Controlled release of linear-dendritic hybrids of carbosiloxane dendrimer: the effect of hybrid's amphiphilicity on drug-incorporation; hybrid-drug interactions and hydrolytic behavior of nanocarriers.

Abstract:

:Dendritic micelles formed from amphiphilic dendritic ABA triblock copolymers based on organic linear poly(ethylene oxide) and inorganic dendritic block containing silicon atoms (OSC-D(Gn)-PEO-D(Gn)-CSO, n=1-3)(1) were evaluated as drug delivery vehicles for a drug in both lipophilic and hydrophilic forms. The physical parameters of the drug-incorporated carriers including the influences of drug:carrier ratio, the release kinetics of the drugs from the micellar solution were measured. The apparent partition constant of drug between the carriers and the external medium was studied as well. It was observed that the loading efficiency and hydrolytic behavior of the hybrids depend on several factors, such as type of interaction between host and guest molecules, generation of the dendritic copolymers and pH. The release profiles of the drugs from the micelle solution were found to be a slow steady release at pH 1, 7.4 and 10. Investigation of the drug release dynamics in buffered media at pH 7.4 showed that the drug released through the carriers with slight deviation follow Fickian and Case II diffusion mechanisms for drugs in lipophilic and hydrophilic forms, respectively.

journal_name

Int J Pharm

authors

Namazi H,Jafarirad S

doi

10.1016/j.ijpharm.2011.01.007

subject

Has Abstract

pub_date

2011-04-04 00:00:00

pages

167-73

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(11)00021-4

journal_volume

407

pub_type

杂志文章
  • Tableting process optimisation with the application of fuzzy models.

    abstract::A quality-by-design (QbD) principle, including process analytical technology, is becoming the principal idea in drug development and manufacturing. The implementation of QbD into product development and manufacturing requires larger resources, both human and financial, however, large-scale production can be establishe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.01.023

    authors: Belic A,Skrjanc I,Bozic DZ,Vrecer F

    更新日期:2010-04-15 00:00:00

  • Emerging trends in the stabilization of amorphous drugs.

    abstract::The number of active pharmaceutical substances having high therapeutic potential but low water solubility is constantly increasing, making it difficult to formulate these compounds as oral dosage forms. The solubility and dissolution rate, and thus potentially the bioavailability, of these poorly water-soluble drugs c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2012.04.066

    authors: Laitinen R,Löbmann K,Strachan CJ,Grohganz H,Rades T

    更新日期:2013-08-30 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

  • Systematic evaluation of design features enables efficient selection of Π electron-stabilized polymeric micelles.

    abstract::Polymeric micelles (PM) based on poly(ethylene glycol)-b-poly(N-2-benzoyloxypropyl methacrylamide) (mPEG-b-p(HPMA-Bz)) loaded with paclitaxel (PTX-PM) have shown promising results in overcoming the suboptimal efficacy/toxicity profile of paclitaxel. To get insight into the stability of PTX-PM formulations upon storage...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119409

    authors: Sheybanifard M,Beztsinna N,Bagheri M,Buhl EM,Bresseleers J,Varela-Moreira A,Shi Y,van Nostrum CF,van der Pluijm G,Storm G,Hennink WE,Lammers T,Metselaar JM

    更新日期:2020-06-30 00:00:00

  • Gastroretentive drug delivery system of DA-6034, a new flavonoid derivative, for the treatment of gastritis.

    abstract::A gastroretentive drug delivery system of DA-6034, a new synthetic flavonoid derivative, for the treatment of gastritis was developed by using effervescent floating matrix system (EFMS). The therapeutic limitations of DA-6034 caused by its low solubility in acidic conditions were overcome by using the EFMS, which was ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.12.042

    authors: Jang SW,Lee JW,Park SH,Kim JH,Yoo M,Na DH,Lee KC

    更新日期:2008-05-22 00:00:00

  • Hydrogel based approaches for cardiac tissue engineering.

    abstract::Heart failure still represents the leading cause of death worldwide. Novel strategies using stem cells and growth factors have been investigated for effective cardiac tissue regeneration and heart function recovery. However, some major challenges limit their translation to the clinic. Recently, biomaterials have emerg...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.10.061

    authors: Saludas L,Pascual-Gil S,Prósper F,Garbayo E,Blanco-Prieto M

    更新日期:2017-05-25 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

  • Selection of high efficient transdermal lipid vesicle for curcumin skin delivery.

    abstract::Curcumin shows effective anti-inflammatory activities but is seldom used in clinic because of its poor solubility in water and vulnerablity to sunshine ultraviolet effect. Novel lipid vesicles have been developed as carriers for skin delivery. In this paper, lipid vesicles-propylene glycol liposomes (PGL), Ethosomes a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.06.052

    authors: Zhao YZ,Lu CT,Zhang Y,Xiao J,Zhao YP,Tian JL,Xu YY,Feng ZG,Xu CY

    更新日期:2013-09-15 00:00:00

  • Glycerosomes: Investigation of role of 1,2-dimyristoyl-sn-glycero-3-phosphatidycholine (DMPC) on the assembling and skin delivery performances.

    abstract::Glycerosomes were formulated using 1,2-dimyristoyl-sn-glycero-3-phosphatidycholine (DMPC), diclofenac sodium salt and 10, 20 or 30% glycerol in the water phase, while corresponding liposomes were prepared with the same amount of DMPC and diclofenac, without glycerol. The aim of the present work was to evaluate the eff...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.09.026

    authors: Manca ML,Manconi M,Zaru M,Valenti D,Peris JE,Matricardi P,Maccioni AM,Fadda AM

    更新日期:2017-10-30 00:00:00

  • Effects of conditions for preparing nanoparticles composed of aminoethylcarbamoyl-beta-cyclodextrin and ethylene glycol diglycidyl ether on trap efficiency of a guest molecule.

    abstract::Nanoparticles comprising copolymers of aminoethylcarbamoyl-beta-cyclodextrin (AEC-beta-CD) and ethylene glycol diglycidyl ether (EGDGE) are prepared by an interfacial polyaddition reaction in a miniemulsion system. Polymers are formed in a W/O emulsion containing 0.25-10.0% (w/w) water and 5.0% (w/w) surfactant (MO-3S...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.12.015

    authors: Eguchi M,Du YZ,Ogawa Y,Okada T,Yumoto N,Kodaka M

    更新日期:2006-03-27 00:00:00

  • Preparation of olanzapine and methyl-β-cyclodextrin complexes using a single-step, organic solvent-free supercritical fluid process: An approach to enhance the solubility and dissolution properties.

    abstract::The purpose of this study was to evaluate a single-step, organic solvent-free supercritical fluid process for the preparation of olanzapine-methyl-β-cyclodextrin complexes with an express goal to enhance the dissolution properties of olanzapine. The complexes were prepared by supercritical carbon dioxide processing, c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.08.062

    authors: Rudrangi SR,Trivedi V,Mitchell JC,Wicks SR,Alexander BD

    更新日期:2015-10-15 00:00:00

  • Application of spherical silicate to prepare solid dispersion dosage forms with aqueous polymers.

    abstract::The objective of this study is to prepare and characterize solid dispersions of nifedipine (NP) using porous spherical silicate micro beads (MB) that were approximately 100 μm in diameter with vinylpyrrolidone/vinyl acetate copolymer (PVP/VA) and a Wurster-type fluidized bed granulator. Compared with previously report...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.07.037

    authors: Nagane K,Kimura S,Ukai K,Takahashi C,Ogawa N,Yamamoto H

    更新日期:2015-09-30 00:00:00

  • Ligand anchored dendrimers based nanoconstructs for effective targeting to cancer cells.

    abstract::Dendrimers are considered versatile carriers especially for the treatment of diseases like cancer, AIDS, malaria etc. Cancer is a worldwide threat particularly in developing countries. A breakthrough research in this regard is a prime requirement. In the present study, folic acid was conjugated to fifth generation pol...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.04.002

    authors: Gupta U,Dwivedi SK,Bid HK,Konwar R,Jain NK

    更新日期:2010-06-30 00:00:00

  • Evaluation of the transdermal permeation of different paraben combinations through a pig ear skin model.

    abstract::Although parabens have several features of ideal preservatives, different studies have shown that they may affect human health due to their estrogenic activity. Therefore, various strategies have been applied to reduce their skin penetration. However, the effect of paraben combinations on transdermal permeation has no...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.02.006

    authors: Caon T,Costa AC,de Oliveira MA,Micke GA,Simões CM

    更新日期:2010-05-31 00:00:00

  • Characterization of Re-188-Sn microparticles used for synovitis treatment.

    abstract::Rhenium-188 labeled tin (Sn) microparticles were developed for pain palliation therapy in the patients suffering from synovitis with acute pain. The rhenium tin microparticles were prepared using stannous chloride and freshly eluted (188)ReO(4)(-) from (188)W/(188)Re generator. The aggregated colloidal particles, pack...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.01.014

    authors: Shukla J,Bandopadhyaya GP,Shamim SA,Kumar R

    更新日期:2007-06-29 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

  • Anion effects on electrostatic charging of sterically stabilized, water insoluble drug particles.

    abstract::Water-insoluble suspensions of itraconazole and budesonide were sterically stabilized using nonionic polymers (poloxamer 188 or polysorbate 80) and probed for polymer-anion interactions by measuring changes in particle zeta potential. Anions comprising a range of functionalities and aqueous solubilities were examined....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.10.004

    authors: Owen H,Graham S,Werling JO,Carter PW

    更新日期:2009-02-23 00:00:00

  • Enhancement of solubility and dissolution rate of baicalein, wogonin and oroxylin A extracted from Radix scutellariae.

    abstract::Baicalein, wogonin, and oroxylin A are three major hydrophobic components in the extract of Radix scutellariae with wide spectrum of pharmacological applications. The purpose of this study was to enhance the solubility, dissolution rate and stability of baicalein, wogonin and oroxylin A by solid dispersion (SD) techni...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.068

    authors: Yu H,Chang JS,Kim SY,Kim YG,Choi HK

    更新日期:2017-08-07 00:00:00

  • Development and in vitro evaluation of novel floating chitosan microcapsules for oral use: comparison with non-floating chitosan microspheres.

    abstract::Floating (F) microcapsules containing melatonin (MT) were prepared by the ionic interaction of chitosan and a negatively charged surfactant, sodium dioctyl sulfosuccinate (DOS). The DOS/chitosan complex formation was confirmed employing infrared spectroscopy, differential scanning calorimetry (DSC), solubility and X-r...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00396-4

    authors: El-Gibaly I

    更新日期:2002-12-05 00:00:00

  • Deoxycholate-hydrogels: novel drug carrier systems for topical use.

    abstract::Na-deoxycholate (Na-DOC) forms a viscous thixotropic gel when in contact with excess buffer systems. The resulting gels have been tested as novel drug carrier systems for topical use. The influence of differing amounts of mannitol, glycerol and xylitol on the viscous modulus (G"/Pa) was evaluated by oscillatory measur...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00170-2

    authors: Valenta C,Nowack E,Bernkop-Schnürch A

    更新日期:1999-08-05 00:00:00

  • Lidocaine-loaded non-ionic surfactant vesicles: characterization and in vitro permeation studies.

    abstract::Our research on topical application of lidocaine-loaded non-ionic surfactant vesicles (NSVs) was prompted by the great interest on new delivery systems for local anaesthetics. This study is focused on a novel formulation of NSVs entrapping lidocaine in the form of a free base (LID) and a hydrochloride (LIDHCl). NSVs w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00828-6

    authors: Carafa M,Santucci E,Lucania G

    更新日期:2002-01-01 00:00:00

  • Dehydration of trehalose dihydrate at low relative humidity and ambient temperature.

    abstract::The physico-chemical behaviour of trehalose dihydrate during storage at low relative humidity and ambient temperature was investigated, using a combination of techniques commonly employed in pharmaceutical research. Weight loss, water content determinations, differential scanning calorimetry and X-ray powder diffracti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.01.026

    authors: Jones MD,Hooton JC,Dawson ML,Ferrie AR,Price R

    更新日期:2006-04-26 00:00:00

  • Interactions between a poorly soluble cationic drug and sodium dodecyl sulfate in dissolution medium and their impact on in vitro dissolution behavior.

    abstract::In the pharmaceutical industry, in vitro dissolution testing ofsolid oral dosage forms is a very important tool for drug development and quality control. However, ion-pairing interaction between the ionic drugand surfactants in dissolution medium often occurs, resulting in inconsistent and incomplete drug release. The...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.10.063

    authors: Huang Z,Parikh S,Fish WP

    更新日期:2018-01-15 00:00:00

  • Are all aciclovir cream formulations bioequivalent?

    abstract::Topical aciclovir cream (ACV, Zovirax Cream) containing 40% propylene glycol (PG), the optimum found for skin penetration, is clinically effective in the treatment of recurrent herpes labialis. One hundred and thirty-nine ACV generic creams were analysed and 80% of these contained less than 20% PG. From this, we hypot...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.07.020

    authors: Trottet L,Owen H,Holme P,Heylings J,Collin IP,Breen AP,Siyad MN,Nandra RS,Davis AF

    更新日期:2005-11-04 00:00:00

  • Microagglomeration of pulverized pharmaceutical powders using the Wurster process I. Preparation of highly drug-incorporated, subsieve-sized core particles for subsequent microencapsulation by film-coating.

    abstract::A novel agglomeration process of pulverized pharmaceutical powders into subsieve-sized agglomerates (microagglomeration) was designed for manufacturing highly drug-incorporated core particles for subsequent microencapsulation by film-coating. The microagglomeration of pulverized phenacetin powder, whose mass median di...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00006-x

    authors: Ichikawa H,Fukumori Y

    更新日期:1999-04-15 00:00:00

  • Controlled release of doxorubicin from polyethylene glycol functionalized melanin nanoparticles for breast cancer therapy: Part I. Production and drug release performance of the melanin nanoparticles.

    abstract::In this study, polyethylene glycol (PEG) conjugated melanin nanoparticles (MNPs) were prepared (PEG-MNPs). A model chemotherapy drug, doxorubicin (DOX), was loaded into the PEG-MNPs with varied concentrations (0.125, 0.250, 0.500 mg/mL). TEM images showed that, DOX-PEG-MNPs are spherical-shaped and 15 ± 2.2 nm in diam...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118613

    authors: Ozlu B,Kabay G,Bocek I,Yilmaz M,Piskin AK,Shim BS,Mutlu M

    更新日期:2019-10-30 00:00:00

  • Physicochemical characterization techniques for lipid based delivery systems for siRNA.

    abstract::siRNA based therapeutics is an emerging class of molecules with a high potential for fulfilling the promise of gene medicine. The high selectivity of siRNAs for their targets and subsequent gene ablation has been effectively demonstrated in a wide range of pre-clinical models. siRNA delivery in vivo has been most succ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2011.09.032

    authors: Kapoor M,Burgess DJ,Patil SD

    更新日期:2012-05-01 00:00:00

  • Comparative study on radiolabeling and biodistribution of core-shell silver/polymeric nanoparticles-based theranostics for tumor targeting.

    abstract::A simple and rapid method for radiolabeling of three types of Ag NPs has been performed using 125I isotope, with high labeling yields, >90% without disturbing the optical properties. All the factors affecting labeling yield were studied. In order to monitor the in-vivo tissue uptake of radiolabeled Ag NPs using γ-rays...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.044

    authors: Farrag NS,El-Sabagh HA,Al-Mahallawi AM,Amin AM,AbdEl-Bary A,Mamdouh W

    更新日期:2017-08-30 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

  • Using deconvolution to understand the mechanism for variable plasma concentration-time profiles after intramuscular injection.

    abstract::To introduce better antibiotics for the treatment of some infectious diseases in sheep and to expand the range of antibiotics available for veterinary medicine, pharmacokinetics of two antibiotics marbofloxacin (MBX) and trovafloxacin (TVX) were investigated in sheep after intramuscular injection. Variable and irregul...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.01.046

    authors: Mahmood AH,Liu X,Grice JE,Medley GA,Roberts MS

    更新日期:2015-03-15 00:00:00