Fabrication of TPGS-Stabilized Liposome-PLGA Hybrid Nanoparticle Via a New Modified Nanoprecipitation Approach: In Vitro and In Vivo Evaluation.

Abstract:

PURPOSE:In this study, a new modified nanoprecipitation approach that more efficient and simpler than conventional approach was developed to synthesize D-alpha-Tocopheryl polyethylene glycol 1000 succinate stabilized liposome-PLGA hybrid nanoparticle, loaded with simvastatin (ST-TLPN). METHODS:The optimum formulation was screened via investigation of the impact of TPGS mass within polymeric core and lipid shell on the physicochemical properties of nanoparticles respectively. FTIR, and drug release of ST-TLPN were also systematically determined. Finally, the cellular internalization was evaluated using the murine macrophage cell line, in vivo pharmacokinetic behavior and antiatherogenic efficacies were elaborately examined in atherosclerotic rabbit models. RESULTS:With the weight ratio of TPGS-to-PLGA in organic phase of 30% and TPGS-to-lipid in aqueous phase of 35%, ST-TLPN exhibited core-shell structure, sub-100 nm size, EE% of over 90% and a slow release profile. The excellent cellular uptake was displayed in RAW264.7 cell line. Improved pharmacokinetic behavior, and enhanced antiatherogenic efficacy of ST-TLPN in the model animals were also revealed compared with ST-loaded PLGA nanoparticles. CONCLUSION:These findings suggest the modified nanoprecipitation method holds great potential for fabricating LPN, aided by the multiple functions of TPGS. And the prepared TLPN is a promising delivery system for use in the pharmaceutical field.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Zhang M,He J,Zhang W,Liu J

doi

10.1007/s11095-018-2485-3

subject

Has Abstract

pub_date

2018-08-30 00:00:00

pages

199

issue

11

eissn

0724-8741

issn

1573-904X

pii

10.1007/s11095-018-2485-3

journal_volume

35

pub_type

杂志文章
  • Permeability characteristics of tetragastrins across intestinal membranes using the Caco-2 monolayer system: comparison between acylation and application of protease inhibitors.

    abstract:PURPOSE:Three types of acyl tetragastrin (TG), acetyl-TG (C2-TG), butyryl-TG (C4-TG) and caproyl-TG (C6-TG) were synthesized and their in vitro intestinal permeability characteristics were examined using Caco-2 monolayers. METHODS:The disappearance of acyl-TGs from the apical side of Caco-2 monolayers was estimated by...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1011997404306

    authors: Fujita T,Kawahara I,Quan Y,Hattori K,Takenaka K,Muranishi S,Yamamoto A

    更新日期:1998-09-01 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

  • D-glucose triggers multidrug resistance-associated protein (MRP)-mediated secretion of fluorescein across rat jejunum in vitro.

    abstract:PURPOSE:To examine the transport characteristics of the multidrug resistance-associated protein (MRP) substrate fluorescein across the isolated rat small intestinal segments. METHODS:The transport of fluorescein was studied in side-by-side diffusion chambers under short-circuited conditions at physiological pH. RESUL...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000022410.89709.c3

    authors: Legen I,Kristl A

    更新日期:2004-04-01 00:00:00

  • Mechanism of the solution oxidation of rofecoxib under alkaline conditions.

    abstract:PURPOSE:The rapid oxidation of rofecoxib under alkaline conditions has been previously reported. The oxidation was reported to involve gamma-lactone ring opening to an alcohol, which further oxidized to a dicarboxyclic acid. The oxidation was suspected to be mediated by peroxy radicals. This work further investigates t...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-005-6947-z

    authors: Harmon PA,Biffar S,Pitzenberger SM,Reed RA

    更新日期:2005-10-01 00:00:00

  • Polydopamine-based surface modification for the development of peritumorally activatable nanoparticles.

    abstract:PURPOSE:To create poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs), where a drug-encapsulating NP core is covered with polyethylene glycol (PEG) in a normal condition but exposes a cell-interactive TAT-modified surface in an environment rich in matrix metalloproteinases (MMPs). METHODS:PLGA NPs were modified w...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-1039-y

    authors: Gullotti E,Park J,Yeo Y

    更新日期:2013-08-01 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

  • Variations of in vitro nitroglycerine permeation through human epidermis.

    abstract::The fluxes of nitroglycerine (NG) through human abdominal epidermis from different individuals were measured in vitro at 32°C. The mean NG flux for the entire group was 16.9 µg/cm(2) × hr, with a standard deviation of 47.7%. There are no significant differences in the means and the variances of NG fluxes between males...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/A:1016381017357

    authors: Langguth P,Spahn H,Mutschler E

    更新日期:1986-02-01 00:00:00

  • Immunopotentiator-Loaded Polymeric Microparticles as Robust Adjuvant to Improve Vaccine Efficacy.

    abstract:PURPOSE:Adjuvants are required to ensure the efficacy of subunit vaccines. Incorporating molecular immunopotentiators within particles could overcome drawbacks of molecular adjuvants (such as solubility and toxicity), and improve adjuvanticity of particles, achieving stronger adjuvant activity. Aim of this study is to ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-015-1666-6

    authors: Zhang W,Wang L,Yang T,Liu Y,Chen X,Liu Q,Jia J,Ma G

    更新日期:2015-09-01 00:00:00

  • Histone H1-mediated transfection: serum inhibition can be overcome by Ca2+ ions.

    abstract:PURPOSE:One of the drawbacks of polycationic and cationic liposomal gene transfer is its sensitivity to serum. Gene therapy requires the transfectant-DNA complex to be resistant to serum as well as blood. Since Ca2+ has proved to be an efficient cofactor of polycationic gene transfer, we decided to investigate its effe...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1007581700996

    authors: Haberland A,Knaus T,Zaitsev SV,Buchberger B,Lun A,Haller H,Böttger M

    更新日期:2000-02-01 00:00:00

  • Structure in dehydrated trehalose dihydrate--evaluation of the concept of partial crystallinity.

    abstract:PURPOSE:(i) To use trehalose as a model compound to evaluate the concept of crystallinity in pharmaceuticals. (ii) To understand the structural nature of dehydrated trehalose dihydrate. MATERIALS AND METHODS:Trehalose dihydrate was dehydrated isothermally at several temperatures below 100 degrees C and the anhydrous p...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-9058-6

    authors: Rani M,Govindarajan R,Surana R,Suryanarayanan R

    更新日期:2006-10-01 00:00:00

  • Rapid determination of methadone in plasma, cerebrospinal fluid, and urine by gas chromatography and its application to routine drug monitoring.

    abstract::Determination of methadone (MET) in biological fluids can serve to adjust dosages in patients suffering from cancer pain or participating in methadone maintenance programs. We developed a gas chromatographic assay using nitrogen-phosphorus detection. The method involves a single-step extraction from alkalized plasma, ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018904825958

    authors: Schmidt N,Sittl R,Brune K,Geisslinger G

    更新日期:1993-03-01 00:00:00

  • Selection of a derivative of the antiviral agent 9-[(1,3-dihydroxy-2-propoxy)-methyl]guanine (DHPG) with improved oral absorption.

    abstract::Various diesters of 9-[(1,3-dihydroxy-2-propoxy)-methyl]guanine (DHPG) were screened in order to identify a derivative with improved oral absorption. The solubilities and dissolution rates decreased with increasing chain length and branching of the ester group. However, the dipropionate ester showed an anomalously fas...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016462801968

    authors: Benjamin EJ,Firestone BA,Bergstrom R,Fass M,Massey I,Tsina I,Lin YY

    更新日期:1987-04-01 00:00:00

  • Machine Learning Platform to Discover Novel Growth Inhibitors of Neisseria gonorrhoeae.

    abstract:PURPOSE:To advance fundamental biological and translational research with the bacterium Neisseria gonorrhoeae through the prediction of novel small molecule growth inhibitors via naïve Bayesian modeling methodology. METHODS:Inspection and curation of data from the publicly available ChEMBL web site for small molecule ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02876-y

    authors: Pereira JC,Daher SS,Zorn KM,Sherwood M,Russo R,Perryman AL,Wang X,Freundlich MJ,Ekins S,Freundlich JS

    更新日期:2020-07-13 00:00:00

  • Pharmaceutical evaluation of gas-filled microparticles as gene delivery system.

    abstract:PURPOSE:To produce and characterize a nonviral ultrasound-controlled release system of plasmid DNA (pDNA) encapsulated in gas-filled poly(D,L-lactide-co-glycolide) microparticles (PLGA-MPs). METHODS:Different cationic polymers were used to form pDNA/polymer complexes to enhance the stability of pDNA during micropartic...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1014430631844

    authors: Seemann S,Hauff P,Schultze-Mosgau M,Lehmann C,Reszka R

    更新日期:2002-03-01 00:00:00

  • Role of appendages in skin resistance and iontophoretic peptide flux: human versus snake skin.

    abstract:PURPOSE:1. The assessment of the role of hair follicles and sweat glands in skin resistance and percutaneous iontophoretic flux of 9-desglycinamide, 8-arginine vasopressin (DGAVP) by comparing two skin species: human stratum corneum which contained hair follicles, sweat and sebaceous glands, and shed snake skin which l...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016243706415

    authors: Craane-van Hinsberg WH,Verhoef JC,Bax LJ,Junginger HE,Boddé HE

    更新日期:1995-10-01 00:00:00

  • The effects of bile salts and lipids on the physicochemical behavior of gemfibrozil.

    abstract::Physicochemical effects caused by intestinal fluids on drugs in the gastrointestinal (GI) tract can be a contributing factor in food induced changes in bioavailability. To identify physicochemical properties of gemfibrozil that may be altered by endogenous and dietary lipids, in vitro studies were conducted in model s...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018967401000

    authors: Luner PE,Babu SR,Radebaugh GW

    更新日期:1994-12-01 00:00:00

  • Analysis of the compression mechanics of pharmaceutical agglomerates of different porosity and composition using the Adams and Kawakita equations.

    abstract:PURPOSE:To analyze the mechanics of some pharmaceutical agglomerates during uniaxial confined compression by using compression parameters derived from the Heckel, Kawakita and Adams equations, and to study the influence of these compression parameters on the tablet-forming ability of agglomerates. METHODS:Force and di...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1007575120817

    authors: Nicklasson F,Alderborn G

    更新日期:2000-08-01 00:00:00

  • SB-239063, a potent and selective inhibitor of p38 map kinase: preclinical pharmacokinetics and species-specific reversible isomerization.

    abstract:PURPOSE:A series of studies was conducted to evaluate the preclinical pharmacokinetics of SB-239063 (trans-1-(4-hydroxycyclohexyl)-4-(4-fluorophenyl)-5-[(2-methoxy)pyrimidin-4-yl] imidazole), a potent and selective p38 MAP kinase inhibitor. METHODS:SB-239063 was administered both i.v. and p.o. in the rat, dog, cynomol...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1013002414678

    authors: Ward KW,Proksch JW,Azzarano LM,Salyers KL,McSurdy-Freed JE,Molnar TM,Levy MA,Smith BR

    更新日期:2001-09-01 00:00:00

  • Human monoclonal antibody fragments targeting matrilin-3 in growth plate cartilage.

    abstract:PURPOSE:Many genetic disorders, including chondrodysplasias, and acquired disorders impair growth plate function, resulting in short and sometimes malformed bones. There are multiple endocrine and paracrine factors that promote chondrogenesis at the growth plate, which could potentially be used to treat these disorders...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-015-1636-z

    authors: Cheung CS,Zhu Z,Lui JC,Dimitrov D,Baron J

    更新日期:2015-07-01 00:00:00

  • Voltage dependence of transepithelial guanidine permeation across Caco-2 epithelia allows determination of the paracellular flux component.

    abstract:PURPOSE:The aim of this study was to investigate transepithelial ionic permeation via the paracellular pathway of human Caco-2 epithelial monolayers and its contribution to absorption of the base guanidine. METHODS:Confluent monolayers of Caco-2 epithelial cells were mounted in Ussing chambers and the transepithelial ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-006-9568-2

    authors: Carr G,Haslam IS,Simmons NL

    更新日期:2006-03-01 00:00:00

  • Biodegradable poly(2-dimethylamino ethylamino)phosphazene for in vivo gene delivery to tumor cells. Effect of polymer molecular weight.

    abstract:PURPOSE:Previously, we have shown that complexes of plasmid DNA with the biodegradable polymer poly(2-dimethylamino ethylamino)phosphazene (p(DMAEA)-ppz) mediated tumor selective gene expression after intravenous administration in mice. In this study, we investigated the effect of p(DMAEA)-ppz molecular weight on both ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9299-z

    authors: de Wolf HK,de Raad M,Snel C,van Steenbergen MJ,Fens MH,Storm G,Hennink WE

    更新日期:2007-08-01 00:00:00

  • Prodrugs of peptides. 11. Chemical and enzymatic hydrolysis kinetics of N-acyloxymethyl derivatives of a peptide-like bond.

    abstract::Various carboxylic acid esters of the N-hydroxymethyl derivative of N-benzyloxycarbonylglycine benzylamide, used as a peptide-like model, were prepared and their decomposition kinetics studied in aqueous solution and in human plasma solutions. These N-acyloxymethylamide derivatives were found to undergo a facile decom...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015839426229

    authors: Bundgaard H,Rasmussen GJ

    更新日期:1991-10-01 00:00:00

  • Population Pharmacokinetics, Efficacy Exposure-response Analysis, and Model-based Meta-analysis of Fenebrutinib in Subjects with Rheumatoid Arthritis [corrected].

    abstract:PURPOSE:Fenebrutinib (GDC-0853), a Bruton's tyrosine kinase (BTK) inhibitor was investigated in a Phase 2 clinical trial in patients with rheumatoid arthritis (RA). Our aim was to apply a model-informed drug development (MIDD) approach to examine the totality of available clinical efficacy data. METHODS:Population pha...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-019-2752-y

    authors: Chan P,Yu J,Chinn L,Prohn M,Huisman J,Matzuka B,Hanley W,Tuckwell K,Quartino A

    更新日期:2020-01-06 00:00:00

  • Changes of Blood-Brain Barrier and Brain Parenchymal Protein Expression Levels of Mice under Different Insulin-Resistance Conditions Induced by High-Fat Diet.

    abstract:PURPOSE:The purpose of the present study was to investigate changes of blood-brain barrier (BBB) and brain parenchymal protein expression due to type II diabetes mellitus (T2DM) induced by a high-fat diet (HFD) by using SWATH-based quantitative proteomics. METHODS:Mice were fed a HFD for 2 or 10 weeks, and then SWATH-...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-019-2674-8

    authors: Ogata S,Ito S,Masuda T,Ohtsuki S

    更新日期:2019-07-31 00:00:00

  • Efficacy of Optimized Treatment Protocol Using LAU-7b Formulation against Ovalbumin (OVA) and House Dust Mite (HDM) -Induced Allergic Asthma in Atopic Hyperresponsive A/J Mice.

    abstract:PURPOSE:To assess the efficacy of the novel clinical formulation of fenretinide (LAU-7b) for the treatment of allergic asthma. To study the association between LAU-7b treatment in allergic asthma and the modulation of very long chain ceramides (VLCC). METHODS:We used two allergens (OVA and HDM) to induce asthma in mou...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-019-2743-z

    authors: Youssef M,De Sanctis JB,Kanagaratham C,Tao S,Ahmed E,Radzioch D

    更新日期:2020-01-08 00:00:00

  • Long-circulating poly(ethylene glycol)-modified gelatin nanoparticles for intracellular delivery.

    abstract:PURPOSE:The objective of this study was to develop and characterize long-circulating, biodegradable, and biocompatible nanoparticulate formulation as an intracellular delivery vehicle. METHODS:Poly(ethylene glycol) (PEG)-modified gelatin was synthesized by reacting Type-B gelatin with PEG-epoxide. The nanoparticles, p...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016486910719

    authors: Kaul G,Amiji M

    更新日期:2002-07-01 00:00:00

  • Nanocarriers.

    abstract::The use of nanoparticulate pharmaceutical carriers to enhance the in vivo efficiency of many drugs well established itself over the past decade both in pharmaceutical research and clinical setting. The current level of engineering pharmaceutical nanocarriers in some cases allows for drug delivery systems (DDS) to demo...

    journal_title:Pharmaceutical research

    pub_type: 社论

    doi:10.1007/s11095-007-9463-5

    authors: Torchilin VP

    更新日期:2007-12-01 00:00:00

  • A fractal approach to heterogeneous drug distribution: calcium pharmacokinetics.

    abstract:PURPOSE:To point out the importance of heterogeneity in drug distribution processes and develop a noncompartmental approach for the description of the distribution of drug in the body. METHODS:A dichotomous branching network of vessels for the arterial tree connected to a similar venous network was used to describe th...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016031129053

    authors: Macheras P

    更新日期:1996-05-01 00:00:00

  • Nonisothermal stability assessment of stable pharmaceuticals: testing of a clindamycin phosphate formulation.

    abstract::The stability of an antibiotic formulation (clindamycin phosphate in dextrose), which is stable at room temperature, was assessed by nonisothermal kinetic analysis at elevated temperatures. A preliminary study, conducted to establish apparent rate order, verified the appropriateness of a first-order kinetic model. The...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015840320410

    authors: Kipp JE,Hlavaty JJ

    更新日期:1991-05-01 00:00:00

  • Unconventional Passive Enhancement of Transdermal Drug Delivery: toward a Mechanistic Understanding of Penetration Enhancers Releasing from Acrylic Pressure-Sensitive Adhesive of Patches.

    abstract:PURPOSE:Penetration enhancers (PEs) enhancing efficacy depends on two processes: PEs release from patches and action on skin. Compared with their action on skin, PEs release process was poorly understood. Therefore, the purpose of this study was to make a mechanistic understanding of PEs release from acrylic pressure-s...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-020-02901-0

    authors: Zeng L,Song W,He W,Zhang J,Wang Y,Bian J,Mao Z,Quan D,Liu J

    更新日期:2020-08-13 00:00:00