scholarly journals Preparation of anti-HER-2 antibody PLGA polymer nano- ultrasound contrast agent In vitro targeting experiment

2019 ◽  
Author(s):  
Ji Lin ◽  
Molly Stevens ◽  
John Smith
Keyword(s):  
Breast Cancer ◽  
Particle Size ◽  
Electron Microscope ◽  
Contrast Agent ◽  
Cancer Cells ◽  
Breast Cancer Cells ◽  
Ultrasound Contrast Agent ◽  
Ultrasound Contrast ◽  
Her 2

AbstractIn this report, we demonstrated a novel method to prepare a hollow nano-targeted ultrasound contrast agent carrying anti-HER-2 antibody with high molecular weight polylactic acid-glycolic acid (PLGA) as a film-forming material, and to investigate in vitro targeting and imaging effects. We utilized the camphor as porogen, PLGA nano-ultrasound contrast agent was prepared by modified double emulsion solvent evaporation method. The general characteristics were characterized by scanning electron microscope, transmission electron microscope and laser particle size analyzer. The angiography was performed by carbodiimide method. The anti-HER-2 antibody was used to prepare the PLGA-targeted nano-ultrasound contrast agent with anti-HER-2 antibody. The in-situ imaging ability was evaluated by laser confocal scanning microscopy. Results indicate that the average particle size of PLGA nano-ultrasound contrast agent was (152.00± 58.08) nm. The particles were regular spherical, uniform in size and good in dispersion. In vitro targeting experiments showed that PLGA-targeted contrast agents with anti-HER-2 antibodies were more strongly aggregated on the surface of breast cancer cells. In vitro imaging experiments showed that the PLGA-targeted nano-ultrasound contrast imaging showed a fine and uniform point-like hyperechoic echo, and no significant attenuation of the posterior echo. This study successfully produced a PLGA-targeted nano-ultrasound contrast agent with anti-HER-2 antibody, which can specifically bind to breast cancer cells with high expression of HER-2 receptor in vitro, and the imaging effect in vitro is better.

Preparation of Microbubble Contrast Material of Sulfhydryl-Maleimide Group and Its Application in Ultrasound Diagnosis of Breast Cancer

2020 ◽  
Vol 12 (9) ◽  
pp. 1361-1370
Author(s):  
Juan Liu ◽  
Wenbin Zhu ◽  
Hongyan Chen ◽  
Ying Lin ◽  
Xueqin Li
Keyword(s):  
Breast Cancer ◽  
Particle Size ◽  
Contrast Agent ◽  
Cancer Cells ◽  
Breast Cancer Cells ◽  
Ultrasound Diagnosis ◽  
Average Particle ◽  
Microbubble Contrast Agent ◽  
Maleimide Group

In this study, an ultrasound microbubble contrast agent with integrin αvβ3 as the target was prepared. It was used for the target-finding diagnosis of breast cancer cells. The sulfhydryl group of iRGD peptide and the maleimide group of DSPE-PEG2000 Maleimides were connected by a thin-film hydration method to obtain a new type of ultrasound microbubble contrast agent (iRGD-DSM). First, a particle size analyzer and an optical microscope were used to characterize the iRGD-DSM. Then, the mouse breast cancer cell 4T1 was used for breast cancer ultrasound diagnosis by in vitro culture, and the binding of the contrast agent to the cells was analyzed. Also, quantitative analysis was performed by flow cytometry. The test results showed that an iRGD peptide, iRGD/DSPE-P2000, was obtained based on the chemical coupling of sulfhydryl-maleimide groups. In terms of average particle size, microbubble distribution, and concentration, the iRGD-DSM contrast agent prepared in this study was similar to conventional microbubble contrast agents. Also, when the DSPC, DSPEPEG, iRGD/DSPE-P2000 molar ratio is 36:3:1, higher peptide content can be obtained. Dynamic/static specific targeting of vascular endothelial cells (bEND.3) adhesion test confirmed that iRGD-DSM contrast agent can be firmly combined with bEND.3. In the target-finding test of breast cancer cells 4T1, the ultrasound microbubble contrast agent proposed based on this study had obvious binding imaging with breast cancer cells 4T1. In numerical analysis, the binding rate of the contrast agent to 4T1 cells reached (95.75 ± 1.43)%. Therefore, it was confirmed that the ultrasound microbubble contrast agent iRGD-DSM with integrin αvβ3 as a target has certain in vitro targeting ability for breast cancer diagnosis.

Novel Difolate Targeting Nano-Level Ultrasound Contrast Agent for Therapy of Breast Cancer Tumor Cells

2021 ◽  
Vol 13 (7) ◽  
pp. 1295-1303
Author(s):  
Guangheng Liu ◽  
Xiangfeng Yang ◽  
Qiming Niu ◽  
Wenkui Sun
Keyword(s):  
Breast Cancer ◽  
Contrast Agent ◽  
Tumor Cells ◽  
Folate Receptor ◽  
Ultrasound Contrast Agent ◽  
Hydroxyl Group ◽  
Binding Ability ◽  
Ultrasound Contrast ◽  
Mcf 7

ABSTRACTA new type of difolate targeting nano-level ultrasound contrast agent ((folate molecule, FOL)2-TUAs) was prepared, so as to investigate its targeted binding effect with human breast cancer mammary carcinoma cells (MCF-7) in vitro. L-2-aminoadipic acid (L-2-AD) as a branch unit was inserted at the hydroxyl end of distearoyl phosphatidylethanolamine (DISP)-PEG2000-COOH to construct a tree structure. At this time, the free hydroxyl group in the distearoyl phosphatidylethanolamine (DISP)-PEG2000-COOH structure modified the FOL with the help of N-Hydroxysuccinimide/N,N'-dicyclohexylcarbodiimide (NHS/DCC). Each 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] (DISP-PEG2000) connected two FOLs to generate difolate targeted nanomaterials. Nano laser particle size (PS) and Zeta potential analyzer (ZPA) were applied to analyze the physical characteristics of the material such as PS and dispersion, and the enhanced development effect in vitro was detected by the ultrasonic diagnostic instrument. Besides, the targeted binding ability of the contrast agent based on this material to folate receptor (FR) overexpressing MCF-7 cells was analyzed by flow cytometry (FCM) and fluorescence microscope. In the experiment, hydrogen-1 nuclear magnetic resonance (1H NMR) demonstrated that (FOL)2-TUAs was successfully synthesized. The surface of this material was round and uniformly distributed without aggregation. According to the relative number of FOL molecules, non-targeted nano-agent (U-TUA), monofolate targeted nano-agent (FOL-TUA), and difolate targeted nano-agent ((FOL)2-TUA) were obtained. The in vitro imaging showed that different materials exhibited enhanced imaging effects in ultrasonic diagnostic equipment. FCM and fluorescence microscopy both indicated that the difolate TUA could achieve a good binding to MCF-7 cells. Most of the nano-agents were attached to the cell membrane, surrounded by red fluorophore, namely increasing the FOL content of DISP-PEG2000 chain could enhance the targeted binding ability of tumor cells.

Preparation and In Vitro Evaluation of a Nano Ultrasound Contrast Agent Targeting Pancreatic Cancer

2021 ◽  
Vol 21 (3) ◽  
pp. 1413-1418
Author(s):  
Wu Chen ◽  
Xiaofang Liu ◽  
Yiying Li ◽  
Yongsheng Yang ◽  
Kun Xu ◽  
...  
Keyword(s):  
Pancreatic Cancer ◽  
Particle Size ◽  
Contrast Agent ◽  
Drug Loading ◽  
Ultrasound Contrast Agent ◽  
Ultrasound Contrast ◽  
Loading Efficiency ◽  
Targeted Ultrasound ◽  
Drug Loading Efficiency

To prepare a nano-sized ultrasound contrast agent that specifically targets pancreatic cancer cells and to evaluate its targeting effect In Vitro. PLGA-PEG-NHS was synthesized using PLGA, NHS, and PEG and detected using 1H-NMR. PLGA-PEG-NHS and PFOB were used to prepare PLGA nano contrast agent coated with PFOB by emulsification and volatilization, and then a hedgehog antibody was conjugated. The morphology of the nano contrast agent was observed using a transmission electron microscope, and its particle size and potential were measured using the dynamic light scattering method. The entrapment and drug loading efficiency of the nano contrast agent was measured using gas chromatography-mass spectrometry. The In Vitro release characteristics of the nano contrast agent was measured using the dialysis method. Human pancreatic cancer cell lines SW1990 and CFPAC1 were cultured in medium containing the nano contrast agent. The targeting ability of the nano contrast agent was qualitatively and quantitatively verified using fluorescence microscopy and flow cytometry. The average particle size of the targeted ultrasound contrast agent was 198.9 nm, zeta potential was −31.8 mv, entrapment rate was 63.7±3.9%, drug loading efficiency was 14.3±0.9%, and drug release was 85.3% in 48 h. In Vitro cell experiments showed that the targeted ultrasound contrast agent strongly bound to SW1990 cells with high expression of hedgehog antigen, but no specific binding was detected in CFPAC-1 cells which lack the hedgehog antigen. The nano ultrasound contrast agent prepared by emulsification and volatilization method can be potentially used for the diagnosis of pancreatic cancer.

N-hexane Extract and Fraction of Green Tea as Antiproliferation of MCM-B2 Breast Cancer Cells In Vitro

2020 ◽  
Vol 6 (2) ◽  
Author(s):  
Lisni Noraida Waruwu ◽  
Maria Bintang ◽  
Bambang Pontjo Priosoeryanto
Keyword(s):  
Breast Cancer ◽  
Cancer Cells ◽  
Green Tea ◽  
Cancer Cell ◽  
Breast Cancer Cells ◽  
Green Tea Extract ◽  
Hexane Fraction ◽  
Phytochemical Screening ◽  
Tea Extract

Green tea (Camellia sinensis) is one of traditional plants that have the potential as an anticancer. The sample used in this research commercial green tea extract. The purpose of this study was to test the antiproliferation activity of green tea extract on breast cancer cell MCM-B2 in vitro. Green tea extract fractionated using three solvents, ie water, ethanol 70%, and n-hexane. Extract and fraction of green tea water have value Lethality Concentration 50 (LC50) more than 1000 ppm. The fraction of ethanol 70% and n-hexane had an LC50 value of 883.48 ppm and 600.56 ppm, respectively. The results of the phytochemical screening of green tea extract are flavonoids, tannins, and saponins, while the phytochemical screening results of n-hexane fraction are flavonoids and tannins. Antiproliferation activity was tested on breast cancer cells MCM-B2 and normal cells Vero by trypan blue staining method. The highest MCM-B2 cell inhibitory activity was achieved at a concentration of 13000 ppm green tea extract and 1000 ppm of n-hexane fraction, 59% and 59%, respectively. The extract and n-hexane fraction of green tea are not toxic to normal Vero cells characterized by not inhibiting normal cell proliferation. Keywords: antiproliferative, cancer cell MCM-B2, commercial green tea, cytotoxicity

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