Effects of skeleton structure on necrosis targeting and clearance properties of radioiodinated dianthrones.

Abstract:

:Necrosis avid agents (NAAs) can be used for diagnose of necrosis-related diseases, evaluation of therapeutic responses and targeted therapeutics of tumor. In order to probe into the effects of molecular skeleton structure on necrosis targeting and clearance properties of radioiodinated dianthrones, four dianthrone compounds with the same substituents but different skeletal structures, namely Hypericin (Hyp), protohypericin (ProHyp), emodin dianthrone mesomer (ED-1) and emodin dianthrone raceme (ED-2) were synthesized and radioiodinated. Then radioiodinated dianthrones were evaluated in vitro for their necrosis avidity in A549 lung cancer cells untreated and treated with H2O2. Their biodistribution and pharmacokinetic properties were determined in rat models of induced necrosis. In vitro cell assay revealed that destruction of rigid skeleton structure dramatically reduced their necrosis targeting ability. Animal studies demonstrated that destruction of rigid skeleton structure dramatically reduced the necrotic tissue uptake and speed up the clearance from the most normal tissues for the studied compounds. Among these (131)I-dianthrones, (131)I-Hyp exhibited the highest uptake and persistent retention in necrotic tissues. Hepatic infarction could be clearly visualized by SPECT/CT using (131)I-Hyp as an imaging probe. The results suggest that the skeleton structure of Hyp is the lead structure for further structure optimization of this class of NAAs.

journal_name

J Drug Target

authors

Zhang D,Jiang C,Yang S,Gao M,Huang D,Wang X,Shao H,Feng Y,Sun Z,Ni Y,Zhang J,Yin Z

doi

10.3109/1061186X.2015.1113541

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

566-77

issue

6

eissn

1061-186X

issn

1029-2330

journal_volume

24

pub_type

杂志文章
  • Influence of coenzyme Q10 on tissue distribution of archaeosomes, and pegylated archaeosomes, administered to mice by oral and intravenous routes.

    abstract::The biodistribution of orally and intravenously administered archaeosomes in mice was compared to that of archaeosomes containing either coenzyme Q10 (archaeosome-CoQ10), polyethylene glycol (archaeosome-PEG), or PEG plus CoQ10 (archaeosome-PEG-CoQ10). The archaeosome formulations were prepared by a reverse-phase evap...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869909085521

    authors: Omri A,Makabi-Panzu B,Agnew BJ,Sprott GD,Patel GB

    更新日期:2000-01-01 00:00:00

  • Recent advances in metal nanoparticles in cancer therapy.

    abstract::Metal nanoparticles (NPs) may have the potential to overcome problems related to conventional chemotherapy. Metal NPs reported to play a beneficial and powerful role in cancer therapy providing better targeting, gene silencing and drug delivery. Functionalised metal NPs with targeting ligands offer a better control of...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1400553

    authors: Sharma A,Goyal AK,Rath G

    更新日期:2018-09-01 00:00:00

  • Virulence-attenuated Salmonella engineered to secrete immunomodulators reduce tumour growth and increase survival in an autochthonous mouse model of breast cancer.

    abstract::The ultimate goal of bacterial based cancer therapy is to achieve non-toxic penetration and colonisation of the tumour microenvironment. To overcome this efficacy-limiting toxicity of anticancer immunotherapy, we have tested a therapy comprised of systemic delivery of a vascular disrupting agent to induce intratumoral...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2020.1850739

    authors: Augustin LB,Milbauer L,Hastings SE,Leonard AS,Saltzman DA,Schottel JL

    更新日期:2020-12-21 00:00:00

  • Liposomes and niosomes as potential carriers for dermal delivery of minoxidil.

    abstract::The aim of this work was to formulate minoxidil loaded liposome and niosome formulations to improve skin drug delivery. Multilamellar liposomes were prepared using soy phosphatidylcholine at different purity degrees (Phospholipon 90, 90% purity, soy lecithin (SL), 75% purity) and cholesterol (Chol), whereas niosomes w...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600991993

    authors: Mura S,Pirot F,Manconi M,Falson F,Fadda AM

    更新日期:2007-02-01 00:00:00

  • Targeting of doxorubicin to the urinary bladder of the rat shows increased cytotoxicity in the bladder urine combined with an absence of renal toxicity.

    abstract::Targeting of anti-tumor drugs to the urinary bladder for the treatment of bladder carcinoma may be useful, since these agents generally have a low degree of urinary excretion and are highly toxic elsewhere in the body. The anti-tumor drug doxorubicin was coupled to the low-molecular weight protein lysozyme via the aci...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860290007568

    authors: Haas M,Moolenaar F,Elsinga A,Van der Wouden EA,de Jong PE,Meijer DK,de Zeeuw D

    更新日期:2002-02-01 00:00:00

  • Local drug delivery in the urinary tract: current challenges and opportunities.

    abstract::Drug delivery is an important consideration in disease treatment. There are many opportunities for novel methods and technologies to hold promising roles in overcoming traditional obstacles. Delivery systems functionalised to boast synergistic antimicrobial effects, specific targeting, and enhanced bioavailability all...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1419356

    authors: Mittal R,Pan DR,Parrish JM,Huang EH,Yang Y,Patel AP,Malhotra AK,Mittal J,Chhibber S,Harjai K

    更新日期:2018-09-01 00:00:00

  • Targeting of the B-lineage leukemia stem cells and their progeny with norcantharidin encapsulated liposomes modified with a novel CD19 monoclonal antibody 2E8 in vitro.

    abstract::This study was aimed to generate a new agent, norcantharidin (NCTD) encapsulated liposomes modified with a novel murine anti-human CD19 monoclonal antibody 2E8 (2E8–NCTD–liposomes), to specifically target the B-lineage leukemia stem cells (B-LSCs) and their progeny in vitro. Our results have shown that the positive pe...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611861003649720

    authors: Zhang J,Tang Y,Li S,Liao C,Guo X

    更新日期:2010-11-01 00:00:00

  • Characterization of oleanolic acid derivative for colon cancer targeting with positron emission tomography.

    abstract::Oleanolic acid (OA) is a pentacyclic triterpenoid found in various plant species. Triterpenoid compounds have been shown to inhibit tumor proliferation and to induce apoptosis in cancer cells. We synthesized an OA derivative and evaluated its inhibitory effects on cell proliferation in human colon cancer. Radioisotope...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2013.851684

    authors: Kim SM,Jeong IH,Yim MS,Chae MK,Kim HN,Kim DK,Kang CM,Choe YS,Lee C,Ryu EK

    更新日期:2014-10-07 00:00:00

  • siRNA: an alternative treatment for diabetes and associated conditions.

    abstract::Diabetes is a condition that is not completely treatable but life of a diabetic patient can be smoothed by preventing or delaying the associate conditions like diabetic retinopathy, nephropathy, impaired wound healing process, etc. Apart from conventional methods to regulate diabetic condition, new techniques using si...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2018.1476518

    authors: Shende P,Patel C

    更新日期:2019-02-01 00:00:00

  • Brain targeting of nerve growth factor using poly(butyl cyanoacrylate) nanoparticles.

    abstract::The nerve growth factor (NGF) is essential for the survival of both peripheral ganglion cells and central cholinergic neurons in the basal forebrain. The accelerated loss of central cholinergic neurons during Alzheimer's disease may be a determinant cause of dementia, and this observation may suggest a possible therap...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860903112842

    authors: Kurakhmaeva KB,Djindjikhashvili IA,Petrov VE,Balabanyan VU,Voronina TA,Trofimov SS,Kreuter J,Gelperina S,Begley D,Alyautdin RN

    更新日期:2009-09-01 00:00:00

  • EGFR-targeted immunoliposomes derived from the monoclonal antibody EMD72000 mediate specific and efficient drug delivery to a variety of colorectal cancer cells.

    abstract::We hypothesized that immunoliposomes (ILs) constructed using Fab' from the humanized anti-EGFR monoclonal antibody, EMD72000, can provide efficient intracellular drug delivery in EGFR-overexpressing colorectal tumor cells.ILs were constructed modularly with various MAb fragments, including Fab' from EMD72000 (matuzuma...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600691049

    authors: Mamot C,Ritschard R,Küng W,Park JW,Herrmann R,Rochlitz CF

    更新日期:2006-05-01 00:00:00

  • Encapsulation of vancomycin and gentamicin within cationic liposomes for inhibition of growth of Staphylococcus epidermidis.

    abstract::Liposomes have been prepared from dipalmitoylphosphatidylcholine (DPPC), cholesterol (Chol) and dimethyldioctadecylammonium bromide (DDAB). The cationic vesicles adsorb to biofilms of the skin-associated bacteria Staphylococcus epidermidis, which have a negative charge. Encapsulation of the antibacterial drug vancomyc...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869609015975

    authors: Sanderson NM,Jones MN

    更新日期:1996-01-01 00:00:00

  • Receptor mediated targeting of lectin conjugated gliadin nanoparticles in the treatment of Helicobacter pylori.

    abstract::The present work describes the potential for using lectin-conjugated gliadin nanoparticles as a means of locating and anchoring a drug delivery system on the carbohydrate receptors of Helicobacter pylori (H. pylori). Gliadin nanoparticles (GNP) bearing acetohydroxamic acid (AHA) were prepared by a desolvation method. ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860310001647771

    authors: Umamaheshwari RB,Jain NK

    更新日期:2003-08-01 00:00:00

  • Gold nanoparticles potentiates N-acetylcysteine effects on neurochemicals alterations in rats after polymicrobial sepsis.

    abstract::Herein, we report the effect of gold nanoparticles (AuNP) and n-acetylcysteine (NAC) isolated or in association as important anti-inflammatory and antioxidant compounds on brain dysfunction in septic rats. Male Wistar rats after sham operation or caecal ligation and perforation (CLP) were treated with subcutaneously i...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2019.1678168

    authors: Petronilho F,Tenfen L,Della Giustina A,Joaquim L,Novochadlo M,de Oliveira Junior AN,Bagio E,Goldim MPS,de Carli RJ,Bonfante SRSA,Metzker KLL,Muttini S,Dos Santos TM,de Oliveira MP,Engel NA,Rezin GT,Kanis LA,Barichello T

    更新日期:2020-04-01 00:00:00

  • Internalization and subcellular fate of aptamer and peptide dual-functioned nanoparticles.

    abstract:PURPOSE:To evaluate the internalization and subcellular fate of AS1411 aptamer (for glioma targeting) and TGN peptide (for blood-brain barrier targeting)-modified nanoparticles (AsTNPs), which was important for optimizing targeted delivery systems and realizing the potential toxicity to cells. METHODS:Organelles were ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2014.886038

    authors: Gao H,Yang Z,Zhang S,Pang Z,Jiang X

    更新日期:2014-06-01 00:00:00

  • Molecular weight-dependent lymphatic transfer of fluorescein isothiocyanate-labeled dextrans after intrapulmonary administration and effects of various absorption enhancers on the lymphatic transfer of drugs in rats.

    abstract::We have developed a new method to evaluate the transfer of macromolecular drugs to intrapulmonary lymph nodes in rats after intrapulmonary administration. By using this method, we observed that the transfer of fluorescein isothiocyanate dextrans (FDs) to the intrapulmonary lymph nodes was markedly higher than that to ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509015955

    authors: Hanatani K,Takada K,Yoshida N,Nakasuji M,Morishita Y,Yasako K,Fujita T,Yamamoto A,Muranishi S

    更新日期:1995-01-01 00:00:00

  • Anti-tumor and anti-metastatic effects of gelatin-doxorubicin and PEGylated gelatin-doxorubicin nanoparticles in SCC7 bearing mice.

    abstract::The goal of this study was to develop a systemically non-toxic and stable circulation based passive targeting system for efficient anticancer treatment. Gelatin-doxorubicin (GD) and PEGylated gelatin-doxorubicin (PGD) nanoparticles were designed and their feasibilities as an anti-cancer drug were evaluated. The sizes ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600935701

    authors: Lee GY,Park K,Nam JH,Kim SY,Byun Y

    更新日期:2006-12-01 00:00:00

  • Phospholipids-based ultrasonic microbubbles for catechins encapsulation and ultrasound-triggered release.

    abstract:OBJECTIVE:The objective of this work was to examine the application of catechins-containing phospholipids-based ultrasonic microbubbles (PUM) in ultrasound-induced delivery. METHODS:Catechins-containing PUM were prepared by dissolving lyophilized PUM powder in catechins solution. Morphologic characteristics of catechi...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802475696

    authors: Lu CT,Zhao YZ

    更新日期:2008-12-01 00:00:00

  • The alpha-fetoprotein third domain receptor binding fragment: in search of scavenger and associated receptor targets.

    abstract::Recent studies have demonstrated that the carboxyterminal third domain of alpha-fetoprotein (AFP-CD) binds with various ligands and receptors. Reports within the last decade have established that AFP-CD contains a large fragment of amino acids that interact with several different receptor types. Using computer softwar...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2015.1015538

    authors: Mizejewski GJ

    更新日期:2015-01-01 00:00:00

  • Application of titanium dioxide (TiO2) nanoparticles in cancer therapies.

    abstract::Cancer is one of the most common diseases all over the world; many people suffer from diverse types of cancer. However, currently there is no exact cure or therapy developed for cancer. On the other hand, nanoparticles are defined as microscopic particles that have dimensions less than 100 nm and they are known for th...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2018.1527338

    authors: Çeşmeli S,Biray Avci C

    更新日期:2019-08-01 00:00:00

  • Synthesis, characterization and in vitro evaluation of dimethyl-beta-cyclodextrin-4-biphenylylacetic acid conjugate.

    abstract::Biphenylylacetic acid (BPAA) was linked to the free hydroxyl group of 2,6-di-O-methyl-beta-Cyclodextrin (DM-beta-CyD) through an ester linkage to obtain the site specific release of the drug to the colon. The conjugate at 1:1 mole ratio was separated from the reaction mixture by semipreparative reverse-phase HPLC and ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860310001615965

    authors: Ventura CA,Paolino D,Pedotti S,Pistarà V,Corsaro A,Puglisi G

    更新日期:2003-05-01 00:00:00

  • Pieter Cullis: an outstanding lipid biophysicist, drug delivery scientist, educator, and entrepreneur.

    abstract::There are much said about Pieter Cullis in this special volume honoring him. He was the pioneer to study the role of hexagonal HII phase in membrane fusion and the one who applied this concept for the design of lipid nanoparticles. He was also the first to utilize remote loading techniques for the delivery of amphipat...

    journal_title:Journal of drug targeting

    pub_type: 传,历史文章,杂志文章

    doi:10.3109/1061186X.2016.1172590

    authors: Huang L,Miao L

    更新日期:2016-11-01 00:00:00

  • Tweaking dendrimers and dendritic nanoparticles for controlled nano-bio interactions: potential nanocarriers for improved cancer targeting.

    abstract::Nanoparticles have shown great promise in the treatment of cancer, with a demonstrated potential in targeted drug delivery. Among a myriad of nanocarriers that have been recently developed, dendrimers have attracted a great deal of scientific interests due to their unique chemical and structural properties that allow ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2015.1052077

    authors: Bugno J,Hsu HJ,Hong S

    更新日期:2015-01-01 00:00:00

  • Dynamics of microparticles inside lipid vesicles: movement in confined spaces.

    abstract::Microparticles and nanoparticles used in drug delivery frequently depend on their movement in confined spaces such as cells. Liposomes containing small numbers of 1-µm diameter polystyrene particles were used to study the dynamics of their movement within the confined space of the liposome interior. The analysis of th...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2010.526228

    authors: Al-Obaidi H,Nasseri B,Florence AT

    更新日期:2010-12-01 00:00:00

  • The human Nox4: gene, structure, physiological function and pathological significance.

    abstract::Increased generation of reactive oxygen species (ROS) has been implicated in the pathogenesis of a variety of diseases such as cardiovascular diseases and cancer. NADPH oxidase (Nox), a multicomponent enzyme, has been identified as one of the key sources of ROS. Nox4, one of the seven members of Nox family (Nox1, Nox2...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2015.1036276

    authors: Guo S,Chen X

    更新日期:2015-12-01 00:00:00

  • Transfection of HEK cells via DNA-loaded PLGA and P(FASA) nanospheres.

    abstract::HEK cells were transfected with the GFP gene using various vectors: naked DNA, lipofectamine, and both PLGA and P(FASA) plasmid-loaded nanospheres. All methods were assessed alone and with the use of chloroquine, a lysosomal enzyme inhibitor. Transfection efficiencies were determined and compared at various times post...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186021000038373

    authors: Sandor M,Mehta S,Harris J,Thanos C,Weston P,Marshall J,Mathiowitz E

    更新日期:2002-09-01 00:00:00

  • Do model polymer therapeutics sufficiently diffuse through articular cartilage to be a viable therapeutic route?

    abstract::The ability of a polymer therapeutic to access the appropriate subcellular location is crucial to its efficacy and is defined to a large part by the many and complex cellular biological and biochemical barriers such that a construct must traverse. It is shown here that model dextrin conjugates are able to pass through...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1378660

    authors: Powell A,Caterson B,Hughes C,Paul A,James C,Hopkins S,Mansour O,Griffiths P

    更新日期:2017-01-01 00:00:00

  • The influence of a colonic microbiota on HPMA copolymer lectin conjugates binding in rodent intestine.

    abstract::Germ-free (GF) animals lack a colonic microflora like that seen in conventional (CV) animals. Bacterial presence plays a role in the development of glycoproteins in the gastrointestinal (GI) tract; the absence of a microbiota has been seen to suppress the production of certain glycoproteins and glycolipids. Binding pa...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860108997920

    authors: Wróblewski S,Ríhová B,Rossmann P,Hudcovicz T,Reháková Z,Kopecková P,Kopecek J

    更新日期:2001-04-01 00:00:00

  • Polymersomes as an effective drug delivery system for glioma--a review.

    abstract::Glioma is one of the most commonly occurring malignant brain tumours which need proper treatment strategy. The current therapies for treating glioma like surgical resection, radiotherapy, and chemotherapy have failed in achieving satisfactory results and this forms a rationale for the development of novel drug deliver...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2014.916712

    authors: Krishnamoorthy B,Karanam V,Chellan VR,Siram K,Natarajan TS,Gregory M

    更新日期:2014-07-01 00:00:00

  • Oral delivery of pathogens from the intestine to the nervous system.

    abstract::Most therapeutic agents are delivered orally. Consequently, the major classes of therapeutically useful chemicals are partially lipophilic, small molecular weight compounds. They have reasonable permeability coefficient values across cell membranes, including those of intestinal epithelia and vascular endothelia. In c...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/10611860410001693715

    authors: Baird AW,Campion DP,O'Brien L,Brayden DJ

    更新日期:2004-02-01 00:00:00