Enhanced Cellular Uptake and Gene Silencing Activity of Survivin-siRNA via Ultrasound-Mediated Nanobubbles in Lung Cancer Cells.

Abstract:

PURPOSE:Paclitaxel is a first-line drug for the therapy of lung cancer, however, drug resistance is a serious limiting factor, related to overexpression of anti-apoptotic proteins like survivin. To overcome this phenomenon, developing novel ultrasound responsive nanobubbles - nanosized drug delivery system- for the delivery of paclitaxel and siRNA in order to silence survivin expression in the presence of ultrasound was aimed. METHODS:Paclitaxel-carrying nanobubble formulation was obtained by modifying the multistep method. Then, the complex formation of the nanobubbles - paclitaxel formulation with survivin-siRNA, was examined in terms of particle size, polydispersity index, zeta potential, and morphology. Furthermore, siRNA binding and protecting ability, cytotoxicity, cellular uptake, gene silencing, and induction of apoptosis studies were investigated in terms of lung cancer cells. RESULTS:Developed nanobubbles have particle sizes of 218.9-369.6 nm, zeta potentials of 27-34 mV, were able to protect siRNA from degradation and delivered siRNA into the lung cancer cells. Survivin expression was significantly lower compared with the control groups and enhanced apoptosis was induced by the co-delivery of survivin-siRNA and paclitaxel. Furthermore, significantly higher effects were obtained in the presence of ultrasound induction. CONCLUSION:The ultrasound responsive nanobubble system carrying paclitaxel and survivin-siRNA is a promising and effective approach against lung cancer cells.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Akbaba H,Erel-Akbaba G,Kotmakçı M,Başpınar Y

doi

10.1007/s11095-020-02885-x

subject

Has Abstract

pub_date

2020-08-05 00:00:00

pages

165

issue

8

eissn

0724-8741

issn

1573-904X

pii

10.1007/s11095-020-02885-x

journal_volume

37

pub_type

杂志文章
  • Assessment of the lateral diffusion and penetration of topically applied drugs in humans using a novel concentric tape stripping design.

    abstract:PURPOSE:To determine the extent of lateral spread and stratum corneum (SC) penetration of caffeine (CAF), hydrocortisone (HC) and ibuprofen (IBU) using a novel concentric tape stripping technique. METHOD:Ethanolic solutions of CAF, HC or IBU were applied to the forearm of 8 volunteers. At various time points, 10 succe...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0731-7

    authors: Gee CM,Nicolazzo JA,Watkinson AC,Finnin BC

    更新日期:2012-08-01 00:00:00

  • Effect of selective lipid extraction from different body regions on epidermal barrier function.

    abstract:PURPOSE:To assess the effects of selective lipid extraction and tape stripping on transepidermal water loss (TEWL) at three body regions in the pig. METHODS:Lipids were extracted from the abdominal, inguinal. and back regions using three different solvent extraction procedures or cellophane tape stripping (15x) on Yor...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1010944529387

    authors: Monteiro-Riviere NA,Inman AO,Mak V,Wertz P,Riviere JE

    更新日期:2001-07-01 00:00:00

  • Evaluation of an enzyme-containing capsular shaped pulsatile drug delivery system.

    abstract:PURPOSE:To develop an enzymatically-controlled pulsatile drug release system based on an impermeable capsule body, which contains the drug and is closed by an erodible pectin/pectinase-plug. METHODS:The plug was prepared by direct compression of pectin and pectinase in different ratios. In addition to the disintegrati...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018959327311

    authors: Krögel I,Bodmeier R

    更新日期:1999-09-01 00:00:00

  • Quantitative assessment of intestinal first-pass metabolism of oral drugs using portal-vein cannulated rats.

    abstract:PURPOSE:To evaluate the impact of intestinal first-pass metabolism (Fg) by cytochrome P4503A (CYP3A) and uridine 5'-diphosphate-glucuronosyltransferases (UGT) on in vivo oral absorption of their substrate drugs. METHODS:CYP3A and UGT substrates were orally administered to portal-vein cannulated (PV) rats to evaluate t...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1489-x

    authors: Matsuda Y,Konno Y,Hashimoto T,Nagai M,Taguchi T,Satsukawa M,Yamashita S

    更新日期:2015-02-01 00:00:00

  • Absorptive-mediated endocytosis of an adrenocorticotropic hormone (ACTH) analogue, ebiratide, into the blood-brain barrier: studies with monolayers of primary cultured bovine brain capillary endothelial cells.

    abstract::The internalization of a neuromodulatory adrenocorticotropic hormone (ACTH) analogue, [125I]ebiratide (H-Met(O2)-Glu[125I]His-Phe-D-Lys-Phe-NH(CH2)2NH2), was examined in cultured monolayers of bovine brain capillary endothelial cells (BCEC). HPLC analysis of the incubation solution showed that [125I]ebiratide was not ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015848531603

    authors: Terasaki T,Takakuwa S,Saheki A,Moritani S,Shimura T,Tabata S,Tsuji A

    更新日期:1992-04-01 00:00:00

  • Jejunal absorption and metabolism of R/S-verapamil in humans.

    abstract:PURPOSE:The purpose of this human intestinal perfusion study was to investigate the transport and metabolism of R/S-verapamil in the human jejunum (in vivo). METHODS:A regional single-pass perfusion of the jejunum was performed using a Loc-I-Gut perfusion tube in 12 healthy volunteers. Each perfusion lasted for 200 mi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1011916329863

    authors: Sandström R,Karlsson A,Knutson L,Lennernäs H

    更新日期:1998-06-01 00:00:00

  • Controlled delivery systems for proteins using polyanhydride microspheres.

    abstract::A method to provide near-constant sustained release of high molecular weight, water-soluble proteins from polyanhydride microspheres is described. The polyanhydrides used were poly(fatty acid dimer) (PFAD), poly(sebacic acid) (PSA), and their copolymers [P(FAD-SA)]. P(FAD-SA) microspheres containing proteins of differ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018929531410

    authors: Tabata Y,Gutta S,Langer R

    更新日期:1993-04-01 00:00:00

  • In vitro and in vivo properties of recombinant human serum albumin from Pichia pastoris purified by a method of short processing time.

    abstract:PURPOSE:Recombinant human serum albumin (rHSA), secreted by a Pichia pastoris expression system, was purified by a fast and efficient method, the essential feature of which is strong but reversible binding of the protein to Blue Sepharose. The structural characteristics, stability, and ligand-binding properties of the ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1013391001141

    authors: Watanabe H,Yamasaki K,Kragh-Hansen U,Tanase S,Harada K,Suenaga A,Otagiri M

    更新日期:2001-12-01 00:00:00

  • Crystalline form information from multiwell plate salt screening by use of Raman microscopy.

    abstract:PURPOSE:The purpose of this study was to establish a useful methodology, possibly providing information on the stoichiometry of pharmaceutical drug salts obtained from salt screening by using a multiwell plate and a Raman microscope. METHODS:Tamoxifen salt screening was conducted with monobasic and polybasic acids on ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-9644-7

    authors: Kojima T,Onoue S,Murase N,Katoh F,Mano T,Matsuda Y

    更新日期:2006-04-01 00:00:00

  • Application of a biomagnetic measurement system (BMS) to the evaluation of gastrointestinal transit of intestinal pressure-controlled colon delivery capsules (PCDCs) in human subjects.

    abstract:PURPOSE:For determination of the transit time through various parts of the gastrointestinal (GI) tract, we developed a method that provides the location of disintegration and drug release. This method involves GI magnetomarkergraphy (GIMG) using a 129-channel Shimadzu vector biomagnetic measurement system (BMS). METHO...

    journal_title:Pharmaceutical research

    pub_type: 临床试验,杂志文章

    doi:10.1023/a:1007561129221

    authors: Hu Z,Mawatari S,Shibata N,Takada K,Yoshikawa H,Arakawa A,Yosida Y

    更新日期:2000-02-01 00:00:00

  • Targeted delivery of doxorubicin by HPMA copolymer-hyaluronan bioconjugates.

    abstract:PURPOSE:Overexpression of hyaluronan (HA) receptors on cancer cells results in enhanced endocytotic uptake of the drug conjugate. An N-(2-hydroxypropyl)methacrylamide (HPMA)-HA polymeric drug delivery system was used for targeted delivery of doxorubicin to cancer cells. METHODS:HA-doxorubicin (DOX) bioconjugates (HA-D...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015170907274

    authors: Luo Y,Bernshaw NJ,Lu ZR,Kopecek J,Prestwich GD

    更新日期:2002-04-01 00:00:00

  • Disparity of in vitro and in vivo oleic acid-enhanced beta-estradiol percutaneous absorption across human skin.

    abstract::The permeation enhancing property of 5% oleic acid in ethanol on beta-estradiol was investigated in vitro and in vivo using symmetrical and asymmetrical side-by-side diffusion cells and the human skin sandwich flap, respectively. beta-Estradiol permeability in vitro and in vivo was similar in 75% ethanol (ETOH). Oleic...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018974131236

    authors: Pershing LK,Parry GE,Lambert LD

    更新日期:1993-12-01 00:00:00

  • Understanding biorelevant drug release from a novel thermoplastic capsule by considering microstructural formulation changes during hydration.

    abstract:PURPOSE:To study the biorelevant drug release from novel starch-based polyvinyl alcohol capsules (S-PVA-C). The effect of the shell material is studied by considering microstructural formulation changes during hydration. METHODS:Two different self-emulsifying systems containing either fenofibrate or probucol were fill...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-1152-y

    authors: Misic Z,Urbani R,Pfohl T,Muffler K,Sydow G,Kuentz M

    更新日期:2014-01-01 00:00:00

  • Overcoming the blood-brain barrier in chemotherapy treatment of pediatric brain tumors.

    abstract::Pediatric brain tumors are most common cancers in childhood and among the leading causes of death in children. Chemotherapy has been used as adjuvant (i.e. after) or neoadjuvant (i.e. before) therapy to surgery and radiotherapy for the management of pediatric brain tumors for more than four decades and gained more att...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-013-1196-z

    authors: Wu L,Li X,Janagam DR,Lowe TL

    更新日期:2014-03-01 00:00:00

  • Protein spray-freeze drying. Effect of atomization conditions on particle size and stability.

    abstract:PURPOSE:To investigate the effect of atomization conditions on particle size and stability of spray-freeze dried protein. METHODS:Atomization variables were explored for excipient-free (no zinc added) and zinc-complexed bovine serum albumin (BSA). Particle size was measured by laser diffraction light scattering follow...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1007570030368

    authors: Costantino HR,Firouzabadian L,Hogeland K,Wu C,Beganski C,Carrasquillo KG,Córdova M,Griebenow K,Zale SE,Tracy MA

    更新日期:2000-11-01 00:00:00

  • NO donor and biological properties of different benzofuroxans.

    abstract:PURPOSE:To investigate the effect of benzofusion on NO donor properties and related biological activities of the furoxan system. The biological properties considered were the ability to increase the cytosolic levels of cGMP in C6 cells and vasodilation. METHODS:NO donor properties were investigated either in the prese...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018974409622

    authors: Medana C,Di Stilo A,Visentin S,Fruttero R,Gasco A,Ghigo D,Bosia A

    更新日期:1999-06-01 00:00:00

  • Nontoxic suramin as a chemosensitizer in patients: dosing nomogram development.

    abstract:PURPOSE:We reported that suramin produced chemosensitization at nontoxic doses. This benefit was lost at the approximately 10-fold higher, maximally tolerated doses (MTD). The aim of the current study was to identify in patients the chemosensitizing suramin dose that delivers 10-50 microM plasma concentrations over 48 ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-0165-1

    authors: Chen D,Song SH,Wientjes MG,Yeh TK,Zhao L,Villalona-Calero M,Otterson GA,Jensen R,Grever M,Murgo AJ,Au JL

    更新日期:2006-06-01 00:00:00

  • PLGA microparticles in respirable sizes enhance an in vitro T cell response to recombinant Mycobacterium tuberculosis antigen TB10.4-Ag85B.

    abstract:PURPOSE:To study the use of poly (lactide-co-glycolide) (PLGA) microparticles in respirable sizes as carriers for recombinant tuberculosis (TB) antigen, TB10.4-Ag85B, with the ultimate goal of pulmonary delivery as vaccine for the prevention of TB. MATERIALS AND METHODS:Recombinant TB antigens were purified from E. co...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-009-0028-7

    authors: Shi S,Hickey AJ

    更新日期:2010-02-01 00:00:00

  • Release of plasmid DNA-encoding IL-10 from PLGA microparticles facilitates long-term reversal of neuropathic pain following a single intrathecal administration.

    abstract:PURPOSE:Interleukin-10 (IL-10) is an anti-inflammatory molecule that has achieved interest as a therapeutic for neuropathic pain. In this work, the potential of plasmid DNA-encoding IL-10 (pDNA-IL-10) slowly released from biodegradable microparticles to provide long-term pain relief in an animal model of neuropathic pa...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-010-0077-y

    authors: Soderquist RG,Sloane EM,Loram LC,Harrison JA,Dengler EC,Johnson SM,Amer LD,Young CS,Lewis MT,Poole S,Frank MG,Watkins LR,Milligan ED,Mahoney MJ

    更新日期:2010-05-01 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

  • The Impact of Inadequate Temperature Storage Conditions on Aggregate and Particle Formation in Drugs Containing Tumor Necrosis Factor-Alpha Inhibitors.

    abstract:PURPOSE:To measure aggregate and particle formation in tumor necrosis factor-alpha (TNF-α) inhibitors etanercept, adalimumab and certolizumab pegol product samples after exposure to freezing temperature conditions similar to storage conditions previously observed in patients' homes. METHODS:TNF-α inhibitors in their o...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2341-x

    authors: Vlieland ND,Nejadnik MR,Gardarsdottir H,Romeijn S,Sediq AS,Bouvy ML,Egberts ACG,van den Bemt BJF,Jiskoot W

    更新日期:2018-02-05 00:00:00

  • Novel beads made of alpha-cyclodextrin and oil for topical delivery of a lipophilic drug.

    abstract:PURPOSE:To investigate the potential of a novel lipid carrier, comprising beads of alpha-cyclodextrin and soybean oil, for topical drug delivery. Adapalene was chosen as a model drug to explore the ability of the beads to encapsulate and release a highly lipophilic compound. MATERIALS AND METHODS:Adapalene-loaded bead...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9395-0

    authors: Trichard L,Delgado-Charro MB,Guy RH,Fattal E,Bochot A

    更新日期:2008-02-01 00:00:00

  • Heat-treated Fungizone retains amphotericin B antifungal activity without renal toxicity in rats infected with Aspergillus fumigatus.

    abstract:PURPOSE:The purpose of this study was to assess the antifungal activity and renal and hepatic toxicity of amphotericin B (AmpB) following administration of Fungizone (FZ) and a heat-treated form of FZ (HFZ) to rats infected with Aspergillus fumigatus. METHODS:Infected rats were administered FZ and HFZ at a dosing regi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000041449.46054.b4

    authors: Sivak O,Bartlett K,Wasan KM

    更新日期:2004-09-01 00:00:00

  • Mechanisms of transport and structure-permeability relationship of sulfasalazine and its analogs in Caco-2 cell monolayers.

    abstract:PURPOSE:To investigate the mechanisms involved in transport of sulfasalazine in Caco-2 cells. METHODS:Permeability coefficients of sulfasalazine and its analogs across Caco-2 cell monolayers were measured as a function of direction of transport, energy and concentration dependence, and in the presence of inhibitors of...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1026450326712

    authors: Liang E,Proudfoot J,Yazdanian M

    更新日期:2000-10-01 00:00:00

  • Pharmacokinetic study of an iridoid glucoside: aucubin.

    abstract::Aucubin, a promising hepatoprotecting iridoid glucoside, was given intravenously (iv), orally (po), intraperitoneally (ip), and hepatoportally (pv) to rats. A linear pharmacokinetic behavior was obtained after iv administation of 400-400 mg/kg of aucubin. The half-life of aucubin in the postdistributive phase (t1/2, b...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015821527621

    authors: Suh NJ,Shim CK,Lee MH,Kim SK,Chang IM

    更新日期:1991-08-01 00:00:00

  • Use of glancing angle X-ray powder diffractometry to depth-profile phase transformations during dissolution of indomethacin and theophylline tablets.

    abstract:PURPOSE:The purpose of this study was (i) to develop glancing angle x-ray powder diffractometry (XRD) as a method for profiling phase transformations as a function of tablet depth; and (ii) to apply this technique to (a) study indomethacin crystallization during dissolution of partially amorphous indomethacin tablets a...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000012163.89163.f8

    authors: Debnath S,Predecki P,Suryanarayanan R

    更新日期:2004-01-01 00:00:00

  • Pectin and Mucin Enhance the Bioadhesion of Drug Loaded Nanofibrillated Cellulose Films.

    abstract:PURPOSE:Bioadhesion is an important property of biological membranes, that can be utilized in pharmaceutical and biomedical applications. In this study, we have fabricated mucoadhesive drug releasing films with bio-based, non-toxic and biodegradable polymers that do not require chemical modifications. METHODS:Nanofibr...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-018-2428-z

    authors: Laurén P,Paukkonen H,Lipiäinen T,Dong Y,Oksanen T,Räikkönen H,Ehlers H,Laaksonen P,Yliperttula M,Laaksonen T

    更新日期:2018-05-22 00:00:00

  • A model for targeting colon carcinoma cells using single-chain variable fragments anchored on virus-like particles via glycosyl phosphatidylinositol anchor.

    abstract:PURPOSE:VLPs displaying tumor targeting single-chain variable fragments (VLP-rscFvs) which targets tumor-associated glycoprotein-72 (TAG-72) marker protein have a potential for immunotherapy against colon carcinoma tumors. In this study, scFvs anchored on VLPs using glycosylphosphatidylinositol (GPI) were prepared to t...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1316-4

    authors: Deo VK,Yui M,Alam J,Yamazaki M,Kato T,Park EY

    更新日期:2014-08-01 00:00:00

  • The effect of cyclodextrins on the stability of peptides in nasal enzymic systems.

    abstract::Leucine enkephalin (YGGFL) undergoes rapid degradation in sheep nasal mucosa to yield GGFL which is further degraded to FL. The activity of the nasal mucosal homogenate against YGGFL and GGFL (t1/2 12 and 7 min) was significantly greater than that observed with a nasal wash fluid (t1/2 40 and 13 min). The effect of cy...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018946829225

    authors: Irwin WJ,Dwivedi AK,Holbrook PA,Dey MJ

    更新日期:1994-12-01 00:00:00

  • Near-infrared image-guided delivery and controlled release using optimized thermosensitive liposomes.

    abstract:PURPOSE:To engineer optimized near-infrared (NIR) active thermosensitive liposomes to potentially achieve image-guided delivery of chemotherapeutic agents. METHODS:Thermosensitive liposomes were surface-coated with either polyethylene glycol or dextran. Differential scanning calorimetry and calcein release studies wer...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0738-0

    authors: Turner DC,Moshkelani D,Shemesh CS,Luc D,Zhang H

    更新日期:2012-08-01 00:00:00