beta-carotene encapsulation in a mannitol matrix as affected by divalent cations and phosphate anion.

Abstract:

:The effects of addition of divalent cations and phosphate buffer on the degree of beta-carotene encapsulation in a mannitol matrix during freeze-drying were analyzed. The degradation rate of encapsulated beta-carotene as a function of % RH and its relationship with the physical state of the matrix during storage at 25 degrees C was also studied. The presence of phosphate salts significantly delayed mannitol crystallization at a highly satisfactory degree during freeze-drying and, consequently, the degree of beta-carotene encapsulation increased. This effect was maintained over quite long time during storage of the freeze-dried samples at 25 degrees C. Unavoidable local variations in water content during 3 years storage caused the decrease of T(g) values and made the crystallization degree to increase. The divalent cations showed a synergistic effect and also modified the kinetics of beta-carotene degradation during storage, increasing its stability. The mechanism of crystallization inhibition likely includes a change in hydrogen bond network or/and change in molecular mobility in the presence of divalent cations and phosphate anions. The degradation rate of beta-carotene in a mannitol/KH(2)PO(4) matrix increased as increasing % RH until a value at which the samples collapsed (75% RH), and then the degradation rate decreased. Collapse phenomena may affect diffusion of oxygen from the surface to the inside of the matrix and increase retention of beta-carotene. Surface color was not an appropriate indicator for beta-carotene degradation, because it was mostly dependent on the optical properties of the matrix, which changed with the degree of matrix hydration and collapse.

journal_name

Int J Pharm

authors

Sutter SC,Buera MP,Elizalde BE

doi

10.1016/j.ijpharm.2006.09.023

subject

Has Abstract

pub_date

2007-03-06 00:00:00

pages

45-54

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(06)00778-2

journal_volume

332

pub_type

杂志文章
  • Gelation of the internal core of liposomes as a strategy for stabilization and modified drug delivery I. Physico-chemistry study.

    abstract::Since the application of nanotechnology to drug delivery, both polymer-based and lipid-based nanocarriers have demonstrated clinical benefits, improving both drug efficacy and safety. However, to further address the challenges of the drug delivery field, hybrid lipid-polymer nanocomposites have been designed to merge ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119467

    authors: Petralito S,Paolicelli P,Nardoni M,Trilli J,Di Muzio L,Cesa S,Relucenti M,Matassa R,Vitalone A,Adrover A,Casadei MA

    更新日期:2020-07-30 00:00:00

  • Effect of electrokinetic stabilizers on the physicochemical properties of propofol emulsions.

    abstract::The aims of the present study were to elucidate the potential mechanism of propofol emulsion destabilization following the addition of lidocaine, and to evaluate the effects of various electrokinetic stabilizers on the physicochemical properties of lidocaine-propofol emulsions. The assessments included pH observations...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.07.011

    authors: Rhee YS,Park CW,Oh TO,Kim JY,Ha JM,Lee BJ,Lee KH,Chi SC,Park ES

    更新日期:2010-10-15 00:00:00

  • Measurement of residence time distributions and material tracking on three continuous manufacturing lines.

    abstract::Over the recent decade, benefits of continuous manufacturing (CM) of pharmaceutical products have been acknowledged widely. In contrast to batch processes, the product is not physically separated into batches in CM, which creates a few challenges. Product release is done for batches that should have a uniform quality ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.03.058

    authors: Karttunen AP,Hörmann TR,De Leersnyder F,Ketolainen J,De Beer T,Hsiao WK,Korhonen O

    更新日期:2019-05-30 00:00:00

  • Reformulation of etoposide with solubility-enhancing rubusoside.

    abstract::Etoposide (ETO), a widely used anti-cancer drug, is constrained by its low aqueous solubility and by side effects from both the drug and its solubilizing excipients. In this study, a recently discovered natural solubilizer rubusoside (RUB) was used to achieve the solubilization of ETO. Dynamic light scattering and fre...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.013

    authors: Zhang F,Koh GY,Hollingsworth J,Russo PS,Stout RW,Liu Z

    更新日期:2012-09-15 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

  • Development of new polymer-based particulate systems for anti-glioma vaccination.

    abstract::Biodegradable and biocompatible microspheres represent a promising alternative to conventional adjuvants for anti-tumour vaccination. Focusing on glioma, we developed two poly(D,L-lactide-co-glycolide) (PLGA)-based particulate systems presenting tumour antigens associated with plasma membranes or with cell lysates. Gl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.046

    authors: Sapin A,Garcion E,Clavreul A,Lagarce F,Benoit JP,Menei P

    更新日期:2006-02-17 00:00:00

  • Development of Ussing model coupled with artificial membrane for predicting intestinal absorption mechanisms of drugs.

    abstract::The absorption mechanisms of drugs play an important role on development and various application of drugs. However, the present methods of absorption mechanisms are not perfect enough. Hence, exploring a novel method to accurately predict the absorption mechanisms is necessary. In this study, we developed an Ussing mo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119170

    authors: Huang S,Huang Y,Yin X,Wang D,Xiang W,Wang M,Xia Z

    更新日期:2020-04-15 00:00:00

  • Preliminary pharmaceutical development of antimalarial-antibiotic cotherapy as a pre-referral paediatric treatment of fever in malaria endemic areas.

    abstract::Artemether (AM) plus azithromycin (AZ) rectal co-formulations were studied to provide pre-referral treatment for children with severe febrile illnesses in malaria-endemic areas. The target profile required that such product should be cheap, easy to administer by non-medically qualified persons, rapidly effective again...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.04.023

    authors: Gaubert A,Kauss T,Marchivie M,Ba BB,Lembege M,Fawaz F,Boiron JM,Lafarge X,Lindegardh N,Fabre JL,White NJ,Olliaro PL,Millet P,Grislain L,Gaudin K

    更新日期:2014-07-01 00:00:00

  • Curcumin nanoparticles containing poloxamer or soluplus tailored by high pressure homogenization using antisolvent crystallization.

    abstract::Curcumin is a natural active constituent of Curcuma longa from Zingiberaceae family that shows many different pharmacological effects such as anticancer, antioxidant, anti-inflammatory, antimicrobial and antiviral effect. However, its bioavailability is profoundly limited by its poor water solubility. In this study an...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.03.038

    authors: Homayouni A,Amini M,Sohrabi M,Varshosaz J,Nokhodchi A

    更新日期:2019-05-01 00:00:00

  • A genetically modified recombinant tumor necrosis factor-alpha conjugated to the distal terminals of liposomal surface grafted polyethyleneglycol chains.

    abstract::A genetically modified recombinant tumor necrosis factor (TNF)-alpha (rKRKTNF) was conjugated to the terminal carboxyl groups of liposome grafted polyethyleneglycol (PEG) chains. The long-circulating liposomes were composed of egg phosphatidylcholine, cholesterol (chol) and 7% carboxyl PEG-phosphatidylethanolamine. Th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00092-7

    authors: Savva M,Duda E,Huang L

    更新日期:1999-07-05 00:00:00

  • Controlled-release triple anti-inflammatory therapy based on novel gastroretentive sponges: characterization and magnetic resonance imaging in healthy volunteers.

    abstract::The current work aimed to develop novel composite sponges of chitosan (CH)-chondroitin sulfate (CS) as a low-density gastroretentive delivery system for lornoxicam (LOR). This triple anti-inflammatory therapy-loaded matrices are expected to expand and float upon contact with gastric fluids for prolonged times. CH and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.06.013

    authors: Tadros MI,Fahmy RH

    更新日期:2014-09-10 00:00:00

  • Optimization of PLG microspheres for tailored drug release.

    abstract::Here we explore the opportunity to design and then produce tailored release of therapeutic drugs from microcapsules. By use of "building blocks," formed from well characterized microcapsule populations, an inverse design algorithm has been developed that provides an optimal (in a least squares sense) combination of bu...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.09.010

    authors: Berchane NS,Jebrail FF,Andrews MJ

    更新日期:2010-01-04 00:00:00

  • Decoding the small size challenges of mini-tablets for enhanced dose flexibility and micro-dosing.

    abstract::Mini-tablets are an age appropriate dosage form for oral administration to pediatric and geriatric patients, either as individual mini-tablets or as composite dosage units. Smaller size mini-tablets than the commonly used 2 mm or larger size would offer more tailored micro-dose delivery of investigational drugs. This ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118905

    authors: Mitra B,Thool P,Meruva S,Aycinena JA,Li J,Patel J,Patel K,Agarwal A,Karki S,Bowen W

    更新日期:2020-01-25 00:00:00

  • In vivo deposition study of a new generation nebuliser utilising hybrid resonant acoustic (HYDRA) technology.

    abstract::Conventional nebulisation has the disadvantages of low aerosol output rate and potential damage to macromolecules due to high shear (jet nebulisation) or cavitation (ultrasonic nebulisation). HYDRA (HYbriD Resonant Acoustics) technology has been shown to overcome these problems by using a hybrid combination of surface...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119196

    authors: Kwok PCL,McDonnell A,Tang P,Knight C,McKay E,Butler SP,Sivarajah A,Quinn R,Fincher L,Browne E,Yeo LY,Chan HK

    更新日期:2020-04-30 00:00:00

  • Poly(acrylic acid) microspheres containing beta-cyclodextrin: loading and in vitro release of two dyes.

    abstract::Microspheres containing poly(acrylic acid) and beta-cyclodextrin or maltose were prepared by a w/o solvent evaporation technique. The dispersed aqueous phase contained poly(acrylic acid) (800 mg) and beta-cyclodextrin or maltose (0, 200 or 800 mg). Food-grade olive oil was the continuous phase. Microsphere particle si...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00190-8

    authors: Bibby DC,Davies NM,Tucker IG

    更新日期:1999-10-05 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

  • Elaborations on the Higuchi model for drug delivery.

    abstract::The Higuchi model for the rate of drug release from matrix devices where the drug loading exceeds the solubility in the matrix medium, whose 50-year anniversary is celebrated in this issue, has proven to be a robust framework and an invaluable tool in developing a significant part of the modern controlled drug deliver...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.037

    authors: Paul DR

    更新日期:2011-10-10 00:00:00

  • Delivery of FK506-loaded PLGA nanoparticles prolongs cardiac allograft survival.

    abstract::In this study, FK506-loaded poly(lactide-co-glycolide) nanoparticles (PLGA-FK506-NPs) were developed using an O/W emulsion solvent evaporation method. The PLGA-FK506-NPs were observed to be monodispersed and spherical by transmission and scanning electron microscopy. The mean size and zeta potential measured by dynami...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118951

    authors: Deng C,Chen Y,Zhang L,Wu Y,Li H,Wu Y,Wang B,Sun Z,Li Y,Lv Q,Yang Y,Wang J,Jin Q,Xie M

    更新日期:2020-02-15 00:00:00

  • Production of dry-state ketoprofen-encapsulated PMMA NPs by coupling micromixer-assisted nanoprecipitation and spray drying.

    abstract::We present a two-step process to produce dry-state Ketoprofen-loaded poly(methyl methacrylate) nanoparticles (NPs) with controllable size and tunable drug release profile. A colloidal suspension of drug-loaded nanoparticles was first obtained from a nanoprecipitation process and then transferred into a commercial spra...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.031

    authors: Ding S,Serra CA,Anton N,Yu W,Vandamme TF

    更新日期:2019-03-10 00:00:00

  • Effects of drying technique on extrusion-spheronisation granules and tablet properties.

    abstract::Extrusion-spheronisation was used to generate smooth, highly spherical granules of a microcrystalline cellulose/propyl gallate/water paste. Freeze-drying retained the shape and size of the granules, whereas oven-drying produced roughened granules due to the uneven shrinkage of the wet powders. Compaction of one size f...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.09.050

    authors: Song B,Rough SL,Wilson DI

    更新日期:2007-03-06 00:00:00

  • In vitro and in vivo evaluation of mucoadhesive microspheres consisting of dextran derivatives and cellulose acetate butyrate.

    abstract::The objective of this study was to evaluate mucoadhesive properties and gastrointestinal transit of microspheres made of oppositely charged dextran derivatives and cellulose acetate butyrate (CAB). The microspheres were prepared by emulsion solvent evaporation method. A reference microsphere was made of lactose instea...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00159-5

    authors: Miyazaki Y,Ogihara K,Yakou S,Nagai T,Takayama K

    更新日期:2003-06-04 00:00:00

  • The influence of plate design on the properties of pellets produced by extrusion and spheronization.

    abstract::The aim of this work was to produce pellets using a standard formulation by means of extrusion and spheronization. Three different spheroniser friction plate patterns (i.e. cross-hatch, radial, striated edge pattern) have been used in order to investigate whether the plate pattern affects physical properties of the pe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.05.050

    authors: Michie H,Podczeck F,Newton JM

    更新日期:2012-09-15 00:00:00

  • GSH responsive nanomedicines self-assembled from small molecule prodrug alleviate the toxicity of cardiac glycosides as potent cancer drugs.

    abstract::Cardiac glycosides (CGs) have been used to treat cancer for hundreds of years. However, the narrow therapeutic window and system toxicity have hindered their wide clinical applications. Herein, the small molecule prodrug strategy and nanotechnology were integrated into one drug delivery system with enhanced therapeuti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118980

    authors: Zhang H,Zhu Y,Sun C,Xie Y,Adu-Frimpong M,Deng W,Yu J,Xu X,Han Z,Qi G

    更新日期:2020-02-15 00:00:00

  • Dose tolerability of chronically inhaled voriconazole solution in rodents.

    abstract::Invasive pulmonary aspergillosis (IPA) is a fungal disease of the lung associated with high mortality rates in immunosuppressed patients despite treatment. Targeted drug delivery of aqueous voriconazole solutions has been shown in previous studies to produce high tissue and plasma drug concentrations as well as improv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.06.003

    authors: Tolman JA,Nelson NA,Bosselmann S,Peters JI,Coalson JJ,Wiederhold NP,Williams RO 3rd

    更新日期:2009-09-08 00:00:00

  • Aptamers as the chaperones (Aptachaperones) of drugs-from siRNAs to DNA nanorobots.

    abstract::Aptamers, nucleic acid ligands that are specific against their corresponding targets are increasingly employed in a variety of applications including diagnostics and therapeutics. The specificity of the aptamers against their targets is also used as the basis for the formulation of the aptamer-based drug delivery syst...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2019.118483

    authors: Citartan M,Kaur H,Presela R,Tang TH

    更新日期:2019-08-15 00:00:00

  • The application of STEP-technology® for particle and protein dispersion detection studies in biopharmaceutical research.

    abstract::Particle detection and analysis techniques are essential in biopharmaceutical industries to evaluate the quality of various parenteral formulations regarding product safety, product quality and to meet the regulations set by the authority agencies. Several particle analysis systems are available on the market, but for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.03.050

    authors: Gross-Rother J,Herrmann N,Blech M,Pinnapireddy SR,Garidel P,Bakowsky U

    更新日期:2018-05-30 00:00:00

  • Physicochemical characteristics of quinupramine in the EVA matrix.

    abstract::Ethylene-vinyl acetate (EVA) is widely used as a membrane or matrix for transdermal drug delivery systems. In an attempt to determine the state of a drug in the EVA matrix, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and thermal analysis of the quinupramine-EVA matrix were carried out and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.06.016

    authors: Cho CW,Choi JS,Shin SC

    更新日期:2006-08-31 00:00:00

  • Diffusion and binding of 5-fluorouracil in non-ionic hydrogels with interpolymer complexation.

    abstract::Hydrogen-bonded interpolymer complexes can be used for development of novel dosage forms. In this study, two types of crosslinked hydrogels, copolymer networks of N-vinyl pyrrolidone and acrylamide (PVP-co-PAM) and interpenetrating polymer networks (IPN) composed of crosslinked PVP-co-PAM and poly(vinyl alcohol) (PVA)...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.04.037

    authors: Zhou W,Lu P,Sun L,Ji C,Dong J

    更新日期:2012-07-15 00:00:00

  • Influence of dry granulation on compactibility and capping tendency of macrolide antibiotic formulation.

    abstract::The effect of dry granulation (roller compaction and slugging) on compactibility and tablet capping tendency in a formulation with macrolide antibiotic and microcrystalline cellulose (MCC) was investigated. Direct tableting of this formulation revealed a pronounced capping tendency. Both dry granulated systems exhibit...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.01.023

    authors: Bozic DZ,Dreu R,Vrecer F

    更新日期:2008-06-05 00:00:00

  • Comparative study of Pluronic(®) F127-modified liposomes and chitosan-modified liposomes for mucus penetration and oral absorption of cyclosporine A in rats.

    abstract::Liposomes modified using cationic and hydrophilic nonionic polymers are 2 popular carriers for improving oral drug absorption. Cationic polymer-modified liposomes can adhere to the intestinal wall mucus (mucoadhesive type), while liposomes modified using hydrophilic nonionic polymers can penetrate across the mucus bar...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.04.002

    authors: Chen D,Xia D,Li X,Zhu Q,Yu H,Zhu C,Gan Y

    更新日期:2013-06-05 00:00:00