Drug release kinetics and transport mechanisms from semi-interpenetrating networks of gelatin and poly(ethylene glycol) diacrylate.

Abstract:

PURPOSE:To elucidate the key parameters affecting solute transport from semi-interpenetrating networks (sIPNs) comprised of poly(ethylene glycol) diacrylate (PEGdA) and gelatin that are partially crosslinked, water-swellable and biodegradable. Effects of material compositions, solute size, solubility, and loading density have been investigated. MATERIALS AND METHODS:sIPNs of following gelatin/PEGdA weight-to-weight ratios were prepared: 10:15, 10:20, 10:30, 15:15, 20:15. Five model solutes of different physicochemical properties were selected, i.e. silver sulfadiazine (AgSD), bupivacaine hydrochloride (Bup), sulfadiazine sodium (NaSD), keratinocyte growth factor (KGF), and bovine serum albumin conjugated with fluorescein isothiocyanate (BSA-FITC). Release studies were performed and the results were analyzed using three hydrogel based common theories (free volume, hydrodynamic and obstruction). RESULTS:The release kinetics of model solutes was influenced by each factor under investigation. Specifically, the initial release rates and intra-gel diffusivity decreased with increasing PEGdA content or increasing solute molecular weight. However, the initial release rate and intra-gel diffusivity increased with increasing gelatin content or increasing solute water solubility, which contradicted with the classical hydrogel based solute transport theories, i.e. increasing polymer volume leads to decreased solute diffusivity within the gel. CONCLUSION:This analysis provides structure-functional information of the sIPN as a potential therapeutic delivery matrix.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Fu Y,Kao WJ

doi

10.1007/s11095-009-9923-1

subject

Has Abstract

pub_date

2009-09-01 00:00:00

pages

2115-24

issue

9

eissn

0724-8741

issn

1573-904X

journal_volume

26

pub_type

杂志文章
  • Initial Drug Dissolution from Amorphous Solid Dispersions Controlled by Polymer Dissolution and Drug-Polymer Interaction.

    abstract:PURPOSE:To identify the key formulation factors controlling the initial drug and polymer dissolution rates from an amorphous solid dispersion (ASD). METHODS:Ketoconazole (KTZ) ASDs using PVP, PVP-VA, HMPC, or HPMC-AS as polymeric matrix were prepared. For each drug-polymer system, two types of formulations with the sa...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-016-1969-2

    authors: Chen Y,Wang S,Wang S,Liu C,Su C,Hageman M,Hussain M,Haskell R,Stefanski K,Qian F

    更新日期:2016-10-01 00:00:00

  • Celiac disease: a challenging disease for pharmaceutical scientists.

    abstract::Celiac disease (CD) is an immune-mediated enteropathy triggered by the ingestion of gluten-containing grains that affects ~1% of the white ethnic population. In the last decades, a rise in prevalence of CD has been observed that cannot be fully explained by improved diagnostics. Genetic predisposition greatly influenc...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0951-x

    authors: Matoori S,Fuhrmann G,Leroux JC

    更新日期:2013-03-01 00:00:00

  • Liposomal co-delivery of omacetaxine mepesuccinate and doxorubicin for synergistic potentiation of antitumor activity.

    abstract:PURPOSE:Anticancer chemotherapy usually involves the administration of several anticancer drugs that differ in their action mechanisms. Here, we aimed to test whether the combination of omacetaxine mepesuccinate (OMT) and doxorubicin (DOX) could show synergism, and whether the liposomal co-delivery of these two drugs c...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1317-3

    authors: Shim G,Lee S,Choi J,Lee S,Kim CW,Oh YK

    更新日期:2014-08-01 00:00:00

  • Immobilization of active urokinase on albumin microspheres: use of a chemical dehydrant and process monitoring.

    abstract::A method of immobilizing urokinase on albumin microspheres has been developed. Laser scattering, which was used to follow particle size from the initial emulsification stage to the final aqueous resuspension of the microsphere stage, showed that particle coalescence and crosslinking were critical parameters in manufac...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015855622459

    authors: Bhargava K,Ando HY

    更新日期:1992-06-01 00:00:00

  • In Vivo performance of ophthalmic preparations of betamethasone and phenylephrine hydrochloride in the rabbit eye: Effect of polyvinyl alcohol.

    abstract::The effect of different concentrations of polyvinyl alcohol 14000 and 72000 (PVA 14 and 72) on the activity of betamethasone and phenylephrine hydrochloride in the rabbit eye was investigated. The polymer of higher molecular weight exerts a more pronounced effect at relatively lower viscosities. Effects on the intraoc...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/A:1016398915965

    authors: Kassem MA,Attia MA,Habib FS,Mohamed AR

    更新日期:1986-08-01 00:00:00

  • A simple rheological method for the in vitro assessment of mucin-polymer bioadhesive bond strength.

    abstract::A simple viscometric method was used to quantify mucin-polymer bioadhesive bond strength. Viscosities of 15% (w/v) porcine gastric mucin dispersions in 0.1 N HCl (pH 1) or 0.1 N acetate buffer (pH 5.5) were measured with a Brookfield viscometer in the absence (eta m) or presence (eta t) of selected neutral, anionic, a...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015812615635

    authors: Hassan EE,Gallo JM

    更新日期:1990-05-01 00:00:00

  • Bisacylphosphonates inhibit hydroxyapatite formation and dissolution in vitro and dystrophic calcification in vivo.

    abstract::Some geminal bisphosphonates are used clinically for a number of important bone/calcium related diseases; however, side effects and lack of selectivity impede their wide use. This work reports the synthesis and evaluation of bisacylphosphonates (e.g., adipoyl- and suberoylbisphosphonate). These compounds were found to...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018956516640

    authors: Golomb G,Schlossman A,Saadeh H,Levi M,Van Gelder JM,Breuer E

    更新日期:1992-01-01 00:00:00

  • Influence of P-glycoprotein modulators on cardiac uptake, metabolism, and effects of idarubicin.

    abstract:PURPOSE:The clinical utility of anthracyclines like idarubicin (IDA) is limited by the occurrence of multidrug resistance and cardiotoxicity. Previous studies have demonstrated that the multidrug transporter P-glycoprotein (P-gp) is present in the heart and have suggested that it exerts a protective function. We sought...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1013022212738

    authors: Kang W,Weiss M

    更新日期:2001-11-01 00:00:00

  • Evaluation of temperature-sensitive, indocyanine green-encapsulating micelles for noninvasive near-infrared tumor imaging.

    abstract:PURPOSE:Indocyanine green (ICG), an FDA-approved near infrared (NIR) dye, has potential application as a contrast agent for tumor detection. Because ICG binds strongly to plasma proteins and exhibits aqueous, photo, and thermal instability, its current applications are largely limited to monitoring blood flow. To addre...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-010-0190-y

    authors: Kim TH,Chen Y,Mount CW,Gombotz WR,Li X,Pun SH

    更新日期:2010-09-01 00:00:00

  • Promoted Antitumor Activity of Myricetin against Lung Carcinoma Via Nanoencapsulated Phospholipid Complex in Respirable Microparticles.

    abstract:PURPOSE:Myricetin (MYR) flavonoid is well-recognized for its antioxidant, anti-inflammatory and anti-tumor potential. Introducing nanomedicine was the ultimate resort to solve the imperfections of this nutraceutical, namely solubility, stability and delivery issues. The study, thus, aims at developing inhalable micropa...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02794-z

    authors: Nafee N,Gaber DM,Elzoghby AO,Helmy MW,Abdallah OY

    更新日期:2020-04-14 00:00:00

  • Improving the selectivity of HAV-peptides in modulating E-cadherin-E-cadherin interactions in the intercellular junction of MDCK cell monolayers.

    abstract:PURPOSE:The objective of this work is to understand the sequence specificity of HAV peptides and to improve their selectivity in regulating E-cadherin-E-cadherin interactions in the intercellular junctions. METHODS:Peptide 1 was modified using an alanine scanning method to give peptides 2-6. The ability of these pepti...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1011094025008

    authors: Makagiansar IT,Avery M,Hu Y,Audus KL,Siahaan TJ

    更新日期:2001-04-01 00:00:00

  • Molecular mobility as a predictor of the water sorption by annealed amorphous trehalose.

    abstract:PURPOSE:The work aims at investigating the correlation of water sorption potential with different measures of molecular mobility in an annealed amorphous model compound (trehalose). METHODS:Amorphous trehalose, prepared by freeze-drying, was annealed at 100°C (17°C < T (g)) for up to 120 h. Global mo...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0910-6

    authors: Bhardwaj SP,Suryanarayanan R

    更新日期:2013-03-01 00:00:00

  • Improved intestinal absorption of an enteric-coated sodium ursodeoxycholate formulation.

    abstract::A new enteric-coated formulation of sodium ursodeoxycholate was prepared and administered to man. The barrier film disintegrates and releases the drug only at pH > or = 5.5. The sodium salt of glycoursodeoxycholate was also prepared and encapsulated like ursodeoxycholate. Serum levels of ursodeoxycholate and glycourso...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018907825281

    authors: Roda A,Roda E,Marchi E,Simoni P,Cerrè C,Pistillo A,Polimeni C

    更新日期:1994-05-01 00:00:00

  • Molecular modeling study of diltiazem mimics at L-type calcium channels.

    abstract:PURPOSE:A theoretical study was performed to generate a pharmacophore model for chemically diverse structures that specifically interact with the diltiazem binding site of L-type calcium channels. METHODS:Via molecular mechanics and quantum chemical methods solvation energies, logP values, conformational and electroni...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015037800903

    authors: Schleifer KJ,Tot E

    更新日期:1999-10-01 00:00:00

  • Dynamic analysis of GI absorption and hepatic distribution processes of telmisartan in rats using positron emission tomography.

    abstract:PURPOSE:To dynamically analyze the processes of oral absorption and hepatobiliary distribution of telmisartan using positron emission tomography (PET). METHODS:(11)C-labeled telmisartan ([(11)C]TEL) was orally administered to rats with or without non-radiolabeled telmisartan (0.5, and 10 mg/kg). PET scanning of abdomi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0768-7

    authors: Kataoka M,Takashima T,Shingaki T,Hashidzume Y,Katayama Y,Wada Y,Oh H,Masaoka Y,Sakuma S,Sugiyama Y,Yamashita S,Watanabe Y

    更新日期:2012-09-01 00:00:00

  • Biodegradable poly(2-dimethylamino ethylamino)phosphazene for in vivo gene delivery to tumor cells. Effect of polymer molecular weight.

    abstract:PURPOSE:Previously, we have shown that complexes of plasmid DNA with the biodegradable polymer poly(2-dimethylamino ethylamino)phosphazene (p(DMAEA)-ppz) mediated tumor selective gene expression after intravenous administration in mice. In this study, we investigated the effect of p(DMAEA)-ppz molecular weight on both ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9299-z

    authors: de Wolf HK,de Raad M,Snel C,van Steenbergen MJ,Fens MH,Storm G,Hennink WE

    更新日期:2007-08-01 00:00:00

  • Stability and solubility of celecoxib-PVP amorphous dispersions: a molecular perspective.

    abstract:PURPOSE:The purpose of the current study is to evaluate the solubility advantage offered by celecoxib (CEL) amorphous systems and to characterize and correlate the physical and thermodynamic properties of CEL and its amorphous molecular dispersions containing poly(vinylpyrrolidone) (PVP). METHODS:The measurement of cr...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000045226.42859.b8

    authors: Gupta P,Kakumanu VK,Bansal AK

    更新日期:2004-10-01 00:00:00

  • Cyclodextrin sulfates: characterization as polydisperse and amorphous mixtures.

    abstract::Alpha- and beta-cyclodextrins and their hydroxypropyl derivatives were converted by the reaction with chlorosulfonic acid in pyridine to the corresponding sulfates. Cyclodextrin sulfates were shown by fast-atom bombardment mass spectrometry (negative ion mode, triethanolamine matrix) to be mixtures with nearly symmetr...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015854402122

    authors: Pitha J,Mallis LM,Lamb DJ,Irie T,Uekama K

    更新日期:1991-09-01 00:00:00

  • Pharmacodynamics of insulin following intravenous and enteral administrations of porcine-zinc insulin to rats.

    abstract::Previous work from this laboratory showed site-dependent variations in the apparent permeability of insulin as measured using the everted rat gut sac technique, with the greatest permeability in the distal jejunum and the lowest in the duodenum (5). To quantify better the rate and extent of insulin absorption from the...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015894125611

    authors: Schilling RJ,Mitra AK

    更新日期:1992-08-01 00:00:00

  • Predicting skin permeability.

    abstract::Published permeability coefficient (Kp) data for the transport of a large group of compounds through mammalian epidermis were analyzed by a simple model based upon permeant size [molecular volume (MV) or molecular weight (MW)] and octanol/water partition coefficient (Koct). The analysis presented is a facile means to ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015810312465

    authors: Potts RO,Guy RH

    更新日期:1992-05-01 00:00:00

  • Use of artificial digestive systems to investigate the biopharmaceutical factors influencing the survival of probiotic yeast during gastrointestinal transit in humans.

    abstract:PURPOSE:To evaluate the influence of the main biopharmaceutical factors on the viability of a new probiotic yeast strain, using dynamic in vitro systems simulating human gastric/small intestinal (TIM) and large intestinal (ARCOL) environments. METHODS:The viability of Saccharomyces cerevisiae CNCM I-3856 throughout th...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-011-0620-5

    authors: Blanquet-Diot S,Denis S,Chalancon S,Chaira F,Cardot JM,Alric M

    更新日期:2012-06-01 00:00:00

  • Cellular handling of a dexamethasone-anti-E-selectin immunoconjugate by activated endothelial cells: comparison with free dexamethasone.

    abstract:PURPOSE:For selective inhibition of endothelial cell activation in chronic inflammation, we have developed a dexamethasone-anti-E-selectin immunoconjugate. The present study was performed to evaluate the cellular handling of this immunoconjugate by activated primary endothelial cells and to compare its drug delivery ca...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1020769716288

    authors: Kok RJ,Everts M,Asgeirsdóttir SA,Meijer DK,Molema G

    更新日期:2002-11-01 00:00:00

  • Liposomes co-Loaded with 6-Phosphofructo-2-Kinase/Fructose-2, 6-Biphosphatase 3 (PFKFB3) shRNA Plasmid and Docetaxel for the Treatment of non-small Cell Lung Cancer.

    abstract:PURPOSE:Non-small cell lung cancer is the leading cause of cancer related deaths globally. Considering the side effects and diminishing chemosensitivity to chemotherapy, novel treatment approaches are sought. Hence, we aim to develop a liposomal co-delivery system of pDNA expressing shRNA against PFKFB3 (pshPFKFB3) and...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2244-x

    authors: Chowdhury N,Vhora I,Patel K,Doddapaneni R,Mondal A,Singh M

    更新日期:2017-11-01 00:00:00

  • Heparin-paclitaxel conjugates using mixed anhydride as intermediate: synthesis, influence of polymer structure on drug release, anticoagulant activity and in vitro efficiency.

    abstract:PURPOSE:The heparin-paclitaxel conjugates using amino acid as linker (HD2), with low anticoagulant activity, the similar anticancer activity as paclitaxel, offer great potential for further investigation. METHODS:Two types of heparin-paclitaxel conjugates (HD) have been developed, in which O-acetylated heparin as carr...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-008-9762-5

    authors: Wang Y,Xin D,Liu K,Xiang J

    更新日期:2009-04-01 00:00:00

  • Current Trends on Medical and Pharmaceutical Applications of Inkjet Printing Technology.

    abstract::Inkjet printing is an attractive material deposition and patterning technology that has received significant attention in the recent years. It has been exploited for novel applications including high throughput screening, pharmaceutical formulations, medical devices and implants. Moreover, inkjet printing has been imp...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-016-1931-3

    authors: Scoutaris N,Ross S,Douroumis D

    更新日期:2016-08-01 00:00:00

  • A novel one-step drug-loading procedure for water-soluble amphiphilic nanocarriers.

    abstract:PURPOSE:The lack of water-solubility hampers the use of many potent pharmaceuticals. Polymeric micelles are self-assembled nanocarriers with versatile properties that can be engineered to solubilize, target, and release hydrophobic drugs in a controlled-release fashion. Unfortunately, their large-scale use is limited b...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000029284.40637.69

    authors: Fournier E,Dufresne MH,Smith DC,Ranger M,Leroux JC

    更新日期:2004-06-01 00:00:00

  • In vitro/in vivo correlation for 14C-methylated lysozyme release from poly(ether-ester) microspheres.

    abstract:PURPOSE:The purpose of this study was to obtain an in vitro/in vivo correlation for the sustained release of a protein from poly(ethylene glycol) terephthalate (PEGT)/poly(butylene terephthalate) (PBT) microspheres. METHODS:Radiolabeled lysozyme was encapsulated in PEGT/PBT microspheres via a water-in-oil-in-water emu...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/B:PHAM.0000019303.12086.d1

    authors: van Dijkhuizen-Radersma R,Wright SJ,Taylor LM,John BA,de Groot K,Bezemer JM

    更新日期:2004-03-01 00:00:00

  • Nebulization of fluids of different physicochemical properties with air-jet and ultrasonic nebulizers.

    abstract:PURPOSE:Empirical formulae relate the mean size of primary droplets from jet and ultrasonic nebulizers to a fluid's physicochemical properties. Although the size selective "filtering" effects of baffling and evaporation may modify the secondary aerosol produced, this research sought to evaluate whether viscosity and su...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016205520044

    authors: McCallion ON,Taylor KM,Thomas M,Taylor AJ

    更新日期:1995-11-01 00:00:00

  • Human monoclonal antibody fragments targeting matrilin-3 in growth plate cartilage.

    abstract:PURPOSE:Many genetic disorders, including chondrodysplasias, and acquired disorders impair growth plate function, resulting in short and sometimes malformed bones. There are multiple endocrine and paracrine factors that promote chondrogenesis at the growth plate, which could potentially be used to treat these disorders...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-015-1636-z

    authors: Cheung CS,Zhu Z,Lui JC,Dimitrov D,Baron J

    更新日期:2015-07-01 00:00:00

  • Enhanced Follicular Delivery of Finasteride to Human Scalp Skin Using Heat and Chemical Penetration Enhancers.

    abstract:PURPOSE:The aim of this work was to evaluate whether improved topical delivery of finasteride, focussed to the hair follicles of human scalp skin could be achieved with application of short durations of heat and use of specific chemical penetration enhancers. METHODS:Franz cell experiments with human scalp skin were p...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02822-y

    authors: Farah HA,Brown MB,McAuley WJ

    更新日期:2020-05-31 00:00:00