Abstract:
:Cross-linked albumin microcapsules were prepared, using a polycondensation interfacial process. Doxorubicin was incorporated in these microcapsules by simple adsorption from aqueous solution. Increasing the extent of cross-linkage of the microcapsule walls by either increasing the cross-linking agent concentration or the time of reaction significantly reduced the absorption ability of these microcapsules. Doxorubicin release kinetic evaluation revealed that the presence of a salt in the release medium was needed to enable much of the drug to be released. Furthermore, the doxorubicin displacement intensity from the microcapsules was dependent on the nature and concentration of the cations used, indicating that an ion-exchange process was involved. Analysis of the various doxorubicin release profiles, using ion-exchange kinetic equation, showed that the release kinetic process is governed by a film diffusion process at low and moderate Na+ ion concentrations in the exchanging solution, and by a particle diffusion process at high Na+ ion concentrations, sufficient to drive the doxorubicin exchange to completion.
journal_name
J Microencapsuljournal_title
Journal of microencapsulationauthors
Sawaya A,Fickat R,Benoit JP,Puisieux F,Benita Sdoi
10.3109/02652048809064170subject
Has Abstractpub_date
1988-07-01 00:00:00pages
255-67issue
3eissn
0265-2048issn
1464-5246journal_volume
5pub_type
杂志文章abstract::Eudragit RS microspheres containing verapamil HCl for oral use were prepared using three different dispersing agents: aluminium tristearate, magnesium stearate and sucrose stearate, by a solvent evaporation method. The effects of the type and concentration of the dispersing agents and the inner phase polymer concentra...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040310001637893
更新日期:2004-03-01 00:00:00
abstract::Emulsions of menhaden oil and sodium caseinate (NaCas) incorporating carbohydrates of varying dextrose equivalence (DE) were spray-dried to yield encapsulated fish oil powders. The effects of carbohydrate DE (5.5-38), core/wall ratio and NaCas/carbohydrate ratio on microencapsulation efficiency (ME) and oxidative stab...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/0265204031000151974
更新日期:2003-09-01 00:00:00
abstract::Enteric diastase spherules were prepared using cellulose acetate phthalate and eudragit RS-100 by emulsion solvent removal method. Factors that could affect the size shape and diastatic activity were studied. The studied factors include pH of aqueous media, temperature of dispersion media and concentration of surface ...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.3109/02652049109021868
更新日期:1991-10-01 00:00:00
abstract::This study optimized and evaluated the conditions for surface coating of microspheres using a spray-dryer. Four formulations of Bromophenol blue (BPB)-loaded albumin microspheres were prepared using a spray-dryer, cross-linked at different concentrations and time periods. One of the optimized formulations with the des...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040802476187
更新日期:2008-12-01 00:00:00
abstract::This paper prepared novel biodegradable and pH-sensitive microgels based on Poly(epsilon-caprolactone)-Pluronic-Poly(epsilon-caprolactone)-dimethacrylate (PCFC-DMA), Poly(ethylene glycol) dimethacrylate (PEG-DMA) and methylacrylic acid (MAA) cross-linked with N,N'-methylenebisacrylamide (BIS), initiated by NaHSO(3), K...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.3109/02652040802610827
更新日期:2009-11-01 00:00:00
abstract::The present research work was aimed at development and optimization of alginate mucoadhesive microspheres of carvedilol for nasal delivery to avoid first pass metabolism and to improve the therapeutic efficacy in the treatment of hypertension and angina pectoris. The microspheres were prepared by a water-in-oil (w/o) ...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040802456726
更新日期:2009-08-01 00:00:00
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
更新日期:1996-11-01 00:00:00
abstract::The aim of this study was to design and develop microspheres of indomethacin with pH and transit time dependent release properties for achieving targeted delivery to the colon. Microspheres containing varying proportions of ethyl cellulose and Eudragit (L100 or S100) either alone or in combination were prepared using ...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040802424021
更新日期:2009-08-01 00:00:00
abstract::This study aims to formulate a microparticle-based system that protects the protein from the harsh gastric conditions and also provides appropriate uptake via M cells for desired immune response upon oral administration. The formulation was derived using a valid statistical model, analysed by JMP® (SAS). The average s...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.3109/02652048.2011.651503
更新日期:2012-01-01 00:00:00
abstract::The sustained delivery of multiple agents to the lung offers potential benefits to patients. This study explores the preparation of highly respirable dual-loaded spray-dried double emulsions. Spray-dried powders were produced from water-in-oil-in-water (w/o/w) double emulsions, containing salbutamol sulphate and/or be...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040903052044
更新日期:2010-01-01 00:00:00
abstract:CONTEXT:Flavonoids show promising anticancer potential but it is limited due to poor solubility. OBJECTIVE:The present investigation was to prepare Chrysin-Phospholipid complex loaded solid lipid nanoparticles (Ch-PC-SLNs) for improving its encapsulation as compared to that of Chrysin loaded SLNs (Ch-SLNs) and evaluat...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652048.2018.1559369
更新日期:2018-09-01 00:00:00
abstract::Bioavailability of oral drugs can be limited by an intestinal excretion process mediated by P-glycoprotein (P-gp). Polyethylene glycol (PEG) is a known P-gp inhibitor. Dispersion of Famotidine (a P-gp substrate) within PEGylated nanoparticles (NPs) was used to improve its oral bioavailability. In this work, we evaluat...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652048.2017.1290155
更新日期:2017-02-01 00:00:00
abstract::The aim of this study was to develop and characterize diclofenac sodium loaded-cellulose acetate butyrate microparticles in order to obtain a controlled-release system. The influence of the type of polymer, the volume and composition of the internal phase, drug loading, surfactant concentration and additive added on m...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040701747928
更新日期:2008-02-01 00:00:00
abstract::Anal fissure is common and painful disease of anorectum. In this study, microparticles containing nifedipine and lidocaine HCl were prepared by spray drying and applied to bio-degradable and bio-stable tampons. Characterization of microparticles was determined by visual analyses, mass yield, particle size measurement,...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652048.2017.1393113
更新日期:2017-12-01 00:00:00
abstract::Liposomes were introduced first in 1980 for topical drug delivery and since then have attracted considerable interest and generated many speculative claims concerning their potential utility both as a drug carrier and reservoir for controlled release of drugs within various layers of the skin. A number of clinical stu...
journal_title:Journal of microencapsulation
pub_type: 杂志文章,评审
doi:10.3109/02652049309104381
更新日期:1993-04-01 00:00:00
abstract::For slow release of tea tree oil (TTO), TTO were encapsulated by urea-formaldehyde (UF) resin via in situ polymerisation. The effects of curing time and drying condition on particle size, and TTO loading of the TTO/UF microcapsules were investigated. The results indicated that TTO/UF resin microcapsules with curing ti...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652048.2020.1735548
更新日期:2020-06-01 00:00:00
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
更新日期:1988-10-01 00:00:00
abstract::Hyaluronidase is a protein whose enzymatic activity is successfully employed in extravasation therapy. Taking into account that several proteins (e.g. gelatin and albumin) have been employed as natural polymers for the preparation of microspheres, this work approaches a comprehensive investigation on hyaluronidase inj...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.3109/02652049809006838
更新日期:1998-01-01 00:00:00
abstract::Alginate bead containing calcium carbonate particle were prepared by dropping the suspension of alginate/calcium carbonate (4/1, w/w) into aqueous solution of CaCl(2) (0.1 M). The pH-dependent release property of the bead was observed for 12 h using blue dextran as a model drug. The release increased up to 4 h in a sa...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040701657820
更新日期:2007-12-01 00:00:00
abstract::Polyisohexylcyanoacrylate nanocapsules containing cyclosporin were prepared by mixing in a 1:2 ratio an oil/ethanol solution of monomer and drug with an aqueous phase. Drug nanoencapsulation rate was controlled by its partition coefficient between the inner (organic) and outer (aqueous) phases. Thus highest encapsulat...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.3109/02652049109021233
更新日期:1992-04-01 00:00:00
abstract:AIM:This study aimed to evaluate the protective effect of flaxseed mucilage on the co-extrusion microencapsulation of Lactobacillus rhamnosus GG. METHODS:Core flow rate, chitosan coating, and flaxseed mucilage concentration were optimised for the microencapsulation of L. rhamnosus. The microbeads were characterised an...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652048.2020.1863490
更新日期:2020-12-28 00:00:00
abstract::This work investigated the means for the efficient encapsulation of muramyl dipeptide (MDP) in poly(epsilon-caprolactone) (PCL) microparticles (MP) by a solvent evaporation method in order to optimize the effect of the adjuvant for oral immunization. Therefore, the influence of MDP concentration in the inner aqueous p...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/026520499288799
更新日期:1999-09-01 00:00:00
abstract::This paper discusses the optimization of the solvent evaporation process to produce double-walled (DW) microspheres in a single-step. Five process variables were studied: polymer solution concentration, polymer weight ratio, polymer solution volume ratios, encapsulation temperature, and air flow rate across the top of...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/026520499289149
更新日期:1999-03-01 00:00:00
abstract::Radioembolization is used in diagnostic imaging of the lungs and for radioembolization therapy of hepatic tumours. Presently, 99mTc labelled macroaggregates or microspheres of human serum albumin (HAM) are used for this purpose. Poly lactic acid (PLA) is biodegradable, like HAM, and, unlike HAM, is not a blood product...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/026520400405750
更新日期:2000-07-01 00:00:00
abstract::In ophthalmic drug delivery, a major problem is retaining an adequate concentration of a therapeutic agent in the pre-corneal area. Polycarboxylic acid carriers such as polyacrylic acid and polyitaconic acid in sub-colloidal, nanoparticulate hydrogel form have a strong potential for sustained release of a drug in ocul...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040400008515
更新日期:2004-12-01 00:00:00
abstract::Optimum conditions for the preparation of non-magnetic and magnetic microspheres of albumin-globulin mix (alglomix) containing mefenamic acid have been standardized. The effect of various parameters has been investigated with regard to the appearance, yield, drug content and encapsulation efficiency. The physicochemic...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.3109/02652049109021856
更新日期:1991-01-01 00:00:00
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
更新日期:2005-02-01 00:00:00
abstract::The objective of this study is to explore the influence of polyvinylpyrrolidone (PVP) quantity on the solubility, crystallinity and oral bioavailability of poorly water-soluble fenofibrate in solvent-evaporated microspheres. Numerous microspheres were prepared with fenofibrate, sodium lauryl sulphate (SLS) and PVP usi...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652048.2016.1194906
更新日期:2016-06-01 00:00:00
abstract::Sub-100-nm nanoparticles were prepared from beta-lactoglobulin (BLG) with a narrow size distribution by a desolvation method using glutaraldehyde for cross-linking. With pre-heating of the BLG solution to 60 degrees C and subsequent pH readjustment to 9.0, nanoparticles of 59 +/- 5 nm were obtained with improved unifo...
journal_title:Journal of microencapsulation
pub_type: 杂志文章
doi:10.1080/02652040601035143
更新日期:2006-12-01 00:00:00
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
更新日期:2015-01-01 00:00:00