids.

    abstract::Non-viral delivery using cationic solid lipid nanoparticles (SLNs) represents a useful strategy to introduce large DNA and RNA molecules to target cells. A careful selection of components and their amounts is critical to improve transfection efficiency. In this work, a selected and optimized formulation of SLNs was us...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.11.026

    authors: Fàbregas A,Prieto-Sánchez S,Suñé-Pou M,Boyero-Corral S,Ticó JR,García-Montoya E,Pérez-Lozano P,Miñarro M,Suñé-Negre JM,Hernández-Munain C,Suñé C

    更新日期:2017-01-10 00:00:00

  • On iontophoretic delivery enhancement: ionization and transport properties of lidocaine hydrochloride in aqueous propylene glycol.

    abstract::The ionization and transport properties of lidocaine hydrochloride (LidHCl) in aqueous propylene glycol (PG) containing 20% PG by weight was studied by means of electrical precision conductometry. For drug concentrations exceeding about 1.7 mM a slight formation of LidH(+)Cl(-) ion-pairs is indicated; ion-pair associa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00400-2

    authors: Karami K,Merclin N,Brounéus F,Beronius P

    更新日期:2000-05-15 00:00:00

  • Biological activity of heterologous murine interleukin-10 and preliminary studies on the use of a dextrin nanogel as a delivery system.

    abstract::Interleukin-10 (IL-10) is an anti-inflammatory cytokine, which active form is a non-covalent homodimer with two intramolecular disulphide bonds essential for its biological activity. A mutated form of murine IL-10 was successfully expressed in E. coli, recovered and purified from inclusion bodies. Its ability to reduc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.08.040

    authors: Carvalho V,Castanheira P,Faria TQ,Gonçalves C,Madureira P,Faro C,Domingues L,Brito RM,Vilanova M,Gama M

    更新日期:2010-11-15 00:00:00

  • A novel approach to avoid capping and/or lamination by application of external lower punch vibration.

    abstract::Capping as well as lamination are two common problems, which affect the resulting product quality of the tablet. Usually, capping and lamination occur during or after tablet manufacturing, and may therefore influence follow-up processes such as the coating. In this context, there is an urgent need for approaches to ov...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119195

    authors: Kalies A,Heinrich T,Leopold CS

    更新日期:2020-04-30 00:00:00

  • Stability and activity of hydroxyethyl starch-coated polyplexes in frozen solutions or lyophilizates.

    abstract::Despite their great potential, gene delivery polyplexes have a number of limitations, including their tendency for aggregation in vivo or upon storage. In previous studies, we could show that hydroxyethyl starch (HES)-decoration of polyplexes reduces aggregation in vitro and in vivo. The current study investigates the...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.04.020

    authors: Noga M,Edinger D,Wagner E,Winter G,Besheer A

    更新日期:2014-07-20 00:00:00

  • Strategies for maintaining the particle size of peptide DNA condensates following freeze-drying.

    abstract::The particle size of peptide DNA condensates were studied after freeze-drying and rehydration as a function of sugar excipient, concentration, pH, DNA concentration, and peptide condensing agent. In the absence of an excipient, freeze-dried 50 microg/ml AlkCWK(18) (iodoacetic acid alkylated Cys-Typ-Lys(18)) DNA conden...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00435-x

    authors: Kwok KY,Adami RC,Hester KC,Park Y,Thomas S,Rice KG

    更新日期:2000-08-10 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

  • A novel particle engineering technology: spray-freezing into liquid.

    abstract::Spray-freezing into liquid (SFL) is a novel particle engineering technology where a feed solution containing an active pharmaceutical ingredient (API) and pharmaceutical excipient(s) is atomized beneath the surface of a cryogenic liquid, such as liquid nitrogen. Intense atomization results from the impingement that oc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00154-0

    authors: Rogers TL,Hu J,Yu Z,Johnston KP,Williams RO 3rd

    更新日期:2002-08-21 00:00:00

  • Cyclodextrin containing biodegradable particles: from preparation to drug delivery applications.

    abstract::Cyclodextrins (CDs) offer a very broad spectrum of applications in diverse fields of drug delivery. They are a family of cyclic α-(1-4)-linked oligosaccharides of α-d-glucopyranose subunits forming a more hydrophobic central cavity and a hydrophilic outer shell. CDs bear cage like supramolecular structures, similar to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2013.12.004

    authors: Zafar N,Fessi H,Elaissari A

    更新日期:2014-01-30 00:00:00

  • Magnetic solid lipid nanoparticles in hyperthermia against colon cancer.

    abstract::A reproducible double emulsion/solvent evaporation procedure is developed to formulate magnetic solid lipid nanoparticles (average size≈180 nm) made of iron oxide cores embedded within a glyceryl trimyristate solid matrix. The physicochemical characterization of the nanocomposites ascertained the efficacy of the prepa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.03.005

    authors: Muñoz de Escalona M,Sáez-Fernández E,Prados JC,Melguizo C,Arias JL

    更新日期:2016-05-17 00:00:00

  • Manufacturing and characterization of long-acting levonorgestrel intrauterine systems.

    abstract::Mirena® is long-acting (5 years) contraceptive intrauterine device. It is composed of a hollow cylindrical drug reservoir (containing Levonorgestrel and polydimethylsiloxane), which is covered with a release rate controlling silicone membrane. This structure presents a manufacturing challenge and to date, there have b...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.09.004

    authors: Bao Q,Gu B,Price CF,Zou Y,Wang Y,Kozak D,Choi S,Burgess DJ

    更新日期:2018-10-25 00:00:00

  • Nanoparticle encapsulation of emulsion droplets.

    abstract::The overall aim of this study is to coat emulsion droplets with nanoparticles using a simple heterocoagulation process in aqueous dispersion and determine: the adsorption behavior and interfacial layer microstructure, droplet physical stability against flocculation and coalescence, and the release profile of a model l...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.06.044

    authors: Prestidge CA,Simovic S

    更新日期:2006-10-31 00:00:00

  • Development of a new system for prediction of drug absorption that takes into account drug dissolution and pH change in the gastro-intestinal tract.

    abstract::A new system for prediction of drug absorption that takes into account drug dissolution and pH change in the gastro-intestinal tract was developed. In this new system, a drug (solid form) is added into a drug-dissolving vessel (pH 1.0) and the dissolved drug is transferred to a pH adjustment vessel (pH 6.0). Then the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00663-9

    authors: Kobayashi M,Sada N,Sugawara M,Iseki K,Miyazaki K

    更新日期:2001-06-19 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

  • 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 ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.05.045

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

    更新日期:2019-07-20 00:00:00

  • Graphene oxide crosslinked-zein nanofibrous scaffolds for prominent Cu-adsorption as tissue regeneration promoters in diabetic rats: Nanofibers optimization and in vivo assessment.

    abstract::Diabetic ulcers are prone to bacterial contamination and can severely affect patient's quality of life. This study is first report to explore copper-grafted graphene oxide-crosslinked zein scaffolds (Cu-GZS) for promoting cutaneous excision wounds healing as a promising therapeutic modality in diabetic male-rats. Cu-G...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119919

    authors: El-Lakany SA,Kamoun EA,Abd-Elhamid AI,Aly RG,Samy WM,Elgindy NA

    更新日期:2020-11-30 00:00:00

  • Combinatorial design of passive drug delivery platforms.

    abstract::We introduce a novel computational approach to designing passive drug delivery systems based on porous materials such as hydrogels. Our approach uses three tools: a method to establish the exact release pattern from all possible loading sites inside a given hydrogel; a method to generate a large number of hydrogel str...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.02.029

    authors: Casault S,Kenward M,Slater GW

    更新日期:2007-07-18 00:00:00

  • Comparison of the IV pharmacokinetics in sheep of miconazole-cyclodextrin solutions and a micellar solution.

    abstract::The pharmacokinetics of miconazole were studied after intravenous administration to six sheep (4 mg/kg) of three aqueous solutions: a marketed micellar solution containing polyoxyl-35 castor oil (Daktarin IV(R)) was compared with two solutions both containing 50 mM lactic acid and a cyclodextrin derivative (100 mM HP-...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(98)00403-7

    authors: Piel G,Evrard B,Van Hees T,Delattre L

    更新日期:1999-03-25 00:00:00

  • smartPearls - Novel physically stable amorphous delivery system for poorly soluble dermal actives.

    abstract::Dermally applied poorly soluble actives whether in cosmetics or pharmaceuticals show insufficient skin penetration. Especially actives being insoluble in both phases of dermal vehicles, i.e. water and oil have no or less real effect. An approach to overcome this obstacle is the use of amorphous actives instead of the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2018.11.018

    authors: Müller RH,Hespeler D,Jin N,Pyo SM

    更新日期:2019-01-30 00:00:00

  • Serum-stable, long-circulating paclitaxel-loaded colloidal carriers decorated with a new amphiphilic PEG derivative.

    abstract::The paper describes sterically stabilized lipid nanocapsules (LNC) and multilamellar liposomes (MLV) coated using a new amphiphilic conjugate of PEG(2000) with a 2-alkyl-lipoamino acid (LAA). A complement activation assay (CH50) and uptake experiments by THP-1 macrophage cells were used to assess in vitro the effectiv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.01.038

    authors: Basile L,Passirani C,Huynh NT,Béjaud J,Benoit JP,Puglisi G,Pignatello R

    更新日期:2012-04-15 00:00:00

  • Evaluation of sorption capacity of antibiotics and antibacterial properties of a cyclodextrin-polymer functionalized hydroxyapatite-coated titanium hip prosthesis.

    abstract::Infection still present as one of common complications after total hip replacement (∼2.5%), which may cause serious outcomes. For preventing such risk, loading antibiotics onto implants for increasing local drug concentration at targeted sites could be a solution. This study aims at modifying the surface of hydroxyapa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.10.026

    authors: Taha M,Chai F,Blanchemain N,Neut C,Goube M,Maton M,Martel B,Hildebrand HF

    更新日期:2014-12-30 00:00:00

  • Spherical agglomerates of lactose with enhanced mechanical properties.

    abstract::The aim of this study was to prepare spherical agglomerates of lactose and to evaluate their physicochemical properties, flow properties, particle friability and compaction properties, and to compare them to commercially available types of lactose for direct compression (spray-dried, granulated and anhydrous β-lactose...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.11.040

    authors: Lamešić D,Planinšek O,Lavrič Z,Ilić I

    更新日期:2017-01-10 00:00:00

  • Solid lipid nanoparticles as drug carriers for topical glucocorticoids.

    abstract::Recent investigations both in vitro and in human subjects proved the benefit/risk ratio of prednicarbate (PC) to exceed those of halogenated topical glucocorticoids about 2-fold. To obtain a further highly desired increase by drug targeting to viable epidermis, PC was incorporated into solid lipid nanoparticles (SLN)....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00413-5

    authors: Maia CS,Mehnert W,Schäfer-Korting M

    更新日期:2000-03-10 00:00:00

  • Evolution of Cyclodextrin Nanosponges.

    abstract::Cyclodextrin-based nanosponges (CD-NSs) are insoluble, highly cross-linked 3D network polymers used in several scientific and technological fields, the main area of investigation concerns the pharmaceutical applications, in which CD-NSs have been mostly employed as drug delivery systems. CD-NSs can be generally groupe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.06.072

    authors: Caldera F,Tannous M,Cavalli R,Zanetti M,Trotta F

    更新日期:2017-10-15 00:00:00

  • Tensile and shear methods for measuring strength of bilayer tablets.

    abstract::Both shear and tensile measurement methods have been used to quantify interfacial bonding strength of bilayer tablets. The shear method is more convenient to perform, but reproducible strength data requires careful control of the placement of tablet and contact point for shear force application. Moreover, data obtaine...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.010

    authors: Chang SY,Li JX,Sun CC

    更新日期:2017-05-15 00:00:00

  • Properties of polyethylene glycol 660 12-hydroxy stearate at a triglyceride/water interface.

    abstract::This study proposed a method to understand the surfactant role in the first step of the formulation of a novel generation of lipidic nanocapsules. A dynamic rheological protocol was applied using a pendant drop tensiometer in order to determine the interfacial properties of the initial mixture implied in the first for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00144-8

    authors: Heurtault B,Saulnier P,Pech B,Proust JE,Benoît JP

    更新日期:2002-08-21 00:00:00

  • Preparation of 4-arm star PELA and its encapsulation of rotavirus for drug delivery.

    abstract::A relatively high molecular weight of 4-arm star PELA was obtained by ring-opening polymerization of l-lactic acid O-carboxyanhydride with 4-arm-PEG in the presence of DMAP as an initiator. The results via(1)H NMR and (13)C NMR show that the end of the star PELA chain is a hydroxyl group and the central core is a PEG ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.05.074

    authors: Qingcong L,Xiaoxia P,Hongli L,Minglong Y

    更新日期:2015-08-01 00:00:00

  • Effects of non-ionic surfactants as permeation enhancers towards piroxicam from the poloxamer gel through rat skins.

    abstract::The enhancing effects of non-ionic surfactants on the permeation of piroxicam from the poloxamer gels were evaluated using Franz diffusion cells fitted with excised rat skins. The effectiveness of penetration enhancers, the ratio of piroxicam flux in the presence or absence of enhancers, was defined as the enhancement...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00699-8

    authors: Shin SC,Cho CW,Oh IJ

    更新日期:2001-07-17 00:00:00

  • Correlation of laboratory and production freeze drying cycles.

    abstract::The purpose of this study was to develop the correlation of cycle parameters between a laboratory and a production freeze-dryer. With the established correlation, key cycle parameters obtained using a laboratory dryer may be converted to those for a production dryer with minimal experimental efforts. In order to devel...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.06.022

    authors: Kuu WY,Hardwick LM,Akers MJ

    更新日期:2005-09-30 00:00:00

  • Optimized conditions of bio-mimetic artificial membrane permeation assay.

    abstract::Effects of pH and co-solvents on the bio-mimetic artificial membrane permeation assay were investigated to determine the optimal conditions for the prediction of oral absorption. The permeability (P(am)) of 33 structurally diverse drugs to the PC/PE/PS/PI/CHO/1,7-octadiene membrane system (bio-mimetic lipid (BML) memb...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00845-6

    authors: Sugano K,Hamada H,Machida M,Ushio H,Saitoh K,Terada K

    更新日期:2001-10-09 00:00:00