Lyotropic liquid crystalline phases formed from glycerate surfactants as sustained release drug delivery systems.

Abstract:

:A new class of surfactants with glycerate headgroups, that form viscous lyotropic liquid crystalline phases in excess water, have been investigated for their potential to provide sustained release matrices for depot drug delivery. Oleyl glycerate and phytanyl glycerate were used as representative surfactants of this new class, and their behaviour compared with that of glyceryl monooleate (GMO). The surfactants were found to form reverse hexagonal phase (H(II)) in excess water, and the matrices were loaded with a series of model hydrophobic and hydrophilic drugs, (paclitaxel, irinotecan, glucose, histidine and octreotide), and the release kinetics determined. In all cases, the release behaviour obeyed Higuchi kinetics, with linear drug release versus square root of time. The H(II) phases released model drugs slower than the GMO cubic phase matrix. The oleyl glycerate matrix was found to consistently release drug faster than the phytanyl glycerate matrix, despite both matrices being based on H(II) phase. To further demonstrate the potential utility of these materials as drug depot delivery systems, an injectable precursor formulation for octreotide was also prepared and demonstrated to provide controlled release for the peptide. The stability of the H(II) phase to likely in vivo breakdown products was also assessed.

journal_name

Int J Pharm

authors

Boyd BJ,Whittaker DV,Khoo SM,Davey G

doi

10.1016/j.ijpharm.2005.11.033

keywords:

subject

Has Abstract

pub_date

2006-02-17 00:00:00

pages

218-26

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(05)00806-9

journal_volume

309

pub_type

杂志文章
  • Influence of monocaprin on the permeability of a diacidic drug BTA-243 across Caco-2 cell monolayers and everted gut sacs.

    abstract::This study explores the potential of the monoglyceride monocaprin as an enhancer of the epithelial permeability of the beta(3)-adrenoceptor agonist BTA-243, as an approach to improving the bioavailability of this drug. The permeabilities of BTA-243 and mannitol (paracellular marker) in Caco-2 cell monolayer and everte...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00343-5

    authors: Brown JR,Collett JH,Attwood D,Ley RW,Sims EE

    更新日期:2002-10-01 00:00:00

  • A chitosan hydrogel-based cancer drug delivery system exhibits synergistic antitumor effects by combining with a vaccinia viral vaccine.

    abstract::Cancer treatment combining chemotherapy and immunotherapy has been vigorously exploited to further improve cancer therapeutic efficacy. This study investigated a new chemoimmunotherapy approach utilizing hydrogel as a local anti-cancer drug delivery system. Chitosan hydrogel containing doxorubicin (CH-DOX) and vaccini...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.08.014

    authors: Han HD,Song CK,Park YS,Noh KH,Kim JH,Hwang T,Kim TW,Shin BC

    更新日期:2008-02-28 00:00:00

  • Knowledge management in secondary pharmaceutical manufacturing by mining of data historians-A proof-of-concept study.

    abstract::In this proof-of-concept study, a methodology is proposed to systematically analyze large data historians of secondary pharmaceutical manufacturing systems using data mining techniques. The objective is to develop an approach enabling to automatically retrieve operation-relevant information that can assist the managem...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.03.035

    authors: Meneghetti N,Facco P,Bezzo F,Himawan C,Zomer S,Barolo M

    更新日期:2016-05-30 00:00:00

  • Sinomenine hydrochloride loaded thermosensitive liposomes combined with microwave hyperthermia for the treatment of rheumatoid arthritis.

    abstract::The conventional medications are still facing a huge challenge for the treatment of rheumatoid arthritis (RA). Thus, looking for an effective therapy of RA has became an urgent issue nowadays. In this study, a novel thermosensitive liposome loaded with sinomenine hydrochloride (SIN-TSL) was developed by a pH gradient ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.119001

    authors: Shen Q,Zhang X,Qi J,Shu G,Du Y,Ying X

    更新日期:2020-02-25 00:00:00

  • Intranasal spray formulation containing rizatriptan benzoate for the treatment of migraine.

    abstract::Rizatriptan produces antimigraine activity by acting as selective agonist of 5-HT1B and 5-HT1D receptors present on intracranial and extracerebral blood vessels. Absorption from oral tablet is slow with Tmax of approximately 1-1.5 h. A few attempts have been made to promote rapid absorption such as oral or sublingual ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118702

    authors: Chokshi A,Vaishya R,Inavolu R,Potta T

    更新日期:2019-11-25 00:00:00

  • Plasticizer di(2-ethylhexyl)phthalate (DEHP) release in wet-primed extracorporeal membrane oxygenation (ECMO) circuits.

    abstract::A wet-primed ready-to-use extracorporeal membrane oxygenation (ECMO) circuit is used in some centres for rapid deployment of ECMO during cardiopulmonary resuscitation. Yet, the potential release of plasticizer di(2-ethylhexyl)phthalate (DEHP) from the polyvinyl chloride tubing in the circuit during storage is a concer...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.01.030

    authors: Han J,Beeton A,Long P,Karimova A,Robertson A,Cross N,Smith L,O'Callaghan M,Goldman A,Brown K,Tuleu C

    更新日期:2005-04-27 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

  • Heat shock protein derivatives for delivery of antigens to antigen presenting cells.

    abstract::Delivery of antigens to antigen presenting cells (APCs) is a key issue for developing effective cancer vaccines. Controlling the tissue distribution of antigens can increase antigen-specific immune responses, including the induction of cytotoxic T lymphocytes (CTL). Heat shock protein 70 (Hsp70) forms complexes with a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2007.09.030

    authors: Nishikawa M,Takemoto S,Takakura Y

    更新日期:2008-04-16 00:00:00

  • Graphene oxide crosslinked-zein nanofibrous scaffolds for prominent Cu-adsorption as tissue regeneration promoters in diabetic rats: Nanofibers optimization and in vivo assessment.

    abstract::Diabetic ulcers are prone to bacterial contamination and can severely affect patient's quality of life. This study is first report to explore copper-grafted graphene oxide-crosslinked zein scaffolds (Cu-GZS) for promoting cutaneous excision wounds healing as a promising therapeutic modality in diabetic male-rats. Cu-G...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119919

    authors: El-Lakany SA,Kamoun EA,Abd-Elhamid AI,Aly RG,Samy WM,Elgindy NA

    更新日期:2020-11-30 00:00:00

  • Exploring optimized methoxy poly(ethylene glycol)-block-poly(ε-caprolactone) crystalline cored micelles in anti-glaucoma pharmacotherapy.

    abstract::Methoxy-poly(ethylene glycol)-b-poly(ε-caprolactone) (mPEG-PCL) polymeric micelles (PMs) open a promising avenue through which ocular drug delivery with superior efficacy and tolerability can be potentially obtained. Methazolamide (MTZ) is an anti-glaucoma drug exhibiting poor corneal penetration, making it an ideal c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.06.011

    authors: Elmowafy E,Gad H,Biondo F,Casettari L,Soliman ME

    更新日期:2019-07-20 00:00:00

  • Effect of structural factors on release profiles of camptothecin from block copolymer conjugates with high load of drug.

    abstract::The aim of the present work was the synthesis and study the kinetics and profiles of camptothecin (CPT) release form block co- and ter-polymer conjugates comprising polylactide (PLA) segments and CPT moieties, structurally diverse by degrees of branching, content of d-PLA units and poly(ethylene glycol) methyl ether m...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.01.022

    authors: Plichta A,Kowalczyk S,Olędzka E,Sobczak M,Strawski M

    更新日期:2018-03-01 00:00:00

  • Dry powdered aerosols of diatrizoic acid nanoparticle agglomerates as a lung contrast agent.

    abstract::Aerosolized contrast agents may improve the resolution of biomedical imaging modalities and enable more accurate diagnosis of lung diseases. Many iodinated compounds, such as diatrizoic acid, have been shown to be safe and useful for radiographic examination of the airways. Formulations of such compounds must be impro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.03.009

    authors: El-Gendy N,Aillon KL,Berkland C

    更新日期:2010-05-31 00:00:00

  • Distinct transduction modes of arginine-rich cell-penetrating peptides for cargo delivery into tumor cells.

    abstract::The application of cell-penetrating peptides (CPPs) for delivering various cargo molecules with biological functions into cells has gained much attention in recent years. However, the internalization mechanisms and delivery properties of CPP-cargo remains controversial. In this study, low- and high-molecular-weight ca...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.08.001

    authors: Ma DX,Shi NQ,Qi XR

    更新日期:2011-10-31 00:00:00

  • Preparation and characterization of two-phase melt systems of lidocaine.

    abstract::The melting point of lidocaine was significantly lowered when mixed with thymol and/or aqueous ethanol. Mixtures of lidocaine and thymol at ratios within the range of 30:70-70:30 (w:w) became homogeneous oils at 25 degrees C. In a pH 9.2 carbonate buffer containing 25% ethanol, lidocaine (5%, w:w) also liquefied at 25...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00689-5

    authors: Kang L,Jun HW,Mani N

    更新日期:2001-07-03 00:00:00

  • Delivery of salmon calcitonin using a microneedle patch.

    abstract::Peptides and polypeptides have important pharmacological properties but only a limited number have been exploited as therapeutics because of problems related to their delivery. Most of these drugs require a parenteral delivery system which introduces the problems of pain, possible infection, and expertise required to ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.11.046

    authors: Tas C,Mansoor S,Kalluri H,Zarnitsyn VG,Choi SO,Banga AK,Prausnitz MR

    更新日期:2012-02-28 00:00:00

  • High loading fragrance encapsulation based on a polymer-blend: preparation and release behavior.

    abstract::The six fragrances, camphor, citronellal, eucalyptol, limonene, menthol and 4-tert-butylcyclohexyl acetate, which represent different chemical functionalities, were encapsulated with a polymer-blend of ethylcellulose (EC), hydroxypropyl methylcellulose (HPMC) and poly(vinyl alcohol) (PV(OH)) using solvent displacement...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.02.020

    authors: Sansukcharearnpon A,Wanichwecharungruang S,Leepipatpaiboon N,Kerdcharoen T,Arayachukeat S

    更新日期:2010-05-31 00:00:00

  • Image-based analysis of the size- and time-dependent penetration of polymeric micelles in multicellular tumor spheroids and tumor xenografts.

    abstract::While the heightened tumor accumulation of systemically administered nanomedicines relative to conventional chemotherapeutic agents has been well established, corresponding improvements in therapeutic efficacy have often been incommensurate. This observation may be attributed to the limited exposure of cancer cells to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.01.010

    authors: Mikhail AS,Eetezadi S,Ekdawi SN,Stewart J,Allen C

    更新日期:2014-04-10 00:00:00

  • Characterization and aerodynamic evaluation of spray dried recombinant human growth hormone using protein stabilizing agents.

    abstract::The effect of the protein stabilizers on the stability and aerosol performance of spray dried recombinant human growth hormone (SD rhGH) was investigated. rhGH solution was spray dried alone, with polysorbate 20 (at three concentrations of 0.05%, 0.01%, and 0.005%), Zn(2+) (by Zn(2+):rhGH molar ratio of 2:1 and 4:1), ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.10.053

    authors: Jalalipour M,Gilani K,Tajerzadeh H,Najafabadi AR,Barghi M

    更新日期:2008-03-20 00:00:00

  • Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes.

    abstract::The purpose of the present study was to evaluate the enhancement of tolbutamide (TBM) oral bioavailability and hypoglycaemic activity through complexation with beta-cyclodextrin (beta-CD) and hydroxypropyl-beta-cyclodextrin (HP-beta-CD). TBM and its freeze-dried inclusion complexes were administered to rabbits (New ze...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00445-2

    authors: Veiga F,Fernandes C,Teixeira F

    更新日期:2000-07-20 00:00:00

  • Mechanistic study on rapid fabrication of fibrous films via centrifugal melt spinning.

    abstract::Fibrous films have attracted considerable attention in the field of drug delivery and wound dressings owing to their porous structure and highly aligned fiber orientation. However, current fabrication methods such as electrospinning have certain limitations, including high voltage requirement and conductivity dependen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.02.005

    authors: Yang Y,Zheng N,Zhou Y,Shan W,Shen J

    更新日期:2019-04-05 00:00:00

  • Effect of cholesterol and temperature on the elastic properties of niosomal membranes.

    abstract::The mechanical characteristics of non-ionic bilayer membranes composed of sorbitan monostearate, cholesterol and poly-24-oxyethylene cholesteryl were studied by measuring the modulus of surface elasticity (mu), a measure of membrane strength, as a function of cholesterol content and temperature. The modulus of surface...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.05.009

    authors: Nasseri B

    更新日期:2005-08-26 00:00:00

  • Achieving delayed release of freeze-dried probiotic strains by extrusion, spheronization and fluid bed coating - evaluated using a three-step in vitro model.

    abstract::Intake of probiotics is associated with many health benefits, which has generated an interest in formulating viable probiotic supplements. The present study had two aims. The first aim was to achieve gastrointestinal protection and delayed release of viable probiotics by pelletizing and coating freeze-dried probiotic ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120022

    authors: Jacobsen NMY,Caglayan I,Caglayan A,Bar-Shalom D,Müllertz A

    更新日期:2020-12-15 00:00:00

  • Parenteral nanoemulsions as promising carriers for brain delivery of risperidone: Design, characterization and in vivo pharmacokinetic evaluation.

    abstract::This paper describes design and evaluation of parenteral lecithin-based nanoemulsions intended for brain delivery of risperidone, a poorly water-soluble psychopharmacological drug. The nanoemulsions were prepared through cold/hot high pressure homogenization and characterized regarding droplet size, polydispersity, su...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.07.007

    authors: Đorđević SM,Cekić ND,Savić MM,Isailović TM,Ranđelović DV,Marković BD,Savić SR,Timić Stamenić T,Daniels R,Savić SD

    更新日期:2015-09-30 00:00:00

  • Magnetic solid lipid nanoparticles in hyperthermia against colon cancer.

    abstract::A reproducible double emulsion/solvent evaporation procedure is developed to formulate magnetic solid lipid nanoparticles (average size≈180 nm) made of iron oxide cores embedded within a glyceryl trimyristate solid matrix. The physicochemical characterization of the nanocomposites ascertained the efficacy of the prepa...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.03.005

    authors: Muñoz de Escalona M,Sáez-Fernández E,Prados JC,Melguizo C,Arias JL

    更新日期:2016-05-17 00:00:00

  • Effective melanoma cancer suppression by iontophoretic co-delivery of STAT3 siRNA and imatinib using gold nanoparticles.

    abstract::Co-delivery of chemotherapeutic agents improve anti-tumor efficacy and reduce cancer resistance. Here, we report development of layer-by-layer assembled gold nanoparticles (LbL-AuNP) containing anti-STAT3 siRNA and imatinib mesylate (IM) to treat melanoma. The combination treatment with STAT3 siRNA and IM in B16F10 me...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.087

    authors: Labala S,Jose A,Chawla SR,Khan MS,Bhatnagar S,Kulkarni OP,Venuganti VVK

    更新日期:2017-06-20 00:00:00

  • Phase behavior of itraconazole-phenol mixtures and its pharmaceutical applications.

    abstract::The aims of this study were to examine the phase behavior of itraconazole-phenol mixtures and assess the feasibility of topical formulations of itraconazole using eutectic mixture systems. Itraconazole-phenol eutectic mixtures were characterized using differential scanning calorimetry, Fourier transform infrared spect...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.07.054

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

    更新日期:2012-10-15 00:00:00

  • Enhanced anti-tumor and anti-metastasis therapy for triple negative breast cancer by CD44 receptor-targeted hybrid self-delivery micelles.

    abstract::Tumor growth and metastasis are multistep processes regulated by multiple signaling pathways. The successful treatment of cancer largely depends on the ability to inhibit metastatic process. Multiphase inhibition of metastasis is a promising approach. Here, we described a targeting delivery system which was constructe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119085

    authors: Yang Y,Long Y,Wang Y,Ren K,Li M,Zhang Z,Xiang B,He Q

    更新日期:2020-03-15 00:00:00

  • Blend uniformity analysis of pharmaceutical products by Broadband Acoustic Resonance Dissolution Spectroscopy (BARDS).

    abstract::Blend uniformity analysis (BUA) is a routine and highly regulated aspect of pharmaceutical production. In most instances, it involves quantitative determination of individual components of a blend in order to ascertain the mixture ratio. This approach often entails the use of costly and sophisticated instrumentation a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.07.073

    authors: Fitzpatrick D,Scanlon E,Krüse J,Vos B,Evans-Hurson R,Fitzpatrick E,McSweeney S

    更新日期:2012-11-15 00:00:00

  • Investigation of properties and recrystallisation behaviour of amorphous indomethacin samples prepared by different methods.

    abstract::The aim of this study was to investigate if amorphous indomethacin samples, prepared using different preparation methods, exhibit different structural and kinetic characteristics and if these differences can be correlated to their physical stability (time to crystallisation). Samples were prepared by melt quenching, s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.12.019

    authors: Karmwar P,Graeser K,Gordon KC,Strachan CJ,Rades T

    更新日期:2011-09-30 00:00:00

  • Solid dispersion of acetaminophen and poly(ethylene oxide) prepared by hot-melt mixing.

    abstract::In this study, a model drug, acetaminophen (APAP), was melt mixed with poly(ethylene oxide) (PEO) using a Brabender mixer. APAP was found to recrystallize upon cooling to room temperature for all the drug loadings investigated. Higher drug loading leads to faster recrystallization rate. However, the morphology of the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.04.033

    authors: Yang M,Wang P,Huang CY,Ku MS,Liu H,Gogos C

    更新日期:2010-08-16 00:00:00