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 and determination of the maximum globule diameter (MGD) and zeta potential (ZP). The MGD of propofol emulsions increased up to several tens mum following the addition of 50 mg of lidocaine to 200mg of propofol, and the proposed destabilization mechanism involves localization of protonated lidocaine molecules between lecithin molecules in propofol emulsions, which consequently leads to increased ZP. The ZP of propofol emulsions containing acidic amino acid or neutral amino acid increased following the addition of lidocaine, and a charge reversal occurred. Therefore, the MGD of emulsions increased to several tens (m. However, the MGD of emulsions that contained basic amino acids or basic compounds remained below 5 (m, despite the addition of large amounts lidocaine (50 mg), and the ZP did not pass through the point of zero charge. In conclusion, our results provide not only further insight into the physical stability of propofol emulsions containing lidocaine, but also a better understanding of the administration of propofol in existing applications.

journal_name

Int J Pharm

authors

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

doi

10.1016/j.ijpharm.2010.07.011

subject

Has Abstract

pub_date

2010-10-15 00:00:00

pages

21-7

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(10)00521-1

journal_volume

398

pub_type

杂志文章
  • Synergistic enhancement of anticancer therapeutic efficacy of HPMA copolymer doxorubicin conjugates via combination of ligand modification and stimuli-response srategies.

    abstract::N-(2-Hydroxypropyl) methacrylamide (HPMA) copolymer has been extensively studied as drug carrier for tumor therapy. Due to the Enhanced Permeability and Retention (EPR) effect, HPMA copolymer drug conjugates are able to be passively accumulated in the tumor site. Currently, efficient uptake of this polymeric system by...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.12.018

    authors: Li L,Zhou M,Huang Y

    更新日期:2018-01-30 00:00:00

  • Influence of different parameters on reconstitution of lyophilized SLN.

    abstract::Drug-loaded solid lipid nanoparticles (SLN) suitable for parenteral administration were freeze-dried. The lipid matrix Imwitor 900 (concentration, 2.5%) was stabilized with Lipoid E 80 and sodium glycocholate. The influence of different parameters of lyophilization like the protective effect of cryoprotectants, freezi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00424-x

    authors: Zimmermann E,Müller RH,Mäder K

    更新日期:2000-03-10 00:00:00

  • Short-term delayed-release microcapsules spraycoated with acrylic terpolymers.

    abstract::A series of poly(ethyl acrylate (EA)/methyl methacrylate (MMA)/2-hydroxyethyl methacrylate (HEMA)) lattices were synthesized to prepare short-term delayed-release microcapsules by employing the Wurster coating process. Latex with a HEMA molar fraction exceeding 60% could not be synthesized as an aqueous suspension due...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.020

    authors: Liu D,Ichikawa H,Cui F,Fukumori Y

    更新日期:2006-01-13 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

  • Preparation and characterization of water-soluble albumin-bound curcumin nanoparticles with improved antitumor activity.

    abstract::Curcumin (CCM), a yellow natural polyphenol extracted from turmeric (Curcuma longa), has potent anti-cancer properties as has been demonstrated in various human cancer cells. However, the widespread clinical application of this efficient agent in cancer and other diseases has been limited by its poor aqueous solubilit...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.041

    authors: Kim TH,Jiang HH,Youn YS,Park CW,Tak KK,Lee S,Kim H,Jon S,Chen X,Lee KC

    更新日期:2011-01-17 00:00:00

  • Systematic modifications of amino acid-based organogelators for the investigation of structure-property correlations in drug delivery system.

    abstract::Thermogels, used as multi-functional drug-loading materials, have properties that mainly rely on their gelator structure. Although a large variety of organogel systems are used as drug delivery carriers, relatively few have been investigated in terms of their structure-property correlations based on amino acid derivat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.06.043

    authors: Hu B,Sun W,Li H,Sui H,Li S

    更新日期:2018-08-25 00:00:00

  • TR146 cells grown on filters as a model of human buccal epithelium: IV. Permeability of water, mannitol, testosterone and beta-adrenoceptor antagonists. Comparison to human, monkey and porcine buccal mucosa.

    abstract::The objective of the present study was to evaluate the TR146 cell culture model as an in vitro model of human buccal epithelium. For this purpose, the permeability of water, mannitol and testosterone across the TR146 cell culture model was compared to the permeability across human, monkey and porcine buccal mucosa. Fu...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00368-3

    authors: Nielsen HM,Rassing MR

    更新日期:2000-01-25 00:00:00

  • Drug interactions with diosmectite: a study using the artificial stomach-duodenum model.

    abstract::Drug interactions with diosmectite, a gastric-protective drug, were studied in vitro using an artificial stomach-duodenum model. The behavior of neutral and ionisable drugs with pKa values ranging between 2 and 8 was monitored to determine the physicochemical characteristics of the interactions. The main neutral (digo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00073-3

    authors: Castela-Papin N,Cai S,Vatier J,Keller F,Souleau CH,Farinotti R

    更新日期:1999-05-10 00:00:00

  • Enhanced oral bioavailability of paclitaxel by D-alpha-tocopheryl polyethylene glycol 400 succinate in mice.

    abstract::Paclitaxel is widely used to treat several types of solid tumors. The commercially available paclitaxel formulation contains Cremophor/ethanol as solubilizers. This study evaluated the effects of D-alpha-tocopheryl polyethylene glycol 400 succinate (TPGS 400) on the oral absorption of paclitaxel in mice. Mice were giv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.04.013

    authors: Ho PY,Yeh TK,Yao HT,Lin HL,Wu HY,Lo YK,Chang YW,Chiang TH,Wu SH,Chao YS,Chen CT

    更新日期:2008-07-09 00:00:00

  • Pharmacokinetics of Gastrodin in rat plasma and CSF after i.n. and i.v.

    abstract::The pharmacokinetic behavior of Gastrodin in rat plasma and cerebrospinal fluid (CSF) after intranasal and intravenous administration (50mg kg(-1)) was investigated. Intranasal administration of Gastrodin provided a comparable AUC in CSF compared with the intravenous administration. But Gastrodin level in plasma was v...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.03.041

    authors: Wang Q,Chen G,Zeng S

    更新日期:2007-08-16 00:00:00

  • PLGA-based drug delivery systems: importance of the type of drug and device geometry.

    abstract::Different types of ibuprofen- and lidocaine-loaded, poly(lactic-co-glycolic acid) (PLGA)-based microparticles and thin, free films of various dimensions were prepared and physico-chemically characterized in vitro. The obtained experimental results were analyzed using mathematical theories based on Fick's second law of...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.10.030

    authors: Klose D,Siepmann F,Elkharraz K,Siepmann J

    更新日期:2008-04-16 00:00:00

  • Zinc delivery from non-woven fibres within a therapeutic nipple shield.

    abstract::A Therapeutic Nipple Shield (TNS) was previously developed to respond to the global need for new infant therapeutic delivery technologies. However, the release efficiency for the same Active Pharmaceutical Ingredient (API) from different therapeutic matrices within the TNS formulation has not yet been investigated. To...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.12.042

    authors: Maier T,Scheuerle RL,Markl D,Bruggraber S,Zeitler A,Fruk L,Slater NKH

    更新日期:2018-02-15 00:00:00

  • Properties of solid dispersions of piroxicam in polyvinylpyrrolidone.

    abstract::Solid dispersions of piroxicam were prepared with polyvinylpyrrolidone (PVP) K-17 PF and PVP K-90 by solvent method. The physical state and drug:PVP interaction of solid dispersions and physical mixtures were characterized by X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy and differential scanning c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00070-8

    authors: Tantishaiyakul V,Kaewnopparat N,Ingkatawornwong S

    更新日期:1999-04-30 00:00:00

  • Engineering of nano-crystalline drug suspensions: employing a physico-chemistry based stabilizer selection methodology or approach.

    abstract::This paper describes a systematic approach to select optimum stabilizer for the preparation of nano-crystalline suspensions of an active pharmaceutical ingredient (API). The stabilizer can be either a dispersant or a combination of dispersant and wetting agent. The proposed screening method is a quick and efficient wa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.09.048

    authors: Nakach M,Authelin JR,Tadros T,Galet L,Chamayou A

    更新日期:2014-12-10 00:00:00

  • Dissolution performance of binary amorphous drug combinations--Impact of a second drug on the maximum achievable supersaturation.

    abstract::An increased number of amorphous formulations of poorly water soluble drugs are being introduced into the market due to their higher transient solubility and thus faster absorption and higher bioavailability. While most amorphous drug products contain a single drug substance, there is a growing trend towards co-formul...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.026

    authors: Trasi NS,Taylor LS

    更新日期:2015-12-30 00:00:00

  • Evaluation of air-interfaced Calu-3 cell layers for investigation of inhaled drug interactions with organic cation transporters in vitro.

    abstract::A physiologically pertinent in vitro model is urgently needed for probing interactions between inhaled drugs and the organic cation transporters (OCT) in the bronchial epithelium. This study evaluated OCT expression, functionality, inhibition by common inhaled drugs and impact on formoterol transepithelial transport i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.12.036

    authors: Mukherjee M,Pritchard DI,Bosquillon C

    更新日期:2012-04-15 00:00:00

  • Influence of surface charge and inner composition of porous nanoparticles to cross blood-brain barrier in vitro.

    abstract::The aim of these studies was to evaluate the binding, uptake and transcytosis of 60 nm porous nanoparticles (NPs) that differed in their surface charge and inner composition on the blood-brain barrier (BBB). They were prepared from maltodextrins derived with or without a cationic ligand. In the cationic NPs an anionic...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.06.023

    authors: Jallouli Y,Paillard A,Chang J,Sevin E,Betbeder D

    更新日期:2007-11-01 00:00:00

  • A prototype 'Infucon' device for continuous infusion of microbubbles in vivo.

    abstract::A device for continuous infusion of microbubbles (MBs) 'Infucon' has been designed, constructed and tested on rabbits. The device prevents MBs from flotation and accumulation in the layer directly below the surface in the syringe injection during i.v. application. Homogenous i.v. application of MBs was tested on 16 ma...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.12.026

    authors: Kauerová Z,Lukáč R,Kohout P,Mašek J,Koudelka Š,Plocková J,Vašíčková M,Vlašín M,Turánek J

    更新日期:2013-01-30 00:00:00

  • Designed sponges based on chitosan and cyclodextrin polymer for a local release of ciprofloxacin in diabetic foot infections.

    abstract::Diabetic foot infections are the most common complications requiring hospitalisation of patients with diabetes. They often result in amputation to extremities and are associated with high morbi-mortality rates, especially when bone is infected. Treatment of these complications is based on surgical procedures, nursing ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119677

    authors: Gauzit Amiel A,Palomino-Durand C,Maton M,Lopez M,Cazaux F,Chai F,Neut C,Foligné B,Martel B,Blanchemain N

    更新日期:2020-09-25 00:00:00

  • A centrifuge technique for the evaluation of the extent of water movement in wet powder masses.

    abstract::A centrifuge method has been applied to the assessment of water retention in pharmaceutical powders. Five drug models and microcrystalline cellulose (MCC) were each mixed with different amounts of water and centrifuged at different speeds. The amount of water retained by the wet mass was evaluated by drying the powder...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00201-x

    authors: Tomer G,Newton JM

    更新日期:1999-10-15 00:00:00

  • Microencapsulation of amorphous solid dispersions of fenretinide enhances drug solubility and release from PLGA in vitro and in vivo.

    abstract::The purpose of this study was to develop solid dispersions of fenretinide(4HPR), incorporate them into poly(lactic-co-glycolic)(PLGA) millicylindrical implants, and evaluate the resulting implants in vitro and in vivo for future applications in oral cancer chemoprevention. Due to the extreme hydrophobicity of 4HPR, 4H...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119475

    authors: Nieto K,Mallery SR,Schwendeman SP

    更新日期:2020-08-30 00:00:00

  • Squalenoyl-gemcitabine/edelfosine nanoassemblies: Anticancer activity in pediatric cancer cells and pharmacokinetic profile in mice.

    abstract::Despite the great advances accomplished in the treatment of pediatric cancers, recurrences and metastases still exacerbate prognosis in some aggressive solid tumors such as neuroblastoma and osteosarcoma. In view of the poor efficacy and toxicity of current chemotherapeutic treatments, we propose a single multitherape...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119345

    authors: Rodríguez-Nogales C,Mura S,Couvreur P,Blanco-Prieto MJ

    更新日期:2020-05-30 00:00:00

  • Functionalized (poly(ɛ-caprolactone))₂-poly(ethylene glycol) nanoparticles with grafting nicotinic acid as drug carriers.

    abstract::Nicotinic acid was grafted on (poly(ɛ-caprolactone))(2)-poly(ethylene glycol) copolymers that were used for the preparation of nanoparticles with the objectives to monitor particle size and to optimize the drug loading capacity as well as the release profile of the particles. Increasing amounts of grafting nicotinic a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.11.033

    authors: Suksiriworapong J,Sripha K,Kreuter J,Junyaprasert VB

    更新日期:2012-02-28 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

  • Formulation strategies for the stabilization of tetanus toxoid in poly(lactide-co-glycolide) microspheres.

    abstract::The development of a single-dose tetanus vaccine based on Poly(Lactic acid) (PLA) or Poly(Lactide-co-Glycolide) (PLGA) microspheres has been complicated due to the instability of tetanus toxoid (TT) inside these systems. Herein we report an attempt to re-design PLGA microspheres by co-encapsulating TT in the dry solid...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00178-7

    authors: Sánchez A,Villamayor B,Guo Y,McIver J,Alonso MJ

    更新日期:1999-08-20 00:00:00

  • Polymer encapsulation of inorganic nanoparticles for biomedical applications.

    abstract::Hybrid inorganic colloidal particles have attracted a great attention in the last years, and they have been largely used in various applications and more particularly in biomedical nanotechnology. Recently, they are used as carriers for biomolecules, and exploited for use in microsystems, microfluidics and in lab-on-a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2013.09.001

    authors: Ladj R,Bitar A,Eissa MM,Fessi H,Mugnier Y,Le Dantec R,Elaissari A

    更新日期:2013-12-15 00:00:00

  • Validation of fluid bed granulation utilizing artificial neural network.

    abstract::Three innovative components (an annular gap spray system, a booster bottom and an outlet filter) have been developed by Innojet Technologies to improve fluid bed technology and to reduce the common interference factors (clogging of nozzles and outlet filters, spray loss, spray drying and fluidized bed heterogeneity). ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.07.051

    authors: Behzadi SS,Klocker J,Hüttlin H,Wolschann P,Viernstein H

    更新日期:2005-03-03 00:00:00

  • Crystallization rate of amorphous nifedipine analogues unrelated to the glass transition temperature.

    abstract::To examine the relative contributions of molecular mobility and thermodynamic factor, the relationship between glass transition temperature (T(g)) and the crystallization rate was examined using amorphous dihydropyridines (nifedipine (NFD), m-nifedipine (m-NFD), nitrendipine (NTR) and nilvadipine (NLV)) with differing...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.11.052

    authors: Miyazaki T,Yoshioka S,Aso Y,Kawanishi T

    更新日期:2007-05-04 00:00:00

  • Gene expression in an intact ex-vivo skin tissue model following percutaneous delivery of cationic liposome-plasmid DNA complexes.

    abstract::The skin represents an attractive site for the localised gene therapy of dermatological pathologies and as a potential antigen bioreactor following transdermal delivery. Potential also exists for the gene therapy of skin as a cosmetic intervention. The most exploited non-viral gene delivery system involves the complex...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00336-7

    authors: Birchall JC,Marichal C,Campbell L,Alwan A,Hadgraft J,Gumbleton M

    更新日期:2000-03-20 00:00:00

  • Lecithin based nanoemulsions: A comparative study of the influence of non-ionic surfactants and the cationic phytosphingosine on physicochemical behaviour and skin permeation.

    abstract::Charged drug delivery systems are interesting candidates for the delivery of drugs through skin. In the present study, it was possible to create negatively and positively charged oil/water nanoemulsions by using sucrose laureate and polysorbate 80 as non-ionic surfactants. The positively charged nanoemulsions were gen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.11.014

    authors: Hoeller S,Sperger A,Valenta C

    更新日期:2009-03-31 00:00:00