Electrophoretic ink using urea-formaldehyde microspheres.

Abstract:

:A kind of electronic ink, which is supported on indium-tin-oxide (ITO) glass before polymerization, is prepared using urea and formaldehyde resin as wall materials, in which TiO(2) modified with PMMA are dispersed in tetrachloroethylene (TCE) using a mixture of oil blue dyes and charge control additive (span80). Rotary viscometer, Fourier transform infrared spectroscopy (FT-IR) and optical microscopy are used to characterize the particles, respectively. The electrophoretic mobility of the microcapsules to electric field is also investigated with two parallel electrodes.

journal_name

J Microencapsul

authors

Wang YT,Zhao XP,Wang DW

doi

10.1080/02652040600788197

subject

Has Abstract

pub_date

2006-11-01 00:00:00

pages

762-8

issue

7

eissn

0265-2048

issn

1464-5246

pii

JK225QQ862843715

journal_volume

23

pub_type

杂志文章
  • Formulation, characterization and evaluation of rotavirus encapsulated PLA and PLGA particles for oral vaccination.

    abstract::Polylactide (PLA) and polylactide-co-glycolide (PLGA) particles entrapping rotavirus (strain SA11) were formulated using a solvent evaporation technique. To minimize denaturation of viral antigen during the emulsification process, serum albumin was used as a stabilizer. Use of NaHCO(3) and sucrose during the primary e...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040802211709

    authors: Nayak B,Panda AK,Ray P,Ray AR

    更新日期:2009-03-01 00:00:00

  • Development of a new delivery system consisting in 'drug-in cyclodextrin-in PLGA nanoparticles'.

    abstract::A combined approach based on drug cyclodextrin (CD) complexation and loading into PLGA nanoparticles (NP) has been developed to improve oxaprozin therapeutic efficiency. This strategy exploits the solubilizing and stabilizing properties of CDs and the prolonged-release and targeting properties of PLGA NPs. Drug-loaded...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652040903515508

    authors: Mura P,Maestrelli F,Cecchi M,Bragagni M,Almeida A

    更新日期:2010-01-01 00:00:00

  • Polymethylene-co-guanidine based capsules: a mechanistic study of the formation using alginate and cellulose sulphate.

    abstract::Capsules have been prepared based on a polyanion blend of sodium alginate and sodium cellulose sulphate, gelled in the presence of calcium chloride and sodium chloride. In a second step a membrane was formed via the addition of polymethylene-co-guanidine (PMCG), an oligocation. A mechanistic study examined the influen...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040601058418

    authors: Renken A,Hunkeler D

    更新日期:2007-02-01 00:00:00

  • Formation of essential oil containing microparticles comprising a hydrogenated vegetable oil matrix and characterisation thereof.

    abstract::Microparticles with different essential oil concentrations 0, 75, 150, 225 and 300 gkg-1, (g of essential oil per kg of microparticles), were produced by dispersing the essential oils within a hydrogenated vegetable fat matrix and forming spherical solid particles by spray-chilling. Size distribution, flowability, sur...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652048.2018.1515998

    authors: Gottschalk P,Brodesser B,Poncelet D,Jaeger H,Rennhofer H,Cole S

    更新日期:2018-09-01 00:00:00

  • Fabrication and characterisation of 2NDPA-loaded poly(lactide-co-glycolide) (PLG) microspheres for explosive safety.

    abstract::We demonstrate the microencapsulation of a double-base (DB) rocket propellant stabiliser, 2-nitrodiphenylamine (2-NDPA), that can potentially increase the shelf life of DB rocket propellants. Poly(lactide-co-glycolide) (PLG) microspheres loaded with 2-NDPA were prepared using the oil-in-water emulsion technique. The m...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2012.668956

    authors: Shorty M,Singh S,Jebrail FF,Andrews MJ

    更新日期:2012-01-01 00:00:00

  • N-lauroyl chitosan surface-modified PLGA nanoparticles as carrier for adriamycin to overcome cancer drug resistance.

    abstract::N-lauroyl chitosan (NLCS) conjugates with different degrees of substitution (DS) of lauroyl group were synthesized and used to prepare surface modified poly(lactic-co-glycolic) acid (NLCS-PLGA) nanoparticles via hydrophobic interaction and ionic bond force. NLCS-PLGA nanoparticles had spherical shape with shell-core s...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2013.824515

    authors: Li J,Zhou P,Wang Y,Chen H,Zhang C,Li R,Yang X,Wang Y

    更新日期:2014-01-01 00:00:00

  • Delivery of rSLPI in a liposomal carrier for inhalation provides protection against cathepsin L degradation.

    abstract::Secretory leukocyte protease inhibitor (SLPI) is an endogenous serine protease inhibitor that protects the lungs from excessive tissue damage caused by leukocyte proteases released during inflammation. Recombinant SLPI (rSLPI) has shown potential as a treatment for inflammatory lung conditions. To date, its clinical a...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040802466535

    authors: Gibbons AM,McElvaney NG,Taggart CC,Cryan SA

    更新日期:2009-09-01 00:00:00

  • Cationic lipid emulsions as potential bioadhesive carriers for ophthalmic delivery of palmatine.

    abstract::Palmatine (PM) is a potent anti-infective agent used to treat eye diseases. However, PM is less effective for ocular application due to short residence time within the eyes. This study aimed to develop a cationic lipid emulsions (CLEs) for ophthalmic delivery of PM and evaluate its suitability in infection treatment. ...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652048.2016.1248512

    authors: Yin J,Xiang C,Lu G

    更新日期:2016-12-01 00:00:00

  • Emulsification preparation of calcium alginate beads in the presence of sequesterant.

    abstract::A biocompatible emulsification method has been developed for microencapsulation of live cells and enzymes within a calcium alginate matrix. Fabrication of alginate beads was achieved by premixing a sequestering agent (sodium polyphosphate) and the calcium source (calcium sulphate) with the hydrogel monomer prior to th...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652049509010294

    authors: Monshipouri M,Price RR

    更新日期:1995-05-01 00:00:00

  • A novel microparticulate vaccine for melanoma cancer using transdermal delivery.

    abstract::In this study, we formulated a microparticulate melanoma cancer vaccine via the transdermal route. The vaccine was delivered using microneedle-based Dermaroller® which is available for cosmetic purposes. Unlike subcutaneous injections, administration using microneedles is painless and in general can increase the perme...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2011.559287

    authors: Bhowmik T,D'Souza B,Shashidharamurthy R,Oettinger C,Selvaraj P,D'Souza MJ

    更新日期:2011-01-01 00:00:00

  • Microencapsulation of drugs by the coacervation technique using ethylcellulose and acrylate-methacrylate copolymer as wall materials.

    abstract::In this study, ethylcellulose and acrylate-methacrylate copolymer (Eudragit RL 100, Eudragit RS 100) membranes were prepared by using appropriate types and amounts of plasticizers. Thirty percent and 20% of triacetin based on polymer weight were found to be appropriate plasticizers for ethylcellulose membranes and acr...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652049609026048

    authors: Nimmannit U,Suwanpatra N

    更新日期:1996-11-01 00:00:00

  • Liposomes as cyclosporin A carriers: positively charged lecithin-cholesterol liposomes associated with cyclosporin A do not inhibit biosynthesis of mitochondrial polyglycerophosphatides and microsomal phosphatidylinositol.

    abstract::Phosphatidylcholine (from egg yolk)-cholesterol-stearylamine (7:2:2.25, molar ratio) liposomes when associated with cyclosporin A (phosphatidylcholine:cyclosporin A = 2:0.07, molar ratio) do not inhibit significantly the biosynthesis of [3H]polyglycerophosphatides and [3H]phosphatidylinositol in mitochondrial and micr...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048909098018

    authors: Stuhne-Sekalec L,Stanacev NZ

    更新日期:1989-04-01 00:00:00

  • Development of a new solid lipid nanoparticle formulation containing retinoic acid for topical treatment of acne.

    abstract::The development of solid lipid nanoparticles (SLN) containing all-trans retinoic acid (RA) is an interesting approach to topical treatment of acne. SLN has potential for controlled release and follicular penetration, which can reduce adverse effects in comparison with conventional formulations. However, the encapsulat...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040701288519

    authors: Castro GA,Oréfice RL,Vilela JM,Andrade MS,Ferreira LA

    更新日期:2007-08-01 00:00:00

  • Preparation of microcapsules from complex coacervation of Gantrez-gelatin. III. Bioavailability of nitrofurantoin microcapsules.

    abstract::The bioavailability of marketed nitrofurantoin capsules was compared to capsules filled with Gantrez-gelatin nitrofurantoin microcapsules of a core:coat ratio of 1:2. The collective results obtained from the analysis of urine samples of five volunteers indicated that nitrofurantoin microcapsules provided a prolonged r...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048809036727

    authors: Mortada SA,el Egaky MA,Motawi AM,el Khodery KA

    更新日期:1988-10-01 00:00:00

  • Labile conjugation of a hydrophilic drug to PLA oligomers to modify a drug delivery system: cephradin in a PLAGA matrix.

    abstract::The physical entrapment of a hydrophilic drug within degradable microspheres is generally difficult because of poor entrapment yield and/or fast release, depending on the microsphere fabrication method. In order to counter the effects of drug hydrophilicity, it is proposed to covalently attach the drug to lactic acid ...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/026520400417667

    authors: Ustariz-Peyret C,Coudane J,Vert M,Kaltsatos V,Boisramené B

    更新日期:2000-09-01 00:00:00

  • Surface characterization by atomic force microscopy of sterilized PLGA microspheres.

    abstract::Atomic force microscopy (AFM) is recognized a suitable and powerful technique for surface and morphological analysis. Even if until now this technique has not been frequently used in the pharmaceutical field, it can contribute to an accurate morphologic characterization of microspheres and nanospheres. In this work, a...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040500435220

    authors: Dorati R,Patrini M,Perugini P,Pavanetto F,Stella A,Modena T,Genta I,Conti B

    更新日期:2006-03-01 00:00:00

  • Impact of microparticle formulation approaches on drug burst release: a level A IVIVC.

    abstract:AIM:To study the effect of poly(d,l-lactic-co-glycolic acid) (PLGA) microparticles (MPs) preparation techniques on particle physical characterization with special emphasis on burst drug release. METHODS:A basic drug clozapine was used in combination with acid-terminated PLGA. Two approaches for MP preparation were com...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2014.913724

    authors: Ishak RA,Mortada ND,Zaki NM,El-Shamy Ael-H,Awad GA

    更新日期:2014-01-01 00:00:00

  • Formulation and in vitro-in vivo evaluation of ketoprofen-loaded albumin microspheres for intramuscular administration.

    abstract::The objective of this work was to prepare and evaluate ketoprofen-loaded albumin microspheres for intramuscular administration. Microspheres were prepared by emulsion cross-linking method using a 2(3) factorial design and the effect of different factors on entrapment efficiency was determined. Microspheres were evalua...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040802420367

    authors: Mathew ST,Devi SG,Prasanth VV,Vinod B

    更新日期:2009-08-01 00:00:00

  • Response surface methodology to obtain naproxen controlled release tablets from its microspheres with Eudragit L100-55.

    abstract:PURPOSE:Naproxen CR tablets have been obtained from its microspheres prepared by coprecipitation with Eudragit L100-55. The purpose of this work was to evaluate the main and interaction effects of deaggregating agent concentration (X1), compression pressure (X2) and amount of precipitating water (X3) on naproxen releas...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040110055630

    authors: Zaghloul AA,Vaithiyalingam SR,Faltinek J,Reddy IK,Khan MA

    更新日期:2001-09-01 00:00:00

  • Functionality of protective colloids affecting the formation, size uniformity and morphology of drug-free polylactic acid microspheres.

    abstract::Drug-free polylactic acid (PLA) microspheres were prepared by an emulsification-solvent evaporation technique using different types of protective colloids. The influence of five types of hydrophilic prolymers (polysaccharides, proteins, synthetic cellulose derivatives, synthetic nonionic polymers and surfactants) on t...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652049809006865

    authors: Lin SY,Chen KS,Teng HH

    更新日期:1998-05-01 00:00:00

  • Solid lipid nanoparticles and nanosuspension formulation of Saquinavir: preparation, characterization, pharmacokinetics and biodistribution studies.

    abstract::Solid lipid nanoparticles (SLNs) and nanosuspensions (NSs) have shown great promise for improving bioavailability of poorly water-soluble drugs. This study was aimed to develop SLNs and NS of Saquinavir (SQ) for improvement in bioavailability. These formulations were characterized and their pharmacokinetics and biodis...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2011.590612

    authors: Dodiya SS,Chavhan SS,Sawant KK,Korde AG

    更新日期:2011-01-01 00:00:00

  • Preparation, statistical optimisation and in vitro characterisation of poly (3-hydroxybutyrate-co-3-hydroxyvalerate)/poly (lactic-co-glycolic acid) blend nanoparticles for prolonged delivery of teriparatide.

    abstract::The purpose of this study was the preparation, optimisation and in vitro characterisation of PHBV and PLGA blend nanoparticles (NPs) for prolonged delivery of Teriparatide. Double emulsion solvent evaporation technique was employed for the fabrication of NPs. The nanoformulation was optimised using the Box-Behnken met...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652048.2016.1208296

    authors: Bahari Javan N,Rezaie Shirmard L,Jafary Omid N,Akbari Javar H,Rafiee Tehrani M,Abedin Dorkoosh F

    更新日期:2016-08-01 00:00:00

  • An investigation of internal phase losses during the microencapsulation of fragrances.

    abstract::Prototype fragrances, prepared from common fragrance components, were extracted with water, recovered, and characterized by gas chromatography before and after the water treatment, revealing a significant loss of the more water-soluble components. Unextracted prototype fragrances were also microencapsulated by a gelat...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652049209021244

    authors: Flores RJ,Wall MD,Carnahan DW,Orofino TA

    更新日期:1992-07-01 00:00:00

  • Studies on the drug release properties of nano-encapsulated indomethacin microparticles.

    abstract::Indomethacin micro-crystals sized approximately 2 microm have been encapsulated with polyelectrolyte multi-layers for the purpose of controlled release. Charged linear poly (dimethyldiallyl ammonium chloride) (PDDA) and poly (styrene sulphonate) (PSS) were alternatively deposited on approximately 2 microm drug micro-c...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652040500044972

    authors: Chen Y,Lin X

    更新日期:2005-02-01 00:00:00

  • Phagocytosis and degradation of human serum albumin microspheres and nanoparticles in human macrophages.

    abstract::Nanoparticles and microspheres made from human serum albumin are biodegradable and, as a physiological material, less cytocidal than cyanoacrylates. Therefore, they should be a suitable carrier system for targeting drugs into cells of the mononuclear phagocyte system. Nevertheless, the process of phagocytic uptake and...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652049409040455

    authors: Schäfer V,von Briesen H,Rübsamen-Waigmann H,Steffan AM,Royer C,Kreuter J

    更新日期:1994-05-01 00:00:00

  • Reinvestigating nanoprecipitation via Box-Behnken design: a systematic approach.

    abstract::This work demonstrates Box-Behnken design (BBD)'s capability in exploring scientific principles governing a process, different from its use in process optimisation. We have investigated nanoprecipitation (NP) of temozolomide with polycaprolactone. Five factors, surfactant, stirring speed (SS), dropping rate (DR), phas...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2014.950710

    authors: Singh Y,Ojha P,Srivastava M,Chourasia MK

    更新日期:2015-01-01 00:00:00

  • Resveratrol solid lipid microparticles as dry powder formulation for nasal delivery, characterization and in vitro deposition study.

    abstract::This study focuses on development and in vitro characterisation of a nasal delivery system based on uncoated or chitosan-coated solid lipid microparticles (SLMs) containing resveratrol, a natural anti-inflammatory molecule, as an effective alternative to the conventional steroidal drugs. The physico-chemical character...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.1080/02652048.2016.1260659

    authors: Martignoni I,Trotta V,Lee WH,Loo CY,Pozzoli M,Young PM,Scalia S,Traini D

    更新日期:2016-12-01 00:00:00

  • Prolonged retention and in vivo evaluation of cationic nanoparticles loaded with Mitomycin C designed for intravesical chemotherapy of bladder tumours.

    abstract::To overcome the recurrence problem in bladder tumours; nanoparticles with positive surface charge may improve interaction with biological membranes for intravesical administration. The aim of this study was to design, develop and evaluate (in vitro-in vivo) cationic nanoparticles based on chitosan, poly-L-lysine or po...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2012.668957

    authors: Erdoğar N,Iskit AB,Mungan NA,Bilensoy E

    更新日期:2012-01-01 00:00:00

  • Influence of the surface properties of low contact angle surfactants on the body distribution of 14C-poly(methyl methacrylate) nanoparticles.

    abstract::The body distribution of surfactant-coated and non-coated poly(methyl methacrylate) nanoparticles with a size of 131 +/- 30 nm after intravenous injection into rats was investigated. The coating materials were poloxamine 904, poloxamine 908, poloxamine 1508, poloxamer 338, and Brij 35. These materials were preselected...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652049209021219

    authors: Tröster SD,Kreuter J

    更新日期:1992-01-01 00:00:00

  • Mucoadhesive drug carrier based on functional-modified cellulose as poorly water-soluble drug delivery system.

    abstract::The purpose of this study was to design and characterise an oral mucoadhesive micellar drug carrier. In this regard, a mucoadhesive hydrophobic cationic aminocellulose was easily synthesised under mild homogeneous conditions with high yield. The cellulose derivative resulted in strongly improved mucoadhesive propertie...

    journal_title:Journal of microencapsulation

    pub_type: 杂志文章

    doi:10.3109/02652048.2015.1046516

    authors: Songsurang K,Siraleartmukul K,Muangsin N

    更新日期:2015-01-01 00:00:00