Anticancer siRNA cocktails as a novel tool to treat cancer cells. Part (B). Efficiency of pharmacological action.

Abstract:

:This paper examines a perspective to use newly engineered nanomaterials as effective and safe carriers for gene therapy of cancer. Three different groups of cationic dendrimers (PAMAM, phosphorus, and carbosilane) were complexed with anticancer siRNA and the biophysical properties of the dendriplexes created were analyzed. The potential of the dendrimers as nanocarriers for anticancer Bcl-xl, Bcl-2, Mcl-1 siRNAs and additionally a scrambled sequence siRNA has been explored. Dendrimer/siRNA complexes were characterised by various methods including fluorescence, zeta potential, dynamic light scattering, circular dichroism, gel electrophoresis and transmission electron microscopy. In this part of study, the transfection of complexes in HeLa and HL-60 cells was analyzed using both single apoptotic siRNAs and a mixture (cocktail) of them. Cocktails were more effective than single siRNAs, allowing one to decrease siRNAs concentration in treating cells. The dendrimers were compared as siRNA carriers, the most effective being the phosphorus-based ones. However, they were also the most cytotoxic on their own, so that in this regard the application of all dendrimers in anticancer therapy will be discussed.

journal_name

Int J Pharm

authors

Dzmitruk V,Szulc A,Shcharbin D,Janaszewska A,Shcharbina N,Lazniewska J,Novopashina D,Buyanova M,Ionov M,Klajnert-Maculewicz B,Gómez-Ramirez R,Mignani S,Majoral JP,Muñoz-Fernández MA,Bryszewska M

doi

10.1016/j.ijpharm.2015.03.034

subject

Has Abstract

pub_date

2015-05-15 00:00:00

pages

288-94

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(15)00250-1

journal_volume

485

pub_type

杂志文章
  • Oral delivery of oleuropein-loaded lipid nanocarriers alleviates inflammation and oxidative stress in acute colitis.

    abstract::Inflammation and oxidative stress pathways have emerged as novel targets in the management of inflammatory bowel diseases (IBD). Targeting the drug to the inflamed colon remains a challenge. Nanostructured lipid carriers (NLCs) have been reported to accumulate in inflamed colonic mucosa. The antioxidant/antiinflamator...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119515

    authors: Huguet-Casquero A,Xu Y,Gainza E,Pedraz JL,Beloqui A

    更新日期:2020-08-30 00:00:00

  • Prediction of drug-packaging interactions via molecular dynamics (MD) simulations.

    abstract::The interaction between packaging materials and drug products is an important issue for the pharmaceutical industry, since during manufacturing, processing and storage a drug product is continuously exposed to various packaging materials. The experimental investigation of a great variety of different packaging materia...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.03.049

    authors: Feenstra P,Brunsteiner M,Khinast J

    更新日期:2012-07-15 00:00:00

  • Enhanced bioavailability of buspirone hydrochloride via cup and core buccal tablets: formulation and in vitro/in vivo evaluation.

    abstract::This work aims to prepare sustained release buccal mucoadhesive tablets of buspirone hydrochloride (BH) to improve its systemic bioavailability. The tablets were prepared according to 5×3 factorial design where polymer type was set at five levels (carbopol, hydroxypropyl methylcellulose, sodium alginate, sodium carbox...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,随机对照试验

    doi:10.1016/j.ijpharm.2014.01.003

    authors: Kassem MA,Elmeshad AN,Fares AR

    更新日期:2014-03-10 00:00:00

  • Modeling of the burst release from PLGA micro- and nanoparticles as function of physicochemical parameters and formulation characteristics.

    abstract::A substantial drug release from poly(lactic-co-glycolic) acid (PLGA) micro- and nanoparticles can occur in the first hours of immersion, which is referred to as burst release. A strong burst release (when not intentional) is to be avoided as it decreases the efficacy of the treatment and could be dangerous to the host...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.08.118

    authors: Rodrigues de Azevedo C,von Stosch M,Costa MS,Ramos AM,Cardoso MM,Danhier F,Préat V,Oliveira R

    更新日期:2017-10-30 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

  • Novel drug delivery strategies for improving econazole antifungal action.

    abstract::Econazole is a commonly used azole antifungal in clinical treatment of superficial fungal infections. It is generally used as conventional cream and gel preparations under the brand names of Spectazole (United States), Ecostatin (Canada), Pevaryl (Western Europe). Treatment efficiency of antifungal drugs depends on th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2015.09.015

    authors: Firooz A,Nafisi S,Maibach HI

    更新日期:2015-11-10 00:00:00

  • Engineered DNA nanodrugs alleviate inflammation in inflammatory arthritis.

    abstract::Rheumatoid arthritis (RA) is an autoimmune disease featured with chronic joint inflammation. Suppression of inflammation is critical to RA treatment and joint protection. In this study, DNA nanodrugs are prepared via the conjugation of NF-κB decoy oligodeoxynucleotides (dODNs) and VCAM-1 targeted peptides (P) onto sel...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119047

    authors: Wang Z,Chu X,Li N,Fu L,Gu H,Zhang N

    更新日期:2020-03-15 00:00:00

  • Cold flow of estradiol transdermal systems: influence of drug loss on the in vitro flux and drug transfer across human epidermis.

    abstract::The objective was to quantify drug loss due to cold flow (CF) in marketed estradiol transdermal drug delivery systems (TDDS), and study its influence on the in vitro flux and drug transfer across contacting skin. TDDS samples (products-A and B) were induced with CF at 25 and 32°C/60% RH by applying 1-kg force for 72h....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.10.013

    authors: Krishnaiah YS,Yang Y,Hunt RL,Khan MA

    更新日期:2014-12-30 00:00:00

  • Dissolution of biomacromolecules in organic solvents by nano-complexing with poly(ethylene glycol).

    abstract::Various biomacromolecules (BMs) such as proteins, DNA, and carbohydrates are extremely difficult to be dissolved in a single organic solvent phase for sustained release or targeted delivery formulation. In this study, three different BMs could be solubilized in selected organic solvents by forming poly(ethylene glycol...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.01.033

    authors: Mok H,Kim HJ,Park TG

    更新日期:2008-05-22 00:00:00

  • Prolonged subcutaneous delivery of low molecular weight heparin based on thermoresponsive hydrogels with chitosan nanocomplexes: Design, in vitro evaluation, and cytotoxicity studies.

    abstract::Low molecular weight heparins (LMWHs) have risen in popularity over the past decades. Owing to their appropriate pharmacokinetic profile, they enable long-term clinical applications, e.g. prophylaxis of deep vein thrombosis. Although the administration of LMWHs is not as frequent as of heparin, it still requires once ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.063

    authors: Radivojša Matanović M,Grabnar I,Gosenca M,Grabnar PA

    更新日期:2015-07-05 00:00:00

  • Performance evaluation of PAMAM dendrimer based simvastatin formulations.

    abstract::The purpose of this investigation was to evaluate the performance of poly (amidoamine) (PAMAM) dendrimers, with three different surface groups, to be used as drug carriers. Drug-dendrimers complexes were investigated for solubility studies, dissolution studies, in vitro drug release studies, and for stability studies....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.12.002

    authors: Kulhari H,Pooja D,Prajapati SK,Chauhan AS

    更新日期:2011-02-28 00:00:00

  • Methotrexate-loaded biodegradable polymeric micelles for lymphoma therapy.

    abstract::Drug resistance and recurrence are the main clinical challenges in chemotherapy of lymphoma. Methotrexate (MTX), especially high dose MTX (HD MTX), is extensively used to treat some aggressive subtypes of lymphoma, such as Burkitt's lymphoma, in order to overcome drug resistance. But poor solubility of the free drug a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.025

    authors: Wang MY,Qu Y,Hu DR,Chen LJ,Shi K,Jia YP,Yi YY,Wei Q,Niu T,Qian ZY

    更新日期:2019-02-25 00:00:00

  • Inhalation of tobramycin in cystic fibrosis. Part 2: optimization of the tobramycin solution for a jet and an ultrasonic nebulizer.

    abstract::The inhalation of tobramycin is part of current cystic fibrosis (CF) therapy. Local therapy with inhaled antibiotics has demonstrated improvements in pulmonary function. Current inhalation therapy is limited by the available drug formulations in combination with the nebulization time. The aim of this study is to devel...

    journal_title:International journal of pharmaceutics

    pub_type: 评论,杂志文章

    doi:10.1016/s0378-5173(99)00252-5

    authors: Le Brun PP,de Boer AH,Gjaltema D,Hagedoorn P,Heijerman HG,Frijlink HW

    更新日期:1999-11-05 00:00:00

  • What level of protection can be obtained using sun protective clothing? Determining effectiveness using an in vitro method.

    abstract::It has been clearly demonstrated that ultraviolet radiation is harmful to the skin and can cause helioderma and cancers. There are different methods of combating ultraviolet radiation: sunscreens formulated with filters and/or screens as well as clothing. For this work, the authors studied different fabrics to evaluat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.06.022

    authors: Ghazi S,Couteau C,Coiffard LJ

    更新日期:2010-09-15 00:00:00

  • Preparation and characterization of stable nanoliposomal formulations of curcumin with high loading efficacy: In vitro and in vivo anti-tumor study.

    abstract::Liposomal formulations were made using Solvent-assisted active loading technology (SALT). Two formulations composed of HSPC:DPPG:Chol:DSPE-mPEG2000 (PG-LipCUR) and HSPC:Chol:DSPE-mPEG2000 (LipCUR) demonstrated good colloidal properties and the CUR-encapsulation of 82% and 89% for PG-LipCUR and LipCUR, respectively. Th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119211

    authors: Karimi M,Gheybi F,Zamani P,Mashreghi M,Golmohammadzadeh S,Darban SA,Badiee A,Jaafari MR

    更新日期:2020-04-30 00:00:00

  • Evaluation of the vibratory feeder method for assessment of powder flow properties.

    abstract::The flow properties of pharmaceutical powders and blends used in solid oral dosage forms are an important consideration during dosage form development. The vibratory feeder method, a flow measurement technique that quantifies avalanche flow, has been adapted for measurement of the flow properties of common pharmaceuti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.09.024

    authors: Bhattachar SN,Hedden DB,Olsofsky AM,Qu X,Hsieh WY,Canter KG

    更新日期:2004-01-28 00:00:00

  • DPI formulations for high dose applications - Challenges and opportunities.

    abstract::This opinion piece gives reasons for high dose DPI applications, points out challenges and shows opportunities and possible solutions for high dose DPI. This piece of work shall set the stage for more in-depth reviews of state of the art and research papers addressing the challenges of high dose DPI which shall be inc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2018.06.038

    authors: Scherließ R,Etschmann C

    更新日期:2018-09-05 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

  • Preparation of spray dried submicron particles: Part B - Particle recovery by electrostatic precipitation.

    abstract::The low bioavailability of poorly water-soluble drugs is currently one of the major focuses of pharmaceutical research. One strategy currently being investigated to overcome this limitation is to decrease the particle size of the active pharmaceutical ingredients (API). An innovative process for this is spray drying w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.06.069

    authors: Dobrowolski A,Strob R,Nietfeld J,Pieloth D,Wiggers H,Thommes M

    更新日期:2018-09-05 00:00:00

  • Relating the tableting behavior of piroxicam polytypes to their crystal structures using energy-vector models.

    abstract::Piroxicam crystallises into two polytypes, α1 and α2, with crystal structures that contain identical molecular layers but differ in the way that these layers are stacked. In spite of having close structural similarity, the polytypes have significantly different powder tabletting behaviour: α2 forms only weak tablets a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.03.040

    authors: Upadhyay PP,Sun CC,Bond AD

    更新日期:2018-05-30 00:00:00

  • Novel self-floating tablet for enhanced oral bioavailability of metformin based on cellulose.

    abstract::Metformin has several problems such as low bioavailability, short half-life, and narrow absorption window, sustained and site-specific drug delivery system is required. Floating drug delivery systems are very useful to achieve these purposes. However, conventional floating systems have several limitations; lag time, a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120113

    authors: Wook Huh H,Na YG,Kang H,Kim M,Han M,Mai Anh Pham T,Lee H,Baek JS,Lee HK,Cho CW

    更新日期:2021-01-05 00:00:00

  • In vitro skin penetration enhancement techniques: A combined approach of ethosomes and microneedles.

    abstract::Dermal administration of different macromolecules, such as nucleic acids, remains a real challenge because of the difficulty of crossing the main skin barrier, the stratum corneum (SC). To overcome this barrier, the use of deformable lipid-based nanovectors were developed to increase topical penetration through the SC...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118793

    authors: Bellefroid C,Lechanteur A,Evrard B,Mottet D,Debacq-Chainiaux F,Piel G

    更新日期:2019-12-15 00:00:00

  • Development and characterisation of sustained release solid dispersion oral tablets containing the poorly water soluble drug disulfiram.

    abstract::Administration of drugs via the oral route is the most common and preferred route due to its ease of administration, cost-effectiveness and flexibility in design. However, if the drug being administered has limited aqueous solubility it can result in poor bioavailability. Furthermore, the low pH of the stomach as well...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.11.029

    authors: Shergill M,Patel M,Khan S,Bashir A,McConville C

    更新日期:2016-01-30 00:00:00

  • An intravenous application of magnetic nanoparticles for osteomyelitis treatment: An efficient alternative.

    abstract::The infection of bone and bone marrow is called osteomyelitis. Treatment is difficult since antibiotics can not reach with enough concentration to the infected area. For the first time in this study, we have developed gentamicin-loaded magnetic gelatin nanoparticles (GMGNPs) for nanocarrier-mediated and magnetically t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119999

    authors: Ak G,Bozkaya ÜF,Yılmaz H,Sarı Turgut Ö,Bilgin İ,Tomruk C,Uyanıkgil Y,Hamarat Şanlıer Ş

    更新日期:2021-01-05 00:00:00

  • Experimental and computational study of the effect of breath-actuated mechanism built in the NEXThaler® dry powder inhaler.

    abstract::The breath-actuated mechanism (BAM) is a mechanical unit included in NEXThaler® with the role of delaying the emission of the drug until the inhalation flow rate of the patient is sufficiently high to detach the drug particles from their carriers. The main objective of this work was to analyse the effect of the presen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.09.057

    authors: Farkas Á,Lewis D,Church T,Tweedie A,Mason F,Haddrell AE,Reid JP,Horváth A,Balásházy I

    更新日期:2017-11-25 00:00:00

  • Risperidone solid dispersion for orally disintegrating tablet: its formulation design and non-destructive methods of evaluation.

    abstract::The focus of present investigation was to assess the utility of non-destructive techniques in the evaluation of risperidone solid dispersions (SD) with methyl-β-cyclodextrin (MBCD) and subsequent incorporation of the SD into orally disintegrating tablets (ODT) for a faster release of risperidone. The SD was prepared b...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.08.025

    authors: Rahman Z,Zidan AS,Khan MA

    更新日期:2010-11-15 00:00:00

  • Evaluation of collagen and methylated collagen as gene carriers.

    abstract::This study explores the potential of DNA complexes prepared with methylated collagen (MC) and unmodified native collagen (NC) to deliver genes into cells. The physicochemical properties and transfection abilities of these two types of complexes are studied in parallel. MC was prepared by methylation of the carboxyl gr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.04.014

    authors: Wang J,Lee IL,Lim WS,Chia SM,Yu H,Leong KW,Mao HQ

    更新日期:2004-07-26 00:00:00

  • Nanodiamonds: Minuscule gems that ferry antineoplastic drugs to resistant tumors.

    abstract::Remarkable efforts are currently devoted to the area of nanodiamonds (NDs) research due to their superior properties viz: biocompatibility, minute size, inert core, and tunable surface chemistry. The use of NDs for the delivery of anticancer drugs has been at the forefront of NDs applications owing to their ability to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2018.12.090

    authors: Ali MS,Metwally AA,Fahmy RH,Osman R

    更新日期:2019-03-10 00:00:00

  • The role of internal and external stimuli in the rational design of skin-specific drug delivery systems.

    abstract::The concept of skin-specific drug delivery with a spatio-temporal control has just recently received concerns in dermatology. Inspired by the progress in smart materials and their perspective application in medicine science, development of stimuli responsive drug delivery systems with skin-specificity has become possi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.120081

    authors: Chen Y,Chen N,Feng X

    更新日期:2021-01-05 00:00:00

  • Gastro intestinal tracking and gastric emptying of solid dosage forms in rats using X-ray imaging.

    abstract::The aim of this research was to study the gastrointestinal transit and gastric emptying of non-disintegrating solid dosage forms in rats using X-ray imaging. Commercial gelatin minicapsules were filled with barium sulfate and enterically coated using Eudragit S100. The capsules were administered orally to rats followe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.01.001

    authors: Saphier S,Rosner A,Brandeis R,Karton Y

    更新日期:2010-03-30 00:00:00