听力与言语-语言病理学

行为科学

医学伦理学

你正在浏览INTERNATIONAL JOURNAL OF PHARMACEUTICS期刊下所有文献
  • 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

  • Liposomal andrographolide dry powder inhalers for treatment of bacterial pneumonia via anti-inflammatory pathway.

    abstract::Andrographolide (AG) is a chemical entity from traditional Chinese herbs and its oral pills have been applied to the treatment of respiratory inflammation. Here we report pulmonary delivery of liposomal AG dry powder inhalers (LADPIs) for treatment of Staphylococcus aureus-induced pneumonia. AG liposomes were prepared...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.005

    authors: Li M,Zhang T,Zhu L,Wang R,Jin Y

    更新日期:2017-08-07 00:00:00

  • Polymer nanoassemblies with hydrophobic pendant groups in the core induce false positive siRNA transfection in luciferase reporter assays.

    abstract::Poly(ethylene glycol)-conjugated polyethylenimine (PEG-PEI) is a widely studied cationic polymer used to develop non-viral vectors for siRNA therapy of genetic disorders including cancer. Cell lines stably expressing luciferase reporter protein typically evaluate the transfection efficacy of siRNA/PEG-PEI complexes, h...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.056

    authors: Rheiner S,Reichel D,Rychahou P,Izumi T,Yang HS,Bae Y

    更新日期:2017-08-07 00:00:00

  • Synbiotic loaded chitosan-Ca-alginate microparticles reduces inflammation in the TNBS model of rat colitis.

    abstract::New therapeutic strategies against inflammatory bowel disease (IBD) consider the usage of probiotics, prebiotics and synbiotics as beneficial for the intestinal microbial balance. Limitations of such an approach are addressed into difference in survival, persistence, colonization and variable effects among different p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.049

    authors: Ivanovska TP,Mladenovska K,Zhivikj Z,Pavlova MJ,Gjurovski I,Ristoski T,Petrushevska-Tozi L

    更新日期:2017-07-15 00:00:00

  • Behaviour of silver nanoparticles in simulated saliva and gastrointestinal fluids.

    abstract::Continuously increasing application of silver nanoparticles (AgNPs) requires information on their safety and performance under biological conditions. Assessment of AgNPs in biological systems is also related to availability of robust toxicological methods for evaluation of toxic potential of AgNPs and information on t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.026

    authors: Pinďáková L,Kašpárková V,Kejlová K,Dvořáková M,Krsek D,Jírová D,Kašparová L

    更新日期:2017-07-15 00:00:00

  • Limited drug solubility can be decisive even for freely soluble drugs in highly swollen matrix tablets.

    abstract::The aim of this study was to elucidate the importance of potential limited solubility effects for the control of drug release from hydrophilic matrix tablets loaded with a freely water-soluble drug. It is often assumed that the considerable amounts of water penetrating into this type of advanced drug delivery systems ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.001

    authors: Siepmann F,Karrout Y,Gehrke M,Penz FK,Siepmann J

    更新日期:2017-06-30 00:00:00

  • Design of nonionic micelle-laden polysaccharide hydrogels for controlled delivery of hydrophobic drugs.

    abstract::The incorporation of micelle self-assembly in hydrogels has been used to produce self-healing materials, materials with tunable mechanical properties, and hydrophilic or hydrophobic drug delivery systems. However, little is known about the connection among formulation - structure - properties (particularly transport) ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.062

    authors: Munoz SZ,Zhadan R,Acosta E

    更新日期:2017-06-30 00:00:00

  • Microemulsion utility in pharmaceuticals: Implications for multi-drug delivery.

    abstract::Emulsion technology has been utilized extensively in the pharmaceutical industry. This article presents a comprehensive review of the literature on an important subcategory of emulsions, microemulsions. Microemulsions are optically transparent, thermodynamically stable colloidal systems, 10-100nm diameter, that form s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.05.005

    authors: Callender SP,Mathews JA,Kobernyk K,Wettig SD

    更新日期:2017-06-30 00:00:00

  • Novel Curcumin loaded nanoparticles engineered for Blood-Brain Barrier crossing and able to disrupt Abeta aggregates.

    abstract::The formation of extracellular aggregates built up by deposits of β-amyloid (Aβ) is a hallmark of Alzheimer's disease (AD). Curcumin has been reported to display anti-amyloidogenic activity, not only by inhibiting the formation of new Aβ aggregates, but also by disaggregating existing ones. However, the uptake of Curc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.015

    authors: Barbara R,Belletti D,Pederzoli F,Masoni M,Keller J,Ballestrazzi A,Vandelli MA,Tosi G,Grabrucker AM

    更新日期:2017-06-30 00:00:00

  • Use of acidifier and solubilizer in tadalafil solid dispersion to enhance the in vitro dissolution and oral bioavailability in rats.

    abstract::The purpose of this study is to improve the solubility, in vitro dissolution, and oral bioavailability in rats of tadalafil (TDF) by using SD technique with a weak acid and a copolymer. TDF-SD was prepared via solvent evaporation, coupled with the incorporation of an acidifier and solubilizer. Tartaric acid enhanced t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.056

    authors: Choi JS,Kwon SH,Lee SE,Jang WS,Byeon JC,Jeong HM,Park JS

    更新日期:2017-06-30 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

  • PEGylated doxorubicin nanoparticles mediated by HN-1 peptide for targeted treatment of oral squamous cell carcinoma.

    abstract::HN-1, a 12-amino acid peptide, has been reported to possess strong capabilities for targeting and penetrating head and neck squamous cell carcinoma. Here, we designed a simple but effective nanoparticle system for the delivery of doxorubicin (DOX) targeting oral squamous cell carcinoma (OSCC) through the mediation of ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.027

    authors: Wang Y,Wan G,Li Z,Shi S,Chen B,Li C,Zhang L,Wang Y

    更新日期:2017-06-15 00:00:00

  • Preparation and characterization of lipid nanoparticle/pDNA complexes for STAT3 downregulation and overcoming chemotherapy resistance in lung cancer cells.

    abstract::Developments in the field of molecular oncology have revealed that resistance to chemotherapeutics is acqured through several mechanisms including overexpression of common oncogenic proteins. Signal Transducer and Activator of Transcription 3 (STAT3) is one of these oncogenes that is overexpressed in many cancer types...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.034

    authors: Kotmakçı M,Çetintaş VB,Kantarcı AG

    更新日期:2017-06-15 00:00:00

  • Surface modification of acetaminophen particles by atomic layer deposition.

    abstract::Active pharmaceutical ingredients (APIs) are predominantly organic solid powders. Due to their bulk properties many APIs require processing to improve pharmaceutical formulation and manufacturing in the preparation for various drug dosage forms. Improved powder flow and protection of the APIs are often anticipated cha...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.031

    authors: Kääriäinen TO,Kemell M,Vehkamäki M,Kääriäinen ML,Correia A,Santos HA,Bimbo LM,Hirvonen J,Hoppu P,George SM,Cameron DC,Ritala M,Leskelä M

    更新日期:2017-06-15 00:00:00

  • Elaboration and evaluation of alginate foam scaffolds for soft tissue engineering.

    abstract::Controlling microarchitecture in polymer scaffolds is a priority in material design for soft tissue applications. This paper reports for the first time the elaboration of alginate foam-based scaffolds for mesenchymal stem cell (MSC) delivery and a comparative study of various surfactants on the final device performanc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.060

    authors: Ceccaldi C,Bushkalova R,Cussac D,Duployer B,Tenailleau C,Bourin P,Parini A,Sallerin B,Girod Fullana S

    更新日期:2017-05-30 00:00:00

  • Polymer sutures for simultaneous wound healing and drug delivery - A review.

    abstract::Drug delivery using suitable polymeric devices has gathered momentum in the recent years due to their remarkable properties. The versatility of polymeric materials makes them reliable candidates for site targeted drug release. Among them biodegradable sutures has received considerable attention because they offer grea...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.03.041

    authors: Joseph B,George A,Gopi S,Kalarikkal N,Thomas S

    更新日期:2017-05-30 00:00:00

  • Downstream drug product processing of itraconazole nanosuspension: Factors influencing drug particle size and dissolution from nanosuspension-layered beads.

    abstract::There is more research required to broaden the knowledge on the downstream processing of nanosuspensions into solid oral dosage forms, especially for coated nanosuspensions onto beads as carriers. This study focuses on bead layering as one approach to solidify nanosuspensions. The aim was to systematically investigate...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.012

    authors: Parmentier J,Tan EH,Low A,Möschwitzer JP

    更新日期:2017-05-30 00:00:00

  • An approach for chemical stability during melt extrusion of a drug substance with a high melting point.

    abstract::Poorly water-soluble drug substances that exhibit high melting points are difficult to process by melt extrusion due to chemical instability at high temperatures required for processing. The purpose of this study was to extrude meloxicam (melting point 255°C) by optimizing processing parameters and formulation composi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.070

    authors: Haser A,Huang S,Listro T,White D,Zhang F

    更新日期:2017-05-30 00:00:00

  • Development of medicated foams that combine incompatible hydrophilic and lipophilic drugs for psoriasis treatment.

    abstract::The focus was on the development of medicated foam for incorporation of two incompatible active agents for psoriasis treatment; i.e., lipophilic cholecalciferol, and hydrophilic salicylic acid. Emphasis was given to formulation of a propellant-free foam, with sufficient foaming properties, physical and chemical stabil...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.061

    authors: Mirtič J,Papathanasiou F,Temova Rakuša Ž,GosencaMatjaž M,Roškar R,Kristl J

    更新日期:2017-05-30 00:00:00

  • PEGylated composite nanoparticles of PLGA and polyethylenimine for safe and efficient delivery of pDNA to lungs.

    abstract::Achieving stable, efficient and non-toxic pulmonary gene delivery is most challenging requirement for successful gene therapy to lung. Composite nanoparticles (NPs) of the poly(lactic-co-glycolic acid) (PLGA) and cationic polymer polyethyleneimine (PEI) is an efficient alternative to viral and liposomal vectors for th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.094

    authors: Kolte A,Patil S,Lesimple P,Hanrahan JW,Misra A

    更新日期:2017-05-30 00:00:00

  • Functionalized single-walled carbon nanotubes: cellular uptake, biodistribution and applications in drug delivery.

    abstract::The unique properties of single-walled carbon nanotubes (SWNTs) enable them to play important roles in many fields. One of their functional roles is to transport cargo into cell. SWNTs are able to traverse amphipathic cell membranes due to their large surface area, flexible interactions with cargo, customizable dimens...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.03.017

    authors: Li Z,de Barros ALB,Soares DCF,Moss SN,Alisaraie L

    更新日期:2017-05-30 00:00:00

  • Investigation of in vitro PDT activities of zinc phthalocyanine immobilised TiO2 nanoparticles.

    abstract::Phthalocyanines (Pcs) are commonly used as Photosensors (PSs) in Photodynamic Therapy (PDT) applications due to their intense absorption in the far red-near IR spectral region with a high extinction coefficient and high ability for generating singlet oxygen. Pcs targetspecifically tumors, and do not show any considera...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.050

    authors: Yurt F,Ince M,Colak SG,Ocakoglu K,Er O,Soylu HM,Gunduz C,Avci CB,Kurt CC

    更新日期:2017-05-30 00:00:00

  • Dropwise additive manufacturing of pharmaceutical products for amorphous and self emulsifying drug delivery systems.

    abstract::The improvements in healthcare systems and the advent of the precision medicine initiative have created the need to develop more innovative manufacturing methods for the delivery and production of individualized dosing and personalized treatments. In accordance with the changes observed in healthcare systems towards m...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.003

    authors: Içten E,Purohit HS,Wallace C,Giridhar A,Taylor LS,Nagy ZK,Reklaitis GV

    更新日期:2017-05-30 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

  • In vitro and in silico characterization of fibrous scaffolds comprising alternate colistin sulfate-loaded and heat-treated polyvinyl alcohol nanofibrous sheets.

    abstract::A multilayer mat for dispensing colistin sulfate through a body surface was prepared by electrospinning. The fabricated system comprised various polyvinyl alcohol fibrous layers prepared with or without the active ingredient. One of the electrospun layers contained water-soluble colistin sulfate and the other was prep...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.044

    authors: Sebe I,Ostorházi E,Bodai Z,Eke Z,Szakács J,Kovács NK,Zelkó R

    更新日期:2017-05-15 00:00:00

  • Tensile and shear methods for measuring strength of bilayer tablets.

    abstract::Both shear and tensile measurement methods have been used to quantify interfacial bonding strength of bilayer tablets. The shear method is more convenient to perform, but reproducible strength data requires careful control of the placement of tablet and contact point for shear force application. Moreover, data obtaine...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.010

    authors: Chang SY,Li JX,Sun CC

    更新日期:2017-05-15 00:00:00

  • Electrospun protein nanofibers in healthcare: A review.

    abstract::Electrospun nanofibers are being utilized for a wide range of healthcare applications. A plethora of natural and synthetic polymers are exploited for their ability to be electrospun and replace the complex habitat provided by the extracellular matrix for the cells. The fabrication of nanofibers can be tuned to act as ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.03.013

    authors: Babitha S,Rachita L,Karthikeyan K,Shoba E,Janani I,Poornima B,Purna Sai K

    更新日期:2017-05-15 00:00:00

  • Nanoincorporation of bioactive compounds from red grape pomaces: In vitro and ex vivo evaluation of antioxidant activity.

    abstract::In this study, the active components of grape pomaces were first extracted by maceration in ethanol and propylene glycol, then in extra virgin olive oil. The main components of the hydrophilic extractive solutions were flavonoids, while monounsaturated fatty acids were the most abundant constituents of the extractive ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.037

    authors: Manconi M,Marongiu F,Manca ML,Caddeo C,Sarais G,Cencetti C,Pucci L,Longo V,Bacchetta G,Fadda AM

    更新日期:2017-05-15 00:00:00

  • Reflectometric monitoring of the dissolution process of thin polymeric films.

    abstract::Pharmaceutical thin films are versatile drug-delivery platforms i.e. allowing transdermal, oral, sublingual and buccal administration. However, dissolution testing of thin films is challenging since the commonly used dissolution tests for conventional dosage forms correspond rather poorly to the physiological conditio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.028

    authors: Laitinen R,Räty J,Korhonen K,Ketolainen J,Peiponen KE

    更新日期:2017-05-15 00:00:00

  • Sustained release ophthalmic dexamethasone: In vitro in vivo correlations derived from the PK-Eye.

    abstract::Corticosteroids have long been used to treat intraocular inflammation by intravitreal injection. We describe dexamethasone loaded poly-DL-lactide-co-glycolide (PLGA) microparticles that were fabricated by thermally induced phase separation (TIPS). The dexamethasone loaded microparticles were evaluated using a two-comp...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.047

    authors: Awwad S,Day RM,Khaw PT,Brocchini S,Fadda HM

    更新日期:2017-04-30 00:00:00

  • One-week in vivo sustained release of a peptide formulated into in situ forming implants.

    abstract::The LR12 peptide has been reported to reduce the size of infarct and improve both cardiac function and survival in myocardial infarction in murine models, after daily repeated intraperitoneal injections. In order to protect peptide from degrading and to prolong its release, in situ implants based on biocompatible biod...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.046

    authors: Parent M,Clarot I,Gibot S,Derive M,Maincent P,Leroy P,Boudier A

    更新日期:2017-04-15 00:00:00

  • Nano-encapsulation of a novel anti-Ran-GTPase peptide for blockade of regulator of chromosome condensation 1 (RCC1) function in MDA-MB-231 breast cancer cells.

    abstract::Ran is a small ras-related GTPase and is highly expressed in aggressive breast carcinoma. Overexpression induces malignant transformation and drives metastatic growth. We have designed a novel series of anti-Ran-GTPase peptides, which prevents Ran hydrolysis and activation, and although they display effectiveness in s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.006

    authors: Haggag YA,Matchett KB,Dakir el-H,Buchanan P,Osman MA,Elgizawy SA,El-Tanani M,Faheem AM,McCarron PA

    更新日期:2017-04-15 00:00:00

  • Core-interlayer-shell Fe3O4@mSiO2@lipid-PEG-methotrexate nanoparticle for multimodal imaging and multistage targeted chemo-photodynamic therapy.

    abstract::Multimodal imaging-guided multistage targeted synergistic combination therapy possesses many advantages including increased tumoricidal effect, reduced toxicity, and retarded drug resistance. Herein, we have elaborately developed a core-interlayer-shell structure Fe3O4@mSiO2@lipid-PEG-methotrexatenanoparticle(FMLM), i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.068

    authors: Liu G,Ma J,Li Y,Li Q,Tan C,Song H,Cai S,Chen D,Hou Z,Chen Q,Zhu X

    更新日期:2017-04-15 00:00:00

  • Lipid nanovehicles with adjustable surface properties for overcoming multiple barriers simultaneously in oral administration.

    abstract::Lipid nanoparticles (LNs) are widely investigated for oral drug delivery, and for achieving significant advantages in colloidal stability, biocompatibility and scaled-up possibility. However, researchers face challenge of developing methods to improve the ability of LNs in overcoming multiple barriers (i.e., mucus and...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.015

    authors: Wu L,Liu M,Shan W,Cui Y,Zhang Z,Huang Y

    更新日期:2017-03-30 00:00:00

  • Development of enteric-coated fixed dose combinations of amorphous solid dispersions of ezetimibe and lovastatin: Investigation of formulation and process parameters.

    abstract::Enteric-coated fixed-dose combinations of ezetimibe and lovastatin were prepared by fluid bed coating aiming to avoid the acidic conversion of lovastatin to its hydroxyacid derivative. In a two-step process, sucrose beads were layered with a glass solution of ezetimibe, lovastatin and Soluplus®, top-coated with an ent...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.053

    authors: Riekes MK,Dereymaker A,Berben P,Augustijns P,Stulzer HK,Van den Mooter G

    更新日期:2017-03-30 00:00:00

  • Continuous direct compression as manufacturing platform for sustained release tablets.

    abstract::This study presents a framework for process and product development on a continuous direct compression manufacturing platform. A challenging sustained release formulation with high content of a poorly flowing low density drug was selected. Two HPMC grades were evaluated as matrix former: standard Methocel CR and direc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.010

    authors: Van Snick B,Holman J,Cunningham C,Kumar A,Vercruysse J,De Beer T,Remon JP,Vervaet C

    更新日期:2017-03-15 00:00:00

  • Amorphization within the tablet: Using microwave irradiation to form a glass solution in situ.

    abstract::In situ amorphization is a concept that allows to amorphize a given drug in its final dosage form right before administration. Hence, this approach can potentially be used to circumvent recrystallization issues that other amorphous formulation approaches are facing during storage. In this study, the feasibility of mic...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.035

    authors: Doreth M,Hussein MA,Priemel PA,Grohganz H,Holm R,Lopez de Diego H,Rades T,Löbmann K

    更新日期:2017-03-15 00:00:00

  • Design of spray dried ternary solid dispersions comprising itraconazole, soluplus and HPMCP: Effect of constituent compositions.

    abstract::A range of 17 ternary formulations of itraconazole (ITZ), HPMCP and Soluplus have been manufactured using spray drying. These amorphous solid dispersions (ASDs) were very stable against crystallisation and ITZ was found to be amorphous in all formulations after one year at 40°C/75% RH. A number of solid state analytic...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.043

    authors: Davis MT,Potter CB,Mohammadpour M,Albadarin AB,Walker GM

    更新日期:2017-03-15 00:00:00

  • A systematic review of the use of dosage form manipulation to obtain required doses to inform use of manipulation in paediatric practice.

    abstract::This study sought to determine whether there is an evidence base for drug manipulation to obtain the required dose, a common feature of paediatric clinical practice. A systematic review of the data sources, PubMed, EMBASE, CINAHL, IPA and the Cochrane database of systematic reviews, was used. Studies that considered t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.12.032

    authors: Richey RH,Hughes C,Craig JV,Shah UU,Ford JL,Barker CE,Peak M,Nunn AJ,Turner MA

    更新日期:2017-02-25 00:00:00

  • Efficient gene delivery to primary human retinal pigment epithelial cells: The innate and acquired properties of vectors.

    abstract::The purpose of this study is designing non-viral gene delivery vectors for transfection of the primary human retinal pigment epithelial cells (RPE). In the design process of gene delivery vectors, considering physicochemical properties of vectors alone does not seem to be enough since they interact with constituents o...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.12.048

    authors: Tasharrofi N,Kouhkan F,Soleimani M,Soheili ZS,Atyabi F,Akbari Javar H,Abedin Dorkoosh F

    更新日期:2017-02-25 00:00:00

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