Enhancing the chemotherapy effect of Apatinib on gastric cancer by co-treating with salidroside to reprogram the tumor hypoxia micro-environment and induce cell apoptosis.

Abstract:

:Hypoxic microenvironment commonly occurred in the solid tumors considerably decreases the chemosensitivity of cancer cells. Salidroside (Sal), the main active ingredient of Rhodiola rosea, was shown to be able of regulating the tumor hypoxia micro-environment and enhancing the chemotherapeutic efficacy of drug-resistant cancer. Therefore, in this study, the Sal was co-loaded with Apatinib (Apa) by the PLGA-based nanoparticles (NPs) to improve the chemosensitivity of gastric cancer cells. Additionally, to improve the drug delivery efficacy, the tumor-homing peptide (iVR1 peptides) was further decorated on the surface of NPs. The tumor targeting ability of the peptides-functionalized nanoparticles (iVR1-NPs-Apa/Sal) was evaluated by in vitro and in vivo experiments. As the obtained results revealed that the iVR1-NPs-Apa/Sal displayed excellent tumor affinity than the unmodified ones (NPs-Apa/Sal), which in turn resulted in more efficient of anti-proliferation of gastric cancer cells and anti-tumor effect in vivo. In addition, compared with the cells or tumor-bearing mice only treaded by monotherapy of Apa, the cells or mice received combinational treatment of Apa and Sal showed obvious lower rate of growth, invasion, and migration or tumor growth and progress. Underlying mechanisms were further investigated and it was revealed that the anti-gastric cancer effect of Apa was signally improved by Sal through down-regulation the proliferation factors and increase the pro-apoptotic genes, as well as reprograming the tumor hypoxia micro-environment. In a word, the study showed that the Sal was able of improving the chemosensitivity of gastric cancer to Apa and the iVR1-NPs-Apa/Sal was capable of realizing highly efficient of tumor-targeting drug delivery.

journal_name

Drug Deliv

journal_title

Drug delivery

authors

Zhang Z,Yang W,Ma F,Ma Q,Zhang B,Zhang Y,Liu Y,Liu H,Hua Y

doi

10.1080/10717544.2020.1754528

subject

Has Abstract

pub_date

2020-12-01 00:00:00

pages

691-702

issue

1

eissn

1071-7544

issn

1521-0464

journal_volume

27

pub_type

杂志文章
  • Chitosan-N-acetyl cysteine conjugates: in vitro evaluation of permeation enhancing and P-glycoprotein inhibiting properties.

    abstract::This study evaluated three chitosan-N-acetyl cysteine (CAC) conjugates of increasing molecular mass as a valuable tool to improve the absorption of drugs by assessing its permeation enhancing effect regarding the active P-gp substrate rhodamine-123 in comparison to the trans- and paracellular marker FD 4 both in rat i...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540802006708

    authors: Schmitz T,Hombach J,Bernkop-Schnürch A

    更新日期:2008-05-01 00:00:00

  • Cleavable PEGylation: a strategy for overcoming the "PEG dilemma" in efficient drug delivery.

    abstract::To prolong the circulation time of drug, PEGylation has been widely used via the enhanced permeability and retention (EPR) effect, thereby providing new hope for better treatment. However, PEGylation also brings the "PEG dilemma", which is difficult for the cellular absorption of drugs and subsequent endosomal escape....

    journal_title:Drug delivery

    pub_type: 杂志文章,评审

    doi:10.1080/10717544.2017.1388451

    authors: Fang Y,Xue J,Gao S,Lu A,Yang D,Jiang H,He Y,Shi K

    更新日期:2017-12-01 00:00:00

  • Assessment of the efficacy of drug transdermal delivery by electro-phonophoresis in treating tuberculous lymphadenitis.

    abstract::Electro-phonophoresis (EP) has been used in various clinical fields. The objective of present study is to evaluate the skin permeability of isoniazid (INH) and rifampicin (RIF) in patients with tuberculous lymphadenitis with the aid of EP to validate the clinical applications of this transdermal delivery system for th...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2015.1124474

    authors: Chen S,Qin M,Han Y,Zhao L,Fu Y,Shang Y,Liu Z,Huang H

    更新日期:2016-06-01 00:00:00

  • PLA/PEG-PPG-PEG/dexamethasone implant prepared by hot-melt extrusion for controlled release of immunosuppressive drug to implantable medical devices, Part 2: in vivo evaluation.

    abstract::Hot-melt extrusion (HME) plays an important role in preparing implants as local drug delivery systems in pharmaceutical fields. Here, a new PLA/PEG-PPG-PEG/Dexamethasone (PLA/F68/Dex) implant prepared by HME has been developed. Importantly, the implant was successfully achieved to control release of immunosuppressive ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2013.801049

    authors: Li D,Guo G,Deng X,Fan R,Guo Q,Fan M,Liang J,Luo F,Qian Z

    更新日期:2013-04-01 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

  • Strategies to deliver microRNAs as potential therapeutics in the treatment of cardiovascular pathology.

    abstract:CONTEXT:MicroRNAs (miRNAs) are important and powerful mediators in a variety of diseases including cardiovascular pathology. Thus, they emerged as interesting new drug targets. However, it is important to develop efficient transfer tools to successfully deliver miRNAs or antisense oligonucleotides (antagomirs) to the t...

    journal_title:Drug delivery

    pub_type: 杂志文章,评审

    doi:10.3109/10717544.2012.738436

    authors: Chistiakov DA,Sobenin IA,Orekhov AN

    更新日期:2012-11-01 00:00:00

  • Immunotherapeutic effect of BCG-polysaccharide nucleic acid powder on Mycobacterium tuberculosis-infected mice using microneedle patches.

    abstract::Polysaccharide nucleic acid fractions of bacillus Calmette-Guérin, termed BCG-PSN, have traditionally been used as immunomodulators in the treatment of dermatitis and allergic diseases. While the sales of injectable BCG-PSN have shown steady growth in recent years, no reports of using BCG-PSN powder or its immunothera...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2017.1391892

    authors: Yan Q,Liu H,Cheng Z,Xue Y,Cheng Z,Dai X,Shan W,Chen F

    更新日期:2017-11-01 00:00:00

  • A novel method to prepare magnetite chitosan microspheres conjugated with methotrexate (MTX) for the controlled release of MTX as a magnetic targeting drug delivery system.

    abstract::The purpose of the present study is to develop a new method to prepare magnetite chitosan microspheres conjugated with methotrexate (MTX) for the controlled release of MTX as a magnetic targeting drug delivery system. MTX was first conjugated to the chitosan chain via a peptide bond and then a suspension cross-linking...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540902989555

    authors: Zhang X,Chen F,Ni J

    更新日期:2009-07-01 00:00:00

  • Alpha-lipoic acid-loaded nanostructured lipid carrier: sustained release and biocompatibility to HaCaT cells in vitro.

    abstract::ALA-loaded nanostructured lipid carrier (ALA-NLC) was designed to improve physicochemical stability and water solubility, and promote sustained release of ALA as well as determine the biocompatibility of ALA-NLC. The ALA-NLC manufactured using hot high-pressure homogenization technique was investigated in terms of siz...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2013.846435

    authors: Wang J,Xia Q

    更新日期:2014-08-01 00:00:00

  • Bisphosphonates: therapeutics potential and recent advances in drug delivery.

    abstract:CONTEXT:Bisphosphonates (BPs) are widely used for prevention and treatment of osteoporosis. BPs are known as gold standard for osteoporosis (OP) treatment due to their positive results in clinical studies. But some serious side effects are associated with BPs like gastrointestinal adverse effect i.e. esophagitis and ul...

    journal_title:Drug delivery

    pub_type: 杂志文章,评审

    doi:10.3109/10717544.2013.870259

    authors: Fazil M,Baboota S,Sahni JK,Ameeduzzafar,Ali J

    更新日期:2015-01-01 00:00:00

  • Liraglutide-loaded multivesicular liposome as a sustained-delivery reduces blood glucose in SD rats with diabetes.

    abstract::Subcutaneous liraglutide-loaded multivesicular liposomes (Lrg-MVLs) were developed as a sustained drug-delivery system for treating diabetes and their properties were characterized. The Lrg-MVLs prepared using a two-step water-in-oil-in-water double emulsification process had a spherical appearance with a mean diamete...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2016.1180723

    authors: Zhang L,Ding L,Tang C,Li Y,Yang L

    更新日期:2016-11-01 00:00:00

  • In vitro characterization of human intact erythrocytes loaded by enalaprilat.

    abstract::In vitro characteristics of the human erythrocytes loaded by enalaprilat have been evaluated. Erythrocytes obtained from a healthy volunteer were loaded by enalaprilat using the hypotonic preswelling method, and the loading parameters, drug-release kinetics, hematological indices, particle size distribution, scanning ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/107175401317245903

    authors: Hamidi M,Tajerzadeh H,Dehpour AR,Rouini MR,Ejtemaee-Mehr S

    更新日期:2001-10-01 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

  • Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer's disease.

    abstract::Alzheimer's disease is a neurodegenerative disorder mainly characterized by β-amyloid deposit and tau hyperphosphorylation with no curative treatments. Curcumin (Cur) has been proved to have potential use in Alzheimer's disease with its anti-amyloid, anti-inflammatory, and anti-oxidant properties, etc. However, its hy...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2018.1461955

    authors: Fan S,Zheng Y,Liu X,Fang W,Chen X,Liao W,Jing X,Lei M,Tao E,Ma Q,Zhang X,Guo R,Liu J

    更新日期:2018-11-01 00:00:00

  • Active pulmonary targeting against tuberculosis (TB) via triple-encapsulation of Q203, bedaquiline and superparamagnetic iron oxides (SPIOs) in nanoparticle aggregates.

    abstract::Tuberculosis (TB) has gained attention over the past few decades by becoming one of the top ten leading causes of death worldwide. This infectious disease of the lungs is orally treated with a medicinal armamentarium. However, this route of administration passes through the body's first-pass metabolism which reduces t...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2019.1676841

    authors: Poh W,Ab Rahman N,Ostrovski Y,Sznitman J,Pethe K,Loo SCJ

    更新日期:2019-12-01 00:00:00

  • Strategies for meloxicam delivery to and across the skin: a review.

    abstract::Although meloxicam (MX) is relatively safer than other NSAIDs, adverse effects relating to the gastro-intestinal tract are still a problem when administrated MX at high doses and on the long-term treatment. Drug delivery via skin provides an attractive alternative to oral administration, but is limited by the first la...

    journal_title:Drug delivery

    pub_type: 杂志文章,评审

    doi:10.3109/10717544.2016.1157839

    authors: Chen J,Gao Y

    更新日期:2016-10-01 00:00:00

  • Optimizing novel penetration enhancing hybridized vesicles for augmenting the in-vivo effect of an anti-glaucoma drug.

    abstract::Usually the topical delivery of ocular drugs poses a great challenge. Accordingly, the work in this study comprised the use of different hybrids of generally regarded as safe (GRAS) oils and surfactants in order to develop and optimize novel acetazolamide (AZD) entrapped-vesicular systems aiming at improving its ocula...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2016.1233588

    authors: Naguib SS,Hathout RM,Mansour S

    更新日期:2017-11-01 00:00:00

  • Solid lipid nanoparticles for ocular drug delivery.

    abstract::Ocular drug delivery remains challenging because of the complex nature and structure of the eye. Conventional systems, such as eye drops and ointments, are inefficient, whereas systemic administration requires high doses resulting in significant toxicity. There is a need to develop novel drug delivery carriers capable...

    journal_title:Drug delivery

    pub_type: 杂志文章,评审

    doi:10.3109/10717544.2010.483257

    authors: Seyfoddin A,Shaw J,Al-Kassas R

    更新日期:2010-09-01 00:00:00

  • 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 invest...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2018.1436097

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

    更新日期:2018-11-01 00:00:00

  • Passive targeting and lung tolerability of enoxaparin microspheres for a sustained antithrombotic activity in rats.

    abstract::Pulmonary bed can retain microparticles (MP) larger than their capillaries' diameter, hence we offer a promising way for lung passive targeting following intravenous (IV) administration. In this study, enoxaparin (Enox)-albumin microspheres (Enox-Alb MS) were, optimally, developed as lung targeted sustained release MP...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717544.2016.1245368

    authors: Ibrahim SS,Osman R,Mortada ND,Geneidy AS,Awad GA

    更新日期:2017-11-01 00:00:00

  • New method for ophthalmic delivery of azithromycin by poloxamer/carbopol-based in situ gelling system.

    abstract::This study focused on preparation and evaluation of a thermosensitive and mucoadhesive in situ gelling ophthalmic system of azithromycin (ATM). Poloxamer 407 (P407) and poloxamer 188 (P188) were used as gelling agents. Addition of Carbopol 974P (CP 974P) to the gelling systems could increase the solubility of ATM by s...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2010.483255

    authors: Cao F,Zhang X,Ping Q

    更新日期:2010-09-01 00:00:00

  • Assessment of simvastatin niosomes for pediatric transdermal drug delivery.

    abstract::The prevalence of childhood dyslipidemia increases and is considered as an important risk factor for the incidence of cardiovascular disease in the adulthood. To improve dosing accuracy and facilitate the determination of dosing regimens in function of the body weight, the proposed study aims at preparing transdermal ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2014.980896

    authors: Zidan AS,Hosny KM,Ahmed OA,Fahmy UA

    更新日期:2016-06-01 00:00:00

  • Formulation and evaluation of dextromethorphan hydrobromide sustained release tablets.

    abstract::Sustained release (SR) matrix tablets of dextromethorphan hydrobromide were prepared by wet granulation using hydroxypropyl methyl cellulose (HPMC-K-100 CR) as the hydrophilic rate controlling polymer. The effect of the concentration of the polymer and different fillers on the in vitro drug release rate was studied. T...

    journal_title:Drug delivery

    pub_type: 杂志文章,随机对照试验

    doi:10.1080/10717540802035301

    authors: Meyyanathan SN,Rajan S,Muralidaharan S,Siddaiah MK,Krishnaraj K,Suresh B

    更新日期:2008-09-01 00:00:00

  • Effects of bile salts on the lovastatin pharmacokinetics following oral administration to rats.

    abstract::This study aimed to examine the effects of bile salts on pharmacokinetics of lovastatin, which has low bioavailability. Lovastatin solid dispersions were prepared using sodium deoxycholate (NaDC) and sodium glycholate (NaGC) at ratios of 1:19, 1:49, and 1:69. The formulated solid dispersions and control (commercial ta...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2010.512024

    authors: Kim K,Yoon I,Chun I,Lee N,Kim T,Gwak HS

    更新日期:2011-01-01 00:00:00

  • Development of lipid nanoparticles for a histone deacetylases inhibitor as a promising anticancer therapeutic.

    abstract:BACKGROUND:Vorinostat (VRS), a histone deacetylases inhibitor, has significant cytotoxic potential in a large number of human cancer cell lines. OBJECTIVE:To clarify its promising anticancer potential and to improve its drawback related to physical properties and in vivo performance of VRS. METHODS:VRS was successful...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2014.991432

    authors: Tran TH,Chu DT,Truong DH,Tak JW,Jeong JH,Hoang VL,Yong CS,Kim JO

    更新日期:2016-05-01 00:00:00

  • Synthesis, characterization and evaluation of tinidazole-loaded mPEG-PDLLA (10/90) in situ gel forming system for periodontitis treatment.

    abstract::Traditional in situ gel forming systems are potential applications for parenteral administration but always accompanied with burst release. To overcome this limitation, the tinidazole (TNZ)-loaded in situ gel forming system using a diblock copolymer, monomethoxy poly(ethylene glycol)-block-poly(d,l-lactide) (mPEG-PDLL...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.3109/10717544.2015.1061069

    authors: Tian Y,Shen Y,Jv M

    更新日期:2016-10-01 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

  • Sustained ocular drug delivery from a temperature and pH triggered novel in situ gel system.

    abstract::Various ocular diseases like glaucoma, conjunctivitis, and dry eye syndrome require frequent drug administration. Poor ocular bioavailability of drugs (< 1%) from conventional eye drops is due mainly to the precorneal loss factors that include rapid tear turnover, nonproductive absorption, transient residence time in ...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540701606426

    authors: Gupta H,Jain S,Mathur R,Mishra P,Mishra AK,Velpandian T

    更新日期:2007-11-01 00:00:00

  • Drug delivery devices based on mesoporous silicate.

    abstract::A mesoporous material based on aluminosilicate mixture was studied to investigate its ability to include drugs and then release them. Nonsteroidal anti-inflammatory agents such as diflunisal, naproxen, ibuprofen and its sodium salt have been used in this study. The preparation of the mesoporous material and its charac...

    journal_title:Drug delivery

    pub_type: 杂志文章

    doi:10.1080/10717540490265252

    authors: Cavallaro G,Pierro P,Palumbo FS,Testa F,Pasqua L,Aiello R

    更新日期:2004-01-01 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