Intracellular processing of poly(ethylene imine)/ribozyme complexes can be observed in living cells by using confocal laser scanning microscopy and inhibitor experiments.

Abstract:

PURPOSE:Critical steps in the subcellular processing of poly(ethylene imine)/nucleic acid complexes, especially endosomal/lysosomal escape, were visualized by using living cell confocal laser scanning microscopy (CSLM) to obtain an insight into their mechanism. METHODS:Living cell confocal microscopy was used to examine the intracellular fate of poly(ethylene imine)/ribozyme and poly(L-lysine)/ribozyme complexes over time, in the presence of and without bafilomycin Al, a selective inhibitor of endosomal/lysosomal acidification. The compartment of complex accumulation was identified by confocal microscopy with a fluorescent acidotropic dye. To confirm microscopic data, luciferase reporter gene expression was determined under similar experimental conditions. RESULTS:Poly(ethylene imine)/ribozyme complexes accumulate in acidic vesicles, most probably lysosomes. Release of complexes occurs in a sudden event, very likely due to bursting of these organelles. After release, poly(ethylene imine) and ribozyme spread throughout the cell, during which slight differences in distribution between cytosol and nucleus are visible. No lysosomal escape was observed with poly(L-lysine)/ribozyme complexes or when poly(ethylene imine)/ ribozyme complexes were applied together with bafilomycin A1. Poly(ethylene imine)/plasmid complexes exhibited a high luciferase expression, which was reduced approximately 200-fold when lysosomal acidification was suppressed with bafilomycin A1. CONCLUSIONS:Our data provide, for the first time, direct experimental evidence for the escape of poly(ethylene imine)/nucleic acid complexes from the endosomal/lysosomal compartment. CLSM, in conjunction with living cell microscopy, is a promising tool for studying the subcellular fate of polyplexes in nucleic acid/gene delivery.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Merdan T,Kunath K,Fischer D,Kopecek J,Kissel T

doi

10.1023/a:1014212630566

subject

Has Abstract

pub_date

2002-02-01 00:00:00

pages

140-6

issue

2

eissn

0724-8741

issn

1573-904X

journal_volume

19

pub_type

杂志文章
  • Textural analysis and flow rheometry of novel, bioadhesive antimicrobial oral gels.

    abstract:PURPOSE:This study examined the rheological and textural characteristics (hardness, compressibilty, adhesiveness and cohesiveness) of bioadhesive oral gels containing the antimicrobial agent chlorhexidine. METHODS:Textural analysis was performed using a Stable Micro Systems texture analyser (model TA-XT 2) in texture ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012091231023

    authors: Jones DS,Woolfson AD,Brown AF

    更新日期:1997-04-01 00:00:00

  • A semi-physiological-based pharmacokinetic/pharmacodynamic model to describe the effects of topotecan on b-lymphocyte lineage cells.

    abstract:PURPOSE:To develop a semi-physiological-based model describing simultaneously the time course of immature and mature B-lymphocytes after topotecan (TPT) administration to tumor-bearing rats. METHODS:Twenty-four tumor-bearing BDIX male rats received a single 6 mg/kg intra-peritoneal dose of TPT or saline. Mature and im...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-009-0025-x

    authors: Vélez de Mendizábal N,Martínez-Forero I,Garrido MJ,Bandrés E,García-Foncillas J,Segura C,Trocóniz IF

    更新日期:2010-03-01 00:00:00

  • Synthesis and in vitro evaluation of a novel chitosan-glutathione conjugate.

    abstract:PURPOSE:It was the aim of this study to synthesize and characterize a novel chitosan-glutathione (GSH) conjugate providing improved mucoadhesive and permeation-enhancing properties. METHODS:Mediated by carbodiimide and N-hydroxysuccinimide, glutathione was covalently attached to chitosan via the formation of an amide ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-005-6248-6

    authors: Kafedjiiski K,Föger F,Werle M,Bernkop-Schnürch A

    更新日期:2005-09-01 00:00:00

  • Using partial area for evaluation of bioavailability and bioequivalence.

    abstract::Assessment of bioavailability/bioequivalence generally relies on the comparison of rate and extent of drug absorption between products. Rate of absorption is commonly expressed by peak concentration (C(max)) and time to peak concentration (T(max)), although these parameters are indirect measures of absorption rate. Re...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-011-0421-x

    authors: Chen ML,Davit B,Lionberger R,Wahba Z,Ahn HY,Yu LX

    更新日期:2011-08-01 00:00:00

  • Major involvement of low-density lipoprotein receptor-related protein 1 in the clearance of plasma free amyloid beta-peptide by the liver.

    abstract:PURPOSE:To identify the molecules responsible for amyloid beta-peptide (1-40) (Abeta(1-40)) uptake by the liver, which play a major role in the systemic clearance of Abeta(1-40). METHODS:The liver uptake index method was used to examine the mechanisms of Abeta(1-40) uptake by the liver in vivo. RESULTS:[125I]Abeta(1-...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-0208-7

    authors: Tamaki C,Ohtsuki S,Iwatsubo T,Hashimoto T,Yamada K,Yabuki C,Terasaki T

    更新日期:2006-07-01 00:00:00

  • Mechanical properties of dry and wet cellulosic and acrylic films prepared from aqueous colloidal polymer dispersions used in the coating of solid dosage forms.

    abstract::The mechanical properties of dry and wet polymeric films prepared from various aqueous polymeric dispersions were evaluated by a puncture test. They were studied with respect to type of polymer dispersion [cellulosic: Aquacoat and Surelease; acrylic: Eudragit NE, L, RS, and RL 30 D], plasticizer type (water-soluble or...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018942127524

    authors: Bodmeier R,Paeratakul O

    更新日期:1994-06-01 00:00:00

  • Recent developments in cyclic acetal biomaterials for tissue engineering applications.

    abstract::At an ever increasing pace, synthetic biomaterials are being developed with specific functionalities for tissue engineering applications. These biomaterials possess properties including biocompatibility, mechanical strength, and degradation as well as functionalities such as specific cell adhesion and directed cell mi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-008-9620-5

    authors: Falco EE,Patel M,Fisher JP

    更新日期:2008-10-01 00:00:00

  • Fuzzy modeling of skin permeability coefficients.

    abstract:PURPOSE:The purpose of this work was to determine whether a new modeling methodology using fuzzy logic c an predict skin permeability coefficients that are given compound descriptors that have been proven to affect percutaneous penetration. METHOD:Three fuzzy inference models were developed using subtractive clusterin...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1022273115847

    authors: Pannier AK,Brand RM,Jones DD

    更新日期:2003-02-01 00:00:00

  • Investigation into the influence of primary crystallization conditions on the mechanical properties and secondary processing behaviour of fluticasone propionate for carrier based dry powder inhaler formulations.

    abstract:PURPOSE:To investigate the influence of primary crystallization conditions on the mechanical properties and secondary processing behaviour of fluticasone propionate (FP) for carrier based dry powder inhaler (DPI) formulations. METHODS:Young's modulus of FP crystals produced using different anti-solvents was determined...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-011-0640-1

    authors: Kubavat HA,Shur J,Ruecroft G,Hipkiss D,Price R

    更新日期:2012-04-01 00:00:00

  • Evaluation of Predictors of Protein Relative Stability Obtained by Solid-State Hydrogen/Deuterium Exchange Monitored by FTIR.

    abstract:PURPOSE:Hydrogen/deuterium (H/D) exchange over a range of temperatures suggests a protein structural/mobility transition in the solid state below the system glass transition temperature (Tg). The purpose of this study was to determine whether solid-state protein stability correlates with the difference between storage ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02897-7

    authors: Fang R,Obeidat W,Pikal MJ,Bogner RH

    更新日期:2020-08-13 00:00:00

  • Effect of treatment regimen on the immunogenicity of human interferon Beta in immune tolerant mice.

    abstract:PURPOSE:Interferon beta is commonly used as therapeutic in the first line of therapy for multiple sclerosis. However, depending on the product, it induces an antibody response in up to 60% of patients. This study evaluated the impact of therapy related factors like dose, route of administration and administration frequ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-0992-9

    authors: Kijanka G,Jiskoot W,Schellekens H,Brinks V

    更新日期:2013-06-01 00:00:00

  • Predicting skin permeability.

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

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015810312465

    authors: Potts RO,Guy RH

    更新日期:1992-05-01 00:00:00

  • Cell-penetrating antimicrobial peptides - prospectives for targeting intracellular infections.

    abstract:PURPOSE:To investigate the suitability of three antimicrobial peptides (AMPs) as cell-penetrating antimicrobial peptides. METHODS:Cellular uptake of three AMPs (PK-12-KKP, SA-3 and TPk) and a cell-penetrating peptide (penetratin), all 5(6)-carboxytetramethylrhodamine-labeled, were tested in HeLa WT cells and analyzed ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1550-9

    authors: Bahnsen JS,Franzyk H,Sayers EJ,Jones AT,Nielsen HM

    更新日期:2015-05-01 00:00:00

  • Nonlinear disposition of intravenous 2',3'-dideoxyinosine in rats.

    abstract::The pharmacokinetics of 2',3'-dideoxyinosine (ddI) were examined in rats given intravenous doses of 8, 40, or 200 mg/kg. The concentrations of ddI in whole blood and plasma were identical. The concentration decline was multiexponential, with mean half-lives of 2 and 20 min for the first and second phases, respectively...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015866714224

    authors: Wientjes MG,Mukherji E,Au JL

    更新日期:1992-08-01 00:00:00

  • A Review of the Emerging Role of Silk for the Treatment of the Eye.

    abstract::Silk is a remarkable biopolymer with a long history of medical use. Silk fabrications have a robust track record for load-bearing applications, including surgical threads and meshes, which are clinically approved for use in humans. The progression of top-down and bottom-up engineering approaches using silk as the basi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-018-2534-y

    authors: Tran SH,Wilson CG,Seib FP

    更新日期:2018-11-05 00:00:00

  • Cyclodextrins as mucosal absorption promoters of insulin. II. Effects of beta-cyclodextrin derivatives on alpha-chymotryptic degradation and enteral absorption of insulin in rats.

    abstract::The relative effectiveness of two beta-cyclodextrin derivatives, i.e., dimethyl-beta-cyclodextrin (DM beta CD) and hydroxypropyl-beta-cyclodextrin (HP beta CD), in enhancing enteral absorption of insulin was evaluated in the lower jejunal/upper ileal segments of the rat by means of an in situ closed loop method. The i...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018997101542

    authors: Shao Z,Li Y,Chermak T,Mitra AK

    更新日期:1994-08-01 00:00:00

  • Effect of moisture content on compression properties of two dextrose-based directly compressible diluents.

    abstract::Moisture sorption characteristics and the effect of moisture content on the compression properties of two dextrose-based directly compressible diluents, namely, Emdex (diluent A) and Sweetrex (diluent B) were studied. Both diluents sorbed moisture rapidly at relative humidities greater than 60%. For both the diluents,...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015889414533

    authors: Shukla AJ,Price JC

    更新日期:1991-03-01 00:00:00

  • Direct observation of single particle electrostatic charging by atomic force microscopy.

    abstract:PURPOSE:To show that atomic force microscopy (AFM) can be used to directly study the electrostatic charging and dissipation of single pharmaceutical particles. MATERIALS AND METHODS:Particles of lactose attached to AFM cantilevers were charged on a glass surface at a relative humidity (RH) of 0.1%. By recording force-...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-9230-z

    authors: Bunker MJ,Davies MC,James MB,Roberts CJ

    更新日期:2007-06-01 00:00:00

  • Sphingosine-based liposome as DNA vector for intramuscular gene delivery.

    abstract:PURPOSE:The aim of this study was to develop a labile sphingosine-based liposome for intramuscular gene delivery. METHODS:Sphingosine-based liposomes were formulated in a range of solutions with phosphatidylcholine, then were associated to DNA. The physico-chemical characteristics of the sphingosine/EPC liposomes and ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1019894008885

    authors: Baraldo K,Leforestier N,Bureau M,Mignet N,Scherman D

    更新日期:2002-08-01 00:00:00

  • In vitro- in vivo correlation's dissolution limits setting.

    abstract:PURPOSE:In vitro in vivo correlation (IVIVC) is a biopharmaceutical tool recommended for use in formulation development. When validated, IVIVC can be used to set dissolution limits and, based on the dissolution limits, as a surrogate for an in vivo study. The purpose of this paper is to study the various methods used t...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-014-1349-8

    authors: Roudier B,Davit BM,Beyssac E,Cardot JM

    更新日期:2014-09-01 00:00:00

  • Population Pharmacokinetics (PK) and Pharmacodynamics (PD) Analysis of LY3015014, a Monoclonal Antibody to Protein Convertase Subtilisin/Kexin Type 9 (PCSK9) in Healthy Subjects and Hypercholesterolemia Patients.

    abstract:PURPOSE:LY3015014 is a humanized immunoglobulin G4 (IgG4) monoclonal antibody that binds to the catalytic domain of PCSK9 and reduce low-density lipoprotein cholesterol (LDL-C) in patients with hypercholesterolemia that is poorly controlled by maximally tolerated statin therapy. The objective of this pharmacokinetic/ph...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-016-2054-6

    authors: Shen T,James DE,Krueger KA

    更新日期:2017-01-01 00:00:00

  • The pharmacokinetics of trilostane and ketotrilostane in an interconverting system in the rat.

    abstract::The pharmacokinetics of trilostane and one of its metabolites ketotrilostane are described and characterized in the rat following the separate intravenous administration of trilostane and ketotrilostane. It was noted during these studies that the parent compound and its metabolite undergo metabolic interconversion-tri...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015828027060

    authors: McGee JP,Shaw PN

    更新日期:1992-04-01 00:00:00

  • Challenging the Relevance of Unbound Tissue-to-Blood Partition Coefficient (Kpuu) on Prediction of Drug-Drug Interactions.

    abstract:PURPOSE:To examine the theoretical/practical utility of the liver-to-blood partition coefficient (Kpuu) for predicting drug-drug interactions (DDIs), and compare the Kpuu-approach to the extended clearance concept AUCR-approach. METHODS:The Kpuu relationship was derived from first principles. Theoretical simulations i...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02797-w

    authors: Sodhi JK,Liu S,Benet LZ

    更新日期:2020-03-25 00:00:00

  • Passive transepithelial absorption of thyrotropin-releasing hormone (TRH) via a paracellular route in cultured intestinal and renal epithelial cell lines.

    abstract::Transport studies using intestinal brush-border membrane vesicles isolated from rats and rabbits have failed to demonstrate proton- or Na(+)-dependent carrier-mediated transport of thyrotropin-releasing hormone (TRH), despite a pharmacologically relevant oral bioavailability. To examine the hypothesis that reported le...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018947430018

    authors: Thwaites DT,Hirst BH,Simmons NL

    更新日期:1993-05-01 00:00:00

  • In Silico Predictions of Human Skin Permeability using Nonlinear Quantitative Structure-Property Relationship Models.

    abstract:PURPOSE:Predicting human skin permeability of chemical compounds accurately and efficiently is useful for developing dermatological medicines and cosmetics. However, previous work have two problems; 1) quality of databases used, and 2) methods for prediction models. In this paper, we attempt to solve these two problems...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-015-1629-y

    authors: Baba H,Takahara J,Mamitsuka H

    更新日期:2015-07-01 00:00:00

  • Body distribution of camptothecin solid lipid nanoparticles after oral administration.

    abstract:PURPOSE:The aim of this study was to investigate the specific changes in body distribution of camptothecin (CA) through incorporation into solid lipid nanoparticles (SLN) by peroral route. METHODS:Camptothecin loaded solid lipid nanoparticles (CA-SLN) coated with poloxamer 188 were produced by high pressure homogeniza...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018888927852

    authors: Yang S,Zhu J,Lu Y,Liang B,Yang C

    更新日期:1999-05-01 00:00:00

  • The use of multiple doses and pharmacodynamic system analysis to distinguish between dispositional delays and time-variant pharmacodynamics.

    abstract::Pharmacokinetic-pharmacodynamic modeling algorithms, in general, rely on hysteresis minimization techniques that assume time-invariant pharmacodynamics (constant biophase concentration-effect relationships). When time-variant pharmacodynamics are observed, a specific model for tolerance or sensitization is required. H...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018940122382

    authors: Gastonguay MR,Schwartz SL

    更新日期:1994-12-01 00:00:00

  • Rapid doxorubicin efflux from the nucleus of drug-resistant cancer cells following extracellular drug clearance.

    abstract:PURPOSE:Following extracellular drug clearance, we analyzed the rate of doxorubicin efflux from the nucleus of three human leukemic cells (K562, Molt4 and CCRF-CEM) and related it to their differential sensitivity to this drug, after a short drug pulse. RESULTS:For many pulse-chase regimes, K562 cell viability was lea...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9369-2

    authors: Chen VY,Posada MM,Zhao L,Rosania GR

    更新日期:2007-11-01 00:00:00

  • Antiangiogenic effect of bile acid acylated heparin derivative.

    abstract:PURPOSE:Chemically modified heparin-DOCA was prepared and found to have markedly lower anticoagulant activity than heparin. In the present study, we elucidated the antiangiogenic and antitumoral activities of heparin-DOCA derivative. METHODS:To evaluate the antiangiogenic and antitumoral effects of heparin-DOCA, capil...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-9139-6

    authors: Park K,Kim YS,Lee GY,Nam JO,Lee SK,Park RW,Kim SY,Kim IS,Byun Y

    更新日期:2007-01-01 00:00:00

  • An ex vivo toe model used to assess applicators for the iontophoretic ungual delivery of terbinafine.

    abstract:PURPOSE:An ex vivo intact toe model was developed to assess two different applicator designs for iontophoretic delivery of terbinafine into the nail only or the nail and surrounding skin. METHODS:Iontophoretic permeation studies were carried out on intact cadaver toes using nail-only and nail/skin applicators with a c...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-009-9934-y

    authors: Nair AB,Kim HD,Davis SP,Etheredge R,Barsness M,Friden PM,Murthy SN

    更新日期:2009-09-01 00:00:00