α-Conotoxin ImI-modified polymeric micelles as potential nanocarriers for targeted docetaxel delivery to α7-nAChR overexpressed non-small cell lung cancer.

Abstract:

:A micelle system modified with α-Conotoxin ImI (ImI), a potently antagonist for alpha7 nicotinic acetylcholine receptor (α7-nAChR) previously utilized for targeting breast cancer, was constructed. Its targeting efficiency and cytotoxicity against non-small cell lung cancer (NSCLC) highly expressing α7-nAChR was investigated. A549, a non-small cell lung cancer cell line, was selected as the cell model. The cellular uptake study showed that the optimal modification ratio of ImI on micelle surface was 5% and ImI-modification increased intracellular delivery efficiency to A549 cells via receptor-mediated endocytosis. Intracellular Ca2+ transient assay demonstrated that ImI modification led to enhanced molecular interaction between nanocarriers and A549 cells. The in vivo near-infrared fluorescence imaging further revealed that ImI-modified micelles could facilitate the drug accumulation in tumor sites compared with non-modified micelles via α7-nAChR mediation. Moreover, docetaxel (DTX) was loaded in ImI-modified nanomedicines to evaluate its in vitro cytotoxicity. As a result, DTX-loaded ImI-PMs exhibited greater anti-proliferation effect on A549 cells compared with non-modified micelles. Generally, our study proved that ImI-modified micelles had targeting ability to NSCLC in addition to breast cancer and it may provide a promising strategy to deliver drugs to NSCLC overexpressing α7-nAChR.

journal_name

Drug Deliv

journal_title

Drug delivery

authors

Mei D,Zhao L,Chen B,Zhang X,Wang X,Yu Z,Ni X,Zhang Q

doi

10.1080/10717544.2018.1436097

subject

Has Abstract

pub_date

2018-11-01 00:00:00

pages

493-503

issue

1

eissn

1071-7544

issn

1521-0464

journal_volume

25

pub_type

杂志文章
  • Effects of vehicles and pressure sensitive adhesives on the penetration of isosorbide dinitrate across the hairless mouse skin.

    abstract::The effects of various vehicles and adhesives on the percutaneous absorption of isosorbide dinitrate (ISDN) were evaluated. Lauroglycol FCC showed the highest flux among vehicles tested. The flux of ISDN from silicone and acrylic adhesive matrices was found to be higher than that from other types of adhesive matrices....

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10426500290095430

    authors: Myoung Y,Choi HK

    更新日期:2002-04-01 00:00:00

  • Cellular effects of antisense c-myc oligodeoxynucleotides are delivery dependent.

    abstract::Among the transcription factors critical for cell cycle regulation is the proto-oncogene c-myc. The expression of c-myc upon vascular injury and its inhibition by antisense oligodeoxynucleotides have demonstrated the importance of this protein in the control of proliferation for many cell types, including vascular smo...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717549609029444

    authors: Koo EW,Edelman ER

    更新日期:1996-01-01 00:00:00

  • Use of biorelevant media for assessment of a poorly soluble weakly basic drug in the form of liquisolid compacts: in vitro and in vivo study.

    abstract::The purpose of this work is to use biorelevant media to evaluate the robustness of a poorly water soluble weakly basic drug to variations along the gastrointestinal tract (GIT) after incorporation in liquisolid compacts and to assess the success of these models in predicting the in vivo performance. Liquisolid tablets...

    journal_title:Drug delivery

    pub_type: 杂志文章,随机对照试验

    doi:10.3109/10717544.2014.917442

    authors: Badawy MA,Kamel AO,Sammour OA

    更新日期:2016-01-01 00:00:00

  • Influence of potential inhalation carriers on stability of thymopentin in rat bronchoalveolar lavage fluid.

    abstract::In the present study, the stability of thymopentin (TP5) in bronchoalveolar lavage fluid (BALF) in presence of potential excipients in inhalation formulation was investigated. The content of TP5 was determined using HPLC method. Commonly used bulking agent, dispersibility enhancers and absorption enhancers in inhalati...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2013.878002

    authors: Cai C,Wang L,Dong W,Tang X

    更新日期:2014-09-01 00:00:00

  • Laser-assisted delivery enhances topical uptake of the anticancer agent cisplatin.

    abstract::Systemic chemotherapy with the anticancer agent cisplatin is approved for advanced non-melanoma skin cancer (NMSC), but topical treatment is limited by insufficient cutaneous penetration. We studied the impact of ablative fractional laser (AFL) exposure on topical cisplatin's pharmacokinetics and biodistribution in sk...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2018.1534896

    authors: Wenande E,Olesen UH,Boesen MR,Persson DP,Lerche CM,Stürup S,Gammelgaard B,Husted S,Anderson RR,Haedersdal M

    更新日期:2018-11-01 00:00:00

  • Preparation and characterization of solid lipid nanoparticles containing cloricromene.

    abstract::This article describes the development of solid lipid nanoparticles (SLN) as colloidal carriers for cloricromene. Nanoparticles were prepared by the microemulsion or precipitation technique. In vitro drug release profile from SLN was studied under various experimental conditions mimicking some body fluids. The drug re...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/drd_10_4_245

    authors: Bondì ML,Fontana G,Carlisi B,Giammona G

    更新日期:2003-10-01 00:00:00

  • In vivo lymphatic targeting of methylene blue with microemulsion and multiple microemulsion.

    abstract::Three formulations including methylene blue solution (MB-S), MB water-in-oil microemulsion (MB-ME), and MB multiple microemulsion (MB-MME) were prepared with the aim to evaluate whether the three formulations can carry MB target to regional lymph nodes and show lymphatic tropism after subcutaneous administration. The ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540903075644

    authors: Wang S,Yang R,Yao H,Zhou G,Zhang Y,Yang B,Ng L,Yan M

    更新日期:2009-10-01 00:00:00

  • In vitro assessment of lidocaine release from aqueous and oil solutions and from preformed and in situ formed aqueous and oil suspensions. Parenteral depots for intra-articular administration.

    abstract::In vitro drug release rates from aqueous and oil solutions as well as preformed and in situ formed aqueous and oil suspensions intended for intra-articular delivery have been investigated using the rotating dialysis cell model. Using lidocaine as a model drug substance the release kinetics from aqueous and oil suspens...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540701828657

    authors: Pedersen BT,Larsen SW,Østergaard J,Larsen C

    更新日期:2008-01-01 00:00:00

  • pH-responsive thiolated chitosan nanoparticles for oral low-molecular weight heparin delivery: in vitro and in vivo evaluation.

    abstract::The aim of present study was to investigate a pH-responsive and mucoadhesive nanoparticle system for oral bioavailability enhancement of low-molecular weight heparin (LMWH). The thioglycolic acid (TGA) was first covalently attached to chitosan (CS) with 396.97 ± 54.54 μmol thiol groups per gram of polymer and then the...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2014.909908

    authors: Fan B,Xing Y,Zheng Y,Sun C,Liang G

    更新日期:2016-01-01 00:00:00

  • Development and characterization of mucoadhesive microspheres bearing salbutamol for nasal delivery.

    abstract::Mucoadhesive drug delivery systems are those that provide intimate contact of the drug with the mucosa for an extended period of time. In our present work, mucoadhesive chitosan microspheres were prepared by emulsion solvent method. Formulations were characterized for various physicochemical attributes, shape, surface...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540490280750

    authors: Jain SK,Chourasia MK,Jain AK,Jain RK,Shrivastava AK

    更新日期:2004-03-01 00:00:00

  • Recent advances in non-ionic surfactant vesicles (niosomes): self-assembly, fabrication, characterization, drug delivery applications and limitations.

    abstract::Non-ionic surfactant vesicles, simply known as niosomes are synthetic vesicles with potential technological applications. Niosomes have the same potential advantages of phospholipid vesicles (liposomes) of being able to accommodate both water soluble and lipid soluble drug molecules control their release and as such s...

    journal_title:Drug delivery

    pub_type: 杂志文章,评审

    doi:10.3109/10717544.2013.838077

    authors: Abdelkader H,Alani AW,Alany RG

    更新日期:2014-03-01 00:00:00

  • The optimized drug delivery systems of treating cancer bone metastatic osteolysis with nanomaterials.

    abstract::Some cancers such as human breast cancer, prostate cancer, and lung cancer easily metastasize to bone, leading to osteolysis and bone destruction accompanied by a complicated microenvironment. Systemic administration of bisphosphonates (BP) or denosumab is the routine therapy for osteolysis but with non-negligible sid...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2020.1856225

    authors: Cheng X,Wei J,Ge Q,Xing D,Zhou X,Qian Y,Jiang G

    更新日期:2021-12-01 00:00:00

  • Anti-tumor effect of local injectable hydrogel-loaded endostatin alone and in combination with radiotherapy for lung cancer.

    abstract::Endostatin (ES) can effectively inhibit neovascularization in most solid tumors and has the potential to make oxygen delivery more efficient and increase the efficacy of radiotherapy (RT). With a short half-life, ES is mainly administered systemically, which leads to low intake in tumor tissue and often toxic systemic...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2020.1869864

    authors: Wang N,Gao Q,Tang J,Jiang Y,Yang L,Shi X,Chen Y,Zhang Y,Fu S,Lin S

    更新日期:2021-12-01 00:00:00

  • Extruded Soluplus/SIM as an oral delivery system: characterization, interactions, in vitro and in vivo evaluations.

    abstract::The aim of this study was to obtain a stable, amorphous solid dispersion (SD) with Soluplus, prepared by hot-melt extrusion (HME) as an effective and stable oral delivery system to improve the physical stability and bioavailability of the poorly water-soluble simvastatin (SIM), a drug with relatively low Tg. The drug ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2014.960982

    authors: Zhang Y,Liu Y,Luo Y,Yao Q,Zhong Y,Tian B,Tang X

    更新日期:2016-07-01 00:00:00

  • Lung cancer combination therapy: co-delivery of paclitaxel and doxorubicin by nanostructured lipid carriers for synergistic effect.

    abstract:CONTEXT:Paclitaxel (PTX) and doxorubicin (DOX) are widely used for the combined chemotherapy of solid tumors. However, free drug combination has lower antitumor efficiency. It is necessary to design a drug delivery system to carry both of them. OBJECTIVE:This study aimed to engineer a nano-drug delivery system for co-...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2015.1055619

    authors: Wang Y,Zhang H,Hao J,Li B,Li M,Xiuwen W

    更新日期:2016-05-01 00:00:00

  • Characterizing monoclonal antibodies to antigenic domains of TCblR/CD320, the receptor for cellular uptake of transcobalamin-bound cobalamin.

    abstract::Monoclonal antibodies (mAbs) were generated to the extracellular domain of transcobalamin receptor (TCblR) and used to identify the regions of the receptor protein involved in antibody binding. Based on the effect of transcobalamin bound cobalamin (TC-Cbl) on antibody binding, this study identified both blocking and b...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2010.509745

    authors: Jiang W,Nakayama Y,Sequeira JM,Quadros EV

    更新日期:2011-01-01 00:00:00

  • Floating microspheres of carvedilol as gastro retentive drug delivery system: 3(2) full factorial design and in vitro evaluation.

    abstract:CONTEXT:Designing a sustained release system for Carvedilol to increase its residence time in the stomach. OBJECTIVE:Preparation of floating microsphere by the emulsion solvent diffusion method, studying the effect of various process parameters and optimize the formulation using full factorial design. METHODS:Differe...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2013.834414

    authors: Nila MV,Sudhir MR,Cinu TA,Aleykutty NA,Jose S

    更新日期:2014-03-01 00:00:00

  • Transdermal delivery of isoniazid and rifampin in guinea pigs by electro-phonophoresis.

    abstract::Electro-phonophoresis (EP) has been used as a drug delivery approach in clinical fields. The objective of the present study is to evaluate the skin permeability of isoniazid and rifampin in guinea pigs by EP to provide reference basis for clinical applications of such transdermal delivery system in the treatment of pa...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2016.1267275

    authors: Chen S,Han Y,Yu D,Huo F,Wang F,Li Y,Dong L,Liu Z,Huang H

    更新日期:2017-11-01 00:00:00

  • Effect of tissue permeability and drug diffusion anisotropy on convection-enhanced delivery.

    abstract::Although convection-enhanced delivery (CED) can successfully facilitate a bypass of the blood brain barrier, its treatment efficacy remains highly limited in clinic. This can be partially attributed to the brain anisotropic characteristics that lead to the difficulties in controlling the drug spatial distribution. Her...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2019.1639844

    authors: Zhan W,Rodriguez Y Baena F,Dini D

    更新日期:2019-12-01 00:00:00

  • Antitumor activities of novel glycyrrhetinic acid-modified curcumin-loaded cationic liposomes in vitro and in H22 tumor-bearing mice.

    abstract::At present, the chemotherapy of advanced inoperable liver cancer is limited with serious side effects. Curcumin possesses multiple cancer preventive activities and low safety concerns. However, its poor solubility and instability in water pose significant pharmacological barriers to its clinical application. In this s...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2018.1526227

    authors: Chang M,Wu M,Li H

    更新日期:2018-11-01 00:00:00

  • Curcumin-loaded lipid nanocarrier for improving bioavailability, stability and cytotoxicity against malignant glioma cells.

    abstract:OBJECTIVE:In the present study, Curcumin (CU)-loaded nanocarrier (NC) such as nanoemulsion (NE) was developed with the objective of increasing its cytotoxicity and bioavailability through lymphatic transport by enhancing its solubility and intestinal permeability. MATERIALS AND METHODS:Based on the area obtained in ps...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2014.909906

    authors: Kumar A,Ahuja A,Ali J,Baboota S

    更新日期:2016-01-01 00:00:00

  • Propolis organogel as a novel topical delivery system for treating wounds.

    abstract:CONTEXT:Propolis has traditionally been used in curing infections and healing wounds and burns. OBJECTIVE:The aim of this study is to formulate pluronic lecithin organogel of propolis to improve its availability and antimicrobial activity. MATERIALS AND METHODS:Different organogels were prepared by using soybean leci...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2013.847032

    authors: Balata G,El Nahas HM,Radwan S

    更新日期:2014-02-01 00:00:00

  • Chemotherapeutic efficacy of nanoparticle encapsulated antitubercular drugs.

    abstract::Our objective was to evaluate the chemotherapeutic potential of oral poly lactide-co-glycolide (PLG, a synthetic polymer) nanoparticle encapsulated ethambutol in combination with PLG-nanoparticle encapsulated-(rifampicin + isoniazid + pyrazinamide) in a murine tuberculosis (TB) model. Our formulation was prepared by t...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540500398076

    authors: Pandey R,Sharma S,Khuller GK

    更新日期:2006-07-01 00:00:00

  • Enhanced skin permeation of 6-methoxy-2-naphthylacetic acid by salt formation.

    abstract::The aim of this work was to prepare salts of 6-methoxy-2-naphthylacetic acid (6-MNA) to improve its physicochemical properties for percutaneous application. 6-MNA, an active metabolite of non-steroidal anti-inflammatory drug nabumetone has long half life and has the tendency to penetrate well into synovial fluid. The ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2014.894595

    authors: Pawar V,Kumar HY,Giridhar R,Yadav MR

    更新日期:2015-05-01 00:00:00

  • N-trimethyl chitosan (TMC)-modified microemulsions for improved oral bioavailability of puerarin: preparation and evaluation.

    abstract::The aim of this research was to increase the oral bioavailability of puerarin by N-trimethyl chitosan-modified microemulsions (TMC-MEs) loaded with puerarin. Different concentrations of TMC-modified microemulsions were prepared in our study, and then evaluated for particle size, zeta potential, morphological observati...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2013.879398

    authors: Liao D,Liu X,Dai W,Tang T,Ou G,Zhang K,Han M,Kang R,Yang S,Xiang D

    更新日期:2015-01-01 00:00:00

  • Carboplatin-Loaded PLGA Microspheres for Intracerebral Implantation: In Vivo Characterization.

    abstract::Carboplatin is a potent anticancer agent that has shown efficacy in clinical trials against malignant glioma, one of the most deadly cancers in humans. However, a high systemic dose is required to achieve an effective concentration in the brain because of the presence of the blood-brain barrier (BBB). Such a high dose...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717549709052017

    authors: Chen W,He J,Olson JJ,Lu DR

    更新日期:1997-01-01 00:00:00

  • Silk fibroin nanoparticles dyeing indocyanine green for imaging-guided photo-thermal therapy of glioblastoma.

    abstract::Silk was easily dyed in traditional textile industry because of its strong affinity to many colorants. Herein, the biocompatible silk fibroin was firstly extracted from Bombyx mori silkworm cocoons. And SF nanoparticles (SFNPs) were prepared for dyeing indocyanine green (ICG) and construct a therapeutic nano-platform ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2018.1428244

    authors: Xu HL,ZhuGe DL,Chen PP,Tong MQ,Lin MT,Jiang X,Zheng YW,Chen B,Li XK,Zhao YZ

    更新日期:2018-11-01 00:00:00

  • In situ evading of phagocytic uptake of stealth solid lipid nanoparticles by mouse peritoneal macrophages.

    abstract::Stealth solid lipid nanoparticles (SSLN) were prepared and evaluated for the effect of evading phagocytic uptake by mouse peritoneal macrophages in situ. Fluorescent SSLNs were prepared by emulsion/evaporation with rhodamine B as the fluorescent marker and polyoxyethylene stearate as stealth agent in a stearic acid ma...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540500315930

    authors: Wang Y,Wu W

    更新日期:2006-05-01 00:00:00

  • Transdermal administration of melatonin coupled to cryopass laser treatment as noninvasive therapy for prostate cancer.

    abstract::Melatonin, a pineal gland hormone, exerts oncostatic activity in several types of human cancer, including prostate, the most common neoplasia and the third most frequent cause of male cancer death in the developed world. The growth of androgen-sensitive LNCaP prostate cancer cells in mice is inhibited by 3 mg/kg/week ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2017.1338793

    authors: Terraneo L,Bianciardi P,Virgili E,Finati E,Samaja M,Paroni R

    更新日期:2017-11-01 00:00:00

  • The effectivity analysis of accumulation of liposomal, micellar, and water-soluble forms of diminazene in cells and in organs.

    abstract::The study was aimed at evaluating the effectiveness of liposomal, micellar, and water-soluble drug forms of diminazene for its localization in cells and selective accumulation at the sites of aggregation of pathogenic organisms. Pharmacological and dynamic properties of a new injection micellar diminazene preparation ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540500459084

    authors: Staroverov SA,Pristensky DV,Yermilov DN,Gabalov KP,Zhemerichkin DA,Sidorkin VA,Shcherbakov AA,Shchyogolev SY,Dykman LA

    更新日期:2006-09-01 00:00:00